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Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
Kichaev, Gleb; Bhatia, Gaurav; Loh, Po-Ru; Gazal, Steven; Burch, Kathryn; Freund, Malika K; Schoech, Armin; Pasaniuc, Bogdan; Price, Alkes L.
Afiliación
  • Kichaev G; Interdepartamental Program in Bioinformatics, University of California, Los Angeles, CA 90095, USA. Electronic address: gkichaev@ucla.edu.
  • Bhatia G; Department of Epidemiology. Harvard T. H. Chan School of Public Health, Boston, MA 02115, USA.
  • Loh PR; Department of Epidemiology. Harvard T. H. Chan School of Public Health, Boston, MA 02115, USA; Program in Medical and Population Genetics, Broad Institute, Cambridge, MA 02142, USA.
  • Gazal S; Department of Epidemiology. Harvard T. H. Chan School of Public Health, Boston, MA 02115, USA; Program in Medical and Population Genetics, Broad Institute, Cambridge, MA 02142, USA.
  • Burch K; Interdepartamental Program in Bioinformatics, University of California, Los Angeles, CA 90095, USA.
  • Freund MK; Department of Human Genetics, University of California, Los Angeles, CA 90095, USA.
  • Schoech A; Department of Epidemiology. Harvard T. H. Chan School of Public Health, Boston, MA 02115, USA; Program in Medical and Population Genetics, Broad Institute, Cambridge, MA 02142, USA.
  • Pasaniuc B; Interdepartamental Program in Bioinformatics, University of California, Los Angeles, CA 90095, USA; Department of Human Genetics, University of California, Los Angeles, CA 90095, USA; Department Pathology and Laboratory Medicine, University of California, Los Angeles, CA 90095, USA.
  • Price AL; Department of Epidemiology. Harvard T. H. Chan School of Public Health, Boston, MA 02115, USA; Program in Medical and Population Genetics, Broad Institute, Cambridge, MA 02142, USA; Department of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, MA 02115, USA. Electronic address: ap
Am J Hum Genet ; 104(1): 65-75, 2019 01 03.
Article en En | MEDLINE | ID: mdl-30595370
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Herencia Multifactorial / Polimorfismo de Nucleótido Simple / Estudio de Asociación del Genoma Completo Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Am J Hum Genet Año: 2019 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Herencia Multifactorial / Polimorfismo de Nucleótido Simple / Estudio de Asociación del Genoma Completo Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Am J Hum Genet Año: 2019 Tipo del documento: Article