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Number of items at this level: 771.

2024

Sage, Sophie E.; Leeb, Tosso; Jagannathan, Vidhya; Gerber, Vinzenz (2024). Single-cell profiling of bronchoalveolar cells reveals a Th17 signature in neutrophilic severe equine asthma. Immunology, 171(4), pp. 549-565. Wiley-Blackwell 10.1111/imm.13745

McFarland, Elizah D; Elsohaby, Ibrahim; Baes, Christine F; Stryhn, Henrik; Keefe, Gregory; McClure, J T (2024). Impacts of preweaning colostrum feeding practices and health measures on dairy cow production, while accounting for genetic potential. (In Press). Journal of animal science Oxford University Press 10.1093/jas/skae061

Houlahan, K; Schenkel, F S; Miglior, F; Jamrozik, J; Stephansen, R B; González-Recio, O; Charfeddine, N; Segelke, D; Butty, A M; Stratz, P; VandeHaar, M J; Tempelman, R J; Weigel, K; White, H; Peñagaricano, F; Koltes, J E; Santos, J E P; Baldwin, R L; Baes, C F (2024). Estimation of genetic parameters for feed efficiency traits using random regression models in dairy cattle. Journal of dairy science, 107(3), pp. 1523-1534. Elsevier 10.3168/jds.2022-23124

van Staaveren, Nienke; Oliveira, Hinayah R; Houlahan, Kerry; Chud, Tatiane C S; Oliveira, Gerson A; Hailemariam, Dagnachew; Kistemaker, Gerrit; Miglior, Filippo; Plastow, Graham; Schenkel, Flavio S; Cerri, Ronaldo; Sirard, Marc-André; Stothard, Paul; Pryce, Jennie; Butty, Adrien; Stratz, Patrick; Abdalla, Emhimad A E; Segelke, Dierck; Stamer, Eckhard; Thaller, Georg; ... (2024). The Resilient Dairy Genome Project - a general overview of methods and objectives related to feed efficiency and methane emissions. Journal of dairy science, 107(3), pp. 1510-1522. Elsevier 10.3168/jds.2022-22951

Makanjuola, Bayode O; Gebhardt-Henrich, Sabine G; Toscano, Michael J; Baes, Christine F (2024). Genetic parameter estimates for the use of an aviary with winter garden by laying hens. Poultry science, 103(3), p. 103369. Elsevier 10.1016/j.psj.2023.103369

Christen, Matthias; Oevermann, Anna; Rupp, Stefan; Vaz, Frédéric M; Wever, Eric J M; Braus, Barbara K; Jagannathan, Vidhya; Kehl, Alexandra; Hytönen, Marjo K; Lohi, Hannes; Leeb, Tosso (2024). PCYT2 deficiency in Saarlooswolfdogs with progressive retinal, central, and peripheral neurodegeneration. Molecular genetics and metabolism, 141(3), p. 108149. Elsevier 10.1016/j.ymgme.2024.108149

Christen, Matthias; Gregor, Anne; Gutierrez-Quintana, Rodrigo; Bongers, Jos; Rupp, Angie; Penderis, Jacques; Shelton, G Diane; Jagannathan, Vidhya; Zweier, Christiane; Leeb, Tosso (2024). NDUFS7 variant in dogs with Leigh syndrome and its functional validation in a Drosophila melanogaster model. Scientific Reports, 14(2975) Nature Publishing Group 10.1038/s41598-024-53314-7

Lopes, L S F; Schenkel, F S; Houlahan, K; Rochus, C M; Oliveira, G A; Oliveira, H R; Miglior, F; Alcantara, L M; Tulpan, D; Baes, C F (2024). Estimates of genetic parameters for rumination time, feed efficiency, and methane production traits in first lactation Holstein cows. (In Press). Journal of dairy science American Dairy Science Association 10.3168/jds.2023-23751

Lynch, C; Schenkel, F S; van Staaveren, N; Miglior, F; Kelton, D; Baes, C F (2024). Investigating the potential for genetic selection of dairy calf disease traits using management data. Journal of dairy science, 107(2), pp. 1022-1034. Elsevier 10.3168/jds.2023-23780

Rudd Garces, Gabriela; Letko, Anna; Häfliger, Irene M; Müller, Jana; Herden, Christiane; Nesseler, Anne; Wagner, Henrik; Schmidt, Martin J; Drögemüller, Cord; Lühken, Gesine (2024). MFSD2A frameshift variant in Kerry Hill sheep with microcephaly. Animal genetics, 55(1), pp. 152-157. Wiley 10.1111/age.13374

Tan, K; Adeniyi, O O; Letko, A; RuddGarces, G; Manz, E; Wagner, H; Zanolari, P; Drögemüller, C; Lühken, G (2024). Identification of genomic regions associated with differences in fleece type in Huacaya and Suri alpacas (Vicugna pacos). Animal genetics, 55(1), pp. 163-167. Wiley 10.1111/age.13377

Jacinto, J G P; Häfliger, I M; Letko, A; Weber, J; Freick, M; Gentile, A; Drögemüller, C; Agerholm, J S (2024). Multiple independent de novo mutations are associated with the development of schistosoma reflexum, a lethal syndrome in cattle. (In Press). The veterinary journal, 304, p. 106069. Elsevier 10.1016/j.tvjl.2024.106069

Rawson, Faye; Christen, Matthias; Rose, Jeremy; Paran, Emilie; Leeb, Tosso; Fadda, Angela (2024). Polioencephalopathy in Eurasier dogs. Journal of veterinary internal medicine, 38(1), pp. 277-284. Wiley 10.1111/jvim.16945

Milia, Sotiria; Leonard, Alexander S.; Mapel, Xena Marie; Bernal Ulloa, Sandra Milena; Drögemüller, Cord; Pausch, Hubert (2024). Taurine pangenome uncovers a segmental duplication upstream of KIT associated with depigmentation in white-headed cattle (bioRxiv). Cold Spring Harbor Laboratory 10.1101/2024.02.02.578587

2023

Signer-Hasler, Heidi; Rohn, Stefanie; Bangerter, Erika; Drögemüller, Cord (1 December 2023). Variantes de protéines dans le lait de chèvre: une mise à jour. Forum Kleinwiederkäuer, 2023(12), pp. 11-17. Verlagsgenossenschaft Caprovis

Widmer, Sarah; Seefried, Franz R; Häfliger, Irene M; Signer-Hasler, Heidi; Flury, Christine; Drögemüller, Cord (2023). WNT10B: A locus increasing risk of brachygnathia inferior in Brown Swiss cattle. Journal of dairy science, 106(12), pp. 8969-8978. Elsevier 10.3168/jds.2023-23315

Frizzarin, M; Miglior, F; Berry, D P; Gormley, I C; Baes, Christine F (2023). Usefulness of mid-infrared spectroscopy as a tool to estimate body condition score change from milk samples in intensively-fed dairy cows. Journal of dairy science, 106(12), pp. 9115-9124. Elsevier 10.3168/jds.2023-23290

Stephansen, R B; Martin, P; Manzanilla-Pech, C I V; Gredler-Grandl, B; Sahana, G; Madsen, P; Weigel, K; Tempelman, R J; Peñagaricano, F; Gaddis, K L Parker; White, H M; Santos, J E P; Koltes, J E; Schenkel, F; Hailemariam, D; Plastow, G; Abdalla, E; VandeHaar, M; Veerkamp, R F; Baes, C; ... (2023). Novel genetic parameters for genetic residual feed intake in dairy cattle using time series data from multiple parities and countries in North America and Europe. Journal of dairy science, 106(12), pp. 9078-9094. Elsevier 10.3168/jds.2023-23330

Meadows, Jennifer R S; Kidd, Jefrey M; Wang, Guo-Dong; Parker, Heidi G; Schall, Peter Z; Bianchi, Matteo; Christmas, Matthew J; Bougiouri, Katia; Buckley, Reuben M; Hitte, Christophe; Nguyen, Anthony K; Wang, Chao; Jagannathan, Vidhya; Niskanen, Julia E; Frantz, Laurent A F; Arumilli, Meharji; Hundi, Sruthi; Lindblad-Toh, Kerstin; Ginja, Catarina; Agustina, Kadek Karang; ... (2023). Author Correction: Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture. Genome biology, 24(1), p. 255. BioMed Central Ltd. 10.1186/s13059-023-03101-w

Bannasch, Danika L; Oertle, Danielle T; Vo, Julia; Batcher, Kevin L; Stern, Joshua A; Kaplan, Joanna L; Li, Ronald H L; Madden, Indiana E; Christen, Matthias; Leeb, Tosso; Joshi, Nikhil (2023). Naturally occurring canine laminopathy leading to a dilated and fibrosing cardiomyopathy in the Nova Scotia Duck Tolling Retriever. Scientific Reports, 13(1), p. 19077. Nature Publishing Group 10.1038/s41598-023-46601-2

Di Lazzaro Filho, Ricardo; Yamamoto, Guilherme Lopes; Silva, Tiago J; Rocha, Leticia A; Linnenkamp, Bianca D W; Castro, Matheus Augusto Araújo; Bartholdi, Deborah; Schaller, André; Leeb, Tosso; Kelmann, Samantha; Utagawa, Claudia Y; Steiner, Carlos E; Steinmetz, Leandra; Honjo, Rachel Sayuri; Kim, Chong Ae; Wang, Lisa; Abourjaili-Bilodeau, Raphaël; Campeau, Philippe; Warman, Matthew; Passos-Bueno, Maria Rita; ... (2023). Biallelic variants in DNA2 cause poikiloderma with congenital cataracts and severe growth failure reminiscent of Rothmund-Thomson syndrome. Journal of medical genetics, 60(11), pp. 1127-1132. BMJ Publishing Group 10.1136/jmg-2022-109119

Schäfer, J; May, A; Wittenberg, J; Hahn, K; Graubner, C; Gerber, V; Drögemüller, C; Unger, Lucia (2023). [DDB2-associated incidence of squamous cell carcinoma in Haflingers: risk minimization by genotyping]. Schweizer Archiv für Tierheilkunde, 165(11), pp. 707-715. Gesellschaft Schweizer Tierärztinnen und Tierärzte 10.17236/sat00409

Sage, Sophie E.; Leeb, Tosso; Jagannathan, Vidhya; Gerber, Vinzenz (28 October 2023). Single-cell transcriptome profiling of bronchoalveolar cells identifies a Th17 signature in severe equine asthma (Unpublished). In: The Annual ECEIM congress 2023. Lyon (F). 28.10.2023.

Leeb, Tosso (2023). (Editorial) Special Issue: "Canine Genetics 2". Genes, 14(10) MDPI, Molecular Diversity Preservation International 10.3390/genes14101930

Lindtke, Dorothea; Seefried, Franz R; Drögemüller, Cord; Neuditschko, Markus (2023). Increased heterozygosity in low-pass sequencing data allows identification of blood chimeras in cattle. Animal genetics, 54(5), pp. 613-618. Wiley 10.1111/age.13334

Littlejohn, Mathew D; Sneddon, Nick; Dittmer, Keren; Keehan, Mike; Stephen, Melissa; Drögemüller, Michaela; Garrick, Dorian (2023). A frameshift-deletion mutation in Reelin causes cerebellar hypoplasia in White Swiss Shepherd dogs. Animal genetics, 54(5), pp. 632-636. Wiley 10.1111/age.13336

Kiener, Sarah; Åhman, Susanne; Jagannathan, Vidhya; Soto, Sara; Leeb, Tosso (2023). Heterozygous KRT10 missense variant in a Chihuahua with severe epidermolytic ichthyosis. Animal genetics, 54(5), pp. 652-654. Wiley 10.1111/age.13341

Rockett, Paige L; Campos, I L; Baes, C F; Tulpan, D; Miglior, F; Schenkel, F S (2023). Genetic evaluation of heat tolerance in Holsteins using test-day production records and NASA POWER weather data. Journal of dairy science, 106(10), pp. 6995-7007. Elsevier 10.3168/jds.2022-22776

P Jacinto, Joana G; Bolcato, Marilena; Häfliger, Irene M; Oevermann, Anna; Gentile, Arcangelo; Drögemüller, Cord (2023). DYRK1B haploinsufficiency in a Holstein cattle with epilepsy. Animal genetics, 54(5), pp. 623-627. Wiley 10.1111/age.13348

Schäfer, J.; Graubner, C.; Gerber, V.; Drögemüller, C.; Underberg, J.; Gurtner, Corinne; Unger, Lucia (2023). [Ocular and non-ocular squamous cell carcinomas in the Haflinger: Eight cases at the Institut Suisse de Médecine Equine (2015-2022)]. Schweizer Archiv für Tierheilkunde, 165(10), pp. 644-655. Gesellschaft Schweizer Tierärztinnen und Tierärzte 10.17236/sat00406

Kiener, Sarah; Troyer, Heather; Ruvolo, Daniel; Grest, Paula; Soto, Sara; Letko, Anna; Jagannathan, Vidhya; Leeb, Tosso; Mauldin, Elizabeth A; Yang, Ching; Rostaher, Ana (2023). Independent COL17A1 Variants in Cats with Junctional Epidermolysis Bullosa. Genes, 14(10) MDPI, Molecular Diversity Preservation International 10.3390/genes14101835

Niskanen, Julia E; Ohlsson, Åsa; Ljungvall, Ingrid; Drögemüller, Michaela; Ernst, Robert F; Dooijes, Dennis; van Deutekom, Hanneke W M; van Tintelen, J Peter; Snijders Blok, Christian J B; van Vugt, Marion; van Setten, Jessica; Asselbergs, Folkert W; Petrič, Aleksandra Domanjko; Salonen, Milla; Hundi, Sruthi; Hörtenhuber, Matthias; Kere, Juha; Pyle, W Glen; Donner, Jonas; Postma, Alex V; ... (2023). Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human. Genome medicine, 15(1), p. 73. BioMed Central 10.1186/s13073-023-01221-3

Jacinto, Joana G. P.; Wohlsein, Peter; Häfliger, Irene M.; Karl, Michael; Pohlers, Michael; Plobner, Lutz; Grünberg, Walter; Drögemüller, Cord (2023). A missense variant in DGKG as a recessive functional variant for hepatic fibrinogen storage disease in Wagyu cattle. Journal of veterinary internal medicine, 37(6), pp. 2631-2637. Wiley 10.1111/jvim.16865

Jacinto, Joana G. P.; Küchler, Leonore Bettina; Peters, Laureen M; Van der Vekens, Elke; Gurtner, Corinne; Seefried, Franz R; Meylan, Mireille; Drögemüller, Cord (2023). MOCOS-associated renal syndrome in a Brown Swiss cattle. Journal of veterinary internal medicine, 37(6), pp. 2603-2609. Wiley 10.1111/jvim.16856

Letko, Anna; Brülisauer, Franz; Häfliger, Irene M; Corr, Eilidh; Scholes, Sandra; Drögemüller, Cord (2023). Loss-of-function variant in the ovine TMCO6 gene in north country Cheviot sheep with motor neuron disease. Genomics, 115(5), p. 110689. Elsevier 10.1016/j.ygeno.2023.110689

Simon, Rebecca; Kiener, Sarah; Thom, Nina; Schäfer, Laura; Müller, Janina; Schlohsarczyk, Elfi K; Gärtner, Ulrich; Herden, Christiane; Leeb, Tosso; Lühken, Gesine (2023). Identification of an ADAMTS2 frameshift variant in a cat family with Ehlers-Danlos syndrome. G3 Genes Genomes Genetics, 13(9) Genetics Society of America 10.1093/g3journal/jkad152

Brunetti, Barbara; Bacci, Barbara; Abbate, Jessica Maria; Tura, Giorgia; Paciello, Orlando; Vaccaro, Emanuela; Prisco, Francesco; Gandini, Gualtiero; Okonji, Samuel; Paola, Andrea di; Letko, Anna; Drögemüller, Cord; Jagannathan, Vidhya; Turba, Maria Elena; Ogundipe, Tolulope Grace; Lorenzini, Luca; Rosati, Marco; Psalla, Dimitra; Leeb, Tosso and Drögemüller, Michaela (2023). SGCD Missense Variant in a Lagotto Romagnolo Dog with Autosomal Recessively Inherited Limb-Girdle Muscular Dystrophy. Genes, 14(8) MDPI, Molecular Diversity Preservation International 10.3390/genes14081641

Meadows, Jennifer R S; Kidd, Jeffrey M; Wang, Guo-Dong; Parker, Heidi G; Schall, Peter Z; Bianchi, Matteo; Christmas, Matthew J; Bougiouri, Katia; Buckley, Reuben M; Hitte, Christophe; Nguyen, Anthony K; Wang, Chao; Jagannathan, Vidhya; Niskanen, Julia E; Frantz, Laurent A F; Arumilli, Meharji; Hundi, Sruthi; Lindblad-Toh, Kerstin; Ginja, Catarina; Agustina, Kadek Karang; ... (2023). Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture. Genome biology, 24(1), p. 187. BioMed Central Ltd. 10.1186/s13059-023-03023-7

Kiener, Sarah; Yang, Ching; Rich, Naomi; Jagannathan, Vidhya; Mauldin, Elizabeth A; Leeb, Tosso (2023). Heterozygous ATP2A2 missense variant identified in a Shih Tzu with Darier disease. Animal genetics, 54(4), pp. 558-561. Wiley 10.1111/age.13314

Pontes Jacinto, Joana Goncalves; Schiavon, Eliana; Häfliger, Irene M; Coin, Patrizio; Seefried, Franz R; Drögemüller, Cord (2023). MYH3-associated non-syndromic palatoschisis (cleft palate, CP) in Limousine cattle. Animal genetics, 54(4), pp. 581-582. Wiley 10.1111/age.13317

Kiener, Sarah; Castilla, Eloy; Jagannathan, Vidhya; Welle, Monika; Leeb, Tosso (2023). SDR9C7 missense variant in a Chihuahua with non-epidermolytic ichthyosis. Animal genetics, 54(4), pp. 562-565. Wiley 10.1111/age.13319

Christen, Matthias; Zdora, Isabel; Leschnik, Michael; Jagannathan, Vidhya; Puff, Christina; Hünerfauth, Enrice; Volk, Holger A; Baumgärtner, Wolfgang; Koch, Tessa C; Schäfer, Wencke; Kleiter, Miriam; Leeb, Tosso (2023). RALGAPA1 Deletion in Belgian Shepherd Dogs with Cerebellar Ataxia. Genes, 14(8) MDPI, Molecular Diversity Preservation International 10.3390/genes14081520

Drögemüller, Michaela; Klein, Nadine; Steffensen, Rikke Lill; Keiner, Miriam; Jagannathan, Vidhya; Leeb, Tosso (2023). PKD1 Nonsense Variant in a Lagotto Romagnolo Family with Polycystic Kidney Disease. Genes, 14(6) MDPI, Molecular Diversity Preservation International 10.3390/genes14061210

Signer-Hasler, Heidi; Casanova, Lucas; Barenco, Alex; Maitre, Blaise; Bagnato, Alessandro; Vevey, Mario; Berger, Beate; Simčič, Mojca; Boichon, Denis; Capitan, Aurélien; Medugorac, Ivica; Bennewitz, Jörn; Mészáros, Gábor; Sölkner, Johann; Drögemüller, Cord; Flury, Christine (2023). Genomic regions underlying positive selection in local, Alpine cattle breeds. Animal genetics, 54(3), pp. 239-253. Blackwell 10.1111/age.13295

Christen, Matthias; Gutierrez-Quintana, Rodrigo; Green, Matthew; Faller, Kiterie M E; Lowrie, Mark; Rusbridge, Clare; Bossens, Kenny; Mellersh, Cathryn; Pettitt, Louise; Heinonen, Tiina; Lohi, Hannes; Jagannathan, Vidhya; Leeb, Tosso (2023). A TNR Frameshift Variant in Weimaraner Dogs with an Exercise-Induced Paroxysmal Movement Disorder. Movement disorders, 38(6), pp. 1094-1099. Wiley 10.1002/mds.29391

Lourdes Frehner, Bianca; Christen, Matthias; Reichler, Iris M; Jagannathan, Vidhya; Novacco, Marilisa; Riond, Barbara; Peters, Laureen M; Suárez Sánchez-Andrade, José; Pieńkowska-Schelling, Aldona; Schelling, Claude; Kipar, Anja; Leeb, Tosso; Balogh, Orsolya (2023). Autosomal recessive hyposegmentation of granulocytes in Australian Shepherd Dogs indicates a role for LMBR1L in myeloid leukocytes. PLoS genetics, 19(6), e1010805. Public Library of Science 10.1371/journal.pgen.1010805

Gutierrez-Quintana, Rodrigo; Christen, Matthias; Faller, Kiterie M E; Guevar, Julien; Jagannathan, Vidhya; Leeb, Tosso (2023). Response to letter regarding "SCN9A variant in a family of mixed breed dogs with congenital insensitivity to pain". Journal of veterinary internal medicine, 37(3), p. 793. Wiley 10.1111/jvim.16707

Kiener, Sarah; McMahill, Barbara G; Affolter, Verena K; Welle, Monika; Yager, Julie A; Jagannathan, Vidhya; Leeb, Tosso (2023). SOAT1 missense variant in two cats with sebaceous gland dysplasia. Molecular genetics and genomics : MGG, 298(4), pp. 837-843. Springer 10.1007/s00438-023-02020-6

Kamalanathan, Stephanie; Houlahan, Kerry; Miglior, Filippo; Chud, Tatiane C S; Seymour, Dave J; Hailemariam, Dagnachew; Plastow, Graham; de Oliveira, Hinayah R; Baes, Christine F; Schenkel, Flavio S (2023). Genetic Analysis of Methane Emission Traits in Holstein Dairy Cattle. Animals, 13(8) MDPI 10.3390/ani13081308

Jenni, Sophia; Ludwig-Peisker, Odette; Jagannathan, Vidhya; Lapsina, Sandra; Stirn, Martina; Hofmann-Lehmann, Regina; Bogdanov, Nikolay; Schetle, Nelli; Giger, Urs; Leeb, Tosso; Bogdanova, Anna (2023). Methemoglobinemia, Increased Deformability and Reduced Membrane Stability of Red Blood Cells in a Cat with a CYB5R3 Splice Defect. Cells, 12(7) MDPI 10.3390/cells12070991

Letko, Anna; Hédan, Benoît; Snell, Anna; Harris, Alexander C; Jagannathan, Vidhya; Andersson, Göran; Holst, Bodil S; Ostrander, Elaine A; Quignon, Pascale; André, Catherine; Leeb, Tosso (2023). Genomic Diversity and Runs of Homozygosity in Bernese Mountain Dogs. Genes, 14(3) MDPI, Molecular Diversity Preservation International 10.3390/genes14030650

Scheemaeker, Stephanie; Inglebert, Marine; Daminet, Sylvie; Dettwiler, Martina; Letko, Anna; Drögemüller, Cord; Kessler, Martin; Ducatelle, Richard; Rottenberg, Sven; Campos, Miguel (2023). Organoids of patient-derived medullary thyroid carcinoma: the first milestone towards a new in vitro model in dogs. Veterinary and comparative oncology, 21(1), pp. 111-122. Wiley 10.1111/vco.12872

Charalambous, Marios; Fischer, Andrea; Potschka, Heidrun; Walker, Matthew C; Raedt, Robrecht; Vonck, Kristl; Boon, Paul; Lohi, Hannes; Löscher, Wolfgang; Worrell, Gregory; Leeb, Tosso; McEvoy, Andrew; Striano, Pasquale; Kluger, Gerard; Galanopoulou, Aristea S; Volk, Holger A; Bhatti, Sofie F M (2023). Translational veterinary epilepsy: A win-win situation for human and veterinary neurology. Veterinary journal, 293(105956), p. 105956. Elsevier 10.1016/j.tvjl.2023.105956

Christen, Matthias; Gonzalo-Nadal, Veronica; Kaczmarska, Adriana; Dyrka, Magdalena; Guevar, Julien; Jagannathan, Vidhya; Leeb, Tosso; Gutierrez-Quintana, Rodrigo (2023). A novel missense variant in the L2HGDH gene in a cat with L-2-hydroxyglutaric aciduria and multicystic cerebral lesions. Journal of veterinary internal medicine, 37(2), pp. 676-680. Wiley 10.1111/jvim.16675

Leeb, Tosso; Bannasch, Danika; Schoenebeck, Jeffrey J (2023). Identification of Genetic Risk Factors for Monogenic and Complex Canine Diseases. Annual Review of Animal Biosciences, 11, pp. 183-205. Annual Reviews 10.1146/annurev-animal-050622-055534

Lenstra, J.A.; Consortium, VarGoats; Nijman, I.J.; Rosen, B.D.; Bardou, P.; Faraut, T.; Cumer, T.; Daly, K.G.; Zheng, Z.; Cai, Y.; Asadollahpour, H.; Kul, Çınar B.; Kul, Çınar B.; Zhang, W.-Y.; E, G.; Ayin, A.; Bakhtin, M.; Balteanu, V.A.; Barfield, D.; Baird, H.; ... (9 February 2023). Y-chromosomal haplogroups from wild and domestic goats reveal ancient migrations and recent introgressions. In: Veerkamp, R. F.; de Haas, Y. (eds.) Proceedings of 12th World Congress on Genetics Applied to Livestock Production (pp. 886-889). The Netherlands: Wageningen Academic Publishers 10.3920/978-90-8686-940-4_208

Widmer, S.; Seefried, F. R.; Drögemüller, C.; von Rohr, P. (9 February 2023). LASSO and SVM: an alternative approach to identify associated genome regions for simple and complex traits in cattle. In: Veerkamp, R. F.; de Haas, Y. (eds.) Proceedings of 12th World Congress on Genetics Applied to Livestock Production (pp. 1664-1667). The Netherlands: Wageningen Academic Publishers 10.3920/978-90-8686-940-4_399

Häfliger, I. M.; Seefried, F. R.; Drögemüller, C. (9 February 2023). Successful trio-based reverse genetic screen in an endangered local cattle breed. In: Veerkamp, R. F.; de Haas, Y. (eds.) Proceedings of 12th World Congress on Genetics Applied to Livestock Production (pp. 1074-1077). The Netherlands: Wageningen Academic Publishers 10.3920/978-90-8686-940-4_254

Abitbol, Marie; Jagannathan, Vidhya; Lopez, Marie; Courtin, Ambre; Dufaure de Citres, Caroline; Gache, Vincent; Leeb, Tosso (2023). A CDH23 missense variant in Beauceron dogs with non-syndromic deafness. Animal genetics, 54(1), pp. 73-77. Wiley 10.1111/age.13273

Massender, Erin; Oliveira, Hinayah R; Brito, Luiz F; Maignel, Laurence; Jafarikia, Mohsen; Baes, Christine F; Sullivan, Brian; Schenkel, Flavio S (2023). Genome-wide association study for milk production and conformation traits in Canadian Alpine and Saanen dairy goats. Journal of dairy science, 106(2), pp. 1168-1189. American Dairy Science Association 10.3168/jds.2022-22223

Rockett, Paige L; Campos, I L; Baes, C F; Tulpan, D; Miglior, F; Schenkel, F S (2023). Phenotypic analysis of heat stress in Holsteins using test-day production records and NASA POWER meteorological data. Journal of dairy science, 106(2), pp. 1142-1158. Elsevier 10.3168/jds.2022-22370

Gutierrez-Quintana, Rodrigo; Christen, Matthias; Faller, Kiterie M E; Guevar, Julien; Jagannathan, Vidhya; Leeb, Tosso (2023). SCN9A variant in a family of mixed breed dogs with congenital insensitivity to pain. Journal of veterinary internal medicine, 37(1), pp. 230-235. Wiley 10.1111/jvim.16610

Duruz, Jules; Sprecher, Marta; Kaldun, Jenifer C; Al-Soudy, Al-Sayed; Tschanz, Heidi E L; van Geest, Geert; Nicholson, Pamela; Bruggmann, Rémy; Sprecher, Simon G (2023). Molecular characterization of cell types in the squid Loligo vulgaris. eLife, 12 eLife Sciences Publications 10.7554/eLife.80670

Leishman, Emily M; Vanderhout, Ryley J; Abdalla, Emhimad A; van Staaveren, Nienke; Naim, Anna; Barbut, Shai; Wood, Benjamin J; Harlander-Matauschek, Alexandra; Baes, Christine F (2023). Genetic parameters of feather corticosterone and fault bars and correlations with production traits in turkeys (Meleagris gallopavo). Scientific reports, 13(1), p. 38. Springer Nature 10.1038/s41598-022-26734-6

Hilton, Stephanie; Christen, Matthias; Bilzer, Thomas; Jagannathan, Vidhya; Leeb, Tosso; Giger, Urs (2023). Dystrophin (DMD) Missense Variant in Cats with Becker-Type Muscular Dystrophy. International journal of molecular sciences, 24(4), p. 3192. MDPI 10.3390/ijms24043192

Christen, Matthias; Ludwig-Peisker, Odette; Jagannathan, Vidhya; Hetzel, Udo; Schönball, Ulrike; Leeb, Tosso (2023). STK36 splice site variant in an Australian Shepherd dog with primary ciliary dyskinesia. Animal genetics, 54(3), pp. 412-415. Wiley 10.1111/age.13306

Batcher, Kevin; Varney, Scarlett; Raudsepp, Terje; Jevit, Matthew; Dickinson, Peter; Jagannathan, Vidhya; Leeb, Tosso; Bannasch, Danika (2023). Ancient segmentally duplicated LCORL retrocopies in equids. PLoS ONE, 18(6), e0286861. Public Library of Science 10.1371/journal.pone.0286861

Dell'Apa, Diletta; Fumeo, Martina; Volta, Antonella; Bernardini, Marco; Fidanzio, Francesca; Buffagni, Valentina; Christen, Matthias; Jagannathan, Vidhya; Leeb, Tosso; Bianchi, Ezio (2023). Case report: Sacral agenesis in two boxer dogs: clinical presentation, diagnostic investigations, and outcome. Frontiers in veterinary science, 10, p. 1201484. Frontiers Media 10.3389/fvets.2023.1201484

Smith, Timothy P. L.; Bickhart, Derek M.; Boichard, Didier; Chamberlain, Amanda J.; Djikeng, Appolinaire; Jiang, Yu; Low, Wai Y.; Pausch, Hubert; Demyda-Peyrás, Sebastian; Prendergast, James; Schnabel, Robert D.; Rosen, Benjamin D. (2023). The Bovine Pangenome Consortium: democratizing production and accessibility of genome assemblies for global cattle breeds and other bovine species. Genome biology, 24(1), p. 139. BioMed Central Ltd. 10.1186/s13059-023-02975-0

Leeb, Tosso (ed.) (2023). Canine Genetics 2, 14. MDPI, Molecular Diversity Preservation International

2022

Martin, Audrey A A; Id-Lahoucine, Samir; Fonseca, Pablo A S; Rochus, Christina M; Alcantara, Lucas M; Tulpan, Dan; LeBlanc, Stephen J; Miglior, Filippo; Casellas, Joaquim; Cánovas, Angela; Baes, Christine F; Schenkel, Flavio S (2022). Unravelling the genetics of non-random fertilization associated with gametic incompatibility. Scientific reports, 12(1), p. 22314. Springer Nature 10.1038/s41598-022-26910-8

Campos, Ivan L; Chud, Tatiane C S; Junior, Gerson A Oliveira; Baes, Christine F; Cánovas, Ángela; Schenkel, Flavio S (2022). Estimation of Genetic Parameters of Heat Tolerance for Production Traits in Canadian Holsteins Cattle. Animals, 12(24) MDPI 10.3390/ani12243585

Signer-Hasler, Heidi; Bangerter, Erika; Drögemüller, Cord (1 December 2022). Aktuelles zur Genetik der Ziegenmilch. Forum Kleinwiederkäuer(12), pp. 6-14. Verlagsgenossenschaft Caprovis

Spinelli, Marialuigia; Zdanowicz, Jarmila A; Keller, Irene; Nicholson, Pamela; Raio, Luigi; Amylidi-Mohr, Sofia; Mosimann, Beatrice; Surbek, Daniel; Mueller, Martin (2022). Hypertensive disorders of pregnancy share common cfDNA methylation profiles. Scientific Reports, 12(1), p. 19837. Nature Publishing Group 10.1038/s41598-022-24348-6

Peters, Laureen; Howard, Judith; Leeb, Tosso; Mevissen, Meike; Graf, Rolf; Reding Graf, Theresia (12 November 2022). Identification Of Regenerating Island-Derived Protein 3E In Dogs. In: 2022 ACVP/ASVCP Annual Meeting.

Leishman, Emily M; Wood, Benjamin J; Baes, Christine F; Harlander-Matauschek, Alexandra; van Staaveren, Nienke (2022). The usual suspects: Co-occurrence of integument injuries in turkey flocks. Poultry science, 101(11), p. 102137. Elsevier 10.1016/j.psj.2022.102137

Peters, Laureen M; Howard, Judith; Leeb, Tosso; Mevissen, Meike; Graf, Rolf; Reding Graf, Theresia (2022). Identification of regenerating island-derived protein 3E in dogs. Frontiers in veterinary science, 9 Frontiers Media 10.3389/fvets.2022.1010809

Inglebert, Marine; Dettwiler, Martina; Hahn, Kerstin; Letko, Anna; Drögemüller, Cord; Doench, John; Brown, Adam; Memari, Yasin; Davies, Helen R; Degasperi, Andrea; Nik-Zainal, Serena; Rottenberg, Sven (2022). A living biobank of canine mammary tumor organoids as a comparative model for human breast cancer. Scientific Reports, 12(1), p. 18051. Nature Publishing Group 10.1038/s41598-022-21706-2

Akyürek, Eylem Emek; Busato, Francesca; Murgiano, Leonardo; Bianchini, Elisa; Carotti, Marcello; Sandonà, Dorianna; Drögemüller, Cord; Gentile, Arcangelo; Sacchetto, Roberta (2022). Differential Analysis of Gly211Val and Gly286Val Mutations Affecting Sarco(endo)plasmic Reticulum Ca2+-ATPase (SERCA1) in Congenital Pseudomyotonia Romagnola Cattle. International journal of molecular sciences, 23(20) MDPI 10.3390/ijms232012364

Widmer, Sarah; Seefried, Franz R; von Rohr, Peter; Häfliger, Irene M; Spengeler, Mirjam; Drögemüller, Cord (2022). Associated regions for multiple birth in Brown Swiss and Original Braunvieh cattle on chromosomes 15 and 11. Animal genetics, 53(5), pp. 557-569. Wiley 10.1111/age.13229

Tan, Kirsty; Roy, Mia; Manz, Eberhard; Wagner, Henrik; Zanolari, Patrik; Drögemüller, Cord; Lühken, Gesine (2022). The KIT:c.376G>A variant in German and Swiss alpacas (Vicugna pacos) with different coat colors. Animal genetics, 53(5), pp. 718-720. Wiley 10.1111/age.13231

Jacinto, Joana G P; Häfliger, Irene M; Caivano, Domenico; Drögemüller, Cord (2022). A germline de novo variant in NUMB associated with a double-outlet right ventricle in Chianina cattle. Animal genetics, 53(5), pp. 713-714. Wiley 10.1111/age.13236

Scheidegger, Milena D; Gerber, Vinzenz; Dolf, Gaudenz; Burger, Dominik; Axiak Flammer, Shannon; Ramseyer, Alessandra (2022). Quantitative gait analysis before and after a cross-country test in a population of elite eventing horses. Journal of equine veterinary science, 117, p. 104077. Elsevier 10.1016/j.jevs.2022.104077

Abitbol, Marie; Jagannathan, Vidhya; Laurent, Nelly; Noblet, Eglantine; Dutil, Guillaume F.; Troupel, Thibaut; de Dufaure de Citres, Caroline; Gache, Vincent; Blot, Stéphane; Escriou, Catherine; Leeb, Tosso (2022). A PNPLA8 frameshift variant in Australian shepherd dogs with hereditary ataxia. Animal genetics, 53(5), pp. 709-712. Wiley 10.1111/age.13245

Martin, Audrey A A; de Oliveira, Gerson; Madureira, Augusto M L; Miglior, Filippo; LeBlanc, Stephen J; Cerri, Ronaldo L A; Baes, Christine F; Schenkel, Flavio S (2022). Reproductive tract size and position score: Estimation of genetic parameters for a novel fertility trait in dairy cows. Journal of dairy science, 105(10), pp. 8189-8198. American Dairy Science Association 10.3168/jds.2021-21651

Hiscock, Heather M; Leishman, Emily M; Vanderhout, Ryley J; Adams, Sarah M; Mohr, Jeff; Wood, Benjamin J; Baes, Christine F; Barbut, Shai (2022). Describing the relationships among meat quality traits in domestic turkey (Meleagris gallopavo) populations. Poultry science, 101(10), p. 102055. Elsevier 10.1016/j.psj.2022.102055

Alcantara, L M; Schenkel, F S; Lynch, C; Oliveira Junior, G A; Baes, C F; Tulpan, D (2022). Machine learning classification of breeding protocol descriptions from Canadian Holsteins. Journal of dairy science, 105(10), pp. 8177-8188. American Dairy Science Association 10.3168/jds.2021-21663

Shadpour, Saeed; Chud, Tatiane C S; Hailemariam, Dagnachew; Oliveira, Hinayah R; Plastow, Graham; Stothard, Paul; Lassen, Jan; Baldwin, Ransom; Miglior, Filippo; Baes, Christine F; Tulpan, Dan; Schenkel, Flavio S (2022). Predicting dry matter intake in Canadian Holstein dairy cattle using milk mid-infrared reflectance spectroscopy and other commonly available predictors via artificial neural networks. Journal of dairy science, 105(10), pp. 8257-8271. American Dairy Science Association 10.3168/jds.2021-21297

Christen, Matthias; Gutierrez-Quintana, Rodrigo; Vandenberghe, Helene; Kaczmarska, Adriana; Penderis, Jacques; José-López, Roberto; Rupp, Angie; Griffiths, Ian R; Jagannathan, Vidhya; Leeb, Tosso (2022). Mitochondrial fission factor (MFF) frameshift variant in Bullmastiffs with mitochondrial fission encephalopathy. Animal genetics, 53(6), pp. 814-820. Wiley 10.1111/age.13263

Pontes Jacinto, Joana Goncalves; Muscatello, Luisa Vera; Häfliger, Irene M; Benazzi, Cinzia; Bolcato, Marilena; Gentile, Arcangelo; Drögemüller, Cord (2022). A Missense Variant in PLP2 in Holstein Cattle with X-Linked Congenital Mast Cell Tumor. Animals, 12(18) MDPI 10.3390/ani12182329

Capuzzello, Giovanni; Pontes Jacinto, Joana Gonçalves; Häfliger, Irene Monika; Chapman, Gail E; Soto Martin, Sara; Viora, Lorenzo; Jonsson, Nicholas N; Drögemüller, Cord (2022). A large deletion encompassing exon 2 of the ectodysplasin A (EDA) gene in a British blue crossbred calf with hypohidrotic ectodermal dysplasia. Acta Veterinaria Scandinavica, 64(1), p. 23. BioMed Central Ltd. 10.1186/s13028-022-00641-2

Bolormaa, Sunduimijid; MacLeod, Iona M; Khansefid, Majid; Marett, Leah C; Wales, William J; Miglior, Filippo; Baes, Christine F; Schenkel, Flavio S; Connor, Erin E; Manzanilla-Pech, Coralia I V; Stothard, Paul; Herman, Emily; Nieuwhof, Gert J; Goddard, Michael E; Pryce, Jennie E (2022). Sharing of either phenotypes or genetic variants can increase the accuracy of genomic prediction of feed efficiency. Genetics, selection, evolution, 54(1), p. 60. BioMed Central 10.1186/s12711-022-00749-z

Mock, Thomas; Bodmer, Michèle; Hirsbrunner, Gabriela; Dettwiler, Martina Andrea; Rodriguez, Sabrina; Hüsler, Rudolf Jürg; Häfliger, Irene Monika; Drögemüller, Cord (September 2022). Evaluation of an investigative model in dairy herds with high calf perinatal mortality rates in Switzerland (Unpublished). In: 31st World Buiatrics Congress. Madrid. 04.09.2022-08.09.2022.

