<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Strom NI</submitter><funding>BLRD VA</funding><funding>NICHD NIH HHS</funding><funding>NCATS NIH HHS</funding><funding>NIDA NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>NIA NIH HHS</funding><funding>NIMH NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NIAAA NIH HHS</funding><funding>HSRD VA</funding><funding>CSRD VA</funding><funding>European Research Council</funding><funding>NHGRI NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>NIGMS NIH HHS</funding><pubmed_abstract>Obsessive-compulsive disorder (OCD) affects ~1% of children and adults and is partly caused by genetic factors. We conducted a genome-wide association study (GWAS) meta-analysis combining 53,660 OCD cases and 2,044,417 controls and identified 30 independent genome-wide significant loci. Gene-based approaches identified 249 potential effector genes for OCD, with 25 of these classified as the most likely causal candidates, including &lt;i>WDR6&lt;/i>, &lt;i>DALRD3&lt;/i>, &lt;i>CTNND1&lt;/i> and multiple genes in the MHC region. We estimated that ~11,500 genetic variants explained 90% of OCD genetic heritability. OCD genetic risk was associated with excitatory neurons in the hippocampus and cortex, along with D1- and D2-type dopamine receptor-containing medium spiny neurons. OCD genetic risk was shared with 6</pubmed_abstract><journal>medRxiv : the preprint server for health sciences</journal><pagination>2024.03.13.24304161</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11071577</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder.</pubmed_title><pmcid>PMC11071577</pmcid><funding_grant_id>R01 MH079488</funding_grant_id><funding_grant_id>R01 MH079489</funding_grant_id><funding_grant_id>IK2 BX005058</funding_grant_id><funding_grant_id>R01 AA026364</funding_grant_id><funding_grant_id>R01 MH079487</funding_grant_id><funding_grant_id>RC2 GM092618</funding_grant_id><funding_grant_id>R56 MH120736</funding_grant_id><funding_grant_id>R01 MH059299</funding_grant_id><funding_grant_id>R01 MH113362</funding_grant_id><funding_grant_id>R01 MH124871</funding_grant_id><funding_grant_id>R01 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identify 30 loci associated with obsessive-compulsive disorder.</name><description>Obsessive-compulsive disorder (OCD) affects ~1% of children and adults and is partly caused by genetic factors. We conducted a genome-wide association study (GWAS) meta-analysis combining 53,660 OCD cases and 2,044,417 controls and identified 30 independent genome-wide significant loci. Gene-based approaches identified 249 potential effector genes for OCD, with 25 of these classified as the most likely causal candidates, including &lt;i>WDR6&lt;/i>, &lt;i>DALRD3&lt;/i>, &lt;i>CTNND1&lt;/i> and multiple genes in the MHC region. We estimated that ~11,500 genetic variants explained 90% of OCD genetic heritability. OCD genetic risk was associated with excitatory neurons in the hippocampus and cortex, along with D1- and D2-type dopamine receptor-containing medium spiny neurons. OCD genetic risk was shared with 6</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2026-07-01T03:24:58.698Z</modification><creation>2026-07-01T03:12:36.075Z</creation></dates><accession>S-EPMC11071577</accession><cross_references><pubmed>38712091</pubmed><doi>10.1101/2024.03.13.24304161</doi></cross_references></HashMap>