نتائج البحث - Farid Radmanesh
- يعرض 1 - 15 نتائج من 15
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Mutations in LAMB1 Cause Cobblestone Brain Malformation without Muscular or Ocular Abnormalities حسب Farid Radmanesh, Ahmet Okay Çağlayan, Jennifer L. Silhavy, Cahide Yılmaz, Vincent Cantagrel, Tarek Omar, Başak Rosti, Hande Kaymakçalan, Stacey Gabriel, Mingfeng Li, Nenad Šestan, Kaya Bilgüvar, William B. Dobyns, Maha S. Zaki, Murat Günel, Joseph G. Gleeson
منشور في 2013Artigo -
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Association of Traumatic Brain Injury With the Risk of Developing Chronic Cardiovascular, Endocrine, Neurological, and Psychiatric Disorders حسب Saef Izzy, Patrick Chen, Zabreen Tahir, Rachel Grashow, Farid Radmanesh, David J. Coté, Taha Yahya, Amar Dhand, Herman A. Taylor, Shirley L. Shih, Omar Albastaki, Craig Rovito, Samuel B. Snider, Michael J. Whalen, David M. Nathan, Karen K. Miller, Frank E. Speizer, Aaron L. Baggish, Marc G. Weisskopf, Ross Zafonte
منشور في 2022Artigo -
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GENOME-WIDE ASSOCIATION STUDY (GWAS) AND GENOME-WIDE BY ENVIRONMENT INTERACTION STUDY (GWEIS) OF DEPRESSIVE SYMPTOMS IN AFRICAN AMERICAN AND HISPANIC/LATINA WOMEN حسب Erin C. Dunn, Anna Wiste, Farid Radmanesh, Lynn M. Almli, Stephanie M. Gogarten, Tamar Sofer, Jessica D. Faul, Sharon L. R. Kardia, Jennifer A. Smith, David R. Weir, Wei Zhao, Thomas W. Soare, Saira Saeed Mirza, Karin Hek, Henning Tiemeier, Joseph S. Goveas, Gloria E. Sarto, Beverly M. Snively, Marilyn C. Cornelis, Karestan C. Koenen, Peter Kraft, Shaun Purcell, Kerry J. Ressler, Jonathan Rosand, Sylvia Wassertheil‐Smoller, Jordan W. Smoller
منشور في 2016Artigo -
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Common variation in <i>COL4A1/COL4A2</i> is associated with sporadic cerebral small vessel disease حسب Kristiina Rannikmäe, Gail Davies, Pippa A. Thomson, Steve Bevan, William J. Devan, Guido J. Falcone, Matthew Traylor, Christopher D. Anderson, Thomas W.K. Battey, Farid Radmanesh, Ranjan Deka, Jessica G. Woo, Lisa J. Martin, Jordi Jiménez-Conde, Magdy Selim, Devin L. Brown, Scott Silliman, Chelsea S. Kidwell, Joan Montaner, Carl D. Langefeld, Agnieszka Słowik, Björn M. Hansen, Cecilia M. Lindgren, James F. Meschia, Myriam Fornage, Joshua C. Bis, Stéphanie Debette, M. Arfan Ikram, W. T. Longstreth, Reinhold Schmidt, Cathy R. Zhang, Qiong Yang, Pankaj Sharma, Steven J. Kittner, Braxton D. Mitchell, Elizabeth Holliday, Christopher Levi, John Attia, Peter M. Rothwell, Deborah Poole, Giorgio B. Boncoraglio, Bruce M. Psaty, Rainer Malik, Natalia S. Rost, Bradford B. Worrall, Martin Dichgans, Tom Van Agtmael, Daniel Woo, Hugh S. Markus, Sudha Seshadri, Jonathan Rosand, Cathie Sudlow
منشور في 2015Revisão -
