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Rare Copy Number Variation Discovery and...
Journal article

Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD

Abstract

Attention deficit hyperactivity disorder (ADHD) is a common and persistent condition characterized by developmentally atypical and impairing inattention, hyperactivity, and impulsiveness. We identified de novo and rare copy number variations (CNVs) in 248 unrelated ADHD patients using million-feature genotyping arrays. We found de novo CNVs in 3 of 173 (1.7%) ADHD patients for whom we had DNA from both parents. These CNVs affected …

Authors

Lionel AC; Crosbie J; Barbosa N; Goodale T; Thiruvahindrapuram B; Rickaby J; Gazzellone M; Carson AR; Howe JL; Wang Z

Journal

Science Translational Medicine, Vol. 3, No. 95,

Publisher

American Association for the Advancement of Science (AAAS)

Publication Date

August 10, 2011

DOI

10.1126/scitranslmed.3002464

ISSN

1946-6234