Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder.

TitleSequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder.
Publication TypeJournal Article
Year of Publication2017
AuthorsKim, DSeung, Burt, AA, Ranchalis, JE, Wilmot, B, Smith, JD, Patterson, KE, Coe, BP, Li, YK, Bamshad, MJ, Nikolas, M, Eichler, EE, Swanson, JM, Nigg, JT, Nickerson, DA, Jarvik, GP
Corporate AuthorsUniversity of Washington Center for Mendelian Genomics
JournalAm J Med Genet B Neuropsychiatr Genet
Date Published2017 Mar 22
ISSN1552-485X
Abstract

Attention-Deficit Hyperactivity Disorder (ADHD) has high heritability; however, studies of common variation account for

DOI10.1002/ajmg.b.32527
Alternate JournalAm. J. Med. Genet. B Neuropsychiatr. Genet.
PubMed ID28332277
Grant ListU54 HG006493 / HG / NHGRI NIH HHS / United States
RC2 HG005608 / HG / NHGRI NIH HHS / United States
T32 HL007312 / HL / NHLBI NIH HHS / United States
F31 MH101905 / MH / NIMH NIH HHS / United States
R01 MH101221 / MH / NIMH NIH HHS / United States