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
Fields of Research (FoR)
Medical Subject Headings (MeSH)
AdolescentAttention Deficit Disorder with HyperactivityAutistic DisorderCase-Control StudiesChildChild, PreschoolDNA Copy Number VariationsFemaleGenetic LociGenetic Predisposition to DiseaseGlycoproteinsHumansMaleNervous System DiseasesPedigreeRisk FactorsSequence Analysis, DNATranscription FactorsTripartite Motif ProteinsUbiquitin-Protein Ligases