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Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis.
Choi, Seung Hoan; Jurgens, Sean J; Haggerty, Christopher M; Hall, Amelia W; Halford, Jennifer L; Morrill, Valerie N; Weng, Lu-Chen; Lagerman, Braxton; Mirshahi, Tooraj; Pettinger, Mary; Guo, Xiuqing; Lin, Henry J; Alonso, Alvaro; Soliman, Elsayed Z; Kornej, Jelena; Lin, Honghuang; Moscati, Arden; Nadkarni, Girish N; Brody, Jennifer A; Wiggins, Kerri L; Cade, Brian E; Lee, Jiwon; Austin-Tse, Christina; Blackwell, Tom; Chaffin, Mark D; Lee, Christina J-Y; Rehm, Heidi L; Roselli, Carolina; Redline, Susan; Mitchell, Braxton D; Sotoodehnia, Nona; Psaty, Bruce M; Heckbert, Susan R; Loos, Ruth J F; Vasan, Ramachandran S; Benjamin, Emelia J; Correa, Adolfo; Boerwinkle, Eric; Arking, Dan E; Rotter, Jerome I; Rich, Stephen S; Whitsel, Eric A; Perez, Marco; Kooperberg, Charles; Fornwalt, Brandon K; Lunetta, Kathryn L; Ellinor, Patrick T; Lubitz, Steven A.
Afiliação
  • Choi SH; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, MA (S.H.C., S.J.J., A.W.H., J.L.H., V.N.M., L.-C.W., M.D.C., C.J.-Y.L., H.L.R., C.R., P.T.E., S.A.L.).
  • Jurgens SJ; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, MA (S.H.C., S.J.J., A.W.H., J.L.H., V.N.M., L.-C.W., M.D.C., C.J.-Y.L., H.L.R., C.R., P.T.E., S.A.L.).
  • Haggerty CM; Department of Translational Data Science and Informatics (C.M.H., B.K.F.), Geisinger, Danville, PA.
  • Hall AW; Heart Institute (C.M.H., B.K.F.), Geisinger, Danville, PA.
  • Halford JL; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, MA (S.H.C., S.J.J., A.W.H., J.L.H., V.N.M., L.-C.W., M.D.C., C.J.-Y.L., H.L.R., C.R., P.T.E., S.A.L.).
  • Morrill VN; Cardiovascular Research Center (A.W.H., V.N.M., L.-C.W., P.T.E., S.A.L.), Boston, MA.
  • Weng LC; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, MA (S.H.C., S.J.J., A.W.H., J.L.H., V.N.M., L.-C.W., M.D.C., C.J.-Y.L., H.L.R., C.R., P.T.E., S.A.L.).
  • Lagerman B; Harvard Medical School (J.L.H., C.A.-T., H.L.R.), Boston, MA.
  • Mirshahi T; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, MA (S.H.C., S.J.J., A.W.H., J.L.H., V.N.M., L.-C.W., M.D.C., C.J.-Y.L., H.L.R., C.R., P.T.E., S.A.L.).
  • Pettinger M; Cardiovascular Research Center (A.W.H., V.N.M., L.-C.W., P.T.E., S.A.L.), Boston, MA.
  • Guo X; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, MA (S.H.C., S.J.J., A.W.H., J.L.H., V.N.M., L.-C.W., M.D.C., C.J.-Y.L., H.L.R., C.R., P.T.E., S.A.L.).
  • Lin HJ; Cardiovascular Research Center (A.W.H., V.N.M., L.-C.W., P.T.E., S.A.L.), Boston, MA.
  • Alonso A; Phenomic Analytics and Clinical Data Core (B.L.), Geisinger, Danville, PA.
  • Soliman EZ; Department of Molecular and Functional Genomics (T.M.), Geisinger, Danville, PA.
  • Kornej J; Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA (M.P., C.K.).
  • Lin H; The Institute for Translational Genomics and Population Sciences, Department of Pediatrics, The Lundquist Insti for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA (X.G., H.J.L., J.I.R.).
  • Moscati A; The Institute for Translational Genomics and Population Sciences, Department of Pediatrics, The Lundquist Insti for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA (X.G., H.J.L., J.I.R.).
  • Nadkarni GN; Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA (A.A.).
  • Brody JA; Epidemiological Cardiology Research Center, Wake Forest School of Medicine, Winston Salem, NC (E.Z.S.).
  • Wiggins KL; NHLBI and Boston University's Framingham Heart Study (J.K., E.J.B., R.S.V).
  • Cade BE; Sections of Cardiovascular Medicine and Preventive Medicine, Boston Medical Center (J.K., R.S.V), Boston University School of Medicine, MA.
  • Lee J; Section of Computational Biomedicine, Department of Medicine (H.L.), Boston University School of Medicine, MA.
  • Austin-Tse C; The Charles Bronfman Institute for Personalized Medicine (A.M., G.N., R.J.F.L.), Icahn School of Medicine, Mount Sinai, New York, NY.
  • Blackwell T; The Charles Bronfman Institute for Personalized Medicine (A.M., G.N., R.J.F.L.), Icahn School of Medicine, Mount Sinai, New York, NY.
  • Chaffin MD; Division of Nephrology, Department of Medicine (G.N.), Icahn School of Medicine, Mount Sinai, New York, NY.
  • Lee CJ; Cardiovascular Health Research Unit, Department of Medicine (J.A.B., K.L.W., N.S., B.M.P., S.R.H.), University of Washington, Seattle.
  • Rehm HL; Cardiovascular Health Research Unit, Department of Medicine (J.A.B., K.L.W., N.S., B.M.P., S.R.H.), University of Washington, Seattle.
  • Roselli C; Massachusetts General Hospital. Division of Sleep Medicine, Department of Medicine (B.E.C.), Boston, MA.
  • Redline S; Division of Sleep and Circadian Disorders (J.L.), Harvard Medical School, Brigham and Women's Hospital, Boston.
  • Mitchell BD; Center for Genomic Medicine (C.A.-T., H.L.R.), Boston, MA.
  • Sotoodehnia N; Harvard Medical School (J.L.H., C.A.-T., H.L.R.), Boston, MA.
  • Psaty BM; Laboratory for Molecular Medicine, Partners Healthcare Personalized Medicine, Cambridge, MA (C.A.-T.).
  • Heckbert SR; Department of Biostatistics, University of Michigan, Ann Arbor (T.B.).
  • Loos RJF; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, MA (S.H.C., S.J.J., A.W.H., J.L.H., V.N.M., L.-C.W., M.D.C., C.J.-Y.L., H.L.R., C.R., P.T.E., S.A.L.).
  • Vasan RS; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, MA (S.H.C., S.J.J., A.W.H., J.L.H., V.N.M., L.-C.W., M.D.C., C.J.-Y.L., H.L.R., C.R., P.T.E., S.A.L.).
  • Benjamin EJ; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, MA (S.H.C., S.J.J., A.W.H., J.L.H., V.N.M., L.-C.W., M.D.C., C.J.-Y.L., H.L.R., C.R., P.T.E., S.A.L.).
  • Correa A; Center for Genomic Medicine (C.A.-T., H.L.R.), Boston, MA.
  • Boerwinkle E; Harvard Medical School (J.L.H., C.A.-T., H.L.R.), Boston, MA.
  • Arking DE; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, MA (S.H.C., S.J.J., A.W.H., J.L.H., V.N.M., L.-C.W., M.D.C., C.J.-Y.L., H.L.R., C.R., P.T.E., S.A.L.).
  • Rich SS; Regeneron Genetics Center, Tarrytown, NY. Departments of Medicine, Brigham and Women's Hospital, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA (S.R.).
  • Whitsel EA; University of Maryland School of Medicine (B.D.M.).
  • Perez M; Geriatrics Research and Education Clinical Center, Baltimore Veterans Administration Medical Center, MD (B.D.M.).
  • Kooperberg C; Cardiovascular Health Research Unit, Department of Medicine (J.A.B., K.L.W., N.S., B.M.P., S.R.H.), University of Washington, Seattle.
  • Fornwalt BK; Division of Cardiology, Department of Epidemiology (N.S.), University of Washington, Seattle.
  • Lunetta KL; Cardiovascular Health Research Unit, Department of Medicine (J.A.B., K.L.W., N.S., B.M.P., S.R.H.), University of Washington, Seattle.
  • Ellinor PT; Department of Epidemiology (B.M.P., S.R.H.), University of Washington, Seattle.
  • Lubitz SA; Department of Health Services (B.M.P.), University of Washington, Seattle.
Circ Genom Precis Med ; 14(4): e003300, 2021 08.
Article em En | MEDLINE | ID: mdl-34319147
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Síndrome do QT Longo / Morte Súbita Cardíaca / Predisposição Genética para Doença / Eletrocardiografia / Heterozigoto Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Síndrome do QT Longo / Morte Súbita Cardíaca / Predisposição Genética para Doença / Eletrocardiografia / Heterozigoto Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article