المؤلفون: Malik, Rainer, Chauhan, Ganesh, Traylor, Matthew, Sargurupremraj, Muralidharan, Okada, Yukinori, Mishra, Aniket, Rutten-Jacobs, Loes, Giese, Anne-Katrin, van der Laan, Sander W, Gretarsdottir, Solveig, Anderson, Christopher D, Chong, Michael, Adams, Hieab HH, Ago, Tetsuro, Almgren, Peter, Amouyel, Philippe, Ay, Hakan, Bartz, Traci M, Benavente, Oscar R, Bevan, Steve, Boncoraglio, Giorgio B, Brown, Robert D, Butterworth, Adam S, Carrera, Caty, Carty, Cara L, Chasman, Daniel I, Chen, Wei-Min, Cole, John W, Correa, Adolfo, Cotlarciuc, Ioana, Cruchaga, Carlos, Danesh, John, de Bakker, Paul IW, DeStefano, Anita L, den Hoed, Marcel, Duan, Qing, Engelter, Stefan T, Falcone, Guido J, Gottesman, Rebecca F, Grewal, Raji P, Gudnason, Vilmundur, Gustafsson, Stefan, Haessler, Jeffrey, Harris, Tamara B, Hassan, Ahamad, Havulinna, Aki S, Heckbert, Susan R, Holliday, Elizabeth G, Howard, George, Hsu, Fang-Chi, Hyacinth, Hyacinth I, Ikram, M Arfan, Ingelsson, Erik, Irvin, Marguerite R, Jian, Xueqiu, Jiménez-Conde, Jordi, Johnson, Julie A, Jukema, J Wouter, Kanai, Masahiro, Keene, Keith L, Kissela, Brett M, Kleindorfer, Dawn O, Kooperberg, Charles, Kubo, Michiaki, Lange, Leslie A, Langefeld, Carl D, Langenberg, Claudia, Launer, Lenore J, Lee, Jin-Moo, Lemmens, Robin, Leys, Didier, Lewis, Cathryn M, Lin, Wei-Yu, Lindgren, Arne G, Lorentzen, Erik, Magnusson, Patrik K, Maguire, Jane, Manichaikul, Ani, McArdle, Patrick F, Meschia, James F, Mitchell, Braxton D, Mosley, Thomas H, Nalls, Michael A, Ninomiya, Toshiharu, O’Donnell, Martin J, Psaty, Bruce M, Pulit, Sara L, Rannikmäe, Kristiina, Reiner, Alexander P, Rexrode, Kathryn M, Rice, Kenneth, Rich, Stephen S, Ridker, Paul M, Rost, Natalia S, Rothwell, Peter M, Rotter, Jerome I, Rundek, Tatjana, Sacco, Ralph L, Sakaue, Saori, Sale, Michele M

المصدر: Nature Genetics. 50(4)

مصطلحات موضوعية: Biological Sciences, Genetics, Human Genome, Stroke, Clinical Research, Brain Disorders, Aetiology, 2.1 Biological and endogenous factors, Cardiovascular, Computational Biology, Databases, Genetic, Epigenesis, Genetic, Female, Gene Regulatory Networks, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, INDEL Mutation, Linkage Disequilibrium, Male, Models, Genetic, Polymorphism, Single Nucleotide, Risk Factors, AFGen Consortium, Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, International Genomics of Blood Pressure (iGEN-BP) Consortium, INVENT Consortium, STARNET, BioBank Japan Cooperative Hospital Group, COMPASS Consortium, EPIC-CVD Consortium, EPIC-InterAct Consortium, International Stroke Genetics Consortium, METASTROKE Consortium, Neurology Working Group of the CHARGE Consortium, NINDS Stroke Genetics Network, UK Young Lacunar DNA Study, MEGASTROKE Consortium, Medical and Health Sciences, Developmental Biology, Agricultural biotechnology, Bioinformatics and computational biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/30v249w4Test

المؤلفون: Larsson, Susanna C, Traylor, Matthew, Burgess, Stephen, Boncoraglio, Giorgio B, Jern, Christina, Michaëlsson, Karl, Markus, Hugh S, MEGASTROKE project of the International Stroke Genetics Consortium

مصطلحات موضوعية: Brain Ischemia, Calcium, Humans, Intracranial Embolism, Magnesium, Mendelian Randomization Analysis, Polymorphism, Single Nucleotide, Stroke

وصف الملف: Print-Electronic; application/pdf

العلاقة: https://www.repository.cam.ac.uk/handle/1810/290715Test

الإتاحة: https://doi.org/10.17863/CAM.37915Test
https://www.repository.cam.ac.uk/handle/1810/290715Test

المؤلفون: Cheng, Yu Ching, Stanne, Tara M., Giese, Anne Katrin, Ho, Weang Kee, Traylor, Matthew, Amouyel, Philippe, Holliday, Elizabeth G., Malik, Rainer, Xu, Huichun, Kittner, Steven J., Cole, John W., O'Connell, Jeffrey R., Danesh, John, Rasheed, Asif, Zhao, Wei, Engelter, Stefan, Grond Ginsbach, Caspar, Kamatani, Yoichiro, Lathrop, Mark, Leys, Didier, Thijs, Vincent, Metso, Tiina M., Tatlisumak, Turgut, Parati, Eugenio A., Norrving, Bo, Bevan, Steve, Rothwell, Peter M., Sudlow, Cathie, Slowik, Agnieszka, Lindgren, Arne, Walters, Matthew R., Jannes, Jim, Shen, Jess, Crosslin, David, Doheny, Kimberly, Laurie, Cathy C., Kanse, Sandip M., Bis, Joshua C., Fornage, Myriam, Mosley, Thomas H., Hopewell, Jemma C., Strauch, Konstantin, Müller Nurasyid, Martina, Gieger, Christian, Waldenberger, Melanie, Peters, Annette, Meisinger, Christine, Ikram, M. Arfan, Longstreth, W. T., Meschia, James F., Seshadri, Sudha, Sharma, Pankaj, Worrall, Bradford, Jern, Christina, Levi, Christopher, Dichgans, Martin, Boncoraglio, Giorgio B., Markus, Hugh S., Debette, Stephanie, Rolfs, Arndt, Saleheen, Danish, Mitchell, Braxton D., PEZZINI, Alessandro

المساهمون: Cheng, Yu Ching, Stanne, Tara M., Giese, Anne Katrin, Ho, Weang Kee, Traylor, Matthew, Amouyel, Philippe, Holliday, Elizabeth G., Malik, Rainer, Xu, Huichun, Kittner, Steven J., Cole, John W., O'Connell, Jeffrey R., Danesh, John, Rasheed, Asif, Zhao, Wei, Engelter, Stefan, Grond Ginsbach, Caspar, Kamatani, Yoichiro, Lathrop, Mark, Leys, Didier, Thijs, Vincent, Metso, Tiina M., Tatlisumak, Turgut, Pezzini, Alessandro, Parati, Eugenio A., Norrving, Bo, Bevan, Steve, Rothwell, Peter M., Sudlow, Cathie, Slowik, Agnieszka, Lindgren, Arne, Walters, Matthew R., Jannes, Jim, Shen, Je, Crosslin, David, Doheny, Kimberly, Laurie, Cathy C., Kanse, Sandip M., Bis, Joshua C., Fornage, Myriam, Mosley, Thomas H., Hopewell, Jemma C., Strauch, Konstantin, Müller Nurasyid, Martina, Gieger, Christian, Waldenberger, Melanie, Peters, Annette, Meisinger, Christine, Ikram, M. Arfan, Longstreth, W. T., Meschia, James F., Seshadri, Sudha, Sharma, Pankaj, Worrall, Bradford, Jern, Christina, Levi, Christopher, Dichgans, Martin, Boncoraglio, Giorgio B., Markus, Hugh S., Debette, Stephanie, Rolfs, Arndt, Saleheen, Danish, Mitchell, Braxton D.

مصطلحات موضوعية: Factor VII, Genetic, Genome-wide analysi, Ischemic stroke, Stroke, Adult, African Continental Ancestry Group, Age of Onset, Aged, Asian Continental Ancestry Group, Brain Ischemia, Chromosomes, Human, Pair 10, Computer Simulation, DNA, Intergenic, European Continental Ancestry Group, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Male, Middle Aged, Odds Ratio, Polymorphism, Single Nucleotide, Serine Endopeptidase, Neurology (clinical), Cardiology and Cardiovascular Medicine, Advanced and Specialized Nursing

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/26732560; info:eu-repo/semantics/altIdentifier/wos/WOS:000377040200014; volume:47; issue:2; firstpage:307; lastpage:316; numberofpages:10; journal:STROKE; http://hdl.handle.net/11379/485221Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84969389433; http://stroke.ahajournals.orgTest/

الإتاحة: https://doi.org/10.1161/STROKEAHA.115.011328Test
http://hdl.handle.net/11379/485221Test
http://stroke.ahajournals.orgTest/

المؤلفون: Traylor, Matthew, Zhang, Cathy R, Adib-Samii, Poneh, Devan, William J, Parsons, Owen E, Lanfranconi, Silvia, Gregory, Sarah, Cloonan, Lisa, Falcone, Guido J, Radmanesh, Farid, Fitzpatrick, Kaitlin, Kanakis, Allison, Barrick, Thomas R, Moynihan, Barry, Lewis, Cathryn M, Boncoraglio, Giorgio B, Lemmens, Robin, Thijs, Vincent, Sudlow, Cathie, Wardlaw, Joanna, Rothwell, Peter M, Meschia, James F, Worrall, Bradford B, Levi, Christopher, Bevan, Steve, Furie, Karen L, Dichgans, Martin, Rosand, Jonathan, Markus, Hugh S, Rost, Natalia, International Stroke Genetics Consortium

مصطلحات موضوعية: Cerebral Small Vessel Diseases, Genetic Predisposition to Disease, Genetic Testing, Genome-Wide Association Study, Humans, Polymorphism, Single Nucleotide, Risk Factors, Stroke, White Matter

وصف الملف: application/pdf

العلاقة: https://www.repository.cam.ac.uk/handle/1810/252831Test

الإتاحة: https://www.repository.cam.ac.uk/handle/1810/252831Test

المؤلفون: Dichgans, Martin, Malik, Rainer, König, Inke R, Rosand, Jonathan, Clarke, Robert, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Mitchell, Braxton D, Assimes, Themistocles L, Levi, Christopher, O'Donnell, Christopher J, Fornage, Myriam, Thorsteinsdottir, Unnur, Psaty, Bruce M, Hengstenberg, Christian, Seshadri, Sudha, Erdmann, Jeanette, Bis, Joshua C, Peters, Annette, Boncoraglio, Giorgio B, März, Winfried, Meschia, James F, Kathiresan, Sekar, Ikram, M Arfan, McPherson, Ruth, Stefansson, Kari, Sudlow, Cathie, Reilly, Muredach P, Thompson, John R, Sharma, Pankaj, Hopewell, Jemma C, Chambers, John C, Watkins, Hugh, Rothwell, Peter M, Roberts, Robert, Markus, Hugh S, Samani, Nilesh J, Farrall, Martin, Schunkert, Heribert

المساهمون: Stroke and Dementia Research, Klinikum der Universität München, Ludwig-Maximilians-Universität, Munich, Germany (M.D., R. Malik), Munich Cluster for Systems Neurology (SyNergy), Munich, Germany (M.D.), Institut für Medizinische Biometrie und Statistik (I.R.K.), and Institut für integrative und experimentelle Genomik (J.E.), Universität zu Lübeck, Lübeck, Germany, Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Germany (I.R.K.), Department of Neurology and Center for Human Genetic Research (J.R.), and Cardiology Division (C.J.O.D.), Massachusetts General Hospital, Boston, Harvard Medical School, Boston, MA (J.R.), Program in Medical and Population Genetics (J.R.), and Program in Medical and Population Genetics (S.K.), Broad Institute of Harvard and MIT, Cambridge, MA, Clinical Trial Service Unit and Epidemiological Studies Unit (R.C., J.C.H.), Wellcome Trust Centre for Human Genetics (H.W., M. Farrall), Department of Cardiovascular Medicine (M. Farrall), and Stroke Prevention Research Unit, Nuffield Department of Clinical Neuroscience (P.M.R.), John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom, deCODE Genetics, Reykjavik, Iceland (S.G., G.T., U.T., K.S.), Department of Medicine, University of Maryland School of Medicine, Baltimore (B.D.M.), Department of Medicine, Stanford University School of Medicine, Stanford, CA (T.L.A.), Center for Translational Neuroscience and Mental Health Research, University of Newcastle, New South Wales, Australia (C.L.), Hunter Medical Research Institute, New South Wales, Australia (C.L.), National Heart, Lung and Blood Institute and NHLBI's Framingham Heart Study, MA (C.J.O.D., S.S.), University of Texas Health Science Center at Houston (M. Fornage), Cardiovascular Health Research Unit, Department of Epidemiology (B.M.P.), Department of Medicine (B.M.P.), Department of Health Services (B.M.P.), and Cardiovascular Health Research Unit, Department of Medicine (J.C.B.), University

