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.

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.

Rosand, Jonathan, Mitchell, Braxton D., Thijs, Vincent, Woo, Daniel, Worrall, Bradford B., Arnett, Donna K., Benavente, Oscar, Cole, John W., Dichgans, Martin, Grewal, Raji P., Jern, Christina, Conde, Jordi Jiménez, Ay, Hakan, Johnson, Julie A., Lee, Jin-Moo, Levi, Christopher, Markus, Hugh S., Melander, Olle, Rexrode, Kathryn, Rothwell, Peter M., Rundek, Tatjana, Sacco, Ralph L., Schmidt, Reinhold, de Bakker, Paul I. W., Sharma, Pankaj, Slowik, Agnieszka, Wasssertheil-Smoller, Sylvia, Gwinn, Katrina, Kittner, Steven J., Lindgren, Anne, Meschia, James F., Pulit, Sarah L., Sudlow, Cathie L. M.. Elsevier; 2016. Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.

Lemmens, Robin, Buysschaert, Ian, Jood, Katarina, Blomstrand, Christian, Jern, Christina, Wnuk, Marcin, Slowik, Agniezska, Lambrechts, Diether, Thijs, Vincent, International Stroke Genetics Consortium,, Geelen, Veerle, Fernandez-Cadenas, Israel, Montaner, Joan, Schmidt, Helena, Schmidt, Reinhold, Attia, John, Maguire, Jane, Levi, Christopher. American Heart Association; 2010. The association of the 4q25 susceptibility variant for atrial fibrillation with stroke is limited to stroke of cardioembolic etiology.

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.

Majersik, Jennifer J., Cole, John W., 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, Golledge, Jonathan, Maguire, Jane, , , , , , , Rost, Natalia S., Chan, Yu-Feng Yvonne, Gurol, M. Edip, Lindgren, Arne G., Woo, Daniel, Fernandez-Cadenas, Israel, Chen, Donna T.. Lippincott Williams & Wilkins; 2015. Recommendations from the international stroke genetics consortium, part 1: standardized phenotypic data collection.

Campbell, Bruce C. V., Mitchell, Peter J., Simpson, Marion, Brooks, Mark, Asadi, Hamed, Wu, Teddy Y., Shah, Darshan G., Wijeratne, Tissa, Ang, Timothy, Miteff, Ferdinand, Levi, Christopher, Krause, Martin, Churilov, Leonid, Parsons, Mark W., , , , , , , , , , Yassi, Nawaf, , , , , , , , , , , Kleinig, Timothy J., , , , , , , , , , , Yan, Bernard, Dowling, Richard J., Bush, Steven J., Dewey, Helen M., Thijs, Vincent. Sage; 2018. Tenecteplase versus alteplase before endovascular thrombectomy (EXTEND-IA TNK): a multicenter, randomized, controlled study.

Bellenguez, Céline, Bevan, Steve, Band, Gavin, Syme, Paul D., Malik, Rainer, Pera, Joanna, Norrving, Bo, Lemmens, Robin, Freeman, Colin, Schanz, Renata, James, Tom, Poole, Deborah, Gschwendtner, Andreas, Murphy, Lee, Segal, Helen, Cortellini, Lynelle, Cheng, Yu-Ching, Woo, Daniel, Nalls, Michael A., Müller-Myhsok, Bertram, Meisinger, Christa, Seedorf, Udo, Ross-Adams, Helen, Spencer, Chris C. A., Boonen, Steven, Wloch-Kopec, Dorota, Valant, Valerie, Slark, Julia, Furie, Karen, Delavaran, Hossein, Langford, Cordelia, Deloukas, Panos, Edkins, Sarah, Hunt, Sarah, Burgess, Annette I., Gray, Emma, Dronov, Serge, Peltonen, Leena, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Stefansson, Kari, Boncoraglio, Giorgio B., Parati, Eugenio A., Attia, John, Pirinen, Matti, Holliday, Elizabeth, Levi, Chris, Franzosi, Maria-Grazia, Goel, Anuj, Helgadottir, Anna, Blackwell, Jenefer M., Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Jackson, Caroline A., Duncanson, Audrey, Jankowski, Janusz, Mathew, Christopher G., Palmer, Colin N. A., Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J., Trembath, Richard C., Viswanathan, Ananth C., Wood, Nicholas W., Traylor, Matthew, Worrall, Bradford B., Kittner, Steven J., Mitchell, Braxton D., Kissela, Brett, Meschia, James F., Thijs, Vincent, Lindgren, Arne, Macleod, Mary Joan, Slowik, Agnieszka, Walters, Matthew, Strange, Amy, Rosand, Jonathan, Sharma, Pankaj, Farrall, Martin, Sudlow, Cathie L. M., Rothwell, Peter M., Dichgans, Martin, Donnelly, Peter, Markus, Hugh S., Su, Zhan. Nature Publishing Group; 2012. Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.

