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Genome-wide analysis identifies a role for common copy number variants in specific language impairment.

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Title: Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
Authors: Simpson NH; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK., Ceroni F; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK., Reader RH; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK., Covill LE; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK., Knight JC; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK., Hennessy ER; University Child Health and DMDE, University of Aberdeen, Aberdeen, UK., Bolton PF; Departments of Child and Adolescent Psychiatry, Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, London, UK., Conti-Ramsden G; School of Psychological Sciences, University of Manchester, Manchester, UK., O'Hare A; Department of Reproductive and Developmental Sciences, University of Edinburgh, Edinburgh, UK., Baird G; Children's Neurosciences Department, Evelina Children's Hospital and King's Health Partners, London, UK., Fisher SE; Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands., Newbury DF; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.; St John's College, University of Oxford, Oxford, UK.
Corporate Authors: SLI Consortium
Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2015 Oct; Vol. 23 (10), pp. 1370-7. Date of Electronic Publication: 2015 Jan 14.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
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  Data: <searchLink fieldCode="AU" term="%22Simpson+NH%22">Simpson NH</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22Ceroni+F%22">Ceroni F</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22Reader+RH%22">Reader RH</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22Covill+LE%22">Covill LE</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22Knight+JC%22">Knight JC</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22Hennessy+ER%22">Hennessy ER</searchLink>; University Child Health and DMDE, University of Aberdeen, Aberdeen, UK.<br /><searchLink fieldCode="AU" term="%22Bolton+PF%22">Bolton PF</searchLink>; Departments of Child and Adolescent Psychiatry, Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, London, UK.<br /><searchLink fieldCode="AU" term="%22Conti-Ramsden+G%22">Conti-Ramsden G</searchLink>; School of Psychological Sciences, University of Manchester, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22O'Hare+A%22">O'Hare A</searchLink>; Department of Reproductive and Developmental Sciences, University of Edinburgh, Edinburgh, UK.<br /><searchLink fieldCode="AU" term="%22Baird+G%22">Baird G</searchLink>; Children's Neurosciences Department, Evelina Children's Hospital and King's Health Partners, London, UK.<br /><searchLink fieldCode="AU" term="%22Fisher+SE%22">Fisher SE</searchLink>; Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Newbury+DF%22">Newbury DF</searchLink>; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.; St John's College, University of Oxford, Oxford, UK.
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  Data: <searchLink fieldCode="JN" term="%229302235%22">European journal of human genetics : EJHG</searchLink> [Eur J Hum Genet] 2015 Oct; Vol. 23 (10), pp. 1370-7. <i>Date of Electronic Publication: </i>2015 Jan 14.
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