Items where Creator is "Bevan, Stephen"

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Malik, Rainer and Dau, Therese and Gonik, Maria and Sivakumar, Anirudh and Deredge, Daniel J. and Edeleva, Evgeniia V. and Götzfried, Jessica and van der Laan, Sander W. and Pasterkamp, Gerard and Beaufort, Nathalie and Seixas, Susana and Bevan, Stephen and Lincz, Lisa F. and Holliday, Elizabeth G. and Burgess, Annette I. and Rannikmäe, Kristiina and Minnerup, Jens and Kriebel, Jennifer and Waldenberger, Melanie and Müller-Nurasyid, Martina and Lichtner, Peter and Saleheen, Danish and Rothwell, Peter M. and Levi, Christopher and Attia, John and Sudlow, Cathie L. M. and Braun, Dieter and Markus, Hugh S. and Wintrode, Patrick L. and Berger, Klaus and Jenne, Dieter E. and Dichgans, Martin (2017) Common coding variant inSERPINA1increases the risk for large artery stroke. Proceedings of the National Academy of Sciences, 114 (14). pp. 3613-3618. ISSN 1091-6490

Ehret, Georg B and Ferreira, Teresa and Chasman, Daniel I and Jackson, Anne U and Schmidt, Ellen M and Johnson, Toby and Thorleifsson, Gudmar and Luan, Jian'an and Donnelly, Louise A and Kanoni, Stavroula and Petersen, Ann-Kristin and Pihur, Vasyl and Strawbridge, Rona J and Shungin, Dmitry and Hughes, Maria F and Meirelles, Osorio and Kaakinen, Marika and Bouatia-Naji, Nabila and Kristiansson, Kati and Shah, Sonia and Kleber, Marcus E and Guo, Xiuqing and Lyytikäinen, Leo-Pekka and Fava, Cristiano and Eriksson, Niclas and Nolte, Ilja M and Magnusson, Patrik K and Salfati, Elias L and Rallidis, Loukianos S and Theusch, Elizabeth and Smith, Andrew J P and Folkersen, Lasse and Witkowska, Kate and Pers, Tune H and Joehanes, Roby and Kim, Stuart K and Lataniotis, Lazaros and Jansen, Rick and Johnson, Andrew D and Warren, Helen and Kim, Young Jin and Zhao, Wei and Wu, Ying and Tayo, Bamidele O and Bochud, Murielle and Absher, Devin and Adair, Linda S and Amin, Najaf and Arking, Dan E and Axelsson, Tomas and Baldassarre, Damiano and Balkau, Beverley and Bandinelli, Stefania and Barnes, Michael R and Barroso, Inês and Bevan, Stephen and Bis, Joshua C and Bjornsdottir, Gyda and Boehnke, Michael and Boerwinkle, Eric and Bonnycastle, Lori L and Boomsma, Dorret I and Bornstein, Stefan R and Brown, Morris J and Burnier, Michel and Cabrera, Claudia P and Chambers, John C and Chang, I-Shou and Cheng, Ching-Yu and Chines, Peter S and Chung, Ren-Hua and Collins, Francis S and Connell, John M and Döring, Angela and Dallongeville, Jean and Danesh, John and de Faire, Ulf and Delgado, Graciela and Dominiczak, Anna F and Doney, Alex S F and Drenos, Fotios and Edkins, Sarah and Eicher, John D and Elosua, Roberto and Enroth, Stefan and Erdmann, Jeanette and Eriksson, Per and Esko, Tonu and Evangelou, Evangelos and Evans, Alun and Fall, Tove and Farrall, Martin and Felix, Janine F and Ferrières, Jean and Ferrucci, Luigi and Fornage, Myriam and Forrester, Terrence and Franceschini, Nora and Franco, Oscar H and Franco-Cereceda, Anders and Fraser, Ross M and Ganesh, Santhi K and Gao, He and Gertow, Karl and Gianfagna, Francesco and Gigante, Bruna and Giulianini, Franco and Goel, Anuj and Goodall, Alison H and Goodarzi, Mark O and Gorski, Mathias and Gräßler, Jürgen and Groves, Christopher J and Gudnason, Vilmundur and Gyllensten, Ulf and Hallmans, Göran and Hartikainen, Anna-Liisa and Hassinen, Maija and Havulinna, Aki S and Hayward, Caroline and Hercberg, Serge and Herzig, Karl-Heinz and Hicks, Andrew A and Hingorani, Aroon D and Hirschhorn, Joel N and Hofman, Albert and Holmen, Jostein and Holmen, Oddgeir Lingaas and Hottenga, Jouke-Jan and Howard, Phil and Hsiung, Chao A and Hunt, Steven C and Ikram, M Arfan and Illig, Thomas and Iribarren, Carlos and Jensen, Richard A and Kähönen, Mika and Kang, Hyun Min and Kathiresan, Sekar and Keating, Brendan J and Khaw, Kay-Tee and Kim, Yun Kyoung and Kim, Eric and Kivimaki, Mika and Klopp, Norman and Kolovou, Genovefa and Komulainen, Pirjo and Kooner, Jaspal S and Kosova, Gulum and Krauss, Ronald M and Kuh, Diana and Kutalik, Zoltan and Kuusisto, Johanna and Kvaløy, Kirsti and Lakka, Timo A and Lee, Nanette R and Lee, I-Te and Lee, Wen-Jane and Levy, Daniel and Li, Xiaohui and Liang, Kae-Woei and Lin, Honghuang and Lin, Li and Lindström, Jaana and Lobbens, Stéphane and Männistö, Satu and Müller, Gabriele and Müller-Nurasyid, Martina and Mach, François and Markus, Hugh S and Marouli, Eirini and McCarthy, Mark I and McKenzie, Colin A and Meneton, Pierre and Menni, Cristina and Metspalu, Andres and Mijatovic, Vladan and Moilanen, Leena and Montasser, May E and Morris, Andrew D and Morrison, Alanna C and Mulas, Antonella and Nagaraja, Ramaiah and Narisu, Narisu and Nikus, Kjell and O'Donnell, Christopher J and O'Reilly, Paul F and Ong, Ken K and Paccaud, Fred and Palmer, Cameron D and Parsa, Afshin and Pedersen, Nancy L and Penninx, Brenda W and Perola, Markus and Peters, Annette and Poulter, Neil and Pramstaller, Peter P and Psaty, Bruce M and Quertermous, Thomas and Rao, Dabeeru C and Rasheed, Asif and Rayner, N William and Renström, Frida and Rettig, Rainer and Rice, Kenneth M and Roberts, Robert and Rose, Lynda M and Rossouw, Jacques and Samani, Nilesh J and Sanna, Serena and Saramies, Jouko and Schunkert, Heribert and Sebert, Sylvain and Sheu, Wayne H-H and Shin, Young-Ah and Sim, Xueling and Smit, Johannes H and Smith, Albert V and Sosa, Maria X and Spector, Tim D and Stančáková, Alena and Stanton, Alice V and Stirrups, Kathleen E and Stringham, Heather M and Sundstrom, Johan and Swift, Amy J and Syvänen, Ann-Christine and Tai, E-Shyong and Tanaka, Toshiko and Tarasov, Kirill V and Teumer, Alexander and Thorsteinsdottir, Unnur and Tobin, Martin D and Tremoli, Elena and Uitterlinden, Andre G and Uusitupa, Matti and Vaez, Ahmad and Vaidya, Dhananjay and van Duijn, Cornelia M and van Iperen, Erik P A and Vasan, Ramachandran S and Verwoert, Germaine C and Virtamo, Jarmo and Vitart, Veronique and Voight, Benjamin F and Vollenweider, Peter and Wagner, Aline and Wain, Louise V and Wareham, Nicholas J and Watkins, Hugh and Weder, Alan B and Westra, Harm-Jan and Wilks, Rainford and Wilsgaard, Tom and Wilson, James F and Wong, Tien Y and Yang, Tsun-Po and Yao, Jie and Yengo, Loic and Zhang, Weihua and Zhao, Jing Hua and Zhu, Xiaofeng and Bovet, Pascal and Cooper, Richard S and Mohlke, Karen L and Saleheen, Danish and Lee, Jong-Young and Elliott, Paul and Gierman, Hinco J and Willer, Cristen J and Franke, Lude and Hovingh, G Kees and Taylor, Kent D and Dedoussis, George and Sever, Peter and Wong, Andrew and Lind, Lars and Assimes, Themistocles L and Njølstad, Inger and Schwarz, Peter E H and Langenberg, Claudia and Snieder, Harold and Caulfield, Mark J and Melander, Olle and Laakso, Markku and Saltevo, Juha and Rauramaa, Rainer and Tuomilehto, Jaakko and Ingelsson, Erik and Lehtimäki, Terho and Hveem, Kristian and Palmas, Walter and März, Winfried and Kumari, Meena and Salomaa, Veikko and Chen, Yii-Der I and Rotter, Jerome I and Froguel, Philippe and Jarvelin, Marjo-Riitta and Lakatta, Edward G and Kuulasmaa, Kari and Franks, Paul W and Hamsten, Anders and Wichmann, H-Erich and Palmer, Colin N A and Stefansson, Kari and Ridker, Paul M and Loos, Ruth J F and Chakravarti, Aravinda and Deloukas, Panos and Morris, Andrew P and Newton-Cheh, Christopher and Munroe, Patricia B (2016) The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nature Genetics, 48 (10). pp. 1171-1184. ISSN 1061-4036

