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: Chauhan, Ganesh, Adams, Hieab H H, Satizabal, Claudia L, Bis, Joshua C, Teumer, Alexander, Sargurupremraj, Muralidharan, Hofer, Edith, Trompet, Stella, Hilal, Saima, Smith, Albert Vernon, Jian, Xueqiu, Malik, Rainer, Traylor, Matthew, Pulit, Sara L, Amouyel, Philippe, Mazoyer, Bernard, Zhu, Yi-Cheng, Kaffashian, Sara, Schilling, Sabrina, Beecham, Gary W, Montine, Thomas J, Schellenberg, Gerard D, Kjartansson, Olafur, Guðnason, Vilmundur, Knopman, David S, Griswold, Michael E, Windham, B Gwen, Gottesman, Rebecca F, Mosley, Thomas H, Schmidt, Reinhold, Saba, Yasaman, Schmidt, Helena, Takeuchi, Fumihiko, Yamaguchi, Shuhei, Nabika, Toru, Kato, Norihiro, Rajan, Kumar B, Aggarwal, Neelum T, De Jager, Philip L, Evans, Denis A, Psaty, Bruce M, Rotter, Jerome I, Rice, Kenneth, Lopez, Oscar L, Liao, Jiemin, Chen, Christopher, Cheng, Ching-Yu, Wong, Tien Y, Ikram, Mohammad K, van der Lee, Sven J, Amin, Najaf, Chouraki, Vincent, DeStefano, Anita L, Aparicio, Hugo J, Romero, Jose R, Maillard, Pauline, DeCarli, Charles, Wardlaw, Joanna M, Hernández, Maria Del C Valdés, Luciano, Michelle, Liewald, David, Deary, Ian J, Starr, John M, Bastin, Mark E, Muñoz Maniega, Susana, Slagboom, P Eline, Beekman, Marian, Deelen, Joris, Uh, Hae-Won, Lemmens, Robin, Brodaty, Henry, Wright, Margaret J, Ames, David, Boncoraglio, Giorgio B, Hopewell, Jemma C, Beecham, Ashley H, Blanton, Susan H, Wright, Clinton B, Sacco, Ralph L, Wen, Wei, Thalamuthu, Anbupalam, Armstrong, Nicola J, Chong, Elizabeth, Schofield, Peter R, Kwok, John B, van der Grond, Jeroen, Stott, David J, Ford, Ian, Jukema, J Wouter, Vernooij, Meike W, Hofman, Albert, Uitterlinden, André G, van der Lugt, Aad, Wittfeld, Katharina, Grabe, Hans J, Hosten, Norbert, von Sarnowski, Bettina, Völker, Uwe, Levi, Christopher, Jimenez-Conde, Jordi, Sharma, Pankaj, Sudlow, Cathie L M, Rosand, Jonathan, Woo, Daniel, Cole, John W, Meschia, James F, Slowik, Agnieszka, Thijs, Vincent, Lindgren, Arne, Melander, Olle, Grewal, Raji P, Rundek, Tatjana, Rexrode, Kathy, Rothwell, Peter M, Arnett, Donna K, Jern, Christina, Johnson, Julie A, Benavente, Oscar R, Wasssertheil-Smoller, Sylvia, Lee, Jin-Moo, Wong, Quenna, Mitchell, Braxton D, Rich, Stephen S, McArdle, Patrick F, Geerlings, Mirjam I, van der Graaf, Yolanda, de Bakker, Paul I W, Asselbergs, Folkert W, Srikanth, Velandai, Thomson, Russell, McWhirter, Rebekah, Moran, Chris, Callisaya, Michele, Phan, Thanh, Rutten-Jacobs, Loes C A, Bevan, Steve, Tzourio, Christophe, Mather, Karen A, Sachdev, Perminder S, van Duijn, Cornelia M, Worrall, Bradford B, Dichgans, Martin, Kittner, Steven J, Markus, Hugh S, Ikram, Mohammad A, Fornage, Myriam, Launer, Lenore J, Seshadri, Sudha, Longstreth, W T, Debette, Stéphanie

