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Meadows, Jennifer R S; Kidd, Jefrey M; Wang, Guo-Dong; Parker, Heidi G; Schall, Peter Z; Bianchi, Matteo; Christmas, Matthew J; Bougiouri, Katia; Buckley, Reuben M; Hitte, Christophe; Nguyen, Anthony K; Wang, Chao; Jagannathan, Vidhya; Niskanen, Julia E; Frantz, Laurent A F; Arumilli, Meharji; Hundi, Sruthi; Lindblad-Toh, Kerstin; Ginja, Catarina; Agustina, Kadek Karang; ... (2023). Author Correction: Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture. Genome biology, 24(1), p. 255. BioMed Central Ltd. 10.1186/s13059-023-03101-w
Littlejohn, Mathew D; Sneddon, Nick; Dittmer, Keren; Keehan, Mike; Stephen, Melissa; Drögemüller, Michaela; Garrick, Dorian (2023). A frameshift-deletion mutation in Reelin causes cerebellar hypoplasia in White Swiss Shepherd dogs. Animal genetics, 54(5), pp. 632-636. Wiley 10.1111/age.13336
Niskanen, Julia E; Ohlsson, Åsa; Ljungvall, Ingrid; Drögemüller, Michaela; Ernst, Robert F; Dooijes, Dennis; van Deutekom, Hanneke W M; van Tintelen, J Peter; Snijders Blok, Christian J B; van Vugt, Marion; van Setten, Jessica; Asselbergs, Folkert W; Petrič, Aleksandra Domanjko; Salonen, Milla; Hundi, Sruthi; Hörtenhuber, Matthias; Kere, Juha; Pyle, W Glen; Donner, Jonas; Postma, Alex V; ... (2023). Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human. Genome medicine, 15(1), p. 73. BioMed Central 10.1186/s13073-023-01221-3
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
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
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
Letko, Anna; Minor, Katie M.; Norton, Elaine M.; Marinescu, Voichita D.; Drögemüller, Michaela; Ivansson, Emma; Megquier, Kate; Noh, Hyun Ji; Starkey, Mike; Friedenberg, Steven G.; Lindblad-Toh, Kerstin; Mickelson, James R.; Drögemüller, Cord (2021). Genome-Wide Analyses for Osteosarcoma in Leonberger Dogs Reveal the CDKN2A/B Gene Locus as a Major Risk Locus. Genes, 12(12), p. 1964. MDPI 10.3390/genes12121964
Drögemüller, Michaela; Letko, Anna; Matiasek, Kaspar; Jagannathan, Vidhya; Corlazzoli, Daniele; Rosati, Marco; Jurina, Konrad; Medl, Susanne; Gödde, Thomas; Rupp, Stefan; Fischer, Andrea; Luján Feliu-Pascual, Alejandro; Drögemüller, Cord (2020). SLC19A3 Loss-of-Function Variant in Yorkshire Terriers with Leigh-Like Subacute Necrotizing Encephalopathy. Genes, 11(10), p. 1215. MDPI 10.3390/genes11101215
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
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
Gentilini, Fabio; Turba, Maria Elena; Giancola, Fiorella; Chiocchetti, Roberto; Bernardini, Chiara; Dajbychova, Markéta; Jagannathan, Vidya; Drögemüller, Michaela; Drögemüller, Cord (2019). A large deletion in the GP9 gene in Cocker Spaniel dogs with Bernard-Soulier syndrome. PLoS ONE, 14(9), e0220625. Public Library of Science 10.1371/journal.pone.0220625
Dürig, Nicole; Letko, Anna; Lepori, Vincent; Hadji Rasouliha, Sheida; Loechel, R; Kehl, A; Hytönen, M K; Lohi, H; Mauri, Nico; Dietrich, Sara Joëlle; Wiedmer, Michaela; Drögemüller, Michaela; Jagannathan, Vidhya; Schmutz, S M; Leeb, Tosso (2018). Two MC1R loss-of-function alleles in cream-coloured Australian Cattle Dogs and white Huskies. Animal genetics, 49(4), pp. 284-290. Blackwell 10.1111/age.12660
Schmidli, Manuel; Fuhrer, Bettina; Kurt, Nadine; Senn, David; Drögemüller, Michaela; Rytz, Ulrich; Spreng, David Emmanuel; Forterre, Simone (2018). Inflammatory pattern of the infrapatellar fat pad in dogs with canine cruciate ligament disease. BMC veterinary research, 14(1), p. 161. BioMed Central 10.1186/s12917-018-1488-y
