05 Veterinary Medicine > Department of Clinical Research and Veterinary Public Health (DCR-VPH) > Institute of Genetics

University of Bern (798)
- 05 Veterinary Medicine (798)
  - Department of Clinical Research and Veterinary Public Health (DCR-VPH) (798)
    - Institute of Genetics (798)

Group by: Date | Name | Item Type | Refereed | No Grouping

Number of items at this level: 2439.

Abril Gaona, Carlos

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

Aebi, Marlis

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

Aeschlimann, Leonore

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

Aguilar Bultet, Lisandra

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

Akouchekian, Mansoureh

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

Alaeddine, Ferial

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

Albrecht, Christiane

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

Alsaaod, Maher

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

Altermatt, Nicole

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

Amylidi-Mohr, Sofia

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

Anderegg, Linda

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

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

Anderegg, Linda; Im Hof Gut, Michelle; Hetzel, Udo; Howerth, Elizabeth W; Leuthard, Fabienne Nadja; Kyöstilä, Kaisa; Lohi, Hannes; Pettitt, Louise; Mellersh, Cathryn; Minor, Katie M; Mickelson, James R; Batcher, Kevin; Bannasch, Danika; Jagannathan, Vidya; Leeb, Tosso (2019). NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesia. PLoS genetics, 15(9), e1008378. Public Library of Science 10.1371/journal.pgen.1008378

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

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

Arnaud, Galichet

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

Awasthi, Nivedita

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

Axiak, Shannon

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

Baes, Christine Francoise

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Nayeri, S.; Schenkel, F.S.; Fleming, A.; Kroezen, V.; Sargolzaei, M.; Baes, C.; Cánovas, A.; Squires, J.; Miglior, F. (2019). Genome-wide association analysis for β-hydroxybutyrate concentration in Milk in Holstein dairy cattle. BMC genetics, 20(1), p. 58. BioMed Central 10.1186/s12863-019-0761-9

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

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

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

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

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

Baes, Christine F.; Makanjuola, B.; Miglior, F.; Marras, G.; Howard, J.T.; Fleming, A.; Maltecca, C. (2019). Symposium review: The genomic architecture of inbreeding: How homozygosity affects health and performance. Journal of dairy science, 102(3), pp. 2807-2817. Elsevier 10.3168/jds.2018-15520

Guarini, A.R.; Lourenco, D.A.L.; Brito, L.F.; Sargolzaei, M.; Baes, C. F.; Miglior, F.; Misztal, I.; Schenkel, F.S. (2019). Genetics and genomics of reproductive disorders in Canadian Holstein cattle. Journal of dairy science, 102(2), pp. 1341-1353. Elsevier 10.3168/jds.2018-15038

Jaton, C.; Schenkel, F. S.; Chud, T. C. S.; Malchiodi, F.; Sargolzaei, M.; Price, C. A.; Canovàs, A.; Baes, C.; Miglior, F. (2019). Genetic and genomic analyses of embryo production in dairy cattle. Reproduction, fertility, and development, 32(2), pp. 50-55. CSIRO Publishing 10.1071/RD19275

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

Guarini, A.R.; Sargolzaei, M.; Brito, L.F.; Kroezen, V.; Lourenco, D.A.L.; Baes, C. F.; Miglior, F.; Cole, J.B.; Schenkel, F.S. (2019). Estimating the effect of the deleterious recessive haplotypes AH1 and AH2 on reproduction performance of Ayrshire cattle. Journal of dairy science, 102(6), pp. 5315-5322. Elsevier 10.3168/jds.2018-15366

Martin, Pauline; Baes, C.; Houlahan, Kerry; Richardson, Caeli; Jamrozik, Janusz; Miglior, Filippo (2019). Genetic Correlations among Selected Traits in Canadian Holsteins. Canadian journal of animal science, 99(4), pp. 693-704. NRC Research Press 10.1139/CJAS-2018-0190

Massender, Erin; Brito, Luiz F; Cánovas, Angela; Baes, Christine F.; Kennedy, Delma; Schenkel, Flavio S (2019). A genetic evaluation of growth, ultrasound, and carcass traits at alternative slaughter endpoints in crossbred heavy lambs. Journal of animal science, 97(2), pp. 521-535. Oxford University Press 10.1093/jas/sky455

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

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

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

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

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

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

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

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

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

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

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

Balmer, Pierre

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

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

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

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

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

Bannasch, Danika

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

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

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

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

Bannöhr, Jeanette

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

Bauer, Anina; Hadji Rasouliha, Sheida; Brunner, Magdalena; Jagannathan, Vidya; Bucher, I; Bannöhr, Jeanette; Varjonen, K; Bond, R; Bergvall, K; Welle, Monika Maria; Roosje, Petra; Leeb, Tosso (2019). A second KRT71 allele in curly coated dogs. Animal genetics, 50(1), pp. 97-100. Blackwell 10.1111/age.12743

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

Barrientos, Laura Soledad

Barrientos, Laura Soledad; Maiolini, Arianna; Häni, Anna Katrin; Jagannathan, Vidya; Leeb, Tosso (2019). NHLRC1 dodecamer repeat expansion demonstrated by whole genome sequencing in a Chihuahua with Lafora disease. Animal genetics, 50(1), pp. 118-119. Blackwell 10.1111/age.12756

Bauer, Anina

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

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

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

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

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

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

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

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

De Lucia, Michela; Bauer, Anina; Spycher, Melina; Jagannathan, Vidya; Romano, Erica; Welle, Monika Maria; Leeb, Tosso (2019). Genetic variant in the NSDHL gene in a cat with multiple congenital lesions resembling inflammatory linear verrucous epidermal nevi. Veterinary dermatology, 30(1), 64-e18. Blackwell Science 10.1111/vde.12699

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

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

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

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

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

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

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

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

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

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

Baumann, Ulrich

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

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

Beaurepaire, Alexis

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

Becker, Doreen

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

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

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

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

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

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

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

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

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

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

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

Beer, Gian

Berenguer Veiga, Inês Margarida

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

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

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

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

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

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

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

Bertoni, Giuseppe

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

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

Besuchet Schmutz, Nathalie

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

Blaszczyk, Klaudia Zofia

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

Blatter, Marlis

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

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

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

Blatter, Sohvi Tuulikki

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

Bley, Tim Hendrik

Bodmer, Michèle

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

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

Bogedale, Kirsten Carolin

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

Borer, Stephanie

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

Bornand, Valérie

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

Botteron, Catherine

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

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

Bouzalas, Ilias

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

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

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

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

Braga, Sophie Marie-Pierre

Braunschweig, Martin

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

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

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

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

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

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

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

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

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

Brehm, Walter

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

Bruckmaier, Rupert

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

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

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

Bruggmann, Rémy

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

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

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

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

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

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

Brunner, Adrian

Brunner, Magdalena Anna Theresa

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

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

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

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

Brünisholz, Hervé Paul

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

Buchs, Natasha

Burger, Dominik Cyrill

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

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

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

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

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

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

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

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

Burger, Nicole Christine

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

Busato, André

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

Bützberger, Charis Fanny

Café Marçal, Valéria

Cardoso Alves, Lisa Alexandra

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

Christen, Garance Anne

Christen, Matthias

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

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

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

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

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

Christen, Matthias Theo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Cosandey, Jeanne

Cvitas, Iva

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

Danilowicz, Emilia

Demmel, Steffi

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

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

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

Dettwiler, Martina Andrea

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

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

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

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

Dietrich, Sara Joëlle

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

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

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

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

Dietschi, Elisabeth

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

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

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

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

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

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

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

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

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

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

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

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

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

Doherr, Marcus

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

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

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

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

Dolf, Gaudenz

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Drögemüller, Cord

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Küttel, Luzia Marlis; Letko, Anna; Häfliger, Irene Monika; Signer-Hasler, Heidi; Joller, Sara; Hirsbrunner, Gabriela; Mészáros, G; Sölkner, J; Flury, C; Leeb, Tosso; Drögemüller, C. (2019). A complex structural variant at the KIT locus in cattle with the Pinzgauer spotting pattern. Animal genetics, 50(5), pp. 423-429. Wiley 10.1111/age.12821

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

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

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

Häfliger, Irene Monika; Behn, Holger; Freick, Markus; Jagannathan, Vidhya; Drögemüller, Cord (2019). A COL2A1 de novo variant in a Holstein bulldog calf. Animal genetics, 50(1), pp. 113-114. Blackwell 10.1111/age.12735

Hofstetter, Sonja; Seefried, F; Häfliger, Irene Monika; Jagannathan, Vidya; Leeb, Tosso; Drögemüller, Cord (2019). A non-coding regulatory variant in the 5'-region of the MITF gene is associated with white-spotted coat in Brown Swiss cattle. Animal genetics, 50(1), pp. 27-32. Blackwell 10.1111/age.12751

Jagannathan, Vidya; Gerber, Vinzenz; Rieder, S; Tetens, J; Thaller, G; Drögemüller, Cord; Leeb, Tosso (2019). Comprehensive characterization of horse genome variation by whole-genome sequencing of 88 horses. Animal genetics, 50(1), pp. 74-77. Blackwell 10.1111/age.12753

