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Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.
Davies, Robert W; Fiksinski, Ania M; Breetvelt, Elemi J; Williams, Nigel M; Hooper, Stephen R; Monfeuga, Thomas; Bassett, Anne S; Owen, Michael J; Gur, Raquel E; Morrow, Bernice E; McDonald-McGinn, Donna M; Swillen, Ann; Chow, Eva W C; van den Bree, Marianne; Emanuel, Beverly S; Vermeesch, Joris R; van Amelsvoort, Therese; Arango, Celso; Armando, Marco; Campbell, Linda E; Cubells, Joseph F; Eliez, Stephan; Garcia-Minaur, Sixto; Gothelf, Doron; Kates, Wendy R; Murphy, Kieran C; Murphy, Clodagh M; Murphy, Declan G; Philip, Nicole; Repetto, Gabriela M; Shashi, Vandana; Simon, Tony J; Suñer, Damiàn Heine; Vicari, Stefano; Scherer, Stephen W; Bearden, Carrie E; Vorstman, Jacob A S.
Afiliación
  • Davies RW; Program in Genetics and Genome Biology and The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Fiksinski AM; Department of Statistics, University of Oxford, Oxford, UK.
  • Breetvelt EJ; Department of Psychiatry, Brain Center, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Williams NM; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
  • Hooper SR; Department of Psychiatry, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Monfeuga T; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.
  • Bassett AS; Department of Allied Health Sciences, School of Medicine, University of North Carolina-Chapel Hill, Chapel Hill, NC, USA.
  • Owen MJ; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.
  • Gur RE; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
  • Morrow BE; Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada.
  • McDonald-McGinn DM; The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.
  • Swillen A; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.
  • Chow EWC; Department of Psychiatry and Lifespan Brain Institute, Penn Medicine-CHOP, University of Pennsylvania, Philadelphia, PA, USA.
  • van den Bree M; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Emanuel BS; Division of Human Genetics, 22q and You Center, Clinical Genetics Center, and Section of Genetic Counseling, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Vermeesch JR; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA, USA.
  • van Amelsvoort T; Center for Human Genetics, University Hospital Gasthuisberg, Leuven, Belgium.
  • Arango C; Department of Human Genetics KU Leuven, Leuven, Belgium.
  • Armando M; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
  • Campbell LE; Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada.
  • Cubells JF; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.
  • Eliez S; Division of Human Genetics, 22q and You Center, Clinical Genetics Center, and Section of Genetic Counseling, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Garcia-Minaur S; Center for Human Genetics, University Hospital Gasthuisberg, Leuven, Belgium.
  • Gothelf D; Department of Psychiatry and Neuropsychology, Maastricht University, Maastricht, the Netherlands.
  • Kates WR; Department of Child and Adolescent Psychiatry, Institute of Psychiatry and Mental Health, Hospital General Universitario Gregorio Marañón, IiSGM, CIBERSAM, School of Medicine, Universidad Complutense, Madrid, Spain.
  • Murphy KC; Developmental Imaging and Psychopathology, Department of Psychiatry, University of Geneva, Geneva, Switzerland.
  • Murphy CM; School of Psychology, University of Newcastle, Newcastle, Australia.
  • Murphy DG; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.
  • Philip N; Emory Autism Center, Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA.
  • Repetto GM; Developmental Imaging and Psychopathology, Department of Psychiatry, University of Geneva, Geneva, Switzerland.
  • Shashi V; Institute of Medical and Molecular Genetics (INGEMM), La Paz University Hospital, Madrid, Spain.
  • Simon TJ; The Child Psychiatry Division, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Israel.
  • Suñer DH; Sackler Faculty of Medicine and Sagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel.
  • Vicari S; Department of Psychiatry and Behavioral Sciences, SUNY Upstate Medical University, Syracuse, NY, USA.
  • Scherer SW; Department of Psychiatry, Royal College of Surgeons in Ireland, Beaumont Hospital, Dublin, Ireland.
  • Bearden CE; Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology & Neuroscience (IoPPN), King's College London, London, UK.
  • Vorstman JAS; Département de Génétique Médicale, APHM, CHU Timone Enfants, Marseille, France.
Nat Med ; 26(12): 1912-1918, 2020 12.
Article en En | MEDLINE | ID: mdl-33169016
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esquizofrenia / Variación Genética / Síndrome de DiGeorge / Discapacidad Intelectual Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Nat Med Asunto de la revista: BIOLOGIA MOLECULAR / MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Canadá
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esquizofrenia / Variación Genética / Síndrome de DiGeorge / Discapacidad Intelectual Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Nat Med Asunto de la revista: BIOLOGIA MOLECULAR / MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Canadá