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DECO: a framework for jointly analyzing de novo and rare case/control variants, and biological pathways.
Nguyen, Tan-Hoang; He, Xin; Brown, Ruth C; Webb, Bradley T; Kendler, Kenneth S; Vladimirov, Vladimir I; Riley, Brien P; Bacanu, Silviu-Alin.
Afiliação
  • Nguyen TH; Virginia Institute for Psychiatric and Behavioral Genetics, Department of Psychiatry, Virginia Commonwealth University, Richmond, VA, USA.
  • He X; The Department of Human Genetics, University of Chicago, IL 60637, USA; Grossman Institute for Neuroscience, Quantitative Biology and Human Behavior, University of Chicago, Chicago, IL 60637, USA.
  • Brown RC; Virginia Institute for Psychiatric and Behavioral Genetics, Department of Psychiatry, Virginia Commonwealth University, Richmond, VA, USA.
  • Webb BT; Virginia Institute for Psychiatric and Behavioral Genetics, Department of Psychiatry, Virginia Commonwealth University, Richmond, VA, USA.
  • Kendler KS; Virginia Institute for Psychiatric and Behavioral Genetics, Department of Psychiatry, Virginia Commonwealth University, Richmond, VA, USA.
  • Vladimirov VI; Virginia Institute for Psychiatric and Behavioral Genetics, Department of Psychiatry, Virginia Commonwealth University, Richmond, VA, USA; Department of Psychiatry & Behavioral Sciences, College of Medicine, Texas A&M University, College Station, TX, USA; and the Lieber Institute for Brain D
  • Riley BP; Virginia Institute for Psychiatric and Behavioral Genetics, Department of Psychiatry, Virginia Commonwealth University, Richmond, VA, USA.
  • Bacanu SA; Virginia Institute for Psychiatric and Behavioral Genetics, Department of Psychiatry, Virginia Commonwealth University, Richmond, VA, USA.
Brief Bioinform ; 22(5)2021 09 02.
Article em En | MEDLINE | ID: mdl-33791774

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esquizofrenia / Predisposição Genética para Doença / Biologia de Sistemas / Transtornos do Neurodesenvolvimento / Mutação Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esquizofrenia / Predisposição Genética para Doença / Biologia de Sistemas / Transtornos do Neurodesenvolvimento / Mutação Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article