학술논문
A Genome-Wide Association Study Identifies LIPAas a Susceptibility Gene for Coronary Artery Disease
Document Type
Article
Author
Wild, Philipp S.; Zeller, Tanja; Schillert, Arne; Szymczak, Silke; Sinning, Christoph R.; Deiseroth, Arne; Schnabel, Renate B.; Lubos, Edith; Keller, Till; Eleftheriadis, Medea S.; Bickel, Christoph; Rupprecht, Hans J.; Wilde, Sandra; Rossmann, Heidi; Diemert, Patrick; Cupples, L. Adrienne; Perret, Claire; Erdmann, Jeanette; Stark, Klaus; Kleber, Marcus E.; Epstein, Stephen E.; Voight, Benjamin F.; Kuulasmaa, Kari; Li, Mingyao; Schäfer, Arne S.; Klopp, Norman; Braund, Peter S.; Sager, Hendrik B.; Demissie, Serkalem; Proust, Carole; König, Inke R.; Wichmann, Heinz-Erich; Reinhard, Wibke; Hoffmann, Michael M.; Virtamo, Jarmo; Burnett, Mary Susan; Siscovick, David; Wiklund, Per Gunnar; Qu, Liming; Mokthari, Nour Eddine El; Thompson, John R.; Peters, Annette; Smith, Albert V.; Yon, Emmanuelle; Baumert, Jens; Hengstenberg, Christian; März, Winfried; Amouyel, Philippe; Devaney, Joseph; Schwartz, Stephen M.; Saarela, Olli; Mehta, Nehal N.; Rubin, Diana; Silander, Kaisa; Hall, Alistair S.; Ferrieres, Jean; Harris, Tamara B.; Melander, Olle; Kee, Frank; Hakonarson, Hakon; Schrezenmeir, Juergen; Gudnason, Vilmundur; Elosua, Roberto; Arveiler, Dominique; Evans, Alun; Rader, Daniel J.; Illig, Thomas; Schreiber, Stefan; Bis, Joshua C.; Altshuler, David; Kavousi, Maryam; Witteman, Jaqueline C.M.; Uitterlinden, Andre G.; Hofman, Albert; Folsom, Aaron R.; Barbalic, Maja; Boerwinkle, Eric; Kathiresan, Sekar; Reilly, Muredach P.; O'Donnell, Christopher J.; Samani, Nilesh J.; Schunkert, Heribert; Cambien, Francois; Lackner, Karl J.; Tiret, Laurence; Salomaa, Veikko; Munzel, Thomas; Ziegler, Andreas; Blankenberg, Stefan
Source
Circulation: Cardiovascular Genetics; August 2011, Vol. 4 Issue: 4 p403-412, 10p
Subject
Language
ISSN
1942325X
Abstract
eQTL analyses are important to improve the understanding of genetic association results. We performed a genome-wide association and global gene expression study to identify functionally relevant variants affecting the risk of coronary artery disease (CAD).