Camille W. Brune

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Joseph Glessner, Kai Wang, Guiqing Cai et al. · Nature · 2009 · 1.4K citations · Full text

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Kai Wang, Haitao Zhang, Deqiong Ma et al. · Nature · 2009 · 968 citations · Full text

Neurodevelopmental Disorders, Syndromic Autism, Genetic Disorder +7

Recurrent 16p11.2 microdeletions in autism

Revati Kumar, Samer Karamohamed, Jyotsna Sudi et al. · Human Molecular Genetics · 2007 · 737 citations · Full text

A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism

Dan E. Arking, David J. Cutler, Camille W. Brune et al. · The American Journal of Human Genetics · 2008 · 589 citations · Full text

Common Genetic Variant, Developmental Biology, Syndromic Autism +6

Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism

Suma Jacob, Camille W. Brune, C. S. Carter et al. · Neuroscience Letters · 2007 · 423 citations · Full text

Syndromic Autism, Caucasian Children, Genetic Epidemiology +7