Hans‐Hilger Ropers

Abnormal Behavior Associated with a Point Mutation in the Structural Gene for Monoamine Oxidase A

Han G. Brunner, Marcel Nelen, Xandra O. Breakefield et al. · Science · 1993 · 1.6K citations

Life Sciences, Genetics, Molecular Genetics +17

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

Hossein Najmabadi, Hao Hu, Masoud Garshasbi et al. · Nature · 2011 · 987 citations

Life Sciences, Genetics, Molecular Genetics +12

X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family

Frédéric Laumonnier, Frédérique Bonnet‐Brilhault, Marie Gomot et al. · The American Journal of Human Genetics · 2004 · 760 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Localization of the gene for Cowden disease to chromosome 10q22–23

Marcel Nelen, G.W. Padberg, E Peeters et al. · Nature Genetics · 1996 · 670 citations

Life Sciences, Genetics, Molecular Genetics +10

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

Patrick Tarpey, Raffaella Smith, Erin Pleasance et al. · Nature Genetics · 2009 · 617 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12