A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease

Autor: Emmi Tikkanen, Elias Salfati, Majid Nikpay, Sonia S. Anand, Heribert Schunkert, Thomas Quertermous, George Dedoussis, Abbas Dehghan, Evelin Mihailov, Danish Saleheen, Lars Lannfelt, M. De Andrade, Daniel I. Chasman, Stanley L. Hazen, Vilmundur Gudnason, Christopher Grace, Christina Willenborg, Xueli Yang, Paul M. Ridker, Panos Deloukas, Hwang S-J., Eric Boerwinkle, Sekar Kathiresan, Lars Bertram, Kim B-J., Yun Kyoung Kim, Lokki M-L., Philippe M. Frossard, Adil Rasheed, Marc Haber, Alistair S. Hall, Kathleen Stirrups, Daniel J. Rader, Christopher B. Granger, Ingrid B. Borecki, Weihua Zhang, Thomas Meitinger, Liming Qu, Maris Alver, Wei Zhao, Samuli Ripatti, Andres Metspalu, Diego Ardissino, Memon F-U-R., Themistocles L. Assimes, Sebastian M. Armasu, Won H-H., L. A. Cupples, Tõnu Esko, Stephen M. Schwartz, Dongfeng Gu, Alanna C. Morrison, Han B-G., Nancy L. Pedersen, Tom R. Webb, Joachim Thiery, Marcus E. Kleber, Ligui Wang, J W Jukema, Thorsten Kessler, Xiangfeng Lu, Frank Beutner, Alison H. Goodall, Loukianos S. Rallidis, Natalia Pervjakova, Loos Rjf., Stavroula Kanoni, Leanne M. Hall, Patrik K. E. Magnusson, John C. Chambers, Christian Hengstenberg, Svati H. Shah, Olle Melander, Richa Saxena, Markus Perola, Alexandre F.R. Stewart, Jeanette Erdmann, Nadeem Hayyat Mallick, N. R. van Zuydam, Omri Gottesman, Jemma C. Hopewell, Hugh Watkins, John R. Thompson, Carlos Iribarren, Anders Hamsten, Rory Collins, Theodosios Kyriakou, Markus Scholz, Dharambir K. Sanghera, Jie Huang, Julie E. Buring, Christopher J. O'Donnell, Anuj Goel, Lynda M. Rose, Martin Farrall, Albert V. Smith, Lyytikäinen L-P., Winfried März, Muredach P. Reilly, Mary F. Feitosa, Andrew Bjonnes, Stella Trompet, John Danesh, Robert Roberts, Stefan Gustafsson, Christian Gieger, Ian Ford, Lingyao Zeng, Lars Lind, David J. Stott, Erik Ingelsson, Colin N. A. Palmer, Markku S. Nieminen, M Samuel, Annette Peters, Kirsi Auro, Dominique Gauguier, Narinder K. Mehra, Khan Shah Zaman, P. De Vries, Nilesh J. Samani, Inke R. König, Juha Sinisalo, Ilja Demuth, Pekka J. Karhunen, Wolfgang Lieb, Andrew P. Morris, Nora Franceschini, Veikko Salomaa, Robert Clarke, Erwin P. Bottinger, Roberto Elosua, Yingchang Lu, André G. Uitterlinden, Shapour Jalilzadeh, Cecilia M. Lindgren, Shufeng Chen, Terho Lehtimäki, Jaspal S. Kooner, Tamara B. Harris, Stephen E. Epstein, Udo Seedorf, Oscar H. Franco, Pierre Zalloua, King Wai Lau, Iftikhar J. Kullo, Albert Hofman, Christopher P. Nelson, MariaGrazia Franzosi, Ruth McPherson

Publikováno v: Nature Genetics, 47(10), 1121
Nature Genetics, 47(10), 1121-1130. Nature Publishing Group
Nature genetics
Nature Genetics

Existing knowledge of genetic variants affecting risk of coronary artery disease (CAD) is largely based on genome-wide association study (GWAS) analysis of common SNPs. Leveraging phased haplotypes from the 1000 Genomes Project, we report a GWAS meta

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e125112055851368aa2c8ef11bf42dd
http://hdl.handle.net/1887/108152