Hofstetter, Sonja; Pieńkowska-Schelling, Aldona; von Rotz, Alois; Drögemüller, Cord (2019). [Unilateral peromelia of the left pelvic limb in a Brown Swiss calf]. Schweizer Archiv für Tierheilkunde, 161(1), pp. 59-64. Gesellschaft Schweizer Tierärztinnen und Tierärzte 10.17236/sat00194

Lucchini, Nadia; Flury, Christine; Drögemüller, Cord (January 2019). Se prévenir de la problématique de l’intersexualité dans l’élevage des chèvres génétiquement mottes? Forum Kleinwiederkäuer = Forum petits ruminants, 2019(1-2), pp. 15-21. Verlagsgenossenschaft Caprovis

Grahofer, Alexander; Letko, Anna; Häfliger, Irene Monika; Jagannathan, Vidya; Ducos, Alain; Richard, Olivia; Peter, Vanessa Georgina; Nathues, Heiko; Drögemüller, Cord (2019). Chromosomal imbalance in pigs showing a syndromic form of cleft palate. BMC Genomics, 20(1), p. 349. BioMed Central 10.1186/s12864-019-5711-4

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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, 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

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

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

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

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

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; 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

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

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

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

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

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

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

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

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

Drögemüller, Michaela

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

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

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

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

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

Hug, Petra

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

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

Huynh-Do, Uyen

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

Häfliger, Irene Monika

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; 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

Häni, Anna Katrin

Hüsler, Jürg

Hüsler, Rudolf Jürg

Inglebert, Marine Hélène Fanny

Jacinto, Joana

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

Jagannathan, Vidya

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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; 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

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

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

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

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

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

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

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

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

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

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

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

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

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

Felkel, Sabine; Vogl, Claus; Rigler, Doris; Dobretsberger, Viktoria; Chowdhary, Bhanu P; Distl, Ottmar; Fries, Ruedi; Jagannathan, Vidya; Janečka, Jan E; Leeb, Tosso; Lindgren, Gabriella; McCue, Molly; Metzger, Julia; Neuditschko, Markus; Rattei, Thomas; Raudsepp, Terje; Rieder, Stefan; Rubin, Carl-Johan; Schaefer, Robert; Schlötterer, Christian; ... (2019). The horse Y chromosome as an informative marker for tracing sire lines. Scientific Reports, 9(1), p. 6095. Nature Publishing Group 10.1038/s41598-019-42640-w

Murgiano, Leonardo; Becker, Doreen; Torjman, Dina; Niggel, Jessica K; Milano, Ausra; Cullen, Cheryl; Feng, Rui; Wang, Fan; Jagannathan, Vidya; Pearce-Kelling, Sue; Katz, Martin L; Leeb, Tosso; Aguirre, Gustavo D (2019). Complex Structural Variant Associated with Non-syndromic Canine Retinal Degeneration. G3 Genes Genomes Genetics, 9(2), pp. 425-437. Genetics Society of America 10.1534/g3.118.200859

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Jaggy, André

Janda, Jozef

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

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

Joller, Sara

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

Jores, Jörg

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

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Jost, Ursula

Juillerat, Valérie

Karli, Philemon

Karol, Agnieszka

Kehrli, Dounia

Keller, Irene

Kiener, Sarah

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

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

Kircher, Patrick Robert

Klebic, Ismar

Klukowska, Jolanta

Koch, Caroline

Koch, Christoph

Koch, Michel Christoph

Kohler, Philipp

Kraft, Matthias Fabian

Kässmeyer, Sabine

Kühni, Kathrin

Küttel, Luzia Marlis

Labroussaa, Fabien

Lang-Fritz, Johann

Lanz, Simone Nicole

Lauber, Beatrice

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

Lauper, Murielle

Leeb, Tosso

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

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

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

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

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

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

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

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

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

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

Leeb, Tosso (ed.) (2023). Canine Genetics 2, 14. MDPI

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

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

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

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

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

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

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

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

Leeb, Tosso (2019). Concern Regarding the Publication by Posbergh et al. “A Nonsynonymous Change in Adhesion G Protein–Coupled Receptor L3 Associated With Risk for Equine Degenerative Myeloencephalopathy in the Caspian Horse,” J Equine Vet Sci 2018;70:96–100. Journal of Equine Veterinary Science, 72, p. 124. W.B. Saunders Co. 10.1016/j.jevs.2018.10.021

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

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

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

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

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

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

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

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.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Lepori, Vincent

Letko, Anna

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

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