المساهمون: 1 Bordeaux Populat Hlth Res Ctr, Bordeaux, France Show more 2 CEA, CNRS, INSERM, U1219,Grp Imagerie Neurofonct,U5293, Bordeaux, France Show more 3 Univ Bordeaux, Bordeaux, France Show more 4 Bordeaux Univ Hosp, Dept Neurol, Bordeaux, France Show more 5 Erasmus MC, Dept Epidemiol, Rotterdam, Netherlands Show more 6 Erasmus MC, Dept Radiol & Nucl Med, Rotterdam, Netherlands Show more 7 Erasmus MC, Dept Internal Med, Rotterdam, Netherlands Show more 8 Erasmus MC, Dept Neurol, Rotterdam, Netherlands Show more 9 Boston Univ, Sch Med, Dept Neurol, Boston, MA 02215 USA Show more 10 Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02215 USA Show more 11 NHLBI, Framingham Heart Study, Bldg 10, Bethesda, MD 20892 USA Show more 12 Univ Washington, Cardiovasc Hlth Res Unit, Dept Med, Seattle, WA 98195 USA Show more 13 Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA Show more 14 Univ Washington, Dept Hlth Serv, Seattle, WA 98195 USA Show more 15 Univ Washington, Dept Biostat, Seattle, WA 98195 USA Show more 16 Univ Washington, Dept Neurol, Seattle, WA 98195 USA Show more 17 Univ Washington, Dept Pathol, Seattle, WA 98195 USA Show more 18 Stanford Univ, Pathol, Stanford, CA 94305 USA Show more 19 Univ Med Greifswald, Inst Community Med, Greifswald, Germany Show more 20 Univ Med Greifswald, Dept Psychiat & Psychotherapy, Greifswald, Germany Show more 21 Univ Med Greifswald, Inst Diagnost Radiol & Neuroradiol, Greifswald, Germany Show more 22 Univ Med Greifswald, Dept Neurol, Greifswald, Germany Show more 23 Med Univ Graz, Clin Div Neurogeriatr, Dept Neurol, Graz, Austria Show more 24 Med Univ Graz, Inst Med Informat Stat & Documentat, Graz, Austria Show more 25 Med Univ Graz, Gottfried Schatz Res Ctr Cell Signaling Metab & A, Inst Mol Biol & Biochem, Graz, Austria Show more 26 Leiden Univ, Med Ctr, Dept Cardiol, Leiden, Netherlands Show more 27 Leiden Univ, Med Ctr, Sect Gerontol & Geriatr, Dept Internal Med, Leiden, Netherlands Show more 28 Leiden Univ, Med Ctr, Mol Epidemiol, Leiden, Netherlands Show more 29 Leiden Univ, Med Ctr, Med Stat & Bioinformat, Leiden, Netherlands Show more 30 Leiden Univ, Med Ctr, Dept Radiol, Leiden, Netherlands Show more 31 Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Pharmacol, Singapore, Singapore Show more 32 Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Ophthalmol, Singapore, Singapore Show more 33 Icelandic Heart Assoc, Kopavogur, Iceland Show more 34 Univ Texas Hlth Sci Ctr Houston, Inst Mol Med, Houston, TX 77030 USA Show more 35 Univ Texas Hlth Sci Ctr Houston, Ctr Human Genet, Houston, TX 77030 USA Show more 36 Ludwig Maximilians Univ Munchen, Klinikum Univ Munchen, Inst Stroke & Dementia Res, Munich, Germany Show more 37 Univ Cambridge, Clin Neurosci, Cambridge, England Show more 38 Univ Lincoln, Sch Life Sci, Lincoln, England Show more 39 German Ctr Neurodegenerat Dis DZNE, Populat Hlth Sci, Bonn, Germany Show more 40 Univ Med Ctr Utrecht, Dept Med Genet, Utrecht, Netherlands Show more 41 Univ Med Ctr Utrecht, Dept Neurol, Brain Ctr Rudolf Magnus, Utrecht, Netherlands Show more 42 Univ Med Ctr Utrecht, Dept Epidemiol, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands Show more 43 Univ Med Ctr Utrecht, Dept Genet, Ctr Mol Med, Utrecht, Netherlands Show more 44 Univ Med Ctr Utrecht, Dept Cardiol, Div Heart & Lungs, Utrecht, Netherlands Show more 45 Univ Utrecht, Utrecht, Netherlands Show more 46 Lille Univ, INSERM, Lille Univ Hosp, Inst Pasteur Lille, Lille, France Show more 47 Peking Union Med Coll Hosp, Dept Neurol, Beijing, Peoples R China Show more 48 Univ Miami, Miller Sch Med, John P Hussman Inst Human Genom, Coral Gables, FL 33124 USA Show more 49 Univ Miami, Miller Sch Med, Dept Neurol, Coral Gables, FL 33124 USA Show more 50 Univ Miami, Miller Sch Med, Evelyn F McKnight Brain Inst, Coral Gables, FL 33124 USA Show more 51 Univ Miami, Miller Sch Med, Dept Epidemiol & Publ Hlth Sci, Coral Gables, FL 33124 USA Show more 52 Univ Miami, Miller Sch Med, Dr John T Macdonald Fdn, Dept Human Genet, Coral Gables, FL 33124 USA Show more 53 Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA Show more 54 Landspitali Natl Univ Hosp, Dept Neurol, Reykjavik, Iceland Show more 55 Landspitali Natl Univ Hosp, Dept Radiol, Reykjavik, Iceland Show more 56 Univ Iceland, Fac Med, Reykjavik, Iceland Show more 57 Mayo Clin, Dept Neurol, Rochester, MN USA Show more 58 Univ Mississippi, Med Ctr, Dept Data Sci, Jackson, MS 39216 USA Show more 59 Univ Mississippi, Med Ctr, Dept Med, Jackson, MS 39216 USA Show more 60 Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA Show more 61 Natl Ctr Global Hlth & Med, Res Inst, Dept Gene Diagnost & Therapeut, Tokyo, Japan Show more 62 Shimane Univ, Sch Med, Dept Internal Med 3, Matsue, Shimane, Japan Show more 63 Shimane Univ, Sch Med, Dept Funct Pathol, Matsue, Shimane, Japan Show more 64 Rush Univ, Med Ctr, Chicago, IL 60612 USA Show more 65 Brigham & Womens Hosp, Boston, MA 02115 USA Show more 66 Columbia Univ, Med Ctr, Ctr Translat & Computat Neuroimmunol, Dept Neurol, New York, NY USA 67 Kaiser Permanente Washington Hlth Res Inst, Seattle, WA USA Show more 68 Harbor UCLA Med Ctr, Inst Translat Genom & Populat Sci, Los Angeles Biomed Res Inst, Torrance, CA 90509 USA Show more 69 Harbor UCLA Med Ctr, Div Genom Outcomes, Dept Pediat, Torrance, CA 90509 USA Show more 70 Univ Calif Los Angeles, Dept Pediat, Los Angeles, CA 90024 USA Show more 71 Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90024 USA Show more 72 Univ Calif Los Angeles, Dept Human Genet, Los Angeles, CA USA Show more 73 Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15260 USA Show more 74 Singapore Eye Res Inst, Singapore, Singapore Show more 75 Duke NUS Grad Med Sch, Singapore, Singapore Show more 76 Singapore Natl Eye Ctr, Singapore Eye Res Inst, Singapore, Singapore Show more 77 Natl Univ Hlth Syst, MACC, Singapore, Singapore Show more 78 Erasmus MC Univ Med Ctr, Genet Epidemiol Unit, Dept Epidemiol & Biostat, Rotterdam, Netherlands Show more 79 Univ Calif Davis, Dept Neurol, Davis, CA 95616 USA Show more 80 Univ Edinburgh, Brain Res Imaging Ctr, Edinburgh, Midlothian, Scotland Show more 81 Univ Edinburgh, Ctr Clin Brain Sci, Edinburgh, Midlothian, Scotland Show more 82 Univ Edinburgh, Edinburgh Dementia Res Ctr, Edinburgh, Midlothian, Scotland Show more 83 Univ Edinburgh, Ctr Cognit Ageing & Cognit Epidemiol, Edinburgh, Midlothian, Scotland Show more 84 Univ Edinburgh, Alzheimer Scotland Dementia Res Ctr, Edinburgh, Midlothian, Scotland Show more 85 Univ Edinburgh, Inst Genet & Mol Med, Edinburgh, Midlothian, Scotland Show more 86 Univ Leuven, KU Leuven, Dept Neurosci, Expt Neurol, Leuven, Belgium Show more 87 Univ Leuven, KU Leuven, Leuven Res Inst Neurosci & Dis LIND, Leuven, Belgium Show more 88 VIB, Ctr Brain & Dis Res, Lab Neurobiol, Leuven, Belgium Show more 89 Univ Hosp Leuven, Dept Neurol, Leuven, Belgium Show more 90 Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Melbourne, Vic, Australia Show more 91 Univ New South Wales, Ctr Hlth Brain Ageing, Psychiat, Sydney, NSW, Australia Show more 92 Univ New South Wales, Dementia Ctr Res Collaborat, Sydney, NSW, Australia Show more 93 Univ New South Wales, Sch Med Sci, Sydney, NSW, Australia Show more 94 Murdoch Univ, Math & Stat, Perth, WA, Australia Show more 95 Neurosci Res Australia, Randwick, NSW, Australia Show more 96 Univ Sydney, Brain & Mind Ctr, Camperdown, NSW, Australia Show more 97 Univ Queensland, Queensland Brain Inst, Brisbane, Qld, Australia Show more 98 Natl Ageing Res Inst, Melbourne, Vic, Australia Show more 99 Univ Melbourne, Acad Unit Psychiat Old Age, Melbourne, Vic, Australia Show more 100 Fdn IRCCS Ist