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Powerful rare variant association testing in a copula-based joint analysis of multiple phenotypes.
Konigorski, Stefan; Yilmaz, Yildiz E; Janke, Jürgen; Bergmann, Manuela M; Boeing, Heiner; Pischon, Tobias.
  • Konigorski S; Molecular Epidemiology Research Group, Max Delbrück Center (MDC) for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
  • Yilmaz YE; Digital Health and Machine Learning Research Group, Hasso Plattner Institute for Digital Engineering, Potsdam, Germany.
  • Janke J; Department of Mathematics and Statistics, Memorial University of Newfoundland, St. John's, NL, Canada.
  • Bergmann MM; Discipline of Genetics, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL, Canada.
  • Boeing H; Discipline of Medicine, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL, Canada.
  • Pischon T; Molecular Epidemiology Research Group, Max Delbrück Center (MDC) for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
Genet Epidemiol ; 44(1): 26-40, 2020 01.
Article en En | MEDLINE | ID: mdl-31732979
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Simulación por Computador / Marcadores Genéticos / Enfermedades Raras / Estudio de Asociación del Genoma Completo / Modelos Genéticos Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article
Texto completo
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XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Simulación por Computador / Marcadores Genéticos / Enfermedades Raras / Estudio de Asociación del Genoma Completo / Modelos Genéticos Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article