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Genetic variants in <i>CETP</i> increase risk of intracerebral hemorrhage حسب Christopher D. Anderson, Guido J. Falcone, Chia‐Ling Phuah, Farid Radmanesh, H. Bart Brouwers, Thomas W.K. Battey, Alessandro Biffi, Gina M. Peloso, Dajiang J. Liu, Alison Ayres, Joshua N. Goldstein, Anand Viswanathan, Steven M. Greenberg, Magdy Selim, James F. Meschia, Devin L. Brown, Bradford B. Worrall, Scott Silliman, David Tirschwell, Matthew L. Flaherty, Peter Kraft, Jeremiasz Jagiełła, Helena Schmidt, Björn M. Hansen, Jordi Jiménez-Conde, Eva Giralt‐Steinhauer, Roberto Elosúa, Elisa Cuadrado‐Godia, Carolina Soriano‐Tárraga, Koen M. van Nieuwenhuizen, Catharina J.M. Klijn, Kristiina Rannikmäe, Neshika Samarasekera, Rustam Al‐Shahi Salman, Cathie Sudlow, Ian J. Deary, Andrea Morotti, Alessandro Pezzini, Joanna Pera, Andrzej Urbanik, Alexander Pichler, Christian Enzinger, Bo Norrving, Joan Montaner, Israel Fernández‐Cadenas, Pilar Delgado, Jaume Roquer, Arne Lindgren, Agnieszka Słowik, Reinhold Schmidt, Chelsea S. Kidwell, Steven J. Kittner, Salina P. Waddy, Carl D. Langefeld, Gonçalo R. Abecasis, Cristen J. Willer, Sekar Kathiresan, Daniel Woo, Jonathan Rosand
منشور في 2016Artigo -
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Meta-analysis of Genome-wide Association Studies Identifies 1q22 as a Susceptibility Locus for Intracerebral Hemorrhage حسب Daniel Woo, Guido J. Falcone, William J. Devan, W. Mark Brown, Alessandro Biffi, Timothy D. Howard, Christopher D. Anderson, H. Bart Brouwers, Valerie Valant, Thomas W.K. Battey, Farid Radmanesh, Miriam R. Raffeld, Sylvia Baedorf-Kassis, Ranjan Deka, Jessica G. Woo, Lisa J. Martin, Mary Haverbusch, Charles J. Moomaw, Guangyun Sun, Joseph P. Broderick, Matthew L. Flaherty, Sharyl Martini, Dawn Kleindorfer, Brett Kissela, Mary E. Comeau, Jeremiasz Jagiełła, Helena Schmidt, Paul Freudenberger, Alexander Pichler, Christian Enzinger, Björn M. Hansen, Bo Norrving, Jordi Jiménez‐Conde, Eva Giralt‐Steinhauer, Roberto Elosúa, Elisa Cuadrado‐Godia, Carolina Soriano‐Tárraga, Jaume Roquer, Peter Kraft, Alison Ayres, Kristin Schwab, Jacob L. McCauley, Joanna Pera, Andrzej Urbanik, Natalia S. Rost, Joshua N. Goldstein, Anand Viswanathan, Eva-Maria Stögerer, David Tirschwell, Magdy Selim, Devin L. Brown, Scott Silliman, Bradford B. Worrall, James F. Meschia, Chelsea S. Kidwell, Joan Montaner, Israel Fernández‐Cadenas, Pilar Delgado, Rainer Malik, Martin Dichgans, Steven M. Greenberg, Peter M. Rothwell, Arne Lindgren, Agnieszka Słowik, Reinhold Schmidt, Carl D. Langefeld, Jonathan Rosand
منشور في 2014Revisão -
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Genetic variation at 16q24.2 is associated with small vessel stroke حسب Matthew Traylor, Rainer Malik, Mike A. Nalls, Ioana Cotlarciuc, Farid Radmanesh, Guðmar Þorleifsson, Ken B. Hanscombe, Carl D. Langefeld, Danish Saleheen, Natalia S. Rost, İdil Yet, Tim D. Spector, Jordana T. Bell, Eilís Hannon, Jonathan Mill, Ganesh Chauhan, Stéphanie Debette, Joshua C. Bis, W.T. Longstreth, M. Arfan Ikram, Lenore J. Launer, Sudha Seshadri, Monica Anne Hamilton‐Bruce, Jordi Jiménez-Conde, John W. Cole, Reinhold Schmidt, Agnieszka Słowik, Robin Lemmens, Cecilia M. Lindgren, Olle Melander, Raji P. Grewal, Ralph L. Sacco, Tatjana Rundek, Kathryn M. Rexrode, Donna K. Arnett, Julie A. Johnson, Oscar Benavente, Sylvia Wasssertheil‐Smoller, Jin‐Moo Lee, Sara L. Pulit, Quenna Wong, Stephen S. Rich, Paul I. W. de Bakker, Patrick F. McArdle, Daniel Woo, Christopher D. Anderson, Huichun Xu, Laura Heitsch, Myriam Fornage, Christina Jern, Hreinn Stefánsson, Unnur Þorsteinsdóttir, Sólveig Grétarsdóttir, Cathryn M. Lewis, Pankaj Sharma, Cathie Sudlow, Peter M. Rothwell, Giorgio B. Boncoraglio, Vincent Thijs, Christopher Levi, James F. Meschia, Jonathan Rosand, Steven J. Kittner, Braxton D. Mitchell, Martin Dichgans, Bradford B. Worrall, Hugh S. Markus
منشور في 2016Artigo -
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A genome-wide association study of outcome from traumatic brain injury حسب Mart Kals, Kevin Kunzmann, Livia Parodi, Farid Radmanesh, Lindsay Wilson, Saef Izzy, Christopher D. Anderson, Ava M. Puccio, David O. Okonkwo, Nancy Temkin, Ewout W. Steyerberg, Murray B. Stein, Geoffrey A. Manley, Andrew I.R. Maas, Sylvia Richardson, Ramon Diaz‐Arrastia, Aarno Palotie, Samuli Ripatti, Jonathan Rosand, David Menon, Cecilia Åkerlund, Krisztina Amrein, Nada Andelic, Lasse Andreassen, Audny Anke, Anna Degli Antoni, Gérard Audibert, Philippe Azouvi, Maria Luisa Azzolini, Ronald Bartels, Pál Barzó, Romuald Beauvais, Ronny Beer, Bo‐Michael Bellander, Antonio Belli, Habib Benali, Maurizio Berardino, Luigi Beretta, Morten Blaabjerg, Peter Bragge, Alexandra Bražinová, Vibeke Brinck, Joanne Brooker, Caroline Brorsson, Andras Buki, Monika Bullinger, Manuel Cabeleira, Alessio Caccioppola, Emiliana Calappi, Maria Rosa Calvi, Peter Cameron, Guillermo Carbayo Lozano, Marco Carbonara, Simona Cavallo, Giorgio Chevallard, Arturo Chieregato, Giuseppe Citerio, Hans Clusmann, Mark Coburn, Jonathan Coles, D. James Cooper, Marta Correia, Amra Čović, Nicola Curry, Endre Czeiter, Marek Czosnyka, Claire Dahyot‐Fizelier, Paul Dark, Helen Dawes, Véronique De Keyser, Vincent Degos, Françesco Della Corte, Hugo den Boogert, Bart Depreitere, Đula Đilvesi, Abhishek Dixit, Emma Donoghue, Jens P. Dreier, Guy‐Loup Dulière, Ari Ercole, Patrick Esser, Erzsébet Ezer, Martin Fabricius, Valery L. Feigin, Kelly Foks, Shirin Frisvold, Alex Furmanov, Pablo Gagliardo, Damien Galanaud, Dashiell Gantner, Guoyi Gao, Pradeep George, Alexandre Ghuysen, Lelde Giga, Ben Glocker, Jagoš Golubović, Pedro A. Gómez, Johannes Gratz, Benjamin Gravesteijn, Francesca Grossi
منشور في 2022Revisão -
