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The individual and global impact of copy-number variants on complex human traits.
Auwerx, Chiara; Lepamets, Maarja; Sadler, Marie C; Patxot, Marion; Stojanov, Milos; Baud, David; Mägi, Reedik; Porcu, Eleonora; Reymond, Alexandre; Kutalik, Zoltán.
Afiliação
  • Auwerx C; Center for Integrative Genomics, University of Lausanne, Lausanne 1015, Switzerland; Department of Computational Biology, University of Lausanne, Lausanne 1015, Switzerland; Swiss Institute of Bioinformatics, Lausanne 1015, Switzerland; University Center for Primary Care and Public Health, Lausanne
  • Lepamets M; Institute of Molecular and Cell Biology, University of Tartu, Tartu 51010, Estonia; Estonian Genome Centre, Institute of Genomics, University of Tartu, Tartu 51010, Estonia.
  • Sadler MC; Swiss Institute of Bioinformatics, Lausanne 1015, Switzerland; University Center for Primary Care and Public Health, Lausanne 1010, Switzerland.
  • Patxot M; Department of Computational Biology, University of Lausanne, Lausanne 1015, Switzerland.
  • Stojanov M; Materno-fetal and Obstetrics Research Unit, Department Woman-Mother-Child, CHUV, Lausanne 1011, Switzerland.
  • Baud D; Materno-fetal and Obstetrics Research Unit, Department Woman-Mother-Child, CHUV, Lausanne 1011, Switzerland.
  • Mägi R; Estonian Genome Centre, Institute of Genomics, University of Tartu, Tartu 51010, Estonia.
  • Porcu E; Center for Integrative Genomics, University of Lausanne, Lausanne 1015, Switzerland; Swiss Institute of Bioinformatics, Lausanne 1015, Switzerland; University Center for Primary Care and Public Health, Lausanne 1010, Switzerland.
  • Reymond A; Center for Integrative Genomics, University of Lausanne, Lausanne 1015, Switzerland. Electronic address: alexandre.reymond@unil.ch.
  • Kutalik Z; Department of Computational Biology, University of Lausanne, Lausanne 1015, Switzerland; Swiss Institute of Bioinformatics, Lausanne 1015, Switzerland; University Center for Primary Care and Public Health, Lausanne 1010, Switzerland. Electronic address: zoltan.kutalik@unil.ch.
Am J Hum Genet ; 109(4): 647-668, 2022 04 07.
Article em En | MEDLINE | ID: mdl-35240056
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Estudo de Associação Genômica Ampla / Variações do Número de Cópias de DNA Limite: Female / Humans 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: Estudo de Associação Genômica Ampla / Variações do Número de Cópias de DNA Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article