Phenotype-genotype analysis of dystrophinopathy caused by duplication mutation in Dystrophin gene in an African patient von Peddareddygari, L R, Pillai, B H, Nochlin, D, Sharer, L R, Grewal, R P

Volltext

Agreement between TOAST and CCS ischemic stroke classification: The NINDS SiGN Study von McArdle, Patrick F, Kittner, Steven J, Ay, Hakan, Brown, Robert D, Meschia, James F, Rundek, Tatjana, Wassertheil-Smoller, Sylvia, Woo, Daniel, Andsberg, Gunnar, Biffi, Alessandro, Brenner, David A, Cole, John W, Corriveau, Roderick, de Bakker, Paul I.W, Delavaran, Hossein, Dichgans, Martin, Grewal, Raji P, Gwinn, Katrina, Huq, Mohammed, Jern, Christina, Jimenez-Conde, Jordi, Jood, Katarina, Kaplan, Robert C, Katschnig, Petra, Katsnelson, Michael, Labovitz, Daniel L, Lemmens, Robin, Li, Linxin, Lindgren, Arne, Markus, Hugh S, Peddareddygari, Leema R, Pedersén, Annie, Pera, Joanna, Redfors, Petra, Roquer, Jaume, Rosand, Jonathan, Rost, Natalia S, Rothwell, Peter M, Sacco, Ralph L, Sharma, Pankaj, Slowik, Agnieszka, Sudlow, Cathie, Thijs, Vincent, Tiedt, Steffen, Valenti, Raffaella, Worrall, Bradford B

Volltext

Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke von Jaworek, Thomas, Xu, Huichun, Cole, John W., Rannikmae, Kristiina, Stanne, Tara M., Tomppo, Liisa, Abedi, Vida, Amouyel, Philippe, Bell, Steven, Benavente, Oscar R., Boncoraglio, Giorgio B., Butterworth, Adam, Carcel-Marquez, Jara, Chong, Michael, Cruchaga, Carlos, Cushman, Mary, Danesh, John, Debette, Stéphanie, Duggan, David J., Engstrom, Gunnar, Enzinger, Chris, Faul, Jessica D., Fecteau, Natalie S., 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, Ilinca, Andreea, Irvin, Marguerite R., Jackson, Rebecca D., Jacob, Mina A., Rabionet, Raquel, Johnson, Julie A., Koido, Masaru, Kubo, Michiaki, Lee, Jin-Moo, Lemmens, Robin, Levi, Christopher R., Li, Jiang, Li, Liming, Lin, Kuang, Lopez, Haley, Luke, Sothear, McArdle, Patrick F., McDonough, Caitrin W., Meschia, James F., Metso, Tiina, Müller-Nurasyid, Martina, O'Connor, Timothy D., O'Donnell, Martin, Peddareddygari, Leema R., Pera, Joanna, Perry, James A., Peters, Annette, Putaala, Jukka, Ray, Debashree, Rexrode, Kathryn, Ribases, Marta, Rosand, Jonathan, Rothwell, Peter M., Sacco, Ralph L., Salomaa, Veikko, Sanchez-Mora, Cristina, Schmidt, Reinhold, Sharma, Pankaj, Slowik, Agnieszka, Smith, Jennifer A., Smith, Nicholas L., Wassertheil-Smoller, Sylvia, Söderholm, Martin, Stine, O. Colin, Strbian, Daniel, Sudlow, Cathie L.M., Tatlisumak, Turgut, Terao, Chikashi, Torres-Aguila, Nuria P., Trégouët, David-Alexandre, Tuladhar, Anil M., Veldink, Jan H., Weir, David R., Woo, Daniel, Worrall, Bradford B., Hong, Charles C., Ross, Owen A., Zand, Ramin, Leeuw, Frank-Erik de, Lindgren, Arne G., Pare, Guillaume, Anderson, Christopher D., Jern, Christina, Malik, Rainer, Dichgans, Martin, Mitchell, Braxton D., Kittner, Steven J.

