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Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD.
Wang, Sheng; Wang, Belinda; Drury, Vanessa; Drake, Sam; Sun, Nawei; Alkhairo, Hasan; Arbelaez, Juan; Duhn, Clif; Bal, Vanessa H; Langley, Kate; Martin, Joanna; Hoekstra, Pieter J; Dietrich, Andrea; Xing, Jinchuan; Heiman, Gary A; Tischfield, Jay A; Fernandez, Thomas V; Owen, Michael J; O'Donovan, Michael C; Thapar, Anita; State, Matthew W; Willsey, A Jeremy.
Affiliation
  • Wang S; Department of Psychiatry and Behavioral Sciences, UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, 94143, USA.
  • Wang B; Department of Psychiatry and Behavioral Sciences, UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, 94143, USA.
  • Drury V; Department of Psychiatry and Behavioral Sciences, UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, 94143, USA.
  • Drake S; Department of Psychiatry and Behavioral Sciences, UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, 94143, USA.
  • Sun N; Department of Psychiatry and Behavioral Sciences, UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, 94143, USA.
  • Alkhairo H; Department of Psychiatry and Behavioral Sciences, UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, 94143, USA.
  • Arbelaez J; Department of Psychiatry and Behavioral Sciences, UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, 94143, USA.
  • Duhn C; Department of Psychiatry and Behavioral Sciences, UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, 94143, USA.
  • Bal VH; Graduate School of Applied and Professional Psychology, Rutgers University, New Brunswick, NJ, USA.
  • Langley K; Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, Wales, UK.
  • Martin J; School of Psychology, Cardiff University School of Medicine, Cardiff, Wales, UK.
  • Hoekstra PJ; Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, Wales, UK.
  • Dietrich A; University of Groningen, University Medical Center Groningen, Department of Child and Adolescent Psychiatry, Groningen, The Netherlands.
  • Xing J; Accare Child Study Center, Groningen, The Netherlands.
  • Heiman GA; University of Groningen, University Medical Center Groningen, Department of Child and Adolescent Psychiatry, Groningen, The Netherlands.
  • Tischfield JA; Accare Child Study Center, Groningen, The Netherlands.
  • Fernandez TV; Department of Genetics and the Human Genetics Institute of New Jersey, Rutgers, the State University of New Jersey, Piscataway, NJ, USA.
  • Owen MJ; Department of Genetics and the Human Genetics Institute of New Jersey, Rutgers, the State University of New Jersey, Piscataway, NJ, USA.
  • O'Donovan MC; Department of Genetics and the Human Genetics Institute of New Jersey, Rutgers, the State University of New Jersey, Piscataway, NJ, USA.
  • Thapar A; Yale Child Study Center and Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
  • State MW; Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, Wales, UK.
  • Willsey AJ; Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, Wales, UK.
Nat Commun ; 14(1): 8077, 2023 Dec 06.
Article in En | MEDLINE | ID: mdl-38057346
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Attention Deficit Disorder with Hyperactivity / Autistic Disorder / Tourette Syndrome / Neurodevelopmental Disorders / Autism Spectrum Disorder Limits: Female / Humans / Male Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2023 Document type: Article Affiliation country: United States Country of publication: United kingdom
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Attention Deficit Disorder with Hyperactivity / Autistic Disorder / Tourette Syndrome / Neurodevelopmental Disorders / Autism Spectrum Disorder Limits: Female / Humans / Male Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2023 Document type: Article Affiliation country: United States Country of publication: United kingdom