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Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome.
Alver, Maris; Mancini, Valentina; Läll, Kristi; Schneider, Maude; Romano, Luciana; Mägi, Reedik; Dermitzakis, Emmanouil T; Eliez, Stephan; Reymond, Alexandre.
Afiliação
  • Alver M; Department of Genetic Medicine and Development, University of Geneva School of Medicine, Geneva, Switzerland. maris.alver@unige.ch.
  • Mancini V; Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia. maris.alver@unige.ch.
  • Läll K; Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland. maris.alver@unige.ch.
  • Schneider M; Developmental Imaging and Psychopathology Laboratory, University of Geneva School of Medicine, Geneva, Switzerland.
  • Romano L; Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia.
  • Mägi R; Clinical Psychology Unit for Intellectual and Developmental Disabilities, Faculty of Psychology and Educational Sciences, University of Geneva, Geneva, Switzerland.
  • Dermitzakis ET; Department of Genetic Medicine and Development, University of Geneva School of Medicine, Geneva, Switzerland.
  • Reymond A; Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia.
Mol Psychiatry ; 27(10): 4191-4200, 2022 10.
Article em En | MEDLINE | ID: mdl-35768638
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Esquizofrenia / Síndrome de DiGeorge / Disfunção Cognitiva Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adolescent / Female / Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Esquizofrenia / Síndrome de DiGeorge / Disfunção Cognitiva Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adolescent / Female / Humans / Male Idioma: En Ano de publicação: 2022 Tipo de documento: Article