Prins, Bram P. and Abbasi, Ali and Wong, Anson and Vaez, Ahmad and Nolte, Ilja and Franceschini, Nora and Stuart, Philip E. and Guterriez Achury, Javier and Mistry, Vanisha and Bradfield, Jonathan P. and Valdes, Ana M. and Bras, Jose and Shatunov, Aleksey and Lu, Chen and Han, Buhm and Raychaudhuri, Soumya and Bevan, Steve and Mayes, Maureen D. and Tsoi, Lam C. and Evangelou, Evangelos and Nair, Rajan P. and Grant, Struan F. A. and Polychronakos, Constantin and Radstake, Timothy R. D. and van Heel, David A. and Dunstan, Melanie L. and Wood, Nicholas W. and Al-Chalabi, Ammar and Dehghan, Abbas and Hakonarson, Hakon and Markus, Hugh S. and Elder, James T. and Knight, Jo and Arking, Dan E. and Spector, Timothy D. and Koeleman, Bobby P. C. and van Duijn, Cornelia M. and Martin, Javier and Morris, Andrew P. and Weersma, Rinse K. and Wijmenga, Cisca and Munroe, Patricia B. and Perry, John R. B. and Pouget, Jennie G. and Jamshidi, Yalda and Snieder, Harold and Alizadeh, Behrooz Z. (2016) Investigating the causal relationship of C-reactive protein with 32 complex somatic and psychiatric outcomes: a large-scale cross-consortium Mendelian randomization study. PLoS medicine, 13 (6). e1001976. ISSN 1549-1277

