Leeb, Tosso

Journal Article

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

Cook, Shawna R; Schwarz, Cleo; Guevar, Julien; Assenmacher, Charles-Antoine; Sheehy, Maeve; Fanzone, Nathan; Church, Molly E; Murgiano, Leonardo; Casal, Margret L; Jagannathan, Vidhya; Gutierrez-Quintana, Rodrigo; Lowrie, Mark; Steffen, Frank; Leeb, Tosso; Ekenstedt, Kari J (2024). Canine RNF170 Single Base Deletion in a Naturally Occurring Model for Human Neuroaxonal Dystrophy. (In Press). Movement disorders Wiley 10.1002/mds.29977

Tammen, Imke; Mather, Marius; Leeb, Tosso; Nicholas, Frank W (2024). Online Mendelian Inheritance in Animals (OMIA): a genetic resource for vertebrate animals. (In Press). Mammalian genome Springer-Verlag 10.1007/s00335-024-10059-y

Kiener, Sarah; Lehner, Georg; Jagannathan, Vidhya; Welle, Monika; Leeb, Tosso (2024). Heterozygous DSP in-frame deletion in a poodle with syndromic ichthyosis involving additional hair and tooth abnormalities. (In Press). Animal genetics Wiley 10.1111/age.13467

Mauldin, Elizabeth; Bradley, Charles; Casal, Margret; Meyer, Jason; Crumrine, Debra; Kiener, Sarah; Leeb, Tosso; Elias, Peter M (2024). Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1-deficient Jack Russell Terriers and response to topical ceramide. (In Press). Veterinary dermatology Wiley 10.1111/vde.13285

Kiener, Sarah; Wildermuth, Brett; Meertens, Nadine M; Jagannathan, Vidhya; Leeb, Tosso (2024). Heterozygous deletion of the NSDHL gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic nevi. Animal genetics, 55(4), pp. 697-699. Wiley 10.1111/age.13436

Rietmann, Stefan J; Nowell, Sarah; Keating, M Kelly; Bauer, Cynthia; Jagannathan, Vidhya; Leeb, Tosso (2024). Heterozygous COL5A1 deletion in a cat with classical Ehlers-Danlos syndrome. Animal genetics, 55(4), pp. 705-707. Wiley 10.1111/age.13446

Kalbfleisch, Theodore S; McKay, Stephanie D; Murdoch, Brenda M; Adelson, David L; Almansa-Villa, Diego; Becker, Gabrielle; Beckett, Linda M; Benítez-Galeano, María José; Biase, Fernando; Casey, Theresa; Chuong, Edward; Clark, Emily; Clarke, Shannon; Cockett, Noelle; Couldrey, Christine; Davis, Brian W; Elsik, Christine G; Faraut, Thomas; Gao, Yahui; Genet, Carine; ... (2024). The Ruminant Telomere-to-Telomere (RT2T) Consortium. Nature genetics, 56(8), pp. 1566-1573. Nature America 10.1038/s41588-024-01835-2

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

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

Rietmann, Stefan J; Lange, Anja; Soto, Sara; Thom, Nina; Manz, Eberhard; Jagannathan, Vidhya; Mayer, Ursula; Leeb, Tosso (2024). KRT5 in-frame deletion in a family of German Shepherd dogs with split paw pad disease resembling localized epidermolysis bullosa simplex in human patients. Animal genetics, 55, pp. 692-696. Wiley 10.1111/age.13444

Christen, Matthias; Gregor, Katharina M; Böttcher-Künneke, Ariane; Lombardo, Mara S; Baumgärtner, Wolfgang; Jagannathan, Vidhya; Puff, Christina; Leeb, Tosso (2024). Intragenic MFSD8 duplication and histopathological findings in a rabbit with neuronal ceroid lipofuscinosis. Animal genetics, 55, pp. 588-598. Wiley 10.1111/age.13441

Suiter, Emma; Baiker, Kerstin; Kaczmarska, Adriana; Christen, Matthias; Leeb, Tosso; Ororbia, Alejandro; Anselmi, Carlo; Minguez, Juan; Gutierrez-Quintana, Rodrigo (2024). Novel MRI and histopathological findings in a young Bullmastiff cross dog with mitochondrial fission encephalopathy. (In Press). Veterinary radiology & ultrasound Wiley 10.1111/vru.13342

Mizukami, Keijiro; Dorsey-Oresto, Angella; Raj, Karthik; Eringis, Anna; Furrow, Eva; Martin, Errolyn; Yamanaka, Daisuke; Kehl, Alexandra; Kolicheski, Ana; Jagannathan, Vidhya; Leeb, Tosso; Lionakis, Michail S; Giger, Urs (2024). Increased susceptibility to Mycobacterium avium complex infection in miniature Schnauzer dogs caused by a codon deletion in CARD9. Scientific reports, 14(10346) Springer Nature 10.1038/s41598-024-61054-x

Kaelin, Christopher B; McGowan, Kelly A; Hutcherson, Anthony D; Delay, John M; Li, Jeremiah H; Kiener, Sarah; Jagannathan, Vidhya; Leeb, Tosso; Murphy, William J; Barsh, Gregory S (2024). Ancestry dynamics and trait selection in a designer cat breed. Current biology, 34(7), 1506-1518.e7. Cell Press 10.1016/j.cub.2024.02.075

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Mühlhause, Franziska; Tipold, Andrea; Rohn, Karl; Lepori, Vincent; Leeb, Tosso; Sewell, Adrian C; Kornberg, Marion (2019). [Follow-up study in German Hunting Terrier dogs with exercise induced metabolic myopathy]. Tierärztliche Praxis. Ausgabe K - Kleintiere, Heimtiere, 47(6), pp. 402-410. Thieme 10.1055/a-1027-2533

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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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

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

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

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

Unger, Lucia; Jagannathan, Vidhya; Pacholewska, Alicja; Leeb, Tosso; Gerber, Vinzenz (2019). Differences in miRNA differential expression in whole blood between horses with sarcoid regression and progression. Journal of veterinary internal medicine, 33(1), pp. 241-250. Wiley-Blackwell 10.1111/jvim.15375

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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

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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

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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

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

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

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

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

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

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

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

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

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

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

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

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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

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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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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; 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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Newspaper or Magazine Article

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

Conference or Workshop Item

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

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.

Working Paper

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

Journal or Series

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