From GWAS Catalog
The Catalog is a quality controlled, manually curated, literature-derived collection of all published genome-wide association studies.
- Genetic association analyses highlight biological pathways underlying mitral valve prolapse.
Nature genetics 2015 Oct 47 (10): 1206-11.
Dina Christian, Bouatia-Naji Nabila, Tucker Nathan, Delling Francesca N, Toomer Katelynn, Durst Ronen, Perrocheau Maelle, Fernandez-Friera Leticia, Solis Jorge, , Le Tourneau Thierry, Chen Ming-Huei, Probst Vincent, Bosse Yohan, Pibarot Philippe, Zelenika Diana, Lathrop Mark, Hercberg Serge, Roussel Ronan, Benjamin Emelia J, Bonnet Fabrice, Lo Su Hao, Dolmatova Elena, Simonet Floriane, Lecointe Simon, Kyndt Florence, Redon Richard, Le Marec Hervé, Froguel Philippe, Ellinor Patrick T, Vasan Ramachandran S, Bruneval Patrick, Markwald Roger R, Norris Russell A, Milan David J, Slaugenhaupt Susan A, Levine Robert A, Schott Jean-Jacques, Hagege Albert A, , Jeunemaitre Xavier, - Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium.
PloS one 2015 10 (10): e0140496.
Bis Joshua C, Sitlani Colleen, Irvin Ryan, Avery Christy L, Smith Albert Vernon, Sun Fangui, Evans Daniel S, Musani Solomon K, Li Xiaohui, Trompet Stella, Krijthe Bouwe P, Harris Tamara B, Quibrera P Miguel, Brody Jennifer A, Demissie Serkalem, Davis Barry R, Wiggins Kerri L, Tranah Gregory J, Lange Leslie A, Sotoodehnia Nona, Stott David J, Franco Oscar H, Launer Lenore J, Stürmer Til, Taylor Kent D, Cupples L Adrienne, Eckfeldt John H, Smith Nicholas L, Liu Yongmei, Wilson James G, Heckbert Susan R, Buckley Brendan M, Ikram M Arfan, Boerwinkle Eric, Chen Yii-Der Ida, de Craen Anton J M, Uitterlinden Andre G, Rotter Jerome I, Ford Ian, Hofman Albert, Sattar Naveed, Slagboom P Eline, Westendorp Rudi G J, Gudnason Vilmundur, Vasan Ramachandran S, Lumley Thomas, Cummings Steven R, Taylor Herman A, Post Wendy, Jukema J Wouter, Stricker Bruno H, Whitsel Eric A, Psaty Bruce M, Arnett Don - Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
Nature genetics 2014 Aug 46 (8): 826-36.
Arking Dan E, Pulit Sara L, Crotti Lia, van der Harst Pim, Munroe Patricia B, Koopmann Tamara T, Sotoodehnia Nona, Rossin Elizabeth J, Morley Michael, Wang Xinchen, Johnson Andrew D, Lundby Alicia, Gudbjartsson Daníel F, Noseworthy Peter A, Eijgelsheim Mark, Bradford Yuki, Tarasov Kirill V, Dörr Marcus, Müller-Nurasyid Martina, Lahtinen Annukka M, Nolte Ilja M, Smith Albert Vernon, Bis Joshua C, Isaacs Aaron, Newhouse Stephen J, Evans Daniel S, Post Wendy S, Waggott Daryl, Lyytikäinen Leo-Pekka, Hicks Andrew A, Eisele Lewin, Ellinghaus David, Hayward Caroline, Navarro Pau, Ulivi Sheila, Tanaka Toshiko, Tester David J, Chatel Stéphanie, Gustafsson Stefan, Kumari Meena, Morris Richard W, Naluai Åsa T, Padmanabhan Sandosh, Kluttig Alexander, Strohmer Bernhard, Panayiotou Andrie G, Torres Maria, Knoflach Michael, Hubacek Jaroslav A, Slowikowski Kamil, Raychaudhuri Soumya, Kumar Runjun D, Harris Tamara B, Launer Lenore J, Shuldiner Alan R, Alonso Alvaro, Bader Joel S, Ehret Georg, Huang Hailiang, Kao W H Linda, Strait James B, Macfarlane Peter W, Brown Morris, Caulfield Mark J, Samani Nilesh J, Kronenberg Florian, Willeit Johann, , , Smith J Gustav, Greiser Karin H, Meyer Zu Schwabedissen Henriette, Werdan Karl, Carella Massimo, Zelante Leopoldo, Heckbert Susan R, Psaty Bruce M, Rotter Jerome I, Kolcic Ivana, Polašek Ozren, Wright Alan F, Griffin Maura, Daly Mark J, , Arnar David O, Hólm Hilma, Thorsteinsdottir Unnur, , Denny Joshua C, Roden Dan M, Zuvich Rebecca L, Emilsson Valur, Plump Andrew S, Larson Martin G, O'Donnell Christopher J, Yin Xiaoyan, Bobbo Marco, D'Adamo Adamo P, Iorio Annamaria, Sinagra Gianfranco, Carracedo Angel, Cummings Steven R, Nalls Michael A, Jula Antti, Kontula Kimmo K, Marjamaa Annukka, Oikarinen Lasse, Perola Markus, Porthan Kimmo, Erbel Raimund, Hoffmann Per, Jöckel