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Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

by Chauhan, Ganesh, Traylor, Matthew, Sargurupremraj, Muralidharan, Okada, Yukinori, Mishra, Aniket, Giese, Anne-Katrin, van der Laan, Sander W., Gretarsdottir, Solveig, Anderson, Christopher D., Almgren, Peter, Amouyel, Philippe, Bartz, Traci M., Benavente, Oscar R., Boncoraglio, Giorgio B., Butterworth, Adam S., Carrera, Caty, Chasman, Daniel I., Cotlarciuc, Ioana, Cruchaga, Carlos, de Bakker, Paul I. W., Duan, Qing, Gottesman, Rebecca F., Harris, Tamara B., Hassan, Ahamad, Havulinna, Aki S., Heckbert, Susan R., Hyacinth, Hyacinth I., Ikram, M. Arfan, Ingelsson, Erik, Jian, Xueqiu, Jukema, J. Wouter, Kanai, Masahiro, Keene, Keith L., Kissela, Brett M., Kleindorfer, Dawn O., Kooperberg, Charles, Lange, Leslie A., Langenberg, Claudia, Launer, Lenore J., Lemmens, Robin, Lewis, Cathryn M., Lin, Wei-Yu, Lorentzen, Erik, Magnusson, Patrik K., Meschia, James F., Mitchell, Braxton D., Mosley, Thomas H., Nalls, Michael A., O’Donnell, Martin J., Pulit, Sara L., Reiner, Alexander P., Ridker, Paul M., Rothwell, Peter M., Rotter, Jerome I., Sale, Michele M., Salomaa, Veikko, Sapkota, Bishwa R., Schmidt, Reinhold, Schmidt, Carsten O., Sharma, Pankaj, Slowik, Agnieszka, Sudlow, Cathie L. M., Tanislav, Christian, Thijs, Vincent N. S., Thorsteinsdottir, Unnur, Tiedt, Steffen, Trompet, Stella, Wareham, Nicholas J., Wassertheil-Smoller, Sylvia, Wilson, James G., Pastinen, Tomi, Ruusalepp, Arno, Koplev, Simon, Björkegren, Johan L. M., Codoni, Veronica, Civelek, Mete, Christophersen, Ingrid E., Roselli, Carolina, Ellinor, Patrick T., Kato, Norihiro, van der Harst, Pim, Elliott, Paul, Takeuchi, Fumihiko, Johnson, Andrew D., Sanghera, Dharambir K., Melander, Olle, Strbian, Daniel, Fernandez-Cadenas, Israel, Rolfs, Arndt, Hata, Jun, Woo, Daniel, Pare, Guillaume, Hopewell, Jemma C., Saleheen, Danish, Stefansson, Kari, Worrall, Bradford B., Seshadri, Sudha, Markus, Hugh S., Debette, Stephanie, Dichgans, Martin
Published in Nature genetics (01.04.2018)

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Multi-ethnic genome-wide association study for atrial fibrillation

by Roselli, Carolina, Chaffin, Mark D., Weng, Lu-Chen, Aeschbacher, Stefanie, Ahlberg, Gustav, Albert, Christine M., Alonso, Alvaro, Anderson, Christopher D., Arking, Dan E., Bartz, Traci M., Benjamin, Emelia J., Bihlmeyer, Nathan A., Bis, Joshua C., Bloom, Heather L., Brody, Jennifer A., Chen, Lin Y., Choi, Eue-Keun, Christophersen, Ingrid E., Conen, David, Cook, James, Damrauer, Scott M., Denny, Joshua C., Dudley, Samuel C., Esko, Tonu, Felix, Stephan B., Franco, Oscar H., Geelhoed, Bastiaan, Grewal, Raji P., Gutmann, Rebecca, Harris, Tamara B., Hofman, Albert, Huang, Jie, Huang, Paul L., Ito, Kaoru, Johnson, Renee, Kääb, Stefan, Kamatani, Yoichiro, Kastrati, Adnan, Katschnig-Winter, Petra, Kessler, Thorsten, Kirchhof, Paulus, Kleber, Marcus E., Kubo, Michiaki, Lin, Henry J., Lindgren, Cecilia M., Loos, Ruth J. F., Lu, Yingchang, Lyytikäinen, Leo-Pekka, Magnusson, Patrik K., Malik, Rainer, Mansur, Alfredo J., Marcus, Gregory M., März, Winfried, Melander, Olle, Müller-Nurasyid, Martina, Nazarian, Saman, Neumann, Benjamin, Newton-Cheh, Christopher, Nilsson, Peter, Noordam, Raymond, Oellers, Heidi, Pak, Hui-Nam, Pedersen, Nancy L., Psaty, Bruce M., Pulit, Sara L., Pullinger, Clive R., Ribasés, Marta, Rienstra, Michiel, Rosand, Jonathan, Rost, Natalia, Saba, Samir, Schramm, Katharina, Schurman, Claudia, Scott, Stuart A., Shaffer, Christian, Shah, Svati, Shalaby, Alaa A., Shim, Jaemin, Shoemaker, M. Benjamin, Sinner, Moritz F., Smith, Albert V., Smith, Blair H., Sun, Han, Tanaka, Toshihiro, Tanriverdi, Kahraman, Taylor, Kent D., Thériault, Sébastien, Trompet, Stella, Tucker, Nathan R., Tveit, Arnljot, Uitterlinden, Andre G., Van Der Harst, Pim, Van Wagoner, David R., Wang, Biqi, Wong, Jorge A., Woo, Daniel, Yoneda, Zachary T., Zeller, Tanja, Zeng, Lingyao, Lubitz, Steven A.
Published in Nature genetics (01.09.2018)