Kiener, Sarah; Mauldin, Elizabeth A; Jagannathan, Vidhya; Casal, Margret L; Leeb, Tosso (2022). KRT5 missense variant in a Cardigan Welsh Corgi with epidermolysis bullosa simplex. Animal genetics, 53(6), pp. 892-896. Wiley 10.1111/age.13257

Jacinto Joana G P, Joana; Häfliger, Irene M; Christen, Matthias; Paris, Julia M; Seefried, Franz R; Drögemüller, Cord (2022). Is a heterozygous missense variant in SGSH the cause of a syndromic form of congenital amastia in an Original Braunvieh calf? Animal genetics, 53(4), pp. 530-531. Wiley 10.1111/age.13207

Nijman, Isaäc J; Rosen, Benjamin D; Bardou, Philippe; Faraut, Thomas; Cumer, Tristan; Daly, Kevin G; Zheng, Zhuqing; Cai, Yudong; Asadollahpour, Hojjat; Kul, Bengi Çınar; Zhang, Wei-Yi; E, Guangxin; Ayin, A; Baird, Hayley; Bakhtin, Meirat; Bâlteanu, Valentin A; Barfield, Diana; Berger, Beate; Blichfeldt, Thor; Boink, Geert; ... (2022). Geographical contrasts of Y-chromosomal haplogroups from wild and domestic goats reveal ancient migrations and recent introgressions. Molecular Ecology, 31(16), pp. 4364-4380. Wiley-Blackwell 10.1111/mec.16579

Kinsey, Nathan A.; Belanger, Janelle M.; Dog Biomedical Variant Database, Consortium; Oberbauer, Anita M. (2022). Canine reference genome accuracy impacts variant calling: Lessons learned from investigating embryonic lethal variants. Animal genetics, 53(5), pp. 706-708. Wiley 10.1111/age.13241

Massender, Erin; Brito, Luiz F; Maignel, Laurence; Oliveira, Hinayah R; Jafarikia, Mohsen; Baes, Christine F; Sullivan, Brian; Schenkel, Flavio S (2022). Single- and multiple-breed genomic evaluations for conformation traits in Canadian Alpine and Saanen dairy goats. Journal of dairy science, 105(7), pp. 5985-6000. American Dairy Science Association 10.3168/jds.2021-21713

Pontes Jacinto, Joana Goncalves; Sbarra, F; Quaglia, A; Gentile, A; Drögemüller, C (2022). Short communication: Prevalence of deleterious variants causing recessive disorders in Italian Chianina, Marchigiana and Romagnola cattle. Animal : an international journal of animal bioscience, 16(7), p. 100569. Elsevier 10.1016/j.animal.2022.100569

Häfliger, Irene M.; Wolf-Hofstetter, Sonja; Casola, Christina; Hetzel, Udo; Seefried, Franz R.; Drögemüller, Cord (2022). A de novo variant in the bovine ADAMTSL4 gene in an Original Braunvieh calf with congenital cataract. Animal genetics, 53(3), pp. 416-421. Wiley 10.1111/age.13178

Hauser, Miriam; Signer-Hasler, Heidi; Küttel, Luzia; Capitan, Aurélien; Guldbrandtsen, Bernt; Hinrichs, Dirk; Flury, Christine; Seefried, Franz R; Drögemüller, Cord (2022). Identification of two new recessive MC1R alleles in red-coloured Evolèner cattle and other breeds. Animal genetics, 53(3), pp. 427-435. Blackwell 10.1111/age.13206

P Jacinto, Joana G; Häfliger, Irene M; Baes, Christine F; de Oliveira, Hinayah R; Drögemüller, Cord (2022). A de novo start-lost variant in ANKRD28 in a Holstein calf with dwarfism. Animal genetics, 53(3), pp. 470-471. 10.1111/age.13204

Kiener, Sarah; Chevallier, Lucie; Jagannathan, Vidhya; Briand, Amaury; Cochet-Faivre, Noëlle; Reyes-Gomez, Edouard; Leeb, Tosso (2022). A COL5A2 In-Frame Deletion in a Chihuahua with Ehlers-Danlos Syndrome. Genes, 13(5) MDPI, Molecular Diversity Preservation International 10.3390/genes13050934

Simon, Rebecca; Drögemüller, Cord; Lühken, Gesine (2022). The Complex and Diverse Genetic Architecture of the Absence of Horns (Polledness) in Domestic Ruminants, including Goats and Sheep. Genes, 13(5) MDPI, Molecular Diversity Preservation International 10.3390/genes13050832

Moshfegh, Cameron; Rambow, Sebastian G; Domenig, Seraina A; Pieńkowska-Schelling, Aldona; Bleul, Ulrich; Vogel, Viola (2022). Differentiation of mouse embryonic stem cells into cells with spermatogonia-like morphology with chemical intervention-dependent increased gene expression of LIM homeobox 1 (Lhx1). Stem cell research, 61, p. 102780. Elsevier 10.1016/j.scr.2022.102780

Neradilová, Silvie; Schauer, Alexandria Marie; Hayward, Jessica J; Brunner, Magdalena Anna Theresa; Bohutínská, Magdalena; Jagannathan, Vidhya; Connell, Laurie B; Boyko, Adam R; Welle, Monika M; Černá Bolfíková, Barbora (2022). Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek. Genes, 13(4) MDPI, Molecular Diversity Preservation International 10.3390/genes13040650

Graber, Jennifer Kalinka; Signer-Hasler, Heidi; Burren, Alexander; Drögemüller, Cord (2022). Evaluation of truncating variants in the LCORL gene in relation to body size of goats from Switzerland. Animal genetics, 53(2), pp. 237-239. Wiley 10.1111/age.13177

Kiener, Sarah; Apostolopoulos, Neoklis; Schissler, Jennifer; Hass, Pascal-Kolja; Leuthard, Fabienne; Jagannathan, Vidhya; Schuppisser, Carole; Soto, Sara; Welle, Monika; Mayer, Ursula; Leeb, Tosso; Fischer, Nina M; Kaessmeyer, Sabine (2022). Independent COL5A1 Variant in Cats with Ehlers-Danlos Syndrome. Genes, 13(5), p. 797. MDPI, Molecular Diversity Preservation International 10.3390/genes13050797

Häfliger, Irene M; Spengeler, Mirjam; Seefried, Franz R; Drögemüller, Cord (2022). Four novel candidate causal variants for deficient homozygous haplotypes in Holstein cattle. Scientific reports, 12(1), p. 5435. Springer Nature 10.1038/s41598-022-09403-6

Bolormaa, S; MacLeod, I M; Khansefid, M; Marett, L C; Wales, W J; Nieuwhof, G J; Baes, C F; Schenkel, F S; Goddard, M E; Pryce, J E (2022). Evaluation of updated Feed Saved breeding values developed in Australian Holstein dairy cattle. JDS communications, 3(2), pp. 114-119. Elsevier 10.3168/jdsc.2021-0150

Bannasch, Danika; Batcher, Kevin; Leuthard, Fabienne; Bannasch, Michael; Hug, Petra; Marcellin-Little, Denis J.; Dickinson, Peter J.; Drögemüller, Michaela; Drögemüller, Cord; Leeb, Tosso (2022). The Effects of FGF4 Retrogenes on Canine Morphology. Genes, 13(2), p. 325. MDPI, Molecular Diversity Preservation International 10.3390/genes13020325

Kiener, Sarah; Wiener, Dominique J; Hopke, Kaitlin; Diesel, Alison B; Jagannathan, Vidhya; Mauldin, Elizabeth A; Casal, Margret L; Leeb, Tosso (2022). ABHD5 frameshift deletion in Golden Retrievers with ichthyosis. G3 Genes Genomes Genetics, 12(2) Genetics Society of America 10.1093/g3journal/jkab397

Rudd Garces, Gabriela; Christen, Matthias; Loechel, Robert; Jagannathan, Vidhya; Leeb, Tosso (2022). FYCO1 Frameshift Deletion in Wirehaired Pointing Griffon Dogs with Juvenile Cataract. Genes, 13(2), p. 334. MDPI, Molecular Diversity Preservation International 10.3390/genes13020334

Leishman, Emily M; Vanderhout, Ryley J; van Staaveren, Nienke; Barbut, Shai; Mohr, Jeff; Wood, Benjamin J; Baes, Christine F (2022). Influence of Post Mortem Muscle Activity on Turkey Meat Quality. Frontiers in veterinary science, 9, p. 822447. Frontiers Media 10.3389/fvets.2022.822447

Signer-Hasler, Heidi; Henkel, Jan; Bangerter, Erika; Bulut, Zafer; Drögemüller, Cord; Leeb, Tosso; Flury, Christine (2022). Runs of homozygosity in Swiss goats reveal genetic changes associated with domestication and modern selection. Genetics, selection, evolution, 54(1), p. 6. BioMed Central 10.1186/s12711-022-00695-w

Vanderhout, Ryley J; Leishman, Emily M; Hiscock, Heather; Abdalla, Emhimad A; Makanjuola, Bayode O; Mohr, Jeff; Harlander-Matauschek, Alexandra; Barbut, Shai; Wood, Benjamin J; Baes, Christine F; van Staaveren, Nienke (2022). Reliability of a White Striping Scoring System and Description of White Striping Prevalence in Purebred Turkey Lines. Animals, 12(3) MDPI 10.3390/ani12030254

Häfliger, Irene M.; Koch, Caroline T.; Michel, Astrid; Rüfenacht, Silvia; Meylan, Mireille; Welle, Monika M.; Drögemüller, Cord (2022). DSP missense variant in a Scottish Highland calf with congenital ichthyosis, alopecia, acantholysis of the tongue and corneal defects. BMC veterinary research, 18(1), p. 20. BioMed Central 10.1186/s12917-021-03113-3

Jacinto, Joana G. P.; Häfliger, Irene M.; Bernardini, Marco; Mandara, Maria Teresa; Bianchi, Ezio; Bolcato, Marilena; Romagnoli, Noemi; Gentile, Arcangelo; Drögemüller, Cord (2022). A homozygous missense variant in laminin subunit beta 1 as candidate causal mutation of hemifacial microsomia in Romagnola cattle. Journal of veterinary internal medicine, 36(1), pp. 292-299. Wiley-Blackwell 10.1111/jvim.16316

Leeb, Tosso; Roosje, Petra; Welle, Monika (2022). Genetics of inherited skin disorders in dogs. Veterinary journal, 279, p. 105782. Elsevier 10.1016/j.tvjl.2021.105782

Kiener, Sarah; Rostaher, Ana; Rüfenacht, Silvia; Jagannathan, Vidhya; Sundberg, John P.; Welle, Monika; Leeb, Tosso (2022). Independent DSG4 frameshift variants in cats with hair shaft dystrophy. Molecular genetics and genomics : MGG, 297(1), pp. 147-154. Springer 10.1007/s00438-021-01842-6

Madureira, A M L; Burnett, T A; Marques, J C S; Moore, A L; Borchardt, S; Heuwieser, W; Guida, T G; Vasconcelos, J L M; Baes, C F; Cerri, R L A (2022). Occurrence and greater intensity of estrus in recipient lactating dairy cows improve pregnancy per embryo transfer. Journal of dairy science, 105(1), pp. 877-888. American Dairy Science Association 10.3168/jds.2021-20437

Abdalla, E. A.; Makanjuola, B. O.; van Staaveren, N.; Wood, B. J.; Baes, C. F. (2022). Accuracy of genomic selection for reducing susceptibility to pendulous crop in turkey (Meleagris gallopavo). Poultry science, 101(2), p. 101601. Elsevier 10.1016/j.psj.2021.101601

Abdalla, Emhimad A E; Makanjuola, Bayode O; Wood, Benjamin J; Baes, Christine F (2022). Genome-wide association study reveals candidate genes relevant to body weight in female turkeys (Meleagris gallopavo). PLoS ONE, 17(3), e0264838. Public Library of Science 10.1371/journal.pone.0264838

Vanderhout, Ryley J; Leishman, Emily M; Abdalla, Emhimad A; Barbut, Shai; Wood, Benjamin J; Baes, Christine F (2022). Genetic Parameters of White Striping and Meat Quality Traits Indicative of Pale, Soft, Exudative Meat in Turkeys (Meleagris gallopavo). Frontiers in genetics, 13, p. 842584. Frontiers Media SA 10.3389/fgene.2022.842584

Christen, Matthias; Rupp, Stefan; Van Soens, Iris; Bhatti, Sofie F. M.; Matiasek, Kaspar; von Klopmann, Thilo; Jagannathan, Vidhya; Madden, Indiana; Batcher, Kevin; Bannasch, Danika; Leeb, Tosso (2022). SLC25A12 Missense Variant in Nova Scotia Duck Tolling Retrievers Affected by Cerebellar Degeneration—Myositis Complex (CDMC). Genes, 13(7), p. 1223. MDPI, Molecular Diversity Preservation International 10.3390/genes13071223

Cvitas, Iva; Oberhaensli, Simone; Leeb, Tosso; Marti, Eliane (2022). Equine keratinocytes in the pathogenesis of insect bite hypersensitivity: Just another brick in the wall? PLoS ONE, 17(8), e0266263. Public Library of Science 10.1371/journal.pone.0266263

Sage, Sophie E.; Nicholson, Pamela; Peters, Laureen M.; Leeb, Tosso; Jagannathan, Vidhya; Gerber, Vinzenz (2022). Single-cell gene expression analysis of cryopreserved equine bronchoalveolar cells (In Press). Frontiers in immunology, 13 Frontiers Research Foundation 10.3389/fimmu.2022.929922

Makanjuola, Bayode O; Abdalla, Emhimad A; Wood, Benjamin J; Baes, Christine F (2022). Applicability of single-step genomic evaluation with a random regression model for reproductive traits in turkeys (Meleagris gallopavo). Frontiers in genetics, 13, p. 923766. Frontiers Media SA 10.3389/fgene.2022.923766

Østergård Jensen, Sarah; Christen, Matthias; Rondahl, Veronica; Holland, Christopher T.; Jagannathan, Vidhya; Leeb, Tosso; Giger, Urs (2022). EHBP1L1 Frameshift Deletion in English Springer Spaniel Dogs with Dyserythropoietic Anemia and Myopathy Syndrome (DAMS) or Neonatal Losses. Genes, 13(9), p. 1533. MDPI, Molecular Diversity Preservation International 10.3390/genes13091533

Sage, Sophie Elena; Nicholson, Pamela; Leeb, Tosso; Gerber, Vinzenz; Jagannathan, Vidhya (2022). Long-Read Transcriptome of Equine Bronchoalveolar Cells. Genes, 13(10), p. 1722. MDPI, Molecular Diversity Preservation International 10.3390/genes13101722

Inglebert, Marine; Dettwiler, Martina; Hahn, Kerstin; Letko, Anna; Drögemüller, Cord; Doench, John; Brown, Adam; Memari, Yasin; Davies, Helen; Degasperi, Andrea; Nik-Zainal, Serena; Rottenberg, Sven (2022). A living biobank of canine mammary tumor organoids as a comparative model for human breast cancer (bioRxiv). Cold Spring Harbor Laboratory 10.1101/2022.09.02.505845

Christen, Matthias; Bongers, Jos; Mathis, Déborah; Jagannathan, Vidya; Quintana, Rodrigo Gutierrez; Leeb, Tosso (2022). ACADM Frameshift Variant in Cavalier King Charles Spaniels with Medium-Chain Acyl-CoA Dehydrogenase Deficiency. Genes, 13(10), p. 1847. MDPI 10.3390/genes13101847

Affolter, Verena K; Kiener, Sarah; Jagannathan, Vidhya; Nagle, Terry; Leeb, Tosso (2022). A de novo variant in the keratin 1 gene (KRT1) in a Chinese shar-pei dog with severe congenital cornification disorder and non-epidermolytic ichthyosis. PLoS ONE, 17(10), e0275367. Public Library of Science 10.1371/journal.pone.0275367

Tengvall, Katarina; Sundström, Elisabeth; Wang, Chao; Bergvall, Kerstin; Wallerman, Ola; Pederson, Eric; Karlsson, Åsa; Harvey, Naomi D.; Blott, Sarah C.; Olby, Natasha; Olivry, Thierry; Brander, Gustaf; Meadows, Jennifer R. S.; Roosje, Petra; Leeb, Tosso; Hedhammar, Åke; Andersson, Göran; Lindblad-Toh, Kerstin (2022). Bayesian model and selection signature analyses reveal risk factors for canine atopic dermatitis. Communications biology, 5(1) Springer Nature 10.1038/s42003-022-04279-8

Ludwig-Peisker, Odette; Ansel, Emily; Schweizer, Daniela; Jagannathan, Vidhya; Loechel, Robert; Leeb, Tosso (2022). PCYT1A Missense Variant in Vizslas with Disproportionate Dwarfism. Genes, 13(12), p. 2354. MDPI, Molecular Diversity Preservation International 10.3390/genes13122354

2021

Braiek, Ben; Moreno-Romieux, Carole; Allain, Charlotte; Bardou, Philippe; Bordes, Arnaud; Debat, Frédéric; Drögemüller, Cord; Plisson-Petit, Florence; Portes, David; Sarry, Julien; Tadi, Némuel; Woloszyn, Florent; Fabre, Stéphane (2021). A Nonsense Variant in CCDC65 Gene Causes Respiratory Failure Associated with Increased Lamb Mortality in French Lacaune Dairy Sheep. Genes, 13(1), p. 45. MDPI, Molecular Diversity Preservation International 10.3390/genes13010045

Häfliger, Irene M.; Seefried, Franz R.; Spengeler, Mirjam; Drögemüller, Cord (2021). Mining massive genomic data of two Swiss Braunvieh cattle populations reveals six novel candidate variants that impair reproductive success. Genetics, selection, evolution, 53(1), p. 95. BioMed Central 10.1186/s12711-021-00686-3

Häfliger, Irene M.; Seefried, Franz R.; Drögemüller, Cord (2021). Reverse Genetic Screen for Deleterious Recessive Variants in the Local Simmental Cattle Population of Switzerland. Animals, 11(12), p. 3535. MDPI 10.3390/ani11123535

Letko, Anna; Minor, Katie M.; Norton, Elaine M.; Marinescu, Voichita D.; Drögemüller, Michaela; Ivansson, Emma; Megquier, Kate; Noh, Hyun Ji; Starkey, Mike; Friedenberg, Steven G.; Lindblad-Toh, Kerstin; Mickelson, James R.; Drögemüller, Cord (2021). Genome-Wide Analyses for Osteosarcoma in Leonberger Dogs Reveal the CDKN2A/B Gene Locus as a Major Risk Locus. Genes, 12(12), p. 1964. MDPI, Molecular Diversity Preservation International 10.3390/genes12121964

Brito, L F; Bedere, N; Douhard, F; Oliveira, H R; Arnal, M; Peñagaricano, F; Schinckel, A P; Baes, C F; Miglior, F (2021). Review: Genetic selection of high-yielding dairy cattle toward sustainable farming systems in a rapidly changing world. Animal, 15 Suppl 1, p. 100292. Elsevier 10.1016/j.animal.2021.100292

Christen, Matthias; Reineking, Wencke; Beineke, Andreas; Jagannathan, Vidhya; Baumgärtner, Wolfgang; Leeb, Tosso (2021). Polyadenine insertion disrupting the G6PC1 gene in German Pinschers with glycogen storage disease type Ia (GSD1A). Animal genetics, 52(6), pp. 900-902. Wiley 10.1111/age.13146

Häfliger, Irene M.; Marchionatti, Emma; Stengard, Michele; Wolf-Hofstetter, Sonja; Paris, Julia M.; Jacinto, Joana G. P.; Watté, Christine; Voelter, Katrin; Occelli, Laurence M.; Komáromy, András M.; Oevermann, Anna; Goepfert, Christine; Borgo, Angelica; Roduit, Raphaël; Spengeler, Mirjam; Seefried, Franz R.; Drögemüller, Cord (2021). CNGB3 Missense Variant Causes Recessive Achromatopsia in Original Braunvieh Cattle. International journal of molecular sciences, 22(22), p. 12440. MDPI 10.3390/ijms222212440

Jacinto, Joana G. P.; Häfliger, Irene M.; Akyürek, Eylem Emek; Sacchetto, Roberta; Benazzi, Cinzia; Gentile, Arcangelo; Drögemüller, Cord (2021). KCNG1-Related Syndromic Form of Congenital Neuromuscular Channelopathy in a Crossbred Calf. Genes, 12(11), p. 1792. MDPI, Molecular Diversity Preservation International 10.3390/genes12111792

Denoyelle, Laure; Talouarn, Estelle; Bardou, Philippe; Colli, Licia; Alberti, Adriana; Danchin, Coralie; Del Corvo, Marcello; Engelen, Stéfan; Orvain, Céline; Palhière, Isabelle; Rupp, Rachel; Sarry, Julien; Salavati, Mazdak; Amills, Marcel; Clark, Emily; Crepaldi, Paola; Faraut, Thomas; Masiga, Clet Wandui; Pompanon, François; Rosen, Benjamin D; ... (2021). VarGoats project: a dataset of 1159 whole-genome sequences to dissect Capra hircus global diversity. Genetics, selection, evolution, 53(1), p. 86. BioMed Central 10.1186/s12711-021-00659-6

Naylor, D; Sharma, A; Li, Z; Monteith, G; Mallard, B A; Bergeron, R; Baes, C; Karrow, N A (2021). Endotoxin-induced cytokine, chemokine and white blood cell profiles of variable stress-responding sheep. Stress - the international journal on the biology of stress, 24(6), pp. 888-897. Taylor & Francis 10.1080/10253890.2021.1954905

Jacinto, Joana G. P.; Häfliger, Irene M.; Veiga, Inês M. B.; Letko, Anna; Gentile, Arcangelo; Drögemüller, Cord (2021). A frameshift insertion in FA2H causes a recessively inherited form of ichthyosis congenita in Chianina cattle. Molecular genetics and genomics : MGG, 296(6), pp. 1313-1322. Springer 10.1007/s00438-021-01824-8

Lynch, C; Oliveira Junior, G A; Schenkel, F S; Baes, C F (2021). Effect of synchronized breeding on genetic evaluations of fertility traits in dairy cattle. Journal of dairy science, 104(11), pp. 11820-11831. American Dairy Science Association 10.3168/jds.2021-20495

Leishman, Emily M; Ellis, Jennifer; van Staaveren, Nienke; Barbut, Shai; Vanderhout, Ryley J; Osborne, Vern R; Wood, Benjamin J; Harlander-Matauschek, Alexandra; Baes, Christine F. (2021). Meta-analysis to predict the effects of temperature stress on meat quality of poultry. Poultry science, 100(11), p. 101471. Elsevier 10.1016/j.psj.2021.101471

Liu, Yuanzhen; Henkel, Jan; Beaurepaire, Alexis; Evans, Jan D.; Neumann, Peter; Huang, Qiang (2021). Comparative genomics suggests local adaptations in the invasive small hive beetle. Ecology and evolution, 11(22), pp. 15780-15791. John Wiley & Sons, Inc. 10.1002/ece3.8242

Leeb, Tosso (2021). Domestic animal genetics. PLoS genetics, 17(10), e1009831. Public Library of Science 10.1371/journal.pgen.1009831

Letko, Anna; Bützberger, Charis; Hirter, Nathalie; Paris, Julia M.; Abril, Carlos; Drögemüller, Cord (2021). Genetic evaluation of small ruminant lentivirus susceptibility in Valais blacknose sheep. Animal genetics, 52(5), pp. 781-782. Wiley 10.1111/age.13108

Jenkins, Christopher A.; Dog Biomedical Variant Database, Consortium; Schofield, Ellen C.; Mellersh, Cathryn S.; De Risio, Luisa; Ricketts, Sally L. (2021). Improving the resolution of canine genome-wide association studies using genotype imputation: A study of two breeds. Animal genetics, 52(5), pp. 703-713. Wiley 10.1111/age.13117

Lühken, Gesine; Drögemüller, Cord (1 September 2021). Pourquoi les moutons et les chèvres ne sont-ils pas tous bicornes? Forum Kleinwiederkäuer, 9, pp. 6-11. Verlagsgenossenschaft Caprovis

Makanjuola, Bayode O.; Maltecca, Christian; Miglior, Filippo; Marras, Gabriele; Abdalla, Emhimad A.; Schenkel, Flavio S.; Baes, Christine F. (2021). Identification of unique ROH regions with unfavorable effects on production and fertility traits in Canadian Holsteins. Genetics selection evolution, 53(1), p. 68. BioMed Central 10.1186/s12711-021-00660-z

Bannasch, Danika L.; Kaelin, Christopher B; Letko, Anna; Loechel, Robert; Hug, Petra; Jagannathan, Vidhya; Henkel, Jan; Roosje, Petra; Hytönen, Marjo K; Lohi, Hannes; Arumilli, Meharji; Minor, Katie M; Mickelson, James R; Drögemüller, Cord; Barsh, Gregory S; Leeb, Tosso (2021). Dog colour patterns explained by modular promoters of ancient canid origin. Nature ecology & evolution, 5(10), pp. 1415-1423. Nature Publishing Group 10.1038/s41559-021-01524-x

Leeb, Tosso (12 August 2021). Genetic enigma solved: Inheritance of coat color patterns in dogs. Medienmitteilung Universität Bern

Tavares-Gomes, Leticia; Monney, Camille; Neuhaus, Géraldine; Francisco, David; Solis, Diana; Summerfield, Artur; Erny, Daniel; Jagannathan, Vidhya; Oevermann, Anna (2021). Transcriptome of microglia reveals a species-specific expression profile in bovines with conserved and new signature genes. GLIA, 69(8), pp. 1932-1949. Wiley-Blackwell 10.1002/glia.24002

Bauer, A.; Hadji Rasouliha, S.; Brunner, M. T.; Jagannathan, V.; Bucher, I.; Bannoehr, J.; Varjonen, K.; Bond, R.; Bergvall, K.; Welle, M. M.; Roosje, P.; Leeb, T. (2021). Corrigendum: A second KRT71 allele in curly coated dogs. Animal genetics, 52(4), p. 575. Wiley 10.1111/age.13098

Christen, Matthias; Högler, Sandra; Kleiter, Miriam; Leschnik, Michael; Weber, Corinna; Thaller, Denise; Jagannathan, Vidya; Leeb, Tosso (2021). Deletion of the SELENOP gene leads to CNS atrophy with cerebellar ataxia in dogs. PLoS genetics, 17(8), e1009716. Public Library of Science 10.1371/journal.pgen.1009716

Seymour, D J; Cánovas, A; Chud, T C S; Cant, J P; Osborne, V R; Baes, C F; Schenkel, F S; Miglior, F (2021). Associations between feed efficiency and aspects of lactation curves in primiparous Holstein dairy cattle. Journal of dairy science, 104(8), pp. 9304-9315. American Dairy Science Association 10.3168/jds.2020-20010

Oliveira Junior, G A; Schenkel, F S; Alcantara, L; Houlahan, K; Lynch, C; Baes, C F (2021). Estimated genetic parameters for all genetically evaluated traits in Canadian Holsteins. Journal of dairy science, 104(8), pp. 9002-9015. American Dairy Science Association 10.3168/jds.2021-20227

Emamgholi Begli, Hakimeh; Schaeffer, Lawrence R; Abdalla, Emhimad; Lozada-Soto, Emmanuel A; Harlander-Matauschek, Alexandra; Wood, Benjamin J; Baes, Christine F (2021). Genetic analysis of egg production traits in turkeys (Meleagris gallopavo) using a single-step genomic random regression model. Genetics, selection, evolution, 53(1), p. 61. BioMed Central 10.1186/s12711-021-00655-w

Laukner, Anna; Truchet, Laura; Manukjan, Georgi; Schulze, Harald; Langbein-Detsch, Ines; Mueller, Elisabeth; Leeb, Tosso; Kehl, Alexandra (2021). Effects of Cocoa Genotypes on Coat Color, Platelets and Coagulation Parameters in French Bulldogs. Genes, 12(7) MDPI, Molecular Diversity Preservation International 10.3390/genes12071092

Jacinto, Joana G. P.; Markey, Alysta D.; Veiga, Inês M. B.; Paris, Julia M.; Welle, Monika; Beever, Jonathan E.; Drögemüller, Cord (2021). A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle. Genes, 12(7), p. 1038. MDPI, Molecular Diversity Preservation International 10.3390/genes12071038

Bögeholz, Anke; Falker-Gieske, Clemens; Guélat, Monika; Gurtner, Corinne; Hunziker, Sibylle; Oevermann, Anna; Thaller, Georg; Drögemüller, Cord; Tetens, Jens (2021). GWAS Hits for Bilateral Convergent Strabismus with Exophthalmos in Holstein Cattle Using Imputed Sequence Level Genotypes. Genes, 12(7), p. 1039. MDPI, Molecular Diversity Preservation International 10.3390/genes12071039

Widmer, Sarah; Seefried, Franz R.; von Rohr, Peter; Häfliger, Irene M.; Spengeler, Mirjam; Drögemüller, Cord (2021). A major QTL at the LHCGR/FSHR locus for multiple birth in Holstein cattle. Genetics selection evolution, 53(1) BioMed Central 10.1186/s12711-021-00650-1

Butty, Adrien M; Chud, Tatiane C S; Cardoso, Diercles F; Lopes, Lucas S F; Miglior, Filippo; Schenkel, Flavio S; Cánovas, Angela; Häfliger, Irene M.; Drögemüller, Cord; Stothard, Paul; Malchiodi, Francesca; Baes, Christine F. (2021). Genome-wide association study between copy number variants and hoof health traits in Holstein dairy cattle. Journal of dairy science, 104(7), pp. 8050-8061. American Dairy Science Association 10.3168/jds.2020-19879

Jacinto, Joana G. P.; Häfliger, Irene M.; Gentile, Arcangelo; Drögemüller, Cord (2021). A Heterozygous Missense Variant in MAP2K2 in a Stillborn Romagnola Calf with Skeletal-Cardio-Enteric Dysplasia. Animals, 11(7), p. 1931. MDPI 10.3390/ani11071931

Leishman, Emily M; van Staaveren, Nienke; Mohr, Jeff; Wood, Benjamin J; Freeman, Nikole E; Newman, Amy E M; Harlander-Matauschek, Alexandra; Baes, Christine F (2021). The Effect of Egg Laying on Feather and Plasma Corticosterone Concentrations in Turkey (Meleagris gallopavo) Hens. Animals, 11(7) MDPI 10.3390/ani11071892

Eager, Katie L.M.; Cauchi, Monique; Willet, Cali E.; Häfliger, Irene M.; Drögemüller, Cord; O’Rourke, Brendon A.; Tammen, Imke (2021). The previously reported LRP4 c.4940C>T variant is not associated with syndactyly in cattle. Animal genetics, 52(3), pp. 380-381. Wiley 10.1111/age.13061

Henkel, Jan; Dubacher, Alexandra; Bangerter, Erika; Herren, Ursula; Ammann, Philippe; Drögemüller, Cord; Flury, Christine; Leeb, Tosso (2021). Introgression of ASIP and TYRP1 Alleles Explains Coat Color Variation in Valais Goats. Journal of heredity, 112(5), pp. 452-457. Oxford University Press 10.1093/jhered/esab024

Allais-Bonnet, Aurélie; Hintermann, Aurélie; Deloche, Marie-Christine; Cornette, Raphaël; Bardou, Philippe; Naval-Sanchez, Marina; Pinton, Alain; Haruda, Ashleigh; Grohs, Cécile; Zakany, Jozsef; Bigi, Daniele; Medugorac, Ivica; Putelat, Olivier; Greyvenstein, Ockert; Hadfield, Tracy; Jemaa, Slim Ben; Bunevski, Gjoko; Menzi, Fiona; Hirter, Nathalie; Paris, Julia M; ... (2021). Analysis of Polycerate Mutants Reveals the Evolutionary Co-option of HOXD1 for Horn Patterning in Bovidae. Molecular Biology and Evolution, 38(6), pp. 2260-2272. Oxford University Press 10.1093/molbev/msab021

Bertani, Valeria; Prioni, Simona; Di Lecce, Rosanna; Gazza, Ferdinando; Ragionieri, Luisa; Merialdi, Giuseppe; Bonilauri, Paolo; Jagannathan, Vidhya; Grassi, Sara; Cabitta, Livia; Paoli, Antonella; Morrone, Amelia; Sonnino, Sandro; Drögemüller, Cord; Cantoni, Anna Maria (2021). A pathogenic HEXA missense variant in wild boars with Tay-Sachs disease. Molecular genetics and metabolism, 133(3), pp. 297-306. Elsevier 10.1016/j.ymgme.2021.05.001

Quitt, Pia R; Brühschwein, Andreas; Matiasek, Kaspar; Wielaender, Franziska; Karkamo, Veera; Hytönen, Marjo K; Meyer-Lindenberg, Andrea; Dengler, Berett; Leeb, Tosso; Lohi, Hannes; Fischer, Andrea (2021). A hypomyelinating leukodystrophy in German Shepherd dogs. Journal of veterinary internal medicine, 35(3), pp. 1455-1465. Wiley-Blackwell 10.1111/jvim.16085

Altermatt, N.; Dolf, G.; Ramseyer, A.; Burger, D.; Gerber, V. (2021). [Prevalence of health problems in midlife Swiss warm-blooded horses]. Schweizer Archiv für Tierheilkunde, 163(5), pp. 339-350. Gesellschaft Schweizer Tierärztinnen und Tierärzte 10.17236/sat00301

Trigo, Beatriz B.; Utsunomiya, Adam T. H.; Fortunato, Alvaro A. A. D.; Milanesi, Marco; Torrecilha, Rafaela B. P.; Lamb, Harrison; Nguyen, Loan; Ross, Elizabeth M.; Hayes, Ben; Padula, Rômulo C. M.; Sussai, Thayla S.; Zavarez, Ludmilla B.; Cipriano, Rafael S.; Caminhas, Maria M. T.; Lopes, Flavia L.; Pelle, Cassiano; Leeb, Tosso; Bannasch, Danika; Bickhart, Derek; Smith, Timothy P. L.; ... (2021). Variants at the ASIP locus contribute to coat color darkening in Nellore cattle. Genetics, selection, evolution, 53(1), p. 40. BioMed Central 10.1186/s12711-021-00633-2

Kuca, Thibaud; Marron, Brandy M; Pontes Jacinto, Joana Goncalves; Paris, Julia M.; Gerspach, Christian; Beever, Jonathan E; Drögemüller, Cord (2021). A Nonsense Variant in Hephaestin Like 1 (HEPHL1) Is Responsible for Congenital Hypotrichosis in Belted Galloway Cattle. Genes, 12(5) MDPI, Molecular Diversity Preservation International 10.3390/genes12050643

Houlahan, Kerry; Schenkel, Flavio S; Hailemariam, Dagnachew; Lassen, Jan; Kargo, Morten; Cole, John B; Connor, Erin E; Wegmann, Silvia; Junior, Oliveira; Miglior, Filippo; Fleming, Allison; Chud, Tatiane C S; Baes, Christine F (2021). Effects of Incorporating Dry Matter Intake and Residual Feed Intake into a Selection Index for Dairy Cattle Using Deterministic Modeling. Animals, 11(4) MDPI 10.3390/ani11041157

Balmer, Pierre; Hariton, William V. J.; Sayar, Beyza; Jagannathan, Vidhya; Galichet, Arnaud; Leeb, Tosso; Roosje, Petra; Müller, Eliane J. (2021). SUV39H2 epigenetic silencing controls fate conversion of epidermal stem and progenitor cells. Journal of cell biology, 220(4) Rockefeller Institute Press 10.1083/jcb.201908178

Jacinto, Joana G. P.; Häfliger, Irene M.; Gentile, Arcangelo; Drögemüller, Cord; Bolcato, Marilena (2021). A 6.7 kb deletion in the COL2A1 gene in a Holstein calf with achondrogenesis type II and perosomus elumbis. Animal genetics, 52(2), pp. 244-245. Wiley 10.1111/age.13033

Brands, Jan; Steffen, Frank; Spennes, Jochen; Leeb, Tosso; Bilzer, Thomas (2021). COL6A1 related muscular dystrophy in Landseer dogs - a canine model for Ullrich congenital muscular dystrophy. Muscle & nerve, 63(4), pp. 608-616. John Wiley & Sons 10.1002/mus.27162

Oliveira Junior, G A; Schaeffer, L R; Schenkel, F; Tiezzi, F; Baes, C F (2021). Potential effects of hormonal synchronized breeding on genetic evaluations of fertility traits in dairy cattle: A simulation study. Journal of dairy science, 104(4), pp. 4404-4412. American Dairy Science Association 10.3168/jds.2020-18944

Gallina, Laura; Koch, Michel C.; Gentile, Arcangelo; Treglia, Ida; Bombardi, Cristiano; Mandrioli, Luciana; Bolcato, Marilena; Scagliarini, Alessandra; Drögemüller, Cord; Seuberlich, Torsten; Ciulli, Sara (2021). Bovine viral diarrhoea virus 1b infection associated with congenital tremor and hypomyelination in Holstein calves. Veterinary microbiology, 256, p. 109047. Elsevier 10.1016/j.vetmic.2021.109047

Flury, Christine; Bangerter, Erika; Drögemüller, Cord (10 March 2021). Efficace et précis: le génotypage SNP ouvre de nouvelles perspectives en sélection caprine. Forum Kleinwiederkäuer(3) Verlagsgenossenschaft Caprovis

Hirter, Nathalie; Drögemüller, Cord (3 March 2021). L’entropion chez le mouton: la génétique décide. Forum Kleinwiederkäuer, 3 Verlagsgenossenschaft Caprovis

O’Toole, Donal; Häfliger, Irene M.; Leuthard, Fabienne; Schumaker, Brant; Steadman, Lynn; Murphy, Brian; Drögemüller, Cord; Leeb, Tosso (2021). X-Linked Hypohidrotic Ectodermal Dysplasia in Crossbred Beef Cattle Due to a Large Deletion in EDA. Animals, 11(3), p. 657. MDPI 10.3390/ani11030657

Jacinto, Joana G. P.; Häfliger, Irene M.; McEvoy, Fintan J.; Drögemüller, Cord; Agerholm, Jørgen S. (2021). A De Novo Mutation in COL1A1 in a Holstein Calf with Osteogenesis Imperfecta Type II. Animals, 11(2) MDPI 10.3390/ani11020561

Abdalla, Emhimad A.; Wood, Benjamin J.; Baes, Christine F. (2021). Accuracy of breeding values for production traits in turkeys (Meleagris gallopavo) using recursive models with or without genomics. Genetics, selection, evolution, 53(1), p. 16. BioMed Central 10.1186/s12711-021-00611-8

Ani, A O; Baes, C; Chemineau, P; Gauly, M; Jiménez-Flores, R; Kashiwazaki, N; Kegley, E B; Kembe, M A; Loh, T C; Maiwashe, A; Medina-Villacìs, M; Rosati, A (2021). Opinion paper: COVID-19 and the livestock sector. Animal, 15(2), p. 100102. Elsevier 10.1016/j.animal.2020.100102

van Staaveren, Nienke; Ellis, Jennifer; Baes, Christine F.; Harlander-Matauschek, Alexandra (2021). A meta-analysis on the effect of environmental enrichment on feather pecking and feather damage in laying hens. Poultry science, 100(2), pp. 397-411. Elsevier 10.1016/j.psj.2020.11.006

Gerber, Nadja; Brunner, Magdalena A. T.; Jagannathan, Vidya; Leeb, Tosso; Gerhards, Nora M.; Welle, Monika M.; Dettwiler, Martina (2021). Transcriptional Differences between Canine Cutaneous Epitheliotropic Lymphoma and Immune-Mediated Dermatoses. Genes, 12(2) MDPI, Molecular Diversity Preservation International 10.3390/genes12020160

Massender, Erin; Brito, Luiz F.; Cánovas, Angela; Baes, Christine F.; Kennedy, Delma; Schenkel, Flavio S. (2021). The value of incorporating carcass trait phenotypes in terminal sire selection indexes to improve carcass weight and quality of heavy lambs. Journal of animal breeding and genetics, 138(1), pp. 91-107. Wiley-Blackwell 10.1111/jbg.12484

Letko, Anna; Strugnell, Ben; Häfliger, Irene M.; Paris, Julia M.; Waine, Katie; Drögemüller, Cord; Scholes, Sandra (2021). Compound heterozygous PLA2G6 loss-of-function variants in Swaledale sheep with neuroaxonal dystrophy. Molecular genetics and genomics : MGG, 296(1), pp. 235-242. Springer 10.1007/s00438-020-01742-1

Unger, Lucia; Abril, Carlos; Gerber, Vinzenz; Jagannathan, Vidhya; Koch, Christoph; Hamza, Eman (2021). Diagnostic potential of three serum microRNAs as biomarkers for equine sarcoid disease in horses and donkeys. Journal of veterinary internal medicine, 35(1), pp. 610-619. Wiley-Blackwell 10.1111/jvim.16027

Richardson, C M; Baes, C F; Amer, P R; Quinton, C; Hely, F; Osborne, V R; Pryce, J E; Hailemariam, D; Miglior, F (2021). Estimating the environmental impact of dairy cattle breeding programs through emission intensity. Animal, 15(1), p. 100005. Elsevier 10.1016/j.animal.2020.100005

De Preux, Mathieu; Gurtner, Corinne; Klebic, Ismar; Waschk, Maja Alice; Drögemüller, Cord; Brünisholz, Hervé Paul (2021). Skeletal metastasis from a squamous cell carcinoma of the nictitating membrane in a Haflinger horse. Equine veterinary education, 33(5) Wiley-Blackwell 10.1111/eve.13180

Letko, Anna; Schauer, Alexandria Marie; Derks, Martijn F. L.; Grau-Roma, Llorenç; Drögemüller, Cord; Grahofer, Alexander (2021). Phenotypic and Genomic Analysis of Cystic Hygroma in Pigs. Genes, 12(2), p. 207. MDPI, Molecular Diversity Preservation International 10.3390/genes12020207

Jacinto, Joana G. P.; Häfliger, Irene M.; Borel, Nicole; Zanolari, Patrik; Drögemüller, Cord; Veiga, Inês M. B. (2021). Clinicopathological and Genomic Characterization of a Simmental Calf with Generalized Bovine Juvenile Angiomatosis. Animals, 11(3) MDPI 10.3390/ani11030624

Christen, Matthias; Janzen, Nils; Fraser, Anne; Sewell, Adrian C.; Jagannathan, Vidhya; Guevar, Julien; Leeb, Tosso; Sanchez-Masian, Daniel (2021). L2HGDH Missense Variant in a Cat with L-2-Hydroxyglutaric Aciduria. Genes, 12(5), p. 682. MDPI, Molecular Diversity Preservation International 10.3390/genes12050682

Jagannathan, Vidya; Hitte, Christophe; Kidd, Jeffrey M.; Masterson, Patrick; Murphy, Terence D.; Emery, Sarah; Davis, Brian; Buckley, Reuben M.; Liu, Yan-Hu; Zhang, Xiang-Quan; Leeb, Tosso; Zhang, Ya-Ping; Ostrander, Elaine A.; Wang, Guo-Dong (2021). Dog10K_Boxer_Tasha_1.0: A Long-Read Assembly of the Dog Reference Genome. Genes, 12(6) MDPI, Molecular Diversity Preservation International 10.3390/genes12060847

Kiener, Sarah; Ribi, Camillo; Keller, Irene; Chizzolini, Carlo; Trendelenburg, Marten; Huynh-Do, Uyen; von Kempis, Johannes; Leeb, Tosso (2021). Variants Affecting the C-Terminal Tail of UNC93B1 Are Not a Common Risk Factor for Systemic Lupus Erythematosus. Genes, 12(8), p. 1268. MDPI, Molecular Diversity Preservation International 10.3390/genes12081268

Kiener, Sarah; Cikota, Robert; Welle, Monika; Jagannathan, Vidhya; Åhman, Susanne; Leeb, Tosso (2021). A Missense Variant in SLC39A4 in a Litter of Turkish Van Cats with Acrodermatitis Enteropathica. Genes, 12(9), p. 1309. MDPI, Molecular Diversity Preservation International 10.3390/genes12091309

Adams, Sarah M.; Derks, Martijn F. L.; Makanjuola, Bayode O.; Marras, Gabriele; Wood, Ben J.; Baes, Christine F. (2021). Investigating inbreeding in the turkey (Meleagris gallopavo) genome. Poultry science, 100(11), p. 101366. Elsevier 10.1016/j.psj.2021.101366

Christen, Matthias; de le Roi, Madeleine; Jagannathan, Vidhya; Becker, Kathrin; Leeb, Tosso (2021). MYO5A Frameshift Variant in a Miniature Dachshund with Coat Color Dilution and Neurological Defects Resembling Human Griscelli Syndrome Type 1. Genes, 12(10), p. 1479. MDPI, Molecular Diversity Preservation International 10.3390/genes12101479

Christen, Matthias; Booij-Vrieling, Henriëtte; Oksa-Minalto, Jelena; de Vries, Cynthia; Kehl, Alexandra; Jagannathan, Vidhya; Leeb, Tosso (2021). MIA3 Splice Defect in Cane Corso Dogs with Dental-Skeletal-Retinal Anomaly (DSRA). Genes, 12(10), p. 1497. MDPI, Molecular Diversity Preservation International 10.3390/genes12101497

Rudd Garces, Gabriela; Turba, Maria Elena; Muracchini, Myriam; Diana, Alessia; Jagannathan, Vidhya; Gentilini, Fabio; Leeb, Tosso (2021). PRKG2 Splice Site Variant in Dogo Argentino Dogs with Disproportionate Dwarfism. Genes, 12(10), p. 1489. MDPI, Molecular Diversity Preservation International 10.3390/genes12101489

Christen, Matthias; Indzhova, Victoria; Guo, Ling T.; Jagannathan, Vidhya; Leeb, Tosso; Shelton, G. Diane; Brocal, Josep (2021). LAMA2 Nonsense Variant in an Italian Greyhound with Congenital Muscular Dystrophy. Genes, 12(11), p. 1823. MDPI, Molecular Diversity Preservation International 10.3390/genes12111823

Rudd Garces, Gabriela; Knebel, Anna; Hülskötter, Kirsten; Jagannathan, Vidhya; Störk, Theresa; Hewicker-Trautwein, Marion; Leeb, Tosso; Volk, Holger A. (2021). LTBP3 Frameshift Variant in British Shorthair Cats with Complex Skeletal Dysplasia. Genes, 12(12), p. 1923. MDPI, Molecular Diversity Preservation International 10.3390/genes12121923

Leishman, Emily M.; van Staaveren, Nienke; Osborne, Vern R.; Wood, Benjamin J.; Baes, Christine F.; Harlander-Matauschek, Alexandra (2021). A Cross-Sectional Study on the Prevalence of Footpad Dermatitis in Canadian Turkeys. Frontiers in animal science, 2 Frontiers Media 10.3389/fanim.2021.726907

Cosandey, Jeanne; Hamza, Eman; Gerber, Vinzenz; Ramseyer, Alessandra; Leeb, Tosso; Jagannathan, Vidhya; Blaszczyk, Klaudia; Unger, Lucia (2021). Diagnostic and prognostic potential of eight whole blood microRNAs for equine sarcoid disease. PLoS ONE, 16(12), e0261076. Public Library of Science 10.1371/journal.pone.0261076

2020

Garcia, Teresa Maria; Kiener, Sarah; Jagannathan, Vidhya; Russell, Duncan S; Leeb, Tosso (2020). A COL7A1 Variant in a Litter of Neonatal Basset Hounds with Dystrophic Epidermolysis Bullosa. Genes, 11(12), p. 1458. MDPI, Molecular Diversity Preservation International 10.3390/genes11121458

Murgiano, Leonardo; Becker, Doreen; Spector, Courtney; Carlin, Kendall; Santana, Evelyn; Niggel, Jessica K; Jagannathan, Vidya; Leeb, Tosso; Pearce-Kelling, Sue; Aguirre, Gustavo D; Miyadera, Keiko (2020). CCDC66 frameshift variant associated with a new form of early-onset progressive retinal atrophy in Portuguese Water Dogs. Scientific reports, 10(1), p. 21162. Springer Nature 10.1038/s41598-020-77980-5

Jost, Stéphanie Mali; Drögemüller, Cord; Zanolari, Patrik (2 December 2020). Particularités génétiques chez les petits camélidés. Forum Kleinwiederkäuer(12), pp. 14-20. Verlagsgenossenschaft Caprovis

Leishman, Emily M; van Staaveren, Nienke; McIntyre, Don R; Mohr, Jeff; Wood, Benjamin J; Baes, Christine F; Harlander-Matauschek, Alexandra (2020). Describing the growth and molt of modern domestic turkey (Meleagris gallopavo) primary wing feathers. Journal of animal science, 98(12) Oxford University Press 10.1093/jas/skaa373

Paris, J. M.; Letko, A.; Häfliger, I. M.; Ammann, P.; Drögemüller, C. (2020). Ear type in sheep is associated with the MSRB3 locus. Animal genetics, 51(6), pp. 968-972. Wiley 10.1111/age.12994

Häfliger, Irene Monika; Agerholm, Jørgen Steen; Drögemüller, Cord (2020). Constitutional trisomy 20 in an aborted Holstein fetus with pulmonary hypoplasia and anasarca syndrome. Animal genetics, 51(6), pp. 988-989. Wiley 10.1111/age.13008

Abdalla, E. A.; Id-Lahoucine, S.; Cánovas, A.; Casellas, J.; Schenkel, F. S.; Wood, B. J.; Baes, C. F. (2020). Discovering lethal alleles across the turkey genome using a transmission ratio distortion approach. Animal genetics, 51(6), pp. 876-889. Wiley 10.1111/age.13003

Letko, Anna; Minor, Katie M; Friedenberg, Steven G; Shelton, G Diane; Salvador, Jill Pesayco; Mandigers, Paul J J; Leegwater, Peter A J; Winkler, Paige A; Petersen-Jones, Simon M; Stanley, Bryden J; Ekenstedt, Kari J; Johnson, Gary S; Hansen, Liz; Jagannathan, Vidya; Mickelson, James R; Drögemüller, Cord (2020). A CNTNAP1 Missense Variant Is Associated with Canine Laryngeal Paralysis and Polyneuropathy. Genes, 11(12) MDPI, Molecular Diversity Preservation International 10.3390/genes11121426

Letko, Anna; Minor, Katie M; Jagannathan, Vidhya; Seefried, Franz R; Mickelson, James R; Oliehoek, Pieter; Drögemüller, Cord (2020). Correction to: Genomic diversity and population structure of the Leonberger dog breed. Genetics, selection, evolution, 52(1), p. 70. BioMed Central 10.1186/s12711-020-00590-2

Monckton, Valerie; van Staaveren, Nienke; Baes, Christine F; Balzani, Agnese; Kwon, Isabelle Y; McBride, Peter; Harlander-Matauschek, Alexandra (2020). Are Turkeys (Meleagris gallopavo) Motivated to Avoid Excreta-Soiled Substrate? Animals, 10(11) MDPI 10.3390/ani10112015

Syrjä, Pernilla; Palviainen, Mari; Jokinen, Tarja; Kyöstilä, Kaisa; Lohi, Hannes; Roosje, Petra; Anderegg, Linda; Leeb, Tosso; Sukura, Antti; Eskelinen, Eeva-Liisa (2020). Altered Basal Autophagy Affects Extracellular Vesicle Release in Cells of Lagotto Romagnolo Dogs With a Variant ATG4D. Veterinary pathology, 57(6), pp. 926-935. Sage 10.1177/0300985820959243

Jacinto, Joana G. P.; Häfliger, Irene M.; Veiga, Inês M. B.; Drögemüller, Cord; Agerholm, Jørgen S. (2020). A de novo mutation in KRT5 in a crossbred calf with epidermolysis bullosa simplex. Journal of veterinary internal medicine, 34(6), pp. 2800-2807. Wiley-Blackwell 10.1111/jvim.15943

Leishman, Emily M.; Freeman, Nikole E.; Newman, Amy E. M.; van Staaveren, Nienke; Wood, Benjamin J.; Harlander-Matauschek, Alexandra; Baes, Christine F. (2020). Research Note: Quantifying corticosterone in turkey (Meleagris gallopavo) feathers using ELISA. Poultry science, 99(11), pp. 5261-5264. Elsevier 10.1016/j.psj.2020.06.075

Pontes Jacinto, Joana Goncalves; Häfliger, Irene M.; Veiga, Inês M. B.; Letko, Anna; Benazzi, Cinzia; Bolcato, Marilena; Drögemüller, Cord (2020). A Heterozygous Missense Variant in the COL5A2 in Holstein Cattle Resembling the Classical Ehlers–Danlos Syndrome. Animals, 10(11), p. 2002. MDPI 10.3390/ani10112002

Christen, Matthias; Austel, Michaela; Banovic, Frane; Jagannathan, Vidhya; Leeb, Tosso (2020). NSDHL Frameshift Deletion in a Mixed Breed Dog with Progressive Epidermal Nevi. Genes, 11(11) MDPI, Molecular Diversity Preservation International 10.3390/genes11111297

Drögemüller, Michaela; Letko, Anna; Matiasek, Kaspar; Jagannathan, Vidhya; Corlazzoli, Daniele; Rosati, Marco; Jurina, Konrad; Medl, Susanne; Gödde, Thomas; Rupp, Stefan; Fischer, Andrea; Luján Feliu-Pascual, Alejandro; Drögemüller, Cord (2020). SLC19A3 Loss-of-Function Variant in Yorkshire Terriers with Leigh-Like Subacute Necrotizing Encephalopathy. Genes, 11(10), p. 1215. MDPI, Molecular Diversity Preservation International 10.3390/genes11101215

Letko, Anna; Minor, Katie M.; Jagannathan, Vidya; Seefried, Franz R.; Mickelson, James R.; Oliehoek, Pieter; Drögemüller, Cord (2020). Genomic diversity and population structure of the Leonberger dog breed. Genetics, selection, evolution, 52(1), p. 61. BioMed Central 10.1186/s12711-020-00581-3

Brunetti, Barbara; Muscatello, Luisa V; Letko, Anna; Papa, Valentina; Cenacchi, Giovanna; Grillini, Marco; Murgiano, Leonardo; Jagannathan, Vidya; Drögemüller, Cord (2020). X-Linked Duchenne-Type Muscular Dystrophy in Jack Russell Terrier Associated with a Partial Deletion of the Canine DMD Gene. Genes, 11(10) MDPI, Molecular Diversity Preservation International 10.3390/genes11101175

Falker-Gieske, Clemens; Iffland, Hanna; Preuß, Siegfried; Bessei, Werner; Drögemüller, Cord; Bennewitz, Jörn; Tetens, Jens (2020). Meta-analyses of genome wide association studies in lines of laying hens divergently selected for feather pecking using imputed sequence level genotypes. BMC genetics, 21(1), p. 114. BioMed Central 10.1186/s12863-020-00920-9

Dettwiler, M.; Leuthard, F.; Bauer, A.; Jagannathan, V.; Lourenço, A. M.; Pereira, H.; Leeb, T.; Welle, M. M. (2020). A nonsense variant in the KRT14 gene in a domestic shorthair cat with epidermolysis bullosa simplex. Animal genetics, 51(5), pp. 829-832. Wiley 10.1111/age.12979

Letko, Anna; Dijkman, Reinie; Strugnell, Ben; Häfliger, Irene M.; Paris, Julia M.; Henderson, Katrina; Geraghty, Tim; Orr, Hannah; Scholes, Sandra; Drögemüller, Cord (2020). Deleterious AGXT Missense Variant Associated with Type 1 Primary Hyperoxaluria (PH1) in Zwartbles Sheep. Genes, 11(10) MDPI, Molecular Diversity Preservation International 10.3390/genes11101147

Hulliger, Matthias F.; Pacholewska, Alicja; Vargas, Amandine; Lavoie, Jean-Pierre; Leeb, Tosso; Gerber, Vinzenz; Jagannathan, Vidya (2020). An Integrative miRNA-mRNA Expression Analysis Reveals Striking Transcriptomic Similarities between Severe Equine Asthma and Specific Asthma Endotypes in Humans. Genes, 11(10) MDPI, Molecular Diversity Preservation International 10.3390/genes11101143

Jost, Stéphanie Mali; Knoll, Andrea; Lühken, Gesine; Drögemüller, Cord; Zanolari, Patrik (2020). Prevalence of coat colour traits and congenital disorders of South American camelids in Austria, Germany and Switzerland. Acta Veterinaria Scandinavica, 62(1), p. 56. BioMed Central Ltd. 10.1186/s13028-020-00554-y

Pontes Jacinto, Joana Goncalves; Häfliger, Irene Monika; Letko, Anna; Drögemüller, Cord; Agerholm, Jørgen Steen (2020). A large deletion in the COL2A1 gene expands the spectrum of pathogenic variants causing bulldog calf syndrome in cattle. Acta Veterinaria Scandinavica, 62(1), p. 49. BioMed Central Ltd. 10.1186/s13028-020-00548-w

Kiener, Sarah; Laprais, Aurore; Mauldin, Elizabeth A; Jagannathan, Vidya; Olivry, Thierry; Leeb, Tosso (2020). LAMB3 Missense Variant in Australian Shepherd Dogs with Junctional Epidermolysis Bullosa. Genes, 11(9) MDPI, Molecular Diversity Preservation International 10.3390/genes11091055

Vernau, Karen M; Struys, Eduard; Letko, Anna; Woolard, Kevin D; Aguilar, Miriam; Brown, Emily A; Cissell, Derek D; Dickinson, Peter J; Shelton, G Diane; Broome, Michael R; Gibson, K Michael; Pearl, Phillip L; König, Florian; Van Winkle, Thomas J; O'Brien, Dennis; Roos, B; Matiasek, Kaspar; Jagannathan, Vidya; Drögemüller, Cord; Mansour, Tamer A; ... (2020). A Missense Variant in ALDH5A1 Associated with Canine Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD) in the Saluki Dog. Genes, 11(9) MDPI, Molecular Diversity Preservation International 10.3390/genes11091033

Hauser, M.; Wolf-Hofstetter, S.; Acklin-Menzi, F.; Studer, E.; Rediger, D.; Seefried, F. R.; Drögemüller, C. (2020). Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed. Schweizer Archiv für Tierheilkunde, 162(9), pp. 551-559. Gesellschaft Schweizer Tierärztinnen und Tierärzte 10.17236/sat00272

Makanjuola, Bayode O.; Maltecca, Christian; Miglior, Filippo; Schenkel, Flavio S.; Baes, Christine F. (2020). Effect of recent and ancient inbreeding on production and fertility traits in Canadian Holsteins. BMC Genomics, 21(1), p. 605. BioMed Central 10.1186/s12864-020-07031-w

Joller, Sara; Häfliger, Irene M.; Drögemüller, Cord; Richard, Olivia K.; Grahofer, Alexander (2020). Thrombocytopenic purpura on an organic farm with pen mating: a case report on the re-emergence of an old disease. Porcine health management, 6(1) BioMed Central 10.1186/s40813-020-00157-z

Wiener, Dominique J.; Groch, Kátia R.; Brunner, Magdalena A. T.; Leeb, Tosso; Jagannathan, Vidya; Welle, Monika M. (2020). Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis. Genes, 11(8) MDPI, Molecular Diversity Preservation International 10.3390/genes11080884

Bannasch, Danika L.; Baes, Christine F.; Leeb, Tosso (2020). Genetic Variants Affecting Skeletal Morphology in Domestic Dogs. Trends in genetics, 36(8), pp. 598-609. Elsevier 10.1016/j.tig.2020.05.005

Rostaher, Ana; Dolf, Gaudenz; Fischer, Nina Maria; Silaghi, Cornelia; Akdis, Cezmi; Zwickl, Lena; Audergon, Sabrina; Favrot, Claude (2020). Atopic dermatitis in a cohort of West Highland white terriers in Switzerland. Part II: estimates of early life factors and heritability. Veterinary dermatology, 31(4), 276-e66. Wiley 10.1111/vde.12843

Batcher, Kevin; Dickinson, Peter; Maciejczyk, Kimberly; Brzeski, Kristin; Hadji Rasouliha, Sheida; Letko, Anna; Drögemüller, Cord; Leeb, Tosso; Bannasch, Danika (2020). Multiple FGF4 Retrocopies Recently Derived within Canids. Genes, 11(8) MDPI, Molecular Diversity Preservation International 10.3390/genes11080839

Nessler, Jasmin; Hug, Petra; Mandigers, Paul J J; Leegwater, Peter A J; Jagannathan, Vidya; Das, Anibh M; Rosati, Marco; Matiasek, Kaspar; Sewell, Adrian C; Kornberg, Marion; Hoffmann, Marina; Wolf, Petra; Fischer, Andrea; Tipold, Andrea; Leeb, Tosso (2020). Mitochondrial PCK2 Missense Variant in Shetland Sheepdogs with Paroxysmal Exercise-Induced Dyskinesia (PED). Genes, 11(7) MDPI, Molecular Diversity Preservation International 10.3390/genes11070774

van Staaveren, Nienke; Leishman, Emily M; Adams, Sarah M; Wood, Benjamin J; Harlander-Matauschek, Alexandra; Baes, Christine F. (2020). Housing and Management of Turkey Flocks in Canada. Animals, 10(7) MDPI 10.3390/ani10071159

Murgiano, Leonardo; Militerno, Gianfranco; Sbarra, Fiorella; Drögemüller, Cord; Jacinto, Joana G. P.; Gentile, Arcangelo; Bolcato, Marilena (2020). KDM2B‐associated paunch calf syndrome in Marchigiana cattle. Journal of veterinary internal medicine, 34(4), pp. 1657-1661. Wiley 10.1111/jvim.15789

Kiener, Sarah; Kehl, Alexandra; Loechel, Robert; Langbein-Detsch, Ines; Müller, Elisabeth; Bannasch, Danika; Jagannathan, Vidya; Leeb, Tosso (2020). Novel Brown Coat Color (Cocoa) in French Bulldogs Results from a Nonsense Variant in HPS3. Genes, 11(6) MDPI, Molecular Diversity Preservation International 10.3390/genes11060636

Brunner, Magdalena A. T.; Berenguer Veiga, Inês Margarida; Niggeler, Allegra; Häfliger, Irene M.; Stettler, Manuela; Meylan, Mireille; Welle, Monika; Drögemüller, Cord (2020). Is a de novo nonsense variant in the ASPDH gene the cause of ulcerative skin lesions in a Holstein calf? Veterinary dermatology, 31(3), 244-e54. Wiley 10.1111/vde.12827

Simon, R; Lischer, H. E. L.; Pieńkowska-Schelling, A.; Keller, I.; Häfliger, I. M.; Letko, A.; Schelling, C; Lühken, G; Drögemüller, C. (2020). New genomic features of the polled intersex syndrome variant in goats unraveled by long-read whole-genome sequencing. Animal genetics, 51(3), pp. 439-448. Wiley 10.1111/age.12918

Häfliger, I. M.; Hirter, N.; Paris, J. M.; Wolf Hofstetter, S.; Seefried, F R; Drögemüller, C. (2020). A de novo germline mutation of KIT in a white-spotted Brown Swiss cow. Animal genetics, 51(3), pp. 449-452. Wiley 10.1111/age.12920

Häfliger, I. M.; Wiedemar, N.; Švara, T; Starič, J; Cociancich, V; Šest, K; Gombač, M; Paller, T; Agerholm, J S; Drögemüller, C. (2020). Identification of small and large genomic candidate variants in bovine pulmonary hypoplasia and anasarca syndrome. Animal genetics, 51(3), pp. 382-390. Wiley 10.1111/age.12923

Häfliger, I. M.; Letko, A.; Murgiano, L.; Drögemüller, C. (2020). De novo stop-lost germline mutation in FGFR3 causes severe chondrodysplasia in the progeny of a Holstein bull. Animal genetics, 51(3), pp. 466-469. Wiley 10.1111/age.12934

Makanjuola, Bayode O.; Miglior, Filippo; Abdalla, Emhimad A.; Maltecca, Christian; Schenkel, Flavio S.; Baes, Christine F. (2020). Effect of genomic selection on rate of inbreeding and coancestry and effective population size of Holstein and Jersey cattle populations. Journal of dairy science, 103(6), pp. 5183-5199. American Dairy Science Association 10.3168/jds.2019-18013

Naylor, D.; Sharma, A.; Li, Z.; Monteith, G.; Sullivan, T.; Canovas, A.; Mallard, B. A.; Baes, C.; Karrow, N. A. (2020). Short communication: Characterizing ovine serum stress biomarkers during endotoxemia. Journal of dairy science, 103(6), pp. 5501-5508. American Dairy Science Association 10.3168/jds.2019-17718

Maltecca, C.; Tiezzi, F.; Cole, J. B.; Baes, C. (2020). Symposium review: Exploiting homozygosity in the era of genomics-Selection, inbreeding, and mating programs. Journal of dairy science, 103(6), pp. 5302-5313. American Dairy Science Association 10.3168/jds.2019-17846

Miglior, F; Baes, C F; Lourenco, D; Penagaricano, F; Heins, B (2020). Introduction: ADSA and Interbull Joint Breeding and Genetics Symposia. Journal of dairy science, 103(6), pp. 5275-5277. American Dairy Science Association 10.3168/jds.2020-18666

Häfliger, Irene M.; Sickinger, Marlene; Holsteg, Mark; Raeder, Leif M.; Henrich, Manfred; Marquardt, Siegfried; Drögemüller, Cord; Lühken, Gesine (2020). An IL17RA frameshift variant in a Holstein cattle family with psoriasis-like skin alterations and immunodeficiency. BMC genetics, 21(1) BioMed Central 10.1186/s12863-020-00860-4

Grilz-Seger, Gertrud; Reiter, Simone; Neuditschko, Markus; Wallner, Barbara; Rieder, Stefan; Leeb, Tosso; Jagannathan, Vidya; Mesarič, Matjaz; Cotman, Markus; Pausch, Hubert; Lindgren, Gabriella; Velie, Brandon; Horna, Michaela; Brem, Gottfried; Druml, Thomas (2020). A Genome-Wide Association Analysis in Noriker Horses Identifies a SNP Associated With Roan Coat Color. Journal of equine veterinary science, 88, p. 102950. Elsevier 10.1016/j.jevs.2020.102950

Alves, Kristen; Brito, Luiz F.; Baes, Christine F.; Sargolzaei, Mehdi; Robinson, John Andrew B.; Schenkel, Flavio S. (2020). Estimation of additive and non-additive genetic effects for fertility and reproduction traits in North American Holstein cattle using genomic information. Journal of animal breeding and genetics, 137(3), pp. 316-330. Wiley-Blackwell 10.1111/jbg.12466

Linek, Monika; Doelle, Maren; Leeb, Tosso; Bauer, Anina; Leuthard, Fabienne; Henkel, Jan; Bannasch, Danika; Jagannathan, Vidya; Welle, Monika M. (2020). ATP2A2 SINE Insertion in an Irish Terrier with Darier Disease and Associated Infundibular Cyst Formation. Genes, 11(5) MDPI, Molecular Diversity Preservation International 10.3390/genes11050481

Backel, Katherine A.; Kiener, Sarah; Jagannathan, Vidya; Casal, Margret L.; Leeb, Tosso; Mauldin, Elizabeth A. (2020). A DSG1 Frameshift Variant in a Rottweiler Dog with Footpad Hyperkeratosis. Genes, 11(4) MDPI, Molecular Diversity Preservation International 10.3390/genes11040469

Baes, Christine; Schenkel, Flavio (2020). The Future of Phenomics. Animal frontiers, 10(2), pp. 4-5. Oxford University Press 10.1093/af/vfaa013

Brito, Luiz; Rojay de Oliveira, Hinaya; Houlahan, Kerry; Fonseca, Pablo; Lam, Stephanie; Butty, Adrien; Seymour, David; Vargas, Giovanna; Chud, Tatiana; Silva, Fabiola; Baes, Christine; Canovas, Angela; Schenkel, Flavio (2020). Genetic mechanisms underlying feed utilization and implementation of genomic selection for improved feed efficiency in dairy cattle. Canadian journal of animal science, 100(4), pp. 587-604. Canadian Science Publishing 10.1139/CJAS-2019-0193

Labroussaa, Fabien; Thomann, Andreas; Nicholson, Pamela; Falquet, Laurent; Jores, Jörg (2020). Complete Genome Sequence of Mycoplasma feriruminatoris Strain IVB14/OD_0535, Isolated from an Alpine Ibex in a Swiss Zoo. Microbiology resource announcements, 9(12) American Society for Microbiology 10.1128/MRA.01528-19

Gurtner, Corinne; Hug, Petra; Kleiter, Miriam; Köhler, Kernt; Dietschi, Elisabeth; Jagannathan, Vidya; Leeb, Tosso (2020). YARS2 Missense Variant in Belgian Shepherd Dogs with Cardiomyopathy and Juvenile Mortality. Genes, 11(3) MDPI 10.3390/genes11030313

Hirter, Nathalie; Letko, Anna; Häfliger, Irene Monika; Becker, Doreen; Greber, Deborah; Drögemüller, Cord (2020). A genome-wide significant association on chromosome 15 for congenital entropion in Swiss White Alpine sheep. Animal genetics, 51(2), pp. 278-283. Wiley 10.1111/age.12903

Nayeri, Shadi; Schenkel, Flavio S.; Martin, Pauline; Fleming, Allison; Jamrozik, Janusz; Malchiodi, Francesca; Brito, Luiz F.; Baes, Christine F.; Sargolzaei, Mehdi; Miglior, Filippo (2020). Estimation of genetic parameters for mid-infrared-predicted lactoferrin and milk fat globule size in Holstein cattle. Journal of dairy science, 103(3), pp. 2487-2497. American Dairy Science Association 10.3168/jds.2019-16850

Saif, Rashid; Henkel, Jan; Jagannathan, Vidya; Drögemüller, Cord; Flury, Christine; Leeb, Tosso (2020). The LCORL Locus is under Selection in Large-Sized Pakistani Goat Breeds. Genes, 11(2) MDPI, Molecular Diversity Preservation International 10.3390/genes11020168

Letko, Anna; Leuthard, Fabienne; Jagannathan, Vidya; Corlazzoli, Daniele; Matiasek, Kaspar; Schweizer, Daniela; Hytönen, Marjo K; Lohi, Hannes; Leeb, Tosso; Drögemüller, Cord (2020). Whole Genome Sequencing Indicates Heterogeneity of Hyperostotic Disorders in Dogs. Genes, 11(2) MDPI, Molecular Diversity Preservation International 10.3390/genes11020163

Leeb, Tosso; Leuthard, Fabienne; Jagannathan, Vidya; Kiener, Sarah; Letko, Anna; Roosje, Petra; Welle, Monika M.; Gailbreath, Katherine L; Cannon, Andrea; Linek, Monika; Banovic, Frane; Olivry, Thierry; White, Stephen D; Batcher, Kevin; Bannasch, Danika; Minor, Katie M; Mickelson, James R; Hytönen, Marjo K; Lohi, Hannes; Mauldin, Elizabeth A; ... (2020). A Missense Variant Affecting the C-Terminal Tail of UNC93B1 in Dogs with Exfoliative Cutaneous Lupus Erythematosus (ECLE). Genes, 11(2) MDPI, Molecular Diversity Preservation International 10.3390/genes11020159

Letko, A.; Ammann, B.; Jagannathan, V.; Henkel, J.; Leuthard, F.; Schelling, C.; Carneiro, M.; Drögemüller, C.; Leeb, T. (2020). A deletion spanning the promoter and first exon of the hair cycle-specific ASIP transcript isoform in black and tan rabbits. Animal genetics, 51(1), pp. 137-140. Wiley 10.1111/age.12881

Torrecilha, R B P; Milanesi, M; Gallana, M; Falbo, A-K; Reichler, I M; Hug, Petra; Jagannathan, Vidya; Trigo, B B; Paulan, S C; Bruno, D B; Garcia, S D; Scaramele, N F; Lopes, F L; Dolf, Gaudenz; Leeb, Tosso; Sölkner, J; Garcia, J F; Pieńkowska-Schelling, A; Schelling, C and Utsunomiya, Y T (2020). Association of missense variants in GDF9 with litter size in Entlebucher Mountain dogs. Animal genetics, 51(1), pp. 78-86. Wiley 10.1111/age.12882

Seymour, D. J.; Cánovas, A.; Chud, T. C. S.; Cant, J. P.; Osborne, V. R.; Baes, C. F.; Schenkel, F. S.; Miglior, F. (2020). The dynamic behavior of feed efficiency in primiparous dairy cattle. Journal of dairy science, 103(2), pp. 1528-1540. American Dairy Science Association 10.3168/jds.2019-17414

Guevar, Julien; Hug, Petra; Giebels, Felix; Durand, Alexane; Jagannathan, Vidya; Leeb, Tosso (2020). A major facilitator superfamily domain 8 frameshift variant in a cat with suspected neuronal ceroid lipofuscinosis. Journal of veterinary internal medicine, 34(1), pp. 289-293. Wiley-Blackwell 10.1111/jvim.15663

Paris, Julia Maria; Letko, Anna; Häfliger, Irene Monika; Švara, Tanja; Gombač, Mitja; Klinc, Primož; Škibin, Andrej; Pogorevc, Estera; Drögemüller, Cord (2020). A de novo variant in OTX2 in a lamb with otocephaly. Acta Veterinaria Scandinavica, 62(1) BioMed Central Ltd. 10.1186/s13028-020-0503-z

Mock, Thomas; Mee, John F.; Dettwiler, Martina; Rodriguez-Campos, Sabrina; Hüsler, Jürg; Michel, Brigitte; Häfliger, Irene Monika; Drögemüller, Cord; Bodmer, Michèle; Hirsbrunner, Gabriela (2020). Evaluation of an investigative model in dairy herds with high calf perinatal mortality rates in Switzerland. Theriogenology, 148, pp. 48-59. Elsevier 10.1016/j.theriogenology.2020.02.039

Bannoehr, Jeanette; Balmer, Pierre; Stoffel, Michael H.; Jagannathan, Vidya; Gaschen, Véronique; Kühni, Kathrin; Sayar, Beyza; Drögemüller, Michaela; Howald, Denise; Wiener, Dominique J.; Leeb, Tosso; Welle, Monika M.; Müller, Eliane J.; Roosje, Petra (2020). Abnormal keratinocyte differentiation in the nasal planum of Labrador Retrievers with hereditary nasal parakeratosis (HNPK). PLoS ONE, 15(3), e0225901. Public Library of Science 10.1371/journal.pone.0225901

Häfliger, Irene Monika; Seefried, Franz; Drögemüller, Cord (2020). Trisomy 29 in a stillborn Swiss Original Braunvieh calf. Animal genetics, 51(3), pp. 483-484. Wiley 10.1111/age.12929

Cvitas, Iva; Oberhänsli, Simone; Leeb, Tosso; Dettwiler, Martina; Müller, Eliane Jasmine; Bruggmann, Rémy; Marti, Eliane Isabelle (2020). Investigating the epithelial barrier and immune signatures in the pathogenesis of equine insect bite hypersensitivity. PLoS ONE, 15(4), e0232189. Public Library of Science 10.1371/journal.pone.0232189

Butty, Adrien M.; Chud, Tatiane C. S.; Miglior, Filippo; Schenkel, Flavio S.; Kommadath, Arun; Krivushin, Kirill; Grant, Jason R.; Häfliger, Irene M.; Drögemüller, Cord; Cánovas, Angela; Stothard, Paul; Baes, Christine F. (2020). High confidence copy number variants identified in Holstein dairy cattle from whole genome sequence and genotype array data. Scientific reports, 10(1), p. 8044. Springer Nature 10.1038/s41598-020-64680-3

Studer, Nicole; Gurtner, Corinne; Levionnois, Olivier Louis Raymond; Drögemüller, Cord; Grahofer, Alexander (2020). Suspected unusual hypermetabolic syndrome after chemical immobilisation in two Mangalica pigs. Veterinary Record Case Reports, 8(1), e001089. British Veterinary Association 10.1136/vetreccr-2020-001089

van Staaveren, Nienke; Leishman, Emily M.; Wood, Benjamin J.; Harlander-Matauschek, Alexandra; Baes, Christine F. (2020). Farmers' Perceptions About Health and Welfare Issues in Turkey Production. Frontiers in veterinary science, 7(332), p. 332. Frontiers Media 10.3389/fvets.2020.00332

2019

Letko, Anna; Zdora, Isabel; Hitzler, Valerie; Jagannathan, Vidya; Beineke, Andreas; Möhrke, Carola; Drögemüller, Cord (2019). A de novo in-frame duplication in the COL1A2 gene in a Lagotto Romagnolo dog with osteogenesis imperfecta. Animal genetics, 50(6), pp. 786-787. Blackwell 10.1111/age.12843

Paris, Julia Maria; Letko, Anna; Häfliger, Irene Monika; Ammann, P; Flury, C; Drögemüller, Cord (2019). Identification of two TYRP1 loss-of-function alleles in Valais Red sheep. Animal genetics, 50(6), pp. 778-782. Wiley 10.1111/age.12863

Woolley, S A; Eager, K L M; Häfliger, Irene Monika; Bauer, Anina; Drögemüller, Cord; Leeb, Tosso; O'Rourke, B A; Tammen, I (2019). An ABCA12 missense variant in a Shorthorn calf with ichthyosis fetalis. Animal genetics, 50(6), pp. 749-752. Wiley 10.1111/age.12856

Leuthard, Fabienne; Lehner, G; Jagannathan, Vidya; Leeb, Tosso; Welle, Monika Maria (2019). A missense variant in the NSDHL gene in a Chihuahua with a congenital cornification disorder resembling inflammatory linear verrucous epidermal nevi. Animal genetics, 50(6), pp. 768-771. Wiley 10.1111/age.12862

Hug, Petra; Jude, R; Henkel, Jan Wolfgang; Jagannathan, Vidya; Leeb, Tosso (2019). A novel KIT deletion variant in a German Riding Pony with white-spotting coat colour phenotype. Animal genetics, 50(6), pp. 761-763. Wiley 10.1111/age.12840

Jagannathan, V.; Drögemüller, C.; Leeb, T. (2019). A comprehensive biomedical variant catalogue based on whole genome sequences of 582 dogs and eight wolves. Animal genetics, 50(6), pp. 695-704. Wiley 10.1111/age.12834

Abdalla, Emhimad; Schenkel, Flavio S.; Emamgholi-Begli, Hakimeh; Willems, Owen; Van As, Pieter; Vanderhout, Ryley; Wood, Ben J.; Baes, Christine F. (2019). Single-step methodology for genomic evaluation in turkeys (Meleagris gallopavo). Frontiers in genetics, 10(1248), p. 1248. Frontiers Media SA 10.3389/fgene.2019.01248

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Henkel, Jan; Saif, Rashid; Jagannathan, Vidya; Schmocker, Corinne; Zeindler, Flurina; Bangerter, Erika; Herren, Ursula; Posantzis, Dimitris; Bulut, Zafer; Ammann, Philippe; Drögemüller, Cord; Flury, Christine; Leeb, Tosso (2019). Selection signatures in goats reveal copy number variants underlying breed-defining coat color phenotypes. PLoS genetics, 15(12), e1008536. Public Library of Science 10.1371/journal.pgen.1008536

Schelling, Claude; Gaillard, Claude; Russenberger, Jane; Moseley, Lou; Dolf, Gaudenz (2019). Heritabilities for the puppy weight at birth in Labrador retrievers. BMC veterinary research, 15(1), p. 395. BioMed Central 10.1186/s12917-019-2146-8

Brenig, Bertram; Steingräber, Lilith; Shan, Shuwen; Xu, Fangzheng; Hirschfeld, Marc; Andag, Reiner; Spengeler, M; Dietschi, Elisabeth; Mischke, Reinhard; Leeb, Tosso (2019). Christmas disease in a Hovawart family resembling human hemophilia B Leyden is caused by a single nucleotide deletion in a highly conserved transcription factor binding site of the F9 gene promoter. Haematologica - the hematology journal, 104(11), pp. 2307-2313. Ferrata-Storti Foundation 10.3324/haematol.2018.215426

Tanaka, Jocelyn; Leeb, Tosso; Rushton, James; Famula, Thomas R; Mack, Maura; Jagannathan, Vidya; Flury, Christine; Bachmann, Iris; Eberth, John; McDonnell, Sue M; Penedo, Maria Cecilia T; Bellone, Rebecca R (2019). Frameshift Variant in MFSD12 Explains the Mushroom Coat Color Dilution in Shetland Ponies. Genes, 10(10) MDPI, Molecular Diversity Preservation International 10.3390/genes10100826

Hug, Petra; Kern, Patricia; Jagannathan, Vidya; Leeb, Tosso (2019). A TAC3 Missense Variant in a Domestic Shorthair Cat with Testicular Hypoplasia and Persistent Primary Dentition. Genes, 10(10), p. 806. MDPI, Molecular Diversity Preservation International 10.3390/genes10100806

Das, Rueben G; Becker, Doreen; Jagannathan, Vidya; Goldstein, Orly; Santana, Evelyn; Carlin, Kendall; Sudharsan, Raghavi; Leeb, Tosso; Nishizawa, Yuji; Kondo, Mineo; Aguirre, Gustavo D; Miyadera, Keiko (2019). Genome-wide association study and whole-genome sequencing identify a deletion in LRIT3 associated with canine congenital stationary night blindness. Scientific reports, 9(1), p. 14166. Springer Nature 10.1038/s41598-019-50573-7

Hirter, Nathalie; Drögemüller, Cord (1 October 2019). Maedi-Visna beim Schaf: Gibt es züchterische Möglichkeiten der Bekämpfung? Forum Kleinwiederkäuer Petits Ruminants, 2019(10), pp. 11-16. Verlagsgenossenschaft Caprovis

Signer-Hasler, Heidi; Burren, Alexander; Ammann, Philippe; Drögemüller, Cord; Flury, Christine (2019). Genomische Inzucht: Wie hoch ist sie in Schweizer Schaf- und Ziegenrassen? Agrarforschung Schweiz, 10(10), pp. 372-379. Agroscope

Bauer, Anina; de Lucia, M; Leuthard, Fabienne Nadja; Jagannathan, Vidya; Leeb, Tosso (2019). Compound heterozygosity for TNXB genetic variants in a mixed-breed dog with Ehlers-Danlos syndrome. Animal genetics, 50(5), pp. 546-549. Wiley 10.1111/age.12830

Störk, Theresa; Nessler, Jasmin; Anderegg, Linda; Hünerfauth, Enrice; Schmutz, Isabelle; Jagannathan, Vidya; Kyöstilä, Kaisa; Lohi, Hannes; Baumgärtner, Wolfgang; Tipold, Andrea; Leeb, Tosso (2019). TSEN54 missense variant in Standard Schnauzers with leukodystrophy. PLoS genetics, 15(10), e1008411. Public Library of Science 10.1371/journal.pgen.1008411

Hadji Rasouliha, Sheida; Barrientos, Laura; Anderegg, Linda; Klesty, Carina; Lorenz, Jessica; Chevallier, Lucie; Jagannathan, Vidya; Rösch, Sarah; Leeb, Tosso (2019). A RAPGEF6 variant constitutes a major risk factor for laryngeal paralysis in dogs. PLoS genetics, 15(10), e1008416. Public Library of Science 10.1371/journal.pgen.1008416

Bauer, Anina; Bateman, John F; Lamandé, Shireen R; Hanssen, Eric; Kirejczyk, Shannon G M; Yee, Mark; Ramiche, Ali; Jagannathan, Vidya; Welle, Monika; Leeb, Tosso; Bateman, Fiona L (2019). Identification of Two Independent COL5A1 Variants in Dogs with Ehlers-Danlos Syndrome. Genes, 10(10) MDPI, Molecular Diversity Preservation International 10.3390/genes10100731

Seymour, D.J.; Cánovas, A.; Baes, C. F.; Chud, T.C.S.; Osborne, V.R.; Cant, J.P.; Brito, L.F.; Gredler-Grandl, B.; Finocchiaro, R.; Veerkamp, R.F.; de Haas, Y.; Miglior, F. (2019). Invited review: Determination of large-scale individual dry matter intake phenotypes in dairy cattle. Journal of dairy science, 102(9), pp. 7655-7663. Elsevier 10.3168/jds.2019-16454

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Gross, Josef Johann; Schwinn, Ann-Catherine Silvia; Schmitz-Hsu, F; Barenco, A; Neuenschwander, T F-O; Drögemüller, Cord; Bruckmaier, Rupert (2019). The APOB loss-of-function mutation of Holstein dairy cattle does not cause a deficiency of cholesterol but decreases the capacity for cholesterol transport in circulation. Journal of dairy science, 102(11), pp. 10564-10572. American Dairy Science Association 10.3168/jds.2019-16852

Häfliger, Irene Monika; Hofstetter, Sonja; Mock, Thomas; Stettler, Manuela Hanna; Meylan, Mireille; Mehinagic, Kemal; Stokar von Neuforn, Nadine; Drögemüller, Cord (2019). APOB-associated cholesterol deficiency in Holstein cattle is not a simple recessive disease. Animal genetics, 50(4), pp. 372-375. Wiley 10.1111/age.12801

De Lucia, Michela; Angileri, Martina; Bauer, Anina; Spycher, Melina; Jagannathan, Vidya; Denti, Daria; Di Diodoro, Francesca; Ferro, Silvia; Mezzalira, Giorgia; Welle, Monika; Leeb, Tosso (2019). X-linked cutaneous mosaicism in a dog. Veterinary dermatology, 30(4), pp. 361-362. Wiley 10.1111/vde.12748

Hauswirth, Regula; Haase, Bianca; Blatter, Marlis; Brooks, Samantha A; Burger, Dominik; Drögemüller, Cord; Gerber, Vinzenz; Henke, Diana; Janda, Jozef; Jude, Rony; Magdesian, K Gary; Matthews, Jacqueline M; Poncet, Pierre-André; Svansson, Vilhjálmur; Tozaki, Teruaki; Wilkinson-White, Lorna; Penedo, M Cecilia T; Rieder, Stefan; Leeb, Tosso (2019). Correction: Mutations in MITF and PAX3 Cause "Splashed White" and Other White Spotting Phenotypes in Horses. PLoS genetics, 15(8), e1008321. Public Library of Science 10.1371/journal.pgen.1008321

Signer-Hasler, Heidi; Burren, A; Ammann, P; Drögemüller, Cord; Flury, C (2019). Runs of homozygosity and signatures of selection: a comparison among eight local Swiss sheep breeds. Animal genetics, 50(5), pp. 512-525. Wiley 10.1111/age.12828

Hug, Petra; Anderegg, Linda; Kehl, Alexandra; Jagannathan, Vidya; Leeb, Tosso (2019). AKNA Frameshift Variant in Three Dogs with Recurrent Inflammatory Pulmonary Disease. Genes, 10(8) MDPI, Molecular Diversity Preservation International 10.3390/genes10080567

Richardson, C.M.; Baes, C. F.; Amer, P.R.; Quinton, C.; Martin, P.; Osborne, V.R.; Pryce, J.E.; Miglior, F. (2019). Determining the economic value of daily dry matter intake and associated methane emissions in dairy cattle. Animal, 14(1), pp. 171-179. Cambridge University Press 10.1017/S175173111900154X

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Guarini, A.R.; Lourenco, D.A.L.; Brito, L.F.; Sargolzaei, M.; Baes, C. F.; Miglior, F.; Tsuruta, S.; Misztal, I.; Schenkel, F.S. (2019). Use of a single-step approach for integrating foreign information into national genomic evaluation in Holstein cattle. Journal of dairy science, 102(9), pp. 8175-8183. Elsevier 10.3168/jds.2018-15819

Ostrander, Elaine A; Wang, Guo-Dong; Larson, Greger; vonHoldt, Bridgett M; Davis, Brian W; Jagannathan, Vidya; Hitte, Christophe; Wayne, Robert K; Zhang, Ya-Ping (2019). Dog10K: an international sequencing effort to advance studies of canine domestication, phenotypes and health. National Science Review, 6(4), pp. 810-824. Oxford University Press 10.1093/nsr/nwz049

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Hug, Petra; Anderegg, Linda; Dürig, Nicole; Lepori, Vincent; Jagannathan, Vidya; Spiess, Bernhard; Richter, Marianne; Leeb, Tosso (2019). A SIX6 Nonsense Variant in Golden Retrievers with Congenital Eye Malformations. Genes, 10(6) MDPI, Molecular Diversity Preservation International 10.3390/genes10060454

Batcher, Kevin; Dickinson, Peter; Giuffrida, Michelle; Sturges, Beverly; Vernau, Karen; Knipe, Marguerite; Hadji Rasouliha, Sheida; Drögemüller, Cord; Leeb, Tosso; Maciejczyk, Kimberly; Jenkins, Christopher A; Mellersh, Cathryn; Bannasch, Danika (2019). Phenotypic Effects of FGF4 Retrogenes on Intervertebral Disc Disease in Dogs. Genes, 10(6) MDPI, Molecular Diversity Preservation International 10.3390/genes10060435

Kommadath, Arun; Grant, Jason R; Krivushin, Kirill; Butty, Adrien M; Baes, Christine Francoise; Carthy, Tara R; Berry, Donagh P; Stothard, Paul (2019). A large interactive visual database of copy number variants discovered in taurine cattle. GigaScience, 8(6) Oxford University Press 10.1093/gigascience/giz073

Bogedale, Kirsten; Jagannathan, Vidya; Gerber, Vinzenz; Unger, Lucia (2019). Differentially expressed microRNAs, including a large microRNA cluster on chromosome 24, are associated with equine sarcoid and squamous cell carcinoma. Veterinary and comparative oncology, 17(2), pp. 155-164. Wiley 10.1111/vco.12458

Paris, Julia Maria; Drögemüller, Cord (June 2019). Mouton Roux du Valais: dignes d’être préservés, roux comme noirs! Forum Kleinwiederkäuer = Forum petits ruminants, 2019(6-7), pp. 11-16. Verlagsgenossenschaft Caprovis

Butty, Adrien M.; Sargolzaei, Mehdi; Miglior, Filippo; Stothard, Paul; Schenkel, Flavio S.; Gredler-Grandl, Birgit; Baes, Christine Francoise (2019). Optimizing Selection of the Reference Population for Genotype Imputation From Array to Sequence Variants. Frontiers in genetics, 10(510), p. 510. Frontiers Media SA 10.3389/fgene.2019.00510

Hédan, Benoit; Cadieu, Edouard; Botherel, Nadine; Dufaure de Citres, Caroline; Letko, Anna; Rimbault, Maud; Drögemüller, Cord; Jagannathan, Vidya; Derrien, Thomas; Schmutz, Sheila; Leeb, Tosso; André, Catherine (2019). Identification of a Missense Variant in MFSD12 Involved in Dilution of Phaeomelanin Leading to White or Cream Coat Color in Dogs. Genes, 10(5) MDPI, Molecular Diversity Preservation International 10.3390/genes10050386

Hitti, Rebekkah J; Oliver, James A C; Schofield, Ellen C; Bauer, Anina; Kaukonen, Maria; Forman, Oliver P; Leeb, Tosso; Lohi, Hannes; Burmeister, Louise M; Sargan, David; Mellersh, Cathryn S (2019). Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration. Genes, 10(5) MDPI, Molecular Diversity Preservation International 10.3390/genes10050385

Vimercati, Sara; Elli, S; Jagannathan, Vidya; Pandey, Amit Vikram; Peduto, Nadja; Leeb, Tosso; Mevissen, Meike (2019). In silico and in vitro analysis of genetic variants of the equine CYP3A94, CYP3A95 and CYP3A97 isoenzymes. Toxicology in vitro, 60, pp. 116-124. Elsevier 10.1016/j.tiv.2019.05.011

Gmel, Annik Imogen; Druml, Thomas; von Niederhäusern, Rudolf; Leeb, Tosso; Neuditschko, Markus (2019). Genome-Wide Association Studies Based on Equine Joint Angle Measurements Reveal New QTL Affecting the Conformation of Horses. Genes, 10(5) MDPI, Molecular Diversity Preservation International 10.3390/genes10050370

Letko, Anna; Dietschi, Elisabeth; Nieburg, Marco; Jagannathan, Vidya; Gurtner, Corinne; Oevermann, Anna; Drögemüller, Cord (2019). A Missense Variant in SCN8A in Alpine Dachsbracke Dogs Affected by Spinocerebellar Ataxia. Genes, 10(5) MDPI, Molecular Diversity Preservation International 10.3390/genes10050362

Marchant, Thomas W; Dietschi, Elisabeth; Rytz, Ulrich; Schawalder, Peter; Jagannathan, Vidya; Hadji Rasouliha, Sheida; Gurtner, Corinne; Waldvogel, Andreas; Harrington, Ronan S; Drögemüller, Michaela; Kidd, Jeffrey; Ostrander, Elaine A; Warr, Amanda; Watson, Mick; Argyle, David; Ter Haar, Gert; Clements, Dylan N; Leeb, Tosso; Schoenebeck, Jeffrey J (2019). An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome. PLoS genetics, 15(5), e1008102. Public Library of Science 10.1371/journal.pgen.1008102

Schmutz, Isabelle; Jagannathan, Vidya; Bartenschlager, Florian; Stein, Veronika M.; Gruber, Achim D; Leeb, Tosso; Katz, Martin L (2019). ATP13A2 missense variant in Australian Cattle Dogs with late onset neuronal ceroid lipofuscinosis. Molecular genetics and metabolism, 127(1), pp. 95-106. Elsevier 10.1016/j.ymgme.2018.11.015

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Fleming, A.; Baes, C. F.; Martin, A.A.A.; Chud, T.C.S.; Malchiodi, F.; Brito, L.; Miglior, F. (2019). Symposium review: The choice and collection of new relevant phenotypes for fertility selection. Journal of dairy science, 102(4), pp. 3722-3734. Elsevier 10.3168/jds.2018-15470

Morath, Ute; Drögemüller, Cord; Stoffel, Michael Hubert; Precht, Maria Christina; Zanolari, Patrik; Spadavecchia, Claudia (2019). Polymelia in a chimeric Simmental calf: nociceptive withdrawal reflex, anaesthetic and analgesic management, anatomic and genetic analysis. BMC veterinary research, 15(1), p. 102. BioMed Central 10.1186/s12917-019-1846-4

Unger, Lucia; Gerber, Vinzenz; Pacholewska, Alicja Elzbieta; Leeb, Tosso; Jagannathan, Vidya (2019). MicroRNA fingerprints in serum and whole blood of sarcoid-affected horses as potential non-invasive diagnostic biomarkers. Veterinary and comparative oncology, 17(1), pp. 107-117. Wiley 10.1111/vco.12451

Decina, Caitlin; Berke, Olaf; van Staaveren, Nienke; Baes, Christine F.; Widowski, Tina; Harlander-Matauschek, Alexandra (2019). An Investigation of Associations Between Management and Feather Damage in Canadian Laying Hens Housed in Furnished Cages. Animals, 9(4), p. 135. MDPI 10.3390/ani9040135

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Brunner, Magdalena; Rüfenacht, Silvia; Bauer, Anina; Erpel, Susanne; Buchs, Natasha; Braga, Sophie Marie-Pierre; Heller, Manfred; Leeb, Tosso; Jagannathan, Vidya; Wiener, Dominique Judith; Welle, Monika Maria (2019). Bald thigh syndrome in sighthounds - Revisiting the cause of a well-known disease. PLoS ONE, 14(2), e0212645. Public Library of Science 10.1371/journal.pone.0212645

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van Staaveren, Nienke van; Decina, Caitlin; Baes, Christine F.; Widowski, Tina M.; Berke, Olaf; Harlander-Matauschek, Alexandra (2019). Housing and Management Practices on 33 Pullet Farms in Canada. Animals, 9(2), p. 49. MDPI 10.3390/ani9020049

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Gentilini, Fabio; Turba, Maria Elena; Giancola, Fiorella; Chiocchetti, Roberto; Bernardini, Chiara; Dajbychova, Markéta; Jagannathan, Vidya; Drögemüller, Michaela; Drögemüller, Cord (2019). A large deletion in the GP9 gene in Cocker Spaniel dogs with Bernard-Soulier syndrome. PLoS ONE, 14(9), e0220625. Public Library of Science 10.1371/journal.pone.0220625

Emamgholi-Begli, H.; Wood, B.; Abdalla, E.; Balzani, A.; Willems, O.; Schenkel, F.S.; Harlander-Matauschek, A.; Baes, C. F. (2019). Genetic parameters for clutch and broodiness traits in turkeys (Meleagris Gallopavo) and their relationship with body weight and egg production. Poultry Science, 98(12), pp. 6263-6269. Oxford University Press 10.3382/ps/pez446

Decina, C.; Berke, O.; van Staaveren, N.; Baes, Christine F.; Harlander-Matauschek, A. (2019). Development of a Scoring System to Assess Feather Damage in Canadian Laying Hen Flocks. Animals, 9(7) MDPI 10.3390/ani9070436

Naji, Maulana; Drögemüller, Cord; Mészáros, Gábor; Sölkner, Johann (2019). Deviation Patterns of Observed and Expected Haplotype Blocks Associated with Potential Recessive Disorders in Tyrol Grey Cattle. Acta Universitatis Agriculturae et Silviculturae Mendelianae Brunensis, 67(5), pp. 1183-1188. Mendel University Press, Brno 10.11118/actaun201967051183

Pontes Jacinto, Joana Goncalves; Bolcato, Marilena; Drögemüller, Cord; Gentile, Arcangelo; Militerno, Gianfranco (2019). Autosomal Cholesterol Deficiency in a Holstein Calf. Pakistan veterinary journal University of Agriculture, Faisalabad 10.29261/pakvetj/2019.120

2018

Genova, F; Longeri, M; Lyons, L A; Bagnato, A; the 99Lives, Consortium; Strillacci, M G (2018). First genome-wide CNV mapping in FELIS CATUS using next generation sequencing data. BMC Genomics, 19(1), p. 895. BioMed Central 10.1186/s12864-018-5297-2

Spycher, M; Bauer, Anina; Jagannathan, Vidhya; Frizzi, M; De Lucia, M; Leeb, Tosso (2018). A frameshift variant in the COL5A1 gene in a cat with Ehlers-Danlos syndrome. Animal genetics, 49(6), pp. 641-644. Wiley 10.1111/age.12727

Hadji Rasouliha, S; Bauer, Anina; Dettwiler, Martina Andrea; Welle, Monika Maria; Leeb, Tosso (2018). A frameshift variant in the EDA gene in Dachshunds with X-linked hypohidrotic ectodermal dysplasia. Animal genetics, 49(6), pp. 651-654. Wiley 10.1111/age.12729

Gallana, M; Utsunomiya, Y T; Dolf, Gaudenz; Pintor Torrecilha, R B; Falbo, A-K; Jagannathan, Vidhya; Leeb, Tosso; Reichler, I; Sölkner, J; Schelling, C (2018). Genome-wide association study and heritability estimate for ectopic ureters in Entlebucher mountain dogs. Animal genetics, 49(6), pp. 645-650. Wiley 10.1111/age.12728

Burns, E N; Bordbari, M H; Mienaltowski, M J; Affolter, V K; Barro, M V; Gianino, F; Gianino, G; Giulotto, E; Kalbfleisch, T S; Katzman, S A; Lassaline, M; Leeb, Tosso; Mack, M; Müller, Eliane Jasmine; MacLeod, J N; Ming-Whitfield, B; Alanis, C R; Raudsepp, T; Scott, E; Vig, S; ... (2018). Generation of an equine biobank to be used for Functional Annotation of Animal Genomes project. Animal genetics, 49(6), pp. 564-570. Wiley 10.1111/age.12717

Stella, Alessandra; Nicolazzi, Ezequiel Luis; Van Tassell, Curtis P; Rothschild, Max F; Colli, Licia; Rosen, Benjamin D; Sonstegard, Tad S; Crepaldi, Paola; Tosser-Klopp, Gwenola; Joost, Stephane (2018). AdaptMap: exploring goat diversity and adaptation. Genetics, selection, evolution, 50(1), p. 61. BioMed Central 10.1186/s12711-018-0427-5

Colli, Licia; Milanesi, Marco; Talenti, Andrea; Bertolini, Francesca; Chen, Minhui; Crisà, Alessandra; Daly, Kevin Gerard; Del Corvo, Marcello; Guldbrandtsen, Bernt; Lenstra, Johannes A; Rosen, Benjamin D; Vajana, Elia; Catillo, Gennaro; Joost, Stéphane; Nicolazzi, Ezequiel Luis; Rochat, Estelle; Rothschild, Max F; Servin, Bertrand; Sonstegard, Tad S; Steri, Roberto; ... (2018). Genome-wide SNP profiling of worldwide goat populations reveals strong partitioning of diversity and highlights post-domestication migration routes. Genetics, selection, evolution, 50(1), p. 58. BioMed Central 10.1186/s12711-018-0422-x

Talenti, Andrea; Palhière, Isabelle; Tortereau, Flavie; Pagnacco, Giulio; Stella, Alessandra; Nicolazzi, Ezequiel L; Crepaldi, Paola; Tosser-Klopp, Gwenola (2018). Functional SNP panel for parentage assessment and assignment in worldwide goat breeds. Genetics, selection, evolution, 50(1), p. 55. BioMed Central 10.1186/s12711-018-0423-9

Bertolini, Francesca; Cardoso, Tainã Figueiredo; Marras, Gabriele; Nicolazzi, Ezequiel L; Rothschild, Max F; Amills, Marcel; AdaptMap, Consortium (2018). Genome-wide patterns of homozygosity provide clues about the population history and adaptation of goats. Genetics, selection, evolution, 50(1), p. 59. BioMed Central 10.1186/s12711-018-0424-8

Cardoso, Taina F; Amills, Marcel; Bertolini, Francesca; Rothschild, Max; Marras, Gabriele; Boink, Geert; Jordana, Jordi; Capote, Juan; Carolan, Sean; Hallsson, Jón H; Kantanen, Juha; Pons, Agueda; Lenstra, Johannes A; AdaptMap, Consortium (2018). Patterns of homozygosity in insular and continental goat breeds. Genetics, selection, evolution, 50(1), p. 56. BioMed Central 10.1186/s12711-018-0425-7

Bertolini, Francesca; Servin, Bertrand; Talenti, Andrea; Rochat, Estelle; Kim, Eui Soo; Oget, Claire; Palhière, Isabelle; Crisà, Alessandra; Catillo, Gennaro; Steri, Roberto; Amills, Marcel; Colli, Licia; Marras, Gabriele; Milanesi, Marco; Nicolazzi, Ezequiel; Rosen, Benjamin D; Van Tassell, Curtis P; Guldbrandtsen, Bernt; Sonstegard, Tad S; Tosser-Klopp, Gwenola; ... (2018). Signatures of selection and environmental adaptation across the goat genome post-domestication. Genetics, selection, evolution, 50(1), p. 57. BioMed Central 10.1186/s12711-018-0421-y

Singer-Berk, M.; Knickelbein, K. E.; Vig, S.; Liu, J.; Bentley, E.; Nunnery, C.; Reilly, C.; Dwyer, A.; Drögemüller, Cord; Unger, Lucia; Gerber, Vinzenz; Lassaline, M.; Bellone, R. R. (2018). Genetic risk for squamous cell carcinoma of the nictitating membrane parallels that of the limbus in Haflinger horses. Animal genetics, 49(5), pp. 457-460. Blackwell 10.1111/age.12695

Guarini, A.R.; Lourenco, D.A.L.; Brito, L.F.; Sargolzaei, M.; Baes, C. F.; Miglior, F.; Misztal, I.; Schenkel, F.S. (2018). Comparison of genomic predictions for lowly heritable traits using multi-step and single-step genomic best linear unbiased predictor in Holstein cattle. Journal of dairy science, 101(9), pp. 8076-8086. Elsevier 10.3168/jds.2017-14193

Neuhauser, Stefanie; Handler, Johannes; Schelling, Claude; Pieńkowska-Schelling, Aldona (2018). Disorder of Sexual Development in a Mare with an Unusual Tentative Mosaic Karyotype: 63,X/64,Xdel(Y). Sexual development, 12(5), pp. 232-238. Karger 10.1159/000490861

Mason, Victor C; Schaefer, Robert J; McCue, Molly E; Leeb, Tosso; Gerber, Vinzenz (2018). eQTL discovery and their association with severe equine asthma in European Warmblood horses. BMC Genomics, 19(1), p. 581. BioMed Central 10.1186/s12864-018-4938-9

Joller, Sara; Ammann, P.; Flury, C.; Drögemüller, Cord (2018). Evaluation of HOXC8 in crested Swiss chicken. Animal genetics, 49(4), pp. 334-336. Blackwell 10.1111/age.12674

Dürig, Nicole; Letko, Anna; Lepori, Vincent; Hadji Rasouliha, Sheida; Loechel, R; Kehl, A; Hytönen, M K; Lohi, H; Mauri, Nico; Dietrich, Sara Joëlle; Wiedmer, Michaela; Drögemüller, Michaela; Jagannathan, Vidhya; Schmutz, S M; Leeb, Tosso (2018). Two MC1R loss-of-function alleles in cream-coloured Australian Cattle Dogs and white Huskies. Animal genetics, 49(4), pp. 284-290. Blackwell 10.1111/age.12660

van Staaveren, Nienke; Decina, Caitlin; Baes, Christine F; Widowski, Tina M; Berke, Olaf; Harlander-Matauschek, Alexandra (2018). A Description of Laying Hen Husbandry and Management Practices in Canada. Animals, 8(7) MDPI 10.3390/ani8070114

Dìez Bernal, Sabina; Lanz, Simone; Schmutz, Isabelle; Leeb, Tosso; Spadavecchia, Claudia (2018). Induction of general anaesthesia by blowpipe darting in a fractious companion horse. Veterinary Record Case Reports, 6(3), e000629. British Veterinary Association 10.1136/vetreccr-2018-000629

Kroezen, V; Schenkel, F S; Miglior, F; Baes, C F; Squires, E J (2018). Candidate gene association analyses for ketosis-resistance in Holsteins. Journal of dairy science, 101(6), pp. 5240-5249. American Dairy Science Association 10.3168/jds.2017-13374

Schmidli, Manuel; Fuhrer, Bettina; Kurt, Nadine; Senn, David; Drögemüller, Michaela; Rytz, Ulrich; Spreng, David Emmanuel; Forterre, Simone (2018). Inflammatory pattern of the infrapatellar fat pad in dogs with canine cruciate ligament disease. BMC veterinary research, 14(1), p. 161. BioMed Central 10.1186/s12917-018-1488-y

Lepori, Vincent; Mühlhause, Franziska; Sewell, Adrian C; Jagannathan, Vidhya; Janzen, Nils; Rosati, Marco; Maximiano Alves de Sousa, Filipe Miguel; Tschopp, Aurélie; Schüpbach, Gertraud; Matiasek, Kaspar; Tipold, Andrea; Leeb, Tosso; Kornberg, Marion (2018). A Nonsense Variant in the ACADVL Gene in German Hunting Terriers with Exercise Induced Metabolic Myopathy. G3 Genes Genomes Genetics, 8(5), pp. 1545-1554. Genetics Society of America 10.1534/g3.118.200084

Riedi, Anna-Katharina; Drögemüller, Cord; Gurtner, Corinne; Meylan, Mireille (2018). Bovine dilated cardiomyopathy: Almost forgotten but still present. Schweizer Archiv für Tierheilkunde, 160(5), pp. 289-293. Gesellschaft Schweizer Tierärztinnen und Tierärzte 10.17236/sat00158

Erles, K; Mugford, A; Barfield, D; Leeb, T.; Kook, P H (2018). Systemic Scedosporium prolificans infection in an 11-month-old Border collie with cobalamin deficiency secondary to selective cobalamin malabsorption (canine Imerslund-Gräsbeck syndrome). Journal of small animal practice, 59(4), pp. 253-256. British Small Animal Veterinary Association 10.1111/jsap.12678

Schmutz, Isabelle; Jagannathan, Vidhya; Dìez Bernal, Sabina; Lanz, Simone; Kalbfleisch, Ted; Leeb, Tosso; Spadavecchia, Claudia (2018). Exclusion of adrenoceptor alpha 2 variants in a horse insensitive to medetomidine. Animal genetics, 49(2), p. 141. Blackwell 10.1111/age.12636

Bauer, Anina; Nimmo, J; Newman, R; Brunner, Magdalena Anna Theresa; Welle, Monika Maria; Jagannathan, Vidhya; Leeb, Tosso (2018). A splice site variant in the SUV39H2 gene in Greyhounds with nasal parakeratosis. Animal genetics, 49(2), pp. 137-140. Blackwell 10.1111/age.12643

Stratz, Patrick; Schiller, Katja Franziska; Wellmann, Robin; Preuss, Siegfried; Baes, Christine Francoise; Bennewitz, Jörn (2018). Genetic parameter estimates and targeted association analyses of growth, carcass, and meat quality traits in German Merinoland and Merinoland-cross lambs. Journal of animal science, 96(2), pp. 398-406. American Society of Animal Science 10.1093/jas/sky012

Joller, Sara; Bertschinger, Flurina; Kump, Erwin; Spiri, Astrid; von Rotz, Alois; Schweizer, Daniela Esther; Drögemüller, Cord; Flury, Christine (2018). Crossed beaks in a local Swiss chicken breed. BMC veterinary research, 14(1), p. 68. BioMed Central 10.1186/s12917-018-1398-z

Joller, Sara; Stettler, Manuela Hanna; Locher, Iwan; Dettwiler, Martina Andrea; Seefried, F; Meylan, Mireille; Drögemüller, Cord (2018). [Fanconi-Bickel-Syndrom: a novel genetic disease in Original Braunvieh]. Schweizer Archiv für Tierheilkunde, 160(3), pp. 179-184. Gesellschaft Schweizer Tierärztinnen und Tierärzte 10.17236/sat00152

Bauer, Anina; Jagannathan, Vidhya; Högler, Sandra; Richter, Barbara; McEwan, Neil A; Thomas, Anne; Cadieu, Edouard; André, Catherine; Hytönen, Marjo K; Lohi, Hannes; Welle, Monika Maria; Roosje, Petra; Mellersh, Cathryn; Casal, Margret L; Leeb, Tosso (2018). MKLN1 splicing defect in dogs with lethal acrodermatitis. PLoS genetics, 14(3), e1007264. Public Library of Science 10.1371/journal.pgen.1007264

Dolf, Gaudenz; Gaillard, Claude; Russenberger, Jane; Moseley, Lou; Schelling, Claude (2018). Factors contributing to the decision to perform a cesarean section in Labrador retrievers. BMC veterinary research, 14(1), p. 57. BioMed Central 10.1186/s12917-018-1381-8

Felkel, S; Vogl, C; Rigler, D; Jagannathan, Vidhya; Leeb, Tosso; Fries, R; Neuditschko, M; Rieder, S; Velie, B; Lindgren, G; Rubin, C-J; Schlötterer, C; Rattei, T; Brem, G; Wallner, B (2018). Asian horses deepen the MSY phylogeny. Animal genetics, 49(1), pp. 90-93. Blackwell 10.1111/age.12635

Bauer, Anina; Kehl, A; Jagannathan, Vidhya; Leeb, Tosso (2018). A novel MLPH variant in dogs with coat colour dilution. Animal genetics, 49(1), pp. 94-97. Blackwell 10.1111/age.12632

Forutan, Mehrnush; Mahyari, Saeid Ansari; Baes, Christine; Melzer, Nina; Schramm Schenkel, Flavio; Sargolzaei, Mehdi (2018). Inbreeding and runs of homozygosity before and after genomic selection in North American Holstein cattle. BMC Genomics, 19(1), p. 98. BioMed Central 10.1186/s12864-018-4453-z

Fleming, Alison; Abdalla, Emhimad A; Maltecca, Christian; Baes, Christine F (2018). Invited review: Reproductive and genomic technologies to optimize breeding strategies for genetic progress in dairy cattle. Archives animal breeding, 61(1), pp. 43-57. Copernicus Publications 10.5194/aab-61-43-2018

Koch, Christoph; Ramsauer, A S; Drögemüller, Michaela; Ackermann, M; Gerber, Vinzenz; Tobler, K (2018). Genomic comparison of bovine papillomavirus 1 isolates from bovine, equine and asinine lesional tissue samples. Virus research, 244, pp. 6-12. Elsevier 10.1016/j.virusres.2017.11.005

Swirski, Sebastian; Röger, Carsten; Pieńkowska-Schelling, Aldona; Ihlenburg, Cynthia; Fischer, Gösta; May, Oliver; Vorm, Mariann; Owczarek-Lipska, Marta; Neidhardt, John (2018). A Novel C-Terminal Mutation in Gsdma3 (C+/H-) Leads to Alopecia and Corneal Inflammatory Response in Mice. Investigative ophthalmology & visual science, 59(1), pp. 561-571. Association for Research in Vision and Ophthalmology 10.1167/iovs.17-22658

Bouwman, Aniek C.; Daetwyler, Hans D.; Chamberlain, Amanda J.; Ponce, Carla Hurtado; Sargolzaei, Mehdi; Schenkel, Flavio S.; Sahana, Goutam; Govignon-Gion, Armelle; Boitard, Simon; Dolezal, Marlies; Pausch, Hubert; Brøndum, Rasmus F.; Bowman, Phil J.; Thomsen, Bo; Guldbrandtsen, Bernt; Lund, Mogens S.; Servin, Bertrand; Garrick, Dorian J.; Reecy, James; Vilkki, Johanna; ... (2018). Meta-analysis of genome-wide association studies for cattle stature identifies common genes that regulate body size in mammals. Nature genetics, 50(3), pp. 362-367. Nature America 10.1038/s41588-018-0056-5

