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Rudd Garces, Gabriela; Farke, Daniela; Schmidt, Martin J; Letko, Anna; Schirl, Katja; Abitbol, Marie; Leeb, Tosso; Lyons, Leslie A; Lühken, Gesine (2024). PAX3 haploinsufficiency in Maine Coon cats with dominant blue eyes and hearing loss resembling the human Waardenburg syndrome. G3 Genes Genomes Genetics, 14(9) Genetics Society of America 10.1093/g3journal/jkae131
Lynch, C; Leishman, E M; Miglior, F; Kelton, D; Schenkel, F S; Baes, C F (2024). Review: Opportunities and challenges for the genetic selection of dairy calf disease traits. Animal : an international journal of animal bioscience, 18 Suppl 2, p. 101141. Elsevier 10.1016/j.animal.2024.101141
Oliveira, Hinayah R; Chud, Tatiane C S; Oliveira, Gerson A; Hermisdorff, Isis C; Narayana, Saranya G; Rochus, Christina M; Butty, Adrien M; Malchiodi, Francesca; Stothard, Paul; Miglior, Filippo; Baes, Christine F; Schenkel, Flavio S (2024). Genome-wide association analyses reveals copy number variant regions associated with reproduction and disease traits in Canadian Holstein cattle. Journal of dairy science, 107(9), pp. 7052-7063. American Dairy Science Association 10.3168/jds.2023-24295
Cook, Shawna R; Schwarz, Cleo; Guevar, Julien; Assenmacher, Charles-Antoine; Sheehy, Maeve; Fanzone, Nathan; Church, Molly E; Murgiano, Leonardo; Casal, Margret L; Jagannathan, Vidhya; Gutierrez-Quintana, Rodrigo; Lowrie, Mark; Steffen, Frank; Leeb, Tosso; Ekenstedt, Kari J (2024). Canine RNF170 Single Base Deletion in a Naturally Occurring Model for Human Neuroaxonal Dystrophy. (In Press). Movement disorders Wiley 10.1002/mds.29977
Tammen, Imke; Mather, Marius; Leeb, Tosso; Nicholas, Frank W (2024). Online Mendelian Inheritance in Animals (OMIA): a genetic resource for vertebrate animals. (In Press). Mammalian genome Springer-Verlag 10.1007/s00335-024-10059-y
Kiener, Sarah; Lehner, Georg; Jagannathan, Vidhya; Welle, Monika; Leeb, Tosso (2024). Heterozygous DSP in-frame deletion in a poodle with syndromic ichthyosis involving additional hair and tooth abnormalities. (In Press). Animal genetics Wiley 10.1111/age.13467
Mauldin, Elizabeth; Bradley, Charles; Casal, Margret; Meyer, Jason; Crumrine, Debra; Kiener, Sarah; Leeb, Tosso; Elias, Peter M (2024). Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1-deficient Jack Russell Terriers and response to topical ceramide. (In Press). Veterinary dermatology Wiley 10.1111/vde.13285
Kiener, Sarah; Wildermuth, Brett; Meertens, Nadine M; Jagannathan, Vidhya; Leeb, Tosso (2024). Heterozygous deletion of the NSDHL gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic nevi. Animal genetics, 55(4), pp. 697-699. Wiley 10.1111/age.13436
Letko, Anna; Gurtner, Corinne; Jagannathan, Vidhya; Drögemüller, Cord (2024). Renal dysplasia in Leonberger dogs - An emerging recessive congenital disorder? Animal genetics, 55(4), pp. 700-701. Wiley 10.1111/age.13439
Rietmann, Stefan J; Nowell, Sarah; Keating, M Kelly; Bauer, Cynthia; Jagannathan, Vidhya; Leeb, Tosso (2024). Heterozygous COL5A1 deletion in a cat with classical Ehlers-Danlos syndrome. Animal genetics, 55(4), pp. 705-707. Wiley 10.1111/age.13446
Kalbfleisch, Theodore S; McKay, Stephanie D; Murdoch, Brenda M; Adelson, David L; Almansa-Villa, Diego; Becker, Gabrielle; Beckett, Linda M; Benítez-Galeano, María José; Biase, Fernando; Casey, Theresa; Chuong, Edward; Clark, Emily; Clarke, Shannon; Cockett, Noelle; Couldrey, Christine; Davis, Brian W; Elsik, Christine G; Faraut, Thomas; Gao, Yahui; Genet, Carine; ... (2024). The Ruminant Telomere-to-Telomere (RT2T) Consortium. Nature genetics, 56(8), pp. 1566-1573. Nature America 10.1038/s41588-024-01835-2
Petretto, Elena; Dettori, Maria Luisa; Luigi-Sierra, María Gracia; Noce, Antonia; Pazzola, Michele; Vacca, Giuseppe Massimo; Molina, Antonio; Martínez, Amparo; Goyache, Félix; Carolan, Sean; The AdaptMap, Consortium; Amills, Marcel (2024). Investigating the footprint of post-domestication dispersal on the diversity of modern European, African and Asian goats. Genetics, selection, evolution, 56(1), p. 55. BioMed Central 10.1186/s12711-024-00923-5
Goncalves Pontes Jacinto, Joana; Letko, Anna; Häfliger, Irene Monika; Drögemüller, Cord; Agerholm, Jørgen Steen (2024). Congenital syndromic Chiari-like malformation (CSCM) in Holstein cattle: towards unravelling of possible genetic causes. Acta Veterinaria Scandinavica, 66(29) BioMed Central Ltd. 10.1186/s13028-024-00752-y
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. Journal of dairy science, 107(7), pp. 4704-4713. American Dairy Science Association 10.3168/jds.2023-23751
Rietmann, Stefan J.; Cochet-Faivre, Noëlle; Dropsy, Helene; Jagannathan, Vidhya; Chevallier, Lucie; Leeb, Tosso (2024). EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia. Genes, 15(7) MDPI 10.3390/genes15070854
Fong, Aisha; Rochus, Christina M; Shandilya, Umesh K; Muniz, Maria M M; Sharma, Ankita; Schenkel, Flavio S; Karrow, Niel A; Baes, Christine F (2024). The role of interleukin-10 receptor alpha (IL10Rα) in Mycobacterium avium subsp. paratuberculosis infection of a mammary epithelial cell line. BMC genomic data, 25(1), p. 58. BMC 10.1186/s12863-024-01234-w
Kiener, Sarah; Åhman, Susanne; Cikota, Robert; Jagannathan, Vidhya; Blatter, Sohvi; Cvitas, Iva; Soto, Sara; Leeb, Tosso (2024). Heterozygous ASPRV1 frameshift variant in a Pembroke Welsh Corgi with ichthyosis. Animal genetics, 55(3), pp. 490-492. Wiley 10.1111/age.13423
Muniz, Maria Malane M; Serrenho, Rita Couto; Duffield, Todd; de Oliveira Junior, Gerson A; McArt, Jessica A A; Baes, Christine F; Schenkel, Flavio Schramm; Squires, E James (2024). Identification of genetic markers associated with hyperketonemia patterns in early lactation Holstein cows. (In Press). Journal of animal breeding and genetics Wiley-Blackwell 10.1111/jbg.12875
Rietmann, Stefan J; Lange, Anja; Soto, Sara; Thom, Nina; Manz, Eberhard; Jagannathan, Vidhya; Mayer, Ursula; Leeb, Tosso (2024). KRT5 in-frame deletion in a family of German Shepherd dogs with split paw pad disease resembling localized epidermolysis bullosa simplex in human patients. Animal genetics, 55, pp. 692-696. Wiley 10.1111/age.13444
Christen, Matthias; Gregor, Katharina M; Böttcher-Künneke, Ariane; Lombardo, Mara S; Baumgärtner, Wolfgang; Jagannathan, Vidhya; Puff, Christina; Leeb, Tosso (2024). Intragenic MFSD8 duplication and histopathological findings in a rabbit with neuronal ceroid lipofuscinosis. Animal genetics, 55, pp. 588-598. Wiley 10.1111/age.13441
Suiter, Emma; Baiker, Kerstin; Kaczmarska, Adriana; Christen, Matthias; Leeb, Tosso; Ororbia, Alejandro; Anselmi, Carlo; Minguez, Juan; Gutierrez-Quintana, Rodrigo (2024). Novel MRI and histopathological findings in a young Bullmastiff cross dog with mitochondrial fission encephalopathy. (In Press). Veterinary radiology & ultrasound Wiley 10.1111/vru.13342
Mizukami, Keijiro; Dorsey-Oresto, Angella; Raj, Karthik; Eringis, Anna; Furrow, Eva; Martin, Errolyn; Yamanaka, Daisuke; Kehl, Alexandra; Kolicheski, Ana; Jagannathan, Vidhya; Leeb, Tosso; Lionakis, Michail S; Giger, Urs (2024). Increased susceptibility to Mycobacterium avium complex infection in miniature Schnauzer dogs caused by a codon deletion in CARD9. Scientific reports, 14(10346) Springer Nature 10.1038/s41598-024-61054-x
Vanderhout, Ryley J; Abdalla, Emhimad A; Leishman, Emily M; Barbut, Shai; Wood, Benjamin J; Baes, Christine F (2024). Genetic architecture of white striping in turkeys (Meleagris gallopavo). Scientific reports, 14(9007) Springer Nature 10.1038/s41598-024-59309-8
Kaelin, Christopher B; McGowan, Kelly A; Hutcherson, Anthony D; Delay, John M; Li, Jeremiah H; Kiener, Sarah; Jagannathan, Vidhya; Leeb, Tosso; Murphy, William J; Barsh, Gregory S (2024). Ancestry dynamics and trait selection in a designer cat breed. Current biology, 34(7), 1506-1518.e7. Cell Press 10.1016/j.cub.2024.02.075
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
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. The veterinary journal, 304, p. 106069. Elsevier 10.1016/j.tvjl.2024.106069
Dini, Filippo M; Jacinto, Joana G P; Cavallini, Damiano; Beltrame, Andrea; Del Re, Flavia S; Abram, Laura; Gentile, Arcangelo; Galuppi, Roberta (2024). Observational longitudinal study on Toxoplasma gondii infection in fattening beef cattle: serology and associated haematological findings. Parasitology research, 123(3) Springer-Verlag 10.1007/s00436-024-08189-y
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
Leeb, Tosso; Pewsner, Mirjam (6 February 2024). RT2T: A Global Collaborative Project to Study Chromosomal Evolution in the Suborder Ruminantia Research Square 10.21203/rs.3.rs-3918604/v2
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
Cook, Shawna R.; Schwarz, Cleo; Guevar, Julien; Assenmacher, Charles-Antoine; Sheehy, Maeve; Fanzone, Nathan; Church, Molly E.; Murgiano, Leonardo; Casal, Margret L.; Jagannathan, Vidhya; Gutierrez-Quintana, Rodrigo; Lowrie, Mark; Steffen, Frank; Leeb, Tosso; Ekenstedt, Kari J. (1 February 2024). RNF170 frameshift deletion in Miniature American Shepherd dogs with neuroaxonal dystrophy provides a naturally occurring model for human RNF170 phenotypic spectrum Research Square 10.21203/rs.3.rs-3914204/v1
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
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. Journal of animal science, 102 Oxford University Press 10.1093/jas/skae061
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
Mehrotra, Arnav; Leonard, Alexander S; Drogemuller, Cord; Grahofer, Alexander; Khayatzadeh, Negar; Hofer, Andreas; Neuenschwander, Stefan; Pausch, Hubert (2024). Genome-Wide Association Testing for Haemorrhagic Bowel Syndrome in a Swiss Large White Pig Population (bioRxiv). Cold Spring Harbor Laboratory 10.1101/2024.04.05.588256
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 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
Jacinto, Joana G P; 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 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, 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 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
Jacinto, Joana G P; 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 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 10.3390/genes14061210
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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 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 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 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 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 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 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 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 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 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 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 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
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 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 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
Jacinto, Joana G P; 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 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 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 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 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 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 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 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 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 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 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 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, Rebecca; 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 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 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
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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 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 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 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
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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
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
Mühlhause, Franziska; Tipold, Andrea; Rohn, Karl; Lepori, Vincent; Leeb, Tosso; Sewell, Adrian C; Kornberg, Marion (2019). [Follow-up study in German Hunting Terrier dogs with exercise induced metabolic myopathy]. Tierärztliche Praxis. Ausgabe K - Kleintiere, Heimtiere, 47(6), pp. 402-410. Thieme 10.1055/a-1027-2533
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 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 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 10.3390/genes10100731
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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
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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
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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 10.3390/genes10080567
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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 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 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 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 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 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 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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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
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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
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
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
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
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
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
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
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
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
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
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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
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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
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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
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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
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
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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
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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
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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
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