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Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke حسب Matthew Traylor, Cathy R. Zhang, Poneh Adib‐Samii, William J. Devan, Owen Parsons, Silvia Lanfranconi, Sarah Gregory, Lisa Cloonan, Guido J. Falcone, Farid Radmanesh, Kaitlin Fitzpatrick, Allison Kanakis, Thomas R. Barrick, Barry Moynihan, Cathryn M. Lewis, Giorgio B. Boncoraglio, Robin Lemmens, Vincent Thijs, Cathie Sudlow, Joanna M. Wardlaw, Peter M. Rothwell, James F. Meschia, Bradford B. Worrall, Christopher Levi, Steve Bevan, Karen L. Furie, Martin Dichgans, Jonathan Rosand, Hugh S. Markus, Natalia S. Rost, Sylvia Smoller, John D. Sorkin, Xingwu Wang, Magdy Selim, Aleksandra Pikula, Philip A. Wolf, Stéphanie Debette, Sudha Seshadri, Paul I. W. de Bakker, Daniel I. Chasman, Kathryn M. Rexrode, Ida Chen, Jerome Rotter, May M. Luke, Michelle Sale, Tsong-Hai Lee, Ku‐Chou Chang, Mitchell S Elkind, Larry Goldstein, Michael L. James, Monique M.B. Breteler, Chris O’Donnell, Didier Leys, Cara L. Carty, Chelsea S. Kidwell, Jes Olesen, Pankaj Sharma, Stephen S. Rich, Turgot Tatlisumak, Olli Häppölä, Philippe Bijlenga, Carolina Soriano‐Tárraga, E. Giralt, Jaume Roquer, Jordi Jiménez‐Conde, Ioana Cotlarcius, John Hardy, Michał Korostyński, Giorgio B. Boncoraglio, Elena Ballabio, Eugenio Parati, Adamski Mateusz, Andrzej Urbanik, Tomasz Dziedzic, Jeremiasz Jagiełła, Jerzy Gąsowski, Marcin Wnuk, Rafał Olszanecki, Joanna Pera, Agnieszka Słowik, Karol Juchniewicz, Christopher Levi, Paul Nyquist, Íscia Lopes‐Cendes, Norberto L. Cabral, Paulo Henrique Condeixa de França, Anderson Gonçalves, Lina Keller, Milita Crisby, Konstantinos Kostulas, Robin Lemmens, Kourosh R. Ahmadi, Christian Opherk, Marco Duering, Martin Dichgans, Rainer Malik, Mariya Gonik, Julie Staals, Olle Melander, Philippe Burri
منشور في 2015Revisão -
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<i>COL4A2</i> is associated with lacunar ischemic stroke and deep ICH حسب Kristiina Rannikmäe, Vhinoth Sivakumaran, Henry Millar, Rainer Malik, Christopher D. Anderson, Michael Chong, Tushar Dave, Guido J. Falcone, Israel Fernández‐Cadenas, Jordi Jiménez-Conde, Cecilia M. Lindgren, Joan Montaner, Martin O’Donnell, Guillaume Paré, Farid Radmanesh, Natalia S. Rost, Agnieszka Słowik, Martin Söderholm, Matthew Traylor, Sara L. Pulit, Sudha Seshadri, Brad Worrall, Daniel Woo, Hugh S. Markus, Braxton D. Mitchell, Martin Dichgans, Jonathan Rosand, Cathie Sudlow, Patrick F. McArdle, Quenna Wong, Katrina Gwinn, Sefanja Achterberg, Ale Algra, Philippe Amouyel, Donna K. Arnett, Ethem Murat Arsava, John Attia, Hakan Ay, Traci M. Bartz, Thomas W.K. Battey, Oscar Benavente, Steve Bevan, Alessandro Biffi, Joshua C. Bis, Susan H. Blanton, Philip St. John, Giorgio B. Boncoraglio, Robert D. Brown, A I Burgess, Caty Carrera, Sherita N. Chapman Smith, Daniel I. Chasman, Ganesh Chauhan, France Wei-Min Chen, Yu‐Ching Cheng, Lisa Cloonan, John W. Cole, Ioana Cotlarciuc, Carlos Cruchaga, Elisa Cuadrado‐Godia, Jesse Dawson, Stéphanie Debette, Hossein Delavaran, Cameron Dell, Kimberly F. Doheny, Chuanhui Dong, David Duggan, Gunnar Engström, Michele K. Evans, Xavier Estivill Pallejà, Jessica D. Faul, Myriam Fornage, Philippe M. Frossard, Karen L. Furie, Dale M. Gamble, Christian Gieger, Anne‐Katrin Giese, Eva Giralt‐Steinhauer, Hector M. González, An Goris, Sólveig Grétarsdóttir, Raji P. Grewal, Ulrike Grittner, Stefan Gustafsson, Buhm Han, Graeme J. Hankey, Laura Heitsch, Peter Higgins, Marc C. Hochberg, Elizabeth Holliday, Jemma C. Hopewell, Richard B. Horenstein, George Howard, M. Arfan Ikram, Andreea Ilinca, Erik Ingelsson, Marguerite R. Irvin, Rebecca D. Jackson, Christina Jern, Julie A. Johnson
منشور في 2017Revisão -
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Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies حسب Ganesh Chauhan, Corey Arnold, Audrey Y. Chu, Myriam Fornage, Azadeh Reyahi, Joshua C. Bis, Aki S. Havulinna, Muralidharan Sargurupremraj, Albert V. Smith, Hieab H.H. Adams, Seung Hoan Choi, Sara L. Pulit, Stella Trompet, Melissa E. Garcia, Ani Manichaikul, Alexander Teumer, Stefan Gustafsson, Traci M. Bartz, Céline Bellenguez, Jean‐Sébastien Vidal, Xueqiu Jian, Ólafur Kjartansson, Kerri L. Wiggins, Claudia L. Satizábal, Flora Xue, Samuli Ripatti, Yongmei Liu, Joris Deelen, Marcel den Hoed, Steve Bevan, Jemma C. Hopewell, Rainer Malik, Susan R. Heckbert, Kenneth Rice, Nicholas L. Smith, Christopher Levi, Pankaj Sharma, Cathie Sudlow, Ali Moussavi Nik, John W. Cole, Reinhold Schmidt, James F. Meschia, Vincent Thijs, Cecilia M. Lindgren, Olle Melander, Raji P. Grewal, Ralph L. Sacco, Tatjana Rundek, Peter M. Rothwell, Donna K. Arnett, Christina Jern, Julie A. Johnson, Oscar Benavente, Sylvia Wassertheil‐Smoller, Jin‐Moo Lee, Quenna Wong, Hugo J. Aparicio, Stefan T. Engelter, Manja Kloß, Didier Leys, Alessandro Pezzini, Julie E. Buring, Paul M. Ridker, Claudine Berr, Jean‐François Dartigues, Anders Hamsten, Patrik K. E. Magnusson, Matthew Traylor, Nancy L. Pedersen, Lars Lannfelt, Lars Lindgren, Cecilia M. Lindgren, Andrew P. Morris, Jordi Jiménez-Conde, Joan Montaner, Farid Radmanesh, Agnieszka Słowik, Daniel Woo, Albert Hofman, Peter J. Koudstaal, Marileen L.P. Portegies, André G. Uitterlinden, Anton J. M. de Craen, Ian Ford, J. Wouter Jukema, David J. Stott, Norrina B. Allen, Michèle M. Sale, Andrew D. Johnson, David A. Bennett, Philip L. De Jager, Charles C. White, Hans J. Grabe, Marcello Ricardo Paulista Markus, Ulf Schminke, Giorgio B. Boncoraglio, Robert Clarke, Yoichiro Kamatani, Jean Dallongeville, Oscar L. López
منشور في 2016Revisão -
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Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation حسب Ingrid E. Christophersen, Michiel Rienstra, Carolina Roselli, Xiaoyan Yin, Bastiaan Geelhoed, John Barnard, Honghuang Lin, Dan E. Arking, Albert V. Smith, Christine M. Albert, Mark Chaffin, Nathan R. Tucker, Molong Li, Derek Klarin, Nathan A. Bihlmeyer, Siew‐Kee Low, Peter Weeke, Martina Müller‐Nurasyid, J. G. Smith, Jennifer A. Brody, Maartje N. Niemeijer, Marcus Dörr, Stella Trompet, Jennifer E. Huffman, Stefan Gustafsson, Claudia Schurmann, Marcus E. Kleber, Leo‐Pekka Lyytikäinen, Ilkka Seppälä, Rainer Malik, Andréa R. V. R. Horimoto, Marco Pérez, Juha Sinisalo, Stefanie Aeschbacher, Sébastien Thériault, Jie Yao, Farid Radmanesh, Stefan Weiß, Alexander Teumer, Seung Hoan Choi, Lu‐Chen Weng, Sebastian Clauß, Rajat Deo, Daniel J. Rader, Svati H. Shah, Albert Y. Sun, Jemma C. Hopewell, Stéphanie Debette, Ganesh Chauhan, Qiong Yang, Bradford B. Worrall, Guillaume Paré, Yoichiro Kamatani, Yanick Hagemeijer, Niek Verweij, Joylene E. Siland, Michiaki Kubo, Jonathan D. Smith, David R. Van Wagoner, Joshua C. Bis, Siegfried Perz, Bruce M. Psaty, Paul M. Ridker, Jared W. Magnani, Tamara B. Harris, Lenore J. Launer, M. Benjamin Shoemaker, Sandosh Padmanabhan, Jeffrey Haessler, Traci M. Bartz, Mélanie Waldenberger, Peter Lichtner, Marina Arendt, José Eduardo Krieger, Mika Kähönen, Lorenz Risch, Alfredo José Mansur, Annette Peters, Blair H. Smith, Lars Lind, Stuart A. Scott, Yingchang Lu, Erwin B. Bottinger, Jussi Hernesniemi, Cecilia M. Lindgren, Jorge Wong, Jie Huang, Markku Eskola, Andrew P. Morris, Ian Ford, Alex P. Reiner, Graciela Delgado, Lin Y. Chen, Yii-Der Ida Chen, Roopinder K. Sandhu, Man Li, Eric Boerwinkle, Lewin Eisele, Lars Lannfelt, Natalia S. Rost
منشور في 2017Revisão -
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Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6 حسب Bram P. Prins, Timothy J. Mead, Jennifer A. Brody, Garðar Sveinbjörnsson, Ιωάννα Ντάλλα, Nathan A. Bihlmeyer, Marten van den Berg, Jette Bork‐Jensen, Stefania Cappellani, Stefan van Duijvenboden, Nikolai Klena, George C. Gabriel, Xiaoqin Liu, Çağrı Güleç, Niels Grarup, Jeffrey Haessler, Leanne M. Hall, Alfonso Iorio, Aaron Isaacs, Ruifang Li‐Gao, Honghuang Lin, Yongmei Liu, Leo‐Pekka Lyytikäinen, Jonathan Marten, Hao Mei, Martina Müller‐Nurasyid, Michele Orini, Sandosh Padmanabhan, Farid Radmanesh, Julia Ramírez, Antonietta Robino, Molly Schwartz, Jessica van Setten, Albert V. Smith, Niek Verweij, Helen R. Warren, Stefan Weiß, Álvaro Alonso, Davíð O. Arnar, Michiel L. Bots, Rudolf A. de Boer, Anna F. Dominiczak, Mark Eijgelsheim, Patrick T. Ellinor, Xiuqing Guo, Stephan B. Felix, Tamara B. Harris, Caroline Hayward, Susan R. Heckbert, Paul L. Huang, J. Wouter Jukema, Mika Kähönen, Jan A. Kors, Pier D. Lambiase, Lenore J. Launer, Man Li, Allan Linneberg, Christopher P. Nelson, Oluf Pedersen, Marco Pérez, Annette Peters, Ozren Polašek, Bruce M. Psaty, Olli T. Raitakari, Kenneth Rice, Jerome I. Rotter, Moritz F. Sinner, Elsayed Z. Soliman, Tim D. Spector, Konstantin Strauch, Unnur Þorsteinsdóttir, Andrew Tinker, Stella Trompet, André G. Uitterlinden, Ilonca Vaartjes, Peter van der Meer, Uwe Völker, Henry Völzke, Mélanie Waldenberger, James Wilson, Zhijun Xie, Folkert W. Asselbergs, Marcus Dörr, Cornelia M. van Duijn, Paolo Gasparini, Daníel F. Guðbjartsson, Vilmundur Guðnason, Torben Hansen, Stefan Kääb, Jørgen K. Kanters, Charles Kooperberg, Terho Lehtimäki, Henry J. Lin, Steven A. Lubitz, Dennis O. Mook‐Kanamori, Francesco J. Conti, Christopher Newton‐Cheh, Jonathan Rosand, Igor Rudan, Nilesh J. Samani
منشور في 2018Artigo -
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Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes حسب Sara L. Pulit, Lu‐Chen Weng, Patrick F. McArdle, Ludovic Trinquart, Seung Hoan Choi, Braxton D. Mitchell, Jonathan Rosand, P. Bakker, Emelia J. Benjamin, Patrick T. Ellinor, Steven J. Kittner, Steven A. Lubitz, Christopher D. Anderson, Ingrid E. Christophersen, Michiel Rienstra, Carolina Roselli, Xiaoyan Yin, Bastiaan Geelhoed, John Barnard, Honghuang Lin, Dan E. Arking, Albert V. Smith, Christine M. Albert, Mark Chaffin, Nathan R. Tucker, Molong Li, Derek Klarin, Nathan A. Bihlmeyer, Siew‐Kee Low, Peter Weeke, Martina Müller‐Nurasyid, J. G. Smith, Jennifer A. Brody, Maartje N. Niemeijer, Marcus Dörr, Stella Trompet, Jennifer E. Huffman, Stefan Gustafsson, Claudia Schurmann, Marcus E. Kleber, Leo‐Pekka Lyytikäinen, Ilkka Seppälä, Rainer Malik, A.R.V.R. Horimoto, Marco Pérez, Juha Sinisalo, Stefanie Aeschbacher, Sébastien Thériault, Jie Yao, Farid Radmanesh, Stefan Weiß, Alexander Teumer, Seung Hoan Choi, Lu‐Chen Weng, Sebastian Clauß, Rajat Deo, Daniel J. Rader, Svati Shah, Joylene E. Siland, Michiaki Kubo, Jonathan D. Smith, David R. Van Wagoner, Joshua C. Bis, Siegfried Perz, Bruce M. Psaty, Paul M. Ridker, Jared W. Magnani, Tamara B. Harris, Lenore J. Launer, M. Benjamin Shoemaker, Sandosh Padmanabhan, Jeffrey Haessler, Traci M. Bartz, Mélanie Waldenberger, Peter Lichtner, Marina Arendt, José Eduardo Krieger, Mika Kähönen, Lorenz Risch, Alfredo José Mansur, Annette Peters, Blair H. Smith, Lars Lind, Stuart A. Scott, Yingchang Lu, Erwin B. Bottinger, Jussi Hernesniemi, Cecilia M. Lindgren, Jorge Wong, Jie Huang, Markku Eskola, Andrew P. Morris, Ian Ford, Alex P. Reiner, Graciela Delgado, Lin Y. Chen, Yii‐Der Ida Chen, Roopinder K. Sandhu, Man Li, Eric Boerwinkle
منشور في 2017Pré-impressão
أدوات البحث:
موضوعات ذات صلة
Medicine
Internal medicine
Biology
Gene
Genetics
Genotype
Single-nucleotide polymorphism
Genetic association
Genome-wide association study
Engineering
Environmental health
Mechanical engineering
Odds ratio
Population
Stroke (engine)
Bioinformatics
Intracerebral hemorrhage
Subarachnoid hemorrhage
Cohort
Heritability
Ischemia
Ischemic stroke
Lacunar stroke
Locus (genetics)
Psychiatry
Traumatic brain injury
Atrial fibrillation
Cardiology
Confidence interval
Disease