Minor, K. M.; Letko, Anna; Becker, Doreen; Drögemüller, Michaela; Mandigers, P. J. J.; Bellekom, S. R.; Leegwater, P. A. J.; Stassen, Q. E. M.; Putschbach, K.; Fischer, A.; Flegel, T.; Matiasek, K.; Ekenstedt, K. J.; Furrow, E.; Patterson, E. E.; Platt, S. R.; Kelly, P. A.; Cassidy, J. P.; Shelton, G. D.; Lucot, K.; ... (2018). Canine NAPEPLD-associated models of human myelin disorders. Scientific Reports, 8(1), p. 5818. Nature Publishing Group 10.1038/s41598-018-23938-7

Lucot, Katherine L.; Dickinson, Peter J.; Finno, Carrie J.; Mansour, Tamer A.; Letko, Anna; Minor, Katherine M.; Mickelson, James R.; Drögemüller, Cord; Brown, C. Titus; Bannasch, Danika L. (2018). A Missense Mutation in the Vacuolar Protein Sorting 11 ( VPS11 ) Gene Is Associated with Neuroaxonal Dystrophy in Rottweiler Dogs. G3 Genes Genomes Genetics, 8(8), pp. 2773-2780. Genetics Society of America 10.1534/g3.118.200376

Jaton, C.; Schenkel, F.S.; Sargolzaei, M.; Cánova, A.; Malchiodi, F.; Price, C.A.; Baes, C.; Miglior, F. (2018). Genome-wide association study and in silico functional analysis of the number of embryos produced by Holstein donors. Journal of dairy science, 101(8), pp. 7248-7257. Elsevier 10.3168/jds.2017-13848

2017

Pacholewska, Alicja Elzbieta; Kraft, Matthias Fabian; Gerber, Vinzenz; Jagannathan, Vidhya (2017). Differential Expression of Serum MicroRNAs Supports CD4⁺ T Cell Differentiation into Th2/Th17 Cells in Severe Equine Asthma. Genes, 8(12) MDPI, Molecular Diversity Preservation International 10.3390/genes8120383

Hofstetter, Sonja; Welle, Monika Maria; Gorgas, Daniela; Balmer, Pierre; Roosje, Petra; Mock, Thomas; Meylan, Mireille; Jagannathan, Vidhya; Drögemüller, Cord (2017). A de novo germline mutation of DLX3 in a Brown Swiss calf with tricho-dento-osseus-like syndrome. Veterinary dermatology, 28(6), 616-e150. Blackwell Science 10.1111/vde.12462

Schnider, Debora; Rieder, S; Leeb, Tosso; Gerber, Vinzenz; Neuditschko, M (2017). A genome-wide association study for equine recurrent airway obstruction in European Warmblood horses reveals a suggestive new quantitative trait locus on chromosome 13. Animal genetics, 48(6), pp. 691-693. Blackwell 10.1111/age.12583

Joller, Sara; Berenguer Veiga, Inês Margarida; Drögemüller, Cord (2017). Dermatosparaxis in White Dorper sheep: confirmation of a causative nonsense mutation in ADAMTS2. Animal genetics, 48(6), pp. 729-730. Blackwell 10.1111/age.12591

Niggeler, Allegra; Tetens, Jens; Stäuble, Anna; Steiner, Adrian; Drögemüller, Cord (2017). A genome-wide significant association on chromosome 2 for footrot resistance/susceptibility in Swiss White Alpine sheep. Animal genetics, 48(6), pp. 712-715. Blackwell 10.1111/age.12614

Vidal, Oriol; Drögemüller, Cord; Obexer, Gaby; Reber, Irene; Jordana, Jordi; Martínez, Amparo; Bâlteanu, Valentin Adrian; Delgado, Juan Vicente; Eghbalsaied, Shahin; Landi, Vincenzo; Goyache, Felix; Traoré, Amadou; Pazzola, Michele; Vacca, Giuseppe Massimo; Badaoui, Bouabid; Pilla, Fabio; D'Andrea, Mariasilvia; Álvarez, Isabel; Capote, Juan; Sharaf, Abdoallah; ... (2017). Differential distribution of Y-chromosome haplotypes in Swiss and Southern European goat breeds. Scientific Reports, 7(1), p. 16161. Nature Publishing Group 10.1038/s41598-017-15593-1

Syrjä, Pernilla; Anwar, Tahira; Jokinen, Tarja; Kyöstilä, Kaisa; Jäderlund, Karin Hultin; Cozzi, Francesca; Rohdin, Cecilia; Hahn, Kerstin; Wohlsein, Peter; Baumgärtner, Wolfgang; Henke, Diana; Oevermann, Anna; Sukura, Antti; Leeb, Tosso; Lohi, Hannes; Eskelinen, Eeva-Liisa (2017). Basal Autophagy Is Altered in Lagotto Romagnolo Dogs with an ATG4D Mutation. Veterinary pathology, 54(6), pp. 953-963. American College of Veterinary Pathologists 10.1177/0300985817712793

Ha, N.-T.; Drögemüller, Cord; Reimer, C.; Schmitz-Hsu, F.; Bruckmaier, Rupert; Simianer, H.; Gross, Josef Johann (2017). Liver transcriptome analysis reveals important factors involved in the metabolic adaptation of the transition cow. Journal of dairy science, 100(11), pp. 9311-9323. American Dairy Science Association 10.3168/jds.2016-12454

Letko, Anna; Drögemüller, Cord (2017). Two brown coat colour-associated TYRP1 variants (b(c) and b(d)) occur in Leonberger dogs. Animal genetics, 48(6), pp. 732-733. Blackwell 10.1111/age.12612

Herder, Vanessa; Ciurkiewicz, Malgorzata; Baumgärtner, Wolfgang; Jagannathan, Vidhya; Leeb, Tosso (2017). Frame-shift variant in the CHRNE gene in a juvenile dog with suspected myasthenia gravis-like disease. Animal genetics, 48(5), p. 625. Blackwell 10.1111/age.12558

Caduff, M; Bauer, Anina; Jagannathan, Vidhya; Leeb, Tosso (2017). A single base deletion in the SLC45A2 gene in a Bullmastiff with oculocutaneous albinism. Animal genetics, 48(5), pp. 619-621. Blackwell 10.1111/age.12582

Bourneuf, E; Otz, P; Pausch, H; Jagannathan, Vidhya; Michot, P; Grohs, C; Piton, G; Ammermüller, S; Deloche, M-C; Fritz, S; Leclerc, H; Péchoux, C; Boukadiri, A; Hozé, C; Saintilan, R; Créchet, F; Mosca, M; Segelke, D; Guillaume, F; Bouet, S; ... (2017). Rapid Discovery of De Novo Deleterious Mutations in Cattle Enhances the Value of Livestock as Model Species. Scientific Reports, 7(1), p. 11466. Nature Publishing Group 10.1038/s41598-017-11523-3

Bauer, Anina; De Lucia, Michela; Jagannathan, Vidhya; Mezzalira, Giorgia; Casal, Margaret L; Welle, Monika Maria; Leeb, Tosso (2017). A Large Deletion in the NSDHL Gene in Labrador Retrievers with a Congenital Cornification Disorder. G3 Genes Genomes Genetics, 7(9), pp. 3115-3121. Genetics Society of America 10.1534/g3.117.1124

Becker, Doreen; Minor, Katie M; Letko, Anna; Ekenstedt, Kari J; Jagannathan, Vidhya; Leeb, Tosso; Shelton, G Diane; Mickelson, James R; Drögemüller, Cord (2017). A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs. BMC Genomics, 18(1), p. 662. BioMed Central 10.1186/s12864-017-4081-z

Mauri, Nico; Kleiter, Miriam; Dietschi, Elisabeth; Leschnik, Michael; Högler, Sandra; Wiedmer, Michaela; Dietrich, Sara Joëlle; Henke, Diana; Steffen, Frank; Schuller, Simone; Gurtner, Corinne; Stokar von Neuforn, Nadine; O'Toole, Donal; Bilzer, Thomas; Herden, Christiane; Oevermann, Anna; Jagannathan, Vidhya; Leeb, Tosso (2017). A SINE Insertion in ATP1B2 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA2). G3 Genes Genomes Genetics, 7(8), pp. 2729-2737. Genetics Society of America 10.1534/g3.117.043018

Agerholm, Jørgen S; McEvoy, Fintan J; Heegaard, Steffen; Charlier, Carole; Jagannathan, Vidhya; Drögemüller, Cord (2017). A de novo missense mutation of FGFR2 causes facial dysplasia syndrome in Holstein cattle. BMC genetics, 18(1), p. 74. BioMed Central 10.1186/s12863-017-0541-3

Dürig, Nicole; Jude, R; Holl, H; Brooks, S A; Lafayette, C; Jagannathan, Vidhya; Leeb, Tosso (2017). Whole genome sequencing reveals a novel deletion variant in the KIT gene in horses with white spotted coat colour phenotypes. Animal genetics, 48(4), pp. 483-485. Blackwell 10.1111/age.12556

Schaefer, Robert J; Schubert, Mikkel; Bailey, Ernest; Bannasch, Danika L; Barrey, Eric; Bar-Gal, Gila Kahila; Brem, Gottfried; Brooks, Samantha A; Distl, Ottmar; Fries, Ruedi; Finno, Carrie J; Gerber, Vinzenz; Haase, Bianca; Jagannathan, Vidhya; Kalbfleisch, Ted; Leeb, Tosso; Lindgren, Gabriella; Lopes, Maria Susana; Mach, Núria; da Câmara Machado, Artur; ... (2017). Developing a 670k genotyping array to tag ~2M SNPs across 24 horse breeds. BMC Genomics, 18(1), p. 565. BioMed Central 10.1186/s12864-017-3943-8

Wallner, Barbara; Palmieri, Nicola; Vogl, Claus; Rigler, Doris; Bozlak, Elif; Druml, Thomas; Jagannathan, Vidhya; Leeb, Tosso; Fries, Ruedi; Tetens, Jens; Thaller, Georg; Metzger, Julia; Distl, Ottmar; Lindgren, Gabriella; Rubin, Carl-Johan; Andersson, Leif; Schaefer, Robert; McCue, Molly; Neuditschko, Markus; Rieder, Stefan; ... (2017). Y Chromosome Uncovers the Recent Oriental Origin of Modern Stallions. Current Biology, 27(13), pp. 2029-2035. Cell Press 10.1016/j.cub.2017.05.086

Marchant, Thomas W; Johnson, Edward J; McTeir, Lynn; Johnson, Craig I; Gow, Adam; Liuti, Tiziana; Kuehn, Dana; Svenson, Karen; Bermingham, Mairead L; Drögemüller, Michaela; Nussbaumer, Marc; Davey, Megan G; Argyle, David J; Powell, Roger M; Guilherme, Sérgio; Lang, Johann; Ter Haar, Gert; Leeb, Tosso; Schwarz, Tobias; Mellanby, Richard J; ... (2017). Canine Brachycephaly Is Associated with a Retrotransposon-Mediated Missplicing of SMOC2. Current Biology, 27(11), 1573-1584.e6. Cell Press 10.1016/j.cub.2017.04.057

Schrack, J; Dolf, G; Reichler, I M; Schelling, C (2017). Factors influencing litter size and puppy losses in the Entlebucher Mountain dog. Theriogenology, 95, pp. 163-170. Elsevier 10.1016/j.theriogenology.2017.03.004

Librado, Pablo; Gamba, Cristina; Gaunitz, Charleen; Der Sarkissian, Clio; Pruvost, Mélanie; Albrechtsen, Anders; Fages, Antoine; Khan, Naveed; Schubert, Mikkel; Jagannathan, Vidhya; Serres-Armero, Aitor; Kuderna, Lukas F K; Povolotskaya, Inna S; Seguin-Orlando, Andaine; Lepetz, Sébastien; Neuditschko, Markus; Thèves, Catherine; Alquraishi, Saleh; Alfarhan, Ahmed H; Al-Rasheid, Khaled; ... (2017). Ancient genomic changes associated with domestication of the horse. Science, 356(6336), pp. 442-445. American Association for the Advancement of Science 10.1126/science.aam5298

Bellone, Rebecca R; Liu, Jiayin; Petersen, Jessica L; Mack, Maura; Singer-Berk, Moriel; Drögemüller, Cord; Malvick, Julia; Wallner, Barbara; Brem, Gottfried; Penedo, M Cecilia; Lassaline, Mary (2017). A missense mutation in damage specific DNA binding protein 2 is a genetic risk factor for limbal squamous cell carcinoma in horses. International journal of cancer, 141(2), pp. 342-353. Wiley-Blackwell 10.1002/ijc.30744

Bauer, Anina Estrella; Hiemesch, Theresa; Jagannathan, Vidhya; Neuditschko, Markus; Bachmann, Iris; Rieder, Stefan; Mikko, Sofia; Penedo, M Cecilia; Tarasova, Nadja; Vitková, Martina; Sirtori, Nicolò; Roccabianca, Paola; Leeb, Tosso; Welle, Monika Maria (2017). A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome. G3 Genes Genomes Genetics, 7(4), pp. 1315-1321. Genetics Society of America 10.1534/g3.117.039511

Oh, Annie; Pearce, Jacqueline W; Gandolfi, Barbara; Creighton, Erica K; Suedmeyer, William K; Selig, Michael; Bosiack, Ann P; Castaner, Leilani J; Whiting, Rebecca E H; Belknap, Ellen B; Lyons, Leslie A; 99 Lives, Consortium (2017). Early-Onset Progressive Retinal Atrophy Associated with an IQCB1 Variant in African Black-Footed Cats (Felis nigripes). Scientific Reports, 7(43918), p. 43918. Nature Publishing Group 10.1038/srep43918

Wielaender, Franziska; Sarviaho, Riika; James, Fiona; Hytönen, Marjo K; Cortez, Miguel A; Kluger, Gerhard; Koskinen, Lotta L E; Arumilli, Meharji; Kornberg, Marion; Bathen-Noethen, Andrea; Tipold, Andrea; Rentmeister, Kai; Bhatti, Sofie F M; Hülsmeyer, Velia; Boettcher, Irene C; Tästensen, Carina; Flegel, Thomas; Dietschi, Elisabeth; Leeb, Tosso; Matiasek, Kaspar; ... (2017). Generalized myoclonic epilepsy with photosensitivity in juvenile dogs caused by a defective DIRAS family GTPase 1. Proceedings of the National Academy of Sciences of the United States of America - PNAS, 114(10), pp. 2669-2674. National Academy of Sciences NAS 10.1073/pnas.1614478114

Hirz, M; Drögemüller, Michaela; Schänzer, A; Jagannathan, Vidhya; Dietschi, Elisabeth; Goebel, H H; Hecht, W; Laubner, S; Schmidt, M J; Steffen, F; Hilbe, M; Köhler, K; Drögemüller, Cord; Herden, C (2017). Neuronal ceroid lipofuscinosis (NCL) is caused by the entire deletion of CLN8 in the Alpenländische Dachsbracke dog. Molecular genetics and metabolism, 120(3), pp. 269-277. Elsevier 10.1016/j.ymgme.2016.12.007

Bauer, Anina Estrella; Waluk, Dominik Pawel; Arnaud, Galichet; Timm, Katrin; Jagannathan, Vidhya; Sayar, Beyza; Wiener, Dominique Judith; Dietschi, Elisabeth; Müller, Eliane Jasmine; Roosje, Petra; Welle, Monika Maria; Leeb, Tosso (2017). A de novo variant in the ASPRV1 gene in a dog with ichthyosis. PLoS genetics, 13(3), e1006651. Public Library of Science 10.1371/journal.pgen.1006651

Mauler, D A; Gandolfi, B; Reinero, C R; O'Brien, D P; Spooner, J L; Lyons, L A; 99 Lives, Consortium (2017). Precision Medicine in Cats: Novel Niemann-Pick Type C1 Diagnosed by Whole-Genome Sequencing. Journal of veterinary internal medicine, 31(2), pp. 539-544. Wiley-Blackwell 10.1111/jvim.14599

Leeb, Tosso; Müller, Eliane Jasmine; Roosje, Petra; Welle, Monika Maria (2017). Genetic testing in veterinary dermatology. Veterinary dermatology, 28(1), 4-e1. Blackwell Science 10.1111/vde.12309

Dürig, Nicole; Jude, Rony; Jagannathan, Vidhya; Leeb, Tosso (2017). A novel MITF variant in a white American Standardbred foal. Animal genetics, 48(1), pp. 123-124. Blackwell 10.1111/age.12484

Aberdein, Danielle; Munday, John S; Gandolfi, Barbara; Dittmer, Keren E; Malik, Richard; Garrick, Dorian J; Lyons, Leslie A; 99 Lives, Consortium (2017). A FAS-ligand variant associated with autoimmune lymphoproliferative syndrome in cats. Mammalian genome, 28(1-2), pp. 47-55. Springer-Verlag 10.1007/s00335-016-9668-1

Pacholewska, Alicja; Marti, Eliane Isabelle; Leeb, Tosso; Jagannathan, Vidhya; Gerber, Vinzenz (2017). LPS-induced modules of co-expressed genes in equine peripheral blood mononuclear cells. BMC Genomics, 18(1), p. 34. BioMed Central 10.1186/s12864-016-3390-y

Wucher, Valentin; Legeai, Fabrice; Hédan, Benoît; Rizk, Guillaume; Lagoutte, Lætitia; Leeb, Tosso; Jagannathan, Vidhya; Cadieu, Edouard; David, Audrey; Lohi, Hannes; Cirera, Susanna; Fredholm, Merete; Botherel, Nadine; Leegwater, Peter A J; Le Béguec, Céline; Fieten, Hille; Johnson, Jeremy; Alföldi, Jessica; André, Catherine; Lindblad-Toh, Kerstin; ... (2017). FEELnc: a tool for long non-coding RNA annotation and its application to the dog transcriptome. Nucleic acids research, 45(8), e57. Information Retrieval Ltd. 10.1093/nar/gkw1306

Lauper, Murielle; Gerber, Vinzenz; Ramseyer, Alessandra; Burger, Dominik; Lüth, A.; Koch, Christoph; Dolf, Gaudenz (2017). Heritabilities of health traits in Swiss Warmblood horses. Equine veterinary journal, 49(1), pp. 15-18. Wiley-Blackwell 10.1111/evj.12537

Neuditschko, Markus; Raadsma, Herman W; Khatkar, Mehar S; Jonas, Elisabeth; Steinig, Eike J; Flury, Christine; Signer-Hasler, Heidi; Frischknecht, Mirjam; von Niederhäusern, Ruedi; Leeb, Tosso; Rieder, Stefan (2017). Identification of key contributors in complex population structures. PLoS ONE, 12(5), e0177638. Public Library of Science 10.1371/journal.pone.0177638

Awasthi, Nivedita; Drögemüller, Cord; Jagannathan, Vidhya; Keller, Irene; Wüthrich, Daniel; Bruggmann, Rémy; Beck, Julia; Schütz, Ekkehard; Brenig, Bertram; Demmel, Steffi; Moser, Simon; Signer-Hasler, Heidi; Pieńkowska-Schelling, Aldona; Schelling, Claude; Sande Melon, Marcos; Rongen, Ronald; Rieder, Stefan; Kelsh, Robert N.; Mercader Huber, Nadia and Leeb, Tosso (2017). A structural variant in the 5’-flanking region of the TWIST2 gene affects melanocyte development in belted cattle. PLoS ONE, 12(6), e0180170. Public Library of Science 10.1371/journal.pone.0180170

Scacco, G.; Rambaldi, A. M.; Roccaro, M.; Peli, A.; Drögemüller, Cord; Gentile, A. (2017). Bilateral Convergent Strabismus with Exophthalmos in cattle - what do we know? Large animal review, 23(2), pp. 67-71. SIVAR - Societa Italiana Veterinari per Animali da Reddito

Balmer, Pierre; Bauer, Anina Estrella; Pujar, Shashikant; McGarvey, Kelly M; Welle, Monika Maria; Galichet, Arnaud; Müller, Eliane Jasmine; Pruitt, Kim D; Leeb, Tosso; Jagannathan, Vidhya (2017). A curated catalog of canine and equine keratin genes. PLoS ONE, 12(8), e0180359. Public Library of Science 10.1371/journal.pone.0180359

Caduff, Madleina; Bauer, Anina Estrella; Jagannathan, Vidhya; Leeb, Tosso (2017). OCA2 splice site variant in German Spitz dogs with oculocutaneous albinism. PLoS ONE, 12(10), e0185944. Public Library of Science 10.1371/journal.pone.0185944

Brunner, Magdalena; Jagannathan, Vidhya; Waluk, Dominik Pawel; Roosje, Petra; Linek, Monika; Panakova, Lucia; Leeb, Tosso; Wiener, Dominique Judith; Welle, Monika Maria (2017). Novel insights into the pathways regulating the canine hair cycle and their deregulation in alopecia X. PLoS ONE, 12(10), e0186469. Public Library of Science 10.1371/journal.pone.0186469

Ha, N.-T.; Gross, Josef Johann; Sharifi, AR; Schlather, M; Drögemüller, Cord; Schnyder, U; Schmitz-Hsu, F; Bruckmaier, Rupert; Simianer, H (2017). Genetische Analyse der metabolischen Adaptation von Milchkühen in der Frühlaktation. Züchtungskunde, 89(1), pp. 48-60. Verlag Eugen Ulmer, Stuttgart

Seuberlich, Torsten; Wüthrich, Daniel; Selimovic-Hamza, Senija; Drögemüller, Cord; Oevermann, Anna; Bruggmann, Remy; Bouzalas, Ilias (2017). Identification of a second encephalitis-associated astrovirus in cattle. Emerging Microbes & Infections, 6(1), p. 1. Nature Publishing Group 10.1038/emi.2017.56

2016

Mauri, Nico; Kleiter, Miriam; Leschnik, Michael; Högler, Sandra; Dietschi, Elisabeth; Wiedmer, Michaela; Dietrich, Sara Joëlle; Henke, Diana; Steffen, Frank; Schuller, Simone; Gurtner, Corinne; Stokar-Regenscheit, Nadine; O'Toole, Donal; Bilzer, Thomas; Herden, Christiane; Oevermann, Anna; Jagannathan, Vidhya; Leeb, Tosso (2016). A Missense Variant in KCNJ10 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA1). G3 Genes Genomes Genetics, 7(2), pp. 663-669. Genetics Society of America 10.1534/g3.116.038455

Murgiano, Leonardo; Jagannathan, Vidhya; Piffer, Christian; Diez-Prieto, Inmaculada; Bolcato, Marilena; Gentile, Arcangelo; Drögemüller, Cord (2016). A frameshift mutation in MOCOS is associated with familial renal syndrome (xanthinuria) in Tyrolean Grey cattle. BMC veterinary research, 12(276), p. 276. BioMed Central 10.1186/s12917-016-0904-4

Pausch, Hubert; Ammermüller, Simon; Wurmser, Christine; Hamann, Henning; Tetens, Jens; Drögemüller, Cord; Fries, Ruedi (2016). A nonsense mutation in the COL7A1 gene causes epidermolysis bullosa in Vorderwald cattle. BMC genetics, 17(149), p. 149. BioMed Central 10.1186/s12863-016-0458-2

Menzi, Fiona (2016). Erste Einblicke in die Genetik der Farbvererbung bei Burenziegen. Forum Kleinwiederkäuer, 2016(11), pp. 11-15. Verlagsgenossenschaft Caprovis, Niederönz

Pacholewska, Alicja Elzbieta; Mach, Núria; Mata, Xavier; Vaiman, Anne; Schibler, Laurent; Barrey, Eric; Gerber, Vincent (2016). Novel equine tissue miRNAs and breed-related miRNA expressed in serum. BMC Genomics, 17(831), p. 831. BioMed Central 10.1186/s12864-016-3168-2

Nolte, Anna; Bello, Aimara; Drögemüller, Michaela; Leeb, Tosso; Brockhaus, Eva; Baumgärtner, Wolfgang; Wohlsein, Peter (2016). Neuronal ceroid lipofuscinosis in an adult American Staffordshire Terrier. Tierärztliche Praxis. Ausgabe K - Kleintiere, Heimtiere, 44(6), pp. 431-436. Schattauer 10.15654/TPK-150766

Kohler, Philipp; Alsaaod, Maher; Dolf, Gaudenz; O'Brien, R; Beer, Gian; Steiner, Adrian (2016). A single prolonged milking interval of 24 h compromises the well-being and health of dairy Holstein cows. Journal of dairy science, 99(11), pp. 9080-9093. American Dairy Science Association 10.3168/jds.2015-10839

Waluk, Dominik Pawel; Zur, Gila; Kaufmann, Ronnie; Welle, Monika Maria; Jagannathan, Vidhya; Drögemüller, Cord; Müller, Eliane Jasmine; Leeb, Tosso; Galichet, Arnaud (2016). A Splice Defect in the EDA Gene in Dogs with an X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED) Phenotype. G3 Genes Genomes Genetics, 6(9), pp. 2949-2954. Genetics Society of America 10.1534/g3.116.033225

Murgiano, Leonardo; Waluk, Dominik Pawel; Towers, Rachel; Wiedemar, Natalie; Dietrich, Sara Joëlle; Jagannathan, Vidhya; Drögemüller, Michaela; Balmer, Pierre; Druet, Tom; Galichet, Arnaud; Penedo, M Cecilia; Müller, Eliane Jasmine; Roosje, Petra; Welle, Monika Maria; Leeb, Tosso (2016). An Intronic MBTPS2 Variant Results in a Splicing Defect in Horses with Brindle Coat Texture. G3 Genes Genomes Genetics, 6(9), pp. 2963-2970. Genetics Society of America 10.1534/g3.116.032433

Burren, A; Neuditschko, Markus; Signer-Hasler, Heidi; Frischknecht, Mirjam; Reber, Irene; Menzi, Fiona; Drögemüller, Cord; Flury, C (2016). Genetic diversity analyses reveal first insights into breed-specific selection signatures within Swiss goat breeds. Animal genetics, 47(6), pp. 727-739. Blackwell 10.1111/age.12476

Mock, Thomas; Mehinagic, Kemal; Menzi, Fiona; Studer, Eveline; Oevermann, Anna; Stoffel, Michael Hubert; Drögemüller, Cord; Meylan, Mireille; Regenscheit, Nadine (2016). Clinicopathological Phenotype of Autosomal Recessive Cholesterol Deficiency in Holstein Cattle. Journal of veterinary internal medicine, 30(4), pp. 1369-1375. Wiley-Blackwell 10.1111/jvim.13976

Švara, Tanja; Cociancich, Vasilij; Šest, Katarina; Gombač, Mitja; Paller, Tomislav; Starič, Jože; Drögemüller, Cord (2016). Pulmonary hypoplasia and anasarca syndrome in Cika cattle. Acta Veterinaria Scandinavica, 58(1), p. 36. BioMed Central Ltd. 10.1186/s13028-016-0220-9

Renner, Swen C.; Suarez-Rubio, Marcela; Wiesner, Kerstin R.; Drögemüller, Cord; Gockel, Sonja; Kalko, Elisabeth K. V.; Ayasse, Manfred; Frantz, Alain C. (2016). Using multiple landscape genetic approaches to test the validity of genetic clusters in a species characterized by an isolation-by-distance pattern. Biological journal of the Linnean Society, 118(2), pp. 292-303. Blackwell Publishing 10.1111/bij.12737

Doelle, Maren; Linder, Keith E; Boche, Janna; Jagannathan, Vidhya; Leeb, Tosso; Linek, Monika (2016). Initial characterization of stiff skin-like syndrome in West Highland white terriers. Veterinary dermatology, 27(3), 210-e53. Blackwell Science 10.1111/vde.12316

Karli, Philemon; Oevermann, Anna; Bauer, Anina Estrella; Jagannathan, Vidhya; Leeb, Tosso (2016). MFSD8 single-base pair deletion in a Chihuahua with neuronal ceroid lipofuscinosis. Animal genetics, 47(5), p. 631. Blackwell 10.1111/age.12449

Hytönen, Marjo K; Arumilli, Meharji; Lappalainen, Anu K; Owczarek, Marta; Jagannathan, Vidhya; Hundi, Sruthi; Salmela, Elina; Venta, Patrick; Sarkiala, Eva; Jokinen, Tarja; Gorgas, Daniela; Kere, Juha; Nieminen, Pekka; Drögemüller, Cord; Lohi, Hannes (2016). Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes. PLoS genetics, 12(5), e1006037. Public Library of Science 10.1371/journal.pgen.1006037

Murgiano, Leonardo; Shirokova, Vera; Welle, Monika Maria; Jagannathan, Vidhya; Plattet, Philippe; Oevermann, Anna; Pienkowska-Schelling, Aldona; Gallo, Daniele; Gentile, Arcangelo; Mikkola, Marja L; Drögemüller, Cord (2016). Correction: Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation. PLoS genetics, 12(5), e1005688. Public Library of Science 10.1371/journal.pgen.1005688

Brinkmann, J; Jagannathan, Vidhya; Drögemüller, Cord; Rieder, S; Leeb, Tosso; Thaller, G; Tetens, J (2016). Genetic variability of the equine casein genes. Journal of dairy science, 99(7), pp. 5486-5497. American Dairy Science Association 10.3168/jds.2015-10652

Gross, Josef Johann; Schwinn, Ann-Catherine; Schmitz-Hsu, F; Menzi, Fiona; Drögemüller, Cord; Albrecht, Christiane; Bruckmaier, Rupert (2016). Rapid Communication: Cholesterol deficiency-associated APOB mutation impacts lipid metabolism in Holstein calves and breeding bulls. Journal of animal science, 94(4), pp. 1761-1766. American Society of Animal Science 10.2527/jas.2016-0439

Frischknecht, Mirjam; Flury, C; Leeb, Tosso; Rieder, S; Neuditschko, M (2016). Selection signatures in Shetland ponies. Animal genetics, 47(3), pp. 370-372. Blackwell 10.1111/age.12416

Aebi, Marlis; Wiedemar, Natalie; Drögemüller, Cord; Zanolari, Patrik (2016). [Inherited thrombopathia in Simmental cattle]. Schweizer Archiv für Tierheilkunde, 158(2), pp. 102-108. Gesellschaft Schweizer Tierärztinnen und Tierärzte

Grahofer, Alexander; Wiedemar, Natalie; Gurtner, Corinne; Drögemüller, Cord; Nathues, Heiko (2016). Diagnosis of diabetes insipidus observed in Swiss Duroc boars. BMC veterinary research, 12(1), p. 22. BioMed Central 10.1186/s12917-016-0645-4

Balogh, Orsolya; Berger, Alice; Pieńkowska-Schelling, Aldona; Willmitzer, Florian; Grest, Paula; Janett, Fredi; Schelling, Claude; Reichler, Iris M (2016). 37,X/38,XY Mosaicism in a Cryptorchid Bengal Cat with Müllerian Duct Remnants. Sexual development, 9(6), pp. 327-332. Karger 10.1159/000443233

Frischknecht, Mirjam; Signer-Hasler, Heidi; Leeb, Tosso; Rieder, S; Neuditschko, M (2016). Genome-wide association studies based on sequence-derived genotypes reveal new QTL associated with conformation and performance traits in the Franches-Montagnes horse breed. Animal genetics, 47(2), pp. 227-229. Blackwell 10.1111/age.12406

Menzi, Fiona; Besuchet Schmutz, Nathalie; Fragnière, Muriel; Hofstetter, S; Jagannathan, Vidhya; Mock, Thomas; Raemy, Andreas; Studer, Eveline; Mehinagic, Kemal; Regenscheit, Nadine; Meylan, Mireille; Schmitz-Hsu, F; Drögemüller, Cord (2016). A transposable element insertion in APOB causes cholesterol deficiency in Holstein cattle. Animal genetics, 47(2), pp. 253-257. Blackwell 10.1111/age.12410

Sayyab, Shumaila; Viluma, Agnese; Bergvall, Kerstin; Brunberg, Emma; Jagannathan, Vidhya; Leeb, Tosso; Andersson, Göran; Bergström, Tomas F (2016). Whole-Genome Sequencing of a Canine Family Trio Reveals a FAM83G Variant Associated with Hereditary Footpad Hyperkeratosis. G3 Genes Genomes Genetics, 6(3), pp. 521-527. Genetics Society of America 10.1534/g3.115.025643

Mach, Núria; Plancade, Sandra; Pacholewska, Alicja Elzbieta; Lecardonnel, Jérôme; Rivière, Julie; Moroldo, Marco; Vaiman, Anne; Morgenthaler, Caroline; Beinat, Marine; Nevot, Alizée; Robert, Céline; Barrey, Eric (2016). Integrated mRNA and miRNA expression profiling in blood reveals candidate biomarkers associated with endurance exercise in the horse. Scientific Reports, 6(22932), p. 22932. Nature Publishing Group 10.1038/srep22932

Brinkmann, J.; Jagannathan, Vidhya; Drögemüller, Cord; Rieder, S.; Leeb, Tosso; Thaller, G.; Tetens, J. (2016). DNA-based analysis of protein variants reveals different genetic variability of the paralogous equine ß-lactoglobulin genes LGB1 and LGB2. Livestock science, 187, pp. 181-185. Elsevier 10.1016/j.livsci.2016.03.014

Seuberlich, Torsten; Wüthrich, Daniel; Selimovic-Hamza, Senija; Drögemüller, Cord; Oevermann, Anna; Bruggmann, Rémy; Bouzalas, Ilias (2016). Identification of a second encephalitis-associated astrovirus in cattle. Emerging Microbes & Infections, 5(8), e71. Nature Publishing Group 10.1038/emi.2016.5

Duart Garcia, Carolina; Plattet, Philippe; Bruggmann, Rémy; Simillion, Cedric André Marie; Irene, Keller; Göran, Andersson; Braunschweig, Martin (2016). Evidence for two protein coding transcripts at the Igf2as locus. Gene Reports, 4, pp. 60-66. Elsevier 10.1016/j.genrep.2016.04.003

Agerholm, Jørgen S.; Menzi, Fiona; McEvoy, Fintan J.; Jagannathan, Vidhya; Drögemüller, Cord (2016). Lethal chondrodysplasia in a family of Holstein cattle is associated with a de novo splice site variant of COL2A1. BMC veterinary research, 12(1), p. 100. BioMed Central 10.1186/s12917-016-0739-z

Menzi, Fiona; Keller, Irene; Reber, Irene; Beck, Julia; Brenig, Bertram; Schütz, Ekkehard; Leeb, Tosso; Drögemüller, Cord (2016). Genomic amplification of the caprine EDNRA locus might lead to a dose dependent loss of pigmentation. Scientific Reports, 6, p. 28438. Nature Publishing Group 10.1038/srep28438

Agerholm, Jørgen S.; McEvoy, Fintan J.; Menzi, Fiona; Jagannathan, Vidhya; Drögemüller, Cord (2016). A CHRNB1 frameshift mutation is associated with familial arthrogryposis multiplex congenita in Red dairy cattle. BMC Genomics, 17(1) BioMed Central 10.1186/s12864-016-2832-x

Unger, Lucia; Fouché, Nathalie Elisa; Leeb, Tosso; Gerber, Vinzenz; Pacholewska, Alicja Elzbieta (2016). Optimized methods for extracting circulating small RNAs from long-term stored equine samples. Acta Veterinaria Scandinavica, 58(1), p. 44. BioMed Central Ltd. 10.1186/s13028-016-0224-5

Tengvall, Katarina; Kozyrev, Sergey; Kierczak, Marcin; Bergvall, Kerstin; Farias, Fabiana H G; Ardesjö-Lundgren, Brita; Olsson, Mia; Murén, Eva; Hagman, Ragnvi; Leeb, Tosso; Pielberg, Gerli; Hedhammar, Åke; Andersson, Göran; Lindblad-Toh, Kerstin (2016). Multiple regulatory variants located in cell type-specific enhancers within the PKP2 locus form major risk and protective haplotypes for canine atopic dermatitis in German shepherd dogs. BMC genetics, 17(1), p. 97. BioMed Central 10.1186/s12863-016-0404-3

Leeb, Tosso (2016). X-chromosomal vererbte ektodermale Dysplasien bei Haustieren. Nova acta Leopoldina, 119(404), pp. 39-46. Wiss. Verl.-Ges.

Bouzalas, Ilias; Wüthrich, Daniel; Selimovic-Hamza, Senija; Drögemüller, Cord; Bruggmann, Rémy; Seuberlich, Torsten (2016). Full-genome based molecular characterization of encephalitis-associated bovine astroviruses. Infection, genetics and evolution, 44, pp. 162-168. Elsevier 10.1016/j.meegid.2016.06.052

2015

Murgiano, Leonardo; Wiedemar, Natalie; Jagannathan, Vidhya; Isling, Louise K; Drögemüller, Cord; Agerholm, Jørgen S (2015). Epidermolysis bullosa in Danish Hereford calves is caused by a deletion in LAMC2 gene. BMC veterinary research, 11(1), p. 334. BioMed Central 10.1186/s12917-015-0334-8

Peters, Martin; Reber, Irene; Jagannathan, Vidhya; Raddatz, Barbara; Wohlsein, Peter; Drögemüller, Cord (2015). DNA-based diagnosis of rare diseases in veterinary medicine: a 4.4 kb deletion of ITGB4 is associated with epidermolysis bullosa in Charolais cattle. BMC veterinary research, 11(1), p. 366. BioMed Central 10.1186/s12917-015-0366-0

Librado, Pablo; Der Sarkissian, Clio; Ermini, Luca; Schubert, Mikkel; Jónsson, Hákon; Albrechtsen, Anders; Fumagalli, Matteo; Yang, Melinda A.; Gamba, Cristina; Seguin-Orlando, Andaine; Mortensen, Cecilie D.; Petersen, Bent; Hoover, Cindi A.; Lorente-Galdos, Belen; Nedoluzhko, Artem; Boulygina, Eugenia; Tsygankova, Svetlana; Neuditschko, Markus; Jagannathan, Vidhya; Thèves, Catherine; ... (2015). Tracking the origins of Yakutian horses and the genetic basis for their fast adaptation to subarctic environments. Proceedings of the National Academy of Sciences of the United States of America - PNAS, 112(50), E6889-E6897. National Academy of Sciences NAS 10.1073/pnas.1513696112

Wiedmer, Michaela; Oevermann, Anna; Borer, Stephanie; Gorgas, Daniela; Shelton, G. Diane; Drögemüller, Michaela; Jagannathan, Vidhya; Henke, Diana; Leeb, Tosso (2015). A RAB3GAP1 SINE Insertion in Alaskan Huskies with Polyneuropathy, Ocular Abnormalities and Neuronal Vacuolation (POANV) Resembling Human Warburg Micro Syndrome 1 (WARBM1). G3 Genes Genomes Genetics, 6(2), pp. 255-262. Genetics Society of America 10.1534/g3.115.022707

Hahn, Kerstin Caroline; Rohdin, Cecilia; Jagannathan, Vidhya; Wohlsein, Peter; Baumgärtner, Wolfgang; Seehusen, Frauke; Spitzbarth, Ingo; Grandon, Rodrigo; Drögemüller, Cord; Jäderlund, Karin Hultin (2015). TECPR2 Associated Neuroaxonal Dystrophy in Spanish Water Dogs. PLoS ONE, 10(11), e0141824. Public Library of Science 10.1371/journal.pone.0141824

Burgstaller, J; Thaller, D; Leeb, Tosso; Schlesinger, P; Kofler, J (2015). Syringomyelia in a Newborn Male Simmental Calf. Journal of veterinary internal medicine, 29(6), pp. 1633-1637. Wiley-Blackwell 10.1111/jvim.13646

Der Sarkissian, Clio; Ermini, Luca; Schubert, Mikkel; Yang, Melinda A; Librado, Pablo; Fumagalli, Matteo; Jónsson, Hákon; Bar-Gal, Gila Kahila; Albrechtsen, Anders; Vieira, Filipe G; Petersen, Bent; Ginolhac, Aurélien; Seguin-Orlando, Andaine; Magnussen, Kim; Fages, Antoine; Gamba, Cristina; Lorente-Galdos, Belen; Polani, Sagi; Steiner, Cynthia; Neuditschko, Markus; ... (2015). Evolutionary Genomics and Conservation of the Endangered Przewalski's Horse. Current Biology, 25(19), pp. 2577-2583. Cell Press 10.1016/j.cub.2015.08.032

Steffen, Frank; Bilzer, Thomas; Brands, Jan; Golini, Lorenzo; Jagannathan, Vidhya; Wiedmer, Michaela; Drögemüller, Michaela; Drögemüller, Cord; Leeb, Tosso (2015). A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular Dystrophy. G3 Genes Genomes Genetics, 5(12), pp. 2611-2617. Genetics Society of America 10.1534/g3.115.021923

Dorotea, Tiziano; Grünberg, Walter; Murgiano, Leonardo; Plattet, Philippe; Drögemüller, Cord; Mascarello, Francesco; Sacchetto, Roberta (2015). Fast-twitch skeletal muscle fiber adaptation to SERCA1 deficiency in a Dutch Improved Red and White calf pseudomyotonia case. Neuromuscular disorders, 25(11), pp. 888-897. Elsevier 10.1016/j.nmd.2015.08.010

Pacholewska, Alicja Elzbieta; Jagannathan, Vidhya; Drögemüller, Michaela; Klukowska-Rötzler, Jolanta; Lanz, Simone; Hamza, Eman; Dermitzakis, Emmanouil T; Marti, Eliane Isabelle; Leeb, Tosso; Gerber, Vinzenz (2015). Impaired Cell Cycle Regulation in a Natural Equine Model of Asthma. PLoS ONE, 10(8), e0136103. Public Library of Science 10.1371/journal.pone.0136103

Wiedemar, Natalie; Riedi, Anna-Katharina; Jagannathan, Vidhya; Drögemüller, Cord; Meylan, Mireille (2015). Genetic Abnormalities in a Calf with Congenital Increased Muscular Tonus. Journal of veterinary internal medicine, 29(5), pp. 1418-1421. Wiley-Blackwell 10.1111/jvim.13599

Bianchi, Matteo; Dahlgren, Stina; Massey, Jonathan; Dietschi, Elisabeth; Kierczak, Marcin; Lund-Ziener, Martine; Sundberg, Katarina; Thoresen, Stein Istre; Kämpe, Olle; Andersson, Göran; Ollier, William E R; Hedhammar, Åke; Leeb, Tosso; Lindblad-Toh, Kerstin; Kennedy, Lorna J; Lingaas, Frode; Rosengren Pielberg, Gerli (2015). A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12. PLoS ONE, 10(8), e0134720. Public Library of Science 10.1371/journal.pone.0134720

Haase, Bianca; Jagannathan, Vidhya; Rieder, Stefan; Leeb, Tosso (2015). A novel KIT variant in an Icelandic horse with white-spotted coat colour. Animal genetics, 46(4), p. 466. Blackwell 10.1111/age.12313

Wiedemar, Natalie; Drögemüller, Cord (2015). A 1.8-kb insertion in the 3'-UTR of RXFP2 is associated with polledness in sheep. Animal genetics, 46(4), pp. 457-461. Blackwell 10.1111/age.12309

Decker, Brennan; Davis, Brian W; Rimbault, Maud; Long, Adrienne H; Karlins, Eric; Parker, Heidi G; Jagannathan, Vidhya; Reiman, Rebecca; Drögemüller, Cord; Corneveaux, Jason J; Chapman, Erica S; Trent, Jeffery M; Leeb, Tosso; Huentelman, Matthew J; Wayne, Robert K; Karyadi, Danielle M; Ostrander, Elaine A (2015). Comparison against 186 canid whole genome sequences reveals survival strategies of an ancient clonally transmissible canine tumor. Genome research, 25(11), pp. 1646-1655. Cold Spring Harbor, N.Y 10.1101/gr.190314.115

Olsson, Mia; Tengvall, Katarina; Frankowiack, Marcel; Kierczak, Marcin; Bergvall, Kerstin; Axelsson, Erik; Tintle, Linda; Marti, Eliane Isabelle; Roosje, Petra; Leeb, Tosso; Hedhammar, Åke; Hammarström, Lennart; Lindblad-Toh, Kerstin (2015). Genome-Wide Analyses Suggest Mechanisms Involving Early B-Cell Development in Canine IgA Deficiency. PLoS ONE, 10(7), e0133844. Public Library of Science 10.1371/journal.pone.0133844

Lindert, Uschi; Weis, Mary Ann; Rai, Jyoti; Seeliger, Frank; Hausser, Ingrid; Leeb, Tosso; Eyre, David; Rohrbach, Marianne; Giunta, Cecilia (2015). Molecular Consequences of the SERPINH1/HSP47 Mutation in the Dachshund Natural Model of Osteogenesis Imperfecta. Journal of biological chemistry, 290(29), pp. 17679-17689. American Society for Biochemistry and Molecular Biology 10.1074/jbc.M115.661025

Dietrich, Joëlle; Menzi, Fiona; Ammann, Philippe; Drögemüller, Cord; Leeb, Tosso (2015). A breeding experiment confirms the dominant mode of inheritance of the brown coat colour associated with the (496) Asp TYRP1 allele in goats. Animal genetics, 46(5), pp. 587-588. Blackwell 10.1111/age.12320

Murgiano, Leonardo; Shirokova, Vera; Welle, Monika Maria; Jagannathan, Vidhya; Plattet, Philippe; Oevermann, Anna; Pienkowska-Schelling, Aldona; Gallo, Daniele; Gentile, Arcangelo; Mikkola, Marja; Drögemüller, Cord (2015). Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation. PLoS genetics, 11(7), e1005427. Public Library of Science 10.1371/journal.pgen.1005427

Muscatello, L V; Benazzi, C; Dittmer, K E; Thompson, K G; Murgiano, Leonardo; Drögemüller, Cord; Avallone, G; Gentile, A; Edwards, J F; Piffer, C; Bolcato, M; Brunetti, B (2015). Ellis-van Creveld Syndrome in Grey Alpine Cattle: Morphologic, Immunophenotypic, and Molecular Characterization. Veterinary pathology, 52(5), pp. 957-966. American College of Veterinary Pathologists 10.1177/0300985815588610

Haase, Bianca; Rieder, S; Leeb, Tosso (2015). Two variants in the KIT gene as candidate causative mutations for a dominant white and a white spotting phenotype in the donkey. Animal genetics, 46(3), pp. 321-324. Blackwell 10.1111/age.12282

Tetens, J; Wiedemar, Natalie; Menoud, Annie; Thaller, G; Drögemüller, Cord (2015). Association mapping of the scurs locus in polled Simmental cattle - evidence for genetic heterogeneity. Animal genetics, 46(2), pp. 224-225. Blackwell 10.1111/age.12237

Kyöstilä, Kaisa; Syrjä, Pernilla; Jagannathan, Vidhya; Chandrasekar, Gayathri; Jokinen, Tarja S; Seppälä, Eija H; Becker, Doreen; Drögemüller, Michaela; Dietschi, Elisabeth; Drögemüller, Cord; Lang, Johann; Steffen, Frank; Rohdin, Cecilia; Jäderlund, Karin H; Lappalainen, Anu K; Hahn, Kerstin; Wohlsein, Peter; Baumgärtner, Wolfgang; Henke, Diana; Oevermann, Anna; ... (2015). A Missense Change in the ATG4D Gene Links Aberrant Autophagy to a Neurodegenerative Vacuolar Storage Disease. PLoS genetics, 11(4), e1005169. Public Library of Science 10.1371/journal.pgen.1005169

Pacholewska, Alicja Elzbieta; Drögemüller, Michaela; Klukowska, Jolanta; Lanz, Simone; Hamza, Eman; Dermitzakis, Emmanouil T; Marti, Eliane Isabelle; Gerber, Vinzenz; Leeb, Tosso; Jagannathan, Vidhya (2015). The transcriptome of equine peripheral blood mononuclear cells. PLoS ONE, 10(3), e0122011. Public Library of Science 10.1371/journal.pone.0122011

Reber, Irene; Keller, Irene; Becker, Doreen; Flury, C; Welle, Monika Maria; Drögemüller, Cord (2015). Wattles in goats are associated with the FMN1/GREM1 region on chromosome 10. Animal genetics, 46(3), pp. 316-320. Blackwell 10.1111/age.12279

Gerber, Martina; Fischer, Andrea; Jagannathan, Vidhya; Drögemüller, Michaela; Drögemüller, Cord; Schmidt, Martin J; Bernardino, Filipa; Manz, Eberhard; Matiasek, Kaspar; Rentmeister, Kai; Leeb, Tosso (2015). A Deletion in the VLDLR Gene in Eurasier Dogs with Cerebellar Hypoplasia Resembling a Dandy-Walker-Like Malformation (DWLM). PLoS ONE, 10(2), e0108917. Public Library of Science 10.1371/journal.pone.0108917

Tassano, Elisa; Jagannathan, Vidhya; Drögemüller, Cord; Leoni, Massimiliano; Hytönen, Marjo K; Severino, Mariasavina; Gimelli, Stefania; Cuoco, Cristina; Rocco, Maja Di; Sanio, Kirsi; Groves, Andrew K; Leeb, Tosso; Gimelli, Giorgio (2015). Congenital aural atresia associated with agenesis of internal carotid artery in a girl with a FOXI3 deletion. American journal of medical genetics. Part A, 167(3), pp. 537-544. Wiley-Liss 10.1002/ajmg.a.36895

Becker, Doreen; Otto, Mandy; Ammann, P; Keller, Irene; Drögemüller, Cord; Leeb, Tosso (2015). The brown coat colour of Coppernecked goats is associated with a non-synonymous variant at the TYRP1 locus on chromosome 8. Animal genetics, 46(1), pp. 50-54. Blackwell 10.1111/age.12240

Drögemüller, Michaela; Jagannathan, Vidhya; Dolf, Gaudenz; Butenhoff, Karin; Kottmann-Berger, Suzanne; Wess, Gerhard; Leeb, Tosso (2015). A single codon insertion in the PICALM gene is not associated with subvalvular aortic stenosis in Newfoundland dogs. Human genetics, 134(1), pp. 127-129. Springer 10.1007/s00439-014-1506-5

Kook, P. H.; Drögemüller, Michaela; Leeb, Tosso; Hinden, Sandro; Ruetten, M.; Howard, J. (2015). Hepatic fungal infection in a young beagle with unrecognised hereditary cobalamin deficiency (Imerslund-Gräsbeck syndrome). Journal of small animal practice, 56(2), pp. 138-141. Pergamon Press 10.1111/jsap.12251

Rupp, Sebastian; Aguilar Bultet, Lisandra; Jagannathan, Vidhya; Guldimann, Claudia; Drögemüller, Cord; Pfarrer, Christiane; Vidondo, Beatriz; Seuberlich, Torsten; Frey, Joachim; Oevermann, Anna (2015). A naturally occurring prfA truncation in a Listeria monocytogenes field strain contributes to reduced replication and cell-to-cell spread. Veterinary microbiology, 179(1-2), pp. 91-101. Elsevier 10.1016/j.vetmic.2015.03.002

van der Kolk, Johannes Hermanus; Pacholewska, Alicja Elzbieta; Gerber, Vinzenz (2015). The role of microRNAs in equine medicine: a review. Veterinary quarterly, 35(2), pp. 88-96. Taylor & Francis 10.1080/01652176.2015.1021186

Wiener, Dominique Judith; Wiedemar, Natalie; Welle, Monika Maria; Drögemüller, Cord (2015). Novel Features of the Prenatal Horn Bud Development in Cattle (Bos taurus). PLoS ONE, 10(5), e0127691. Public Library of Science 10.1371/journal.pone.0127691

Frischknecht, Mirjam; Jagannathan, Vidhya; Plattet, Philippe; Neuditschko, Markus; Signer-Hasler, Heidi; Bachmann, Iris; Pacholewska, Alicja Elzbieta; Drögemüller, Cord; Dietschi, Elisabeth; Flury, Christine; Rieder, Stefan; Leeb, Tosso (2015). A Non-Synonymous HMGA2 Variant Decreases Height in Shetland Ponies and Other Small Horses. PLoS ONE, 10(10), e0140749. Public Library of Science 10.1371/journal.pone.0140749

Burren, Alexander; Wiedemar, Natalie; Drögemüller, Cord; Jörg, Hannes (2015). Genetik der Hornlosigkeit beim Rind. Agrarforschung Schweiz, 6(2), pp. 72-75. Agroscope

2014

Frischknecht, Mirjam; Jagannathan, Vidhya; Leeb, Tosso (2014). Whole genome sequencing confirms KIT insertions in a white cat. Animal genetics, 46(1), p. 98. Blackwell 10.1111/age.12246

Wiedemar, Natalie; Drögemüller, Cord (2014). A 19-Mb de novo deletion on BTA 22 including MITF leads to microphthalmia and the absence of pigmentation in a Holstein calf. Animal genetics, 45(6), pp. 868-870. Blackwell 10.1111/age.12213

Drögemüller, Michaela; Jagannathan, Vidhya; Welle, Monika Maria; Graubner, Claudia; Straub, Reto; Gerber, Vinzenz; Burger, Dominik; Signer-Hasler, Heidi; Poncet, Pierre-André; Klopfenstein, Stéphane; von Niederhäusern, Ruedi; Tetens, Jens; Rieder, Stefan; Thaller, Georg; Drögemüller, Cord; Leeb, Tosso (2014). Congenital Hepatic Fibrosis in the Franches-Montagnes Horse Is Associated with the Polycystic Kidney and Hepatic Disease 1 (PKHD1) Gene. PLoS ONE, 9(10), e1004635. Public Library of Science 10.1371/journal.pone.0110125

Ekenstedt, Kari J; Becker, Doreen; Minor, Katie M; Shelton, G Diane; Patterson, Edward E; Bley, Tim Hendrik; Oevermann, Anna; Bilzer, Thomas; Leeb, Tosso; Drögemüller, Cord; Mickelson, James R (2014). An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogs. PLoS genetics, 10(10), e1004635. Public Library of Science 10.1371/journal.pgen.1004635

Herder, V.; Kummrow, M.; Leeb, Tosso; Sewell, A. C.; Hansmann, F.; Lehmbecker, A.; Wohlsein, P.; Baumgärtner, W. (2014). Polycystic Kidneys and GM2 Gangliosidosis-Like Disease in Neonatal Springboks (Antidorcas marsupialis). Veterinary pathology, 52(3), pp. 543-552. American College of Veterinary Pathologists 10.1177/0300985814549210

Mählmann, Kathrin; Hamza, Eman; Marti, Eliane Isabelle; Dolf, Gaudenz; Klukowska, Jolanta; Gerber, Vinzenz; Koch, Christoph (2014). Increased FOXP3 expression in tumour-associated tissues of horses affected with equine sarcoid disease. Veterinary journal, 202(3), pp. 516-521. Elsevier 10.1016/j.tvjl.2014.09.003

Karli, Philemon; Karol, Agnieszka; Oevermann, Anna; Drögemüller, Cord; Gorgas, Daniela; Henke, Diana (2014). The canine neuronal ceroid-lipofuscinosis: a review. Schweizer Archiv für Tierheilkunde, 156(9), pp. 417-423. Huber 10.1024/0036-7281/a000623

Bouzalas, Ilias G; Wüthrich, Daniel; Walland, Julia Gianna Marlene; Drögemüller, Cord; Zurbriggen, Andreas; Vandevelde, Marc; Oevermann, Anna; Bruggmann, Rémy; Seuberlich, Torsten (2014). Neurotropic astrovirus in cattle with nonsuppurative encephalitis in Europe. Journal of clinical microbiology, 52(9), pp. 3318-3324. American Society for Microbiology 10.1128/JCM.01195-14

Menzi, Fiona (2014). Erbfehler bei Ziegen: ein Problem? Forum Kleinwiederkäuer, 2014(9), pp. 12-19. Verlagsgenossenschaft Caprovis, Niederönz

Fariello, Maria-Ines; Servin, Bertrand; Tosser-Klopp, Gwenola; Rupp, Rachel; Moreno, Carole; San Cristobal, Magali; Boitard, Simon; Drögemüller, Cord; The International Sheep Genomics Consortium, ISGC (2014). Selection signatures in worldwide sheep populations. PLoS ONE, 9(8), e103813. Public Library of Science 10.1371/journal.pone.0103813

Müller, Eliane Jasmine; Galichet, Arnaud; Wiener, Dominique Judith; Marti, Eliane Isabelle; Drögemüller, Cord; Welle, Monika Maria; Roosje, Petra; Leeb, Tosso; Suter, Maja (2014). Keratinocyte biology and pathology. Veterinary dermatology, 25(4), pp. 236-238. Blackwell Science 10.1111/vde.12158

Tetens, J L; Qanbari, S; Drögemüller, Cord; Pimentel, E C G; Bennewitz, J; Thaller, G; Tetens, J (2014). Bos indicus introgression into (peri-)alpine cattle breeds - evidence from the analysis of bovine whey protein variants. Animal genetics, 45(4), pp. 585-588. Blackwell 10.1111/age.12185

O'Brien, D. P.; Leeb, Tosso (2014). DNA testing in neurologic diseases. Journal of veterinary internal medicine, 28(4), pp. 1186-1198. Wiley-Blackwell 10.1111/jvim.12383

Murgiano, Leonardo; Drögemüller, Cord; Sbarra, F; Bolcato, M; Gentile, A (2014). Prevalence of paunch calf syndrome carriers in Italian Romagnola cattle. Veterinary journal, 200(3), pp. 459-461. Elsevier 10.1016/j.tvjl.2014.03.020

Becker, Doreen; Luther, Henning; Hofer, Andreas; Leeb, Tosso (2014). A variant in MYO10 is associated with hind limb conformation in Swiss Large White boars. Animal genetics, 45(2), p. 308. Blackwell 10.1111/age.12111

Fritsche, R.; Dolf, Gaudenz; Schelling, C.; Hungerbuehler, S. O.; Hagen, R.; Reichler, I. M. (2014). Inheritance of ectopic ureters in Entlebucher Mountain Dogs. Journal of animal breeding and genetics, 131(2), pp. 146-152. Wiley-Blackwell 10.1111/jbg.12055

Murgiano, Leonardo; Jagannathan, Vidhya; Benazzi, Cinzia; Bolcato, Marilena; Brunetti, Barbara; Muscatello, Luisa Vera; Dittmer, Keren; Piffer, Christian; Gentile, Arcangelo; Drögemüller, Cord (2014). Deletion in the EVC2 gene causes chondrodysplastic dwarfism in Tyrolean Grey cattle. PLoS ONE, 9(4), e94861. Public Library of Science 10.1371/journal.pone.0094861

Kook, P. H.; Drögemüller, Michaela; Leeb, Tosso; Howard, J.; Ruetten, M. (2014). Degenerative liver disease in young Beagles with hereditary cobalamin malabsorption because of a mutation in the cubilin gene. Journal of veterinary internal medicine, 28(2), pp. 666-671. Wiley-Blackwell 10.1111/jvim.12295

Christen, Garance Anne; Gerber, Vinzenz; Dolf, Gaudenz; Burger, Dominik; Koch, Christoph (2014). Inheritance of equine sarcoid disease in Franches-Montagnes horses. Veterinary journal, 199(1), pp. 68-71. Elsevier 10.1016/j.tvjl.2013.09.053

Drögemüller, Michaela; Jagannathan, Vidhya; Howard, J.; Bruggmann, Rémy; Drögemüller, Cord; Ruetten, Maja; Leeb, Tosso; Kook, Peter H. (2014). A frameshift mutation in the cubilin gene (CUBN) in Beagles with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption). Animal genetics, 45(1), pp. 148-150. Blackwell 10.1111/age.12094

Signer-Hasler, Heidi; Neuditschko, Markus; Koch, Christoph; Froidevaux, Sylvie Marie; Flury, Christine; Burger, Dominik; Leeb, Tosso; Rieder, Stefan (2014). A chromosomal region on ECA13 is associated with maxillary prognathism in horses. PLoS ONE, 9(1), e86607. Public Library of Science 10.1371/journal.pone.0086607

Drögemüller, Michaela; Jagannathan, Vidhya; Becker, Doreen; Drögemüller, Cord; Schelling, Claude; Plassais, Jocelyn; Kaerle, Cécile; Dufaure de Citres, Caroline; Thomas, Anne; Müller, Eliane Jasmine; Welle, Monika Maria; Roosje, Petra; Leeb, Tosso (2014). A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH). PLoS genetics, 10(5), e1004370. Public Library of Science 10.1371/journal.pgen.1004370

Heaton, Michael P.; Leymaster, Kreg A.; Kalbfleisch, Theodore S.; Kijas, James W.; Clarke, Shannon M.; McEwan, John.; Maddox, Jillian F.; Basnayake, Veronica; Petrik, Dustin T.; Simpson, Barry; Smith, Timothy P. L.; Chitko-McKown, Carol G.; Drögemüller, Cord; The International Sheep Genomics Consortium, ISGC (2014). SNPs for parentage testing and traceability in globally diverse breeds of sheep. PLoS ONE, 9(4), e94851. Public Library of Science 10.1371/journal.pone.0094851

Braun, Ueli; Jacober, Simon; Drögemüller, Cord (2014). Congenital nasolacrimal duct fistula in Brown Swiss cattle. BMC veterinary research, 10, p. 44. BioMed Central 10.1186/1746-6148-10-44

Wiedemar, Natalie; Tetens, Jens; Jagannathan, Vidhya; Menoud, Annie; Neuenschwander, Samuel; Bruggmann, Rémy; Thaller, Georg; Drögemüller, Cord (2014). Independent polled mutations leading to complex gene expression differences in cattle. PLoS ONE, 9(3), e93435. Public Library of Science 10.1371/journal.pone.0093435

Murgiano, Leonardo; Jagannathan, Vidhya; Calderoni, Valerio; Joechler, Monika; Gentile, Arcangelo; Drögemüller, Cord (2014). Looking the cow in the eye: deletion in the NID1 gene is associated with recessive inherited cataract in Romagnola cattle. PLoS ONE, 9(10), e110628. Public Library of Science 10.1371/journal.pone.0110628

Burren, Alexander; Signer-Hasler, Heidi; Neuditschko, Markus; Tetens, Jens; Kijas, James; Drögemüller, Cord; Flury, Christine (2014). Fine-scale population structure analysis of seven local Swiss sheep breeds using genome-wide SNP data. Animal genetic resources, 55, pp. 67-76. Cambridge University Press 10.1017/S2078633614000253

Rampoldi, A; Bertschinger, H U; Bürgi, E; Dolf, Gaudenz; Sidler, X; Bratus, A; Vögeli, P; Neuenschwander, S (2014). Inheritance of porcine receptors for enterotoxigenic Escherichia coli with fimbriae F4ad and their relation to other F4 receptors. Animal, 8(6), pp. 859-866. Cambridge University Press 10.1017/S1751731114000779

Frischknecht, Mirjam; Neuditschko, Markus; Jagannathan, Vidhya; Drögemüller, Cord; Tetens, Jens; Thaller, Georg; Leeb, Tosso; Rieder, Stefan (2014). Imputation of sequence level genotypes in the Franches-Montagnes horse breed. Genetics, selection, evolution, 46(1), p. 63. BioMed Central 10.1186/s12711-014-0063-7

Wiewiórka, Marek S; Messina, Antonio; Pacholewska, Alicja Elzbieta; Maffioletti, Sergio; Gawrysiak, Piotr; Okoniewski, Michał J (2014). SparkSeq: fast, scalable and cloud-ready tool for the interactive genomic data analysis with nucleotide precision. Bioinformatics, 30(18), pp. 2652-2653. Oxford University Press 10.1093/bioinformatics/btu343

Haberland, A. M.; Luther, H.; Hofer, A.; Tholen, E.; Simianer, H.; Lind, B.; Baes, C. (2014). Efficiency of different selection strategies against boar taint in pigs. Animal, 8(1), pp. 11-19. Cambridge University Press 10.1017/S1751731113001857

2013

Shakhsi Niaei, Mostafa; Drögemüller, Michaela; Jagannathan, Vidhya; Gerber, Vinzenz; Leeb, Tosso (2013). IL26 gene inactivation in Equidae. Animal genetics, 44(6), pp. 770-772. Blackwell 10.1111/age.12069

Gendron, Karine; Owczarek-Lipska, Marta; Lang, Johann; Leeb, Tosso (2013). Maine Coon renal screening: ultrasonographical characterisation and preliminary genetic analysis for common genes in cats with renal cysts. Journal of feline medicine and surgery, 15(12), pp. 1079-1085. Sage 10.1177/1098612X13492164

Hauswirth, Regula; Jude, Rony; Haase, Bianca; Bellone, Rebecca R; Archer, Sheila; Holl, Heather; Brooks, Samantha A; Tozaki, Teruaki; Penedo, Maria Cecilia T; Rieder, Stefan; Leeb, Tosso (2013). Novel variants in the KIT and PAX3 genes in horses with white-spotted coat colour phenotypes. Animal genetics, 44(6), pp. 763-765. Blackwell 10.1111/age.12057

Kijas, J. W.; Serrano, M.; McCulloch, R.; Li, Y.; Salces Ortiz, J.; Calvo, J. H.; Pérez-Guzmán, M. D.; Drögemüller, Cord; The International Sheep Genomics Consortium, ISGC (2013). Genomewide association for a dominant pigmentation gene in sheep. Journal of animal breeding and genetics, 130(6), pp. 468-475. Wiley-Blackwell 10.1111/jbg.12048

Bruggmann, Rémy; Jagannathan, Vidhya; Braunschweig, Martin (2013). In search of epigenetic marks in testes and sperm cells of differentially fed boars. PLoS ONE, 8(11), e78691. Public Library of Science 10.1371/journal.pone.0078691

Greber, Deborah; Steiner, Adrian; Drögemüller, Cord (September 2013). Entropium und andere Missbildungen in der Schweizer Schafzucht. Forum Kleinwiederkäuer, 2013(9), pp. 6-12. Verlagsgenossenschaft Caprovis, Niederönz

Leeb, Tosso (2013). The Spanish Riding School and the Haute Ecole of complex trait genetics. Pigment cell & melanoma research, 26(4), pp. 439-440. Wiley 10.1111/pcmr.12116

Shirokova, Vera; Jussila, Maria; Hytönen, Marjo K.; Perälä, Nina; Drögemüller, Cord; Leeb, Tosso; Lohi, Hannes; Sainio, Kirsi; Thesleff, Irma; Mikkola, Marja L. (2013). Expression of Foxi3 is regulated by ectodysplasin in skin appendage placodes. Developmental dynamics, 242(6), pp. 593-603. John Wiley & Sons 10.1002/dvdy.23952

Tengvall, Katarina; Kierczak, Marcin; Bergvall, Kerstin; Olsson, Mia; Frankowiack, Marcel; Farias, Fabiana H G; Pielberg, Gerli; Carlborg, Örjan; Leeb, Tosso; Andersson, Göran; Hammarström, Lennart; Hedhammar, Åke; Lindblad-Toh, Kerstin (2013). Genome-wide analysis in German shepherd dogs reveals association of a locus on CFA 27 with atopic dermatitis. PLoS genetics, 9(5), e1003475. Public Library of Science 10.1371/journal.pgen.1003475

Blatter, Marlis; Haase, Bianca; Gerber, Vinzenz; Poncet, P.-A.; Leeb, Tosso; Rieder, S.; Henke, Diana; Janett, F.; Burger, Dominik (2013). Clinical evaluation of the new coat colour macchiato in a male Franches-Montagnes horse. Schweizer Archiv für Tierheilkunde, 155(4), pp. 229-232. Huber 10.1024/0036-7281/a000451

Wiener, Dominique Judith; Gurtner, Corinne; Panakova, Lucia; Mausberg, Theresa-Bernadette; Müller, Eliane Jasmine; Drögemüller, Cord; Leeb, Tosso; Welle, Monika Maria (2013). Clinical and histological characterization of hair coat and glandular tissue of Chinese crested dogs. Veterinary dermatology, 24(2), 274-e62. Blackwell Science 10.1111/vde.12008

Owczarek-Lipska, Marta; Mausberg, Theresa-Bernadette; Stephenson, Hannah; Dukes-McEwan, Joanna; Wess, Gerhard; Leeb, Tosso (2013). A 16-bp deletion in the canine PDK4 gene is not associated with dilated cardiomyopathy in a European cohort of Doberman Pinschers. Animal genetics, 44(2), p. 239. Blackwell 10.1111/j.1365-2052.2012.02396.x

Reber, Irene (2013). Glöckchen-Vererbung bei Ziegen. Forum Kleinwiederkäuer, 2013(4), pp. 18-23. Verlagsgenossenschaft Caprovis, Niederönz

Schütz, Ekkehard; Brenig, Bertram; Scharfenstein, Melanie; Drögemüller, Cord; Leeb, Tosso (2013). Osteogenesis imperfecta in dachshunds. Veterinary record, 172(12), p. 319. British Veterinary Association 10.1136/vr.f1823

Murgiano, Leonardo; Testoni, S.; Drögemüller, Cord; Bolcato, M.; Gentile, A. (2013). Frequency of bovine congenital pseudomyotonia carriers in selected Italian Chianina sires. Veterinary journal, 195(2), pp. 238-240. Elsevier 10.1016/j.tvjl.2012.04.021

Peters, Laureen Michèle; Demmel, Steffi; Pusch, G.; Buters, J. T. M.; Thormann, W.; Zielinski, Jana; Leeb, Tosso; Mevissen, Meike; Schmitz, Andrea (2013). Equine cytochrome P450 2B6--genomic identification, expression and functional characterization with ketamine. Toxicology and Applied Pharmacology, 266(1), pp. 101-8. Elsevier 10.1016/j.taap.2012.10.028

Gallinat, J. L.; Qanbari, S.; Drögemüller, Cord; Pimentel, E. C. G.; Thaller, G.; Tetens, J. (2013). DNA-based identification of novel bovine casein gene variants. Journal of dairy science, 96(1), pp. 699-709. American Dairy Science Association 10.3168/jds.2012-5908

Towers, Rachel E; Murgiano, Leonardo; Millar, David S; Glen, Elise; Topf, Ana; Jagannathan, Vidhya; Drögemüller, Cord; Goodship, Judith A; Clarke, Angus J; Leeb, Tosso (2013). A Nonsense Mutation in the IKBKG Gene in Mares with Incontinentia Pigmenti. PLoS ONE, 8(12), e81625. Public Library of Science 10.1371/journal.pone.0081625

Bellone, Rebecca R; Holl, Heather; Setaluri, Vijayasaradhi; Devi, Sulochana; Maddodi, Nityanand; Archer, Sheila; Sandmeyer, Lynne; Ludwig, Arne; Foerster, Daniel; Pruvost, Melanie; Reissmann, Monika; Bortfeldt, Ralf; Adelson, David L; Lim, Sim Lin; Nelson, Janelle; Haase, Bianca; Engensteiner, Martina; Leeb, Tosso; Forsyth, George; Mienaltowski, Michael J; ... (2013). Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse. PLoS ONE, 8(10), e78280. Public Library of Science 10.1371/journal.pone.0078280

Haase, Bianca; Signer-Hasler, Heidi; Binns, Matthew M; Obexer-Ruff, Gabriela; Hauswirth, Regula; Bellone, Rebecca R; Burger, Dominik; Rieder, Stefan; Wade, Claire M; Leeb, Tosso (2013). Accumulating mutations in series of haplotypes at the KIT and MITF loci are major determinants of white markings in Franches-Montagnes horses. PLoS ONE, 8(9), e75071. Public Library of Science 10.1371/journal.pone.0075071

Jagannathan, Vidhya; Bannoehr, Jeanette; Plattet, Philippe; Hauswirth, Regula; Drögemüller, Cord; Drögemüller, Michaela; Wiener, Dominique Judith; Doherr, Marcus; Owczarek-Lipska, Marta; Galichet, Arnaud; Welle, Monika Maria; Tengvall, Katarina; Bergvall, Kerstin; Lohi, Hannes; Rüfenacht, Silvia; Linek, Monika; Paradis, Manon; Müller, Eliane Jasmine; Roosje, Petra and Leeb, Tosso (2013). A mutation in the SUV39H2 gene in Labrador Retrievers with hereditary nasal parakeratosis (HNPK) provides insights into the epigenetics of keratinocyte differentiation. PLoS genetics, 9(10), e1003848. Public Library of Science 10.1371/journal.pgen.1003848

Owczarek-Lipska, Marta; Jagannathan, Vidhya; Drögemüller, Cord; Lutz, Sabina; Glanemann, Barbara; Leeb, Tosso; Kook, Peter H. (2013). A frameshift mutation in the cubilin gene (CUBN) in Border Collies with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption). PLoS ONE, 8(4), e61144. Public Library of Science 10.1371/journal.pone.0061144

Frischknecht, Mirjam; Niehof-Oellers, Helena; Jagannathan, Vidhya; Owczarek-Lipska, Marta; Drögemüller, Cord; Dietschi, Elisabeth; Dolf, Gaudenz; Tellhelm, Bernd; Lang, Johann; Tiira, Katriina; Lohi, Hannes; Leeb, Tosso (2013). A COL11A2 mutation in Labrador retrievers with mild disproportionate dwarfism. PLoS ONE, 8(3), e60149. Public Library of Science 10.1371/journal.pone.0060149

Becker, Doreen; Wimmers, Klaus; Luther, Henning; Hofer, Andreas; Leeb, Tosso (2013). A genome-wide association study to detect QTL for commercially important traits in Swiss Large White boars. PLoS ONE, 8(2), e55951. Public Library of Science 10.1371/journal.pone.0055951

Petersen, Jessica L; Mickelson, James R; Cothran, E Gus; Andersson, Lisa S; Axelsson, Jeanette; Bailey, Ernie; Bannasch, Danika; Binns, Matthew M; Borges, Alexandre S; Brama, Pieter; da Câmara Machado, Artur; Distl, Ottmar; Felicetti, Michela; Fox-Clipsham, Laura; Graves, Kathryn T; Guérin, Gérard; Haase, Bianca; Hasegawa, Telhisa; Hemmann, Karin; Hill, Emmeline W; ... (2013). Genetic diversity in the modern horse illustrated from genome-wide SNP data. PLoS ONE, 8(1), e54997. Public Library of Science 10.1371/journal.pone.0054997

Petersen, Jessica L; Mickelson, James R; Rendahl, Aaron K; Valberg, Stephanie J; Andersson, Lisa S; Axelsson, Jeanette; Bailey, Ernie; Bannasch, Danika; Binns, Matthew M; Borges, Alexandre S; Brama, Pieter; da Câmara Machado, Artur; Capomaccio, Stefano; Cappelli, Katia; Cothran, E Gus; Distl, Ottmar; Fox-Clipsham, Laura; Graves, Kathryn T; Guérin, Gérard; Haase, Bianca; ... (2013). Genome-wide analysis reveals selection for important traits in domestic horse breeds. PLoS genetics, 9(1), e1003211. Public Library of Science 10.1371/journal.pgen.1003211

Koch, Caroline Tina; Bruggmann, Rémy; Tetens, Jens; Drögemüller, Cord (2013). A non-coding genomic duplication at the HMX1 locus is associated with crop ears in highland cattle. PLoS ONE, 8(10), e77841. Public Library of Science 10.1371/journal.pone.0077841

Hirschvogel, Katrin; Matiasek, Kaspar; Flatz, Katharina; Drögemüller, Michaela; Drögemüller, Cord; Reiner, Bärbel; Fischer, Andrea (2013). Magnetic resonance imaging and genetic investigation of a case of Rottweiler leukoencephalomyelopathy. BMC veterinary research, 9(57), p. 57. BioMed Central 10.1186/1746-6148-9-57

Greber, Deborah; Doherr, Marcus; Drögemüller, Cord; Steiner, Adrian (2013). Occurrence of congenital disorders in Swiss sheep. Acta Veterinaria Scandinavica, 55(27), p. 27. BioMed Central Ltd. 10.1186/1751-0147-55-27

Bruun, Camilla S; Jäderlund, Karin H; Berendt, Mette; Jensen, Kristine B; Spodsberg, Eva H; Gredal, Hanne; Shelton, G Diane; Mickelson, James R; Minor, Katie M; Lohi, Hannes; Bjerkås, Inge; Stigen, Oyvind; Espenes, Arild; Rohdin, Cecilia; Edlund, Rebecca; Ohlsson, Jennie; Cizinauskas, Sigitas; Leifsson, Páll S; Drögemüller, Cord; Moe, Lars; ... (2013). A Gly98Val mutation in the N-Myc downstream regulated gene 1 (NDRG1) in Alaskan Malamutes with polyneuropathy. PLoS ONE, 8(2), e54547. Public Library of Science 10.1371/journal.pone.0054547

Heaton, Michael P; Kalbfleisch, Theodore S; Petrik, Dustin T; Simpson, Barry; Kijas, James W; Clawson, Michael L; Chitko-McKown, Carol G; Harhay, Gregory P; Leymaster, Kreg A; Drögemüller, Cord; The International Sheep Genomics Consortium, ISGC (2013). Genetic testing for TMEM154 mutations associated with lentivirus susceptibility in sheep. PLoS ONE, 8(2), e55490. Public Library of Science 10.1371/journal.pone.0055490

Gallana, Milena; Ryser-Degiorgis, Marie-Pierre; Wahli, Thomas; Segner, Helmut (2013). Climate change and infectious diseases of wildlife: Altered interactions between pathogens, vectors and hosts. Current zoology, 59(3), pp. 427-437. Chinese Academy of sciences

Shakhsi Niaei, Mostafa; Klukowska-Rötzler, Jolanta; Drögemüller, Cord; Gerber, Vinzenz; Leeb, Tosso (2013). The equine DNAH3 gene: SNP discovery and exclusion of an involvement in recurrent airway obstruction (RAO) in European Warmblood horses. Archiv Tierzucht / Archives animal breeding, 56(1), pp. 1-10. Leibniz Institute for Farm Animal Biology FBN 10.7482/0003-9438-56-001

Baes, C.; Mattei, S.; Luther, H.; Ampuero, S.; Sidler, X.; Bee, G.; Spring, P.; Hofer, A. (2013). A performance test for boar taint compounds in live boars. Animal, 7(5), pp. 714-720. Cambridge University Press 10.1017/S1751731112002273

Duart Garcia, Carolina; Braunschweig, Martin (2013). The Igf2as Transcript is Exported into Cytoplasm and Associated with Polysomes. Biochemical Genetics, 51(1-2), pp. 119-130. Springer 10.1007/s10528-012-9547-8

2012

Murgiano, Leonardo; Tammen, Imke; Harlizius, Barbara; Drögemüller, Cord (2012). A de novo germline mutation in MYH7 causes a progressive dominant myopathy in pigs. BMC genetics, 13, p. 99. BioMed Central 10.1186/1471-2156-13-99

Murgiano, Leonardo; Sacchetto, Roberta; Testoni, Stefania; Dorotea, Tiziano; Mascarello, Francesco; Liguori, Rocco; Gentile, Arcangelo; Drögemüller, Cord (2012). Pseudomyotonia in Romagnola cattle caused by novel ATP2A1 mutations. BMC veterinary research, 8, p. 186. BioMed Central 10.1186/1746-6148-8-186

Shakhsi-Niaei, M; Klukowska-Rötzler, Jolanta; Drögemüller, Cord; Swinburne, J; Ehrmann, C; Saftic, Dounia; Ramseyer, Alessandra; Gerber, Vinzenz; Dolf, Gaudenz; Leeb, Tosso (2012). Replication and fine-mapping of a QTL for recurrent airway obstruction in European Warmblood horses. Animal genetics, 43(5), pp. 627-631. Blackwell 10.1111/j.1365-2052.2011.02315.x

Lauber, Beatrice; Molitor, Vivianne; Meury, Sabrina; Doherr, Marcus G; Favrot, Claude; Tengvall, Katarina; Bergvall, Kerstin; Leeb, Tosso; Roosje, Petra; Marti, Eliane Isabelle (2012). Total IgE and allergen-specific IgE and IgG antibody levels in sera of atopic dermatitis affected and non-affected Labrador- and Golden retrievers. Veterinary immunology and immunopathology, 149(1-2), pp. 112-118. Elsevier 10.1016/j.vetimm.2012.05.018

Potocki, Leszek; Lewinska, Anna; Klukowska-Rötzler, Jolanta; Bugno-Poniewierska, Monika; Koch, Christoph; Mählmann, Kathrin; Janda, Jozef; Wnuk, Maciej (2012). DNA hypomethylation and oxidative stress-mediated increase in genomic instability in equine sarcoid-derived fibroblasts. Biochimie, 94(9), pp. 2013-2024. Elsevier Masson SAS 10.1016/j.biochi.2012.05.026

Widmer, Christine; Gebauer, Jan M; Brunstein, Elena; Rosenbaum, Sabrina; Zaucke, Frank; Drögemüller, Cord; Leeb, Tosso; Baumann, Ulrich (2012). Molecular basis for the action of the collagen-specific chaperone Hsp47/SERPINH1 and its structure-specific client recognition. Proceedings of the National Academy of Sciences of the United States of America - PNAS, 109(33), pp. 13243-13247. National Academy of Sciences NAS 10.1073/pnas.1208072109

Klukowska-Rötzler, Jolanta; Swinburne, J.E.; Drögemüller, Cord; Dolf, Gaudenz; Janda, Jozef; Leeb, Tosso; Gerber, Vinzenz (2012). The interleukin 4 receptor gene and its role in recurrent airway obstruction in Swiss Warmblood horses. Animal genetics, 43(4), pp. 450-453. Oxford: Blackwell 10.1111/j.1365-2052.2011.02277.x

Signer-Hasler, Heidi; Flury, Christine; Haase, Bianca; Burger, Dominik; Simianer, Henner; Leeb, Tosso; Rieder, Stefan (2012). A Genome-Wide Association Study Reveals Loci Influencing Height and Other Conformation Traits in Horses. PLoS ONE, 7(5), e37282. Public Library of Science 10.1371/Journal.pone.0037282

Braun, U.; Spiess, B.; Matheis, F.; Schnetzler, C.; Trösch, L.; Drögemüller, C.; Gerspach, C. (2012). Bilateral congenital lacrimal fistula in a Brown Swiss bull. Schweizer Archiv für Tierheilkunde, 154(3), pp. 121-123. Gesellschaft Schweizer Tierärztinnen und Tierärzte 10.1024/0036-7281/a000310

Durkin, Keith; Coppieters, Wouter; Drögemüller, Cord; Ahariz, Naima; Cambisano, Nadine; Druet, Tom; Fasquelle, Corinne; Haile, Aynalem; Horin, Petr; Huang, Lusheng; Kamatani, Yohichiro; Karim, Latifa; Lathrop, Mark; Moser, Simon; Oldenbroek, Kor; Rieder, Stefan; Sartelet, Arnaud; Sölkner, Johann; Stålhammar, Hans; Zelenika, Diana; ... (2012). Serial translocation by means of circular intermediates underlies colour sidedness in cattle. Nature, 482(7383), pp. 81-84. Macmillan Journals Ltd. 10.1038/nature10757

Kijas, James W; Lenstra, Johannes A; Hayes, Ben; Boitard, Simon; Porto Neto, Laercio R; San Cristobal, Magali; Servin, Bertrand; McCulloch, Russell; Whan, Vicki; Gietzen, Kimberly; Paiva, Samuel; Barendse, William; Ciani, Elena; Raadsma, Herman; McEwan, John; Dalrymple, Brian; Drögemüller, Cord (2012). Genome-wide analysis of the world's sheep breeds reveals high levels of historic mixture and strong recent selection. PLoS biology, 10(2), pp. 1-14. Public Library of Science 10.1371/journal.pbio.1001258

Testoni, S; Mazzariol, S; Drögemüller, Cord; Piffer, C; Aresu, L; Gentile, A (2012). Renal dysplasia in grey Alpine breed cattle unrelated to CLDN16 mutations. Veterinary record, 170(1), p. 22. London: British Veterinary Association 10.1136/vr.100209

Wijnberg, I D; Owczarek-Lipska, Marta; Sacchetto, R; Mascarello, F; Pascoli, F; Grunberg, W; van der Kolk J. H., ; Drögemüller, Cord (2012). A missense mutation in the skeletal muscle chloride channel 1 (CLCN1) as candidate causal mutation for congenital myotonia in a New Forest pony. Neuromuscular disorders, 22(4), pp. 361-7. Amsterdam: Elsevier 10.1016/j.nmd.2011.10.001

Testoni, Stefania; Bartolone, Elena; Rossi, Marco; Patrignani, Andrea; Bruggmann, Rémy; Lichtner, Peter; Tetens, Jens; Gentile, Arcangelo; Drögemüller, Cord (2012). KDM2B is implicated in bovine lethal multi-organic developmental dysplasia. PLoS ONE, 7(9), e45634. Lawrence, Kans.: Public Library of Science 10.1371/journal.pone.0045634

Owczarek-Lipska, Marta; Lauber, Béatrice; Molitor, Vivianne; Meury, Sabrina; Kierczak, Marcin; Tengvall, Katarina; Webster, Matthew T.; Jagannathan, Vidhya; Schlotter, Yvette; Willemse, Ton; Hendricks, Anke; Bergvall, Kerstin; Hedhammar, Åke; Andersson, Göran; Lindblad-Toh, Kerstin; Favrot, Claude; Roosje, Petra; Marti, Eliane; Leeb, Tosso and Singh, Shree Ram (2012). Two Loci on Chromosome 5 Are Associated with Serum IgE Levels in Labrador Retrievers. PLoS ONE, 7(6), e39176. Public Library of Science 10.1371/journal.pone.0039176

Menoud, Annie; Welle, Monika Maria; Tetens, Jens; Lichtner, Peter; Drögemüller, Cord; Szecsi, Pal Bela (2012). A COL7A1 Mutation Causes Dystrophic Epidermolysis Bullosa in Rotes Höhenvieh Cattle. PLoS ONE, 7(6), e38823. Public Library of Science 10.1371/journal.pone.0038823

Guldimann, Claudia; Gsponer, M.; Drögemüller, Cord; Oevermann, Anna; Seuberlich, Torsten (2012). Atypical H-Type Bovine Spongiform Encephalopathy in a Cow Born after the Reinforced Feed Ban on Meat-and-Bone Meal in Europe. Journal of clinical microbiology, 50(12), pp. 4171-4174. American Society for Microbiology 10.1128/JCM.02178-12

Hauswirth, Regula; Haase, Bianca; Blatter, Marlis; Brooks, Samantha A.; Burger, Dominik; Drögemüller, Cord; Gerber, Vincent; Henke, Diana; Janda, Jozef; Jude, Rony; Magdesian, K. Gary; Matthews, Jacqueline M.; Poncet, Pierre-André; Svansson, Vilhjálmur; Tozaki, Teruaki; Wilkinson-White, Lorna; Penedo, M. Cecilia T.; Rieder, Stefan; Leeb, Tosso and Barsh, Gregory S. (2012). Mutations in MITF and PAX3 Cause “Splashed White” and Other White Spotting Phenotypes in Horses. PLoS genetics, 8(4), e1002653. Public Library of Science 10.1371/journal.pgen.1002653

Seuberlich, Torsten; Gsponer, Michaela; Drögemüller, Cord; Polak, Miroslaw P.; McCutcheon, Sandra; Heim, Dagmar; Oevermann, Anna; Zurbriggen, Andreas (2012). Novel Prion Protein in BSE-affected Cattle, Switzerland. Emerging infectious diseases, 18(1), pp. 158-159. U.S. National Center for Infectious Diseases 10.3201/eid1801.111225

Schütz, Ekkehard; Drögemüller, Cord; Leeb, Tosso; Scharfenstein, Melanie; Brenig, Bertram (2012). Osteogenesis imperfecta beim Dackel. Kleintierpraxis, 57(2), pp. 57-62. Schaper

2011

Alves, Lisa; Hulsmeyer, V.; Jaggy, André; Fischer, A.; Leeb, Tosso; Drögemüller, Michaela (2011). Polymorphisms in the ABCB1 gene in phenobarbital responsive and resistant idiopathic epileptic Border Collies. Journal of veterinary internal medicine, 25(3), pp. 484-9. Oxford: Wiley-Blackwell 10.1111/j.1939-1676.2011.0718.x

Braunschweig, M.H.; Owczarek-Lipska, M.; Stahlberger-Saitbekova, N. (2011). Relationship of porcine IGF2 imprinting status to DNA methylation at the H19 DMD and the IGF2 DMRs 1 and 2. BMC genetics, 12(1), p. 47. London: BioMed Central 10.1186/1471-2156-12-47

Owczarek-Lipska, Marta; Plattet, Philippe; Zipperle, Ljerka; Drögemüller, Cord; Posthaus, Horst; Dolf, Gaudenz; Braunschweig, Martin (2011). A nonsense mutation in the optic atrophy 3 gene (OPA3) causes dilated cardiomyopathy in Red Holstein cattle. Genomics, 97(1), pp. 51-7. San Diego, Calif.: Elsevier 10.1016/j.ygeno.2010.09.005

Drögemüller, Cord; Reichart, U.; Seuberlich, Torsten; Oevermann, Anna; Baumgartner, M.; Kühni Boghenbor, Kathrin; Stoffel, Michael Hubert; Syring, Claudia; Meylan, Mireille; Muller, S.; Muller, M.; Gredler, B.; Solkner, J.; Leeb, Tosso (2011). An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle. PLoS ONE, 6(4), e18931. Lawrence, Kans.: Public Library of Science 10.1371/journal.pone.0018931

Nussbaumer, Päivi; Frey, Caroline; Gottstein, Bruno; Swinburne, J.E.; Dolf, Gaudenz; Gerber, Vinzenz (2011). Resistance against strongylid nematodes in two high prevalence Equine Recurrent Airway Obstruction families has a genetic basis. Pferdeheilkunde, 27(6), pp. 664-669. Baden-Baden: Hippiatrika Verlagsgesellschaft

Meury, S.; Molitor, Vivianne; Doherr, Marcus; Roosje, Petra; Leeb, Tosso; Hobi, S.; Wilhelm, S.; Favrot, C. (2011). Role of the environment in the development of canine atopic dermatitis in Labrador and golden retrievers. Veterinary dermatology, 22(4), pp. 327-34. Oxford: Blackwell Science 10.1111/j.1365-3164.2010.00950.x

Haase, Bianca; Rieder, S.; Tozaki, T.; Hasegawa, T.; Penedo, M.C.; Jude, R.; Leeb, Tosso (2011). Five novel KIT mutations in horses with white coat colour phenotypes. Animal genetics, 42(3), pp. 337-9. Oxford: Blackwell 10.1111/j.1365-2052.2011.02173.x

Haring, T.; Wichert, B.; Dolf, G.; Haase, B. (2011). Segregation analysis of overweight body condition in an experimental cat population. Journal of heredity, 102(Suppl 1), S28-S31. Oxford: Oxford University Press 10.1093/jhered/esr029

Hasler, H.; Flury, C.; Menet, S.; Haase, Bianca; Leeb, Tosso; Simianer, H.; Poncet, P.A.; Rieder, S. (2011). Genetic diversity in an indigenous horse breed: implications for mating strategies and the control of future inbreeding. Journal of animal breeding and genetics, 128(5), pp. 394-406. Berlin: Wiley-Blackwell 10.1111/j.1439-0388.2011.00932.x

Lequarre, A.S.; Andersson, L.; Andre, C.; Fredholm, M.; Hitte, C.; Leeb, Tosso; Lohi, H.; Lindblad-Toh, K.; Georges, M. (2011). LUPA: a European initiative taking advantage of the canine genome architecture for unravelling complex disorders in both human and dogs. Veterinary journal, 189(2), pp. 155-9. Amsterdam: Elsevier 10.1016/j.tvjl.2011.06.013

Klukowska-Rotzler, Jolanta; Gerber, Vinzenz; Leeb, Tosso (2011). Association analysis of SNPs in the IL21R gene with recurrent airway obstruction (RAO) in Swiss Warmblood horses. Animal genetics, 43(4), pp. 475-476. Oxford: Blackwell 10.1111/j.1365-2052.2011.02289.x

Matiasek, K.; Drögemüller, Cord (2011). Charcot-Marie-Tooth disease: inherited neuropathies revisited. Veterinary journal, 188(3), pp. 254-5. Amsterdam: Elsevier 10.1016/j.tvjl.2011.03.002

Mausberg, T.B.; Wess, G.; Simak, J.; Keller, L.; Drögemüller, Michaela; Drögemüller, Cord; Webster, M.T.; Stephenson, H.; Dukes-McEwan, J.; Leeb, Tosso (2011). A locus on chromosome 5 is associated with dilated cardiomyopathy in Doberman Pinschers. PLoS ONE, 6(5), e20042. Lawrence, Kans.: Public Library of Science 10.1371/journal.pone.0020042

Owczarek-Lipska, Marta; Thomas, A.; Andre, C.; Holzer, S.; Leeb, Tosso (2011). [Frequency of gene defects in selected European retriever populations]. Schweizer Archiv für Tierheilkunde, 153(9), pp. 418-20. Bern: Huber 10.1024/0036-7281/a000236

Seppala, E.H.; Jokinen, T.S.; Fukata, M.; Fukata, Y.; Webster, M.T.; Karlsson, E.K.; Kilpinen, S.K.; Steffen, F.; Dietschi, Elisabeth; Leeb, Tosso; Eklund, R.; Zhao, X.; Rilstone, J.J.; Lindblad-Toh, K.; Minassian, B.A.; Lohi, H. (2011). LGI2 truncation causes a remitting focal epilepsy in dogs. PLoS genetics, 7(7), e1002194. San Francisco, Calif.: Public Library of Science 10.1371/journal.pgen.1002194

Edwards, Ceiridwen J.; Ginja, Catarina; Kantanen, Juha; Perez-Pardal, Lucía; Tresset, Anne; Stock, Frauke; Gama, Luis T.; Penedo, M. Cecilia T.; Bradley, Daniel G.; Lenstra, Johannes A.; Nijman, Isaäc J.; Dolf, Gaudenz (2011). Dual origins of dairy cattle farming - evidence from a comprehensive survey of European Y-chromosomal variation. PLoS ONE, 6(1), e15922. Lawrence, Kans.: Public Library of Science 10.1371/journal.pone.0015922

2010

Drögemüller, Cord (September 2010). Augenerkrankungen bei Jungtieren: ein Problem für die Zucht? Forum Kleinwiederkäuer, 2010(9), pp. 13-19. Verlagsgenossenschaft Caprovis, Niederönz

Bellone, Rebecca R; Forsyth, George; Leeb, Tosso; Archer, Sheila; Sigurdsson, Snaevar; Imsland, Freyja; Mauceli, Evan; Engensteiner, Martina; Bailey, Ernest; Sandmeyer, Lynne; Grahn, Bruce; Lindblad-Toh, Kerstin; Wade, Claire M (2010). Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses. Briefings in functional genomics, 9(3), pp. 193-207. Oxford University Press 10.1093/bfgp/elq002

Syring, Claudia; Drögemüller, Cord; Oevermann, Anna; Pfister, Patrizia; Henke, Diana; Muller, S.; Solkner, J.; Leeb, Tosso; Meylan, Mireille (2010). Degenerative axonopathy in a Tyrolean grey calf. Journal of veterinary internal medicine, 24(6), pp. 1519-23. Oxford: Wiley-Blackwell 10.1111/j.1939-1676.2010.0607.x

Timm, Katrin; Rüfenacht, Silvia; von Tscharner, C.; Bornand, Valérie F.; Doherr, Marcus; Oevermann, Anna; Flury, C.; Rieder, S.; Hirsbrunner, Gabriela; Drögemüller, Cord; Roosje, Petra (2010). Alopecia areata in Eringer cows. Veterinary dermatology, 21(6), pp. 545-53. Oxford: Blackwell Science 10.1111/j.1365-3164.2010.00906.x

Morina, R.; Knorr, C.; Haase, Bianca; Leeb, Tosso; Seuberlich, Torsten; Zurbriggen, Andreas; Brem, G.; Schutz, E.; Brenig, B. (2010). Molecular analysis of carbohydrate N-acetylgalactosamine 4-O sulfotransferase 8 (CHST8) as a candidate gene for bovine spongiform encephalopathy susceptibility. Animal genetics, 41(1), pp. 85-8. Oxford: Blackwell 10.1111/j.1365-2052.2009.01951.x

Becker, Doreen; Tetens, J.; Brunner, A.; Burstel, D.; Ganter, M.; Kijas, J.; Drögemüller, Cord (2010). Microphthalmia in Texel sheep is associated with a missense mutation in the paired-like homeodomain 3 (PITX3) gene. PLoS ONE, 5(1), e8689. Lawrence, Kans.: Public Library of Science 10.1371/journal.pone.0008689

Drögemüller, Cord; Becker, Doreen; Kessler, B.; Kemter, E.; Tetens, J.; Jurina, K.; Jaderlund, K.H.; Flagstad, A.; Perloski, M.; Lindblad-Toh, K.; Matiasek, K. (2010). A deletion in the N-myc downstream regulated gene 1 (NDRG1) gene in Greyhounds with polyneuropathy. PLoS ONE, 5(6), e11258. Lawrence, Kans.: Public Library of Science 10.1371/journal.pone.0011258

Danilowicz, E.; Martinez-Arias, R.; Dolf, Gaudenz; Singh, M.; Probst, I.; Tummler, B.; Holtig, D.; Waldmann, K.H.; Gerlach, G.F.; Stanke, F.; Leeb, Tosso (2010). Characterization of the porcine transferrin gene (TF) and its association with disease severity following an experimental Actinobacillus pleuropneumoniae infection. Animal genetics, 41(4), pp. 424-7. Oxford: Blackwell 10.1111/j.1365-2052.2009.02012.x

Haase, Bianca; Obexer-Ruff, G.; Dolf, Gaudenz; Rieder, S.; Burger, D.; Poncet, P.A.; Gerber, Vinzenz; Howard, J.; Leeb, Tosso (2010). Haematological parameters are normal in dominant white Franches-Montagnes horses carrying a KIT mutation. Veterinary journal, 184(3), pp. 315-7. Amsterdam: Elsevier 10.1016/j.tvjl.2009.02.017

Drögemüller, Cord; Demmel, Steffi; Engensteiner, M.; Rieder, S.; Leeb, Tosso (2010). A shared 336 kb haplotype associated with the belt pattern in three divergent cattle breeds. Animal genetics, 41(3), pp. 304-7. Oxford: Blackwell 10.1111/j.1365-2052.2009.01987.x

Drögemüller, Cord; Tetens, J.; Sigurdsson, S.; Gentile, A.; Testoni, S.; Lindblad-Toh, K.; Leeb, Tosso (2010). Identification of the bovine Arachnomelia mutation by massively parallel sequencing implicates sulfite oxidase (SUOX) in bone development. PLoS genetics, 6(8), e1001079. San Francisco, Calif.: Public Library of Science 10.1371/journal.pgen.1001079

Flury, C; Tapio, M; Sonstegard, T; Drögemüller, Cord; Leeb, Tosso; Simianer, H; Hanotte, O; Rieder, S (2010). Effective population size of an indigenous Swiss cattle breed estimated from linkage disequilibrium. Journal of animal breeding and genetics, 127(5), pp. 339-47. Berlin: Wiley-Blackwell 10.1111/j.1439-0388.2010.00862.x

Grunberg, W.; Sacchetto, R.; Wijnberg, I.; Neijenhuis, K.; Mascarello, F.; Damiani, E.; Drögemüller, Cord (2010). Pseudomyotonia, a muscle function disorder associated with an inherited ATP2A1 (SERCA1) defect in a Dutch Improved Red and White cross-breed calf. Neuromuscular disorders, 20(7), pp. 467-70. Amsterdam: Elsevier 10.1016/j.nmd.2010.04.010

Karol, A.; Drögemüller, Cord; Wimmers, K.; Schellander, K.; Leeb, Tosso (2010). Molecular characterization of five porcine candidate genes for drip loss in pork. Animal biotechnology, 21(2), pp. 114-21. New York, N.Y.: Marcel Dekker 10.1080/10495390903534457

Schmitz, Andrea; Demmel, Steffi; Peters, Laureen Michèle; Leeb, Tosso; Mevissen, Meike; Haase, Bianca (2010). Comparative human-horse sequence analysis of the CYP3A subfamily gene cluster. Animal genetics, 41(s2), pp. 72-79. Oxford: Blackwell 10.1111/j.1365-2052.2010.02111.x

Shakhsi-Niaei, Mostafa; Klukowska-Rötzler, Jolanta; Drögemüller, Cord; Swinburne, J.E.; Gerber, Vinzenz; Leeb, Tosso (2010). Characterization of the equine ITGAX gene and its association with recurrent airway obstruction in European Warmblood horses. Animal genetics, 41(5), pp. 559-60. Oxford: Blackwell 10.1111/j.1365-2052.2010.02066.x

Klukowska-Rötzler, Jolanta; Marti, Eliane Isabelle; Bugno, M.; Leeb, Tosso; Janda, Jozef (2010). Molecular cloning and characterization of equine thymic stromal lymphopoietin. Veterinary immunology and immunopathology, 136(3-4), pp. 346-9. Amsterdam: Elsevier 10.1016/j.vetimm.2010.03.021

2009

Hasler, Heidi; Flury, Christine; Reist, Sabine; Braunschweig, Martin; Dolf, Gaudenz; Drögemüller, Cord; Drögemüller, Michaela; Haase, Bianca; Klukowska-Rötzler, Jolanta; Burger, Dominik; Poncet, Pierre-André; Rieder, Stefan; Leeb, Tosso (2009). Aktuelle Beispiele der Tierzuchtforschung in der Schweiz. Agrarforschung Schweiz, 16(9), pp. 336-341. Agroscope

Alfalah, Marwan; Keiser, Markus; Leeb, Tosso; Zimmer, Klaus-Peter; Naim, Hassen Y. (2009). Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency. Gastroenterology, 136(3), pp. 883-892. Philadelphia, Pa.: Elsevier 10.1053/j.gastro.2008.11.038

Drögemüller, Cord; Becker, Doreen; Brunner, Adrian; Haase, Bianca; Kircher, Patrick Robert; Seeliger, Frank; Fehr, Michael; Baumann, Ulrich; Lindblad-Toh, Kerstin; Leeb, Tosso (2009). A Missense Mutation in the SERPINH1 Gene in Dachshunds with Osteogenesis Imperfecta. PLoS genetics, 5(7), e1000579. San Francisco, Calif.: Public Library of Science 10.1371/journal.pgen.1000579

Tester, Seraina; Juillerat, Valérie; Doherr, Marcus; Haase, Bianca; Polak, M.; Ehrensperger, F.; Leeb, Tosso; Zurbriggen, Andreas; Seuberlich, Torsten (2009). Biochemical typing of pathological prion protein in aging cattle with BSE. Virology journal, 6(1), p. 64. London: BioMed Central 10.1186/1743-422X-6-64

Wade, C.M.; Giulotto, E.; Sigurdsson, S.; Zoli, M.; Gnerre, S.; Imsland, F.; Lear, T.L.; Adelson, D.L.; Bailey, E.; Bellone, R.R.; Blocker, H.; Distl, O.; Edgar, R.C.; Garber, M.; Leeb, Tosso; Mauceli, E.; MacLeod, J.N.; Penedo, M.C.; Raison, J.M.; Sharpe, T.; ... (2009). Genome sequence, comparative analysis, and population genetics of the domestic horse. Science, 326(5954), pp. 865-7. Washington, D.C.: American Association for the Advancement of Science 10.1126/science.1178158

Swinburne, J.E.; Bogle, H.; Klukowska-Rötzler, Jolanta; Drögemüller, Cord; Leeb, Tosso; Temperton, E.; Dolf, Gaudenz; Gerber, Vinzenz (2009). A whole-genome scan for recurrent airway obstruction in Warmblood sport horses indicates two positional candidate regions. Mammalian genome, 20(8), pp. 504-15. New York, N.Y.: Springer 10.1007/s00335-009-9214-5

Sacchetto, R.; Testoni, S.; Gentile, A.; Damiani, E.; Rossi, M.; Liguori, R.; Drögemüller, Cord; Mascarello, R. (2009). A defective SERCA1 protein is responsible for congenital pseudomyotonia in Chianina cattle. American journal of pathology, 174(2), pp. 565-73. New York, N.Y.: Elsevier 10.2353/ajpath.2009.080659

Piras, F.M.; Nergadze, S.G.; Poletto, V.; Cerutti, F.; Ryder, O.A.; Leeb, Tosso; Raimondi, E.; Giulotto, E. (2009). Phylogeny of horse chromosome 5q in the genus Equus and centromere repositioning. Cytogenetic and genome research, 126(1-2), pp. 165-72. Basel: Karger 10.1159/000245916

Owczarek-Lipska, Marta; Denis, C.; Eggen, A.; Leeb, Tosso; Posthaus, Horst; Dolf, Gaudenz; Braunschweig, Martin (2009). The bovine dilated cardiomyopathy locus maps to a 1.0-Mb interval on chromosome 18. Mammalian genome, 20(3), pp. 187-92. New York, N.Y.: Springer-Verlag 10.1007/s00335-009-9171-z

Meller, R.; Brandes, G.; Drögemüller, Cord; Fritz, F.; Schiborra, F.; Fehr, M.; Hankemeier, S.; Krettek, C.; Hurschler, C. (2009). Graft remodeling during growth following anterior cruciate ligament reconstruction in skeletally immature sheep. Archives of orthopaedic and trauma surgery, 129(8), pp. 1037-46. Berlin: Springer 10.1007/s00402-008-0784-6

Kreutzer, R.; Kreutzer, M.; Sewell, A.C.; Techangamsuwan, S.; Leeb, Tosso; Baumgartner, W. (2009). Impact of beta-galactosidase mutations on the expression of the canine lysosomal multienzyme complex. Biochimica et biophysica acta - molecular basis of disease, 1792(10), pp. 982-7. New York, N.Y.: Elsevier 10.1016/j.bbadis.2009.07.004

Haase, Bianca; Brooks, S.A.; Tozaki, T.; Burger, D.; Poncet, P.A.; Rieder, S.; Hasegawa, T.; Penedo, C.; Leeb, Tosso (2009). Seven novel KIT mutations in horses with white coat colour phenotypes. Animal genetics, 40(5), pp. 623-9. Oxford: Blackwell 10.1111/j.1365-2052.2009.01893.x

Goldammer, T.; Di Meo, G.P.; Luhken, G.; Drögemüller, Cord; Wu, C.H.; Kijas, J.; Dalrymple, B.P.; Nicholas, F.W.; Maddox, J.F.; Iannuzzi, L.; Cockett, N.E. (2009). Molecular cytogenetics and gene mapping in sheep (Ovis aries, 2n = 54). Cytogenetic and genome research, 126(1-2), pp. 63-76. Basel: Karger 10.1159/000245907

Glowatzki-Mullis, M.L.; Muntwyler, J.; Baumle, E.; Gaillard, C. (2009). Genetic diversity of Swiss sheep breeds in the focus of conservation research. Journal of animal breeding and genetics, 126(2), pp. 164-75. Berlin: Wiley-Blackwell 10.1111/j.1439-0388.2008.00768.x

Drögemüller, Cord; Rossi, M.; Gentile, A.; Testoni, S.; Jorg, H.; Stranzinger, G.; Drögemüller, Michaela; Glowatzki-Mullis, M.L.; Leeb, Tosso (2009). Arachnomelia in Brown Swiss cattle maps to chromosome 5. Mammalian genome, 20(1), pp. 53-59. Springer-Verlag 10.1007/s00335-008-9157-2

Drögemüller, Cord; Engensteiner, M.; Moser, S.; Rieder, S.; Leeb, Tosso (2009). Genetic mapping of the belt pattern in Brown Swiss cattle to BTA3. Animal genetics, 40(2), pp. 225-9. Oxford: Blackwell 10.1111/j.1365-2052.2008.01826.x

Welle, Monika Maria; Philipp, U.; Rüfenacht, S.; Roosje, Petra; Scharfenstein, M.; Schütz, E.; Brenig, B.; Linek, M.; Mecklenburg, L.; Grest, P.; Drögemüller, Michaela; Haase, Bianca; Leeb, Tosso; Drögemüller, Cord (2009). MLPH Genotype—Melanin Phenotype Correlation in Dilute Dogs. Journal of heredity, 100(Suppl 1), S75-S79. Oxford University Press 10.1093/jhered/esp010

2008

Anistoroaei, R; Fredholm, M; Christensen, K; Leeb, Tosso (2008). Albinism in the American mink (Neovison vison) is associated with a tyrosinase nonsense mutation. Animal genetics, 39(6), pp. 645-648. Blackwell 10.1111/j.1365-2052.2008.01788.x

Drögemüller, Cord; Drögemüller, Michaela; Leeb, Tosso; Mascarello, Francesco; Testoni, Stefania; Rossi, Marco; Gentile, Arcangelo; Damiani, Ernesto; Sacchetto, Roberta (2008). Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease. Genomics, 92(6), pp. 474-477. Elsevier 10.1016/j.ygeno.2008.07.014

Höltig, D; Hennig-Pauka, I; Beyerbach, M; Thies, K; Rehm, T; Gerlach, G-F; Waldmann, K-H; FUGATO-Konsortium, IRAS (2008). Comparison of the diagnostic significance of clinical, radiographic and ultrasonographic results after an experimental aerosol infection of pigs with Actinobacillus pleuropneumoniae. Berliner und Münchener tierärztliche Wochenschrift, 121(11-12), pp. 422-431. Schlütersche 10.2376/0005-9366-121-422

Mömke, S; Fink, S; Wöhlke, A; Drögemüller, C.; Distl, O (2008). Linkage of bilateral convergent strabismus with exophthalmus (BCSE) to BTA5 and BTA18 in German Brown cattle. Animal genetics, 39(5), pp. 544-549. Wiley 10.1111/j.1365-2052.2008.01771.x

Drögemüller, Cord; Karlsson, Elinor K; Hytönen, Marjo K; Perloski, Michele; Dolf, Gaudenz; Sainio, Kirsi; Lohi, Hannes; Lindblad-Toh, Kerstin; Leeb, Tosso (2008). A mutation in hairless dogs implicates FOXI3 in ectodermal development. Science, 321(5895), p. 1462. American Association for the Advancement of Science 10.1126/science.1162525

Baars, Cordula; Leeb, Tosso; von Klopmann, Thilo; Tipold, Andrea; Potschka, Heidrun (2008). Allele-specific polymerase chain reaction diagnostic test for the functional MDR1 polymorphism in dogs. Veterinary journal, 177(3), pp. 394-397. Elsevier 10.1016/j.tvjl.2007.05.020

Kreutzer, Robert; Kreutzer, Mihaela; Leeb, Tosso; Baumgärtner, Wolfgang (2008). Rapid and accurate G M1-gangliosidosis diagnosis using a parentage testing microsatellite. Molecular and cellular probes, 22(4), pp. 252-254. Elsevier 10.1016/j.mcp.2008.05.001

Mausberg, Eva-Maria; Drögemüller, Cord; Dolf, Gaudenz; Rüfenacht, Silvia; Welle, Monika Maria; Leeb, Tosso (2008). Exclusion of patched homolog 2 (PTCH2) as a candidate gene for alopecia X in Pomeranians and Keeshonden. Veterinary record, 163(4), pp. 121-123. British Veterinary Association 10.1136/vr.163.4.121

Gerber, Vinzenz; Swinburne, J E; Blott, S C; Nussbaumer, Päivi; Ramseyer, Alessandra; Klukowska-Rötzler, J; Dolf, Gaudenz; Marti, Eliane Isabelle; Burger, Dominik; Leeb, Tosso (2008). Genetics of recurrent airway obstruction (RAO). DTW. Deutsche tierärztliche Wochenschrift, 115(7), pp. 271-275. Verlag M. & H. Schaper 10.2376/0341-6593-115-271

Haase, Bianca; Jude, R; Brooks, S A; Leeb, Tosso (2008). An equine chromosome 3 inversion is associated with the tobiano spotting pattern in German horse breeds. Animal genetics, 39(3), pp. 306-309. Blackwell 10.1111/j.1365-2052.2008.01715.x

Mele, Mirjam; Ramseyer, Alessandra; Burger, Dominik; Leeb, Tosso; Gerber, Vinzenz (2008). Hereditary diseases in the horse: I. Monogenetic diseases. Schweizer Archiv für Tierheilkunde, 150(4), pp. 167-171. Huber 10.1024/0036-7281.150.4.167

Reinshagen, Konrad; Keller, Klaus M; Haase, Bianca; Leeb, Tosso; Naim, Hassan Y; Zimmer, Klaus P (2008). Mosaic pattern of sucrase isomaltase deficiency in two brothers. Pediatric research, 63(1), pp. 79-83. Nature Publishing Group 10.1203/PDR.0b013e31815b4bac

Raudsepp, T; Gustafson-Seabury, A; Durkin, K; Wagner, M L; Goh, G; Seabury, C M; Brinkmeyer-Langford, C; Lee, E-J; Agarwala, R; Stallknecht-Rice, E; Schäffer, A A; Skow, L C; Tozaki, T; Yasue, H; Penedo, M C T; Lyons, L A; Khazanehdari, K A; Binns, M M; MacLeod, J N; Distl, O; ... (2008). A 4,103 marker integrated physical and comparative map of the horse genome. Cytogenetic and genome research, 122(1), pp. 28-36. Karger 10.1159/000151313

Danilowicz, Emilia; Akouchekian, Mansoureh; Drögemüller, Cord; Haase, Bianca; Leeb, Tosso; Kuiper, Heidi; Distl, Ottmar; Iras, Fugato-Consortium (2008). Molecular characterization and SNP development for the porcine IL6 and IL10 genes. Animal biotechnology, 19(3), pp. 159-165. Marcel Dekker 10.1080/10495390802088621

Drögemüller, Michaela; Tetens, Jens; Dalrymple, B; Goldammer, T; Wu, C H; Cockett, N E; Leeb, Tosso; Drögemüller, Cord (2008). A comparative radiation hybrid map of sheep chromosome 10. Cytogenetic and genome research, 121(1), pp. 35-40. Karger 10.1159/000124379

Rieder, Stefan; Hagger, Christian; Obexer-Ruff, Gabriela; Leeb, Tosso; Poncet, Pierre-André (2008). Genetic analysis of white facial and leg markings in the Swiss Franches-Montagnes Horse Breed. Journal of heredity, 99(2), pp. 130-136. Oxford University Press 10.1093/jhered/esm115

Kreutzer, R; Kreutzer, M; Pröpsting, M J; Sewell, A C; Leeb, Tosso; Naim, H Y; Baumgärtner, W (2008). Insights into post-translational processing of beta-galactosidase in an animal model resembling late infantile human G-gangliosidosis. Journal of Cellular and Molecular Medicine, 12(5A), pp. 1661-1671. Wiley 10.1111/j.1582-4934.2007.00204.x

2007

Prause, Andrea; Guionaud, C T; Klukowska-Rötzler, J; Giulotto, E; Magnani, E; Chowdhary, B P; Philipp, U; Leeb, Tosso; Mevissen, Meike (2007). Chromosomal assignment of five equine HTR genes by FISH and RH mapping. Animal genetics, 38(1), pp. 83-4. Oxford: Blackwell 10.1111/j.1365-2052.2006.01546.x

Geigy, Caroline A; Heid, Silvia; Steffen, Frank; Danielson, Kristen; Jaggy, André; Gaillard, Claude (2007). Does a pleiotropic gene explain deafness and blue irises in white cats? Veterinary journal, 173(3), pp. 548-553. Amsterdam: Elsevier 10.1016/j.tvjl.2006.07.021

Mausberg, E M; Drögemüller, Cord; Rüfenacht, S; Welle, Monika Maria; Roosje, Petra; Suter, M; Leeb, Tosso (2007). [Inherited alopecia X in Pomeranians]. DTW. Deutsche tierärztliche Wochenschrift, 114(4), pp. 129-34. Alfeld: Verlag M. & H. Schaper 10.2377/0341-6593-114-129

Dierks, Claudia; Löhring, Kathrin; Lampe, Virginie; Wittwer, Catherine; Drögemüller, Cord; Distl, Ottmar (2007). Genome-wide search for markers associated with osteochondrosis in Hanoverian warmblood horses. Mammalian genome, 18(10), pp. 739-47. New York, N.Y.: Springer 10.1007/s00335-007-9058-9

Tetens, Jens; Ganter, Martin; Müller, Gundi; Drögemüller, Cord (2007). Linkage mapping of ovine microphthalmia to chromosome 23, the sheep orthologue of human chromosome 18. Investigative ophthalmology & visual science, 48(8), pp. 3506-15. Hagerstown, Md.: Association for Research in Vision and Ophthalmology 10.1167/iovs.07-0041

Barlund, Christy S; Clark, Edward G; Leeb, Tosso; Drögemüller, Cord; Palmer, Colin W (2007). Congenital hypotrichosis and partial anodontia in a crossbred beef calf. Canadian veterinary journal - Revue vétérinaire canadienne, 48(6), pp. 612-4. Ottawa: Canadian Veterinary Medical Association

Wittwer, C; Löhring, K; Drögemüller, Cord; Hamann, H; Rosenberger, E; Distl, O (2007). Mapping quantitative trait loci for osteochondrosis in fetlock and hock joints and palmar/plantar osseus fragments in fetlock joints of South German Coldblood horses. Animal genetics, 38(4), pp. 350-7. Oxford: Blackwell 10.1111/j.1365-2052.2007.01610.x

Drögemüller, Cord; Philipp, Ute; Haase, Bianca; Günzel-Apel, Anne-Rose; Leeb, Tosso (2007). A noncoding melanophilin gene (MLPH) SNP at the splice donor of exon 1 represents a candidate causal mutation for coat color dilution in dogs. Journal of heredity, 98(5), pp. 468-73. Oxford: Oxford University Press 10.1093/jhered/esm021

Aberle, K S; Hamann, H; Drögemüller, Cord; Distl, O (2007). Phylogenetic relationships of German heavy draught horse breeds inferred from mitochondrial DNA D-loop variation. Journal of animal breeding and genetics, 124(2), pp. 94-100. Berlin: Wiley-Blackwell 10.1111/j.1439-0388.2007.00636.x

Haase, Bianca; Doherr, Marcus G; Seuberlich, Torsten; Drögemüller, Cord; Dolf, Gaudenz; Nicken, Petra; Schiebel, Katrin; Ziegler, Ute; Groschup, Martin H; Zurbriggen, Andreas; Leeb, Tosso (2007). PRNP promoter polymorphisms are associated with BSE susceptibility in Swiss and German cattle. BMC genetics, 8, p. 15. London: BioMed Central 10.1186/1471-2156-8-15

Drögemüller, Cord; Rüfenacht, S; Wichert, B; Leeb, Tosso (2007). Mutations within the FGF5 gene are associated with hair length in cats. Animal genetics, 38(3), pp. 218-21. Oxford: Blackwell 10.1111/j.1365-2052.2007.01590.x

Tetens, J; Goldammer, T; Maddox, J F; Cockett, N E; Leeb, Tosso; Drögemüller, Cord (2007). A radiation hybrid map of sheep chromosome 23 based on ovine BAC-end sequences. Animal genetics, 38(2), pp. 132-40. Oxford: Blackwell 10.1111/j.1365-2052.2007.01572.x

Drögemüller, Cord; Leeb, Tosso; Harlizius, Barbara; Tammen, Imke; Distl, Ottmar; Höltershinken, Martin; Gentile, Arcangelo; Duchesne, Amandine; Eggen, André (2007). Congenital syndactyly in cattle: four novel mutations in the low density lipoprotein receptor-related protein 4 gene (LRP4). BMC genetics, 8, p. 5. London: BioMed Central 10.1186/1471-2156-8-5

Mausberg, Eva-Maria; Drögemüller, Cord; Leeb, Tosso; Dolf, Gaudenz; Rüfenacht, Silvia; Welle, Monika Maria (2007). Evaluation of the CTSL2 gene as a candidate gene for alopecia X in Pomeranians and Keeshonden. Animal biotechnology, 18(4), pp. 291-6. New York, N.Y.: Marcel Dekker 10.1080/10495390701547461

Bugno, M; Klukowska-Rötzler, Jolanta; S¿ota, E; Witarski, W; Gerber, Vinzenz; Leeb, Tosso (2007). Fluorescent in situ hybridization mapping of the epidermal growth factor receptor gene in donkey. Journal of animal breeding and genetics, 124(3), pp. 172-4. Berlin: Wiley-Blackwell 10.1111/j.1439-0388.2007.00652.x

Hamann, H; Jude, R; Sieme, H; Mertens, U; Töpfer-Petersen, E; Distl, O; Leeb, Tosso (2007). A polymorphism within the equine CRISP3 gene is associated with stallion fertility in Hanoverian warmblood horses. Animal genetics, 38(3), pp. 259-64. Oxford: Blackwell 10.1111/j.1365-2052.2007.01594.x

Guziewicz, K E; Owczarek, Marta; Küffer, J; Schelling, C; Tontis, A; Denis, C; Eggen, A; Leeb, Tosso; Dolf, Gaudenz; Braunschweig, Martin (2007). The locus for bovine dilated cardiomyopathy maps to chromosome 18. Animal genetics, 38(3), pp. 265-9. Oxford: Blackwell 10.1111/j.1365-2052.2007.01596.x

Ekhlasi-Hundrieser, Mahnaz; Schäfer, Bettina; Philipp, Ute; Kuiper, Heidi; Leeb, Tosso; Mehta, Meenal; Kirchhoff, Christiane; Töpfer-Petersen, Edda (2007). Sperm-binding fibronectin type II-module proteins are genetically linked and functionally related. Gene, 392(1-2), pp. 253-65. Amsterdam: Elsevier 10.1016/j.gene.2007.01.002

Haase, Bianca; Brooks, Samantha A; Schlumbaum, Angela; Azor, Pedro J; Bailey, Ernest; Alaeddine, Ferial; Mevissen, Meike; Burger, Dominik; Poncet, Pierre-André; Rieder, Stefan; Leeb, Tosso (2007). Allelic Heterogeneity at the Equine KIT Locus in Dominant White (W) Horses. PLoS genetics, 3(11), e195. San Francisco, Calif.: Public Library of Science 10.1371/journal.pgen.0030195

Kashkevich, Kseniya; Humeny, Andreas; Ziegler, Ute; Groschup, Martin H; Nicken, Petra; Leeb, Tosso; Fischer, Christine; Becker, Cord-Michael; Schiebel, Katrin (2007). Functional relevance of DNA polymorphisms within the promoter region of the prion protein gene and their association to BSE infection. FASEB journal, 21(7), pp. 1547-55. Bethesda, Md.: Federation of American Societies for Experimental Biology 10.1096/fj.06-7522com

Leeb, Tosso (2007). The horse genome project - sequence based insights into male reproductive mechanisms. Reproduction in domestic animals, 42(Suppl. S2), pp. 45-50. Berlin: Blackwell 10.1111/j.1439-0531.2007.00897.x

Uhlmann, Beatrice; Kuiper, H; Distl, O; Leeb, Tosso (2007). Molecular characterization of the porcine DNAL4 gene. Archiv Tierzucht / Archives animal breeding(50), pp. 267-272. Dummerstorf: Leibniz Institute for Farm Animal Biology FBN

Braunschweig, M. H. (2007). Short communication: duplication in the 5'-flanking region of the beta-lactoglobulin gene is linked to the BLG A allele. Journal of dairy science, 90(12), pp. 5780-3. Savoy, Ill.: American Dairy Science Association 10.3168/jds.2007-0491

Glowatzki-Mullis, M L; Muntwyler, J; Gaillard, C (2007). Cost-effective parentage verification with 17-plex PCR for goats and 19-plex PCR for sheep. Animal genetics, 38(1), pp. 86-8. Oxford: Blackwell 10.1111/j.1365-2052.2006.01550.x

Urfer, S R; Gaillard, C; Steiger, A (2007). Lifespan and disease predispositions in the Irish Wolfhound: a review. Veterinary quarterly, 29(3), pp. 102-11. Germantown, NY: Taylor & Francis

Nenci, Chiara; Zahno, Marie-Luise; Vogt, Hans-Rudolf; Obexer-Ruff, Gaby; Doherr, Marcus G; Zanoni, Reto; Peterhans, Ernst; Bertoni, Giuseppe (2007). Vaccination with a T-cell-priming Gag peptide of caprine arthritis encephalitis virus enhances virus replication transiently in vivo. Journal of general virology, 88(Pt 5), pp. 1589-93. Reading: Society for General Microbiology 10.1099/vir.0.82800-0

Nentwig, Alice; Oevermann, Anna; Heim, Dagmar; Botteron, Catherine; Zellweger, Karola; Drögemüller, Cord; Zurbriggen, Andreas; Seuberlich, Torsten (2007). Diversity in neuroanatomical distribution of abnormal prion protein in atypical scrapie. PLoS pathogens, 3(6), e82. San Francisco, Calif.: Public Library of Science 10.1371/journal.ppat.0030082

Ramseyer, Alessandra; Gaillard, Claude; Burger, Dominik; Straub, Reto; Jost, Ursula; Boog, Cornel; Marti, Eliane; Gerber, Vincent (2007). Effects of genetic and environmental factors on chronic lower airway disease in horses. Journal of veterinary internal medicine, 21(1), pp. 149-56. Oxford: Wiley-Blackwell 10.1892/0891-6640(2007)21[149:EOGAEF]2.0.CO;2

Jost, U; Klukowska-Rötzler, J; Dolf, G; Swinburne, J E; Ramseyer, A; Bugno, M; Burger, D; Blott, S; Gerber, V (2007). A region on equine chromosome 13 is linked to recurrent airway obstruction in horses. Equine veterinary journal, 39(3), pp. 236-41. Oxford: Wiley-Blackwell 10.2746/042516407X171110

Skorczyk, Anna; Stachowiak, Monika; Szczerbal, Izabela; Klukowska-Roetzler, Jolanta; Schelling, Claude; Dolf, Gaudenz; Switonski, Marek (2007). Polymorphism and chromosomal location of the MC4R (melanocortin-4 receptor) gene in the dog and red fox. Gene, 392(1-2), pp. 247-52. Amsterdam: Elsevier 10.1016/j.gene.2006.12.027

Mele, M; Gerber, V; Studer, S; Straub, R; Brehm, W; Gaillard, C; Lüth, A; Burger, D (2007). [Prevalence of hereditary diseases in three-year-old Swiss Warmblood horses]. Schweizer Archiv für Tierheilkunde, 149(4), pp. 161-71. Bern: Huber 10.1024/0036-7281.149.4.161

Kreutzer, R; Müller, G; Leeb, Tosso; Brenig, B; Moritz, A; Baumgärtner, W (2007). Ein Gentest für die GM1-Gangliosidose beim Alaskan Husky. Tierärztliche Praxis. Ausgabe K - Kleintiere, Heimtiere(35), pp. 193-199. Stuttgart: Schattauer

Meinecke, B; Drögemüller, Cord; Kuiper, H; Bürstel, D; Wohlsein, P; Ebeling, S; Wehrend, S; Meinecke-Tillmann, S (2007). A diploid-triploid (60,XX/90,XXY) intersex in a Holstein heifer. Sexual development, 1(1), pp. 59-65. Basel: Karger 10.1159/000096239

Wöhlke, A; Drögemüller, Cord; Distl, O (2007). Prävalenz der Mutation für neuronale Ceroid-Lipofuszinose (NCL) in der europäischen American-Bulldog-Population. Tierärztliche Praxis. Ausgabe K - Kleintiere, Heimtiere(35), pp. 351-355. Stuttgart: Schattauer

Szczerbal, I; Nowacka-Woszuk, J; Racka, M; Klukowska-Rötzler, J; Schelling, C; Dolf, G; Switonski, M (2007). Cytogenic mapping and STR polymorphism of two candidate genes (DRD2 and HTR1D) for behaviour traits in four canids. Archiv Tierzucht / Archives animal breeding(50), pp. 412-417. Dummerstorf: Leibniz Institute for Farm Animal Biology FBN

Tetens, J; Bürstel, D; Ganter, M; Döpke, C; Müller, G; Krause, A; Meyer-Lindenberg, A; Drögemüller, Cord (2007). Untersuchungen zur kongenitalen Mikrophthalmie bei Texelschaf. Tierärztliche Praxis. Ausgabe G - Grosstiere, Nutztiere(35), pp. 211-218. Stuttgart: Schattauer

Peter, C; Bruford, M; Perez, T; Dalamitra, S; Hewitt, G; Erhardt, G; Obexer-Rugg, Gaby; ECONOGENE, Consortium (2007). Genetic diversity and subdivision of 57 European and Middle-Eastern sheep breeds. Animal genetics, 38(1), pp. 37-44. Oxford: Blackwell 10.1111/j.1365-2052.2007.01561.x

Naderi, S; Rezaei, HR; Taberlet, P; Zundel, S; Rafat, SA; Naghash, HR; el-Barody, MA; Ertugrul, O; Pompanon, F; Obexer-Ruff, Gaby; Econogene, Consortium (2007). Large-scale mitochondrial DNA analysis of the domestic goat reveals six haplogroups with high diversity. PLoS ONE, 10(2), e1012. Lawrence, Kans.: Public Library of Science 10.1371/journal.pone.0001012

2006

Ravazzolo, Ana Paula; Nenci, Chiara; Vogt, Hans-Rudolf; Waldvogel, Andreas; Obexer-Ruff, Gaby; Peterhans, Ernst; Bertoni, Giuseppe (2006). Viral load, organ distribution, histopathological lesions, and cytokine mRNA expression in goats infected with a molecular clone of the caprine arthritis encephalitis virus. Virology, 350(1), pp. 116-27. New York, N.Y.: Academic Press 10.1016/j.virol.2006.02.014

Fluri, Alexandra; Nenci, Chiara; Zahno, Marie-Luise; Vogt, Hans-Rudolf; Charan, Shiv; Busato, André; Pancino, Gianfranco; Peterhans, Ernst; Obexer-Ruff, Gaby; Bertoni, Giuseppe (2006). The MHC-haplotype influences primary, but not memory, immune responses to an immunodominant peptide containing T- and B-cell epitopes of the caprine arthritis encephalitis virus Gag protein. Vaccine, 24(5), pp. 597-606. Amsterdam: Elsevier 10.1016/j.vaccine.2005.08.043

Seuberlich, Torsten; Botteron, Catherine; Wenker, Christian; Café Marçal, Valéria; Oevermann, Anna; Haase, Bianca; Leeb, Tosso; Heim, Dagmar; Zurbriggen, Andreas (2006). Spongiform encephalopathy in a miniature zebu. Emerging infectious diseases, 12(12), pp. 1950-1953. Atlanta, Ga.: U.S. National Center for Infectious Diseases 10.3201/eid1212.060750

Leeb, Tosso; Dolle, K; Haase, Bianca (2006). Sequence analysis of the porcine IFNAR1 and IFNGR2 genes. Cytogenetic and genome research, 115(2), pp. 134-7. Basel: Karger 10.1159/000095233

Baars, Cordula; Löscher, Wolfgang; Leeb, Tosso; Becker, Albert; Potschka, Heidrun (2006). Polymorphic variants of the multidrug resistance gene Mdr1a and response to antiepileptic drug treatment in the kindling model of epilepsy. European journal of pharmacology, 550(1-3), pp. 54-61. Amsterdam: Elsevier 10.1016/j.ejphar.2006.08.040

Braunschweig, Martin; Leeb, Tosso (2006). Aberrant low expression level of bovine beta-lactoglobulin is associated with a C to A transversion in the BLG promoter region. Journal of dairy science, 89(11), pp. 4414-9. Savoy, Ill.: American Dairy Science Association

Dierks, C; Mömke, S; Drögemüller, Cord; Leeb, Tosso; Chowdhary, B P; Distl, O (2006). A high-resolution comparative radiation hybrid map of equine chromosome 4q12-q22. Animal genetics, 37(5), pp. 513-7. Oxford: Blackwell 10.1111/j.1365-2052.2006.01510.x

Drögemüller, Cord; Dolf, Gaudenz; Leeb, Tosso (2006). [A database of available DNA tests in the dog]. Schweizer Archiv für Tierheilkunde, 148(8), pp. 409-11. Bern: Huber 10.1024/0036-7281.148.08.409

Klukowska-Rötzler, Jolanta; Jost, U; Schelling, C; Dolf, Gaudenz; Chowdhary, B P; Leeb, Tosso; Gerber, Vinzenz (2006). Characterization and RH mapping of six gene-associated equine microsatellite markers. Animal genetics, 37(3), pp. 305-6. Oxford: Blackwell 10.1111/j.1365-2052.2006.01445.x

Looft, Christian; Paul, Sven; Philipp, Ute; Regenhard, Petra; Kuiper, Heidi; Distl, Ottmar; Chowdhary, Bhanu P; Leeb, Tosso (2006). Sequence analysis of a 212 kb defensin gene cluster on ECA 27q17. Gene, 376(2), pp. 192-8. Amsterdam: Elsevier 10.1016/j.gene.2006.03.006

von Bomhard, Wolf; Mauldin, Elizabeth A; Schmutz, Sheila M; Leeb, Tosso; Casal, Margret L (2006). Black hair follicular dysplasia in Large Münsterländer dogs: clinical, histological and ultrastructural features. Veterinary dermatology, 17(3), pp. 182-8. Oxford: Blackwell Science 10.1111/j.1365-3164.2006.00517.x

Haase, Bianca; Humphray, Sean J; Lyer, Stefan; Renner, Marcus; Poustka, Annemarie; Mollenhauer, Jan; Leeb, Tosso (2006). Molecular characterization of the porcine deleted in malignant brain tumors 1 gene (DMBT1). Gene, 376(2), pp. 184-91. Amsterdam: Elsevier 10.1016/j.gene.2006.03.002

Leeb, Tosso; Vogl, Claus; Zhu, Baoli; de Jong, Pieter J; Binns, Matthew M; Chowdhary, Bhanu P; Scharfe, Maren; Jarek, Michael; Nordsiek, Gabriele; Schrader, Frank; Blöcker, Helmut (2006). A human-horse comparative map based on equine BAC end sequences. Genomics, 87(6), pp. 772-6. San Diego, Calif.: Elsevier 10.1016/j.ygeno.2006.03.002

Drögemüller, Cord; Giese, Alexander; Martins-Wess, Flávia; Wiedemann, Sabine; Andersson, Leif; Brenig, Bertram; Fries, Ruedi; Leeb, Tosso (2006). The mutation causing the black-and-tan pigmentation phenotype of Mangalitza pigs maps to the porcine ASIP locus but does not affect its coding sequence. Mammalian genome, 17(1), pp. 58-66. New York, N.Y.: Springer-Verlag 10.1007/s00335-005-0104-1

Sander, Petra; Alfalah, Marwan; Keiser, Markus; Korponay-Szabo, Ilma; Kovács, Judit B; Leeb, Tosso; Naim, Hassan Y (2006). Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption. Human mutation, 27(1), p. 119. Hoboken, N.J.: Wiley-Blackwell

Swinburne, June E; Boursnell, Mike; Hill, Gemma; Pettitt, Louise; Allen, Twink; Chowdhary, Bhanu; Hasegawa, Telhisa; Kurosawa, Masahiko; Leeb, Tosso; Mashima, Suguru; Mickelson, James R; Raudsepp, Terje; Tozaki, Teruaki; Binns, Matthew (2006). Single linkage group per chromosome genetic linkage map for the horse, based on two three-generation, full-sibling, crossbred horse reference families. Genomics, 87(1), pp. 1-29. San Diego, Calif.: Elsevier 10.1016/j.ygeno.2005.09.001

Jann, Oliver C; Aerts, Jan; Jones, Michelle; Hastings, Nicola; Law, Andy; McKay, Stephanie; Marques, Elisa; Prasad, Aparna; Yu, Jody; Moore, Stephen S; Floriot, Sandrine; Mahé, Marie-Françoise; Eggen, André; Silveri, Licia; Negrini, Riccardo; Milanesi, Elisabetta; Ajmone-Marsan, Paolo; Valentini, Alessio; Marchitelli, Cinzia; Savarese, Maria C; ... (2006). A second generation radiation hybrid map to aid the assembly of the bovine genome sequence. BMC Genomics, 7, p. 283. London: BioMed Central 10.1186/1471-2164-7-283

Wöhlke, A; Kuiper, H; Distl, O; Drögemüller, Cord (2006). The bovine aristaless-like homeobox 4 (ALX4) as a candidate gene for syndactyly. Cytogenetic and genome research, 115(2), pp. 123-8. Basel: Karger 10.1159/000095231

Boneker, C; Kuiper, H; Drögemüller, Cord; Chowdhary, B P; Distl, O (2006). Molecular characterization of the equine collagen, type IX, alpha 2 (COL9A2) gene on horse chromosome 2p16-->p15. Cytogenetic and genome research, 115(2), pp. 107-14. Basel: Karger 10.1159/000095229

Meadows, J R S; Hanotte, O; Drögemüller, Cord; Calvo, J; Godfrey, R; Coltman, D; Maddox, J F; Marzanov, N; Kantanen, J; Kijas, J W (2006). Globally dispersed Y chromosomal haplotypes in wild and domestic sheep. Animal genetics, 37(5), pp. 444-53. Oxford: Blackwell 10.1111/j.1365-2052.2006.01496.x

Sild, E; Volskiene, R; Viinalass, H; Miceikiene, I; Grislis, Z; Distl, O; Drögemüller, Cord (2006). Detection of prion protein gene polymorphisms in Baltic breeds of sheep. Veterinary record, 159(8), pp. 247-50. London: British Veterinary Association 10.1136/vr.159.8.247

de Vries, F; Hamann, H; Drögemüller, Cord; Distl, O (2006). Associations between prion protein genotype and type traits in East Friesian milk sheep. Veterinary record, 158(25), pp. 849-52. London: British Veterinary Association 10.1136/vr.158.25.849

Müller, D; Kuiper, H; Mömke, S; Böneker, C; Drögemüller, Cord; Swinburne, J E; Binns, M; Chowdhary, B P; Distl, O (2006). Physical mapping of the ATP2A2 gene to equine chromosome 8p14-->p12 by FISH and confirmation by linkage and RH mapping. Cytogenetic and genome research, 114(1), 94G. Basel: Karger 10.1159/000091941

Schulze, U; Koch, R; Köchling, M; Wohlsein, P; Drögemüller, Cord; Meyer, W; Distl, O; Waibl, H (2006). [Case report: an exceptional case of a monozygotic thoracopagus parasiticus in a German Holstein calf]. DTW. Deutsche tierärztliche Wochenschrift, 113(2), pp. 72-8. Alfeld: Verlag M. & H. Schaper

Wohlke, Anne; Distl, Ottmar; Drögemüller, Cord (2006). Characterization of the canine CLCN3 gene and evaluation as candidate for late-onset NCL. BMC genetics, 7, p. 13. London: BioMed Central 10.1186/1471-2156-7-13

Drögemüller, Cord; Distl, Ottmar (2006). Genetic analysis of syndactyly in German Holstein cattle. Veterinary journal, 171(1), pp. 120-5. Amsterdam: Elsevier 10.1016/j.tvjl.2004.09.009

Schaschl, H; Wandeler, P; Suchentrunk, F; Obexer-Ruff, Gaby; Goodman, S J (2006). Selection and recombination drive the evolution of MHC class II DRB diversity in ungulates. Heredity, 97(6), pp. 427-37. London: Oliver and Boyd 10.1038/sj.hdy.6800892

Cañón, J; García, D; García-Atance, MA; Obexer-Ruff, Gaby; Lenstra, JA; Ajmone-Marsan, P; Dunner, S; ECONOGENE, Consortium (2006). Geographical partitioning of goat diversity in Europe and the Middle East. Animal genetics, 37(4), pp. 327-34. Oxford: Blackwell 10.1111/j.1365-2052.2006.01461.x

Pariset, L; Cappuccio, I; Ajmone Marsan, P; Dunner, S; Luikart, G; England, PR; Obexer-Ruff, Gaby; Peter, C; Marletta, D; Pilla, F; Valentini, A; ECONOGENE, Consortium (2006). Assessment of population structure by single nucleotide polymorphisms (SNPs) in goat breeds. Journal of chromatography. B - analytical technologies in the biomedical and life sciences, 833(1), pp. 117-20. New York, N.Y.: Elsevier 10.1016/j.jchromb.2006.01.011

Karlskov-Mortensen, P; Bruun, C S; Braunschweig, M H; Sawera, M; Markljung, E; Enfält, A C; Hedebro-Velander, I; Josell, A; Lindahl, G; Lundström, K; von Seth, G; Jørgensen, C B; Andersson, L; Fredholm, M (2006). Genome-wide identification of quantitative trait loci in a cross between Hampshire and Landrace I: carcass traits. Animal genetics, 37(2), pp. 156-62. Oxford: Blackwell 10.1111/j.1365-2052.2005.01405.x

Poncet, P A; Pfister, W; Muntwyler, J; Glowatzki-Mullis, M L; Gaillard, C (2006). Analysis of pedigree and conformation data to explain genetic variability of the horse breed Franches-Montagnes. Journal of animal breeding and genetics, 123(2), pp. 114-21. Berlin: Wiley-Blackwell 10.1111/j.1439-0388.2006.00569.x

Glowatzki-Mullis, M L; Muntwyler, J; Pfister, W; Marti, E; Rieder, S; Poncet, P A; Gaillard, C (2006). Genetic diversity among horse populations with a special focus on the Franches-Montagnes breed. Animal genetics, 37(1), pp. 33-9. Oxford: Blackwell 10.1111/j.1365-2052.2005.01376.x

Sasaki, Y; Miyake, T; Gaillard, C; Oguni, T; Matsumoto, M; Ito, M; Kurahara, T; Sasae, Y; Fujinaka, K; Ohtagaki, S; Dougo, T (2006). Comparison of genetic gains per year for carcass traits among breeding programs in the Japanese Brown and the Japanese Black cattle. Journal of animal science, 84(2), pp. 317-23. Savoy, Ill.: American Society of Animal Science

Voegeli, E; Welle, M; Hauser, B; Dolf, G; Flückiger, M (2006). [Histiocytic sarcoma in the Swiss population of Bernese mountain dogs: a retrospective study of its genetic predisposition]. Schweizer Archiv für Tierheilkunde, 148(6), pp. 281-8. Bern: Huber 10.1024/0036-7281.148.6.281

Drögemüller, Cord; Barlund, CS; Palmer, CW; Leeb, Tosso (2006). A novel mutation in the bovine EDA gene causing anhidrotic ectodermal dysplasia. Archiv Tierzucht / Archives animal breeding(49), pp. 615-616. Dummerstorf: Leibniz Institute for Farm Animal Biology FBN

Burger, N; Busato, A; Nesvadba, JZ; Gottstein, B (2006). Epidemiologische Untersuchungen zum Vorkommen von Dicorcoelium dendriticum im Emmental. Berliner und Münchener tierärztliche Wochenschrift(119), pp. 324-329. Hannover: Schlütersche

Leeb, Tosso; Sander, P (2006). Genetische Einflüsse auf die BSE-Empfänglichkeit beim rind - Mythos oder Realität? Nova acta Leopoldina(94), pp. 227-235. Stuttgart: Wiss. Verl.-Ges.

Klukowska-Rötzler, Jolanta; Bugno, M; Sander, P; Slota, E; Dolf, Gaudenz; Chowdhary, B P; Leeb, Tosso; Gerber, Vinzenz (2006). Chromosomal assignment of the two candidate genes (EGFR, CLCA1) for equine recurrent airway obstruction (RAO) by FISH and RH mapping. Hereditas, 143(2006), pp. 138-41. Lund: Mendelian Society of Lund 10.1111/j.2006.0018-0661.01947.x

Szczerbal, I; Klukowska-Roetzler, J; Dolf, G; Schelling, C; Switonski, M (2006). FISH mapping of 10 canine BAC clones harbouring genes and microsatellites in the arctic fox and the Chinese raccoon dog genomes. Journal of animal breeding and genetics, 123(5), pp. 337-42. Berlin: Wiley-Blackwell 10.1111/j.1439-0388.2006.00608.x

Pariset, L; Cappuccio, I; Joost, S; D'Andrea, M; Marletta, D; Ajmone Marsan, P; Valentini, A; Obexer-Rugg, Gaby; ECONOGENE, Consortium (2006). Characterization of single nucleotide polymorphismus in sheep and their variation as evidence of selection. Animal genetics, 37(3), pp. 290-2. Oxford: Blackwell 10.1111/j.1365-2052.2006.01441.x

Pariset, L; Cappuccio, I; Ajmone-Marsan, P; Bruford, M; Dunner, S; Cortes, O et al; Obexer-Ruff, Gaby; ECONOGENE, Consortium (2006). Characterization of 37 breed-specific single-nucleotide polymorphisms in sheep. Journal of heredity, 97(5), pp. 531-4. Oxford: Oxford University Press 10.1093/jhered/es1020

2005

Töpfer-Petersen, E; Ekhlasi-Hundrieser, M; Tsolova, M; Leeb, Tosso; Kirchhoff, C; Müller, P (2005). Structure and function of secretory proteins of the male genital tract. Andrologia, 37(6), pp. 202-204. Wiley-Blackwell 10.1111/j.1439-0272.2005.00688.x

Sander, Petra; Hamann, Henning; Drögemüller, Cord; Kashkevich, Kseniya; Schiebel, Katrin; Leeb, Tosso (2005). Bovine prion protein gene (PRNP) promoter polymorphisms modulate PRNP expression and may be responsible for differences in bovine spongiform encephalopathy susceptibility. Journal of biological chemistry, 280(45), pp. 37408-37414. American Society for Biochemistry and Molecular Biology 10.1074/jbc.M506361200

Leeb, Tosso; Sieme, H; Töpfer-Petersen, E (2005). Genetic markers for stallion fertility - lessons from humans and mice. Animal reproduction science, 89(1-4), pp. 21-29. Elsevier 10.1016/j.anireprosci.2005.06.021

Kreutzer, Robert; Leeb, Tosso; Müller, Gundi; Moritz, Andreas; Baumgärtner, Wolfgang (2005). A duplication in the canine beta-galactosidase gene GLB1 causes exon skipping and GM1-gangliosidosis in Alaskan huskies. Genetics, 170(4), pp. 1857-1861. Genetics Society of America 10.1534/genetics.105.042580

Haase, Bianca; Schlötterer, Christian; Hundrieser, Mahnaz Ekhlasi; Kuiper, Heidi; Distl, Ottmar; Töpfer-Petersen, Edda; Leeb, Tosso (2005). Evolution of the spermadhesin gene family. Gene, 352, pp. 20-29. Elsevier 10.1016/j.gene.2005.04.015

Leeb, Tosso; Brenig, B; Rohrer, G A (2005). Characterization and linkage mapping of four gene-associated porcine microsatellites. Animal genetics, 36(3), pp. 279-280. Blackwell 10.1111/j.1365-2052.2005.01291.x

Seeliger, F; Drögemüller, Cord; Tegtmeier, P; Baumgärtner, W; Distl, O; Leeb, Tosso (2005). Ectodysplasin-1 deficiency in a German Holstein bull associated with loss of respiratory mucous glands and chronic rhinotracheitis. Journal of comparative pathology, 132(4), pp. 346-349. Elsevier 10.1016/j.jcpa.2004.11.001

Sander, P; Drögemüller, Cord; Cadieu, E; André, C; Leeb, Tosso (2005). Analysis of the canine EDAR gene and exclusion as a candidate for the hairless phenotype in the Chinese Crested dog. Animal genetics, 36(2), pp. 168-171. Blackwell 10.1111/j.1365-2052.2005.01242.x

Wöhlke, Anne; Drögemüller, Cord; Kuiper, Heidi; Leeb, Tosso; Distl, Ottmar (2005). Molecular characterization and chromosomal assignment of the bovine glycinamide ribonucleotide formyltransferase (GART) gene on cattle chromosome 1q12.1-q12.2. Gene, 348, pp. 73-81. Elsevier 10.1016/j.gene.2004.12.038

Drögemüller, Cord; Wöhlke, Anne; Leeb, Tosso; Distl, Ottmar (2005). A 4 Mb high resolution BAC contig on bovine chromosome 1q12 and comparative analysis with human chromosome 21q22. Comparative and functional genomics, 6(4), pp. 194-203. Hindawi 10.1002/cfg.476

Kemter, E; Philipp, U; Klose, R; Kuiper, H; Boelhauve, M; Distl, O; Wolf, E; Leeb, Tosso (2005). Molecular cloning, expression analysis and assignment of the porcine tumor necrosis factor superfamily member 10 gene (TNFSF10) to SSC13q34-->q36 by fluorescence in situ hybridization and radiation hybrid mapping. Cytogenetic and genome research, 111(1), pp. 74-78. Karger 10.1159/000085673

Philipp, Ute; Hamann, Henning; Mecklenburg, Lars; Nishino, Seiji; Mignot, Emmanuel; Günzel-Apel, Anne-Rose; Schmutz, Sheila M; Leeb, Tosso (2005). Polymorphisms within the canine MLPH gene are associated with dilute coat color in dogs. BMC genetics, 6(34), p. 34. BioMed Central 10.1186/1471-2156-6-34

Philipp, U; Quignon, P; Scott, A; André, C; Breen, M; Leeb, Tosso (2005). Chromosomal assignment of the canine melanophilin gene (MLPH): a candidate gene for coat color dilution in Pinschers. Journal of heredity, 96(7), pp. 774-776. Oxford University Press 10.1093/jhered/esi079

Leeb, Tosso; Bruhn, O; Philipp, U; Kuiper, H; Regenhard, P; Paul, S; Distl, O; Chowdhary, B P; Kalm, E; Looft, C (2005). Assignment of the equine S100A7 gene (psoriasin 1) to chromosome 5p12-->p13 by fluorescence in situ hybridization and radiation hybrid mapping. Cytogenetic and genome research, 109(4), p. 533. Karger 10.1159/000084216

Drögemüller, Cord; Kuiper, H; Spötter, A; Martins-Wess, F; Williams, J L; Lassnig, C; Distl, O; Müller, M; Leeb, Tosso (2005). Assignment of the bovine TYK2 and PDE4A genes to bovine chromosome 7q15 by fluorescence in situ hybridization and radiation hybrid mapping. Cytogenetic and genome research, 108(4), p. 363. Karger 10.1159/000081540

2004

Howard, J.; Jaggy, A.; Busato, A.; Gaschen, F. (2004). Electrodiagnostic evaluation in feline hypertrophic muscular dystrophy. Veterinary journal, 1168(1), pp. 87-92. Elsevier 10.1016/S1090-0233(03)00080-7

2003

Rogalska-Niznik, N.; Szczerbal, I.; Dolf, G.; Schläpfer, J.; Schelling, C.; Switonski, M. (2003). Canine-Derived Cosmid Probes Containing Microsatellites Can Be Used in Physical Mapping of Arctic Fox (Alopex lagopus) and Chinese Raccoon Dog (Nyctereutes procyonoides procyonoides) Genomes. Journal of heredity, 94(1), pp. 89-93. Oxford University Press 10.1093/jhered/esg005

2002

Magee, D. A.; Meghen, C.; Harrison, S.; Troy, C. S.; Cymbron, T.; Gaillard, C.; Morrow, A.; Maillard, J. C.; Bradley, D. G. (2002). A Partial African Ancestry for the Creole Cattle Populations of the Caribbean. Journal of heredity, 93(6), pp. 429-432. Oxford University Press 10.1093/jhered/93.6.429

1999

Dolf, G. (1999). DogMap: an international collaboration toward a low-resolution canine genetic marker map. Journal of heredity, 90(1), pp. 3-6. Oxford University Press 10.1093/jhered/90.1.3

1997

Schawalder, Peter; Spreng, David; Dietschi, Elisabeth; Dolf, Gaudenz; Gaillard, Claude (1997). The biomechanics of the hip joint using new diagnostic aspects in the field of hip dysplasia. Constructive critical thoughts on hip dysplasia diagnosis and today's marketable breeding methods with an outlook on future perspectives and possibilities. Part II. Schweizer Archiv für Tierheilkunde, 139(6), pp. 265-270. Huber

Schläpfer, J.; Yang, Y.; Rexroad Iii, C.; Womack, J. E. (1997). A radiation hybrid framework map of bovine chromosome 13. Chromsome research, 5(8), pp. 511-519. Springer 10.1023/A:1018485401403

1996

Schawalder, Peter; Spreng, David; Dietschi, Elisabeth; Dolf, Gaudenz; Gaillard, Claude (1996). The biomechanics of the hip joint using new diagnostic aspects in the field of hip joint dysplasia. Constructive criticism of hip dysplasia diagnosis and present marketable breeding methods with an outlook on future perspectives and possibilities. Part I. Schweizer Archiv für Tierheilkunde, 138(11), pp. 511-522. Huber

Schawalder, Peter; Spreng, David; Dietschi, Elisabeth; Dolf, Gaudenz; Gaillard, Claude (1996). Die Hüftgelenksdysplasie im Umfeld von sekundären Einflüssen und ektopischen Ursachen. Kleintierpraxis, 41, pp. 625-638. Schaper

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