Chauhan, Ganesh and Arnold, Corey R. and Chu, Audrey Y. and Fornage, Myriam and Reyahi, Azadeh and Bis, Joshua C. and Havulinna, Aki S. and Sargurupremraj, Muralidharan and Smith, Albert Vernon and Adams, Hieab H. H. and Choi, Seung Hoan and Pulit, Sara L. and Trompet, Stella and Garcia, Melissa E. and Manichaikul, Ani and Teumer, Alexander and Gustafsson, Stefan and Bartz, Traci M. and Bellenguez, Céline and Vidal, Jean Sebastien and Jian, Xueqiu and Kjartansson, Olafur and Wiggins, Kerri L. and Satizabal, Claudia L. and Xue, Flora and Ripatti, Samuli and Liu, Yongmei and Deelen, Joris and den Hoed, Marcel and Bevan, Steve and Hopewell, Jemma C. and Malik, Rainer and Heckbert, Susan R. and Rice, Kenneth and Smith, Nicholas L. and Levi, Christopher and Sharma, Pankaj and Sudlow, Cathie LM and Nik, Ali Moussavi and Cole, John W. and Schmidt, Reinhold and Meschia, James and Thijs, Vincent and Lindgren, Arne and Melander, Olle and Grewal, Raji P. and Sacco, Ralph L. and Rundek, Tatjana and Rothwell, Peter M. and Arnett, Donna K. and Jern, Christina and Johnson, Julie A. and Benavente, Oscar R. and Wassertheil-Smoller, Sylvia and Lee, Jin-Moo and Wong, Quenna and Aparicio, Hugo J. and Engelter, Stefan T. and Kloss, Manja and Leys, Didier and Pezzini, Alessandro and Buring, Julie E. and Ridker, Paul M. and Berr, Claudine and Dartigues, Jean-François and Hamsten, Anders and Magnusson, Patrik K. and Traylor, Matthew and Pedersen, Nancy L. and Lannfelt, Lars and Lindgren, Lars and Lindgren, Cecilia M. and Morris, Andrew P. and Jimenez-Conde, Jordi and Montaner, Joan and Radmanesh, Farid and Slowik, Agnieszka and Woo, Daniel and Hofman, Albert and Koudstaal, Peter J. and Portegies, Marileen L. P. and Uitterlinden, André G. and de Craen, Anton J. M. and Ford, Ian and Jukema, J. Wouter and Stott, David J. and Allen, Norrina B. and Sale, Michele M. and Johnson, Andrew D. and Bennett, David A. and De Jager, Philip L. and White, Charles C. and Grabe, Hans Jörgen and Markus, Marcello Ricardo Paulista and Schminke, Ulf and Boncoraglio, Giorgio B. and Clarke, Robert and Kamatani, Yoichiro and Dallongeville, Jean and Lopez, Oscar L. and Rotter, Jerome I. and Nalls, Michael A. and Gottesman, Rebecca F. and Griswold, Michael E. and Knopman, David S. and Windham, B. Gwen and Beiser, Alexa and Markus, Hugh S. and Vartiainen, Erkki and French, Curtis R. and Dichgans, Martin and Pastinen, Tomi and Lathrop, Mark and Gudnason, Vilmundur and Kurth, Tobias and Psaty, Bruce M. and Harris, Tamara B. and Rich, Stephen S. and deStefano, Anita L. and Schmidt, Carsten Oliver and Worrall, Bradford B. and Rosand, Jonathan and Salomaa, Veikko and Mosley, Thomas H. and Ingelsson, Erik and van Duijn, Cornelia M. and Tzourio, Christophe and Rexrode, Kathryn M. and Lehmann, Ordan J. and Launer, Lenore J. and Ikram, M. Arfan and Carlsson, Peter and Chasman, Daniel I. and Childs, Sarah J. and Longstreth, William T. and Seshadri, Sudha and Debette, Stéphanie (2016) Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies. The Lancet Neurology, 15 (7). pp. 695-707. ISSN 1474-4422

Traylor, Matthew and Rutten-Jacobs, Loes C. A. and Thijs, Vincent and Holliday, Elizabeth G. and Levi, Chris and Bevan, Steve and Malik, Rainer and Boncoraglio, Giorgio and Sudlow, Cathie and Rothwell, Peter M. and Dichgans, Martin and Markus, Hugh S. (2016) Genetic associations with white matter hyperintensities confer risk of lacunar stroke. Stroke: a Journal of Cerebral Circulation, 47 (5). pp. 1174-9. ISSN 0039-2499