Neurol Carlo Besta, Dept Cerebrovasc Dis, Milan, Italy Show more 101 Univ Oxford, CTSU, Nuffield Dept Populat Hlth, Oxford, England Show more 102 Univ Oxford, Nuffield Dept Clin Neurosci, Oxford, England Show more 103 NINDS, NIH, Bldg 36,Rm 4D04, Bethesda, MD 20892 USA Show more 104 Univ Glasgow, Inst Cardiovasc & Med Sci, Fac Med, Glasgow, Lanark, Scotland Show more 105 Univ Glasgow, Robertson Ctr Biostat, Glasgow, Lanark, Scotland Show more 106 German Ctr Neurodegenerat Dis DZNE, Site Rostock, Greifswald, Germany Show more 107 Ernst Moritz Arndt Univ Greifswald, Interfac Inst Genet & Funct Genom, Greifswald, Germany Show more 108 John Hunter Hosp, Hunter Med Res Inst, Callaghan, NSW, Australia Show more 109 Univ Newcastle, Callaghan, NSW, Australia Show more 110 Hosp del Mar, IMIM, Dept Neurol, Neurovasc Res Grp NEU VAS, Barcelona, Spain Show more 111 Royal Holloway Univ London, Inst Cardiovasc Res, London, England 112 St Peters & Ashford Hosp, Chertsey, Surrey, England Show more 113 Harvard Med Sch, Ctr Human Genet Res, Massachusetts Gen Hosp, Program Med & Populat Genet,Broad Inst, Boston, MA 02115 USA Show more 114 Harvard Med Sch, Dept Neurol, Massachusetts Gen Hosp, Program Med & Populat Genet,Broad Inst, Boston, MA 02115 USA Show more 115 Univ Cincinnati, Coll Med, Cincinnati, OH 45221 USA Show more 116 Univ Maryland, Sch Med, Dept Neurol, Baltimore, MD 21201 USA 117 Baltimore VAMC, Baltimore, MD USA Show more 118 Mayo Clin Jacksonville, Dept Neurol, 4500 San Pablo Rd, Jacksonville, FL 32224 USA Show more 119 Jagiellonian Univ, Dept Neurol, Krakow, Poland Show more 120 Lund Univ, Dept Clin Sci Lund, Neurol, Lund, Sweden Show more 121 Skane Univ Hosp, Dept Neurol & Rehabil Med, Malmo, Sweden Show more 122 Lund Univ, Dept Clin Sci Malmo, Lund, Sweden Show more 123 Seton Hall Univ, Neurosci Inst, Sch Hlth & Med Sci, St Francis Med Ctr, S Orange, NJ 07079 USA Show more 124 Univ Kentucky, Coll Publ Hlth, Lexington, KY USA Show more 125 Univ Gothenburg, Sahlgrenska Acad, Inst Biomed, Gothenburg, Sweden Show more 126 Univ Florida, Dept Pharmacotherapy & Translat Res, Gainesville, FL USA Show more 127 Univ Florida, Ctr Pharmacogen, Coll Pharm, Gainesville, FL USA Show more 128 Univ Florida, Coll Med, Div Cardiovasc Med, Gainesville, FL USA Show more 129 Univ British Columbia, Dept Neurol, Vancouver, BC, Canada Show more 130 Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, Bronx, NY 10467 USA Show more 131 Washington Univ, Sch Med, Dept Neurol, Stroke Ctr, St Louis, MO 63110 USA Show more 132 Univ Maryland, Sch Med, Dept Med, Baltimore, MD 21201 USA Show more 133 Univ Virginia, Sch Med, Ctr Publ Hlth Genom, Charlottesville, VA 22908 USA 134 Netherlands Heart Inst, Durrer Ctr Cardiovasc Res, Utrecht, Netherlands Show more 135 UCL, Fac Populat Hlth Sci, Inst Cardiovasc Sci, London, England Show more 136 UCL, Farr Inst Hlth Informat Res, London, England Show more 137 UCL, Inst Hlth Informat, London, England Show more 138 Monash Univ, Monash Hlth, Peninsula Clin Sch, Melbourne, Vic, Australia Show more 139 Monash Univ, Monash Hlth, Frankston Hosp, Cent Clin Sch, Melbourne, Vic, Australia Show more 140 Monash Univ, Monash Hlth, Sch Clin Sci, Melbourne, Vic, Australia Show more 141 Univ Tasmania, Menzies Inst Med Res, Hobart, Tas, Australia Show more 142 Western Sydney Univ, Penrith, NSW, Australia Show more 143 Univ Virginia, Dept Neurol, Charlottesville, VA USA Show more 144 Univ Virginia, Dept Publ Hlth Sci, Charlottesville, VA USA 145 Prince Wales Hosp, Neuropsychiat Inst, Randwick, NSW, Australia Show more 146 Munich Cluster Syst Neurol SyNergy, Munich, Germany Show more 147 NIA, Intramural Res Program, NIH, Bethesda, MD 20892 USA Show more 148 Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX 78229 USA 149 Glenn Biggs Inst Alzheimers & Neurodegenerat Dis, San Antonio, TX USA

المصدر: Neurology

مصطلحات موضوعية: Heilablóðfall, Gen, Lífshættir, Brain Infarction, Genetic Loci, Genome-Wide Association Study, Life Style

العلاقة: https://n.neurology.org/content/92/5/e486Test; Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting. 2019, 92(5): E486-E503 Neurology; http://hdl.handle.net/2336/620903Test; Neurology

الإتاحة: https://doi.org/10.1212/WNL.0000000000006851Test
http://hdl.handle.net/2336/620903Test

المؤلفون: Traylor, Matthew, Malik, Rainer, Nalls, Mike A, Cotlarciuc, Ioana, Radmanesh, Farid, Thorleifsson, Gudmar, Hanscombe, Ken B, Langefeld, Carl, Saleheen, Danish, Rost, Natalia S, Yet, Idil, Spector, Tim D, Bell, Jordana T, Hannon, Eilis, Mill, Jonathan, Chauhan, Ganesh, Debette, Stephanie, Bis, Joshua C, Longstreth, WT, Ikram, M Arfan, Launer, Lenore J, Seshadri, Sudha, METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium, Hamilton-Bruce, Monica Anne, Jimenez-Conde, Jordi, Cole, John W, Schmidt, Reinhold, Słowik, Agnieszka, Lemmens, Robin, Lindgren, Arne, Melander, Olle, Grewal, Raji P, Sacco, Ralph L, Rundek, Tatjana, Rexrode, Kathryn, Arnett, Donna K, Johnson, Julie A, Benavente, Oscar R, Wasssertheil-Smoller, Sylvia, Lee, Jin-Moo, Pulit, Sara L, Wong, Quenna, Rich, Stephen S, de Bakker, Paul IW, McArdle, Patrick F, Woo, Daniel, Anderson, Christopher D, Xu, Huichun, Heitsch, Laura, Fornage, Myriam, Jern, Christina, Stefansson, Kari, Thorsteinsdottir, Unnur, Gretarsdottir, Solveig, Lewis, Cathryn M, Sharma, Pankaj, Sudlow, Cathie LM, Rothwell, Peter M, Boncoraglio, Giorgio B, Thijs, Vincent, Levi, Chris, Meschia, James F, Rosand, Jonathan, Kittner, Steven J, Mitchell, Braxton D, Dichgans, Martin, Worrall, Bradford B, Markus, Hugh S, International Stroke Genetics Consortium

مصطلحات موضوعية: Adult, Aged, 80 and over, Cerebral Small Vessel Diseases, Chromosomes, Human, Pair 16, Female, Genetic Loci, Genetic Variation, Genome-Wide Association Study, Humans, Male, Middle Aged, Stroke, Lacunar, Zinc Fingers

وصف الملف: Print; application/pdf

العلاقة: https://www.repository.cam.ac.uk/handle/1810/262766Test

الإتاحة: https://doi.org/10.17863/CAM.8057Test
https://www.repository.cam.ac.uk/handle/1810/262766Test

