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Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue.
Wong, Chloe C Y; Smith, Rebecca G; Hannon, Eilis; Ramaswami, Gokul; Parikshak, Neelroop N; Assary, Elham; Troakes, Claire; Poschmann, Jeremie; Schalkwyk, Leonard C; Sun, Wenjie; Prabhakar, Shyam; Geschwind, Daniel H; Mill, Jonathan.
Afiliación
  • Wong CCY; King's College London, Institute of Psychiatry, Psychology and Neuroscience, De Crespigny Park, London, UK.
  • Smith RG; University of Exeter Medical School, University of Exeter, Exeter, UK.
  • Hannon E; University of Exeter Medical School, University of Exeter, Exeter, UK.
  • Ramaswami G; Center for Autism Research and Treatment, and Program in Neurobehavioral Genetics, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
  • Parikshak NN; Center for Autism Research and Treatment, and Program in Neurobehavioral Genetics, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
  • Assary E; Department of Biological and Experimental Psychology, School of Biological and Chemical Sciences, Queen Mary University of London, London, UK.
  • Troakes C; King's College London, Institute of Psychiatry, Psychology and Neuroscience, De Crespigny Park, London, UK.
  • Poschmann J; Centre de Recherche en Transplantation et Immunologie, Institut de Transplantation Urologie Néphrologie (ITUN), CHU Nantes, Inserm, Université de Nantes, Nantes, France.
  • Schalkwyk LC; School of Biological Sciences, University of Essex, Colchester UK.
  • Sun W; Computational and Systems Biology, Genome Institute of Singapore, Singapore.
  • Prabhakar S; Computational and Systems Biology, Genome Institute of Singapore, Singapore.
  • Geschwind DH; Center for Autism Research and Treatment, and Program in Neurobehavioral Genetics, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
  • Mill J; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, USA.
Hum Mol Genet ; 28(13): 2201-2211, 2019 07 01.
Article en En | MEDLINE | ID: mdl-31220268
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastorno Autístico / Lóbulo Temporal / Cerebelo / Corteza Prefrontal / Metilación de ADN Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastorno Autístico / Lóbulo Temporal / Cerebelo / Corteza Prefrontal / Metilación de ADN Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Reino Unido