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
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
PubMed ID28332277
PubMed Central IDPMC5467442
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
R01 MH099064 / MH / NIMH NIH HHS / United States
F31 MH101905 / MH / NIMH NIH HHS / United States
UM1 HG006493 / HG / NHGRI NIH HHS / United States
R01 MH101221 / MH / NIMH NIH HHS / United States