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Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia.
Lin, Jhih-Rong; Zhao, Yingjie; Jabalameli, M Reza; Nguyen, Nha; Mitra, Joydeep; Swillen, Ann; Vorstman, Jacob A S; Chow, Eva W C; van den Bree, Marianne; Emanuel, Beverly S; Vermeesch, Joris R; Owen, Michael J; Williams, Nigel M; Bassett, Anne S; McDonald-McGinn, Donna M; Gur, Raquel E; Bearden, Carrie E; Morrow, Bernice E; Lachman, Herbert M; Zhang, Zhengdong D.
Afiliação
  • Lin JR; Department of Genetics, Albert Einstein College of Medicine, New York, NY, USA.
  • Zhao Y; Department of Genetics, Albert Einstein College of Medicine, New York, NY, USA.
  • Jabalameli MR; Department of Genetics, Albert Einstein College of Medicine, New York, NY, USA.
  • Nguyen N; Department of Genetics, Albert Einstein College of Medicine, New York, NY, USA.
  • Mitra J; Department of Genetics, Albert Einstein College of Medicine, New York, NY, USA.
  • Swillen A; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Vorstman JAS; Department of Psychiatry, University of Toronto, Toronto, ON, Canada.
  • Chow EWC; Department of Psychiatry, University of Toronto, Toronto, ON, Canada.
  • van den Bree M; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.
  • Emanuel BS; Division of Human Genetics and 22q and You Center, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Vermeesch JR; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Owen MJ; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.
  • Williams NM; 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 Psychiatry, University of Toronto, Toronto, ON, Canada.
  • McDonald-McGinn DM; Division of Human Genetics and 22q and You Center, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Gur RE; Department of Psychiatry and Lifespan Brain Institute, Penn Medicine-CHOP, University of Pennsylvania, Philadelphia, PA, USA.
  • Bearden CE; Departments of Psychiatry and Biobehavioral Sciences and Psychology, Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, CA, USA.
  • Morrow BE; Department of Genetics, Albert Einstein College of Medicine, New York, NY, USA.
  • Lachman HM; Department of Genetics, Albert Einstein College of Medicine, New York, NY, USA.
  • Zhang ZD; Department of Genetics, Albert Einstein College of Medicine, New York, NY, USA. zhengdong.zhang@einsteinmed.edu.
Mol Psychiatry ; 28(5): 2071-2080, 2023 May.
Article em En | MEDLINE | ID: mdl-36869225
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esquizofrenia / Síndrome de DiGeorge Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans Idioma: En Revista: Mol Psychiatry Assunto da revista: BIOLOGIA MOLECULAR / PSIQUIATRIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esquizofrenia / Síndrome de DiGeorge Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans Idioma: En Revista: Mol Psychiatry Assunto da revista: BIOLOGIA MOLECULAR / PSIQUIATRIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos