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dc.date.accessioned2015-10-07T08:09:17Z
dc.date.available2015-10-07T08:09:17Z
dc.date.created2015-09-28T14:04:36Z
dc.date.issued2015
dc.identifier.citationChen, Chi-Hua Peng, Qian Schork, Andrew J. Lo, Min-Tzu Fan, Chun-Chieh Wang, Yunpeng Desikan, Rahul S. Bettella, Franscesco Hagler, Donald J. Westlye, Lars Tjelta Kremen, William S. Jernigan, Terry L. Le Hellard, Stephanie Steen, Vidar Martin Espeseth, Thomas Huentelman, Matt Håberg, Asta Agartz, Ingrid Djurovic, Srdjan Andreassen, Ole Andreas Schork, Nicholas Dale, Anders . Large-scale genomics unveil polygenic architecture of human cortical surface area. Nature Communications. 2015, 6:7549
dc.identifier.urihttp://hdl.handle.net/10852/46212
dc.description.abstractLittle is known about how genetic variation contributes to neuroanatomical variability, and whether particular genomic regions comprising genes or evolutionarily conserved elements are enriched for effects that influence brain morphology. Here, we examine brain imaging and single-nucleotide polymorphisms (SNPs) data from ~2,700 individuals. We show that a substantial proportion of variation in cortical surface area is explained by additive effects of SNPs dispersed throughout the genome, with a larger heritable effect for visual and auditory sensory and insular cortices (h2~0.45). Genome-wide SNPs collectively account for, on average, about half of twin heritability across cortical regions (N=466 twins). We find enriched genetic effects in or near genes. We also observe that SNPs in evolutionarily more conserved regions contributed significantly to the heritability of cortical surface area, particularly, for medial and temporal cortical regions. SNPs in less conserved regions contributed more to occipital and dorsolateral prefrontal cortices.en_US
dc.languageEN
dc.language.isoenen_US
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleLarge-scale genomics unveil polygenic architecture of human cortical surface areaen_US
dc.typeJournal articleen_US
dc.creator.authorChen, Chi-Hua
dc.creator.authorPeng, Qian
dc.creator.authorSchork, Andrew J.
dc.creator.authorLo, Min-Tzu
dc.creator.authorFan, Chun-Chieh
dc.creator.authorWang, Yunpeng
dc.creator.authorDesikan, Rahul S.
dc.creator.authorBettella, Franscesco
dc.creator.authorHagler, Donald J.
dc.creator.authorWestlye, Lars Tjelta
dc.creator.authorKremen, William S.
dc.creator.authorJernigan, Terry L.
dc.creator.authorLe Hellard, Stephanie
dc.creator.authorSteen, Vidar Martin
dc.creator.authorEspeseth, Thomas
dc.creator.authorHuentelman, Matt
dc.creator.authorHåberg, Asta
dc.creator.authorAgartz, Ingrid
dc.creator.authorDjurovic, Srdjan
dc.creator.authorAndreassen, Ole Andreas
dc.creator.authorSchork, Nicholas
dc.creator.authorDale, Anders
cristin.unitcode185,53,10,70
cristin.unitnameNORMENT part UiO
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin1276092
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Nature Communications&rft.volume=6:7549&rft.spage=&rft.date=2015
dc.identifier.jtitleNature Communications
dc.identifier.volume6:7549
dc.identifier.doihttp://dx.doi.org/10.1038/ncomms8549
dc.identifier.urnURN:NBN:no-50369
dc.subject.nviVDP::Medisinsk genetikk: 714
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn2041-1723
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/46212/2/ncomms8549.pdf
dc.type.versionPublishedVersion


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