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dc.contributor.authorSimpson, Nuala H
dc.contributor.authorCeroni, Fabiola
dc.contributor.authorReader, Rose H
dc.contributor.authorCovill, Laura E
dc.contributor.authorKnight, Julian C
dc.contributor.authorHennessy, Elizabeth R
dc.contributor.authorBolton, Patrick F
dc.contributor.authorConti-Ramsden, Gina
dc.contributor.authorO'Hare, Anne
dc.contributor.authorBaird, Gillian
dc.contributor.authorFisher, Simon E
dc.contributor.authorNewbury, Dianne F
dc.contributor.authorThe SLI Consortium
dc.date.accessioned2015-11-20T15:49:01Z
dc.date.available2015-11-20T15:49:01Z
dc.date.issued2015
dc.identifier.citationSimpson , N H , Ceroni , F , Reader , R H , Covill , L E , Knight , J C , Hennessy , E R , Bolton , P F , Conti-Ramsden , G , O'Hare , A , Baird , G , Fisher , S E , Newbury , D F & The SLI Consortium 2015 , ' Genome-wide analysis identifies a role for common copy number variants in specific language impairment ' , EJHG : European journal of human genetics : the official journal of the European Society of Human Genetics. , vol. 23 , no. 10 , pp. 1370-1377 . https://doi.org/10.1038/ejhg.2014.296en
dc.identifier.issn1018-4813
dc.identifier.otherPURE: 48403425
dc.identifier.otherPURE UUID: 1fb1688c-bd51-409c-9621-dad376389275
dc.identifier.otherPubMed: 25585696
dc.identifier.otherScopus: 84938993365
dc.identifier.urihttp://hdl.handle.net/2164/5235
dc.descriptionAcknowledgements We would like to thank all the families, professionals and individuals who participated in this research. DNF is an MRC Career Development Fellow and a Junior Research Fellow at St John’s College, University of Oxford. The work of the Newbury lab is funded by the Medical Research Council (G1000569/1 and MR/J003719/1). The collection of the SLIC samples was supported by the Wellcome Trust (060774 and 076566). The genotyping of samples was funded by the Max Planck Society. Recruitment of controls was supported by the Wellcome Trust (074318 and 088891), the European Research Council under the European Union’s Seventh Framework Programme (FP7/2007-2013; 281824) and the National Institute for Health Research (NIHR), Oxford Biomedical Research Centre. FC was supported by the PhD Programme in Molecular and Cellular Biology of the University of Bologna. PFB is supported by a National Institute of Health Research (UK) Senior Investigator award and the Biomedical Research Centre in Mental Health at the South London and Maudsley NHS Trust Hospital, London, UK. The work of the Wellcome Trust Centre in Oxford is supported by the Wellcome Trust (090532/Z/09/Z).en
dc.format.extent8
dc.language.isoeng
dc.relation.ispartofEJHG : European journal of human genetics : the official journal of the European Society of Human Genetics.en
dc.rightsThis work is licensed under a Creative Commons Attribution 3.0 Unported License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/.en
dc.subjectQH426 Geneticsen
dc.subject.lccQH426en
dc.titleGenome-wide analysis identifies a role for common copy number variants in specific language impairmenten
dc.typeJournal articleen
dc.contributor.institutionUniversity of Aberdeen.Medical Educationen
dc.description.statusPeer revieweden
dc.description.versionPublisher PDFen
dc.identifier.doihttps://doi.org/10.1038/ejhg.2014.296


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