<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Vrshek-Schallhorn S</submitter><funding>William T. Grant Foundation</funding><funding>Williams College</funding><funding>NIMH NIH HHS</funding><funding>UNCG</funding><funding>National Institute of Mental Health</funding><pagination>776-90</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4948188</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>124(4)</volume><pubmed_abstract>Behavioral genetic research supports polygenic models of depression in which many genetic variations each contribute a small amount of risk, and prevailing diathesis-stress models suggest gene-environment interactions (G×E). Multilocus profile scores of additive risk offer an approach that is consistent with polygenic models of depression risk. In a first demonstration of this approach in a G×E predicting depression, we created an additive multilocus profile score from 5 serotonin system polymorphisms (1 each in the genes HTR1A, HTR2A, HTR2C, and 2 in TPH2). Analyses focused on 2 forms of interpersonal stress as environmental risk factors. Using 5 years of longitudinal diagnostic and life stress interviews from 387 emerging young adults in the Youth Emotion Project, survival analyses show </pubmed_abstract><journal>Journal of abnormal psychology</journal><pubmed_title>Additive genetic risk from five serotonin system polymorphisms interacts with interpersonal stress to predict depression.</pubmed_title><pmcid>PMC4948188</pmcid><funding_grant_id>R01 MH065651</funding_grant_id><funding_grant_id>F32 MH091955</funding_grant_id><funding_grant_id>F32-MH091955</funding_grant_id><funding_grant_id>R01 MH065652</funding_grant_id><funding_grant_id>R01-MH065651</funding_grant_id><funding_grant_id>R01-MH065652</funding_grant_id><pubmed_authors>Redei EE</pubmed_authors><pubmed_authors>Mineka S</pubmed_authors><pubmed_authors>Zinbarg RE</pubmed_authors><pubmed_authors>Craske MG</pubmed_authors><pubmed_authors>Stroud CB</pubmed_authors><pubmed_authors>Adam EK</pubmed_authors><pubmed_authors>Hammen C</pubmed_authors><pubmed_authors>Vrshek-Schallhorn S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Additive genetic risk from five serotonin system polymorphisms interacts with interpersonal stress to predict depression.</name><description>Behavioral genetic research supports polygenic models of depression in which many genetic variations each contribute a small amount of risk, and prevailing diathesis-stress models suggest gene-environment interactions (G×E). Multilocus profile scores of additive risk offer an approach that is consistent with polygenic models of depression risk. In a first demonstration of this approach in a G×E predicting depression, we created an additive multilocus profile score from 5 serotonin system polymorphisms (1 each in the genes HTR1A, HTR2A, HTR2C, and 2 in TPH2). Analyses focused on 2 forms of interpersonal stress as environmental risk factors. Using 5 years of longitudinal diagnostic and life stress interviews from 387 emerging young adults in the Youth Emotion Project, survival analyses show </description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Nov</publication><modification>2025-04-25T17:49:07.114Z</modification><creation>2019-03-27T02:18:34Z</creation></dates><accession>S-EPMC4948188</accession><cross_references><pubmed>26595467</pubmed><doi>10.1037/abn0000098</doi></cross_references></HashMap>