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

المصدر: Sudlow, C 2016, ' Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies ', Lancet Neurology . https://doi.org/10.1016/S1474-4422Test(16)00102-2

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Adolescent, Population, Genome-wide association study, Biology, Bioinformatics, Article, Brain ischemia, Mice, Young Adult, 03 medical and health sciences, 0302 clinical medicine, SDG 3 - Good Health and Well-being, medicine, Animals, Humans, Child, education, Allele frequency, Stroke, Aged, Aged, 80 and over, education.field_of_study, Cerebral infarction, Forkhead Transcription Factors, Odds ratio, Middle Aged, 16. Peace & justice, medicine.disease, R1, 3. Good health, Minor allele frequency, 030104 developmental biology, Genetic Loci, Cerebral Small Vessel Diseases, Child, Preschool, Female, Neurology (clinical), 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c331412547cee1d7c32a26f93ef5bf6Test
https://pure.eur.nl/en/publications/952f5faf-294e-4331-bea7-fe7bd1766c83Test

المؤلفون: Matthew, Traylor, Rainer, Malik, Mike A, Nalls, Ioana, Cotlarciuc, Farid, Radmanesh, Gudmar, Thorleifsson, Ken B, Hanscombe, Carl, Langefeld, Danish, Saleheen, Natalia S, Rost, Idil, Yet, Tim D, Spector, Jordana T, Bell, Eilis, Hannon, Jonathan, Mill, Ganesh, Chauhan, Stephanie, Debette, Joshua C, Bis, W T, Longstreth, M Arfan, Ikram, Lenore J, Launer, Sudha, Seshadri, Monica Anne, Hamilton-Bruce, Jordi, Jimenez-Conde, John W, Cole, Reinhold, Schmidt, Agnieszka, Słowik, Robin, Lemmens, Arne, Lindgren, Olle, Melander, Raji P, Grewal, Ralph L, Sacco, Tatjana, Rundek, Kathryn, Rexrode, Donna K, Arnett, Julie A, Johnson, Oscar R, 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, Kari, Stefansson, Unnur, Thorsteinsdottir, Solveig, Gretarsdottir, Cathryn M, Lewis, Pankaj, Sharma, Cathie L M, Sudlow, Peter M, Rothwell, Giorgio B, Boncoraglio, Vincent, Thijs, Chris, Levi, James F, Meschia, Jonathan, Rosand, Steven J, Kittner, Braxton D, Mitchell, Martin, Dichgans, Bradford B, Worrall, Hugh S, Markus

المساهمون: Epidemiology, Radiology & Nuclear Medicine

المصدر: Annals of Neurology, 81(3), 383-394. John Wiley & Sons Inc.
Traylor, M, Malik, R, Nalls, M A, Cotlarciuc, I, Radmanesh, F, Thorleifsson, G, Hanscombe, K B, Langefeld, C, Saleheen, D, Rost, N S, Yet, I, Spector, T D, Bell, J T, Hannon, E, Mill, J, Chauhan, G, Debette, S, Bis, J C, Longstreth, W T, Ikram, M A, Launer, L J, Seshadri, S, Hamilton-Bruce, M A, Jimenez-Conde, J, Cole, J W, Schmidt, R, Słowik, A, Lemmens, R, Lindgren, A, Melander, O, Grewal, R P, Sacco, R L, Rundek, T, Rexrode, K, Arnett, D K, Johnson, J A, Benavente, O R, Wasssertheil-Smoller, S, Lee, J M, Pulit, S L, Wong, Q, Rich, S S, de Bakker, P I W, McArdle, P F, Woo, D, Anderson, C D, Xu, H, Heitsch, L, Fornage, M, Jern, C, Stefansson, K, Thorsteinsdottir, U, Gretarsdottir, S, Lewis, C M, Sharma, P, Sudlow, C L M, Rothwell, P M, Boncoraglio, G B, Thijs, V, Levi, C, Meschia, J F, Rosand, J, Kittner, S J, Mitchell, B D, Dichgans, M, Worrall, B B & Markus, H S 2017, ' Genetic variation at 16q24.2 is associated with small vessel stroke ', Annals of Neurology, vol. 81, no. 3, pp. 383-394 . https://doi.org/10.1002/ana.24840Test
Annals of Neurology

مصطلحات موضوعية: Adult, Aged, 80 and over, Male, Genetic Variation, Zinc Fingers, Middle Aged, Stroke, Genetic Loci, Cerebral Small Vessel Diseases, Stroke, Lacunar, Humans, Female, Chromosomes, Human, Pair 16, Research Articles, Aged, Genome-Wide Association Study, Research Article

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::c74f1e4bd983a2a7ae170e25ed5391a3Test
https://ruj.uj.edu.pl/xmlui/handle/item/93442Test

المؤلفون: Parolo, Silvia, Lisa, Antonella, Gentilini, Davide, Di Blasio, Anna Maria, Barlera, Simona, Nicolis, Enrico B., Boncoraglio, Giorgio B., Parati, Eugenio A., Bione, Silvia

المساهمون: Parolo, Silvia, Lisa, Antonella, Gentilini, Davide, Di Blasio, Anna Maria, Barlera, Simona, Nicolis, Enrico B., Boncoraglio, Giorgio B., Parati, Eugenio A., Bione, Silvia

مصطلحات موضوعية: Immunity, Latitude, LincRNA, Pathogen, Chromosomes, Human, Pair 13, Gene Ontology, Genetic Loci, Genome, Italy, Principal Component Analysi, Selection, Genetic, Biological Phenomena, Genetics, Population, Genetics (clinical)

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/26553317; info:eu-repo/semantics/altIdentifier/wos/WOS:000364364900001; volume:16; issue:1; firstpage:132; journal:BMC GENETICS; http://hdl.handle.net/11571/1210554Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84946565656; http://www.biomedcentral.com/bmcgenetTest/

الإتاحة: https://doi.org/10.1186/s12863-015-0293-xTest
http://hdl.handle.net/11571/1210554Test
http://www.biomedcentral.com/bmcgenetTest/

المؤلفون: Simona Barlera, Enrico Nicolis, Eugenio Parati, Silvia Bione, Antonella Lisa, Giorgio B. Boncoraglio, Davide Gentilini, Silvia Parolo, Anna Maria Di Blasio

المصدر: BMC Genetics

مصطلحات موضوعية: Population, Locus (genetics), Context (language use), Biology, 03 medical and health sciences, 0302 clinical medicine, Genetic variation, Genetics, Humans, Genetics(clinical), Genetic variability, Selection, Genetic, education, Allele frequency, LincRNA, Genetics (clinical), Biological Phenomena, 030304 developmental biology, Principal Component Analysis, 0303 health sciences, education.field_of_study, Latitude, Natural selection, Chromosomes, Human, Pair 13, Pathogen, Genome, Human, Immunity, Gene Ontology, Genetics, Population, Italy, Genetic Loci, Evolutionary biology, Genetic structure, 030217 neurology & neurosurgery, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c98e24e2ad9f3066f7d74f056028466fTest
https://doi.org/10.1186/s12863-015-0293-xTest

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

المساهمون: The University of Newcastle. Faculty of Health & Medicine, School of Medicine and Public Health

مصطلحات موضوعية: ischemic stroke, arteries, permutation, genome-wide association, meta-analysis, genetic loci, genetics of disease, atherosclerosis

العلاقة: PLoS Genetics Vol. 10, Issue 7; http://hdl.handle.net/1959.13/1061477Test; uon:16959

الإتاحة: http://hdl.handle.net/1959.13/1061477Test

المؤلفون: Jonathan Rosand, Matthew Traylor, Sudha Seshadri, Veikko Salomaa, Robert Clarke, Anita L. DeStefano, Rodney J. Scott, Steve Bevan, Braxton D. Mitchell, Alun Evans, Philippe Amouyel, Myriam Fornage, Hugh S. Markus, Olli Saarela, Peter Wagner, Dylan Hodgkiss, Angela M. Carter, Giorgio B. Boncoraglio, Catherine Sudlow, K. L. Furie, Will Longstreth, Nicole Soranzo, Peter M. Rothwell, Jean Ferrières, John Attia, Bruce M. Psaty, Martin Dichgans, Christopher Levi, M. Arfan Ikram, Jarmo Virtamo, Gudmar Thorleifsson, Frances M K Williams, Pankaj Sharma, Martin Farrall, Kari Kuulasmaa, Per-Gunnar Wiklund, Elizabeth G. Holliday, James F. Meschia, Anna Helgadottir, Unnur Thorsteinsdottir, Michael A. Nalls, Peter J. Grant, Marco M Ferrario, Dominique Arveiler, Tim D. Spector, Andreas Gschwendtner, Eugenio Parati, Mari A. Kaunisto, Gabriela L. Surdulescu, Joshua C. Bis, Solveig Gretarsdottir, Kaisa Silander, Kari Stefansson, Thomas H. Mosely, Albert Hofman, Pirro G. Hysi, Yu-Ching Cheng, Aarno Palotie

المساهمون: Radiology & Nuclear Medicine, Epidemiology

المصدر: Annals of Neurology; Vol 73
Annals of Neurology
Williams, F M K, Carter, A M, Hysi, P G, Surdulescu, G, Hodgkiss, D, Soranzo, N, Traylor, M, Bevan, S, Dichgans, M, Rothwell, P M W, Sudlow, C, Farrall, M, Silander, K, Kaunisto, M, Wagner, P, Saarela, O, Kuulasmaa, K, Virtamo, J, Salomaa, V, Amouyel, P, Arveiler, D, Ferrieres, J, Wiklund, P, Arfan Ikram, M, Hofman, A, Boncoraglio, G B, Parati, E A, Helgadottir, A, Gretarsdottir, S, Thorsteinsdottir, U, Thorleifsson, G, Stefansson, K, Seshadri, S, Destefano, A, Gschwendtner, A, Psaty, B, Longstreth, W, Mitchell, B D, Cheng, Y, Clarke, R, Ferrario, M, Bis, J C, Levi, C, Attia, J, Holliday, E G, Scott, R J, Fornage, M, Sharma, P, Furie, K L, Rosand, J, Nalls, M, Meschia, J, Mosely, T H, Evans, A, Palotie, A, Markus, H S, Grant, P J & Spector, T D 2013, ' Ischemic stroke is associated with the ABO locus: the EuroCLOT study. ', Annals of Neurology, vol. 73, no. 1, pp. 16-31 . https://doi.org/10.1002/ana.23838Test
Annals of Neurology, 73(1), 16-31. John Wiley & Sons Inc.

مصطلحات موضوعية: Male, Neurology, Genome-wide association study, 030204 cardiovascular system & hematology, Bioinformatics, Brain Ischemia, Brain ischemia, Coronary artery disease, Pathogenesis, Cohort Studies, 0302 clinical medicine, 80 and over, genetics, Genetics, Aged, 80 and over, biology, Atrial fibrillation, Single Nucleotide, Middle Aged, 3. Good health, Europe, Stroke, epidemiology, Female, Rapid Communication, Adult, medicine.medical_specialty, Adolescent, Polymorphism, Single Nucleotide, Fibrin, methods, ABO Blood-Group System, 03 medical and health sciences, Young Adult, ABO blood group system, medicine, Humans, Genetic Predisposition to Disease, Polymorphism, Blood Coagulation, Aged, epidemiology/genetics, diagnosis/epidemiology/genetics, genetics, Adolescent, Adult, Aged, Aged, 80 and over, Blood Coagulation, genetics, Brain Ischemia, diagnosis/epidemiology/genetics, Cohort Studies, Europe, epidemiology, Female, Genetic Loci, genetics, Genetic Predisposition to Disease, epidemiology/genetics, Genetic Variation, genetics, Genome-Wide Association Study, methods, Humans, Male, Middle Aged, Polymorphism, genetics, Stroke, diagnosis/epidemiology/genetics, Young Adult, Genetic Variation, medicine.disease, Genetic Loci, biology.protein, Neurology (clinical), 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6608414d9f9f00d9c383049e49fd4018Test
http://ora.ox.ac.uk/objects/uuid:273d54ad-f9b4-4bdc-bca6-7667a92c622dTest

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

المصدر: Lancet Neurology, 15(2), 174. Lancet Publishing Group

مصطلحات موضوعية: 0301 basic medicine, Adult, medicine.medical_specialty, Adolescent, Tetraspanins, Clinical Neurology, Locus (genetics), Single-nucleotide polymorphism, Genome-wide association study, Nerve Tissue Proteins, Bioinformatics, Brain Ischemia, Cohort Studies, 03 medical and health sciences, Young Adult, 0302 clinical medicine, medicine, Journal Article, Humans, Stroke, Genetic association, Aged, Aged, 80 and over, Neurology & Neurosurgery, business.industry, Case-control study, Odds ratio, Middle Aged, medicine.disease, 030104 developmental biology, Genetic Loci, Case-Control Studies, Medical genetics, Neurology (clinical), business, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf; image/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c29eee423fd89a047d0ae6bc637d79aTest
https://hdl.handle.net/1874/342770Test