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Genome- wide association analyses of child genotype effects and parent- of- origin effects in specific language impairment

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dc.contributor.authorNudel, R.
dc.contributor.authorSimpson, N. H.
dc.contributor.authorBaird, G.
dc.contributor.authorO'Hare, A.
dc.contributor.authorConti-Ramsden, G.
dc.contributor.authorBolton, P. F.
dc.contributor.authorHennessy, E. R.
dc.contributor.authorRing, S. M.
dc.contributor.authorSmith, G. Davey
dc.contributor.authorFrancks, C.
dc.contributor.authorParacchini, S.
dc.contributor.authorMonaco, A. P.
dc.contributor.authorFisher, S. E.
dc.contributor.authorNewbury, D. F.
dc.contributor.authorSLI Consortium
dc.contributor.institutionUniversity of Aberdeen.Medical Educationen
dc.date.accessioned2015-02-06T16:37:01Z
dc.date.available2015-02-06T16:37:01Z
dc.date.issued2014-04
dc.descriptionFunded by •Medical Research Council. Grant Numbers: G1000569/1, MR/J003719/1, G0800523/86473 •University of Oxford Nuffield Department of Medicine Prize Studentship •Max Planck Society •Wellcome Trust. Grant Numbers: 060774, 076566, 090532/Z/09/Z, 092731 •National Institute of Health Research (UK) Senior Investigator award •Biomedical Research Centre in Mental Healthen
dc.description.statusPeer revieweden
dc.format.extent12
dc.format.extent1025630
dc.identifier45922067
dc.identifier559ea20a-5ae0-4cdc-9d25-618f47c94ee1
dc.identifier000333887500007
dc.identifier84897958382
dc.identifier.citationNudel, R, Simpson, N H, Baird, G, O'Hare, A, Conti-Ramsden, G, Bolton, P F, Hennessy, E R, Ring, S M, Smith, G D, Francks, C, Paracchini, S, Monaco, A P, Fisher, S E, Newbury, D F & SLI Consortium 2014, 'Genome- wide association analyses of child genotype effects and parent- of- origin effects in specific language impairment', Genes, Brain, and Behavior, vol. 13, no. 4, pp. 418-429. https://doi.org/10.1111/gbb.12127en
dc.identifier.doi10.1111/gbb.12127
dc.identifier.iss4en
dc.identifier.issn1601-1848
dc.identifier.urihttp://hdl.handle.net/2164/4249
dc.identifier.vol13en
dc.language.isoeng
dc.relation.ispartofGenes, Brain, and Behavioren
dc.subjectALSPACen
dc.subjectGWASen
dc.subjectimprintingen
dc.subjectneurodevelopmental disorderen
dc.subjectspecific language impairmenten
dc.subjectattention-deficit/hyperactivity disorderen
dc.subjectnucleotide exchange factoren
dc.subjectRHO-GTPASESen
dc.subjectcommunication checklisten
dc.subjecthyperactivity disorderen
dc.subjectdevelopmental dyslexiaen
dc.subjectsusceptibility locusen
dc.subjectsuggestive linkageen
dc.subjectmental-retardationen
dc.subjectreading-disabilityen
dc.subjectR Medicineen
dc.subjectMedical Research Council (MRC)en
dc.subjectG1000569/1en
dc.subjectG0800523/86473en
dc.subjectMR/J003719/1en
dc.subjectWellcome Trusten
dc.subject060774en
dc.subject076566en
dc.subject090532/Z/09/Zen
dc.subject092731en
dc.subject.lccRen
dc.titleGenome- wide association analyses of child genotype effects and parent- of- origin effects in specific language impairmenten
dc.typeJournal articleen

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