Search Results - Beiser, Erik J

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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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    Genetic variants for head size share genes and pathways with cancer by Knol, Maria J., Mishra, Aniket, van der Auwera, Sandra, Duperron, Marie-Gabrielle, Pawlak, Mikolaj A., Shin, Jean, Li, Gloria H.Y., Amod, Alyssa R., Tsuchida, Ami, Aygün, Nil, Beyer, Frauke, Bis, Joshua C., Bos, Daniel, Caspers, Svenja, Catheline, Gwenaëlle, Enlund-Cerullo, Maria, Helmer, Catherine, Jack, Clifford R., Jahanshad, Neda, Li, Shuo, Longstreth, W.T., Arfanakis, Konstantinos, Aribisala, Benjamin S., Bastin, Mark E., Cheng, Ching-Yu, Gottesman, Rebecca F., Liewald, David C.M., Lopez, Lorna M., Lopez, Oscar, Niessen, Wiro J., Sacco, Ralph L., Völzke, Henry, Yanek, Lisa, Yang, Jingyun, Bernard, Manon, Boomsma, Dorret I., Brickman, Adam M., Brodaty, Henry, Buitelaar, Jan K., Carr, Vaughan J., Chakravarty, M. Mallar, Ching, Christopher R.K., Corvin, Aiden, Curran, Joanne E., den Braber, Anouk, Erk, Susanne, Fedko, Iryna O., Fernández, Guillén, Fisher, Simon E., Ge, Tian, Goldman, Aaron L., Green, Robert C., Greven, Corina U., Hashimoto, Ryota, Henskens, Frans, Ho, Beng-Choon, Holmes, Avram J., Jablensky, Assen, Jia, Tianye, Kwok, John B., Lawrie, Stephen M., McDonald, Colm, McMahon, Katie L., McWhirter, Olvera, Rene L., Pandolfo, Massimo, Pantelis, Christos, Pappa, Irene, Reppermund, Simone, Rose, Emma Jane, Schall, Ulrich, Schumann, Gunter, Shen, Li, Soininen, Hilkka, Sprooten, Emma, Turner, Jessica A., Van Haren, Neeltje E.M., van 't Ent, Dennis, Wen, Wei, Wright, Margaret J., Wu, Jingqin, Medland, Sarah E., Miyamoto, Susumu, Moebus, Susanne, Muetzel, Ryan, Nagata, Manabu, Palmer, Nicholette D., Quidé, Yann, Roshchupkin, Gennady V., Schreiner, Pamela J., Shapland, Chin Yang, Sidney, Stephen, Uhlmann, Anne, Wittfeld, Katharina, Yang, Qiong, Brunner, Han G., Le Grand, Quentin, Bowden, Donald W., Cheung, Ching-Lung, Thompson, Paul M.

    Published in Cell reports. Medicine
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