Your browser doesn't support javascript.
loading
Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study.
Wolstencroft, Jeanne; Wicks, Francesca; Srinivasan, Ramya; Wynn, Sarah; Ford, Tamsin; Baker, Kate; Chawner, Samuel J R A; Hall, Jeremy; van den Bree, Marianne B M; Owen, Michael J; Skuse, David; Raymond, F Lucy.
Afiliação
  • Wolstencroft J; NIHR BRC Great Ormond Street Institute of Child Health, University College London, London, UK.
  • Wicks F; School of Clinical Medicine, University of Cambridge, Cambridge, UK.
  • Srinivasan R; NIHR BRC Great Ormond Street Institute of Child Health, University College London, London, UK; UCL Division of Psychiatry, University College London, London, UK.
  • Wynn S; UNIQUE Charity, Oxted, UK.
  • Ford T; School of Clinical Medicine, University of Cambridge, Cambridge, UK.
  • Baker K; School of Clinical Medicine, University of Cambridge, Cambridge, UK; Cambridge University Hospitals NHS Foundation Trust, Cambridge Biomedical Campus, Cambridge, UK; MRC Cognition and Brain Sciences Unit, University of Cambridge, Cambridge, UK.
  • Chawner SJRA; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK; Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff, UK; Cardiff University Centre for Human Developm
  • Hall J; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK; Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff, UK.
  • van den Bree MBM; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK; Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff, UK.
  • Owen MJ; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK; Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff, UK.
  • Skuse D; NIHR BRC Great Ormond Street Institute of Child Health, University College London, London, UK.
  • Raymond FL; School of Clinical Medicine, University of Cambridge, Cambridge, UK; Cambridge University Hospitals NHS Foundation Trust, Cambridge Biomedical Campus, Cambridge, UK; NIHR Bioresource, Cambridge Biomedical Campus, Cambridge, UK. Electronic address: flr24@cam.ac.uk.
Lancet Psychiatry ; 9(9): 715-724, 2022 09.
Article em En | MEDLINE | ID: mdl-35932790
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno do Espectro Autista / Deficiência Intelectual Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: Lancet Psychiatry Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno do Espectro Autista / Deficiência Intelectual Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: Lancet Psychiatry Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido