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Comparing Within- and Between-Family Polygenic Score Prediction.
Selzam, Saskia; Ritchie, Stuart J; Pingault, Jean-Baptiste; Reynolds, Chandra A; O'Reilly, Paul F; Plomin, Robert.
Afiliação
  • Selzam S; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 8AF, UK. Electronic address: saskia.selzam@kcl.ac.uk.
  • Ritchie SJ; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 8AF, UK.
  • Pingault JB; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 8AF, UK; Division of Psychology and Language Sciences, University College London, London WC1H 0AP, UK.
  • Reynolds CA; Department of Psychology, University of California Riverside, Riverside, CA 92521, USA.
  • O'Reilly PF; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 8AF, UK; Icahn School of Medicine, Mount Sinai, New York, NY 10029, USA.
  • Plomin R; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 8AF, UK.
Am J Hum Genet ; 105(2): 351-363, 2019 08 01.
Article em En | MEDLINE | ID: mdl-31303263
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esquizofrenia / Transtornos Cognitivos / Herança Multifatorial / Polimorfismo de Nucleotídeo Único / Doenças em Gêmeos / Transtornos do Neurodesenvolvimento / Genes Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Am J Hum Genet Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esquizofrenia / Transtornos Cognitivos / Herança Multifatorial / Polimorfismo de Nucleotídeo Único / Doenças em Gêmeos / Transtornos do Neurodesenvolvimento / Genes Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Am J Hum Genet Ano de publicação: 2019 Tipo de documento: Article