Michaela Drögemüller

PKD1 Nonsense Variant in a Lagotto Romagnolo Family with Polycystic Kidney Disease

V. Jagannathan, T. Leeb, M. Keiner, 2023, Genes.

Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture

K. Lindblad-Toh, J. Kidd, E. Ostrander, 2023, Genome Biology.

A frameshift-deletion mutation in Reelin causes cerebellar hypoplasia in White Swiss Shepherd dogs.

K. Dittmer, D. Garrick, M. Littlejohn, 2023, Animal genetics.

Canine NAPEPLD-associated models of human myelin disorders

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

Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human

C. Mellersh, S. Katayama, K. Krjutškov, 2023, Genome Medicine.

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.

Genome sequencing of 2000 canids by the Dog10K consortium advances the understanding of demography, genome function and architecture

K. Lindblad-Toh, J. Kidd, E. Ostrander, 2023, Genome Biology.

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.