Volltext

Phenotype-Genotype analysis of dystrophinopathy caused by duplication mutation in duplication mutation in Dystrophin gene in an African patient von Peddareddygari, LR, Pillai, BH, Nochlin, D, Sharer, LR, Grewal, RP

Volltext

Stroke genetics informs drug discovery and risk prediction across ancestries von Jürgenson, Tuuli, Namba, Shinichi, Posner, Daniel C., Kamanu, Frederick K., Koido, Masaru, He, Yunye, Caro, Ilana, Krebs, Kristi, Liaw, Yi-Ching, Parodi, Livia, Bae, Hee-Joon, Chong, Michael R., Tomppo, Liisa, Akinyemi, Rufus, Roshchupkin, Gennady V., Habib, Naomi, Jee, Yon Ho, Thomassen, Jesper Qvist, Abedi, Vida, Cárcel-Márquez, Jara, Nygaard, Marianne, Yonova-Doing, Ekaterina, Knol, Maria J., Lewis, Adam J., Judy, Renae L., Amouyel, Philippe, Bakker, Mark K., Bennett, David A., Bis, Joshua C., Bordes, Constance, Børte, Sigrid, Cain, Anael, Ridker, Paul M., Cho, Kelly, Chen, Zhengming, Cruchaga, Carlos, Cole, John W., de Cid, Rafael, Ferreira, Leslie E., He, Jing, Jeon, Christina E., Jern, Christina, Kamouchi, Masahiro, Keene, Keith L., Konuma, Takahiro, Kumar, Amit, Launer, Lenore J., Lee, Keon-Joo, Li, Jiang, Li, Liming, Manichaikul, Ani, Markus, Hugh S., Meitinger, Thomas, Mitchell, Braxton D., Morisaki, Takayuki, O’Donnell, Martin J., Onland-Moret, N. Charlotte, Ovbiagele, Bruce, Peters, Annette, Rosand, Jonathan, Sabatine, Marc S., Sacco, Ralph L., Saleheen, Danish, Schmidt, Carsten O., Smith, Nicholas L., Sloane, Kelly L., Sutoh, Yoichi, Tiwari, Hemant K., Wennberg, Patrik, Wilson, Peter W. F., Yang, Qiong, Yoon, Kyungheon, Gieger, Christian, Ninomiya, Toshiharu, Grabe, Hans J., Jukema, J. Wouter, Kim, Young Jin, Chen, Pei-Hsin, Mayerhofer, Ernst, Ikram, Mohammad A., Worrall, Bradford B., Lathrop, G. Mark, Riaz, Moeen, Simonsick, Eleanor M., Kõrv, Janika, Zand, Ramin, Prasad, Kameshwar, Frikke-Schmidt, Ruth, Liman, Thomas, Ruigrok, Ynte M., Bastarache, Lisa, Damrauer, Scott M., Rotter, Jerome I., Niiranen, Teemu J., Walters, Robin G., Owolabi, Mayowa O., Huffman, Jennifer E., Kamatani, Yoichiro, Dichgans, Martin, Debette, Stephanie

Volltext

Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke von Keene, Keith L., Hyacinth, Hyacinth I., Bis, Joshua C., Kittner, Steven J., Mitchell, Braxton D., Cheng, Yu-Ching, Pare, Guillaume, Chong, Michael, O’Donnell, Martin, Meschia, James F., Chen, Wei-Min, Sale, Michèle M., Rich, Stephen S., Nalls, Mike A., Zonderman, Alan B., Evans, Michele K., Wilson, James G., Correa, Adolfo, Markus, Hugh S., Traylor, Matthew, Lewis, Cathryn M., Carty, Cara L., Reiner, Alexander, Haessler, Jeff, Langefeld, Carl D., Gottesman, Rebecca, Mosley, Thomas H., Woo, Daniel, Yaffe, Kristine, Liu, YongMei, Longstreth, William T., Psaty, Bruce M., Kooperberg, Charles, Lange, Leslie A., Sacco, Ralph, Rundek, Tatjana, Lee, Jin-Moo, Cruchaga, Carlos, Furie, Karen L., Arnett, Donna K., Benavente, Oscar R., Grewal, Raji P., Peddareddygari, Leema Reddy, Dichgans, Martin, Malik, Rainer, Worrall, Bradford B., Fornage, Myriam

