Wolfgang Berger

Positional cloning of the gene for X-linked retinitis pigmentosa 2

Uwe Schwahn, Steffen Lenzner, Juan Dong et al. · Nature Genetics · 1998 · 382 citations

Life Sciences, Genetics, Molecular Genetics +7

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

Nandita Quaderi, Susann Schweiger, Karin Gaudenz et al. · Nature Genetics · 1997 · 370 citations

Life Sciences, Genetics, Molecular Genetics +10

A Genetic Variation in the Adenosine A2A Receptor Gene (ADORA2A) Contributes to Individual Sensitivity to Caffeine Effects on Sleep

Julia Rétey, Martin Adam, Ramin Khatami et al. · Clinical Pharmacology & Therapeutics · 2007 · 280 citations

Medicine, Genetics, Pharmacology +17

TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness

Isabelle Audo, Susanne Kohl, Bart P. Leroy et al. · The American Journal of Human Genetics · 2009 · 262 citations · Full text

Life Sciences, Genetics, Neuroscience +10

A functional genetic variation of adenosine deaminase affects the duration and intensity of deep sleep in humans

Julia Rétey, Martin Adam, E. Honegger et al. · Proceedings of the National Academy of Sciences · 2005 · 261 citations · Full text

Life Sciences, Genetics, Neuroscience +16