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Research Article

A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene

  • Megan Y. Dennis,

    Affiliations: Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom, Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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  • Silvia Paracchini,

    Affiliation: Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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  • Thomas S. Scerri,

    Affiliation: Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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  • Ludmila Prokunina-Olsson,

    Affiliation: Laboratory of Translational Genomics, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Gaithersburg, Maryland, United States of America

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  • Julian C. Knight,

    Affiliation: Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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  • Richard Wade-Martins,

    Affiliation: Department of Physiology, Anatomy, and Genetics, University of Oxford, Oxford, United Kingdom

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  • Penny Coggill,

    Affiliation: Wellcome Trust Sanger Institute, Genome Campus, Hinxton, Cambridge, United Kingdom

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  • Stephan Beck,

    Affiliation: UCL Cancer Institute, University College London, London, United Kingdom

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  • Eric D. Green mail,

    egreen@nhgri.nih.gov (EDG); anthony.monaco@well.ox.ac.uk (APM)

    Affiliation: Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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  • Anthony P. Monaco mail

    egreen@nhgri.nih.gov (EDG); anthony.monaco@well.ox.ac.uk (APM)

    Affiliation: Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom

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  • Published: March 27, 2009
  • DOI: 10.1371/journal.pgen.1000436

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