Koch, Christoph; Ramsauer, A S; Drögemüller, Michaela; Ackermann, M; Gerber, Vinzenz; Tobler, K (2018). Genomic comparison of bovine papillomavirus 1 isolates from bovine, equine and asinine lesional tissue samples. Virus research, 244, pp. 6-12. Elsevier 10.1016/j.virusres.2017.11.005
Minor, K. M.; Letko, Anna; Becker, Doreen; Drögemüller, Michaela; Mandigers, P. J. J.; Bellekom, S. R.; Leegwater, P. A. J.; Stassen, Q. E. M.; Putschbach, K.; Fischer, A.; Flegel, T.; Matiasek, K.; Ekenstedt, K. J.; Furrow, E.; Patterson, E. E.; Platt, S. R.; Kelly, P. A.; Cassidy, J. P.; Shelton, G. D.; Lucot, K.; ... (2018). Canine NAPEPLD-associated models of human myelin disorders. Scientific Reports, 8(1), p. 5818. Nature Publishing Group 10.1038/s41598-018-23938-7
Marchant, Thomas W; Johnson, Edward J; McTeir, Lynn; Johnson, Craig I; Gow, Adam; Liuti, Tiziana; Kuehn, Dana; Svenson, Karen; Bermingham, Mairead L; Drögemüller, Michaela; Nussbaumer, Marc; Davey, Megan G; Argyle, David J; Powell, Roger M; Guilherme, Sérgio; Lang, Johann; Ter Haar, Gert; Leeb, Tosso; Schwarz, Tobias; Mellanby, Richard J; ... (2017). Canine Brachycephaly Is Associated with a Retrotransposon-Mediated Missplicing of SMOC2. Current Biology, 27(11), 1573-1584.e6. Cell Press 10.1016/j.cub.2017.04.057
Hirz, M; Drögemüller, Michaela; Schänzer, A; Jagannathan, Vidhya; Dietschi, Elisabeth; Goebel, H H; Hecht, W; Laubner, S; Schmidt, M J; Steffen, F; Hilbe, M; Köhler, K; Drögemüller, Cord; Herden, C (2017). Neuronal ceroid lipofuscinosis (NCL) is caused by the entire deletion of CLN8 in the Alpenländische Dachsbracke dog. Molecular genetics and metabolism, 120(3), pp. 269-277. Elsevier 10.1016/j.ymgme.2016.12.007
Nolte, Anna; Bello, Aimara; Drögemüller, Michaela; Leeb, Tosso; Brockhaus, Eva; Baumgärtner, Wolfgang; Wohlsein, Peter (2016). Neuronal ceroid lipofuscinosis in an adult American Staffordshire Terrier. Tierärztliche Praxis. Ausgabe K - Kleintiere, Heimtiere, 44(6), pp. 431-436. Schattauer 10.15654/TPK-150766
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
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
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
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
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
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
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
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
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
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
Hirschvogel, Katrin; Matiasek, Kaspar; Flatz, Katharina; Drögemüller, Michaela; Drögemüller, Cord; Reiner, Bärbel; Fischer, Andrea (2013). Magnetic resonance imaging and genetic investigation of a case of Rottweiler leukoencephalomyelopathy. BMC veterinary research, 9(57), p. 57. BioMed Central 10.1186/1746-6148-9-57
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
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
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
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
Welle, Monika Maria; Philipp, U.; Rüfenacht, S.; Roosje, Petra; Scharfenstein, M.; Schütz, E.; Brenig, B.; Linek, M.; Mecklenburg, L.; Grest, P.; Drögemüller, Michaela; Haase, Bianca; Leeb, Tosso; Drögemüller, Cord (2009). MLPH Genotype—Melanin Phenotype Correlation in Dilute Dogs. Journal of heredity, 100(Suppl 1), S75-S79. Oxford University Press 10.1093/jhered/esp010
Drögemüller, Cord; Drögemüller, Michaela; Leeb, Tosso; Mascarello, Francesco; Testoni, Stefania; Rossi, Marco; Gentile, Arcangelo; Damiani, Ernesto; Sacchetto, Roberta (2008). Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease. Genomics, 92(6), pp. 474-477. Elsevier 10.1016/j.ygeno.2008.07.014
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
