Publications by:
Bradford B. Worrall
Also publishes as (Bradford Worrall)
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Majersik, Jennifer J., Cole, John W., Golledge, Jonathan, Rost, Natalia S., Chan, Yu-Feng, Gurol, M. Edip, Lindgren, Arne G., Woo, Daniel, Fernandez-Cadenas, Israel, Chen, Donna T., Thijs, Vincent, Worrall, Bradford B., Kamal, Ayeesha, Bentley, Paul, Wardlaw, Joanna M., Ruigrok , Ynte M., Battey, Thomas W.K., Schmidt , Reinhold, Montaner , Joan, Giese, Anne-Katrin, Roquer, Jaume, Jiménez-Conde, Jordi, Lee, Chaeyoung, Ay, Hakan, Martin , Juan Jose, Rosand, Jonathan, and Maguire, Jane (2015) Recommendations from the international stroke genetics consortium, part 1: standardized phenotypic data collection. Stroke, 46 (1). pp. 279-284.
Traylor, Matthew, Farrall, Martin, Holliday, Elizabeth G., Sudlow, Cathie, Hopewell, Jemma C., Cheng, Yu-Ching, Fornage, Myriam, Ikram, M Arfan, Malik, Rainer, Bevan, Steve, Thorsteinsdottir, Unnur, Nalls, Mike A., Longstreth, W.T., Wiggins, Kerri L., Yadav, Sunaina, Parati, Eugenio A., DeStefano, Anita L., Worrall, Bradford B., Kittner, Steven J., Khan, Muhammad Saleem, Reiner, Alex P., Helgadottir, Anna, Achterberg, Sefanja, Fernandez-Cadenas, Israel, Abboud, Sherine, Schmidt, Reinhold, Walters, Matthew, Chen, Wei-Min, Ringelstein, E Bernd, O'Donnell, Martin, Kee, Weang, Pera, Joanna , Lemmens, Robin, Norrving, Bo, Higgins, Peter, Benn, Marianne, Sale, Michele, Kuhlenbäumer, Gregor, Doney, Alexander S.F., Vicente, Astrid M., Delavaran, Hossein, Algra, Ale, Davies, Gail, Oliveira, Sofia A., Palmer, Colin N.A., Deary, Ian, Schmidt, Helena, Pandolfo, Massimo, Montaner, Joan, Carty, Cara, de Bakker, Paul I.W., Kostulas, Konstantinos, Ferro, Jose M., van Zuydam, Natalie R., Valdimarsson, Einar, Nordestgaard, Børge G., Lindgren, Arne, Thijs, Vincent, Slowik, Agnieszka, Saleheen, Danish, Paré, Guillaume, Berger, Klaus, Thorleifsson, Gudmar, The Australian Stroke Genetics Collaborative, including Jonathan Golledge, Wellcome Trust Case Control Consortium 2 (WTCCC2), Hofman, Albert, Mosley, Thomas H., Mitchell, Braxton D., Furie, Karen, Clarke, Robert, Levi, Christopher, Seshadri, Sudha, Gschwendtner, Andreas, Boncoraglio, Giorgio B., Sharma, Pankaj, Bis, Joshua C., Gretarsdottir, Solveig, Psaty, Bruce M., Rothwell, Peter M., Rosand, Jonathan, Meschia, James F., Stefansson, Kari, Dichgans, Martin, and Markus, Hugh S. (2012) Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies. Lancet Neurology, 11 (11). pp. 951-962.
Cheng, Yu-Ching, Anderson, Christopher D., Bione, Silvia, Keene, Keith, Maguire, Jane M., Nalls, Michael, Rasheed, Asif, Zeginigg, Marion, Attia, John, Baker, Ross, Barlera, Simona, Biffi, Alessandro, Bookman, Ebony, Brott, Thomas G., Brown, Robert D., Chen , Fang, Chen, Wei-Min, Ciusani, Emilio, Cole, John W., Cortellini, Lynelle, Danesh, John, Doheny, Kimberly, Ferrucci, Luigi, Franzosi, Maria Grazia, Frosshard, Philippe, Furie, Karen L., Golledge, Jonathan, Hankey, Graeme J., Hernandez, Dena, Holliday, Elizabeth G., Hsu , Fang-Chi, Jannes, Jim, Kamal, Ayeesha, Khan, Muhammad Saleem, Kittner, Steven J., Koblar, Simon A., Lewis, Martin, Lincz, Lisa, Lisa, Antonella, Matarin, Mar, Moscato, Pablo, Mychaleckyj, Josyf C., Parati, Eugenio A., Parolo, Silvia, Pugh, Elizabeth, Rost, Natalia S., Schallert, Michael, Schmidt, Helena, Scott, Rodney J., Sturm, Jonathan W., Yadav, Sunaina, Zaidi, Moazzam, Boncoraglio, Giorgio B., Levi, Christopher Royce, Meschia, James F., Rosand, Jonathan, Sale, Michele, Saleheen, Danish, Schmidt, Reinhold, Sharma, Pankaj, Worrall, Bradford, Mitchell, Braxton D., GARNET Collaborative Research Group, and GENEVA Consortium (2012) Are myocardial infarction-associated single nucleotide polymorphisms associated with ischemic stroke? Stroke, 43 (4). pp. 980-986.
Holliday, Elizabeth G., Maguire, Jane M., Evans, Tiffany-Jane, Koblar, Simon A., Jannes, Jim, Sturm, Jonathan W., Hankey, Graeme J., Baker, Ross, Golledge, Jonathan, Parsons, Mark W., Malik, Rainer, McEvoy, Mark, Biros, Erik, Lewis, Martin D., Lincz, Lisa F., Peel, Roseanne, Oldmeadow, Christopher, Smith, Wayne, Moscato, Pablo, Barlera, Simona, Bevan, Steve, Bis, Joshua C., Boerwinkle, Eric, Boncoraglio, Giorgio B., Brott, Thomas G., Brown, Robert D., Cheng, Yu-Ching, Cole, John W., Cotlarciuc, Ioanna, Devan, William J., Fornage, Myriam, Furie, Karen L., Grétarsdóttir, Sólveig, Gschwendtner, Andreas, Ikram, M. Arfan, Longstreth, W.T., Meschia, James F., Mitchell, Braxton D., Mosley, Thomas H., Nalls, Michael A., Parati, Eugenio A., Psaty, Bruce M., Sharma, Pankaj, Stefansson, Kari, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Traylor, Matthew, Verhaaren, Benjamin F.J., Wiggins, Kerri L., Worrall, Bradford B., Sudlow, Cathie, Rothwell, Peter M., Farrall, Martin, Dichgans, Martin, Rosand, Jonathan, Markus, Hugh S., Scott, Rodney J., Levi, Christopher, and Attia, John (2012) Common variants at 6p21.1 are associated with large artery atherosclerotic stroke. Nature Genetics, 44 (10). pp. 1147-1151.