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Ellinor, P.T.* ; Lunetta, K.L.* ; Albert, C.M.* ; Glazer, N.L.* ; Ritchie, M.D.* ; Smith, A.V.* ; Arking, D.E.* ; Müller-Nurasyid, M. ; Krijthe, B.P.* ; Lubitz, S.A.* ; Bis, J.C.* ; Chung, M.K.* ; Doerr, M.* ; Ozaki, K.* ; Roberts, J.D.* ; Smith, J.G.* ; Pfeufer, A. ; Sinner, M.F.* ; Lohman, K.* ; Ding, J.Z.* ; Smith, N.L.* ; Smith, J.D.* ; Rienstra, M.* ; Rice, K.M.* ; van Wagoner, D.R.* ; Magnani, J.W.* ; Wakili, R.* ; Clauss, S.* ; Rotter, J.I.* ; Steinbeck, G.* ; Launer, L.J.* ; Davies, R.W.* ; Borkovich, M.* ; Harris, T.B.* ; Lin, H.H.* ; Völker, U.* ; Völzke, H.* ; Milan, D.J.* ; Hofman, A.* ; Boerwinkle, E.* ; Chen, L.Y.* ; Soliman, E.Z.* ; Voight, B.F.* ; Li, G.* ; Chakravarti, A.* ; Kubo, M.* ; Tedrow, U.B.* ; Rose, L.M.* ; Ridker, P.M.* ; Conen, D.* ; Tsunoda, T.* ; Furukawa, T.* ; Sotoodehnia, N.* ; Xu, S.Y.* ; Kamatani, N.* ; Levy, D.* ; Nakamura, Y.* ; Parvez, B.* ; Mahida, S.* ; Furie, K.L.* ; Rosand, J.* ; Muhammad, R.* ; Psaty, B.M.* ; Meitinger, T. ; Perz, S. ; Wichmann, H.-E. ; Witteman, J.C.M.* ; Kao, W.H.L.* ; Kathiresan, S.* ; Roden, D.M.* ; Uitterlinden, A.G.* ; Rivadeneira, F.* ; McKnight, B.* ; Sjögren, M.* ; Newman, A.B.* ; Liu, Y.M.* ; Gollob, M.H.* ; Melander, O.* ; Tanaka, T.* ; Stricker, B.H.C. ; Felix, S.B.* ; Alonso, A.* ; Darbar, D.* ; Barnard, J.* ; Chasman, D.I.* ; Heckbert, S.R.* ; Benjamin, E.J.* ; Gudnason, V.* ; Kääb, S.*

Meta-analysis identifies six new susceptibility loci for atrial fibrillation.

Nat. Genet. 44, 670-675 (2012)
Verlagsversion DOI PMC
Atrial fibrillation is a highly prevalent arrhythmia and a major risk factor for stroke, heart failure and death(1). We conducted a genome-wide association study (GWAS) in individuals of European ancestry, including 6,707 with and 52,426 without atrial fibrillation. Six new atrial fibrillation susceptibility loci were identified and replicated in an additional sample of individuals of European ancestry, including 5,381 subjects with and 10,030 subjects without atrial fibrillation (P < 5 x 10(-8)). Four of the loci identified in Europeans were further replicated in silico in a GWAS of Japanese individuals, including 843 individuals with and 3,350 individuals without atrial fibrillation. The identified loci implicate candidate genes that encode transcription factors related to cardiopulmonary development, cardiac-expressed ion channels and cell signaling molecules.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter GENOME-WIDE ASSOCIATION; CHROMOSOME 4Q25; DILATED CARDIOMYOPATHY; PACEMAKER CHANNEL; COMMON VARIANTS; PR INTERVAL; CAVEOLIN-1; REPLICATION; MUTATIONS; PROTEINS
ISSN (print) / ISBN 1061-4036
e-ISSN 1546-1718
Zeitschrift Nature Genetics
Quellenangaben Band: 44, Heft: 6, Seiten: 670-675 Artikelnummer: , Supplement: ,
Verlag Nature America
Verlagsort New York, NY
Begutachtungsstatus