Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation-Reference-Cited by-同舟云学术

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

Published:2017-04-17 Issue:6 Volume:49 Page:946-952
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Christophersen Ingrid E^ORCID, ,Rienstra Michiel,Roselli Carolina,Yin Xiaoyan,Geelhoed Bastiaan,Barnard John^ORCID,Lin Honghuang^ORCID,Arking Dan E,Smith Albert V^ORCID,Albert Christine M,Chaffin Mark,Tucker Nathan R^ORCID,Li Molong,Klarin Derek,Bihlmeyer Nathan A^ORCID,Low Siew-Kee,Weeke Peter E,Müller-Nurasyid Martina,Smith J Gustav,Brody Jennifer A^ORCID,Niemeijer Maartje N,Dörr Marcus,Trompet Stella,Huffman Jennifer^ORCID,Gustafsson Stefan^ORCID,Schurmann Claudia,Kleber Marcus E^ORCID,Lyytikäinen Leo-Pekka^ORCID,Seppälä Ilkka^ORCID,Malik Rainer,Horimoto Andrea R V R,Perez Marco,Sinisalo Juha,Aeschbacher Stefanie,Thériault Sébastien,Yao Jie,Radmanesh Farid,Weiss Stefan^ORCID,Teumer Alexander^ORCID,Choi Seung Hoan,Weng Lu-Chen,Clauss Sebastian,Deo Rajat,Rader Daniel J,Shah Svati H,Sun Albert,Hopewell Jemma C,Debette Stephanie,Chauhan Ganesh,Yang Qiong^ORCID,Worrall Bradford B,Paré Guillaume,Kamatani Yoichiro,Hagemeijer Yanick P^ORCID,Verweij Niek,Siland Joylene E,Kubo Michiaki,Smith Jonathan D^ORCID,Van Wagoner David R^ORCID,Bis Joshua C,Perz Siegfried,Psaty Bruce M,Ridker Paul M,Magnani Jared W,Harris Tamara B,Launer Lenore J,Shoemaker M Benjamin,Padmanabhan Sandosh,Haessler Jeffrey,Bartz Traci M,Waldenberger Melanie,Lichtner Peter,Arendt Marina,Krieger Jose E^ORCID,Kähönen Mika,Risch Lorenz,Mansur Alfredo J,Peters Annette,Smith Blair H^ORCID,Lind Lars,Scott Stuart A^ORCID,Lu Yingchang,Bottinger Erwin B,Hernesniemi Jussi,Lindgren Cecilia M,Wong Jorge A,Huang Jie,Eskola Markku,Morris Andrew P,Ford Ian,Reiner Alex P,Delgado Graciela,Chen Lin Y,Chen Yii-Der Ida,Sandhu Roopinder K,Li Man^ORCID,Boerwinkle Eric,Eisele Lewin,Lannfelt Lars,Rost Natalia,Anderson Christopher D,Taylor Kent D,Campbell Archie^ORCID,Magnusson Patrik K,Porteous David,Hocking Lynne J,Vlachopoulou Efthymia,Pedersen Nancy L,Nikus Kjell,Orho-Melander Marju,Hamsten Anders,Heeringa Jan,Denny Joshua C,Kriebel Jennifer^ORCID,Darbar Dawood,Newton-Cheh Christopher,Shaffer Christian,Macfarlane Peter W,Heilmann-Heimbach Stefanie,Almgren Peter,Huang Paul L,Sotoodehnia Nona,Soliman Elsayed Z^ORCID,Uitterlinden Andre G,Hofman Albert,Franco Oscar H,Völker Uwe,Jöckel Karl-Heinz,Sinner Moritz F,Lin Henry J,Guo Xiuqing,Dichgans Martin,Ingelsson Erik,Kooperberg Charles,Melander Olle,Loos Ruth J F,Laurikka Jari,Conen David,Rosand Jonathan,van der Harst Pim,Lokki Marja-Liisa,Kathiresan Sekar,Pereira Alexandre,Jukema J Wouter^ORCID,Hayward Caroline,Rotter Jerome I,März Winfried,Lehtimäki Terho,Stricker Bruno H,Chung Mina K,Felix Stephan B,Gudnason Vilmundur,Alonso Alvaro,Roden Dan M,Kääb Stefan,Chasman Daniel I,Heckbert Susan R,Benjamin Emelia J^ORCID,Tanaka Toshihiro^ORCID,Lunetta Kathryn L,Lubitz Steven A,Ellinor Patrick T^ORCID, ,

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.3843.pdf

Reference39 articles.

1. Chugh, S.S. et al. Worldwide epidemiology of atrial fibrillation: a Global Burden of Disease 2010 Study. Circulation 129, 837–847 (2014).

2. January, C.T. et al. 2014 AHA/ACC/HRS guideline for the management of patients with atrial fibrillation: executive summary: a report of the American College of Cardiology/American Heart Association Task Force on practice guidelines and the Heart Rhythm Society. J. Am. Coll. Cardiol. 65, 2246–2280 (2014).

3. Gudbjartsson, D.F. et al. Variants conferring risk of atrial fibrillation on chromosome 4q25. Nature 448, 353–357 (2007).

4. Benjamin, E.J. et al. Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. Nat. Genet. 41, 879–881 (2009).

5. Ellinor, P.T. et al. Common variants in KCNN3 are associated with lone atrial fibrillation. Nat. Genet. 42, 240–244 (2010).

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