Karl-Heinz, Kälsch Hagen, Nöthen Markus M, , den Hoed Marcel, Loos Ruth J F, Thelle Dag S, Gieger Christian, Meitinger Thomas, Perz Siegfried, Peters Annette, Prucha Hanna, Sinner Moritz F, Waldenberger Melanie, de Boer Rudolf A, Franke Lude, van der Vleuten Pieter A, Beckmann Britt Maria, Martens Eimo, Bardai Abdennasser, Hofman Nynke, Wilde Arthur A M, Behr Elijah R, Dalageorgou Chrysoula, Giudicessi John R, Medeiros-Domingo Argelia, Barc Julien, Kyndt Florence, Probst Vincent, Ghidoni Alice, Insolia Roberto, Hamilton Robert M, Scherer Stephen W, Brandimarto Jeffrey, Margulies Kenneth, Moravec Christine E, del Greco M Fabiola, Fuchsberger Christian, O'Connell Jeffrey R, Lee Wai K, Watt Graham C M, Campbell Harry, Wild Sarah H, El Mokhtari Nour E, Frey Norbert, Asselbergs Folkert W, Mateo Leach Irene, Navis Gerjan, van den Berg Maarten P, van Veldhuisen Dirk J, Kellis Manolis, Krijthe Bouwe P, Franco Oscar H, Hofman Albert, Kors Jan A, Uitterlinden André G, Witteman Jacqueline C M, Kedenko Lyudmyla, Lamina Claudia, Oostra Ben A, Abecasis Gonçalo R, Lakatta Edward G, Mulas Antonella, Orrú Marco, Schlessinger David, Uda Manuela, Markus Marcello R P, Völker Uwe, Snieder Harold, Spector Timothy D, Ärnlöv Johan, Lind Lars, Sundström Johan, Syvänen Ann-Christine, Kivimaki Mika, Kähönen Mika, Mononen Nina, Raitakari Olli T, Viikari Jorma S, Adamkova Vera, Kiechl Stefan, Brion Maria, Nicolaides Andrew N, Paulweber Bernhard, Haerting Johannes, Dominiczak Anna F, Nyberg Fredrik, Whincup Peter H, Hingorani Aroon D, Schott Jean-Jacques, Bezzina Connie R, Ingelsson Erik, Ferrucci Luigi, Gasparini Paolo, Wilson James F, Rudan Igor, Franke Andre, Mühleisen Thomas W, Pramstaller Peter P, Lehtimäki Terho J, Paterson Andrew D, Parsa Afshin, Liu Yongmei, van Duijn Cornelia M, Siscovick David S, Gudnason Vilmundur, Jamshidi Yalda, Salomaa Veikko, Felix Stephan B, Sanna Serena, Ritchie Marylyn D, Stricker Bruno H, Stefansson Kari, Boyer Laurie A, Cappola Thomas P, Olsen Jesper V, Lage Kasper, Schwartz Peter J, Kääb Stefan, Chakravarti Aravinda, Ackerman Michael J, Pfeufer Arne, de Bakker Paul I W, Newton-Cheh Christoph - Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality.
European heart journal 2014 Feb 35 (8): 524-31.
Seppälä Ilkka, Kleber Marcus E, Lyytikäinen Leo-Pekka, Hernesniemi Jussi A, Mäkelä Kari-Matti, Oksala Niku, Laaksonen Reijo, Pilz Stefan, Tomaschitz Andreas, Silbernagel Günther, Boehm Bernhard O, Grammer Tanja B, Koskinen Tuomas, Juonala Markus, Hutri-Kähönen Nina, Alfthan Georg, Viikari Jorma S A, Kähonen Mika, Raitakari Olli T, März Winfried, Meinitzer Andreas, Lehtimäki Terho, - Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Nature genetics 2013 Sep 45 (9): 1044-9.
Bezzina Connie R, Barc Julien, Mizusawa Yuka, Remme Carol Ann, Gourraud Jean-Baptiste, Simonet Floriane, Verkerk Arie O, Schwartz Peter J, Crotti Lia, Dagradi Federica, Guicheney Pascale, Fressart Véronique, Leenhardt Antoine, Antzelevitch Charles, Bartkowiak Susan, Borggrefe Martin, Schimpf Rainer, Schulze-Bahr Eric, Zumhagen Sven, Behr Elijah R, Bastiaenen Rachel, Tfelt-Hansen Jacob, Olesen Morten Salling, Kääb Stefan, Beckmann Britt M, Weeke Peter, Watanabe Hiroshi, Endo Naoto, Minamino Tohru, Horie Minoru, Ohno Seiko, Hasegawa Kanae, Makita Naomasa, Nogami Akihiko, Shimizu Wataru, Aiba Takeshi, Froguel Philippe, Balkau Beverley, Lantieri Olivier, Torchio Margherita, Wiese Cornelia, Weber David, Wolswinkel Rianne, Coronel Ruben, Boukens Bas J, Bézieau Stéphane, Charpentier Eric, Chatel Stéphanie, Despres Aurore, Gros Françoise, Kyndt Florence, Lecointe Simon, Lindenbaum Pierre, Portero Vincent, Violleau Jade, Gessler Manfred, Tan Hanno L, Roden Dan M, Christoffels Vincent M, Le Marec Hervé, Wilde Arthur A, Probst Vincent, Schott Jean-Jacques, Dina Christian, Redon Richa
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