M. Drögemüller

发表

Impaired Cell Cycle Regulation in a Natural Equine Model of Asthma

E. Dermitzakis, T. Leeb, V. Jagannathan, 2015, PloS one.

Polymorphisms in the ABCB1 gene in phenobarbital responsive and resistant idiopathic epileptic Border Collies.

T. Leeb, A. Fischer, Lisa Alves, 2011, Journal of veterinary internal medicine.

The Effects of FGF4 Retrogenes on Canine Morphology

C. Drögemüller, T. Leeb, P. Dickinson, 2022, Genes.

A Locus on Chromosome 5 Is Associated with Dilated Cardiomyopathy in Doberman Pinschers

M. Webster, C. Drögemüller, T. Leeb, 2011, PloS one.

An Intronic MBTPS2 Variant Results in a Splicing Defect in Horses with Brindle Coat Texture

T. Leeb, M. Penedo, V. Jagannathan, 2016, G3: Genes, Genomes, Genetics.

The Transcriptome of Equine Peripheral Blood Mononuclear Cells

E. Dermitzakis, T. Leeb, V. Jagannathan, 2015, PloS one.

A Mutation in the FAM83G Gene in Dogs with Hereditary Footpad Hyperkeratosis (HFH)

C. Drögemüller, T. Leeb, J. Plassais, 2014, PLoS genetics.

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

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

Genomic comparison of bovine papillomavirus 1 isolates from bovine, equine and asinine lesional tissue samples.

M. Ackermann, K. Tobler, V. Gerber, 2018, Virus research.

IL26 gene inactivation in Equidae.

T. Leeb, V. Jagannathan, M. Drögemüller, 2013, Animal genetics.

Degenerative Liver Disease in Young Beagles with Hereditary Cobalamin Malabsorption Because of a Mutation in the Cubilin Gene

T. Leeb, M. Drögemüller, P. Kook, 2014, Journal of veterinary internal medicine.

Directed Synthesis of Nonsymmetrical Bis‐Steroidal Pyrazines and the First Biologically Active Cephalostatin Analogues

E. Winterfeldt, M. Drögemüller, R. Jautelat, 1996 .

MLPH Genotype—Melanin Phenotype Correlation in Dilute Dogs

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

Microchip capillary electrophoresis-based genetic comparison of closely related cyathostomin nematode parasites of horses using randomly amplified polymorphic DNA polymerase chain reaction

T. Schnieder, J. Höglund, G. Samson-Himmelstjerna, 2004, Parasitology Research.

Hepatic fungal infection in a young beagle with unrecognised hereditary cobalamin deficiency (Imerslund-Gräsbeck syndrome).

T. Leeb, M. Drögemüller, P. Kook, 2015, The Journal of small animal practice.

Abnormal keratinocyte differentiation in the nasal planum of Labrador Retrievers with hereditary nasal parakeratosis (HNPK)

T. Leeb, M. Stoffel, V. Gaschen, 2020, PloS one.

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.

A RAB3GAP1 SINE Insertion in Alaskan Huskies with Polyneuropathy, Ocular Abnormalities, and Neuronal Vacuolation (POANV) Resembling Human Warburg Micro Syndrome 1 (WARBM1)

T. Leeb, G. Shelton, V. Jagannathan, 2015, G3: Genes, Genomes, Genetics.

Neuronale Zeroidlipofuszinose bei einem adulten American Staffordshire Terrier Neuronal ceroid lipofuscinosis in an adult American Staffordshire Terrier

P. Wohlsein, T. Leeb, W. Baumgärtner, 2016, Tierärztliche Praxis K: Kleintiere/Heimtiere.

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.

Synthesis of Cephalostatin Analogues by Symmetrical and Non‐Symmetrical Routes

E. Winterfeldt, M. Drögemüller, U. Scholz, 1998 .

A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular Dystrophy

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

An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome

J. Kidd, E. Ostrander, M. Watson, 2019, PLoS genetics.

Two MC1R loss‐of‐function alleles in cream‐coloured Australian Cattle Dogs and white Huskies

T. Leeb, H. Lohi, A. Letko, 2018, Animal genetics.

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

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

A RAB3GAP1 SINE Insertion in Alaskan Huskies with Polyneuropathy, Ocular Abnormalities, and Neuronal Vacuolation (POANV) Resembling Human Warburg Micro Syndrome 1 (WARBM1)

T. Leeb, G. Shelton, V. Jagannathan, 2015, G3: Genes, Genomes, Genetics.

Canine Brachycephaly Is Associated with a Retrotransposon-Mediated Missplicing of SMOC2

K. Svenson, M. Bermingham, D. Argyle, 2017, Current Biology.

A whole-genome scan for recurrent airway obstruction in Warmblood sport horses indicates two positional candidate regions

T. Leeb, J. Swinburne, M. Drögemüller, 2009, Mammalian Genome.

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 comparative radiation hybrid map of sheep chromosome 10

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

Arachnomelia in Brown Swiss cattle maps to chromosome 5

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

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.

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

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

Canine NAPEPLD-associated models of human myelin disorders

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

Inflammatory pattern of the infrapatellar fat pad in dogs with canine cruciate ligament disease

M. Drögemüller, D. Spreng, S. Forterre, 2018, BMC Veterinary Research.

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.

Correction: The Transcriptome of Equine Peripheral Blood Mononuclear Cells

E. Dermitzakis, T. Leeb, V. Jagannathan, 2015, PloS one.

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 .

A single codon insertion in the PICALM gene is not associated with subvalvular aortic stenosis in Newfoundland dogs

T. Leeb, V. Jagannathan, M. Drögemüller, 2014, Human Genetics.