C. Drögemüller

R. Bruggmann, C. Drögemüller, D. Wüthrich, 2016, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

Identification of a second encephalitis-associated astrovirus in cattle

R. Bruggmann, C. Drögemüller, D. Wüthrich, 2016, Emerging Microbes & Infections.

A living biobank of canine mammary tumor organoids as a comparative model for human breast cancer

S. Nik-Zainal, H. Davies, J. Doench, 2022, bioRxiv.

Multiple FGF4 Retrocopies Recently Derived within Canids

Kristin E. Brzeski, C. Drögemüller, T. Leeb, 2020, Genes.

Digital Commons @ Michigan Tech Digital Commons @ Michigan Tech Multiple FGF4 retrocopies recently derived within canids Multiple FGF4 retrocopies recently derived within canids

Kristin E. Brzeski, C. Drögemüller, T. Leeb, 2020 .

A GJA9 frameshift variant is associated with polyneuropathy in Leonberger dogs

J. Mickelson, C. Drögemüller, T. Leeb, 2017, BMC Genomics.

Magnetic resonance imaging and genetic investigation of a case of rottweiler leukoencephalomyelopathy

C. Drögemüller, K. Matiasek, A. Fischer, 2013, BMC Veterinary Research.

A de novo mutation in KRT5 in a crossbred calf with epidermolysis bullosa simplex

C. Drögemüller, I. Häfliger, I. Veiga, 2020, Journal of veterinary internal medicine.

A genome-wide significant association on chromosome 15 for congenital entropion in Swiss White Alpine sheep.

C. Drögemüller, I. Häfliger, A. Letko, 2020, Animal genetics.

New genomic features of the polled intersex syndrome variant in goats unraveled by long-read whole-genome sequencing.

C. Drögemüller, H. Lischer, R. Simon, 2020, Animal genetics.

Analysis of Polycerate Mutants Reveals the Evolutionary Co-option of HOXD1 to Determine the Number and Topology of Horns in Bovidae

D. Duboule, G. Tosser-Klopp, J. Lenstra, 2020, bioRxiv.

Molecular characterization of the equine collagen, type IX, alpha 2 (COL9A2) gene on horse chromosome 2p16→p15

C. Drögemüller, O. Distl, B. Chowdhary, 2006, Cytogenetic and Genome Research.

Molecular characterization and chromosomal assignment of the bovine glycinamide ribonucleotide formyltransferase (GART) gene on cattle chromosome 1q12.1-q12.2.

C. Drögemüller, O. Distl, T. Leeb, 2005, Gene.

Evaluation of truncating variants in the LCORL gene in relation to body size of goats from Switzerland

C. Drögemüller, A. Burren, H. Signer-Hasler, 2022, Animal genetics.

Evaluation of HOXC8 in crested Swiss chicken.

C. Drögemüller, C. Flury, P. Ammann, 2018, Animal genetics.

Characterization and comparative mapping of the porcine CTSL gene indicates a novel synteny between HSA9q21→q22 and SSC10q11→q12

B. Brenig, C. Drögemüller, O. Distl, 2002, Cytogenetic and Genome Research.

The Complex and Diverse Genetic Architecture of the Absence of Horns (Polledness) in Domestic Ruminants, including Goats and Sheep

C. Drögemüller, G. Lühken, R. Simon, 2022, Genes.

Assignment of the calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene (CACNA1A), and the ataxin 7 gene (ATXN7) to canine chromosome 20 by fluorescence in situ hybridization and confirmation by radiation hybrid mapping

C. Drögemüller, O. Distl, C. André, 2005, Cytogenetic and Genome Research.

Chromosomal assignment of 20 candidate genes for canine congenital sensorineural deafness by FISH and RH mapping

P. Quignon, C. Drögemüller, O. Distl, 2003, Cytogenetic and Genome Research.

Assignment of the canine tectorin alpha gene (TECTA) to CFA5q12→q13 by FISH and confirmation by radiation hybrid mapping

F. Galibert, P. Quignon, C. Drögemüller, 2002, Cytogenetic and Genome Research.

A homozygous missense variant in laminin subunit beta 1 as candidate causal mutation of hemifacial microsomia in Romagnola cattle

C. Drögemüller, I. Häfliger, M. Bolcato, 2021, Journal of veterinary internal medicine.

Canine reference genome accuracy impacts variant calling: Lessons learned from investigating embryonic lethal variants.

C. Mellersh, J. Mickelson, C. Drögemüller, 2022, Animal genetics.

Physical mapping of the PTHR1 gene to equine chromosome 16q21.2.

C. Drögemüller, O. Distl, B. Chowdhary, 2005, Animal genetics.

A defective SERCA1 protein is responsible for congenital pseudomyotonia in Chianina cattle.

C. Drögemüller, R. Liguori, F. Mascarello, 2009, The American journal of pathology.

Review X-linked Anhidrotic Ectodermal Dysplasia (ed1) in Men, Mice, and Cattle 1. Anhidrotic Ectodermal Dysplasia in Men and Mice 1.1. Phenotype

C. Drögemüller, O. Distl, T. Leeb, 2022 .

A nonsense mutation in the optic atrophy 3 gene (OPA3) causes dilated cardiomyopathy in Red Holstein cattle.

C. Drögemüller, H. Posthaus, M. Braunschweig, 2011, Genomics.

Genetic variability of the equine casein genes.

C. Drögemüller, T. Leeb, J. Tetens, 2016, Journal of dairy science.

DNA-based identification of novel ovine milk protein gene variants

C. Drögemüller, J. Tetens, G. Thaller, 2014 .

Congenital aural atresia associated with agenesis of internal carotid artery in a girl with a FOXI3 deletion

S. Gimelli, G. Gimelli, A. Groves, 2015, American journal of medical genetics. Part A.

Large Animal Models

G. Johnson, C. Drögemüller, M. Katz, 2011 .

[Unilateral peromelia of the left pelvic limb in a Brown Swiss calf].

C. Drögemüller, A. von Rotz, S. Hofstetter, 2019, Schweizer Archiv fur Tierheilkunde.

A Non-Coding Genomic Duplication at the HMX1 Locus Is Associated with Crop Ears in Highland Cattle

R. Bruggmann, C. Drögemüller, J. Tetens, 2013, PloS one.

Exclusion of patched homolog 2 (PTCH2) as a candidate gene for alopecia X in pomeranians and keeshonden

C. Drögemüller, T. Leeb, M. Welle, 2008, Veterinary Record.

Evaluation of the CTSL2 Gene as a Candidate Gene For Alopecia X in Pomeranians and Keeshonden

C. Drögemüller, T. Leeb, M. Welle, 2007, Animal biotechnology.

Abstracts of the 37th American Cytogenetics Conference

C. Steinlein, M. Schmid, S. Antonarakis, 2002, Cytogenetic and Genome Research.

Congenital hypotrichosis and partial anodontia in a crossbred beef calf.

C. Drögemüller, T. Leeb, C. Palmer, 2007, The Canadian veterinary journal = La revue veterinaire canadienne.

Novel Features of the Prenatal Horn Bud Development in Cattle (Bos taurus)

C. Drögemüller, M. Welle, N. Wiedemar, 2015, PloS one.

Independent Polled Mutations Leading to Complex Gene Expression Differences in Cattle

R. Bruggmann, C. Drögemüller, S. Neuenschwander, 2014, PloS one.

Whole Genome Sequencing Indicates Heterogeneity of Hyperostotic Disorders in Dogs

C. Drögemüller, T. Leeb, H. Lohi, 2020, Genes.

DNA-based identification of novel bovine casein gene variants.

C. Drögemüller, S. Qanbari, J. Tetens, 2013, Journal of dairy science.

Effective population size of an indigenous Swiss cattle breed estimated from linkage disequilibrium.

T. Sonstegard, O. Hanotte, H. Simianer, 2010, Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie.

Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes

J. Kere, C. Drögemüller, H. Lohi, 2016, PLoS genetics.

Evaluation of an investigative model in dairy herds with high calf perinatal mortality rates in Switzerland.

C. Drögemüller, T. Mock, J. Mee, 2020, Theriogenology.

Genetic Abnormalities in a Calf with Congenital Increased Muscular Tonus

C. Drögemüller, M. Meylan, A. Riedi, 2015, Journal of veterinary internal medicine.

Chromosomal imbalance in pigs showing a syndromic form of cleft palate

H. Nathues, C. Drögemüller, I. Häfliger, 2019, BMC Genomics.

Bovine Prion Protein Gene (PRNP) Promoter Polymorphisms Modulate PRNP Expression and May Be Responsible for Differences in Bovine Spongiform Encephalopathy Susceptibility*

C. Drögemüller, T. Leeb, P. Sander, 2005, Journal of Biological Chemistry.

Identification of the Bovine Arachnomelia Mutation by Massively Parallel Sequencing Implicates Sulfite Oxidase (SUOX) in Bone Development

K. Lindblad-Toh, C. Drögemüller, S. Sigurdsson, 2010, PLoS genetics.

Alopecia areata in Eringer cows.

C. Drögemüller, C. Flury, A. Oevermann, 2010, Veterinary dermatology.

MLPH Genotype—Melanin Phenotype Correlation in Dilute Dogs

B. Brenig, C. Drögemüller, T. Leeb, 2009 .

A Mutation in the SUV39H2 Gene in Labrador Retrievers with Hereditary Nasal Parakeratosis (HNPK) Provides Insights into the Epigenetics of Keratinocyte Differentiation

C. Drögemüller, T. Leeb, H. Lohi, 2013, PLoS genetics.

Skeletal metastasis from a squamous cell carcinoma of the nictitating membrane in a Haflinger horse

C. Drögemüller, C. Gurtner, I. Klebić, 2019, Equine Veterinary Education.

A missense mutation in damage‐specific DNA binding protein 2 is a genetic risk factor for limbal squamous cell carcinoma in horses

J. Petersen, G. Brem, M. Singer-Berk, 2017, International journal of cancer.

Pulmonary hypoplasia and anasarca syndrome in Cika cattle

C. Drögemüller, J. Starič, T. Švara, 2015, Acta Veterinaria Scandinavica.

DSP missense variant in a Scottish Highland calf with congenital ichthyosis, alopecia, acantholysis of the tongue and corneal defects

C. Drögemüller, I. Häfliger, M. Welle, 2022, BMC Veterinary Research.

A frameshift insertion in FA2H causes a recessively inherited form of ichthyosis congenita in Chianina cattle

C. Drögemüller, I. Häfliger, I. Veiga, 2021, Molecular Genetics and Genomics.

KDM2B‐associated paunch calf syndrome in Marchigiana cattle

C. Drögemüller, M. Bolcato, A. Gentile, 2020, Journal of Veterinary Internal Medicine.

Breeding German sheep for resistance to scrapie

C. Drögemüller, O. Distl, T. Leeb, 2004, Veterinary Record.

Epidermolysa bullosa in Danish Hereford calves is caused by a deletion in LAMC2 gene

C. Drögemüller, V. Jagannathan, L. K. Isling, 2015, BMC Veterinary Research.

Crossed beaks in a local Swiss chicken breed

C. Drögemüller, C. Flury, A. von Rotz, 2018, BMC Veterinary Research.

Microphthalmia in Texel Sheep Is Associated with a Missense Mutation in the Paired-Like Homeodomain 3 (PITX3) Gene

J. Kijas, A. Brunner, C. Drögemüller, 2010, PloS one.

Linkage mapping of ovine microphthalmia to chromosome 23, the sheep orthologue of human chromosome 18.

C. Drögemüller, J. Tetens, M. Ganter, 2007, Investigative ophthalmology & visual science.

Looking the Cow in the Eye: Deletion in the NID1 Gene Is Associated with Recessive Inherited Cataract in Romagnola Cattle

C. Drögemüller, V. Jagannathan, A. Gentile, 2014, PloS one.

Dermatosparaxis in White Dorper sheep: confirmation of a causative nonsense mutation in ADAMTS2.

C. Drögemüller, I. Berenguer Veiga, S. Joller, 2017, Animal genetics.

Genetic risk for squamous cell carcinoma of the nictitating membrane parallels that of the limbus in Haflinger horses.

M. Singer-Berk, C. Drögemüller, C. Reilly, 2018, Animal genetics.

[Diprosopus in calves of different breeds].

C. Drögemüller, O. Distl, A. Beineke, 2004, DTW. Deutsche tierarztliche Wochenschrift.

Identification of small and large genomic candidate variants in bovine pulmonary hypoplasia and anasarca syndrome.

C. Drögemüller, J. Starič, I. Häfliger, 2020, Animal genetics.

Clinicopathological and Genomic Characterization of a Simmental Calf with Generalized Bovine Juvenile Angiomatosis

C. Drögemüller, I. Häfliger, I. Veiga, 2021, Animals : an open access journal from MDPI.

An ABCA12 missense variant in a Shorthorn calf with ichthyosis fetalis.

C. Drögemüller, T. Leeb, I. Häfliger, 2019, Animal genetics.

Short communication: Prevalence of deleterious variants causing recessive disorders in Italian Chianina, Marchigiana and Romagnola cattle.

C. Drögemüller, A. Gentile, J. G. Jacinto, 2022, Animal : an international journal of animal bioscience.

A Heterozygous Missense Variant in MAP2K2 in a Stillborn Romagnola Calf with Skeletal-Cardio-Enteric Dysplasia

C. Drögemüller, I. Häfliger, A. Gentile, 2021, Animals : an open access journal from MDPI.

Prevalence of paunch calf syndrome carriers in Italian Romagnola cattle.

C. Drögemüller, M. Bolcato, A. Gentile, 2014, Veterinary journal.

Frequency of bovine congenital pseudomyotonia carriers in selected Italian Chianina sires.

C. Drögemüller, M. Bolcato, S. Testoni, 2013, Veterinary journal.

Pseudomyotonia in Romagnola cattle caused by novel ATP2A1 mutations

C. Drögemüller, R. Liguori, F. Mascarello, 2012, BMC Veterinary Research.

Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease.

C. Drögemüller, T. Leeb, F. Mascarello, 2008, Genomics.

An IL17RA frameshift variant in a Holstein cattle family with psoriasis-like skin alterations and immunodeficiency

C. Drögemüller, I. Häfliger, M. Holsteg, 2020, BMC Genetics.

Genetic evaluation of small ruminant lentivirus susceptibility in Valais blacknose sheep

C. Drögemüller, C. Abril, A. Letko, 2021, Animal genetics.

A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle

C. Drögemüller, J. Beever, I. Veiga, 2021, Genes.

A Nonsense Variant in Hephaestin Like 1 (HEPHL1) Is Responsible for Congenital Hypotrichosis in Belted Galloway Cattle

C. Drögemüller, J. Beever, B. Marron, 2021, Genes.

Clinical and histological characterization of hair coat and glandular tissue of Chinese crested dogs.

C. Drögemüller, T. Leeb, C. Gurtner, 2013, Veterinary dermatology.

A Mutation in Hairless Dogs Implicates FOXI3 in Ectodermal Development

K. Lindblad-Toh, E. Karlsson, C. Drögemüller, 2008, Science.

Mutations within the FGF5 gene are associated with hair length in cats.

C. Drögemüller, T. Leeb, S. Rüfenacht, 2007, Animal genetics.

Identification of two new recessive MC1R alleles in red‐coloured Evolèner cattle and other breeds

B. Guldbrandtsen, C. Drögemüller, F. Seefried, 2022, Animal genetics.

A mola hydatidosa coexistent with a foetus in a bovine freemartin pregnancy.

C. Drögemüller, T. Leeb, B. Meinecke, 2003, Placenta.

Chromosome Research : An International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology

Keith Durkin, Michel Georges, Arnaud Sartelet, 2011 .

A major QTL at the LHCGR/FSHR locus for multiple birth in Holstein cattle

P. von Rohr, C. Drögemüller, F. Seefried, 2021, Genetics, selection, evolution : GSE.

Phenotypic Effects of FGF4 Retrogenes on Intervertebral Disc Disease in Dogs

C. Mellersh, C. Drögemüller, T. Leeb, 2019, Genes.

Molecular basis for the action of the collagen-specific chaperone Hsp47/SERPINH1 and its structure-specific client recognition

U. Baumann, C. Drögemüller, T. Leeb, 2012, Proceedings of the National Academy of Sciences.

A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular Dystrophy

C. Drögemüller, T. Leeb, V. Jagannathan, 2015, G3: Genes, Genomes, Genetics.

A COL11A2 Mutation in Labrador Retrievers with Mild Disproportionate Dwarfism

C. Drögemüller, T. Leeb, H. Lohi, 2013, PloS one.

Differential distribution of Y-chromosome haplotypes in Swiss and Southern European goat breeds

B. Badaoui, C. Drögemüller, S. Eghbalsaied, 2017, Scientific Reports.

Imputation of sequence level genotypes in the Franches-Montagnes horse breed

C. Drögemüller, T. Leeb, J. Tetens, 2014, Genetics Selection Evolution.

Runs of homozygosity in Swiss goats reveal genetic changes associated with domestication and modern selection

C. Drögemüller, T. Leeb, C. Flury, 2022, Genetics, selection, evolution : GSE.

Mutations in MITF and PAX3 Cause “Splashed White” and Other White Spotting Phenotypes in Horses

J. Matthews, C. Drögemüller, T. Leeb, 2012, PLoS Genetics.

Genomic regions underlying positive selection in local, Alpine cattle breeds.

C. Drögemüller, J. Sölkner, J. Bennewitz, 2023, Animal genetics.

Meta-analysis of genome-wide association studies for cattle stature identifies common genes that regulate body size in mammals

R. Veerkamp, B. Guldbrandtsen, M. Lund, 2018, Nature Genetics.

Animal Cytogenetics and Comparative Mapping

G. Elgar, T. Haaf, B. Brenig, 2002 .

The canine CTSD gene as a candidate for late-onset neuronal ceroid lipofuscinosis.

C. Drögemüller, O. Distl, A. Wöhlke, 2005, Animal genetics.

Characterization of candidate genes for neuronal ceroid lipofuscinosis in dog.

C. Drögemüller, O. Distl, A. Wöhlke, 2005, The Journal of heredity.

Evaluation of the canine TPP1 gene as a candidate for neuronal ceroid lipofuscinosis in Tibetan Terrier and Polish Owczarek Nizinny dogs.

C. Drögemüller, O. Distl, A. Wöhlke, 2005, Animal genetics.

A Missense Variant in ALDH5A1 Associated with Canine Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD) in the Saluki Dog

C. T. Brown, T. Mansour, C. Drögemüller, 2020, Genes.

Comparative mapping of the canine diaphanous homologue 1 (Drosophila) gene (DIAPH1 ) to CFA2q23-q24.2.

P. Quignon, C. Drögemüller, O. Distl, 2002, Animal genetics.

Assignment of the canine cadherin related 23 gene (CDH23) to chromosome 4q12→q13 by fluorescence in situ hybridization and radiation hybrid mapping

F. Galibert, P. Quignon, C. Drögemüller, 2002, Cytogenetic and Genome Research.

An ARHGEF10 Deletion Is Highly Associated with a Juvenile-Onset Inherited Polyneuropathy in Leonberger and Saint Bernard Dogs

E. Patterson, J. Mickelson, C. Drögemüller, 2014, PLoS genetics.

Rapid Discovery of De Novo Deleterious Mutations in Cattle Enhances the Value of Livestock as Model Species

D. Boichard, C. Péchoux, B. Hayes, 2017, Scientific Reports.

A large deletion in the GP9 gene in Cocker Spaniel dogs with Bernard-Soulier syndrome

C. Drögemüller, F. Giancola, V. Jagannathan, 2019, PloS one.

Identification of a Missense Variant in MFSD12 Involved in Dilution of Phaeomelanin Leading to White or Cream Coat Color in Dogs

T. Derrien, É. Cadieu, C. Drögemüller, 2019, Genes.

Comprehensive characterization of horse genome variation by whole-genome sequencing of 88 horses.

