Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/22063
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dc.contributor.authorVinkhuyzen, A A Een
dc.contributor.authorPedersen, N Len
dc.contributor.authorPayton, Aen
dc.contributor.authorHoran, Men
dc.contributor.authorOllier, Wen
dc.contributor.authorPendleton, Nen
dc.contributor.authorDeary, I Jen
dc.contributor.authorMontgomery, G Wen
dc.contributor.authorMartin, N Gen
dc.contributor.authorVisscher, P Men
dc.contributor.authorWray, N Ren
dc.contributor.authorYang, Jen
dc.contributor.authorLee, Sang Hongen
dc.contributor.authorMagnusson, P K Een
dc.contributor.authorIacono, W Gen
dc.contributor.authorMcGue, Men
dc.contributor.authorMadden, P A Fen
dc.contributor.authorHeath, A Cen
dc.contributor.authorLuciano, Men
dc.date.accessioned2017-10-27T14:40:00Z-
dc.date.issued2012-
dc.identifier.citationTranslational Psychiatry, 2(4), p. 1-7en
dc.identifier.issn2158-3188en
dc.identifier.urihttps://hdl.handle.net/1959.11/22063-
dc.description.abstractThe personality traits of neuroticism and extraversion are predictive of a number of social and behavioural outcomes and psychiatric disorders. Twin and family studies have reported moderate heritability estimates for both traits. Few associations have been reported between genetic variants and neuroticism/extraversion, but hardly any have been replicated. Moreover, the ones that have been replicated explain only a small proportion of the heritability (oB2%). Using genome-wide single-nucleotide polymorphism (SNP) data from B12 000 unrelated individuals we estimated the proportion of phenotypic variance explained by variants in linkage disequilibrium with common SNPs as 0.06 (s.e. ¼ 0.03) for neuroticism and 0.12 (s.e. ¼ 0.03) for extraversion. In an additional series of analyses in a family-based sample, we show that while for both traits B45% of the phenotypic variance can be explained by pedigree data (that is, expected genetic similarity) one third of this can be explained by SNP data (that is, realized genetic similarity). A part of the so-called 'missing heritability' has now been accounted for, but some of the reported heritability is still unexplained. Possible explanations for the remaining missing heritability are that:(i) rare variants that are not captured by common SNPs on current genotype platforms make a major contribution; and/ or (ii) the estimates of narrow sense heritability from twin and family studies are biased upwards, for example, by not properly accounting for nonadditive genetic factors and/or (common) environmental factors.en
dc.languageenen
dc.publisherNature Publishing Groupen
dc.relation.ispartofTranslational Psychiatryen
dc.titleCommon SNPs explain some of the variation in the personality dimensions of neuroticism and extraversionen
dc.typeJournal Articleen
dc.identifier.doi10.1038/tp.2012.27en
dcterms.accessRightsGolden
dc.subject.keywordsGene Expression (incl. Microarray and other genome-wide approaches)en
local.contributor.firstnameA A Een
local.contributor.firstnameN Len
local.contributor.firstnameAen
local.contributor.firstnameMen
local.contributor.firstnameWen
local.contributor.firstnameNen
local.contributor.firstnameI Jen
local.contributor.firstnameG Wen
local.contributor.firstnameN Gen
local.contributor.firstnameP Men
local.contributor.firstnameN Ren
local.contributor.firstnameJen
local.contributor.firstnameSang Hongen
local.contributor.firstnameP K Een
local.contributor.firstnameW Gen
local.contributor.firstnameMen
local.contributor.firstnameP A Fen
local.contributor.firstnameA Cen
local.contributor.firstnameMen
local.subject.for2008060405 Gene Expression (incl. Microarray and other genome-wide approaches)en
local.subject.seo2008920110 Inherited Diseases (incl. Gene Therapy)en
local.profile.schoolSchool of Environmental and Rural Scienceen
local.profile.emailslee38@une.edu.auen
local.output.categoryC1en
local.record.placeauen
local.record.institutionUniversity of New Englanden
local.identifier.epublicationsrecordune-20171024-181855en
local.publisher.placeUnited Kingdomen
local.format.startpage1en
local.format.endpage7en
local.url.openhttps://www.nature.com/tp/journal/v2/n4/full/tp201227a.htmlen
local.peerreviewedYesen
local.identifier.volume2en
local.identifier.issue4en
local.access.fulltextYesen
local.contributor.lastnameVinkhuyzenen
local.contributor.lastnamePedersenen
local.contributor.lastnamePaytonen
local.contributor.lastnameHoranen
local.contributor.lastnameOllieren
local.contributor.lastnamePendletonen
local.contributor.lastnameDearyen
local.contributor.lastnameMontgomeryen
local.contributor.lastnameMartinen
local.contributor.lastnameVisscheren
local.contributor.lastnameWrayen
local.contributor.lastnameYangen
local.contributor.lastnameLeeen
local.contributor.lastnameMagnussonen
local.contributor.lastnameIaconoen
local.contributor.lastnameMcGueen
local.contributor.lastnameMaddenen
local.contributor.lastnameHeathen
local.contributor.lastnameLucianoen
dc.identifier.staffune-id:slee38en
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local.identifier.unepublicationidune:22253en
local.identifier.handlehttps://hdl.handle.net/1959.11/22063en
dc.identifier.academiclevelAcademicen
local.title.maintitleCommon SNPs explain some of the variation in the personality dimensions of neuroticism and extraversionen
local.output.categorydescriptionC1 Refereed Article in a Scholarly Journalen
local.search.authorVinkhuyzen, A A Een
local.search.authorPedersen, N Len
local.search.authorPayton, Aen
local.search.authorHoran, Men
local.search.authorOllier, Wen
local.search.authorPendleton, Nen
local.search.authorDeary, I Jen
local.search.authorMontgomery, G Wen
local.search.authorMartin, N Gen
local.search.authorVisscher, P Men
local.search.authorWray, N Ren
local.search.authorYang, Jen
local.search.authorLee, Sang Hongen
local.search.authorMagnusson, P K Een
local.search.authorIacono, W Gen
local.search.authorMcGue, Men
local.search.authorMadden, P A Fen
local.search.authorHeath, A Cen
local.search.authorLuciano, Men
local.uneassociationUnknownen
local.year.published2012en
local.subject.for2020310505 Gene expression (incl. microarray and other genome-wide approaches)en
local.subject.seo2020200101 Diagnosis of human diseases and conditionsen
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