A genome-wide association study of total child psychiatric problems scores

dc.contributor.authorNeumann Alexander
dc.contributor.authorNolte Iilja.M
dc.contributor.authorPappa Iirene
dc.contributor.authorAhluwalia Tarunveer S.
dc.contributor.authorPettersson Eerik
dc.contributor.authorRodriguez Alina
dc.contributor.authorWhitehouse Andrew
dc.contributor.authorvan Beijsterveldt Ccatrina E.M.
dc.contributor.authorBenyamin B.
dc.contributor.authorHammerschlag A.R.
dc.contributor.authorHelmer Q.
dc.contributor.authorKarhunen V.
dc.contributor.authorKrapohl E.
dc.contributor.authorLu Y.
dc.contributor.authorvan der Most P.J.
dc.contributor.authorPalviainen T.
dc.contributor.authorSt Pourcain B.
dc.contributor.authorSeppälä I.
dc.contributor.authorSuarez A.
dc.contributor.authorVilor-Tejedor N.
dc.contributor.authorTiesler C.M.T.
dc.contributor.authorWang C.
dc.contributor.authorWills A.
dc.contributor.authorZhou A.
dc.contributor.authorAlemany S.
dc.contributor.authorBisgaard H.
dc.contributor.authorBønnelykke K.
dc.contributor.authorDavies G.E.
dc.contributor.authorHakulinen C.
dc.contributor.authorHenders A.K.
dc.contributor.authorHyppönen E.
dc.contributor.authorStokholm J.
dc.contributor.authorBartels M.
dc.contributor.authorHottenga J.J.
dc.contributor.authorHeinrich J.
dc.contributor.authorHewitt J.
dc.contributor.authorKeltikangas-Järvinen L.
dc.contributor.authorKorhonen T.
dc.contributor.authorKaprio J.
dc.contributor.authorLahti J.
dc.contributor.authorLahti-Pulkkinen M.
dc.contributor.authorLehtimäki T.
dc.contributor.authorMiddeldorp C.M.
dc.contributor.authorNajman J.M.
dc.contributor.authorPennell C.
dc.contributor.authorPower C.
dc.contributor.authorOldehinkel A.J.
dc.contributor.authorPlomin R.
dc.contributor.authorRäikkönen K.
dc.contributor.authorRaitakari Olli T.
dc.contributor.authorRimfeld K.
dc.contributor.authorSass L.
dc.contributor.authorSnieder H.
dc.contributor.authorStandl M.
dc.contributor.authorSunyer J.
dc.contributor.authorWilliams G.M.
dc.contributor.authorBakermans-Kranenburg M.J.
dc.contributor.authorBoomsma D.I.
dc.contributor.authorvan IJzendoorn M.H.
dc.contributor.authorHartman C.A.
dc.contributor.authorTiemeier H.
dc.contributor.organizationfi=InFLAMES Lippulaiva|en=InFLAMES Flagship|
dc.contributor.organizationfi=sydäntutkimuskeskus|en=Cardiovascular Medicine (CAPC)|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organizationfi=väestötutkimuskeskus|en=Centre for Population Health Research (POP Centre)|
dc.contributor.organization-code1.2.246.10.2458963.20.35734063924
dc.contributor.organization-code1.2.246.10.2458963.20.42471027641
dc.contributor.organization-code1.2.246.10.2458963.20.68445910604
dc.converis.publication-id176200492
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/176200492
dc.date.accessioned2025-08-28T00:45:52Z
dc.date.available2025-08-28T00:45:52Z
dc.description.abstract<p>Substantial genetic correlations have been reported across psychiatric disorders and numerous cross-disorder genetic variants have been detected. To identify the genetic variants underlying general psychopathology in childhood, we performed a genome-wide association study using a total psychiatric problem score. We analyzed 6,844,199 common SNPs in 38,418 school-aged children from 20 population-based cohorts participating in the EAGLE consortium. The SNP heritability of total psychiatric problems was 5.4% (SE = 0.01) and two loci reached genome-wide significance: rs10767094 and rs202005905. We also observed an association of SBF2, a gene associated with neuroticism in previous GWAS, with total psychiatric problems. The genetic effects underlying the total score were shared with common psychiatric disorders only (attention-deficit/hyperactivity disorder, anxiety, depression, insomnia) (rG > 0.49), but not with autism or the less common adult disorders (schizophrenia, bipolar disorder, or eating disorders) (rG < 0.01). Importantly, the total psychiatric problem score also showed at least a moderate genetic correlation with intelligence, educational attainment, wellbeing, smoking, and body fat (rG > 0.29). The results suggest that many common genetic variants are associated with childhood psychiatric symptoms and related phenotypes in general instead of with specific symptoms. Further research is needed to establish causality and pleiotropic mechanisms between related traits.<br></p>
dc.identifier.eissn1932-6203
dc.identifier.jour-issn1932-6203
dc.identifier.olddbid206362
dc.identifier.oldhandle10024/189389
dc.identifier.urihttps://www.utupub.fi/handle/11111/45553
dc.identifier.urlhttps://doi.org/10.1371/journal.pone.0273116
dc.identifier.urnURN:NBN:fi-fe2022091258521
dc.language.isoen
dc.okm.affiliatedauthorRaitakari, Olli
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherPublic Library of Science
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.articlenumbere0273116
dc.relation.doi10.1371/journal.pone.0273116
dc.relation.ispartofjournalPLoS ONE
dc.relation.issue8
dc.relation.volume17
dc.source.identifierhttps://www.utupub.fi/handle/10024/189389
dc.titleA genome-wide association study of total child psychiatric problems scores
dc.year.issued2022

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