C. Drögemüller, T. Leeb, J. Tetens, 2018, Animal Genetics.

A de novo missense mutation of FGFR2 causes facial dysplasia syndrome in Holstein cattle

C. Drögemüller, C. Charlier, S. Heegaard, 2017, BMC Genetics.

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

L. Andersson, B. Brenig, C. Drögemüller, 2006, Mammalian Genome.

Evidence of a new leukemia inhibitory factor-associated genetic marker for litter size in a synthetic pig line.

C. Drögemüller, O. Distl, A. Spötter, 2005, Journal of animal science.

Molecular characterization and chromosome assignment of the porcine gene for leukemia inhibitory factor LIF

B. Brenig, C. Drögemüller, O. Distl, 2001, Cytogenetic and Genome Research.

Mapping and microsatellite marker development for the porcine leukemia inhibitory factor receptor (LIFR) and epidermal growth factor receptor (EGFR) genes

B. Brenig, C. Drögemüller, O. Distl, 2003, Cytogenetic and Genome Research.

Assignment of the porcine epidermal growth factor (EGF) gene to SSC8q2.3-q2.4 by fluorescence in situ hybridization and radiation hybrid mapping.

B. Brenig, C. Drögemüller, O. Distl, 2002, Animal Genetics.

An AvaI and a MspA1I polymorphism at the porcine oestrogen receptor (ESR) gene.

C. Drögemüller, B. Harlizius, U. Thieven, 1997, Animal genetics.

Genome-Wide Analyses for Osteosarcoma in Leonberger Dogs Reveal the CDKN2A/B Gene Locus as a Major Risk Locus

Voichita D. Marinescu, K. Lindblad-Toh, J. Mickelson, 2021, Genes.

A radiation hybrid map of sheep chromosome 23 based on ovine BAC-end sequences.

J. Maddox, N. Cockett, C. Drögemüller, 2007, Animal Genetics.

Spider Lamb Syndrome (SLS) mutation frequency in German Suffolk sheep.

C. Drögemüller, O. Distl, A. Wöhlke, 2005, Animal genetics.

Molecular Characterization and SNP Development for the Porcine Il6 and Il10 Genes

C. Drögemüller, O. Distl, T. Leeb, 2008, Animal biotechnology.

A Diploid-Triploid (60,XX/90,XXY) Intersex in a Holstein Heifer

P. Wohlsein, C. Drögemüller, S. Ebeling, 2006, Sexual Development.

Four novel candidate causal variants for deficient homozygous haplotypes in Holstein cattle

C. Drögemüller, F. Seefried, I. Häfliger, 2022, Scientific Reports.

Brief Gene Mapping Reports A / B / C / D / E / F / G

C. Auffray, A. Zinn, K. Kratochwil, 2002, Cytogenetic and Genome Research.

Analysis of associations between the prion protein genotypes and production traits in East Friesian milk sheep.

C. Drögemüller, O. Distl, M. Ganter, 2005, Journal of dairy science.

[Possible uses of genetic markers for improving fertility and health in swine production].

C. Drögemüller, O. Distl, H. Hamann, 2003, DTW. Deutsche tierarztliche Wochenschrift.

GWAS Hits for Bilateral Convergent Strabismus with Exophthalmos in Holstein Cattle Using Imputed Sequence Level Genotypes

C. Drögemüller, J. Tetens, G. Thaller, 2021, Genes.

PRNP promoter polymorphisms are associated with BSE susceptibility in Swiss and German cattle

C. Drögemüller, T. Leeb, M. Groschup, 2007, BMC Genetics.

Detection of prion protein gene polymorphisms in Baltic breeds of sheep

C. Drögemüller, O. Distl, I. Miceikienė, 2006, Veterinary Record.

Analysis of associations between the prion protein genotype and reproduction traits in meat sheep breeds

C. Drögemüller, O. Distl, M. Ganter, 2004 .

Associations between prion protein genotype and type traits in East Friesian milk sheep

C. Drögemüller, O. Distl, H. Hamann, 2006, Veterinary Record.

Fine mapping of the polled locus to a 1-Mb region on bovine Chromosome 1q12

C. Drögemüller, O. Distl, S. Mömke, 2005, Mammalian Genome.

Bovine viral diarrhoea virus 1b infection associated with congenital tremor and hypomyelination in Holstein calves.

C. Drögemüller, C. Bombardi, M. Bolcato, 2021, Veterinary microbiology.

Sexual selection, multiple mating and paternity in grey mouse lemurs, Microcebus murinus

E. Zimmermann, C. Drögemüller, U. Radespiel, 2002, Animal Behaviour.

Echinococcus multilocularis in Svalbard, Norway: microsatellite genotyping to investigate the origin of a highly focal contamination.

C. Drögemüller, N. Yoccoz, J. Bart, 2012, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

The canine FRDA gene maps to CFA 1q31.1→q31.3

P. Quignon, C. Drögemüller, O. Distl, 2003, Cytogenetic and Genome Research.

Characterization and chromosome localization of a processed pseudogene related to the bovine laminin receptor gene family

B. Brenig, C. Drögemüller, C. Knorr, 2004, Cytogenetic and Genome Research.

Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation

C. Drögemüller, M. Mikkola, V. Jagannathan, 2015, PLoS genetics.

Polymelia in a chimeric Simmental calf: nociceptive withdrawal reflex, anaesthetic and analgesic management, anatomic and genetic analysis

C. Drögemüller, M. Stoffel, C. Spadavecchia, 2019, BMC Veterinary Research.

Neurotropic Astrovirus in Cattle with Nonsuppurative Encephalitis in Europe

R. Bruggmann, C. Drögemüller, J. Walland, 2014, Journal of Clinical Microbiology.

A pathogenic HEXA missense variant in wild boars with Tay-Sachs disease.

C. Drögemüller, S. Sonnino, V. Jagannathan, 2021, Molecular genetics and metabolism.

Bilateral congenital lacrimal fistula in a Brown Swiss bull.

C. Drögemüller, U. Braun, B. Spiess, 2012, Schweizer Archiv fur Tierheilkunde.

Prevalence of coat colour traits and congenital disorders of South American camelids in Austria, Germany and Switzerland

C. Drögemüller, G. Lühken, P. Zanolari, 2020, Acta Veterinaria Scandinavica.

Phenotypic and Genomic Analysis of Cystic Hygroma in Pigs

C. Drögemüller, A. Letko, L. Grau-Roma, 2021, Genes.

Runs of homozygosity and signatures of selection: a comparison among eight local Swiss sheep breeds.

C. Drögemüller, A. Burren, C. Flury, 2019, Animal genetics.

Chromosomal imbalance in pigs showing a syndromic form of cleft palate

H. Nathues, C. Drögemüller, I. Häfliger, 2019, BMC Genomics.

A single point mutation within the ED1 gene disrupts correct splicing at two different splice sites and leads to anhidrotic ectodermal dysplasia in cattle

C. Drögemüller, O. Distl, T. Leeb, 2002, Journal of Molecular Medicine.

A structural variant in the 5’-flanking region of the TWIST2 gene affects melanocyte development in belted cattle

R. Kelsh, R. Bruggmann, B. Brenig, 2016, bioRxiv.

X-Linked Hypohidrotic Ectodermal Dysplasia in Crossbred Beef Cattle Due to a Large Deletion in EDA

C. Drögemüller, T. Leeb, I. Häfliger, 2021, Animals : an open access journal from MDPI.

X-Linked Duchenne-Type Muscular Dystrophy in Jack Russell Terrier Associated with a Partial Deletion of the Canine DMD Gene

C. Drögemüller, A. Letko, V. Jagannathan, 2020, Genes.

Genome-wide association study between copy number variants and hoof health traits in Holstein dairy cattle.

F. Schenkel, C. Drögemüller, A. Butty, 2021, Journal of dairy science.

TECPR2 Associated Neuroaxonal Dystrophy in Spanish Water Dogs

P. Wohlsein, C. Drögemüller, W. Baumgärtner, 2015, PloS one.

Selection signatures in goats reveal copy number variants underlying breed-defining coat color phenotypes

C. Drögemüller, T. Leeb, C. Flury, 2019, PLoS genetics.

Identification of two TYRP1 loss-of-function alleles in Valais Red sheep.

C. Drögemüller, C. Flury, I. Häfliger, 2019, Animal genetics.

X-linked anhidrotic ectodermal dysplasia (ED1) in men, mice, and cattle

C. Drögemüller, O. Distl, T. Leeb, 2003, Genetics Selection Evolution.

Congenital hypotrichosis with anodontia in cattle: a genetic, clinical and histological analysis.

C. Drögemüller, O. Distl, T. Leeb, 2002, Veterinary dermatology.

Partial deletion of the bovine ED1 gene causes anhidrotic ectodermal dysplasia in cattle.

C. Drögemüller, O. Distl, T. Leeb, 2001, Genome research.

A comparative radiation hybrid map of sheep chromosome 10

B. Dalrymple, N. Cockett, C. Drögemüller, 2008, Cytogenetic and Genome Research.

Genetic diversity analyses reveal first insights into breed-specific selection signatures within Swiss goat breeds.

F. Menzi, C. Drögemüller, A. Burren, 2016, Animal genetics.

Ear type in sheep is associated with the MSRB3 locus.

C. Drögemüller, I. Häfliger, A. Letko, 2020, Animal genetics.

A non‐coding regulatory variant in the 5′‐region of the MITF gene is associated with white‐spotted coat in Brown Swiss cattle

C. Drögemüller, T. Leeb, F. Seefried, 2018, Animal Genetics.

Molecular Characterization of Five Porcine Candidate Genes for Drip Loss in Pork

C. Drögemüller, T. Leeb, K. Wimmers, 2010, Animal biotechnology.

Lethal chondrodysplasia in a family of Holstein cattle is associated with a de novo splice site variant of COL2A1

F. Menzi, C. Drögemüller, V. Jagannathan, 2016, BMC Veterinary Research.

A de novo germline mutation in MYH7 causes a progressive dominant myopathy in pigs

C. Drögemüller, B. Harlizius, L. Murgiano, 2012, BMC Genetics.

Genomic amplification of the caprine EDNRA locus might lead to a dose dependent loss of pigmentation

B. Brenig, F. Menzi, C. Drögemüller, 2016, Scientific Reports.

Genetic mapping of the belt pattern in Brown Swiss cattle to BTA3.

C. Drögemüller, T. Leeb, S. Moser, 2009, Animal genetics.

A Splice Defect in the EDA Gene in Dogs with an X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED) Phenotype

C. Drögemüller, T. Leeb, V. Jagannathan, 2016, G3: Genes, Genomes, Genetics.

A novel mutation in the bovine EDA gene causing anhidrotic ectodermal dysplasia

C. Drögemüller, T. Leeb, C. Palmer, 2006 .

Ectodysplasin-1 deficiency in a German Holstein bull associated with loss of respiratory mucous glands and chronic rhinotracheitis.

C. Drögemüller, O. Distl, T. Leeb, 2005, Journal of comparative pathology.

Analysis of the canine EDAR gene and exclusion as a candidate for the hairless phenotype in the Chinese Crested dog.

É. Cadieu, C. Drögemüller, T. Leeb, 2005, Animal genetics.

Identification of a highly polymorphic microsatellite within the bovine ectodysplasin A (ED1) gene on BTA Xq22-24.

C. Drögemüller, O. Distl, T. Leeb, 2000, Animal genetics.

A Non-Synonymous HMGA2 Variant Decreases Height in Shetland Ponies and Other Small Horses

C. Drögemüller, T. Leeb, C. Flury, 2015, PloS one.

An Unusual Splice Defect in the Mitofusin 2 Gene (MFN2) Is Associated with Degenerative Axonopathy in Tyrolean Grey Cattle

Johann Sölkner, Martin Baumgartner, Michael H. Stoffel, 2011, PloS one.

Arachnomelia in Brown Swiss cattle maps to chromosome 5

C. Drögemüller, T. Leeb, G. Stranzinger, 2008, Mammalian Genome.

A Missense Mutation in the SERPINH1 Gene in Dachshunds with Osteogenesis Imperfecta

K. Lindblad-Toh, A. Brunner, C. Drögemüller, 2009, PLoS genetics.

Genome-wide search for markers associated with osteochondrosis in Hanoverian warmblood horses

C. Drögemüller, O. Distl, C. Dierks, 2007, Mammalian Genome.

Mapping quantitative trait loci for osteochondrosis in fetlock and hock joints and palmar/plantar osseus fragments in fetlock joints of South German Coldblood horses.

C. Drögemüller, O. Distl, H. Hamann, 2007, Animal genetics.

Is a heterozygous missense variant in SGSH the cause of a syndromic form of congenital amastia in an Original Braunvieh calf?

C. Drögemüller, F. Seefried, I. Häfliger, 2022, Animal genetics.

Introgression of ASIP and TYRP1 Alleles Explains Coat Color Variation in Valais Goats.

C. Drögemüller, T. Leeb, C. Flury, 2021, The Journal of heredity.

Prenatally engineered autologous amniotic fluid stem cell-based heart valves in the fetal circulation.

Markus Rudin, Peter Modregger, Marco Stampanoni, 2012, Biomaterials.

Assignment of the canine potassium voltage-gated channel, KQT-like subfamily, member 3 (KCNQ3) gene to CFA 13 by radiation hybrid mapping.

