Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study

Autor: Pulit, Sara L, McArdle, Patrick F, Wong, Quenna, Malik, Rainer, Gwinn, Katrina, Achterberg, Sefanja, Algra, Ale, Amouyel, Philippe, Anderson, Christopher D, Arnett, Donna K, Arsava, Ethem Murat, Attia, John, Ay, Hakan, Bartz, Traci M, Battey, Thomas, Benavente, Oscar R, Bevan, Steve, Biffi, Alessandro, Bis, Joshua C, Blanton, Susan H, Boncoraglio, Giorgio B, Brown, Robert D, Jr, Burgess, Annette I, Carrera, Caty, Chapman Smith, Sherita N, Chasman, Daniel I, Chauhan, Ganesh, Chen, Wei-Min, Cheng, Yu-Ching, Chong, Michael, Cloonan, Lisa K, Cole, John W, Cotlarciuc, Ioana, Cruchaga, Carlos, Cuadrado-Godia, Elisa, Dave, Tushar, Dawson, Jesse, Debette, Stéphanie, Delavaran, Hossein, Dell, Cameron A, Dichgans, Martin, Doheny, Kimberly F, Dong, Chuanhui, Duggan, David J, Engström, Gunnar, Evans, Michele K, Pallejà, Xavier Estivill, Faul, Jessica D, Fernández-Cadenas, Israel, Fornage, Myriam, Frossard, Philippe M, Furie, Karen, Gamble, Dale M, Gieger, Christian, Giese, Anne-Katrin, Giralt-Steinhauer, Eva, González, Hector M, Goris, An, Gretarsdottir, Solveig, Grewal, Raji P, Grittner, Ulrike, Gustafsson, Stefan, Han, Buhm, Hankey, Graeme J, Heitsch, Laura, Higgins, Peter, Hochberg, Marc C, Holliday, Elizabeth, Hopewell, Jemma C, Horenstein, Richard B, Howard, George, Ikram, M Arfan, Ilinca, Andreea, Ingelsson, Erik, Irvin, Marguerite R, Jackson, Rebecca D, Jern, Christina, Conde, Jordi Jiménez, Johnson, Julie A, Jood, Katarina, Kahn, Muhammad S, Kaplan, Robert, Kappelle, L Jaap, Kardia, Sharon L R, Keene, Keith L, Kissela, Brett M, Kleindorfer, Dawn O, Koblar, Simon, Labovitz, Daniel, Launer, Lenore J, Laurie, Cathy C, Laurie, Cecelia A, Lee, Cue Hyunkyu, Lee, Jin-Moo, Lehm, Manuel, Lemmens, Robin, Levi, Christopher, Leys, Didier, Lindgren, Arne, Longstreth, W T, Jr, Maguire, Jane, Manichaikul, Ani, Markus, Hugh S, McClure, Leslie A, McDonough, Caitrin W, Meisinger, Christa, Melander, Olle, Meschia, James F, Mola-Caminal, Marina, Montaner, Joan, Mosley, Thomas H, Müller-Nurasyid, Martina, Nalls, Mike A, O'Connell, Jeffrey R, O'Donnell, Martin, Ois, ángel, Papanicolaou, George J, Paré, Guillaume, Peddareddygari, Leema Reddy, Pedersén, Annie, Pera, Joanna, Peters, Annette, Poole, Deborah, Psaty, Bruce M, Rabionet, Raquel, Raffeld, Miriam R, Rannikmäe, Kristiina, Rasheed, Asif, Redfors, Petra, Reiner, Alex P, Rexrode, Kathryn, Ribasés, Marta, Rich, Stephen S, Robberecht, Wim, Rodriguez-Campello, Ana, Rolfs, Arndt, Roquer, Jaume, Rose, Lynda M, Rosenbaum, Daniel, Rost, Natalia S, Rothwell, Peter M, Rundek, Tatjana, Ryan, Kathleen A, Sacco, Ralph L, Sale, Michèle M, Saleheen, Danish, Salomaa, Veikko, Sánchez-Mora, Cristina, Schmidt, Carsten Oliver, Schmidt, Helena, Schmidt, Reinhold, Schürks, Markus, Scott, Rodney, Segal, Helen C, Seiler, Stephan, Seshadri, Sudha, Sharma, Pankaj, Shuldiner, Alan R, Silver, Brian, Slowik, Agnieszka, Smith, Jennifer A, Söderholm, Martin, Soriano, Carolina, Sparks, Mary J, Stanne, Tara, Stefansson, Kari, Stine, O Colin, Strauch, Konstantin, Sturm, Jonathan, Sudlow, Cathie LM, Tajuddin, Salman M, Talbert, Robert L, Tatlisumak, Turgut, Thijs, Vincent, Thorleifsson, Gudmar, Thorsteindottir, Unnur, Tiedt, Steffen, Traylor, Matthew, Trompet, Stella, Valant, Valerie, Waldenberger, Melanie, Walters, Matthew, Wang, Liyong, Wassertheil-Smoller, Sylvia, Weir, David R, Wiggins, Kerri L, Williams, Stephen R, Wloch-Kopec, Dorota, Woo, Daniel, Woodfield, Rebecca, Wu, Ona, Xu, Huichun, Zonderman, Alan B, Worrall, Bradford B, de Bakker, Paul IW, Kittner, Steven J, Mitchell, Braxton D, Rosand, Jonathan, Sudlow, Cathie L M, Worrall, Bradford B Worrall, Arnett, Donna K Arnett, Benavente, Oscar, Wasssertheil-Smoller, Sylvia

Publikováno v: In The Lancet Neurology February 2016 15(2):174-184

Meta-analysis of Genome-wide Association Studies Identifies 1q22 as a Susceptibility Locus for Intracerebral Hemorrhage

Autor: Woo, Daniel, Falcone, Guido J., Devan, William J., Brown, W. Mark, Biffi, Alessandro, Howard, Timothy D., Anderson, Christopher D., Brouwers, H. Bart, Valant, Valerie, Battey, Thomas W.K., Radmanesh, Farid, Raffeld, Miriam R., Baedorf-Kassis, Sylvia, Deka, Ranjan, Woo, Jessica G., Martin, Lisa J., Haverbusch, Mary, Moomaw, Charles J., Sun, Guangyun, Broderick, Joseph P., Flaherty, Matthew L., Martini, Sharyl R., Kleindorfer, Dawn O., Kissela, Brett, Comeau, Mary E., Jagiella, Jeremiasz M., Schmidt, Helena, Freudenberger, Paul, Pichler, Alexander, Enzinger, Christian, Hansen, Björn M., Norrving, Bo, Jimenez-Conde, Jordi, Giralt-Steinhauer, Eva, Elosua, Roberto, Cuadrado-Godia, Elisa, Soriano, Carolina, Roquer, Jaume, Kraft, Peter, Ayres, Alison M., Schwab, Kristin, McCauley, Jacob L., Pera, Joanna, Urbanik, Andrzej, Rost, Natalia S., Goldstein, Joshua N., Viswanathan, Anand, Stögerer, Eva-Maria, Tirschwell, David L., Selim, Magdy, Brown, Devin L., Silliman, Scott L., Worrall, Bradford B., Meschia, James F., Kidwell, Chelsea S., Montaner, Joan, Fernandez-Cadenas, Israel, Delgado, Pilar, Malik, Rainer, Dichgans, Martin, Greenberg, Steven M., Rothwell, Peter M., Lindgren, Arne, Slowik, Agnieszka, Schmidt, Reinhold, Langefeld, Carl D., Rosand, Jonathan

Publikováno v: In The American Journal of Human Genetics 3 April 2014 94(4):511-521

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