Malik, Rainer and Traylor, Matthew and Pulit, Sara L. and Bevan, Steve and Hopewell, Jemma C. and Holliday, Elizabeth G. and Zhao, Wei and Abrantes, Patricia and Amouyel, Philippe and Attia, John R. and Battey, Thomas W.K. and Berger, Klaus and Boncoraglio, Giorgio B. and Chauhan, Ganesh and Cheng, Yu-Ching and Chen, Wei-Min and Clarke, Robert and Cotlarciuc, Ioana and Debette, Stephanie and Falcone, Guido J. and Ferro, Jose M. and Gamble, Dale M. and Ilinca, Andreea and Kittner, Steven J. and Kourkoulis, Christina E. and Lemmens, Robin and Levi, Christopher R. and Lichtner, Peter and Lindgren, Arne and Liu, Jingmin and Meschia, James F. and Mitchell, Braxton D. and Oliveira, Sofia A. and Pera, Joana and Reiner, Alex P. and Rothwell, Peter M. and Sharma, Pankaj and Slowik, Agnieszka and Sudlow, Cathie L.M. and Tatlisumak, Turgut and Thijs, Vincent and Vicente, Astrid M. and Woo, Daniel and Seshadri, Sudha and Saleheen, Danish and Rosand, Jonathan and Markus, Hugh S. and Worrall, Bradford B. and Dichgans, Martin (2016) Low-frequency and common genetic variation in ischemic stroke. Neurology, 86 (13). pp. 1217-1226. ISSN 0028-3878

Malik, Rainer and Traylor, Matthew and Pulit, Sara L. and Bevan, Steve and Hopewell, Jemma C. and Holliday, Elizabeth G. and Zhao, Wei and Abrantes, Patricia and Amouyel, Philippe and Attia, John R. and Battey, Thomas W. K. and Berger, Klaus and Boncoraglio, Giorgio B. and Chauhan, Ganesh and Cheng, Yu-Ching and Chen, Wei-Min and Clarke, Robert and Cotlarciuc, Ioana and Debette, Stephanie and Falcone, Guido J. and Ferro, Jose M. and Gamble, Dale M. and Ilinca, Andreea and Kittner, Steven J. and Kourkoulis, Christina E. and Lemmens, Robin and Levi, Christopher R. and Lichtner, Peter and Lindgren, Arne and Liu, Jingmin and Meschia, James F. and Mitchell, Braxton D. and Oliveira, Sofia A. and Pera, Joana and Reiner, Alex P. and Rothwell, Peter M. and Sharma, Pankaj and Slowik, Agnieszka and Sudlow, Cathie L. M. and Tatlisumak, Turgut and Thijs, Vincent and Vicente, Astrid M. and Woo, Daniel and Seshadri, Sudha and Saleheen, Danish and Rosand, Jonathan and Markus, Hugh S. and Worrall, Bradford B. and Dichgans, Martin (2016) Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration. Neurology, 86 (13). pp. 1217-1226. ISSN 0028-3878

Seppälä, Ilkka and Kleber, Marcus E. and Bevan, Steve and Lyytikäinen, Leo-Pekka and Oksala, Niku and Hernesniemi, Jussi A. and Mäkelä, Kari-Matti and Rothwell, Peter M. and Sudlow, Cathie and Dichgans, Martin and Mononen, Nina and Vlachopoulou, Efthymia and Sinisalo, Juha and Delgado, Graciela E. and Laaksonen, Reijo and Koskinen, Tuomas and Scharnagl, Hubert and Kähönen, Mika and Markus, Hugh S. and März, Winfried and Lehtimäki, Terho (2016) Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke. Scientific Reports, 6 . p. 23207. ISSN 2045-2322

Seppälä, Ilkka and Kleber, Marcus E. and Bevan, Stephen and Lyytikäinen, Leo-Pekka and Oksala, Niku and Hernesniemi, Jussi A. and Mäkelä, Kari-Matti and Rothwell, Peter M. and Sudlow, Cathie and Dichgans, Martin and Mononen, Nina and Vlachopoulou, Efthymia and Sinisalo, Juha and Delgado, Graciela E. and Laaksonen, Reijo and Koskinen, Tuomas and Scharnagl, Hubert and Kähönen, Mika and Markus, Hugh S. and März, Winfried and Lehtimäki, Terho (2016) Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke. Scientific Reports, 6 (1). ISSN 2045-2322

Rutten-Jacobs, Loes C. A. and Traylor, Matthew and Adib-Samii, Poneh and Thijs, Vincent and Sudlow, Cathie and Rothwell, Peter M. and Boncoraglio, Giorgio and Dichgans, Martin and Meschia, James and Maguire, Jane and Levi, Christopher and Rost, Natalia S. and Rosand, Jonathan and Hassan, Ahamad and Bevan, Steve and Markus, Hugh S. (2016) Association of MTHFR C677T genotype with ischemic stroke is confined to cerebral small vessel disease subtype. Stroke: a Journal of Cerebral Circulation, 47 (3). pp. 646-651. ISSN 0039-2499

Rutten-Jacobs, Loes C. A. and Traylor, Matthew and Adib-Samii, Poneh and Thijs, Vincent and Sudlow, Cathie and Rothwell, Peter M. and Boncoraglio, Giorgio and Dichgans, Martin and Meschia, James and Maguire, Jane and Levi, Christopher and Rost, Natalia S. and Rosand, Jonathan and Hassan, Ahamad and Bevan, Steve and Markus, Hugh S. (2016) Association of MTHFRC677T genotype With ischemic stroke Is confined to cerebral small vessel disease subtype. Stroke . STROKEAHA.115.011545. ISSN 0039-2499

Harris, Sarah E. and Malik, Rainer and Marioni, Riccardo and Campbell, Archie and Seshadri, Sudha and Worrall, Bradford B. and Sudlow, Cathie L. M. and Hayward, Caroline and Bastin, Mark E. and Starr, John M. and Porteous, David J. and Wardlaw, Joanna M. and Deary, Ian J. and METASTROKE Consortium, . (2016) Polygenic risk of ischemic stroke is associated with cognitive ability. Neurology, 86 (7). pp. 611-618. ISSN 0028-3878

Cheng, Yu-Ching and Stanne, Tara M. and Giese, Anne-Katrin and Ho, Weang Kee and Traylor, Matthew and Amouyel, Philippe and Holliday, Elizabeth G. and Malik, Rainer and Xu, Huichun and Kittner, Steven J. and Cole, John W. and O'Connell, Jeffrey R. and Danesh, John and Rasheed, Asif and Zhao, Wei and Engelter, Stefan and Grond-Ginsbach, Caspar and Kamatani, Yoichiro and Lathrop, Mark and Leys, Didier and Thijs, Vincent and Metso, Tiina M and Tatlisumak, Turgut and Pezzini, Alessandro and Parati, Eugenio A and Norrving, Bo and Bevan, Steve and Rothwell, Peter M. and Sudlow, Cathie and Slowik, Agnieszka and Lindgren, Arne and Walters, Matthew R. and Jannes, Jim and Shen, Jess and Crosslin, David and Doheny, Kimberly and Laurie, Cathy C. and Kanse, Sandip M. and Bis, Joshua C. and Fornage, Myriam and Mosley, Thomas H. and Hopewell, Jemma C. and Strauch, Konstantin and Müller-Nurasyid, Martina and Gieger, Christian and Waldenberger, Melanie and Peters, Annette and Meisinger, Christine and Ikram, M Arfan and Longstreth, W. T. and Meschia, James F. and Seshadri, Sudha and Sharma, Pankaj and Worrall, Bradford and Jern, Christina and Levi, Christopher and Dichgans, Martin and Boncoraglio, Giorgio B. and Markus, Hugh S. and Debette, Stephanie and Rolfs, Arndt and Saleheen, Danish and Mitchell, Braxton D. (2016) Genome-wide association analysis of young-onset stroke identifies a locus on chromosome 10q25 near HABP2. Stroke: a Journal of Cerebral Circulation, 47 (2). pp. 307-16. ISSN 0039-2499