Traylor, Matthew, Zhang, Cathy R., Fitzpatrick, Kaitlin, Kanakis, Allison, Barrick, Thomas R., Moynihan, Barry, Lewis, Cathryn M., Boncoraglio, Giorgio B., Lemmens, Robin, Thijs, Vincent, Sudlow, Cathie, Wardlaw, Joanna, Adib-Samii, Poneh, Levi, Christopher, Bevan, Steve, Devan, William J., Parsons, Owen E., Lanfranconi, Silvia, Gregory, Sarah, Cloonan, Lisa, Falcone, Guido J., Radmanesh, Fadrid. Lippincott Williams & Wilkins; 2016. Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke.

Traylor, Matthew, Rutten-Jacobs, Loes C. A., Dichgans, Martin, Markus, Hugh S., Thijs, Vincent, Holliday, Elizabeth G., Levi, Chris, Bevan, Steve, Malik, Rainer, Boncoraglio, Giorgio, Sudlow, Cathie, Rothwell, Peter M.. Lippincott Williams & Wilkins; 2016. Genetic associations with white matter hyperintensities confer risk of lacunar stroke.

Rutten-Jacobs, Loes C. A., Traylor, Matthew, Levi, Christopher, Rost, Natalia S., Rosand, Jonathan, Hassan, Ahamad, Markus, Hugh S., Adib-Samii, Poneh, Thijs, Vincent, Sudlow, Cathie, Rothwell, Peter M., Boncoraglio, Giorgio, Dichgans, Martin, Bevan, Steve, Meschia, James. Lippincott Williams & Wilkins; 2015. Common NOTCH3 variants and cerebral small-vessel disease.

Ay, Hakan, Arsava, Ethem Murat, Giralt-Steinhauer, Eva, Grewal, Raji P., Gwinn, Katrina, Jern, Christina, Jimenez-Conde, Jordi, Jood, Katarina, Katsnelson, Michael, Kissela, Brett, Kittner, Steven J., Kleindorfer, Dawn O., Andsberg, Gunnar, Labovitz, Daniel L., Lanfranconi, Silvia, Lee, Jin-Moo, Lehm, Manuel, Lemmens, Robin, Levi, Chris, Li, Linxin, Lindgren, Arne, Markus, Hugh S., McArdle, Patrick F., Benner, Thomas, Melander, Olle, Norrving, Bo, Peddareddygari, Leema Reddy, Pedersen, Annie, Pera, Joanna, Rannikmaee, Kristiina, Rexrode, Kathyrn M., Rhodes, David, Rich, Stephen S., Roquer, Jaume, BrownJr, Robert D., Rosand, Jonathan, Rothwell, Peter M., Rundek, Tatjana, Sacco, Ralph L., Schmidt, Reinhold, Schurks, Markus, Seiler, Stephan, Sharma, Pankaj, Slowik, Agnieszka, Sudlow, Cathie, Chapman, Sherita N., Thijs, Vincent, Woodfield, Rebecca, Worrall, Bradford B., Meschia, James F., Cole, John W., Delavaran, Hossein, Dichgans, Martin, Engstroem, Gunnar. Lippincott Williams & Wilkins; 2014. Pathogenic ischemic stroke phenotypes in the NINDS-Stroke Genetics Network.

Rutten-Jacobs, Loes C. A., Traylor, Matthew, Levi, Christopher, Rost, Natalia S., Rosand, Jonathan, Hassan, Ahamad, Bevan, Steve, Markus, Hugh S., Adib-Samii, Ppneh, Thijs, Vincent, Sudlow, Cathie, Rothwell, Peter M., Boncoraglio, Giorgio, Dichgans, Martin, Meschia, James, Maguire, Jane. Lippincott Williams & Wilkins; 2016. Association of MTHFR C677T genotype with ischemic stroke is confined to cerebral small vessel disease subtype.