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.

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.