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dc.contributor.authorHill, W. D.
dc.contributor.authorDavies, G.
dc.contributor.authorLiewald, D. C.
dc.contributor.authorPayton, A.
dc.contributor.authorMcNeil, C. J.
dc.contributor.authorWhalley, L. J.
dc.contributor.authorHoran, M.
dc.contributor.authorOllier, W.
dc.contributor.authorStarr, J. M.
dc.contributor.authorPendleton, N.
dc.contributor.authorHansel, N. K.
dc.contributor.authorMontgomery, G. W.
dc.contributor.authorMedland, S. E.
dc.contributor.authorMartin, N. G.
dc.contributor.authorWright, M. J.
dc.contributor.authorBates, T. C.
dc.contributor.authorDeary, I. J.
dc.date.accessioned2016-02-29T14:00:14Z
dc.date.available2016-02-29T14:00:14Z
dc.date.issued2016-01
dc.identifier63074741
dc.identifier715cd36e-814c-42bf-bbb9-67223cf59b6a
dc.identifier84953911588
dc.identifier.citationHill , W D , Davies , G , Liewald , D C , Payton , A , McNeil , C J , Whalley , L J , Horan , M , Ollier , W , Starr , J M , Pendleton , N , Hansel , N K , Montgomery , G W , Medland , S E , Martin , N G , Wright , M J , Bates , T C & Deary , I J 2016 , ' Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences ' , Intelligence , vol. 54 , pp. 80-89 . https://doi.org/10.1016/j.intell.2015.11.005en
dc.identifier.issn0160-2896
dc.identifier.urihttp://hdl.handle.net/2164/5569
dc.descriptionAcknowledgements We thank the cohort participants who contributed to these studies and the research staff who collected phenotypic data. Genotyping of the CAGES cohorts and the analyses conducted here were supported by the UK's Biotechnology and Biological Sciences Research Council (BBSRC). Phenotype collection in the Lothian Birth Cohort 1921 was supported by the BBSRC, The Royal Society and The Chief Scientist Office of the Scottish Government. Phenotype collection in the Lothian Birth Cohort 1936 was supported by Research Into Ageing (continues as part of Age UK's The Disconnected Mind project). Phenotype collection in the Aberdeen Birth Cohort 1936 was supported by BBSRC, the Wellcome Trust and Alzheimer's Research UK. Phenotype collection in the Manchester and Newcastle Longitudinal Studies of Cognitive Ageing cohorts was supported by Social Science Research Council, Medical Research Council, Economic and Social Research Council, Research Into Ageing, Wellcome Trust and Unilever plc. The work was undertaken in The University of Edinburgh Centre for Cognitive Ageing and Cognitive Epidemiology, part of the cross council Lifelong Health and Wellbeing Initiative (MR/K026992/1). Funding from the BBSRC, EPSRC, ESRC and MRC is gratefully acknowledged. Authors MJ Wright, N K Hansell, SE Medland, NG Martin, and GW Montgomery would like to acknowledge and thank their twin sample for their participation; the Australian Research Council (ARC) for supporting data collection (A7960034, A79906588, A79801419, DP0212016, DP0343921, DP0664638, DP1093900), and the National Health & Medical Research Council (NHMRC) for funding genotyping (Medical Bioinformatics Genomics Proteomics Programme, 389891). SE Medland is supported by an ARC Future Fellowship. Statistical analyses were carried out on the GenEpi Cluster which is financially supported by contributions from grants from the NHMRC (389892;496682;496688;496739;613672) and ARC (FT0991022;FT0991360).en
dc.format.extent10
dc.format.extent423993
dc.language.isoeng
dc.relation.ispartofIntelligenceen
dc.subjectGene set analysisen
dc.subjectGeneticsen
dc.subjectGWASen
dc.subjectIntellectual disabilitiesen
dc.subjectRC0321 Neuroscience. Biological psychiatry. Neuropsychiatryen
dc.subjectExperimental and Cognitive Psychologyen
dc.subjectArts and Humanities (miscellaneous)en
dc.subjectDevelopmental and Educational Psychologyen
dc.subjectMedical Research Council (MRC)en
dc.subjectBiotechnology and Biological Sciences Research Council (BBSRC)en
dc.subjectEngineering and Physical Sciences Research Council (EPSRC)en
dc.subjectEconomic and Social Research Council (ESRC)en
dc.subject.lccRC0321en
dc.titleExamining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differencesen
dc.typeJournal articleen
dc.contributor.institutionUniversity of Aberdeen.Applied Medicineen
dc.contributor.institutionUniversity of Aberdeen.Institute of Medical Sciencesen
dc.contributor.institutionUniversity of Aberdeen.Aberdeen Biomedical Imaging Centreen
dc.description.statusPeer revieweden
dc.identifier.doi10.1016/j.intell.2015.11.005
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=84953911588&partnerID=8YFLogxKen


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