Please use this identifier to cite or link to this item: https://doi.org/10.1038/tp.2016.246
DC FieldValue
dc.titleMolecular genetic aetiology of general cognitive function is enriched in evolutionarily conserved regions
dc.contributor.authorHill, W.D
dc.contributor.authorDavies, G
dc.contributor.authorHarris, S.E
dc.contributor.authorHagenaars, S.P
dc.contributor.authorLiewald, D.C
dc.contributor.authorPenke, L
dc.contributor.authorGale, C.R
dc.contributor.authorDeary, I.J
dc.contributor.authorDebette, S
dc.contributor.authorVerbaas, C.I
dc.contributor.authorBressler, J
dc.contributor.authorSchuur, M
dc.contributor.authorSmith, A.V
dc.contributor.authorBis, J.C
dc.contributor.authorBennett, D.A
dc.contributor.authorIkram, M.A
dc.contributor.authorLauner, L.J
dc.contributor.authorFitzpatrick, A.L
dc.contributor.authorSeshadri, S
dc.contributor.authorVan Duijn, C.M
dc.contributor.authorMosley, T.H
dc.date.accessioned2020-11-17T06:42:16Z
dc.date.available2020-11-17T06:42:16Z
dc.date.issued2016
dc.identifier.citationHill, W.D, Davies, G, Harris, S.E, Hagenaars, S.P, Liewald, D.C, Penke, L, Gale, C.R, Deary, I.J, Debette, S, Verbaas, C.I, Bressler, J, Schuur, M, Smith, A.V, Bis, J.C, Bennett, D.A, Ikram, M.A, Launer, L.J, Fitzpatrick, A.L, Seshadri, S, Van Duijn, C.M, Mosley, T.H (2016). Molecular genetic aetiology of general cognitive function is enriched in evolutionarily conserved regions. Translational Psychiatry 6 (12) : e980. ScholarBank@NUS Repository. https://doi.org/10.1038/tp.2016.246
dc.identifier.issn2158-3188
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/183585
dc.description.abstractDifferences in general cognitive function have been shown to be partly heritable and to show genetic correlations with several psychiatric and physical disease states. However, to date, few single-nucleotide polymorphisms (SNPs) have demonstrated genome-wide significance, hampering efforts aimed at determining which genetic variants are most important for cognitive function and which regions drive the genetic associations between cognitive function and disease states. Here, we combine multiple large genome-wide association study (GWAS) data sets, from the CHARGE cognitive consortium (n =53 949) and UK Biobank (n=36 035), to partition the genome into 52 functional annotations and an additional 10 annotations describing tissuespecific histone marks. Using stratified linkage disequilibrium score regression we show that, in two measures of cognitive function, SNPs associated with cognitive function cluster in regions of the genome that are under evolutionary negative selective pressure. These conserved regions contained ?2.6% of the SNPs from each GWAS but accounted for ? 40% of the SNP-based heritability. The results suggest that the search for causal variants associated with cognitive function, and those variants that exert a pleiotropic effect between cognitive function and health, will be facilitated by examining these enriched regions. © The Author(s) 2016.
dc.publisherSpringer Nature
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjecthistone
dc.subjectArticle
dc.subjectbiobank
dc.subjectcognition
dc.subjectgene linkage disequilibrium
dc.subjectgenome
dc.subjectgenome-wide association study
dc.subjectmolecular genetics
dc.subjectpleiotropy
dc.subjectsingle nucleotide polymorphism
dc.subjectaged
dc.subjectbrain
dc.subjectcognition
dc.subjectconserved sequence
dc.subjectfemale
dc.subjectgenetic variation
dc.subjectgenetics
dc.subjecthuman
dc.subjectmale
dc.subjectmiddle aged
dc.subjectmolecular biology
dc.subjectmolecular evolution
dc.subjectneuropsychological test
dc.subjectphenotype
dc.subjectphysiology
dc.subjectproblem solving
dc.subjectstatistics
dc.subjectAged
dc.subjectBrain
dc.subjectCognition
dc.subjectConserved Sequence
dc.subjectEvolution, Molecular
dc.subjectFemale
dc.subjectGenetic Variation
dc.subjectGenome-Wide Association Study
dc.subjectHumans
dc.subjectLinkage Disequilibrium
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectMolecular Biology
dc.subjectNeuropsychological Tests
dc.subjectPhenotype
dc.subjectPolymorphism, Single Nucleotide
dc.subjectProblem Solving
dc.subjectStatistics as Topic
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1038/tp.2016.246
dc.description.sourcetitleTranslational Psychiatry
dc.description.volume6
dc.description.issue12
dc.description.pagee980
dc.published.statePublished
Appears in Collections:Elements
Staff Publications

Show simple item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_1038_tp_2016_246.pdf399.29 kBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons