Objects
Malik, Rainer, Bevan, Steve, de Stefano, Anita L., Fornage, Myriam, Psaty, Bruce M., Ikram, M. Afran, Launer, Lenore J., Van Duijn, Cornelia M., Sharma, Pankaj, Mitchell, Braxton D., Rosand, Jonathan, Meschia, James F., Nalls, Michael A., Levi, Christopher, Rothwell, Peter M., Sudlow, Cathie, Markus, Hugh S., Seshadri, Sudha, Dichgans, Martin, MD Wellcome Trust Case Control Consortium 2,, Holliday, Elizabeth G., Devan, William J., Cheng, Yu-Ching, Ibrahim-Verbaas, Carla A., Verhaaren, Benjamin F. J., Bis, Joshua C., Joon, Aron Y.. Lippincott Williams & Wilkins; 2014. Multilocus genetic risk score associates with ischemic stroke in case-control and prospective cohort studies.
Dichgans, Martin, Malik, Rainer, Ódonnell, Christopher J., Fornage, Myriam, Thorsteinsdottir, Unnur, Psaty, Bruce M., Hengstenberg, Christian, Seshadri, Sudha, Erdmann, Jeanette, Bis, Joshua C., Peters, Annette, Boncoraglio, Giorgio B., König, Inke R., März, Winfred, Meschia, James F., Kathiresan, Sekar, Ikram, M. Arfan, McPherson, Ruth, Stefansson, Kari, Sudlow, Cathie, Reilly, Muredach, Thompson, John R., Sharma, Pankaj, Rosand, Jonathon, Hopewell, Jemma C., Chambers, John C., Watkins, Hugh, Rothwell, Peter M., Roberts, Robert, Markus, Hugh S., Samani, Nilesh J., Farrall, Martin, Schunkert, Heribert, Clarke, Robert, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Mitchell, Branxton D., Assimes, Themistocles L., Levi, Christopher. Lippincott Williams & Wilkins; 2014. Shared genetic susceptibility to ischemic stroke and coronary artery disease : a genome-wide analysis of common variants.
Williams, Frances M. K., Carter, Angela M., Sudlow, Cathie, Farrall, Martin, Silander, Kaisa, Kaunisto, Mari, Wagner, Peter, Saarela, Olli, Kuulasmaa, Kari, Virtamo, Jarmo, Salomaa, Veikko, Amouyel, Philippe, Hysi, Pirro G., Bis, Joshua C., Levi, Christopher, Attia, John, Holliday, Elizabeth G., Scott, Rodney J., , , , , , Surdulescu, Gabriela, , , , , , , , , , , Hodgkiss, Dylan, , , , , , , , , , , Soranzo, Nicole, , , , , , , , , , , Traylor, Matthew, , Bevan, Steve, Dichgans, Martin, Rothwell, Peter M. W.. John Wiley & Sons; 2013. Ischemic stroke is associated with the ABO locus: the EuroCLOT Study.
Holliday, Elizabeth G., Traylor, Matthew, Boncoraglio, Giorgio B., Clarke, Robert, Cole, John W., Fornage, Myriam, Furie, Karen L., Ikram, M. Arfan, Jannes, Jim, Kittner, Steven J., Lincz, Lisa F., Maguire, Jane M., Malik, Rainer, Oldmeadow, Christopher, Scott, Rodney J., Levi, Christopher, Attia, John, , , , , , , Bevan, Steve, , , , , , , , , , , Falcone, Guido, , Hopewell, Jemma C., Cheng, Yu-Ching, Cotlarciuc, Ioana, Bis, Joshua C., Boerwinkle, Eric. Lippincott Williams & Wilkins; 2015. Genetic overlap between diagnostic subtypes of ischemic stroke.
Debette, Stéphanie, Ibrahim Verbaas, Carla A., Yang, Qiong, , , , , , , , , , , deStefano, Anita L., , , , , , , , , , , de Quervain, Dominique J. F., , , , , , Srikanth, Velandai, Lahti, Jari, Grabe, Hans J., Smith, Jennifer A., Priebe, Lutz, Yu, Lei, Karbalai, Nazanin, Bressler, Jan, Oldmeadow, Christopher, Holliday, Elizabeth G., Schofield, Peter, Attia, John, , , , , , , Schuur, Maaike, , , , , , , , , , , Smith, Albert, , , , , , , , , , , Bis, Joshua C., , , , , , , , , , , Davies, Gail, , , , , , , , , , , Wolf, Christiane, , , , , , , , , , , Gudnason, Vilmundur, , , , , , , , , , , Chibnik, Lori B., , , , , , , , , , . Elsevier; 2015. Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium.
Chauhan, Ganesh, Adams, Hieab H. H., Satizabal, Claudia L., Bis, Joshua C., Teumer, Alexander, Sargurupremraj, Muralidharan, Hofer, Edith, Trompet, Stella, Hilal, Saima, Smith, Albert Vernon, Jian, Xueqiu, Malik, Rainer, Traylor, Matthew, Pulit, Sara L., Amouyel, Philippe, Mazoyer, Bernard, Zhu, Yi-Cheung, Kaffashian, Sara, Schilling, Sabrina, Beecham, Gary W., Montine, Thomas J., Schellenberg, G. D., Kjartansson, O., Guðnason, V., Knopman, D. S., Griswold, M. E., Windham, B. G., Gottesman, R. F., Mosley, T. H., Schmidt, R., Saba, Y., Schmidt, H., Takeuchi, F., Yamaguchi, S., Nabika, T., Kato, N, Rajan, K. B., Aggarwal, N. T., De Jager, P. L., Evans, D. A., Psaty, B M., Rotter, J. I., Rice, K., Lopez, O. L., Liao, J., Chen, C., Cheng, C.Y., Wong, T. Y., Ikram, M. K., van der Lee, S. J., Amin, N., Chouraki, V., Destefano, A. L., Aparicio, H. J., Romero, J. R., Maillard, P., Decarli, C., Wardlaw, J. M., Del C. Valdés Hernández, M., Luciano, M., Liewald, D., Deary, I. J., Starr, J. M., Bastin, M. E., Maniega, S. M., Slagboom, P. E., Beekman, M., Deelen, J., Uh, H. W., Lemmens, R., Brodaty, H., Wright, MJ., Ames, D., Boncoraglio, G. B., Hopewell, J. C., Beecham, A. H., Blanton, S. H., Wright, C. B., Sacco, R. L., Wen, W., Thalamuthu, A., Armstrong, N. J., Chong, E., Schofield, P. R., Kwok, J. B., van der Grond, J., Stott, D. J., Ford, I., Jukema, J. W., Vernooij, M. W., Hofman, A., Uitterlinden, A. G., van der Lugt, A., Wittfeld, K., Grabe, H. J., Hosten, N., von Sarnowski, B., Völker, U., Levi, Christopher, Jimenez-Conde, J., Sharma, P., Sudlow, C. L. M., Rosand, J., Woo, D., Cole, J. W., Mechia, J. F., Rosand, J., Slowik, A., Thijs, V., Lindgren, A., Melander, O., Grewal, R. P., Rundek, T., Rexrode, K., Arnett, D. K., Jern, C., Johnson, J. A., Benavente, O. R., Rexrode, K., Asselbergs, F. R., Srikanth, V., Thomson, R., McWhirter, R., Moran, C., Callisaya, M., Phan, T., Rutten-Jacobs, L. C. A., Bevan, S., Tzourio, C., Mather, K. A., Sachdev, P. S., van Duijn, C. M., Worrall, B. B., Dichgans, M., Kittner, S. J., Markus, H. S., Ikram, M. A., Fornage, M., Launer, L. J., Seshadri, S., Longstreth, W. T., Debette, S.. Lippincott Williams & Wilkins; 2019. Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting.
Malik, Rainer, Freilinger, Tobias, Bis, Joshua C., Hopewell, Jemma C., Ferrari, Michel D., Rannikmae, Kristiina, Wessman, Maija, Kallela, Mikko, Kubisch, Christian, Fornage, Myriam, Meschia, James F., Lehtimäki, Terho, Winsvold, Bendik S., Sudlow, Cathie, Clarke, Robert, Chasman, Daniel I., Mitchell, Braxton D., Maguire, Jane, Kaprio, Jakko, Farrall, Martin, Raitakari, Olli T., Kurth, Tobias, Ikram, M. Arfan, Anttila, Verneri, Reiner, Alex P., Longstreth, W. T., Rothwell, Peter M., Strachan, David P., Sharma, Pankaj, Seshadri, Sudha, Quaye, Lydia, Cherkas, Lynn, Schürks, Markus, Rosand, Jonathan, Vander Heiden, Jason, Ligthart, Lannie, Boncoraglio, Giorgio B., Davey Smith, George, van Duijn, Cornelia M., Stefansson, Kari, Worrall, Bradford B., Nyholt, Dale R., Markus, Hugh S., van den Maagdenberg, Arn M. J. M., Cotsapas, Chris, Traylor, Matthew, Zwart, John A., Palotie, Aarno, Dichgans, Martin, de Vries, Boukje, Holliday, Elizabeth G., Terwindt, Gisela M., Sturm, Jonathan. Lippincott Williams & Wilkins; 2015. Shared genetic basis for migraine and ischemic stroke: a genome-wide analysis of common variants.
Achterberg, Sefanja, Kappelle, L. Jaap, Mali, W.P.T.M., Doevendans, P.A., Farrall, Martin, Holliday, Elizabeth G., Sudlow, Cathie, Hopewell, Jemma C., Cheng, Yu-Ching, Fornage, Myriam, Ikram, M. Arfan, Malik, Rainer, De Bakker, Paul I. W., Bevan, Steve, Thorsteinsdottir, Unnur, DeStefano, Anita L., Worrall, Bradford B., Reiner, Alex P., Mitchell, Braxtin D., Clarke, Robert, Levi, Christopher, Seshadri, Sudha, Boncoraglio, Giorgio B., Traylor, Matthew, Sharma, Pankaj, Bis, Joshua C., Gretarsdottir, Solveig, Psaty, Bruce M., Rothwell, Peter M., Rosand, Jonathan, Meschia, James F., Stefansson, Kari, Dichgans, Martin, Markus, Hugh S., Algra, Ale, Van Der Graaf, Y., Grobbee, D.E., Rutten, G.E.H.M., Visseren, F.L.J., Moll, F.L.. Public Library of Science; 2015. No additional prognostic value of genetic information in the prediction of vascular events after cerebral ischemia of arterial origin: The PROMISe study.
Holliday, Elizabeth G., Maguire, Jane M., Malik, Rainer, McEvoy, Mark, Biros, Erik, Lewis, Martin D., Lincz, Lisa F., Peel, Roseanne, Oldmeadow, Christopher, Smith, Wayne, Moscato, Pablo, Barlera, Simona, Evans, Tiffany-Jane, Bevan, Steve, Bis, Joshua C., Boerwinkle, Eric, Boncoraglio, Giorgio B., Brott, Thomas G., Scott, Rodney J., Levi, Christopher, Attia, John, Koblar, Simon A., Jannes, Jim, Sturm, Jonathan W., Hankey, Graeme J., Baker, Ross, Golledge, Jonathan, Parsons, Mark W.. Nature Publishing Group; 2012. Common variants at 6p21.1 are associated with large artery atherosclerotic stroke.
Traylor, Matthew, Mäkelä, Kari-Matti, Malik, Rainer, Sudlow, Cathie, Bevan, Steve, Raitoharju, Emma, , Oksala, Niku, Thijs, Vincent, Lemmens, Robin, Lindgren, Arne, Slowik, Agnieszka, Kilarski, Laura L., Maguire, Jane M., Walters, Matthew, Algra, Ale, Sharma, Pankaj, Attia, John R., Boncoraglio, Giorgio B., Rothwell, Peter M., de Bakker, Paul I. W., Bis, Joshua C., Saleheen, Danish, Holliday, ELizabeth G., Kittner, Steven J., Mitchell, Braxton D., Rosand, Jonathan, Meschia, James F., Levi, Christopher, Dichgans, Martin, Lehtimäki, Terho, Lewis, Cathryn M., Markus, Hugh S., Devan, William J., Nalls, Mike A., Wiggins, Kerri L., Zhao, Wei, Cheng, Yu-Ching, Achterberg, Sefanja. Public Library of Science; 2014. A novel MMP12 locus Is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach.
Traylor, Matthew, Farrall, Martin, 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, Holliday, Elizabeth G., 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, Sudlow, Cathie, Ho, Weang Kee, Pera, Joanna, Lemmens, Robin, Norrving, Bo, Higgins, Peter, Benn, Marianne, Sale, Michele, Kuhlenbaumer, Gregor, Doney, Alexander S. F., Vicente, Astrid M., Hopewell, Jemma C., Delavaran, Hossein, Algra, Ale, Davies, Gail, Oliveira, Sophia A., Palmer, Colin N. A., Deary, Ian, Schmidt, Helena, Pandolfo, Massimo, Montaner, Joan, Carty, Cara, Cheng, Yu-Ching, De Bakker, Paul I. W., Kostulas, Konstantinos, Ferro, Jose M., Van Zuydam, Natalie R., Valdimarsson, Einar, Nordestgaard, Berge G., Lindgren, Anne, Thijs, Vincent, Slowik, Agnieszka, Saleheen, Danish, Fornage, Myriam, Paré, Guillaume, Berger, Klaus, Thorleifsson, Gudmar, Astc, W., Hofman, Albert, Mosley, Thomas H., Mitchell, Branxton D., Furie, Karen, Clarke, Robert, Levi, Christopher, Arfan Ikram, M,, 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., Malik, Rainer, Stefansson, Kari, Dichgans, Martin, Markus, Hugh S., Bevan, Steve. The Lancet Publishing Group; 2012. Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies.
Kilarski, Laura L., Achterberg, Sefanja, Walters, Matthew, Worrall, Bradford B., Sale, Michele M., Algra, Ale, Kappelle, L. Jaap, Wijmenga, Cisca, Norrving, Bo, Sandling, Johanna K., Röennblom, Lars, Goris, An, Devan, William J., Franke, Andre, Sudlow, Cathie, Rothwell, Peter M., Levi, Christopher, Holliday, Elizabeth G., Fornage, Myriam, Psaty, Bruce, Gretarsdottir, Solveig, Thorsteinsdottir, Unnar, Seshadri, Sudha, Traylor, Matthew, Mitchell, Braxton D., Kittner, Steven, Clarke, Robert, Hopewell, Jemma C., Bis, Joshua C., Boncoraglio, Giorgio B., Meschia, James, Ikram, M. Arfan, Hansen, Bjorn M., Montaner, Joan, Malik, Rainer, Thorleifsson, Gudmar, Stefanson, Kari, Rosand, Jonathan, de Bakker, Paul I. W., Farrall, Martin, Dichgans, Martin, Markus, Hugh S., Bevan, Steve, Lindgren, Arne, Pare, Guillame, Sharma, Pankaj, Slowik, Agniescka, Thijs, Vincent. Lippincott Williams & Wilkins; 2014. Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12.
Cole, John W., Xu, Huichun, Ryan, Kathleen, Jaworek, Thomas, Dueker, Nicole, McArdle, Patrick, Gaynor, Brady, Cheng, Yu-Ching, O'Connell, Jeffrey, Bevan, Steve, Malik, Rainer, Ahmed, Naveed Uddin, Amouyel, Philippe, Anjum, Sheraz, Bis, Joshua C., , , , , , , , , Crosslin, David, , , , , , , , , , , Danesh, John, , , , , , , , , , , Engelter, Stefan T., , , , , , , , , , , Fornage, Myriam, , , , , , , , , , , Frossard, Philippe, , , , , , , , , Holliday, Elizabeth, Levi, Christopher. Public Library of Science (PLoS); 2018. Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke.
Traylor, Matthew, Malik, Rainer, Yet, Idil, Spector, Tim D., Bell, Jordana T., Hannon, Ellis, Mill, Jonathan, Chauhan, Ganesh, Debette, Stephanie, Bis, Joshua C., Longstreth, W. T., Ikram, M. Arfan, Nalls, Mike A., Levi, Chris, , , , , , , , , , Cotlarciuc, Iona, , , , , , , , , , , Radmanesh, Farid, , , , , , , , , , , Thorleifsson, Gudmar, , , , , , , , , , , Hanscombe, Ken B., , , , , , , , , Langefeld, Carl, Saleheen, Danish, Rost, Natalia S.. John Wiley & Sons; 2017. Genetic variation at 16q24.2 is associated with small vessel stroke.