Pulit, Sara L. and McArdle, Patrick F. and Wong, Quenna and Malik, Rainer and Gwinn, Katrina and Achterberg, Sefanja and Algra, Ale and Amouyel, Philippe and Anderson, Christopher D. and Arnett, Donna K. and Arsava, Ethem Murat and Attia, John and Ay, Hakan and Bartz, Traci M. and Battey, Thomas and Benavente, Oscar R. and Bevan, Steve and Biffi, Alessandro and Bis, Joshua C. and Blanton, Susan H. and Boncoraglio, Giorgio B. and Brown, Robert D. and Burgess, Annette I. and Carrera, Caty and Chapman Smith, Sherita N. and Chasman, Daniel I. and Chauhan, Ganesh and Chen, Wei-Min and Cheng, Yu-Ching and Chong, Michael and Cloonan, Lisa K. and Cole, John W. and Cotlarciuc, Ioana and Cruchaga, Carlos and Cuadrado-Godia, Elisa and Dave, Tushar and Dawson, Jesse and Debette, Stéphanie and Delavaran, Hossein and Dell, Cameron A. and Dichgans, Martin and Doheny, Kimberly F. and Dong, Chuanhui and Duggan, David J. and Engström, Gunnar and Evans, Michele K. and Pallejà, Xavier Estivill and Faul, Jessica D. and Fernández-Cadenas, Israel and Fornage, Myriam and Frossard, Philippe M. and Furie, Karen and Gamble, Dale M. and Gieger, Christian and Giese, Anne-Katrin and Giralt-Steinhauer, Eva and González, Hector M. and Goris, An and Gretarsdottir, Solveig and Grewal, Raji P. and Grittner, Ulrike and Gustafsson, Stefan and Han, Buhm and Hankey, Graeme J. and Heitsch, Laura and Higgins, Peter and Hochberg, Marc C. and Holliday, Elizabeth and Hopewell, Jemma C. and Horenstein, Richard B. and Howard, George and Ikram, M. Arfan and Ilinca, Andreea and Ingelsson, Erik and Irvin, Marguerite R. and Jackson, Rebecca D. and Jern, Christina and Conde, Jordi Jiménez and Johnson, Julie A. and Jood, Katarina and Kahn, Muhammad S. and Kaplan, Robert and Kappelle, L Jaap and Kardia, Sharon L. R. and Keene, Keith L. and Kissela, Brett M. and Kleindorfer, Dawn O. and Koblar, Simon and Labovitz, Daniel and Launer, Lenore J. and Laurie, Cathy C. and Laurie, Cecelia A. and Lee, Cue Hyunkyu and Lee, Jin-Moo and Lehm, Manuel and Lemmens, Robin and Levi, Christopher and Leys, Didier and Lindgren, Arne and Longstreth, W. T. and Maguire, Jane and Manichaikul, Ani and Markus, Hugh S. and McClure, Leslie A. and McDonough, Caitrin W. and Meisinger, Christa and Melander, Olle and Meschia, James F. and Mola-Caminal, Marina and Montaner, Joan and Mosley, Thomas H. and Müller-Nurasyid, Martina and Nalls, Mike A. and O'Connell, Jeffrey R. and O'Donnell, Martin and Ois, ángel and Papanicolaou, George J. and Paré, Guillaume and Peddareddygari, Leema Reddy and Pedersén, Annie and Pera, Joanna and Peters, Annette and Poole, Deborah and Psaty, Bruce M. and Rabionet, Raquel and Raffeld, Miriam R. and Rannikmäe, Kristiina and Rasheed, Asif and Redfors, Petra and Reiner, Alex P. and Rexrode, Kathryn and Ribasés, Marta and Rich, Stephen S. and Robberecht, Wim and Rodriguez-Campello, Ana and Rolfs, Arndt and Roquer, Jaume and Rose, Lynda M. and Rosenbaum, Daniel and Rost, Natalia S. and Rothwell, Peter M. and Rundek, Tatjana and Ryan, Kathleen A. and Sacco, Ralph L. and Sale, Michèle M. and Saleheen, Danish and Salomaa, Veikko and Sánchez-Mora, Cristina and Schmidt, Carsten Oliver and Schmidt, Helena and Schmidt, Reinhold and Schürks, Markus and Scott, Rodney and Segal, Helen C. and Seiler, Stephan and Seshadri, Sudha and Sharma, Pankaj and Shuldiner, Alan R. and Silver, Brian and Slowik, Agnieszka and Smith, Jennifer A. and Söderholm, Martin and Soriano, Carolina and Sparks, Mary J. and Stanne, Tara and Stefansson, Kari and Stine, O. Colin and Strauch, Konstantin and Sturm, Jonathan and Sudlow, Cathie L. M. and Tajuddin, Salman M. and Talbert, Robert L. and Tatlisumak, Turgut and Thijs, Vincent and Thorleifsson, Gudmar and Thorsteindottir, Unnur and Tiedt, Steffen and Traylor, Matthew and Trompet, Stella and Valant, Valerie and Waldenberger, Melanie and Walters, Matthew and Wang, Liyong and Wassertheil-Smoller, Sylvia and Weir, David R. and Wiggins, Kerri L. and Williams, Stephen R. and Wloch-Kopec, Dorota and Woo, Daniel and Woodfield, Rebecca and Wu, Ona and Xu, Huichun and Zonderman, Alan B. and Worrall, Bradford B. and de Bakker, Paul I. W. and Kittner, Steven J. and Mitchell, Braxton D. and Rosand, Jonathan and Mitchell, Braxton D. and Ay, Hakan and Gwinn, Katrina and Kittner, Steven J. and Lindgren, Arne and Meschia, James F. and Pulit, Sara L. and Sudlow, Cathie L. M. and Thijs, Vincent and Woo, Daniel and Worrall, Bradford B. Worrall and Arnett, Donna K. Arnett and Benavente, Oscar and Cole, John W. and Dichgans, Martin and Grewal, Raji P. and Jern, Christina and Conde, Jordi Jiménez and Johnson, Julie A. and Kittner, Steven J. and Lee, Jin-Moo and Levi, Christopher and Lindgren, Arne and Markus, Hugh S. and Melander, Olle and Meschia, James F. and Rexrode, Kathryn and Rosand, Jonathan and Rothwell, Peter M. and Rundek, Tatjana and Sacco, Ralph L. and Schmidt, Reinhold and Sharma, Pankaj and Slowik, Agnieszka and Sudlow, Cathie L. M. and Thijs, Vincent and Wasssertheil-Smoller, Sylvia and Woo, Daniel and Worrall, Bradford B. (2016) Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study. The Lancet Neurology, 15 (2). pp. 174-184. ISSN 1474-4422

Harris, Sarah E. and Malik, Rainer and Marioni, Riccardo and Campbell, Archie and Seshadri, Sudha and Worrall, Bradford B. and Sudlow, Cathie L.M. and Hayward, Caroline and Bastin, Mark E. and Starr, John M. and Porteous, David J. and Wardlaw, Joanna M. and Deary, Ian J. and UNSPECIFIED (2016) Polygenic risk of ischemic stroke is associated with cognitive ability. Neurology, 86 (7). pp. 611-618. ISSN 0028-3878

Traylor, Matthew and Zhang, Cathy R. and Adib-Samii, Poneh and Devan, William J. and Parsons, Owen E. and Lanfranconi, Silvia and Gregory, Sarah and Cloonan, Lisa and Falcone, Guido J. and Radmanesh, Farid and Fitzpatrick, Kaitlin and Kanakis, Allison and Barrick, Thomas R. and Moynihan, Barry and Lewis, Cathryn M. and Boncoraglio, Giorgio B. and Lemmens, Robin and Thijs, Vincent and Sudlow, Cathie and Wardlaw, Joanna and Rothwell, Peter M. and Meschia, James F. and Worrall, Bradford B. and Levi, Christopher and Bevan, Steve and Furie, Karen L. and Dichgans, Martin and Rosand, Jonathan and Markus, Hugh S. and Rost, Natalia (2016) Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke. Neurology, 86 (2). pp. 146-153. ISSN 0028-3878

Traylor, Matthew and Zhang, Cathy R. and Adib-Samii, Poneh and Devan, William J. and Parsons, Owen E. and Lanfranconi, Silvia and Gregory, Sarah and Cloonan, Lisa and Falcone, Guido J. and Radmanesh, Farid and Fitzpatrick, Kaitlin and Kanakis, Allison and Barrick, Thomas R. and Moynihan, Barry and Lewis, Cathryn M. and Boncoraglio, Giorgio B. and Lemmens, Robin and Thijs, Vincent and Sudlow, Cathie and Wardlaw, Joanna and Rothwell, Peter M. and Meschia, James F. and Worrall, Bradford B. and Levi, Christopher and Bevan, Steve and Furie, Karen L. and Dichgans, Martin and Rosand, Jonathan and Markus, Hugh S. and Rost, Natalia (2016) Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke. Neurology, 86 (2). pp. 146-153. ISSN 0028-3878

