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A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.
Emdin, Connor A; Haas, Mary E; Khera, Amit V; Aragam, Krishna; Chaffin, Mark; Klarin, Derek; Hindy, George; Jiang, Lan; Wei, Wei-Qi; Feng, Qiping; Karjalainen, Juha; Havulinna, Aki; Kiiskinen, Tuomo; Bick, Alexander; Ardissino, Diego; Wilson, James G; Schunkert, Heribert; McPherson, Ruth; Watkins, Hugh; Elosua, Roberto; Bown, Matthew J; Samani, Nilesh J; Baber, Usman; Erdmann, Jeanette; Gupta, Namrata; Danesh, John; Saleheen, Danish; Chang, Kyong-Mi; Vujkovic, Marijana; Voight, Ben; Damrauer, Scott; Lynch, Julie; Kaplan, David; Serper, Marina; Tsao, Philip; Mercader, Josep; Hanis, Craig; Daly, Mark; Denny, Joshua; Gabriel, Stacey; Kathiresan, Sekar.
Afiliación
  • Emdin CA; Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
  • Haas ME; Department of Medicine, Harvard Medical School, Boston, Massachusetts, United States of America.
  • Khera AV; Program in Medical and Population Genetics, Broad Institute, Cambridge, Massachusetts, United States of America.
  • Aragam K; Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
  • Chaffin M; Department of Medicine, Harvard Medical School, Boston, Massachusetts, United States of America.
  • Klarin D; Program in Medical and Population Genetics, Broad Institute, Cambridge, Massachusetts, United States of America.
  • Hindy G; Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
  • Jiang L; Department of Medicine, Harvard Medical School, Boston, Massachusetts, United States of America.
  • Wei WQ; Program in Medical and Population Genetics, Broad Institute, Cambridge, Massachusetts, United States of America.
  • Feng Q; Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
  • Karjalainen J; Department of Medicine, Harvard Medical School, Boston, Massachusetts, United States of America.
  • Havulinna A; Program in Medical and Population Genetics, Broad Institute, Cambridge, Massachusetts, United States of America.
  • Kiiskinen T; Program in Medical and Population Genetics, Broad Institute, Cambridge, Massachusetts, United States of America.
  • Bick A; Program in Medical and Population Genetics, Broad Institute, Cambridge, Massachusetts, United States of America.
  • Ardissino D; Program in Medical and Population Genetics, Broad Institute, Cambridge, Massachusetts, United States of America.
  • Wilson JG; Departments of Biomedical Informatics, Vanderbilt University, Vanderbilt, Tennessee, United States of America.
  • Schunkert H; Departments of Medicine, Vanderbilt University, Vanderbilt, Tennessee, United States of America.
  • McPherson R; Departments of Biomedical Informatics, Vanderbilt University, Vanderbilt, Tennessee, United States of America.
  • Watkins H; Departments of Medicine, Vanderbilt University, Vanderbilt, Tennessee, United States of America.
  • Elosua R; Program in Medical and Population Genetics, Broad Institute, Cambridge, Massachusetts, United States of America.
  • Bown MJ; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, FI, Helsinki, Finland.
  • Samani NJ; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, FI, Helsinki, Finland.
  • Baber U; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, FI, Helsinki, Finland.
  • Erdmann J; Program in Medical and Population Genetics, Broad Institute, Cambridge, Massachusetts, United States of America.
  • Gupta N; Division of Cardiology, Azienda Ospedaliero-Universitaria di Parma, Parma, Italy.
  • Danesh J; Associazione per lo Studio Della Trombosi in Cardiologia, Pavia, Italy.
  • Saleheen D; Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi, United States of America.
  • Chang KM; Deutsches Herzzentrum München, Technische Universität München, Deutsches Zentrum für Herz-Kreislauf-Forschung, München, Germany.
  • Vujkovic M; University of Ottawa Heart Institute, Ottawa, Ontario, Canada.
  • Voight B; Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.
  • Damrauer S; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
  • Lynch J; Cardiovascular Epidemiology and Genetics, Hospital del Mar Research Institute, Barcelona, Spain.
  • Kaplan D; CIBER Enfermedades Cardiovasculares (CIBERCV), Barcelona, Spain.
  • Serper M; Facultat de Medicina, Universitat de Vic-Central de Cataluña, Vic, Spain.
  • Tsao P; Department of Cardiovascular Sciences, University of Leicester, and NIHR Leicester Biomedical Research Centre, Leicester, United Kingdom.
  • Mercader J; The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York, United States of America.
  • Hanis C; Institute for Cardiogenetics, University of Lübeck, Lübeck, Germany.
  • Daly M; DZHK (German Research Centre for Cardiovascular Research), partner site Hamburg/Lübeck/Kiel, Lübeck, Germany.
  • Denny J; Program in Medical and Population Genetics, Broad Institute, Cambridge, Massachusetts, United States of America.
  • Gabriel S; Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
  • Kathiresan S; Wellcome Trust Sanger Institute, Hinxton, Cambridge, United Kingdom.
PLoS Genet ; 16(4): e1008629, 2020 04.
Article en En | MEDLINE | ID: mdl-32282858
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Oxidorreductasas / Predisposición Genética a la Enfermedad / Mutación Missense / Proteínas Mitocondriales / Hígado Graso / Cirrosis Hepática Límite: Female / Humans / Male / Middle aged Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Oxidorreductasas / Predisposición Genética a la Enfermedad / Mutación Missense / Proteínas Mitocondriales / Hígado Graso / Cirrosis Hepática Límite: Female / Humans / Male / Middle aged Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos