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 ,

  * E-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

  * E-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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