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

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abstract

A high-resolution analysis of copy number variation in patients with ADHD reveals new gene associations, few de novo mutations, and overlap with genes implicated in other disorders such as autism.

authors

Lionel, Anath C
Crosbie, Jennifer
Barbosa, Nicole
Goodale, Tara
Thiruvahindrapuram, Bhooma
Rickaby, Jessica
Gazzellone, Matthew
Carson, Andrew R
Howe, Jennifer L
Wang, Zhuozhi
Wei, John
Stewart, Alexandre FR
Roberts, Robert
McPherson, Ruth
Fiebig, Andreas
Franke, Andre
Schreiber, Stefan
Zwaigenbaum, Lonnie
Fernandez, Bridget A
Roberts, Wendy
Arnold, Paul D
Szatmari, Peter
Marshall, Christian R
Schachar, Russell
Scherer, Stephen W

status

published

publication date

August 10, 2011

has subject area

06 Biological Sciences (FoR)
11 Medical and Health Sciences (FoR)
Adolescent (MeSH)
Attention Deficit Disorder with Hyperactivity (MeSH)
Autistic Disorder (MeSH)
Case-Control Studies (MeSH)
Child (MeSH)
Child, Preschool (MeSH)
DNA Copy Number Variations (MeSH)
Female (MeSH)
Genetic Loci (MeSH)
Genetic Predisposition to Disease (MeSH)
Glycoproteins (MeSH)
Humans (MeSH)
Male (MeSH)
Nervous System Diseases (MeSH)
Pedigree (MeSH)
Risk Factors (MeSH)
Sequence Analysis, DNA (MeSH)
Transcription Factors (MeSH)
Tripartite Motif Proteins (MeSH)
Ubiquitin-Protein Ligases (MeSH)

published in

Science Translational Medicine Journal