P. Quignon, C. Drögemüller, O. Distl, 2002, Animal Genetics.

Molecular characterization of the porcine gene CAPNS1 encoding the small subunit 1 of calpain on SSC6q1.1→q1.2

C. Drögemüller, T. Leeb, C. Drögemüller, 2003, Cytogenetic and Genome Research.

A 4 Mb High Resolution BAC Contig on Bovine Chromosome 1q12 and Comparative Analysis With Human Chromosome 21q22

C. Drögemüller, O. Distl, T. Leeb, 2005, Comparative and Functional Genomics.

A high-resolution comparative RH map of the proximal part of bovine chromosome 1.

C. Drögemüller, O. Distl, T. Leeb, 2002, Animal genetics.

A TaqI PCR-RFLP at the bovine myogenic factor (MYF5) gene.

C. Drögemüller, A. Kempers, 2000, Animal genetics.

A missense mutation in the skeletal muscle chloride channel 1 (CLCN1) as candidate causal mutation for congenital myotonia in a New Forest pony

I. Wijnberg, C. Drögemüller, F. Mascarello, 2012, Neuromuscular Disorders.

Assignment1 of the porcine inter-α trypsin inhibitor heavy chain 4 (ITIH4) gene to SSC13q2.1→q2.2 by fluorescence in situ hybridization and radiation hybrid mapping

B. Brenig, C. Drögemüller, O. Distl, 2002, Cytogenetic and Genome Research.

Generation of a 5.5-Mb BAC/PAC contig of pig chromosome 6q1.2 and its integration with existing RH, genetic and comparative maps

D. Milan, G. Rohrer, M. Yerle, 2004, Cytogenetic and Genome Research.

A high resolution physical and RH map of pig chromosome 6q1.2 and comparative analysis with human chromosome 19q13.1

D. Milan, M. Yerle, B. Brenig, 2003, BMC Genomics.

Werner Schmid, 1930–2002

C. Auffray, A. Zinn, K. Kratochwil, 2002, Cytogenetic and Genome Research.

Degenerative axonopathy in a Tyrolean grey calf.

C. Drögemüller, T. Leeb, J. Sölkner, 2010, Journal of veterinary internal medicine.

DNA-based analysis of protein variants reveals different genetic variability of the paralogous equine ß-lactoglobulin genes LGB1 and LGB2

C. Drögemüller, T. Leeb, J. Tetens, 2016 .

Constitutional trisomy 20 in an aborted Holstein fetus with pulmonary hypoplasia and anasarca syndrome.

C. Drögemüller, I. Häfliger, J. Agerholm, 2020, Animal genetics.

Trisomy 29 in a stillborn Swiss Original Braunvieh calf.

C. Drögemüller, F. Seefried, I. Häfliger, 2020, Animal Genetics.

A naturally occurring prfA truncation in a Listeria monocytogenes field strain contributes to reduced replication and cell-to-cell spread.

C. Drögemüller, C. Pfarrer, V. Jagannathan, 2015, Veterinary microbiology.

A Frameshift Mutation in the Cubilin Gene (CUBN) in Border Collies with Imerslund-Gräsbeck Syndrome (Selective Cobalamin Malabsorption)

C. Drögemüller, T. Leeb, V. Jagannathan, 2013, PloS one.

The interleukin 4 receptor gene and its role in recurrent airway obstruction in Swiss Warmblood horses.

C. Drögemüller, T. Leeb, J. Swinburne, 2012, Animal genetics.

Genetic analysis of syndactyly in German Holstein cattle.

C. Drögemüller, O. Distl, 2006, The Veterinary Journal.

A CHRNB1 frameshift mutation is associated with familial arthrogryposis multiplex congenita in Red dairy cattle

F. Menzi, C. Drögemüller, V. Jagannathan, 2016, BMC Genomics.

Mining massive genomic data of two Swiss Braunvieh cattle populations reveals six novel candidate variants that impair reproductive success

C. Drögemüller, F. Seefried, I. Häfliger, 2021, Genetics Selection Evolution.

Reverse Genetic Screen for Deleterious Recessive Variants in the Local Simmental Cattle Population of Switzerland

C. Drögemüller, F. Seefried, I. Häfliger, 2021, Animals : an open access journal from MDPI.

Occurrence of congenital disorders in Swiss sheep

C. Drögemüller, A. Steiner, M. Doherr, 2013, Acta Veterinaria Scandinavica.

Diagnosis of diabetes insipidus observed in Swiss Duroc boars

H. Nathues, C. Drögemüller, C. Gurtner, 2016, BMC Veterinary Research.

Diagnosis of diabetes insipidus observed in

H. Nathues, C. Drögemüller, C. Gurtner, 2016 .

Deletion in the EVC2 Gene Causes Chondrodysplastic Dwarfism in Tyrolean Grey Cattle

C. Drögemüller, K. Dittmer, C. Benazzi, 2014, PloS one.

A Missense Change in the ATG4D Gene Links Aberrant Autophagy to a Neurodegenerative Vacuolar Storage Disease

J. Kere, P. Wohlsein, C. Drögemüller, 2015, PLoS genetics.

A Deletion in the VLDLR Gene in Eurasier Dogs with Cerebellar Hypoplasia Resembling a Dandy-Walker-Like Malformation (DWLM)

C. Drögemüller, T. Leeb, K. Matiasek, 2015, PloS one.

A frameshift mutation in the cubilin gene (CUBN) in Beagles with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption).

R. Bruggmann, C. Drögemüller, T. Leeb, 2014, Animal Genetics.

A complex structural variant at the KIT locus in cattle with the Pinzgauer spotting pattern.

C. Drögemüller, T. Leeb, J. Sölkner, 2019, Animal genetics.

SLC19A3 Loss-of-Function Variant in Yorkshire Terriers With Leigh-Like Subacute Necrotizing Encephalopathy

C. Drögemüller, K. Matiasek, A. Fischer, 2020, Genes.

A transposable element insertion in APOB causes cholesterol deficiency in Holstein cattle

F. Schmitz-Hsu, F. Menzi, C. Drögemüller, 2016, Animal genetics.

A de novo variant in OTX2 in a lamb with otocephaly

C. Drögemüller, I. Häfliger, A. Letko, 2020, Acta Veterinaria Scandinavica.

Thrombocytopenic purpura on an organic farm with pen mating: a case report on the re-emergence of an old disease

C. Drögemüller, I. Häfliger, Olivia K. Richard, 2020, Porcine Health Management.

Genetic diversity in German draught horse breeds compared with a group of primitive, riding and wild horses by means of microsatellite DNA markers.

C. Drögemüller, O. Distl, H. Hamann, 2004, Animal genetics.

The LCORL Locus Is under Selection in Large-Sized Pakistani Goat Breeds

C. Drögemüller, T. Leeb, C. Flury, 2020, Genes.

Mining massive genomic data of two Swiss Braunvieh cattle populations reveals six novel candidate variants that impair reproductive success

C. Drögemüller, F. Seefried, I. Häfliger, 2021, Genetics, selection, evolution : GSE.

A de novo germline mutation of KIT in a white-spotted Brown Swiss cow.

C. Drögemüller, F. Seefried, I. Häfliger, 2020, Animal genetics.

A Nonsense Variant in CCDC65 Gene Causes Respiratory Failure Associated with Increased Lamb Mortality in French Lacaune Dairy Sheep

C. Drögemüller, S. Fabre, F. Plisson-Petit, 2021, Genes.

254. Successful trio-based reverse genetic screen in an endangered local cattle breed

C. Drögemüller, F. Seefried, I. Häfliger, 2022, Proceeding of 12th World Congress on Genetics Applied to Livestock Production (WCGALP).

CNGB3 Missense Variant Causes Recessive Achromatopsia in Original Braunvieh Cattle

C. Drögemüller, F. Seefried, I. Häfliger, 2021, International journal of molecular sciences.

[Fanconi-Bickel-Syndrom: a novel genetic disease in Original Braunvieh].

C. Drögemüller, F. Seefried, M. Meylan, 2018, Schweizer Archiv fur Tierheilkunde.

Improving the resolution of canine genome-wide association studies using genotype imputation: A study of two breeds

C. Wade, C. Mellersh, U. Giger, 2021, Animal Genetics.

Phylogenetic relationships of German heavy draught horse breeds inferred from mitochondrial DNA D-loop variation.

C. Drögemüller, O. Distl, H. Hamann, 2007, Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie.

Analysis of Polycerate Mutants Reveals the Evolutionary Co-option of HOXD1 for Horn Patterning in Bovidae

D. Duboule, G. Tosser-Klopp, J. Lenstra, 2021, Molecular biology and evolution.

Meta-analyses of genome wide association studies in lines of laying hens divergently selected for feather pecking using imputed sequence level genotypes

W. Bessei, C. Drögemüller, J. Tetens, 2020, BMC genetics.

Meta-analyses of genome wide association studies in lines of laying hens divergently selected for feather pecking using imputed sequence level genotypes

W. Bessei, C. Drögemüller, J. Tetens, 2020, BMC Genetics.

Using multiple landscape genetic approaches to test the validity of genetic clusters in a species characterized by an isolation-by-distance pattern

C. Drögemüller, Marcela Suarez-Rubio, S. Gockel, 2016 .

A Missense Mutation in the Vacuolar Protein Sorting 11 (VPS11) Gene Is Associated with Neuroaxonal Dystrophy in Rottweiler Dogs

C. T. Brown, T. Mansour, J. Mickelson, 2018, G3: Genes, Genomes, Genetics.

Canine NAPEPLD-associated models of human myelin disorders

E. Patterson, J. Mickelson, C. Drögemüller, 2018, Scientific Reports.

A Nonsense Mutation in the IKBKG Gene in Mares with Incontinentia Pigmenti

J. Goodship, A. Clarke, C. Drögemüller, 2013, PloS one.

High confidence copy number variants identified in Holstein dairy cattle from whole genome sequence and genotype array data

F. Schenkel, A. Kommadath, C. Drögemüller, 2020, Scientific Reports.

Congenital hypotrichosis and oligodontia in cattle

C. Drögemüller, O. Distl, T. Leeb, 2003 .

Breeding for resistance to scrapie: Detection of polymorphisms in the prion protein gene in German sheep breeds

C. Drögemüller, O. Distl, T. Leeb, 2001 .

A CNTNAP1 Missense Variant Is Associated with Canine Laryngeal Paralysis and Polyneuropathy

G. Johnson, J. Mickelson, C. Drögemüller, 2020, Genes.

A deletion spanning the promoter and first exon of the hair cycle-specific ASIP transcript isoform in black and tan rabbits.

C. Drögemüller, T. Leeb, M. Carneiro, 2019, Animal genetics.

Bos indicus introgression into (peri-)alpine cattle breeds - evidence from the analysis of bovine whey protein variants.

C. Drögemüller, S. Qanbari, J. Tetens, 2014, Animal genetics.

Neuronal ceroid lipofuscinosis (NCL) is caused by the entire deletion of CLN8 in the Alpenländische Dachsbracke dog.

H. Goebel, K. Köhler, C. Drögemüller, 2017, Molecular genetics and metabolism.

Novel Prion Protein in BSE-affected Cattle, Switzerland

C. Drögemüller, A. Zurbriggen, A. Oevermann, 2012, Emerging Infectious Diseases.

Graft remodeling during growth following anterior cruciate ligament reconstruction in skeletally immature sheep

C. Krettek, C. Drögemüller, C. Hurschler, 2009, Archives of Orthopaedic and Trauma Surgery.

A de novo in-frame duplication in the COL1A2 gene in a Lagotto Romagnolo dog with osteogenesis imperfecta.

C. Drögemüller, A. Beineke, A. Letko, 2019, Animal genetics.

A De Novo Mutation in COL1A1 in a Holstein Calf with Osteogenesis Imperfecta Type II

C. Drögemüller, I. Häfliger, F. McEvoy, 2021, Animals : an open access journal from MDPI.

A de novo mutation in col1a1 in a holstein calf with osteogenesis imperfecta type II Jacinto,

C. Drögemüller, I. Häfliger, F. McEvoy, 2021 .

A frameshift mutation in MOCOS is associated with familial renal syndrome (xanthinuria) in Tyrolean Grey cattle

C. Drögemüller, M. Bolcato, V. Jagannathan, 2016, BMC Veterinary Research.

Renal dysplasia in grey Alpine breed cattle unrelated to CLDN16 mutations

C. Drögemüller, L. Aresu, S. Mazzariol, 2011, The Veterinary Record.

Deviation Patterns of Observed and Expected Haplotype Blocks Associated with Potential Recessive Disorders in Tyrol Grey Cattle

C. Drögemüller, J. Sölkner, G. Mészáros, 2019, Acta Universitatis Agriculturae et Silviculturae Mendelianae Brunensis.

A COL2A1 de novo variant in a Holstein bulldog calf.

C. Drögemüller, I. Häfliger, V. Jagannathan, 2018, Animal genetics.

A large deletion in the COL2A1 gene expands the spectrum of pathogenic variants causing bulldog calf syndrome in cattle

C. Drögemüller, I. Häfliger, A. Letko, 2020, Acta Veterinaria Scandinavica.

De novo stop-lost germline mutation in FGFR3 causes severe chondrodysplasia in the progeny of a Holstein bull.

