Carsten M. Pusch

New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing

Andreas Keller, Angela Graefen, Markus Ball et al. · Nature Communications · 2012 · 462 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

Carsten M. Pusch, Christina Zeitz, Oliver Brandau et al. · Nature Genetics · 2000 · 260 citations

Medicine, Genetics, Molecular Genetics +13

Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and Mutated in Patients Affected by Autosomal Dominant Hearing Impairment (DFNA4)

Francesca Donaudy, Rik L. Snoeckx, Markus Pfister et al. · The American Journal of Human Genetics · 2004 · 170 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

The SOX10 / Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factor

Carsten M. Pusch, Elisabeth Hustert, Dietmar Pfeifer et al. · Human Genetics · 1998 · 134 citations · Full text

Life Sciences, Genetics, Molecular Genetics +4

Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell

P. Heidrych, Ulrike Zimmermann, Stephanie Kuhn et al. · Human Molecular Genetics · 2009 · 108 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +15