Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome

Anne S. BassettChelsea LowtherDaniele MericoGregory CostainEva W. C. ChowTherese van AmelsvoortDonna McDonald-McGinnRaquel E. GurAnn SwillenMarianne Van den BreeKieran MurphyDoron GothelfCarrie E. BeardenStephan EliezWendy KatesNicole PhilipVandana SashiLinda CampbellJacob VorstmanJoseph CubellsGabriela M. RepettoTony SimonErik BootTracy HeungRens EversClaudia VingerhoetsEsther van DuinElaine ZackaiElfi VergaelenKoen DevriendtJoris R. VermeeschMichael OwenClodagh MurphyElena MichaelovoskyLeila KushanMaude SchneiderWanda FremontTiffany BusaStephen HooperKathryn McCabeSasja DuijffKarin IsaevGiovanna PellecchiaJohn WeiMatthew J. GazzelloneStephen W. SchererBeverly S. EmanuelTingwei GuoBernice E. MorrowChristian R. Marshall2024-05-082024-05-082017http://hdl.handle.net/11447/1869https://investigadores.udd.cl/handle/123456789/932110.1176/appi.ajp.2017.161214172-s2.0-85032969720WOS:000414240700007chromosomal microarrayriskvariantsdisordersmicroduplicationsintegrationmechanismschildhoodmutationsburdenRare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion SyndromeResource Types::text::journal::journal article