C. Drögemüller, I. Häfliger, A. Letko, 2020, Animal genetics.

A Missense Variant in PLP2 in Holstein Cattle with X-Linked Congenital Mast Cell Tumor

C. Drögemüller, I. Häfliger, C. Benazzi, 2022, Animals : an open access journal from MDPI.

C. Drögemüller, I. Häfliger, C. Benazzi, 2021, Genes.

A CHRNB1 frameshift mutation is associated with familial arthrogryposis multiplex congenita in Red dairy cattle

F. Menzi, C. Drögemüller, V. Jagannathan, 2016, BMC Genomics.

DNA-based diagnosis of rare diseases in veterinary medicine: a 4.4 kb deletion of ITGB4 is associated with epidermolysis bullosa in Charolais cattle

P. Wohlsein, C. Drögemüller, V. Jagannathan, 2015, BMC Veterinary Research.

Congenital Hepatic Fibrosis in the Franches-Montagnes Horse Is Associated with the Polycystic Kidney and Hepatic Disease 1 (PKHD1) Gene

C. Drögemüller, T. Leeb, J. Tetens, 2014, PloS one.

Congenital Hepatic Fibrosis in the Franches-Montagnes Horse Is Associated with the Polycystic Kidney and Hepatic Disease 1 ( PKHD 1 ) Gene

C. Drögemüller, T. Leeb, J. Tetens, 2014 .

Mutations in MITF and PAX3 Cause “Splashed White” and Other White Spotting Phenotypes in Horses

J. Matthews, C. Drögemüller, T. Leeb, 2012, PLoS genetics.

A genome-wide significant association on chromosome 2 for footrot resistance/susceptibility in Swiss White Alpine sheep.

C. Drögemüller, J. Tetens, A. Steiner, 2017, Animal genetics.

Persistent Mullerian duct syndrome causing male pseudohermaphroditism in a mixed-breed dog

C. Drögemüller, O. Distl, H. Kuiper, 2004, Veterinary Record.

A Gly98Val Mutation in the N-Myc Downstream Regulated Gene 1 (NDRG1) in Alaskan Malamutes with Polyneuropathy

S. Cirera, J. Mickelson, M. Fredholm, 2013, PloS one.

Assignment of the COL16A1 gene to equine chromosome 2p15.1-p15.3 by FISH and confirmation by RH mapping.

C. Drögemüller, O. Distl, B. Chowdhary, 2005, Animal genetics.

Characterization of the equine ITGAX gene and its association with recurrent airway obstruction in European Warmblood horses.

C. Drögemüller, T. Leeb, J. Swinburne, 2010, Animal genetics.

A breeding experiment confirms the dominant mode of inheritance of the brown coat colour associated with the (496) Asp TYRP1 allele in goats.

F. Menzi, C. Drögemüller, T. Leeb, 2015, Animal genetics.

Correction: Mutations in MITF and PAX3 Cause “Splashed White” and Other White Spotting Phenotypes in Horses

J. Matthews, C. Drögemüller, T. Leeb, 2019, PLoS Genetics.

DYRK1B haploinsufficiency in a Holstein cattle with epilepsy.

C. Drögemüller, I. Häfliger, M. Bolcato, 2023, Animal genetics.

Imputation of sequence level genotypes in the Franches-Montagnes horse breed

C. Drögemüller, T. Leeb, J. Tetens, 2014, Genetics Selection Evolution.

A high-resolution comparative radiation hybrid map of equine chromosome 4q12-q22.

C. Drögemüller, O. Distl, T. Leeb, 2006, Animal genetics.

Linkage of bilateral convergent strabismus with exophthalmus (BCSE) to BTA5 and BTA18 in German Brown cattle.

C. Drögemüller, O. Distl, S. Mömke, 2008, Animal genetics.

WNT10B: A locus increasing risk of brachygnathia inferior in Brown Swiss cattle.

C. Drögemüller, F. Seefried, C. Flury, 2023, Journal of dairy science.

Cloning and chromosomal localization of MYO15A to chromosome 5 of the dog (Canis familiaris)

P. Quignon, C. Drögemüller, O. Distl, 2004, Chromosome Research.

Pseudomyotonia, a muscle function disorder associated with an inherited ATP2A1 (SERCA1) defect in a Dutch Improved Red and White cross-breed calf

I. Wijnberg, C. Drögemüller, F. Mascarello, 2010, Neuromuscular Disorders.

Osteogenesis imperfecta in dachshunds

B. Brenig, C. Drögemüller, T. Leeb, 2013, Veterinary Record.

Assignment1 of the bovine ectodysplasin A gene (ED1) to bovine Xq22→q24 by fluorescence in situ hybridization

C. Drögemüller, O. Distl, T. Leeb, 2001, Cytogenetic and Genome Research.

Genetic analysis of congenital hypotrichosis with anodontia in cattle.

C. Drögemüller, O. Distl, H. Kuiper, 2000 .

Assignment of the COL8A2 gene to equine chromosome 2p15-p16 by FISH and confirmation by RH mapping.

C. Drögemüller, O. Distl, B. Chowdhary, 2005, Animal genetics.

Assignment of the COMP gene to equine chromosome 21q12-q14 by FISH and confirmation by RH mapping.

C. Drögemüller, O. Distl, B. Chowdhary, 2005, Animal genetics.

Animal Cytogenetics and Comparative Mapping

B. Brenig, C. Drögemüller, H. Kuiper, 2001 .

Animal Cytogenetics and Comparative Mapping

P. Quignon, C. Drögemüller, A. Scott, 2003 .

Identification of a second encephalitis-associated astrovirus in cattle

R. Bruggmann, C. Drögemüller, D. Wüthrich, 2016, Emerging Microbes &Infections.

Molecular Characterization of Five Porcine Candidate Genes for Drip Loss in Pork

C. Drögemüller, T. Leeb, K. Wimmers, 2010, Animal biotechnology.

Molecular Cytogenetics and Gene Mapping in Sheep (Ovis aries, 2n = 54)

B. Dalrymple, J. Maddox, F. Nicholas, 2009, Cytogenetic and Genome Research.

Comparison against 186 canid whole-genome sequences reveals survival strategies of an ancient clonally transmissible canine tumor

Jason J. Corneveaux, J. Trent, E. Ostrander, 2015, Genome research.

Remediation of TENORM residues: risk communication in practice

C. Drögemüller, B. Riebe, Claudia König, 2014, Journal of radiological protection : official journal of the Society for Radiological Protection.

Meta-analysis of genome-wide association studies for cattle stature identifies common genes that regulate body size in mammals

R. Veerkamp, B. Guldbrandtsen, M. Lund, 2018, Nature Genetics.

A germline de novo variant in NUMB associated with a double‐outlet right ventricle in Chianina cattle

C. Drögemüller, I. Häfliger, D. Caivano, 2022, Animal genetics.

A nonsense mutation in the COL7A1 gene causes epidermolysis bullosa in Vorderwald cattle

C. Drögemüller, C. Wurmser, R. Fries, 2016, BMC Genetics.