<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Termorshuizen JD</submitter><funding>NIMH NIH HHS</funding><pubmed_abstract>Eating disorders -including anorexia nervosa (AN), bulimia nervosa, and binge eating disorder-are clinically distinct but exhibit symptom overlap and diagnostic crossover. Genomic analyses have mostly examined AN. We conducted the first genomic meta-analysis of binge eating behaviour (BE; 39,279 cases, 1,227,436 controls), alongside new analyses of AN (24,223 cases, 1,243,971 controls) and its subtypes (all European ancestries). We identified six loci associated with BE, including loci associated with higher body mass index (BMI) and impulse-control behaviours. AN GWAS yielded eight loci, validating six loci. Subsequent polygenic risk score analysis demonstrated an association with AN in two East Asian ancestry cohorts. BE and AN exhibited similar positive genetic correlations with psychia</pubmed_abstract><journal>medRxiv : the preprint server for health sciences</journal><pagination>2025.01.31.25321397</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12083633</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Genome-wide association studies of binge eating behaviour and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypes.</pubmed_title><pmcid>PMC12083633</pmcid><funding_grant_id>R01 MH124851</funding_grant_id><pubmed_authors>Ayorech Z</pubmed_authors><pubmed_authors>Palviainen T</pubmed_authors><pubmed_authors>Woodside DB</pubmed_authors><pubmed_authors>Havdahl A</pubmed_authors><pubmed_authors>Gorwood P</pubmed_authors><pubmed_authors>Kaprio J</pubmed_authors><pubmed_authors>Thornton LM</pubmed_authors><pubmed_authors>Martin NG</pubmed_authors><pubmed_authors>Danner 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Genomic analyses have mostly examined AN. We conducted the first genomic meta-analysis of binge eating behaviour (BE; 39,279 cases, 1,227,436 controls), alongside new analyses of AN (24,223 cases, 1,243,971 controls) and its subtypes (all European ancestries). We identified six loci associated with BE, including loci associated with higher body mass index (BMI) and impulse-control behaviours. AN GWAS yielded eight loci, validating six loci. Subsequent polygenic risk score analysis demonstrated an association with AN in two East Asian ancestry cohorts. BE and AN exhibited similar positive genetic correlations with psychia</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 May</publication><modification>2026-04-13T03:23:39.446Z</modification><creation>2026-04-13T03:12:33.667Z</creation></dates><accession>S-EPMC12083633</accession><cross_references><pubmed>40385383</pubmed><doi>10.1101/2025.01.31.25321397</doi></cross_references></HashMap>