Wolfgang Berger

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

Uwe Schwahn, Steffen Lenzner, Juan Dong et al. · Nature Genetics · 1998 · 381 citations

Natural Sciences, Genetics, Genomic Mechanism +10

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 · 367 citations

Developmental Anomaly, Opitz G/bbb Syndrome, Developmental Biology +7

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 · 274 citations

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 · 259 citations

Developmental Anomaly, Mendelian Disorder, Ophthalmology +9

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 · 258 citations · Full text