مصطلحات موضوعية: Kransæðasjúkdómar, Heilablóðfall, Arfgengi, Áhættuþættir, Brain Ischemia, Coronary Artery Disease, Data Interpretation, Statistical, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Phenotype, Polymorphism, Single Nucleotide, Reproducibility of Results, Risk Factors, Stroke

العلاقة: info:eu-repo/grantAgreement/EC/FP7/279143; http://dx.doi.orgTest/ 10.1161/STROKEAHA.113.002707; http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4112102Test/; Stroke 2014, 45 (1):24-36; http://hdl.handle.net/2336/550810Test; Stroke; a journal of cerebral circulation

الإتاحة: https://doi.org/10.1161/STROKEAHA.113.002707Test
http://hdl.handle.net/2336/550810Test

المؤلفون: Traylor, Matthew, Mäkelä, Kari-Matti, Kilarski, Laura L, Holliday, Elizabeth G, Devan, William J, Nalls, Mike A, Wiggins, Kerri L, Zhao, Wei, Cheng, Yu-Ching, Achterberg, Sefanja, Malik, Rainer, Sudlow, Cathie, Bevan, Steve, Raitoharju, Emma, METASTROKE, International Stroke Genetics Consortium, Wellcome Trust Case Consortium 2 (WTCCC2), Oksala, Niku, Thijs, Vincent, Lemmens, Robin, Lindgren, Arne, Slowik, Agnieszka, Maguire, Jane M, Walters, Matthew, Algra, Ale, Sharma, Pankaj, Attia, John R, Boncoraglio, Giorgio B, Rothwell, Peter M, de Bakker, Paul IW, Bis, Joshua C, Saleheen, Danish, Kittner, Steven J, Mitchell, Braxton D, Rosand, Jonathan, Meschia, James F, Levi, Christopher, Dichgans, Martin, Lehtimäki, Terho, Lewis, Cathryn M, Markus, Hugh S

مصطلحات موضوعية: Adult, Age of Onset, Aged, Arteries, Coronary Artery Disease, Female, Genome-Wide Association Study, Glycosaminoglycans, Humans, Male, Matrix Metalloproteinase 12, Middle Aged, Myocardial Infarction, Polymorphism, Single Nucleotide

وصف الملف: Electronic-eCollection; application/pdf

العلاقة: https://www.repository.cam.ac.uk/handle/1810/284875Test

الإتاحة: https://doi.org/10.17863/CAM.32248Test
https://www.repository.cam.ac.uk/handle/1810/284875Test

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

المصدر: Neurology EpiHealth: Epidemiology for Health. 86(13):26-1217

مصطلحات موضوعية: Brain Ischemia, Case-Control Studies, Cooperative Behavior, Genetic Variation, Genome-Wide Association Study, Humans, Polymorphism, Single Nucleotide, Stroke, Journal Article, Meta-Analysis, Research Support, N.I.H., Extramural, Intramural, Non-U.S. Gov't, U.S. Gov't, Non-P.H.S., P.H.S., Medicin och hälsovetenskap, Klinisk medicin, Neurologi, Medical and Health Sciences, Clinical Medicine, Neurology

الوصول الحر: https://lup.lub.lu.se/record/95b30b07-4ef0-412b-a3b1-535d16124e54Test
http://dx.doi.org/10.1212/WNL.0000000000002528Test

المؤلفون: Debette, Stéphanie, Kamatani, Yoichiro, Metso, Tiina M, Kloss, Manja, Chauhan, Ganesh, Engelter, Stefan T, PEZZINI, Alessandro, Thijs, Vincent, Markus, Hugh S, Dichgans, Martin, Wolf, Christiane, Dittrich, Ralf, Touzé, Emmanuel, Southerland, Andrew M, Samson, Yves, Abboud, Shérine, Béjot, Yannick, Caso, Valeria, Bersano, Anna, Gschwendtner, Andreas, Sessa, Maria, Cole, John, Lamy, Chantal, Medeiros, Elisabeth, Beretta, Simone, Bonati, Leo H, Grau, Armin J, Michel, Patrik, Majersik, Jennifer J, Sharma, Pankaj, Kalashnikova, Ludmila, Nazarova, Maria, Dobrynina, Larisa, Bartels, Eva, Guillon, Benoit, van den Herik, Evita G, Fernandez Cadenas, Israel, Jood, Katarina, Nalls, Michael A, De Leeuw, Frank Erik, Jern, Christina, Cheng, Yu Ching, Werner, Inge, Metso, Antti J, Lichy, Christoph, Lyrer, Philippe A, Brandt, Tobias, Boncoraglio, Giorgio B, Wichmann, Heinz Erich, Gieger, Christian, Johnson, Andrew D, Böttcher, Thomas, CASTELLANO, Maurizio, Arveiler, Dominique, Ikram, M. Arfan, Breteler, Monique M. B, PADOVANI, Alessandro, Meschia, James F, Kuhlenbäumer, Gregor, Rolfs, Arndt, Worrall, Bradford B, Ringelstein, Erich Bernd, Zelenika, Diana, Tatlisumak, Turgut, Lathrop, Mark, Leys, Didier, Amouyel, Philippe, Dallongeville, Jean

المساهمون: Debette, Stéphanie, Kamatani, Yoichiro, Metso, Tiina M, Kloss, Manja, Chauhan, Ganesh, Engelter, Stefan T, Pezzini, Alessandro, Thijs, Vincent, Markus, Hugh S, Dichgans, Martin, Wolf, Christiane, Dittrich, Ralf, Touzé, Emmanuel, Southerland, Andrew M, Samson, Yve, Abboud, Shérine, Béjot, Yannick, Caso, Valeria, Bersano, Anna, Gschwendtner, Andrea, Sessa, Maria, Cole, John, Lamy, Chantal, Medeiros, Elisabeth, Beretta, Simone, Bonati, Leo H, Grau, Armin J, Michel, Patrik, Majersik, Jennifer J, Sharma, Pankaj, Kalashnikova, Ludmila, Nazarova, Maria, Dobrynina, Larisa, Bartels, Eva, Guillon, Benoit, van den Herik, Evita G, Fernandez Cadenas, Israel, Jood, Katarina, Nalls, Michael A, De Leeuw, Frank Erik, Jern, Christina, Cheng, Yu Ching, Werner, Inge, Metso, Antti J, Lichy, Christoph, Lyrer, Philippe A, Brandt, Tobia, Boncoraglio, Giorgio B, Wichmann, Heinz Erich, Gieger, Christian, Johnson, Andrew D, Böttcher, Thoma, Castellano, Maurizio, Arveiler, Dominique, Ikram, M. Arfan, Breteler, Monique M. B, Padovani, Alessandro, Meschia, James F, Kuhlenbäumer, Gregor, Rolfs, Arndt, Worrall, Bradford B, Ringelstein, Erich Bernd, Zelenika, Diana, Tatlisumak, Turgut, Lathrop, Mark, Leys, Didier, Amouyel, Philippe, Dallongeville, Jean

مصطلحات موضوعية: Adult, Brain Ischemia, Carotid Artery, Internal, Dissection, Female, Finland, Follow-Up Studie, Genetic Pleiotropy, Genetic Predisposition to Disease, Genome-Wide Association Study, Human, Hypercholesterolemia, Hypertension, Male, Microfilament Protein, Middle Aged, Migraine Disorder, Myocardial Infarction, Obesity, Odds Ratio, Risk Factor, Vertebral Artery Dissection, Allele, Polymorphism, Single Nucleotide

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000346990400015; volume:47; issue:1; firstpage:78; lastpage:83; numberofpages:6; journal:NATURE GENETICS; https://hdl.handle.net/11381/2964611Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84928478209

الإتاحة: https://doi.org/10.1038/ng.3154Test
https://hdl.handle.net/11381/2964611Test

المؤلفون: Keenan, Tanya, Zhao, Wei, Rasheed, Asif, Ho, Weang K., Malik, Rainer, Felix, Janine F., Young, Robin, Shah, Nabi, Samuel, Maria, Sheikh, Nasir, Mucksavage, Megan L, Shah, Omar, Morley, Michael, Laser, Annika, Mallick, Nadeem Hayat, Zaman, Khan Shah, Ishaq, Mohammad, Rasheed, Syed Zahed, Memon, Fazal-Ur-Rehman, Ahmed, Faisal, Hanif, Bashir, Lakhani, Muhammad Shakir, Fahim, Muhammad, Ishaq, Madiha, Shardha, Naresh Kumar, Ahmed, Naveeduddin, Mahmood, Khalid, Iqbal, Waseem, Akhtar, Saba, Raheel, Rabia, O'Donnell, Christopher J., Hengstenberg, Christian, März, Winifred, Kathiresan, Sekar, Samani, Nilesh, Goel, Anuj, Hopewell, Jemma C., Chambers, John, Cheng, Yu-Ching, Sharma, Pankaj, Yang, Qiong, Rosand, Jonathan, Boncoraglio, Giorgio B., Kazmi, Shahana Urooj, Hakonarson, Hakon, Köttgen, Anna, Kalogeropoulos, Andreas, Frossard, Philippe, Kamal, Ayeesha, Dichgans, Martin, Cappola, Thomas P., Reilly, Muredach P., Danesh, John, Rader, Daniel J., Voight, Benjamin F., Saleheen, Danish

المصدر: Keenan , T , Zhao , W , Rasheed , A , Ho , W K , Malik , R , Felix , J F , Young , R , Shah , N , Samuel , M , Sheikh , N , Mucksavage , M L , Shah , O , Morley , M , Laser , A , Mallick , N H , Zaman , K S , Ishaq , M , Rasheed , S Z , Memon , F-U-R , Ahmed , F , Hanif , B , Lakhani , M S , Fahim , M , ....

مصطلحات موضوعية: Coronary Disease/blood, Diabetes Mellitus, Type 2/blood, Global Health, Humans, Mendelian Randomization Analysis/methods, Morbidity/trends, Odds Ratio, Polymorphism, Single Nucleotide, Prognosis, Risk Assessment/methods, Risk Factors, Stroke/blood, Uric Acid/blood

العلاقة: https://discovery.dundee.ac.uk/en/publications/2c742774-18d2-4bbe-88b2-02de406c2b92Test

الإتاحة: https://doi.org/10.1016/j.jacc.2015.10.086Test
https://discovery.dundee.ac.uk/en/publications/2c742774-18d2-4bbe-88b2-02de406c2b92Test

المؤلفون: Eugenio Parati, David R. Crosslin, Thomas H. Mosley, Kimberly F. Doheny, Yu-Ching Cheng, Didier Leys, Turgut Tatlisumak, Christina Jern, Peter M. Rothwell, Sudha Seshadri, Cathie Sudlow, Bradford B. Worrall, W. T. Longstreth, Stéphanie Debette, Anne-Katrin Giese, Weang Kee Ho, Jess Shen, Braxton D. Mitchell, Arne Lindgren, Tiina M. Metso, Mark Lathrop, Danish Saleheen, Yoichiro Kamatani, John W. Cole, Vincent Thijs, Elizabeth G. Holliday, Jemma C. Hopewell, Konstantin Strauch, Cathy C. Laurie, Caspar Grond-Ginsbach, M. Arfan Ikram, Pankaj Sharma, Arndt Rolfs, Alessandro Pezzini, John Danesh, Martin Dichgans, Christopher R Levi, Stefan T. Engelter, Christine Meisinger, Steven J. Kittner, Philippe Amouyel, Jim Jannes, Wei Zhao, Jeffrey R. O'Connell, Matthew Walters, Annette Peters, Agnieszka Slowik, Martina Müller-Nurasyid, Christian Gieger, Rainer Malik, Bo Norrving, Hugh S. Markus, Joshua C. Bis, Sandip M. Kanse, Tara M. Stanne, Myriam Fornage, Huichun Xu, James F. Meschia, Melanie Waldenberger, Matthew Traylor, Steve Bevan, Giorgio B. Boncoraglio, Asif Rasheed

المساهمون: Epidemiology, Neurology

المصدر: Stroke, 47(2), 307-316. Lippincott Williams & Wilkins

مصطلحات موضوعية: Male, Factor VII, Genetics, Genome-wide analysis, Ischemic stroke, Stroke, Adult, African Continental Ancestry Group, Age of Onset, Aged, Asian Continental Ancestry Group, Brain Ischemia, Chromosomes, Human, Pair 10, Computer Simulation, DNA, Intergenic, European Continental Ancestry Group, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Middle Aged, Odds Ratio, Polymorphism, Single Nucleotide, Serine Endopeptidases, Neurology (clinical), Cardiology and Cardiovascular Medicine, Advanced and Specialized Nursing, Genome-wide association study, 030204 cardiovascular system & hematology, 0302 clinical medicine, Medicine, Pair 10, Single Nucleotide, Human, Black People, Single-nucleotide polymorphism, Locus (genetics), Chromosomes, White People, Article, 03 medical and health sciences, Asian People, Genetic predisposition, Polymorphism, Genetic association, Intergenic, business.industry, DNA, Odds ratio, C400 Genetics, Age of onset, business, TCF7L2, 030217 neurology & neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbfe3dcb953fd2a0ca9d68fabf488398Test