Search Results - Levi, Ralph S.

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    Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies by Chauhan, Ganesh, Arnold, Corey R, Chu, Audrey Y, Reyahi, Azadeh, Bis, Joshua C, Havulinna, Aki S, Trompet, Stella, Manichaikul, Ani, Teumer, Alexander, Gustafsson, Stefan, Bartz, Traci M, Bellenguez, Céline, Vidal, Jean Sebastien, Kjartansson, Olafur, Satizabal, Claudia L, Xue, Flora, Liu, Yongmei, Bevan, Steve, Hopewell, Jemma C, Heckbert, Susan R, Rice, Kenneth, Smith, Nicholas L, Levi, Christopher, Sharma, Pankaj, Sudlow, Cathie LM, Cole, John W, Schmidt, Reinhold, Meschia, James, Thijs, Vincent, Melander, Olle, Grewal, Raji P, Sacco, Ralph L, Rundek, Tatjana, Rothwell, Peter M, Jern, Christina, Johnson, Julie A, Benavente, Oscar R, Lee, Jin-Moo, Wong, Quenna, Aparicio, Hugo J, Engelter, Stefan T, Kloss, Manja, Pezzini, Alessandro, Buring, Julie E, Ridker, Paul M, Berr, Claudine, Dartigues, Jean-François, Hamsten, Anders, Traylor, Matthew, Pedersen, Nancy L, Lannfelt, Lars, Morris, Andrew P, Jimenez-Conde, Jordi, Montaner, Joan, Slowik, Agnieszka, Woo, Daniel, Hofman, Albert, Koudstaal, Peter J, Portegies, Marileen L P, Uitterlinden, André G, Ford, Ian, Jukema, J Wouter, Stott, David J, Allen, Norrina B, Johnson, Andrew D, De Jager, Philip L, White, Charles C, Markus, Marcello Ricardo Paulista, Schminke, Ulf, Boncoraglio, Giorgio B, Clarke, Robert, Kamatani, Yoichiro, Dallongeville, Jean, Rotter, Jerome I, Nalls, Michael A, Griswold, Michael E, Knopman, David S, Windham, B Gwen, Beiser, Alexa, Vartiainen, Erkki, French, Curtis R, Pastinen, Tomi, Gudnason, Vilmundur, Kurth, Tobias, Harris, Tamara B, Rich, Stephen S, deStefano, Anita L, Rosand, Jonathan, Mosley, Thomas H, Ingelsson, Erik, van Duijn, Cornelia M, Tzourio, Christophe, Rexrode, Kathryn M, Lehmann, Ordan J, Launer, Lenore J, Carlsson, Peter, Chasman, Daniel I, Childs, Sarah J, Seshadri, Sudha, Debette, Stéphanie

    Published in Lancet neurology
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    Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study by McArdle, Patrick F, Malik, Rainer, Algra, Ale, Amouyel, Philippe, Anderson, Christopher D, Arsava, Ethem Murat, Ay, Hakan, Blanton, Susan H, Brown, Robert D, Burgess, Annette I, Chasman, Daniel I, Chen, Wei-Min, Cheng, Yu-Ching, Cotlarciuc, Ioana, Cruchaga, Carlos, Dave, Tushar, Dawson, Jesse, Delavaran, Hossein, Dell, Cameron A, Dichgans, Martin, Doheny, Kimberly F, Dong, Chuanhui, Duggan, David J, Fornage, Myriam, Frossard, Philippe M, Gamble, Dale M, Giralt-Steinhauer, Eva, Grewal, Raji P, Han, Buhm, Hankey, Graeme J, Heitsch, Laura, Higgins, Peter, Hopewell, Jemma C, Horenstein, Richard B, Howard, George, Ingelsson, Erik, Jackson, Rebecca D, Jern, Christina, Jood, Katarina, Kahn, Muhammad S, Kappelle, L Jaap, Kardia, Sharon L R, Keene, Keith L, Kissela, Brett M, Labovitz, Daniel, Lee, Cue Hyunkyu, Lee, Jin-Moo, Lehm, Manuel, Levi, Christopher, Leys, Didier, Maguire, Jane, Manichaikul, Ani, McClure, Leslie A, Mola-Caminal, Marina, Montaner, Joan, Müller-Nurasyid, Martina, Nalls, Mike A, O'Connell, Jeffrey R, O'Donnell, Martin, Papanicolaou, George J, Paré, Guillaume, Pera, Joanna, Peters, Annette, Rabionet, Raquel, Raffeld, Miriam R, Rannikmäe, Kristiina, Rasheed, Asif, Rexrode, Kathryn, Rolfs, Arndt, Rose, Lynda M, Sacco, Ralph L, Schmidt, Reinhold, Schürks, Markus, Segal, Helen C, Seiler, Stephan, Shuldiner, Alan R, Silver, Brian, Slowik, Agnieszka, Smith, Jennifer A, Söderholm, Martin, Sparks, Mary J, Sudlow, Cathie LM, Tajuddin, Salman M, Talbert, Robert L, Tatlisumak, Turgut, Thorsteindottir, Unnur, Tiedt, Steffen, Trompet, Stella, Waldenberger, Melanie, Wang, Liyong, Wassertheil-Smoller, Sylvia, Weir, David R, Wiggins, Kerri L, Wloch-Kopec, Dorota, Woodfield, Rebecca, Xu, Huichun, Zonderman, Alan B, Worrall, Bradford B, Kittner, Steven J, Arnett, Donna K Arnett

    Published in Lancet neurology
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