Tosso Leeb

Evidence for a Retroviral Insertion in TRPM1 as the Cause of Congenital Stationary Night Blindness and Leopard Complex Spotting in the Horse

Arne Ludwig, David L. Adelson, Padmanabhan Mahadevan, 2013, PloS one.

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

Keith Durkin, Michel Georges, Arnaud Sartelet, 2011 .

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.

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.

A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12

Göran Andersson, Marcin Kierczak, Lorna J. Kennedy, 2015, PloS one.

Expression of Foxi3 is regulated by ectodysplasin in skin appendage placodes

Hannes Lohi, C. Drögemüller, I. Thesleff, 2013, Developmental dynamics : an official publication of the American Association of Anatomists.

Ancient genomic changes associated with domestication of the horse

Arne Ludwig, Anders Albrechtsen, Markus Neuditschko, 2017, Science.

Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency.

Klaus-Peter Zimmer, T. Leeb, H. Naim, 2009, Gastroenterology.