Cheng, Yu-Ching, Anderson, Christopher D., Barlera, Simona, Biffi, Alessandro, Bookman, Ebony, Brott, Thomas G., Brown, Robert D., Chen, Fang, Chen, Wei-Min, Ciusani, Emilio, Cole, John W., Cortellini, Lynelle, Bione, Silvia, Danesh, John, Doheny, Kimberley, Ferrucci, Luigi, Franzosi, Maria Grazia, Frossard, Philippe, Furie, Karen L., Golledge, Jonathan, Hankey, Graeme J., Hernandez, Dena, Holliday, Elizabeth G., Keene, Keith, Hsu, Fang-Chi, Jannes, Jim, Kamal, Ayeesha, Khan, Muhammad Saleem, Kittner, Steven J., Koblar, Simon A., Lewis, Martin, Lincz, Lisa, Lisa, Antonella, Matarin, Mar, Maguire, Jane M., 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., Nalls, Michael, Yadav, Sunaina, Zaidi, Moazzam, Boncoraglio, Giorgio B., Levi, Christopher Royce, Meschia, James F., Rosand, Jonathan, Sale, Michele, Saleheen, Danish, Schmidt, Reinhold, Sharma, Pankaj, Rasheed, Asif, Worrall, Bradford, Mitchell, Branxton D., Zeginigg, Marion, Attia, John, Baker, Ross. Lippincott Williams & Wilkins; 2012. Are myocardial infarction-associated single-nucleotide polymorphisms associated with ischemic stroke?.

Battey, Thomas W. K., Valant, Valerie, Kassis, Sylvia Baedorf, Kourkoulis, Christina, Lee, Chaeyoung, Anderson, Christopher D., Falcone, Guido J., Jimenez-Conde, Jordi, Fernandez-Cadenas, Israel, Pare, Guillaume, Rundek, Tatjana, James, Michael L., Lemmens, Robin, Lee, Tsong-Hai, Tatlisumak, Turgut, Kittner, Steven J., Lindgren, Arne, Mateen, Farrah J., Berkowitz, Aaron L., Holliday, Elizabeth G., Maguire, Jane. Lippincott Williams & Wilkins; 2015. Recommendations from the international stroke genetics consortium, part 2: biological sample collection and storage.

Malik, Rainer, Chauhan, Ganesh, Anderson, Christopher D., Chong, Michael, Adams, Hieab H. H., Ago, Tetsuro, Almgren, Peter, Amouyel, Philippe, Ay, Hakan, Bartz, Traci M., Benavente, Oscar R., Bevan, Steve, Traylor, Matthew, Holliday, Elizabeth G., Attia, John, Levi, Christopher R., Carrera, C, Carty, CL, Chasman, DI, Chen, W-M, Cole, JW, Correa, A, Cotlarciuc, I, Sargurupremraj, Muralidharan, Cruchaga, C, Danesh, J, de Bakker, PIW, DeStefano, AL, Den Hoed, M, Duan, Q, Engelter, ST, Falcone, GJ, Gottesman, RF, Grewal, RP, Okada, Yukinori, Gudnason, V, Gustafsson, S, Haessler, J, Harris, TB, Hassan, A, Havulinna, AS, Heckbert, SR, Holliday, EG, Howard, G, Hsu, F-C, Mishra, Aniket, Hyacinth, HI, Ikram, MA, Ingelsson, E, Irvin, MR, Jian, X, Jiménez-Conde, J, Johnson, JA, Jukema, JW, Kanai, M, Keene, KL, Rutten-Jacobs, Loes, Kissela, BM, Kleindorfer, DO, Kooperberg, C, Kubo, M, Lange, LA, Langefeld, CD, Langenberg, C, Launer, LJ, Lee, J-M, Lemmens, R, Giese, Anne-Katrin, van der Laan, Sander W., Gretarsdottir, Solveig. Nature Publishing Group; 2018. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.

Rannikmäe, Kristiina, Davies, Gail, Deka, Ranjan, Woo, Jessica G., Martin, Lisa J., Jimenez-Conde, Jordi, Selim, Magdy, Brown, Devin L., Silliman, Scott L., Kidwell, Chelsea S., Montaner, Joan, Langefeld, Carl D., Thomson, Pippa A., Holliday, Elizabeth G., Levi, Christopher R., Attia, John, Rothwell, Peter M., Poole, Deborah L., , , , , , Bevan, Steve, , , , , , , , , , , Devan, William J., , , , , , , , , , , Falcone, Guido J., , , Traylor, Matthew, Anderson, Christopher D., Battey, Thomas W. K., Radmanesh, Farid. Lippincott Williams & Wilkins; 2015. Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease.