Drögemüller, Cord

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Jacinto, Joana G. P.; Häfliger, Irene M.; Gentile, Arcangelo; Drögemüller, Cord; Bolcato, Marilena (2020). A 6.7 kb deletion in the COL2A1 gene in a Holstein calf with achondrogenesis type II and perosomus elumbis (In Press). Animal genetics Wiley 10.1111/age.13033

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

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

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

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

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

Letko, Anna; Strugnell, Ben; Häfliger, Irene M.; Paris, Julia M.; Waine, Katie; Drögemüller, Cord; Scholes, Sandra (2020). Compound heterozygous PLA2G6 loss-of-function variants in Swaledale sheep with neuroaxonal dystrophy. (In Press). Molecular genetics and genomics : MGG Springer 10.1007/s00438-020-01742-1

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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


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

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

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

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

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

De Preux, Mathieu; Gurtner, Corinne; Klebic, Ismar; Waschk, Maja Alice; Drögemüller, Cord; Brünisholz, Hervé Paul (2019). Skeletal metastasis from a squamous cell carcinoma of the nictitating membrane in a Haflinger horse (In Press). Equine veterinary education Wiley-Blackwell 10.1111/eve.13180

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

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

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

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

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

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

Küttel, Luzia Marlis; Letko, Anna; Häfliger, Irene Monika; Signer-Hasler, H; 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

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

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

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

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

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

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

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

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

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

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

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

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

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

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


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

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

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

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

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

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

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

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


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

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

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

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

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

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

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

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

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

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

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

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

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

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

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


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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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


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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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


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

Becker, Doreen; Otto, Mandy; Ammann, P; Keller, Irene; Drögemüller, Cord; Leeb, Tosso (2014). 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; Welle, Monika Maria; Graubner, Claudia; Straub, Reto; Gerber, Vinzenz; Burger, Dominik; Signer-Hasler, H.; Poncet, PA; Klopfenstein, S.; von Niederhäusern, R.; Tetens, J.; Rieder, S.; 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

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

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

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

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

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

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

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

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

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

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

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

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

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

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, p. 63. BioMed Central 10.1186/s12711-014-0063-7


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

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

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

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

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

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

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

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

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

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

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

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

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

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

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


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

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

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

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

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

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

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

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

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

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

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

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

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


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

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

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

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


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

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

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

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

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

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

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

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

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

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

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


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

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

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

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

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

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

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

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


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

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

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

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


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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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


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

Drögemüller, Cord; 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

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

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

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

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

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

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

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

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

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

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

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

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


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

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

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

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

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

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

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