000 01498 a2200433 4500
005 20250518005004.0
264 0 _c20191023
008 201910s 0 0 eng d
022 _a1535-7228
024 7 _a10.1176/appi.ajp.2018.17040467
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBergen, Sarah E
245 0 0 _aJoint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.
_h[electronic resource]
260 _bThe American journal of psychiatry
_c01 2019
300 _a29-35 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural
650 0 4 _aAdult
650 0 4 _aAlgorithms
650 0 4 _aDNA Copy Number Variations
650 0 4 _aFemale
650 0 4 _aGenetic Predisposition to Disease
650 0 4 _aGenome-Wide Association Study
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMultifactorial Inheritance
650 0 4 _aPolymorphism, Single Nucleotide
650 0 4 _aRisk Assessment
_xmethods
650 0 4 _aSchizophrenia
_xgenetics
700 1 _aPloner, Alexander
700 1 _aHowrigan, Daniel
700 1 _aO'Donovan, Michael C
700 1 _aSmoller, Jordan W
700 1 _aSullivan, Patrick F
700 1 _aSebat, Jonathan
700 1 _aNeale, Benjamin
700 1 _aKendler, Kenneth S
773 0 _tThe American journal of psychiatry
_gvol. 176
_gno. 1
_gp. 29-35
856 4 0 _uhttps://doi.org/10.1176/appi.ajp.2018.17040467
_zAvailable from publisher's website
999 _c29008833
_d29008833