Volltext

Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting von Bis, Joshua C, Smith, Albert Vernon, Saba, Yasaman, Luciano, Michelle, Bastin, Mark E, Lemmens, Robin, Ames, David, Chong, Elizabeth, van der Lugt, Aad, Jimenez-Conde, Jordi, Rundek, Tatjana, Arnett, Donna K, Jern, Christina, Johnson, Julie A, Benavente, Oscar R, Geerlings, Mirjam I, Tzourio, Christophe, Sachdev, Perminder S, Markus, Hugh S, Seshadri, Sudha, Anderson, Christopher D, de Bakker, Paul IW, Engström, Gunnar, Kissela, Brett M, Pera, Joanna, Soriano-Tárraga, Carolina, Stanne, Tara, Nyquist, Paul, Drazyk, Anna, Markus, Hugh, Chasman, Daniel, Elkind, Mitchell, Bijlenga, Philippe, Yue, Suo, Mateen, Farrah, Meschia, James, Pare, Guillaume, Klijn, Karin, Kamatani, Yoichiro, Tregouet, David, Carrera, Caty, Ruigrok, Ynte, Sargurupremraj, Murali, Liebeskind, David, Tan, Rhea, Broderick, Joseph, Sale, Michele, Konrad, Jan, Nordestgaard, Børge G, Psaty, Bruce M, Benn, Marianne, Farrall, Martin, Nalls, Mike, Oliveira, Sofia A, Becker, James T, Carlsson, Cynthia M, Carney, Regina M, Crocco, Elizabeth A, Faber, Kelley M, Farlow, Martin R, Farrer, Lindsay A, Gearing, Marla, Gilbert, John R, Hamilton-Nelson, Kara L, Haroutunian, Vahram, Huebinger, Ryan M, Kukull, Walter A, Lah, James J, Li, Ge, Lunetta, Kathryn L, Mack, Wendy J, Manly, Jennifer J, Masliah, Eliezer, Miller, Carol A, Pierce, Aimee, Potter, Huntington, Raj, Ashok, Sano, Mary, Spina, Salvatore, Tanzi, Rudolph E, Vinters, Harry V, Yu, Chang-En, Yu, Lei, Liu, Yongmei, Johnson, Andrew D, deStefano, Anita L, van Buchem, Mark A, Boerwinkle, Eric, de Craen, Anton J.M, Ibrahim-Verbaas, Carla A, Oostra, Ben A, Cupples, L Adrienne, Meisinger, Christa, Nambi, Vijay, Halperin, Eran, Orru, Marco, Ernst, Florian, Chilukoti, Ravi Kumar, Wilson, James F, Gudnason, Vilmundur

Volltext

Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries von Jürgenson, Tuuli, Namba, Shinichi, Posner, Daniel C., Kamanu, Frederick K., Koido, Masaru, He, Yunye, Caro, Ilana, Krebs, Kristi, Liaw, Yi-Ching, Parodi, Livia, Bae, Hee-Joon, Chong, Michael R., Tomppo, Liisa, Akinyemi, Rufus, Roshchupkin, Gennady V., Habib, Naomi, Jee, Yon Ho, Thomassen, Jesper Qvist, Abedi, Vida, Cárcel-Márquez, Jara, Nygaard, Marianne, Yonova-Doing, Ekaterina, Knol, Maria J., Lewis, Adam J., Judy, Renae L., Amouyel, Philippe, Bakker, Mark K., Bennett, David A., Bis, Joshua C., Bordes, Constance, Børte, Sigrid, Cain, Anael, Ridker, Paul M., Cho, Kelly, Chen, Zhengming, Cruchaga, Carlos, Cole, John W., de Cid, Rafael, Ferreira, Leslie E., He, Jing, Jeon, Christina E., Jern, Christina, Kamouchi, Masahiro, Keene, Keith L., Konuma, Takahiro, Kumar, Amit, Launer, Lenore J., Lee, Keon-Joo, Li, Jiang, Li, Liming, Manichaikul, Ani, Markus, Hugh S., Meitinger, Thomas, Mitchell, Braxton D., Morisaki, Takayuki, O’Donnell, Martin J., Onland-Moret, N. Charlotte, Ovbiagele, Bruce, Peters, Annette, Rosand, Jonathan, Sabatine, Marc S., Sacco, Ralph L., Saleheen, Danish, Schmidt, Carsten O., Smith, Nicholas L., Sloane, Kelly L., Sutoh, Yoichi, Tiwari, Hemant K., Wennberg, Patrik, Wilson, Peter W. F., Yang, Qiong, Yoon, Kyungheon, Gieger, Christian, Ninomiya, Toshiharu, Grabe, Hans J., Jukema, J. Wouter, Kim, Young Jin, Chen, Pei-Hsin, Mayerhofer, Ernst, Ikram, Mohammad A., Worrall, Bradford B., Lathrop, G. Mark, Riaz, Moeen, Simonsick, Eleanor M., Kõrv, Janika, Zand, Ramin, Prasad, Kameshwar, Frikke-Schmidt, Ruth, Liman, Thomas, Ruigrok, Ynte M., Bastarache, Lisa, Damrauer, Scott M., Rotter, Jerome I., Niiranen, Teemu J., Walters, Robin G., Owolabi, Mayowa O., Huffman, Jennifer E., Kamatani, Yoichiro, Dichgans, Martin, Debette, Stephanie

Volltext

Contribution of Common Genetic Variants to Risk of Early Onset Ischemic Stroke von Jaworek, Thomas, Xu, Huichun, Gaynor, Brady J, Cole, John W., Stanne, Tara M, Amouyel, Philippe, Armstrong, Nicole D, Attia, John, Bell, Steven, Benavente, Oscar R, Boncoraglio, Giorgio B, Butterworth, Adam, Chen, Zhengming, Chong, Michael, Cruchaga, Carlos, Cushman, Mary, Danesh, John, Debette, Stephanie, Duggan, David J, Durda, Jon Peter, Engstrom, Gunnar, Enzinger, Chris, Faul, Jessica D, Fecteau, Natalie S, 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, Ilinca, Andreea, Irvin, Marguerite R, Jackson, Rebecca D, Jacob, Mina A., Janssen, Raquel Rabionet, Jimenez-Conde, Jordi, Johnson, Julie A, Kamatani, Yoichiro, Kardia, Sharon L, Koido, Masaru, Kubo, Michiaki, Lange, Leslie, Lee, Jin-Moo, Lemmens, Robin, Levi, Christopher R, Li, Jiang, Li, Liming, Lin, Kuang, Luke, Sothear, Maguire, Jane, McArdle, Patrick F, McDonough, Caitrin W., Meschia, James F, Metso, Tiina, O'Connor, Timothy D, O'Donnell, Martin, Peddareddygari, Leema R, Pera, Joanna, Perry, James A, Peters, Annette, Putaala, Jukka, Ray, Debashree, Rexrode, Kathryn, Ribases, Marta, Rothwell, Peter M, Rundek, Tatjana, Ryan, Kathleen A, Sacco, Ralph L., Sanchez-Mora, Cristina, Schmidt, Reinhold, Sharma, Pankaj, Slowik, Agnieszka, Smith, Jennifer A, Smith, Nicholas L, Wassertheil-Smoller, Sylvia, Soederholm, Martin, Sudlow, Cathie L, Tatlisumak, Turgut, Terao, Chikashi, Torres-Aguila, Nuria P, Tuladhar, Anil M., Veldink, Jan H, Woo, Daniel, Worrall, Bradford B, Hong, Charles C, Ross, Owen, Zand, Ramin, Leeuw, Frank-Erik de, Lindgren, Arne G, Pare, Guillaume, Markus, Hugh S, Jern, Christina, Malik, Rainer, Dichgans, Martin, Mitchell, Braxton D, Kittner, Steven J

Volltext

Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke von Jaworek, Thomas, Xu, Huichun, Gaynor, Brady J, Cole, John W, Rannikmae, Kristiina, Stanne, Tara M, Tomppo, Liisa, Abedi, Vida, Amouyel, Philippe, Armstrong, Nicole D, Attia, John, Bell, Steven, Benavente, Oscar R, Boncoraglio, Giorgio B, Butterworth, Adam, Carcel-Marquez, Jara, Chen, Zhengming, Chong, Michael, Cruchaga, Carlos, Cushman, Mary, Danesh, John, Debette, Stephanie, Duggan, David J, Durda, Jon Peter, Engstrom, Gunnar, Enzinger, Chris, Faul, Jessica D, Fecteau, Natalie S, 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, Ilinca, Andreea, Irvin, Marguerite R, Jackson, Rebecca D, Jacob, Mina A, Rabionet, Raquel, Jimenez-Conde, Jordi, Johnson, Julie A, Kamatani, Yoichiro, Kardia, Sharon L.R, Koido, Masaru, Kubo, Michiaki, Lange, Leslie, Lee, Jin-Moo, Lemmens, Robin, Levi, Christopher R, Li, Jiang, Li, Liming, Lin, Kuang, Lopez, Haley, Luke, Sothear, Maguire, Jane, McArdle, Patrick F, McDonough, Caitrin W, Meschia, James F, Metso, Tiina, Mueller-Nurasyid, Martina, O'Connor, Timothy D, O'Donnell, Martin, Peddareddygari, Leema R, Pera, Joanna, Perry, James A, Peters, Annette, Putaala, Jukka, Ray, Debashree, Rexrode, Kathryn, Ribases, Marta, Rosand, Jonathan, Rothwell, Peter M, Rundek, Tatjana, 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, Soderholm, Martin, Stine, O. Colin, Strbian, Daniel, Sudlow, Cathie L.M, Tatlisumak, Turgut, Terao, Chikashi, Thijs, Vincent, Torres-Aguila, Nuria P, Tregouet, David-Alexandre, Tuladhar, Anil M, Veldink, Jan H, Walters, Robin G, Weir, David R

Volltext

Stroke Genetics Network (SiGN) Study: Design and Rationale for a Genome-Wide Association Study of Ischemic Stroke Subtypes von Meschia, James F., Arnett, Donna K., Ay, Hakan, Brown, Robert D., Benavente, Oscar R., Cole, John W., de Bakker, Paul I.W., Dichgans, Martin, Fornage, Myriam, Grewal, Raji P., Gwinn, Katrina, Jern, Christina, Conde, Jordi Jimenez, Johnson, Julie A., Jood, Katarina, Laurie, Cathy C., Lee, Jin-Moo, Lindgren, Arne, Markus, Hugh S., McArdle, Patrick F., McClure, Leslie A., Mitchell, Braxton D., Schmidt, Reinhold, Rexrode, Kathryn M., Rich, Stephen S., Rosand, Jonathan, Rothwell, Peter M., Rundek, Tatjana, Sacco, Ralph L., Sharma, Pankaj, Shuldiner, Alan R., Slowik, Agnieszka, Wassertheil-Smoller, Sylvia, Sudlow, Cathie, Thijs, Vincent N.S., Woo, Daniel, Worrall, Bradford B., Wu, Ona, Kittner, Steven J., Anderson, Christopher D., Andren, Kerstin, Andsberg, Gunnar, Arsava, Ethem, Barrett, Kevin M., Benner, Thomas, Bentley, Paul, Bevan, Steven, Biffi, Alessandro, Brenner, David, Chapman, Sherita, Cheng, Yu-Ching, Delavaran, Hossein, Deline, Christopher, Dziedzic, Tomasz, Gamble, Dale, Giralt, Eva, Hegge, Caityln, Heitsch, Laura, Helenius, Johanna, Holmegaard, Lukas, Huq, Mohammed, Irie, Robert E., Jackson, Rebecca, Katschnig, Petra, Katsnelson, Michael, Khoury, Naim, Kilinc, Selma, Kumar, Gyanendra, Labovitz, Daniel, Lanfranconi, Silvia, Langefeld, Carl D., Lemmens, Robin, Li, Linxin, Malik, Shaneela, Melander, Olle, Nordstrom, Sara, Norrving, Bo, Ois, Angel, Ossi, Raid, Peddareddygari, Leema Reddy, Pedersén, Annie, Pera, Joanna, Pucek, Mateusz, Rannikmae, Kristiina, Redfors, Petra, Rhodes, J. David, Ribasés, Marta, Saraf, Neha, Schuerks, Markus, Seiler, Stephan, Sheikh, Huma, Southerland, Andrew M, Sparks, Mary J., Stoegerer, Eva, Sunyer, Jordi, Temple, Ella, Valenti, Raffaella, Weir, David, Weissman, Darren, Woodfield, Rebecca

Volltext

A GWAS Meta-Analysis of Stroke in 22,000 individuals of African descent identifies novel associations with stroke von Keene, Keith L., Hyacinth, Hyacinth I., Bis, Joshua C., Kittner, Steven J., Mitchell, Braxton D., Cheng, Yu-Ching, Pare, Guillaume, Chong, Michael, O’Donnell, Martin, Meschia, James F., Chen, Wei-Min, Sale, Michele M., Rich, Stephen S., Nalls, Mike A., Zonderman, Alan B., Evans, Michele K., Wilson, James G., Correa, Adolfo, Markus, Hugh S., Traylor, Matthew, Lewis, Cathryn M., Carty, Cara L., Reiner, Alexander, Haessler, Jeff, Langefeld, Carl D., Gottesman, Rebecca, Mosley, Thomas H., Woo, Daniel, Yaffe, Kristine, Liu, YongMei, Longstreth, WT, Psaty, Bruce M., Kooperberg, Charles, Lange, Leslie A., Sacco, Ralph, Rundek, Tatjana, Lee, Jin-Moo, Cruchaga, Carlos, Furie, Karen L., Arnett, Donna K., Benavente, Oscar R., Grewal, Raji P., Peddareddygari, Leema Reddy, Dichgans, Martin, Malik, Rainer, Worrall, Bradford B., Fornage, Myriam

Volltext

Abstract TMP49: Yield of Diagnostic Evaluation in Major Stroke Phenoytypes von Majersik, Jennifer J, Arsava, Ethem M, Brown, Robert D, Grewal, Raji, Jern, Christina, Jiménez-Conde, Jordi, Jood, Katarina, Kittner, Steven J, Labovitz, Daniel L, Lindgren, Arne, Meschia, James F, Peddareddygari, Leema R, Pera, Joanna, Rhodes, J. D, Rosand, Jonathan, Rundek, Tatjana, Slowik, Agnieszka, Southerland, Andrew M, Woo, Daniel, Worrall, Bradford B, Ay, Hakan

Volltext

Stroke genetics informs drug discovery and risk prediction across ancestries von Kamanu, F.K., Koido, M., Caro, I., Lin, K., Winsvold, B.S., Parodi, L., Tomppo, L., Jee, Y.H., Abedi, V., Lewis, A.J., Ago, T., Amouyel, P., Bis, J.C., Bordes, C., Borte, S., Cain, A., Cruchaga, C., Cole, J.W., Cid, R. de, Endres, M., Gudnason, V., Havulinna, A.S., Hyacinth, H.I., Jacob, M.A., Jeon, C.E., Jern, C., Kamouchi, M., Keene, K.L., Kittner, S.J., Kumar, A., Launer, L.J., Lee, K.J., Li, L.M., Manichaikul, A., Markus, H.S., Meitinger, T., Nalls, M.A., Nordestgaard, B.G., Onland-Moret, N.C., Peters, A., Sacco, R.L., Saleheen, D., Sandset, E.C., Salomaa, V., Sasaki, M., Schmidt, C.O., Smith, N.L., Tiedt, S., Trompet, S., Vugt, M. van, Verma, S.S., Wiggins, K.L., Woo, D., Wilson, P.W.F., Xu, H.C., Yang, Q., Yoon, K., Meschia, J.F., Traylor, M., Carty, C.L., Reiner, A., Gottesman, R.F., Furie, K.L., Arnett, D.K., Benavente, O.R., Grewal, R.P., Peddareddygari, L.R., Lindstrom, S., Smith, E.N., Vlieg, A.V., Brody, J.A., Pattee, J.W., Giulianini, F., Ibrahim, M., McCauley, B.M., Kraft, P., Hansen, J.B., Morange, P.E., Kabrhel, C., Dijk, E.J. van, Luijckx, G.J., Oostenbrugge, R.J. van, Leeuw, F.E. de, Levi, C.R., Ilinca, A., Rothwell, P.M., Butterworth, A.S., Rolfs, A., Weir, D., Jood, K., Linkohr, B., Lee, T.H., Anderson, C.D., Jian, X.Q., Schminke, U., Ibanez, L., Muino, E., Roquer, J., Sarnowski, C., Kanai, M.

Volltext bestellen

Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke von Jaworek, Thomas, Xu, Huichun, Gaynor, Brady J, Cole, John W, Rannikmae, Kristiina, Stanne, Tara M, Tomppo, Liisa, Abedi, Vida, Amouyel, Philippe, Armstrong, Nicole D, Attia, John, Bell, Steven, Benavente, Oscar R, Boncoraglio, Giorgio B, Carcel-Marquez, Jara, Chen, Zhengming, Chong, Michael, Cruchaga, Carlos, Cushman, Mary, Danesh, John, Duggan, David J, Durda, Jon Peter, Engstrom, Gunnar, Enzinger, Chris, Faul, Jessica D, Fecteau, Natalie S, 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, Jacob, Mina A, Rabionet, Raquel, Jimenez-Conde, Jordi, Johnson, Julie A, Kamatani, Yoichiro, Koido, Masaru, Kubo, Michiaki, Lange, Leslie, Lee, Jin-Moo, Lemmens, Robin, Levi, Christopher R, Li, Liming, Lin, Kuang, Lopez, Haley, Luke, Sothear, Maguire, Jane, McArdle, Patrick F, McDonough, Caitrin W, Meschia, James F, Metso, Tiina, Müller-Nurasyid, Martina, O'Donnell, Martin, Peddareddygari, Leema R, Peters, Annette, Putaala, Jukka, Rexrode, Kathryn, Ribases, Marta, Rosand, Jonathan, Rothwell, Peter M, 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, Stine, O. Colin, Strbian, Daniel, Sudlow, Cathie L. M, Tatlisumak, Turgut, Terao, Chikashi, Thijs, Vincent, Torres-Aguila, Nuria P, Tregouet, David-Alexandre, Tuladhar, Anil M, Veldink, Jan H, Walters, Robin G, Weir, David R, Woo, Daniel, Worrall, Bradford B, Hong, Charles C, Ross, Owen A, Leeuw, Frank-Erik de, Lindgren, Arne G, Pare, Guillaume, Markus, Hugh S, Jern, Christina, Malik, Rainer, Dichgans, Martin, Mitchell, Braxton D, Kittner, Steven J

Volltext bestellen

Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke von Jaworek, Thomas, Xu, Huichun, Gaynor, Brady, Cole, John W, Rannikmae, Kristiina, Stanne, Tara M, Tomppo, Liisa, Abedi, Vida, Amouyel, Philippe, Armstrong, Nicole D, Attia, John, Bell, Steven, Benavente, Oscar R, Boncoraglio, Giorgio B, Cárcel-Márquez, Jara, Chen, Zhengming, Cruchaga, Carlos, Cushman, Mary, Danesh, John, Debette, Stéphanie, Duggan, David J, Durda, Jon Peter, Engstrom, Gunnar, Enzinger, Chris, Faul, Jessica D, Fecteau, Natalie S, 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, Jacob, Mina A, Rabionet, Raquel, Jimenez-Conde, Jordi, Johnson, Julie A, Kamatani, Yoichiro, Kardia, Sharon L.R, Koido, Masaru, Kubo, Michiaki, Lange, Leslie, Lee, Jin-Moo, Lemmens, Robin, Levi, Christopher R, Li, Liming, Lin, Kuang, Lopez, Haley, Luke, Sothear, Maguire, Jane, McArdle, Patrick F, McDonough, Caitrin W, Meschia, James F, Metso, Tiina, Müller-Nurasyid, Martina, Dichgans, Martin, O'Donnell, Martin, Peddareddygari, Leema R, Peters, Annette, Putaala, Jukka, Rexrode, Kathryn, Ribasés Haro, Marta, Rosand, Jonathan, Rothwell, Peter M, Ryan, Kathleen A, Sacco, Ralph L, Salomaa, Veikko, Sánchez-Mora, Cristina, Schmidt, Reinhold, Sharma, Pankaj, Slowik, Agnieszka, Smith, Jennifer A, Smith, Nicholas L, Wassertheil-Smoller, Sylvia, Söderholm, Martin, Stine, O. Colin, Strbian, Daniel, Tatlisumak, Turgut, Terao, Chikashi, Torres-Aguila, Nuria P, Trégouët, David-Alexandre, Tuladhar, Anil M, Veldink, Jan H, Walters, Robin G, Weir, David R, Woo, Daniel, Worrall, Bradford B, Hong, Charles C, Ross, Owen A, de Leeuw, Frank-Erik, Lindgren, Arne G, Paré, Guillaume, Markus, Hugh S, Jern, Christina, Malik, Rainer, Mitchell, Braxton D, Universitat Autònoma de Barcelona

Volltext bestellen

Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke von Jaworek, Thomas, Xu, Huichun, Gaynor, Brady, Cole, John W, Rannikmae, Kristiina, Stanne, Tara M, Tomppo, Liisa, Abedi, Vida, Amouyel, Philippe, Armstrong, Nicole D, Attia, John, Bell, Steven, Benavente, Oscar R, Boncoraglio, Giorgio B, Cárcel-Márquez, Jara, Chen, Zhengming, Cruchaga, Carlos, Cushman, Mary, Danesh, John, Debette, Stéphanie, Duggan, David J, Durda, Jon Peter, Engström, Gunnar, Enzinger, Chris, Faul, Jessica D, Fecteau, Natalie S, 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, Jacob, Mina A, Rabionet, Raquel, Jimenez-Conde, Jordi, Johnson, Julie A, Kamatani, Yoichiro, Kardia, Sharon L.R, Koido, Masaru, Kubo, Michiaki, Lange, Leslie, Lee, Jin-Moo, Lemmens, Robin, Levi, Christopher R, Li, Liming, Lin, Kuang, Lopez, Haley, Luke, Sothear, Maguire, Jane, McArdle, Patrick F, McDonough, Caitrin W, Meschia, James F, Metso, Tiina, Müller-Nurasyid, Martina, Dichgans, Martin, O'Donnell, Martin, Peddareddygari, Leema R, Peters, Annette, Putaala, Jukka, Rexrode, Kathryn, Ribasés Haro, Marta, Rosand, Jonathan, Rothwell, Peter M, Ryan, Kathleen A, Sacco, Ralph L, Salomaa, Veikko, Sánchez-Mora, Cristina, Schmidt, Reinhold, Sharma, Pankaj, Slowik, Agnieszka, Smith, Jennifer A, Smith, Nicholas L, Wassertheil-Smoller, Sylvia, Söderholm, Martin, Stine, O. Colin, Strbian, Daniel, Tatlisumak, Turgut, Terao, Chikashi, Torres-Aguila, Nuria P, Trégouët, David-Alexandre, Tuladhar, Anil M, Veldink, Jan, Walters, Robin G, Weir, David R, Woo, Daniel, Worrall, Bradford B, Hong, Charles C, Ross, Owen A, de Leeuw, Frank-Erik, Lindgren, Arne G, Paré, Guillaume, Markus, Hugh S, Jern, Christina, Malik, Rainer, Mitchell, Braxton, Universitat Autònoma de Barcelona

Volltext bestellen

Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke von Keene, Keith L, Hyacinth, Hyacinth I, Bis, Joshua C, Kittner, Steven J, Mitchell, Braxton D, Cheng, Yu-Ching, Pare, Guillaume, Chong, Michael, O'Donnell, Martin, Meschia, James F, Chen, Wei-Min, Sale, Michèle M, Rich, Stephen S, Nalls, Mike A, Zonderman, Alan B, Evans, Michele K, Wilson, James G, Correa, Adolfo, Markus, Hugh S, Traylor, Matthew, Lewis, Cathryn M, Carty, Cara L, Reiner, Alexander, Haessler, Jeff, Langefeld, Carl D, Gottesman, Rebecca, Mosley, Thomas H, Woo, Daniel, Yaffe, Kristine, Liu, YongMei, Longstreth, William T, Psaty, Bruce M, Kooperberg, Charles, Lange, Leslie A, Sacco, Ralph, Rundek, Tatjana, Lee, Jin-Moo, Cruchaga, Carlos, Furie, Karen L, Arnett, Donna K, Benavente, Oscar R, Grewal, Raji P, Peddareddygari, Leema Reddy, Dichgans, Martin, Malik, Rainer, Worrall, Bradford B, Fornage, Myriam, COMPASS, SiGN, and METASTROKE Consortia

Volltext bestellen

Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke von Keene, Keith L, Hyacinth, Hyacinth I, Bis, Joshua C, Kittner, Steven J, Mitchell, Braxton D, Cheng, Yu-Ching, Pare, Guillaume, Chong, Michael, O'Donnell, Martin, Meschia, James F, Chen, Wei-Min, Sale, Michele M, Rich, Stephen S, Nalls, Mike A, Zonderman, Alan B, Evans, Michele K, Wilson, James G, Correa, Adolfo, Markus, Hugh S, Traylor, Matthew, Lewis, Cathryn M, Carty, Cara L, Reiner, Alexander, Haessler, Jeff, Langefeld, Carl D, Gottesman, Rebecca, Mosley, Thomas H, Woo, Daniel, Yaffe, Kristine, Liu, YongMei, Longstreth, William T, Psaty, Bruce M, Kooperberg, Charles, Lange, Leslie A, Sacco, Ralph, Rundek, Tatjana, Lee, Jin-Moo, Cruchaga, Carlos, Furie, Karen L, Arnett, Donna K, Benavente, Oscar R, Grewal, Raji P, Peddareddygari, Leema Reddy, Dichgans, Martin, Malik, Rainer, Worrall, Bradford B, Fornage, Myriam

Volltext bestellen