Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/3088
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dc.contributor.authorEhli, E. A.en
dc.contributor.authorTong, X.en
dc.contributor.authorAndreassen, O. A.en
dc.contributor.authorBoomsma, D. I.en
dc.contributor.authorBrown, S. A.en
dc.contributor.authorBurt, S. A.en
dc.contributor.authorCopeland, W.en
dc.contributor.authorDick, D. M.en
dc.contributor.authorHarden, K. P.en
dc.contributor.authorHarris, K. M.en
dc.contributor.authorHartman, C. A.en
dc.contributor.authorHeinrich, J.en
dc.contributor.authorHewitt, J. K.en
dc.contributor.authorHopfer, C.en
dc.contributor.authorHypponen, E.en
dc.contributor.authorJarvelin, M. R.en
dc.contributor.authorKaprio, J.en
dc.contributor.authorKeltikangas-Järvinen, L.en
dc.contributor.authorKlump, K. L.en
dc.contributor.authorKrauter, K.en
dc.contributor.authorKuja-Halkola, R.en
dc.contributor.authorLarsson, H.en
dc.contributor.authorLehtimäki, T.en
dc.contributor.authorLichtenstein, P.en
dc.contributor.authorLundström, S.en
dc.contributor.authorMaes, H. H.en
dc.contributor.authorMagnus, P.en
dc.contributor.authorMunafò, M. R.en
dc.contributor.authorNajman, J. M.en
dc.contributor.authorNjølstad, P. R.en
dc.contributor.authorOldehinkel, A. J.en
dc.contributor.authorPennell, C. E.en
dc.contributor.authorPlomin, R.en
dc.contributor.authorReichborn-Kjennerud, T.en
dc.contributor.authorReynolds, C.en
dc.contributor.authorRose, R. J.en
dc.contributor.authorSmolen, A.en
dc.contributor.authorSnieder, H.en
dc.contributor.authorStallings, M.en
dc.contributor.authorStandl, M.en
dc.contributor.authorSunyer, J.en
dc.contributor.authorTiemeier, H.en
dc.contributor.authorWadsworth, S. J.en
dc.contributor.authorWall, T. L.en
dc.contributor.authorWilliams, G. M.en
dc.contributor.authorYstrøm, E.en
dc.contributor.authorNivard, M. G.en
dc.contributor.authorBartels, M.en
dc.contributor.authorMiddeldorp, C. M.en
dc.contributor.authorHenders, A. K.en
dc.contributor.authorWhitehouse, A. J. O.en
dc.contributor.authorJami, E. S.en
dc.contributor.authorHammerschlag, A. R.en
dc.contributor.authorIp, H. F.en
dc.contributor.authorAllegrini, A. G.en
dc.contributor.authorBenyamin, B.en
dc.contributor.authorBorder, R.en
dc.contributor.authorDiemer, E. W.en
dc.contributor.authorJiang, C.en
dc.contributor.authorKarhunen, V.en
dc.contributor.authorLu, Y.en
dc.contributor.authorLu, Q.en
dc.contributor.authorMallard, T. T.en
dc.contributor.authorMishra, P. P.en
dc.contributor.authorNolte, I. M.en
dc.contributor.authorPalviainen, T.en
dc.contributor.authorPeterson, R. E.en
dc.contributor.authorSallis, H. M.en
dc.contributor.authorShabalin, A. A.en
dc.contributor.authorTate, A. E.en
dc.contributor.authorThiering, E.en
dc.contributor.authorVilor-Tejedor, N.en
dc.contributor.authorWang, C.en
dc.contributor.authorZhou, A.en
dc.contributor.authorAdkins, D. E.en
dc.contributor.authorAlemany, S.en
dc.contributor.authorAsk, H.en
dc.contributor.authorChen, Q.en
dc.contributor.authorCorley, R. P.en
dc.contributor.authorEvans, L. M.en
dc.contributor.authorHavdahl, A.en
dc.contributor.authorHagenbeek, F. A.en
dc.contributor.authorHakulinen, C.en
dc.contributor.authorHottenga, J. J.en
dc.contributor.authorKorhonen, T.en
dc.contributor.authorMamun, A.en
dc.contributor.authorMarrington, S.en
dc.contributor.authorNeumann, A.en
dc.contributor.authorRimfeld, K.en
dc.contributor.authorRivadeneira, F.en
dc.contributor.authorSilberg, J. L.en
dc.contributor.authorvan Beijsterveldt, C. E.en
dc.contributor.authorVuoksimaa, E.en
dc.contributor.authorWhipp, A. M.en
dc.date.accessioned2022-11-07T23:38:30Z-
dc.date.available2022-11-07T23:38:30Z-
dc.date.issued2022en
dc.identifier.citation, 2022en
dc.identifier.otherRISen
dc.identifier.urihttp://dora.health.qld.gov.au/qldresearchjspui/handle/1/3088-
dc.description.abstractObjective: To investigate the genetic architecture of internalizing symptoms in childhood and adolescence. Method: In 22 cohorts, multiple univariate genome-wide association studies (GWASs) were performed using repeated assessments of internalizing symptoms, in a total of 64,561 children and adolescents between 3 and 18 years of age. Results were aggregated in meta-analyses that accounted for sample overlap, first using all available data, and then using subsets of measurements grouped by rater, age, and instrument. Results: The meta-analysis of overall internalizing symptoms (INToverall) detected no genome-wide significant hits and showed low single nucleotide polymorphism (SNP) heritability (1.66%, 95% CI = 0.84-2.48%, neffective = 132,260). Stratified analyses indicated rater-based heterogeneity in genetic effects, with self-reported internalizing symptoms showing the highest heritability (5.63%, 95% CI = 3.08%-8.18%). The contribution of additive genetic effects on internalizing symptoms appeared to be stable over age, with overlapping estimates of SNP heritability from early childhood to adolescence. Genetic correlations were observed with adult anxiety, depression, and the well-being spectrum (<br />rg<br /> > 0.70), as well as with insomnia, loneliness, attention-deficit/hyperactivity disorder, autism, and childhood aggression (range <br />rg<br /> = 0.42-0.60), whereas there were no robust associations with schizophrenia, bipolar disorder, obsessive-compulsive disorder, or anorexia nervosa. Conclusion: Genetic correlations indicate that childhood and adolescent internalizing symptoms share substantial genetic vulnerabilities with adult internalizing disorders and other childhood psychiatric traits, which could partially explain both the persistence of internalizing symptoms over time and the high comorbidity among childhood psychiatric traits. Reducing phenotypic heterogeneity in childhood samples will be key in paving the way to future GWAS success.L20177108082022-04-22 <br />en
dc.language.isoenen
dc.relation.ispartofJournal of the American Academy of Child and Adolescent Psychiatryen
dc.titleGenome-wide Association Meta-analysis of Childhood and Adolescent Internalizing Symptomsen
dc.typeArticleen
dc.identifier.doi10.1016/j.jaac.2021.11.035en
dc.subject.keywordscomorbidityen
dc.subject.keywordscontrolled studyen
dc.subject.keywordsdepressionen
dc.subject.keywordsfemaleen
dc.subject.keywordsgenetic associationen
dc.subject.keywordsgenetic correlationen
dc.subject.keywordsgenetic epidemiologyen
dc.subject.keywordsgenome-wide association studyen
dc.subject.keywordsheredityen
dc.subject.keywordswellbeingen
dc.subject.keywordsadolescenceadolescenten
dc.subject.keywordsadulten
dc.subject.keywordsaggressionen
dc.subject.keywordsanorexia nervosaen
dc.subject.keywordsanxietyen
dc.subject.keywordsarticleen
dc.subject.keywordsattention deficit hyperactivity disorderen
dc.subject.keywordsautismen
dc.subject.keywordsbipolar disorderen
dc.subject.keywordschilden
dc.subject.keywordschildhooden
dc.subject.keywordscohort analysisen
dc.subject.keywordssingle nucleotide polymorphismen
dc.subject.keywordsvulnerabilityen
dc.subject.keywordsheritabilityen
dc.subject.keywordshumanen
dc.subject.keywordsinfanten
dc.subject.keywordsinsomniaen
dc.subject.keywordsinternalizing disorderen
dc.subject.keywordslonelinessen
dc.subject.keywordsmaleen
dc.subject.keywordsmeta analysisen
dc.subject.keywordsmolecular geneticsen
dc.subject.keywordsobsessive compulsive disorderen
dc.subject.keywordsschizophreniaen
dc.relation.urlhttps://www.embase.com/search/results?subaction=viewrecord&id=L2017710808&from=exporthttp://dx.doi.org/10.1016/j.jaac.2021.11.035 |en
dc.identifier.risid3001en
local.message.claim2024-06-13T14:15:19.409+1000|||rp04980|||submit_approve|||dc_contributor_author|||None*
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
item.fulltextNo Fulltext-
Appears in Sites:Children's Health Queensland Publications
Queensland Health Publications
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