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Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

by Rienstra, Michiel, Roselli, Carolina, Yin, Xiaoyan, Geelhoed, Bastiaan, Lin, Honghuang, Arking, Dan E, Smith, Albert V, Albert, Christine M, Chaffin, Mark, Tucker, Nathan R, Li, Molong, Klarin, Derek, Low, Siew-Kee, Müller-Nurasyid, Martina, Dörr, Marcus, Trompet, Stella, Gustafsson, Stefan, Kleber, Marcus E, Lyytikäinen, Leo-Pekka, Seppälä, Ilkka, Malik, Rainer, Perez, Marco, Sinisalo, Juha, Thériault, Sébastien, Radmanesh, Farid, Teumer, Alexander, Weng, Lu-Chen, Deo, Rajat, Rader, Daniel J, Shah, Svati H, Yang, Qiong, Worrall, Bradford B, Kamatani, Yoichiro, Hagemeijer, Yanick P, Siland, Joylene E, Kubo, Michiaki, Smith, Jonathan D, Bis, Joshua C, Perz, Siegfried, Psaty, Bruce M, Ridker, Paul M, Magnani, Jared W, Harris, Tamara B, Launer, Lenore J, Shoemaker, M Benjamin, Padmanabhan, Sandosh, Haessler, Jeffrey, Kähönen, Mika, Risch, Lorenz, Mansur, Alfredo J, Smith, Blair H, Lu, Yingchang, Bottinger, Erwin B, Hernesniemi, Jussi, Lindgren, Cecilia M, Huang, Jie, Ford, Ian, Delgado, Graciela, Chen, Lin Y, Chen, Yii-Der Ida, Li, Man, Lannfelt, Lars, Rost, Natalia, Taylor, Kent D, Campbell, Archie, Porteous, David, Hocking, Lynne J, Nikus, Kjell, Orho-Melander, Marju, Hamsten, Anders, Denny, Joshua C, Kriebel, Jennifer, Newton-Cheh, Christopher, Shaffer, Christian, Macfarlane, Peter W, Heilmann-Heimbach, Stefanie, Huang, Paul L, Sotoodehnia, Nona, Soliman, Elsayed Z, Uitterlinden, Andre G, Hofman, Albert, Franco, Oscar H, Völker, Uwe, Lin, Henry J, Ingelsson, Erik, Kooperberg, Charles, Conen, David, Rosand, Jonathan, van der Harst, Pim, Kathiresan, Sekar, Stricker, Bruno H, Chung, Mina K, Felix, Stephan B, Gudnason, Vilmundur, Alonso, Alvaro, Kääb, Stefan, Chasman, Daniel I, Benjamin, Emelia J, Tanaka, Toshihiro, Lunetta, Kathryn L
Published in Nature genetics (01.06.2017)

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Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk

by Choi, Seung Hoan, Jurgens, Sean J., Xiao, Ling, Hill, Matthew C., Haggerty, Christopher M., Sveinbjörnsson, Garðar, Morrill, Valerie N., Marston, Nicholas A., Weng, Lu-Chen, Pirruccello, James P., Arnar, David O., Gudbjartsson, Daniel Fannar, Mantineo, Helene, von Falkenhausen, Aenne S., Natale, Andrea, Tveit, Arnljot, Geelhoed, Bastiaan, Roselli, Carolina, Van Wagoner, David R., Darbar, Dawood, Haase, Doreen, Soliman, Elsayed Z., Davogustto, Giovanni E., Jun, Goo, Calkins, Hugh, Anderson, Jeffrey L., Halford, Jennifer L., Barnard, John, Hokanson, John E., Smith, Jonathan D., Bis, Joshua C., Young, Kendra, Johnson, Linda S. B., Risch, Lorenz, Gula, Lorne J., Kwee, Lydia Coulter, Chaffin, Mark D., Kühne, Michael, Preuss, Michael, Gupta, Namrata, Nafissi, Navid A., Smith, Nicholas L., Nilsson, Peter M., van der Harst, Pim, Wells, Quinn S., Judy, Renae L., Schnabel, Renate B., Johnson, Renee, Smit, Roelof A. J., Gabriel, Stacey, Knight, Stacey, Furukawa, Tetsushi, Blackwell, Thomas W., Nauffal, Victor, Wang, Xin, Min, Yuan-I, Yoneda, Zachary T., Laksman, Zachary W. M., Bezzina, Connie R., Alonso, Alvaro, Albert, Christine M., Arking, Dan E., Roden, Dan M., Chasman, Daniel I., Rader, Daniel J., Conen, David, McManus, David D., Fatkin, Diane, Benjamin, Emelia J., Boerwinkle, Eric, Marcus, Gregory M., Christophersen, Ingrid E., Roberts, Jason D., Raffield, Laura M., Shoemaker, M. Benjamin, Cho, Michael H., Cutler, Michael J., Rienstra, Michiel, Chung, Mina K., S. Olesen, Morten, Sinner, Moritz F., Sotoodehnia, Nona, Kirchhof, Paulus, Loos, Ruth J. F., Nazarian, Saman, Mohanty, Sanghamitra, Damrauer, Scott M., Kaab, Stefan, Heckbert, Susan R., Redline, Susan, Shah, Svati H., Tanaka, Toshihiro, Ebana, Yusuke, Holm, Hilma, Stefansson, Kari, Ruff, Christian T., Sabatine, Marc S., Lunetta, Kathryn L., Lubitz, Steven A., Ellinor, Patrick T.
Published in Nature genetics (01.03.2025)

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Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases

by Roselli, Carolina, Sveinbjornsson, Gardar, Marston, Nicholas A., Choi, Seung Hoan, Chaffin, Mark, Gudbjartsson, Daniel, Hill, Matthew C., Alonso, Alvaro, Anderson, Christopher D., Arking, Dan E., Benjamin, Emelia J., Brumpton, Ben, Chasman, Daniel I., Cho, Kelly, Choi, Eue-Keun, Chung, Mina K., Conen, David, Damrauer, Scott M., Dörr, Marcus, Dudink, Elton, Duong, ThuyVy, Erikstrup, Christian, Esko, Tõnu, Fatkin, Diane, Faul, Jessica D., Ferreira, Manuel, Ganesh, Santhi K., Geelhoed, Bastiaan, Gieger, Christian, Giulianini, Franco, Guo, Xiuqing, Hayward, Caroline, Heckbert, Susan R., Ito, Kaoru, Johnson, Renee, Jukema, J. Wouter, Jurgens, Sean J., Kääb, Stefan, Kardia, Sharon L. R., Khurshid, Shaan, Kamanu, Frederick K., Kirchhof, Paulus, Kleber, Marcus E., Knight, Stacey, Launer, Lenore J., Li, Dadong, Lin, Henry J., Loos, Ruth J. F., Lotta, Luca, Malik, Rainer, Mantineo, Helene, Marcus, Gregory M., März, Winfried, McManus, David D., Melander, Olle, Melloni, Giorgio E. M., Meyre, Pascal B., Mohanty, Sanghamitra, Monfort, Laia M., Müller-Nurasyid, Martina, Nafissi, Navid A., Natale, Andrea, Ostrowski, Sisse R., Pedersen, Ole B., Preuss, Michael, Psaty, Bruce M., Pullinger, Clive R., Rader, Daniel J., Ridker, Paul M., Rienstra, Michiel, Risch, Lorenz, Roden, Dan M., Sabatine, Marc S., Schunkert, Heribert, Shim, Jaemin, Smit, Roelof A. J., Smith, Jennifer A., Smith, Nicholas L., Smith, J. Gustav, Sørensen, Erik, Sotoodehnia, Nona, Strbian, Daniel, Stricker, Bruno H., Teder-Laving, Maris, Sun, Yan V., Thériault, Sébastien, Thorolfsdottir, Rosa B., Thorsteinsdottir, Unnur, Tveit, Arnljot, van der Harst, Pim, van Meurs, Joyce, Wang, Biqi, Weiss, Stefan, Yang, Pil-Sung, Yao, Jie, Zeller, Tanja, Zeng, Lingyao, Zhao, Wei, Zhou, Xiang, Ellinor, Patrick T.
Published in Nature genetics (01.03.2025)

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