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Chunk #4 — Materials and Methods — Sample

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Associations between Polygenic Risk for Psychiatric Disorders and Substance Involvement.
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Non-Hispanic European–American adults who completed the Study of Addiction: Genetics and Environment (SAGE; Bierut et al., 2010) were included in analyses (N = 2573; see Table 1 for demographic information; see Supplementary Materials and Methods for details regarding ancestry determination). Alcohol dependent (n = 1160; required 12-month clustering of DSM-IV symptoms) and control (n = 1413) participants were recruited from three large, complementary datasets ascertained for alcohol (Collaborative Study of the Genetics of Alcoholism; Reich et al., 1998; Foroud et al., 2000), nicotine (Collaborative Study of the Genetics of Nicotine Dependence; Bierut et al., 2007; Saccone et al., 2007), and cocaine (Family Study of Cocaine Dependence; Bierut et al., 2008) dependence. Alcohol dependent cases often met criteria for a variety of other substance use disorders. Controls did not meet criteria for alcohol dependence or for cocaine, cannabis, and opioid dependence (nicotine dependence was allowed) but may have used these substances and endorsed some symptoms at non-diagnostic levels. The Institutional Review Board at each contributing institution (i.e., Henry Ford Health Sciences Center, Howard University, Indiana University, SUNY Health Sciences Center at