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The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype.

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Title: The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype.
Authors: Stanaway IB; Department of Biomedical Informatics Medical Education, School of Medicine, University of Washington, Seattle, Washington., Hall TO; Department of Biomedical Informatics Medical Education, School of Medicine, University of Washington, Seattle, Washington., Rosenthal EA; Division of Medical Genetics, School of Medicine, University of Washington, Seattle, Washington., Palmer M; Division of Medical Genetics, School of Medicine, University of Washington, Seattle, Washington., Naranbhai V; Department of Biomedical Informatics Medical Education, School of Medicine, University of Washington, Seattle, Washington.; Harvard Medical School, Harvard University, Cambridge, Massachusetts., Knevel R; Harvard Medical School, Harvard University, Cambridge, Massachusetts., Namjou-Khales B; Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio., Carroll RJ; Departments of Biomedical Informatics and Medicine, Vanderbilt University, Nashville, Tennessee., Kiryluk K; Department of Medicine, Columbia University, New York City, New York., Gordon AS; Division of Medical Genetics, School of Medicine, University of Washington, Seattle, Washington., Linder J; Vanderbilt Institute for Clinical and Translational Research, School of Medicine, Vanderbilt University, Nashville, Tennessee., Howell KM; Vanderbilt Institute for Clinical and Translational Research, School of Medicine, Vanderbilt University, Nashville, Tennessee., Mapes BM; Vanderbilt Institute for Clinical and Translational Research, School of Medicine, Vanderbilt University, Nashville, Tennessee., Lin FTJ; Feinberg School of Medicine, Northwestern University, Chicago, Illinois., Joo YY; Feinberg School of Medicine, Northwestern University, Chicago, Illinois., Hayes MG; Feinberg School of Medicine, Northwestern University, Chicago, Illinois., Gharavi AG; Department of Medicine, Columbia University, New York City, New York., Pendergrass SA; Geisinger Research, Rockville, Marland., Ritchie MD; Department of Genetics, University of Pennsylvania, Philadelphia, Pennsylvania., de Andrade M; Mayo Clinic, Rochester, Minnesota., Croteau-Chonka DC; Harvard Medical School, Harvard University, Cambridge, Massachusetts., Raychaudhuri S; Harvard Medical School, Harvard University, Cambridge, Massachusetts.; Program in Medical and Population Genetics, Broad Institute of Massachusetts Technical Institute and Harvard University, Cambridge, Massachusetts., Weiss ST; Harvard Medical School, Harvard University, Cambridge, Massachusetts., Lebo M; Harvard Medical School, Harvard University, Cambridge, Massachusetts., Amr SS; Harvard Medical School, Harvard University, Cambridge, Massachusetts., Carrell D; Kaiser Permanente Washington Health Research Institute (Formerly Group Health Cooperative-Seattle), Kaiser Permanente, Seattle, Washington., Larson EB; Kaiser Permanente Washington Health Research Institute (Formerly Group Health Cooperative-Seattle), Kaiser Permanente, Seattle, Washington., Chute CG; Schools of Medicine, Public Health, and Nursing, Johns Hopkins University, Baltimore, Maryland., Rasmussen-Torvik LJ; Feinberg School of Medicine, Northwestern University, Chicago, Illinois., Roy-Puckelwartz MJ; Feinberg School of Medicine, Northwestern University, Chicago, Illinois., Sleiman P; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania., Hakonarson H; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania., Li R; National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland., Karlson EW; Department of Genetics, University of Pennsylvania, Philadelphia, Pennsylvania., Peterson JF; Departments of Biomedical Informatics and Medicine, Vanderbilt University, Nashville, Tennessee., Kullo IJ; Mayo Clinic, Rochester, Minnesota., Chisholm R; Feinberg School of Medicine, Northwestern University, Chicago, Illinois., Denny JC; Departments of Biomedical Informatics and Medicine, Vanderbilt University, Nashville, Tennessee., Jarvik GP; Division of Medical Genetics, School of Medicine, University of Washington, Seattle, Washington., Crosslin DR; Department of Biomedical Informatics Medical Education, School of Medicine, University of Washington, Seattle, Washington.
Corporate Authors: eMERGE Network; National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.
Source: Genetic epidemiology [Genet Epidemiol] 2019 Feb; Vol. 43 (1), pp. 63-81. Date of Electronic Publication: 2018 Oct 08.
Publication Type: Journal Article; Research Support, N.I.H., Extramural
Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8411723 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-2272 (Electronic) Linking ISSN: 07410395 NLM ISO Abbreviation: Genet Epidemiol Subsets: MEDLINE
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  Data: The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype.
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