Traylor, Matthew and Anderson, Christopher D. and Hurford, Robert and Bevan, Steve and Markus, Hugh S. (2016) Oxidative phosphorylation and lacunar stroke. Neurology, 86 (2). pp. 141-145. ISSN 0028-3878

Traylor, Matthew and Anderson, Christopher D. and Hurford, Robert and Bevan, Steve and Markus, Hugh S. (2016) Oxidative phosphorylation and lacunar stroke: genome-wide enrichment analysis of common variants. Neurology, 86 (2). pp. 141-145. ISSN 0028-3878

Gesierich, Benno and Opherk, Christian and Rosand, Jonathan and Gonik, Mariya and Malik, Rainer and Jouvent, Eric and Hervé, Dominique and Adib-Samii, Poneh and Bevan, Steve and Pianese, Luigi and Silvestri, Serena and Dotti, Maria T. and De Stefano, Nicola and van der Grond, Jeroen and Boon, Elles M. J. and Pescini, Francesca and Rost, Natalia and Pantoni, Leonardo and Lesnik Oberstein, Saskia A. and Federico, Antonio and Ragno, Michele and Markus, Hugh S. and Tournier-Lasserve, Elisabeth and Chabriat, Hugues and Dichgans, Martin and Duering, Marco and Ewers, Michael (2016) APOE ɛ2 is associated with white matter hyperintensity volume in CADASIL. Journal of Cerebral Blood Flow & Metabolism . ISSN 0271-678X

Rutten-Jacobs, Loes C.A. and Traylor, Matthew and Adib-Samii, Poneh and Thijs, Vincent and Sudlow, Cathie and Rothwell, Peter M. and Boncoraglio, Giorgio and Dichgans, Martin and Bevan, Steve and Meschia, James and Levi, Christopher and Rost, Natalia S. and Rosand, Jonathan and Hassan, Ahamad and Markus, Hugh S. (2015) Common NOTCH3 variants and cerebral small-vessel disease. Stroke, 46 (6). pp. 1482-1487. ISSN 0039-2499

Hanscombe, Ken B. and Traylor, Matthew and Hysi, Pirro G. and Bevan, Stephen and Dichgans, Martin and Rothwell, Peter M. and Worrall, Bradford B. and Seshadri, Sudha and Sudlow, Cathie and Williams, Frances M. K. and Markus, Hugh S. and Lewis, Cathryn M. (2015) Genetic factors influencing coagulation factor XIII B-subunit contribute to risk of ischemic stroke. Stroke, 46 (8). pp. 2069-2074. ISSN 0039-2499

Traylor, Matthew and Rutten-Jacobs, Loes C. A. and Holliday, Elizabeth G. and Malik, Rainer and Sudlow, Cathie and Rothwell, Peter M. and Maguire, Jane M. and Koblar, Simon A. and Bevan, Steve and Boncoraglio, Giorgio and Dichgans, Martin and Levi, Chris and Lewis, Cathryn M. and Markus, Hugh S. (2015) Differences in common genetic predisposition to ischemic stroke by age and sex. Stroke: a journal of cerebral circulation, 46 (11). pp. 3042-7. ISSN 0039-2499

Traylor, Matthew and Bevan, Stephen and Baron, Jean-Claude and Hassan, Ahamad and Lewis, Cathryn M. and Markus, Hugh S. (2015) Genetic architecture of lacunar stroke. Stroke; a journal of cerebral circulation, 46 (9). pp. 2407-2412. ISSN 0039-2499

Kilarski, Laura L. and Rutten-Jacobs, Loes C. A. and Bevan, Stephen and Baker, Rob and Hassan, Ahamad and Hughes, Derralynn A. and Markus, Hugh S. (2015) Prevalence of CADASIL and Fabry disease in a cohort of MRI defined younger onset lacunar stroke. PloS one, 10 (8). e0136352. ISSN 1932-6203

Rannikmae, K. and Davies, G. and Thomson, P. A. and Bevan, S. and Devan, W. J. and Falcone, G. J. and Traylor, M. and Anderson, C. D. and Battey, T. W. K. and Radmanesh, F. and Deka, R. and Woo, J. G. and Martin, L. J. and Jimenez-Conde, J. and Selim, M. and Brown, D. L. and Silliman, S. L. and Kidwell, C. S. and Montaner, J. and Langefeld, C. D. and Slowik, A. and Hansen, B. M. and Lindgren, A. G. and Meschia, J. F. and Fornage, M. and Bis, J. C. and Debette, S. and Ikram, M. A. and Longstreth, W. T. and Schmidt, R. and Zhang, C. R. and Yang, Q. and Sharma, P. and Kittner, S. J. and Mitchell, B. D. and Holliday, E. G. and Levi, C. R. and Attia, J. and Rothwell, P. M. and Poole, D. L. and Boncoraglio, G. B. and Psaty, B. M. and Malik, R. and Rost, N. and Worrall, B. B. and Dichgans, M. and Van Agtmael, T. and Woo, D. and Markus, H. S. and Seshadri, S. and Rosand, J. and Sudlow, C. L. M. (2015) Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease. Neurology, 84 (9). pp. 918-926. ISSN 0028-3878

Adib-Samii, Poneh and Devan, William and Traylor, Matthew and Lanfranconi, Silvia and Zhang, Cathy R. and Cloonan, Lisa and Falcone, Guido J. and Radmanesh, Farid and Fitzpatrick, Kaitlin and Kanakis, Allison and Rothwell, Peter M. and Sudlow, Cathie and Boncoraglio, Giorgio B. and Meschia, James F. and Levi, Chris and Dichgans, Martin and Bevan, Steve and Rosand, Jonathan and Rost, Natalia S. and Markus, Hugh S. (2015) Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke. Stroke, 46 (2). pp. 348-353. ISSN 0039-2499

Holliday, Elizabeth G. and Traylor, Matthew and Malik, Rainer and Bevan, Stephen and Maguire, Jane and Koblar, Simon A. and Sturm, Jonathan and Hankey, Graeme J. and Oldmeadow, Christopher and McEvoy, Mark and Sudlow, Cathie and Rothwell, Peter M. and Coresh, Josef and Hamet, Pavel and Tremblay, Johanne and Turner, Stephen T. and de Andrade, Mariza and Rao, Madhumathi and Schmidt, Reinhold and Crick, Peter A. and Robino, Antonietta and Peralta, Carmen A. and Jukema, J. Wouter and Mitchell, Paul and Rosas, Sylvia E. and Wang, Jie Jin and Scott, Rodney J. and Dichgans, Martin and Mitchell, Braxton D. and Kao, W.H. Linda and Fox, Caroline S. and Levi, Christopher and Attia, John and Markus, Hugh S. (2014) Polygenic overlap between kidney function and large artery atherosclerotic stroke. Stroke, 45 (12). pp. 3508-3513. ISSN 0039-2499

Markus, Hugh S. and Bevan, Steve (2014) Mechanisms and treatment of ischaemic stroke: insights from genetic associations. Nature Reviews Neurology, 10 (12). pp. 723-730. ISSN 1759-4758

Kilarski, L. L. and Achterberg, S. and Devan, W. J. and Traylor, M. and Malik, R. and Lindgren, A. and Pare, G. and Sharma, P. and Slowik, A. and Thijs, V. and Walters, M. and Worrall, B. B. and Sale, M. M. and Algra, A. and Kappelle, L. J. and Wijmenga, C. and Norrving, B. and Sandling, J. K. and Ronnblom, L. and Goris, A. and Franke, A. and Sudlow, C. and Rothwell, P. M. and Levi, C. and Holliday, E. G. and Fornage, M. and Psaty, B. and Gretarsdottir, S. and Thorsteinsdottir, U. and Seshadri, S. and Mitchell, B. D. and Kittner, S. and Clarke, R. and Hopewell, J. C. and Bis, J. C. and Boncoraglio, G. B. and Meschia, J. and Ikram, M. A. and Hansen, B. M. and Montaner, J. and Thorleifsson, G. and Stefanson, K. and Rosand, J. and de Bakker, P. I. W. and Farrall, M. and Dichgans, M. and Markus, H. S. and Bevan, S. (2014) Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12. Neurology, 83 (8). pp. 678-685. ISSN 0028-3878

Frayling, Timothy M. and Traylor, Matthew and Mäkelä, Kari-Matti and Kilarski, Laura L. and Holliday, Elizabeth G. and Devan, William J. and Nalls, Mike A. and Wiggins, Kerri L. and Zhao, Wei and Cheng, Yu-Ching and Achterberg, Sefanja and Malik, Rainer and Sudlow, Cathie and Bevan, Steve and Raitoharju, Emma and Oksala, Niku and Thijs, Vincent and Lemmens, Robin and Lindgren, Arne and Slowik, Agnieszka and Maguire, Jane M. and Walters, Matthew and Algra, Ale and Sharma, Pankaj and Attia, John R. and Boncoraglio, Giorgio B. and Rothwell, Peter M. and de Bakker, Paul I. W. and Bis, Joshua C. and Saleheen, Danish and Kittner, Steven J. and Mitchell, Braxton D. and Rosand, Jonathan and Meschia, James F. and Levi, Christopher and Dichgans, Martin and Lehtimäki, Terho and Lewis, Cathryn M. and Markus, Hugh S. (2014) A novel MMP12 locus Is associated with large artery atherosclerotic stroke Using a genome-wide age-at-onset informed approach. PLoS Genetics, 10 (7). e1004469. ISSN 1553-7390

Opherk, C. and Gonik, M. and Duering, M. and Malik, R. and Jouvent, E. and Herve, D. and Adib-Samii, P. and Bevan, S. and Pianese, L. and Silvestri, S. and Dotti, M. T. and De Stefano, N. and Liem, M. and Boon, E. M. J. and Pescini, F. and Pachai, C. and Bracoud, L. and Muller-Myhsok, B. and Meitinger, T. and Rost, N. and Pantoni, L. and Lesnik Oberstein, S. and Federico, A. and Ragno, M. and Markus, H. S. and Tournier-Lasserve, E. and Rosand, J. and Chabriat, H. and Dichgans, M. (2014) Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL. Stroke, 45 (4). pp. 968-972. ISSN 0039-2499

This list was generated on Sat Sep 23 01:05:09 2017 BST.