Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke

Autor: Jaworek, Thomas, Xu, Huichun, Attia, John, Veldink, Jan H, Walters, Robin G, Weir, David R, Woo, Daniel, Worrall, Bradford B, Hong, Charles C, Ross, Owen, Zand, Ramin, Leeuw, Frank-Erik de, Lindgren, Arne G, Bell, Steven, Pare, Guillaume, Anderson, Christopher D, Markus, Hugh S, Jern, Christina, Malik, Rainer, Dichgans, Martin, Mitchell, Braxton D, Kittner, Steven J, Consortium, Early Onset Stroke Genetics Consortium of the International Stroke Genetics, Benavente, Oscar R, Boncoraglio, Giorgio B, Butterworth, Adam, Dissections, Cervical Artery, Patients, Ischemic Stroke, Carcel-Marquez, Jara, Chen, Zhengming, Chong, Michael, Gaynor, Brady J, Cruchaga, Carlos, Cushman, Mary, Danesh, John, Debette, Stephanie, Duggan, David J, Durda, Jon Peter, Engstrom, Gunnar, Enzinger, Chris, Faul, Jessica D, Fecteau, Natalie S, Cole, John W, Fernandez-Cadenas, Israel, Gieger, Christian, Giese, Anne-Katrin, Grewal, Raji P, Grittner, Ulrike, Havulinna, Aki S, Heitsch, Laura, Hochberg, Marc C, Holliday, Elizabeth, Hu, Jie, Rannikmae, Kristiina, Ilinca, Andreea, Consortium, INVENT, Irvin, Marguerite R, Jackson, Rebecca D, Jacob, Mina A, Janssen, Raquel Rabionet, Jimenez-Conde, Jordi, Johnson, Julie A, Kamatani, Yoichiro, Kardia, Sharon L, Stanne, Tara M, Koido, Masaru, Kubo, Michiaki, Lange, Leslie, Lee, Jin-Moo, Lemmens, Robin, Levi, Christopher R, Li, Jiang, Li, Liming, Lin, Kuang, Lopez, Haley, Tomppo, Liisa, Luke, Sothear, Maguire, Jane, McArdle, Patrick F, McDonough, Caitrin W, Meschia, James F, Metso, Tiina, Muller-Nurasyid, Martina, O'Connor, Timothy D, O'Donnell, Martin, Peddareddygari, Leema R, Abedi, Vida, Pera, Joanna, Perry, James A, Peters, Annette, Putaala, Jukka, Ray, Debashree, Rexrode, Kathryn, Ribases, Marta, Rosand, Jonathan, Rothwell, Peter M, Rundek, Tatjana, Amouyel, Philippe, Ryan, Kathleen A, Sacco, Ralph L, Salomaa, Veikko, Sanchez-Mora, Cristina, Schmidt, Reinhold, Sharma, Pankaj, Slowik, Agnieszka, Smith, Jennifer A, Smith, Nicholas L, Wassertheil-Smoller, Sylvia, Armstrong, Nicole D, Soederholm, Martin, Stine, O. C., Strbian, Daniel, Sudlow, Cathie L, Tatlisumak, Turgut, Terao, Chikashi, Thijs, Vincent, Torres-Aguila, Nuria P, Tregouet, David-Alexandre, Tuladhar, Anil M

Publikováno v: Neurology 99(16), e1738-e1754 (2022). doi:10.1212/WNL.0000000000201006
Jaworek, T, Xu, H, Gaynor, B, Cole, J, Rannikmae, K, Stanne, T M, Tomppo, L, Abedi, V, Amouyel, P, Armstrong, N, Attia, J, Bell, S, Benavente, O R, Boncoraglio, G B, Butterworth, A S, Carcel-Marquez, J, Chen, Z, Chong, M, Cruchaga, C, Cushman, M, Danesh, J, Debette, S, Duggan, D, Durda, J P, Engstrom, G, Enzinger, C, Faul, J D, Fecteau, N, Fernandez-Cadenas, I, Gieger, C, Giese, A-K, Grewal, R P, Grittner, U, Havulinna, A S, Heitsch, L, Hochberg, M, Holliday, E G, Zhu, J, Llinca, A, Irvin, M R, Jackson, R D, Jacob, M, Rabionet-Janssen, R, Jimenez-Conde, J, Johnson, J A, Kamatani, Y, Kardia, S L R, Koido, M, Kubo, M, Lange, L A, Lee, J-M, Lemmens, R, Levi, C, Li, J, Lin, K, Lopez, H, Maguire, J M, Luke, S, McArdle, P F, McDonough, C W, Meschia, J, Metso, T M, Müller-Nurasyid, M, O'Connor, T, Peddareddygari, L R, O'Donnell, M, Pera, J, Perry, J, Peters, A, Putaala, J, Ray, D, Rexrode, K M, Ribases, M, Rosand, J, Rothwell, P M, Rundek, T, Ryan, K, Sacco, R L, Salomaa, V, Sánchez-Mora, C, Schmidt, R, Sharma, P, Slowik, A, Smith, J, Smith, N L, Wassertheil-Smoller, S, Söderholm, M, Stine, C, Strbian, D, Sudlow, C L M, Tatlisumak, T, Terao, C, Thijs, V, Torres-Aguila, N, Tregouet, D-A, Tuladhar, A M, Veldink, J H, Walters, R G, Weir, D R, Woo, D, Worrall, B B, Hong, C, Ross, O A, Zand, R, de Leeuw, F-E, Lindgren, A, Pare, G, Anderson, C D, Markus, H S, Jern, C, Malik, R, Dichgans, M, Mitchell, B D & Kittner, S J 2022, ' Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke ', Neurology, vol. 99, no. 16, pp. e1738-e1754 . https://doi.org/10.1212/WNL.0000000000201006

Background and Objectives:Current genome-wide association studies of ischemic stroke have focused primarily on late onset disease. As a complement to these studies, we sought to identifythe contribution of common genetic variants to risk of early ons

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https://lirias.kuleuven.be/handle/20.500.12942/716243