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Discovery of 42 genome-wide significant loci associated with dyslexia.
Doust, Catherine; Fontanillas, Pierre; Eising, Else; Gordon, Scott D; Wang, Zhengjun; Alagöz, Gökberk; Molz, Barbara; Pourcain, Beate St; Francks, Clyde; Marioni, Riccardo E; Zhao, Jingjing; Paracchini, Silvia; Talcott, Joel B; Monaco, Anthony P; Stein, John F; Gruen, Jeffrey R; Olson, Richard K; Willcutt, Erik G; DeFries, John C; Pennington, Bruce F; Smith, Shelley D; Wright, Margaret J; Martin, Nicholas G; Auton, Adam; Bates, Timothy C; Fisher, Simon E; Luciano, Michelle.
Afiliación
  • Doust C; Department of Psychology, University of Edinburgh, Edinburgh, UK.
  • Fontanillas P; 23andMe, Inc., Sunnyvale, CA, USA.
  • Eising E; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands.
  • Gordon SD; Genetic Epidemiology Laboratory, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Wang Z; School of Psychology, Shaanxi Normal University and Shaanxi Key Research Center of Child Mental and Behavioral Health, Xi'an, China.
  • Alagöz G; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands.
  • Molz B; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands.
  • Pourcain BS; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands.
  • Francks C; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, the Netherlands.
  • Marioni RE; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
  • Zhao J; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands.
  • Paracchini S; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, the Netherlands.
  • Talcott JB; Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.
  • Monaco AP; School of Psychology, Shaanxi Normal University and Shaanxi Key Research Center of Child Mental and Behavioral Health, Xi'an, China.
  • Stein JF; School of Medicine, University of St Andrews, St Andrews, UK.
  • Gruen JR; Institute of Health and Neurodevelopment, Aston University, Birmingham, UK.
  • Olson RK; Office of the President, Tufts University, Medford, MA, USA.
  • Willcutt EG; Department of Physiology, Anatomy and Genetics, Oxford University, Oxford, UK.
  • DeFries JC; Departments of Pediatrics and Genetics, Yale Medical School, New Haven, CT, USA.
  • Pennington BF; Department of Psychology and Neuroscience, University of Colorado, Boulder, CO, USA.
  • Smith SD; Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA.
  • Wright MJ; Department of Psychology and Neuroscience, University of Colorado, Boulder, CO, USA.
  • Martin NG; Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA.
  • Auton A; Department of Psychology and Neuroscience, University of Colorado, Boulder, CO, USA.
  • Bates TC; Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA.
  • Fisher SE; Department of Psychology, University of Denver, Denver, CO, USA.
  • Luciano M; Department of Neurological Sciences, College of Medicine, University of Nebraska Medical Center, Omaha, NE, USA.
Nat Genet ; 54(11): 1621-1629, 2022 11.
Article en En | MEDLINE | ID: mdl-36266505
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dislexia / Estudio de Asociación del Genoma Completo Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adult / Child / Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dislexia / Estudio de Asociación del Genoma Completo Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adult / Child / Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos