Brett S. Abrahams

Functional impact of global rare copy number variation in autism spectrum disorders

Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei et al. · Nature · 2010 · 2K citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits

Olga Peñagarikano, Brett S. Abrahams, Edward I. Herman et al. · Cell · 2011 · 1.1K citations · Full text

Medicine, Neurobiology, Neuroscience +16

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

Kai Wang, Haitao Zhang, Deqiong Ma et al. · Nature · 2009 · 973 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)

Brett S. Abrahams, Dan E. Arking, Heather C. Mefford et al. · Molecular Autism · 2013 · 940 citations · Full text

Life Sciences, Bioinformatics, Genetics +13

Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene

Maricela Alarcón, Brett S. Abrahams, Jennifer Stone et al. · The American Journal of Human Genetics · 2008 · 825 citations · Full text

Life Sciences, Genetics, Neuroscience +12