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: Malik, Rainer, Chauhan, Ganesh, Anderson, Christopher D, Salomaa, Veikko, Sapkota, Bishwa R, Schmidt, Reinhold, Schmidt, Carsten O, Schminke, Ulf, Sharma, Pankaj, Slowik, Agnieszka, Sudlow, Cathie L M, Tanislav, Christian, Tatlisumak, Turgut, Chong, Michael, Taylor, Kent D, Thijs, Vincent N S, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Tiedt, Steffen, Trompet, Stella, Tzourio, Christophe, van Duijn, Cornelia M, Walters, Matthew, Wareham, Nicholas J, Adams, Hieab H H, Wassertheil-Smoller, Sylvia, Wilson, James G, Wiggins, Kerri L, Yang, Qiong, Yusuf, Salim, Consortium, AFGen, Epidemiology, Cohorts for Heart and Aging Research in Genomic, Pressure, International Genomics of Blood, Consortium, INVENT, STARNET, Ago, Tetsuro, Bis, Joshua C, Pastinen, Tomi, Ruusalepp, Arno, Schadt, Eric E, Koplev, Simon, Björkegren, Johan L M, Codoni, Veronica, Civelek, Mete, Smith, Nicholas L, Trégouët, David A, Almgren, Peter, Christophersen, Ingrid E, Roselli, Carolina, Lubitz, Steven A, Ellinor, Patrick T, Tai, E Shyong, Kooner, Jaspal S, Kato, Norihiro, He, Jiang, van der Harst, Pim, Elliott, Paul, Amouyel, Philippe, Chambers, John C, Takeuchi, Fumihiko, Johnson, Andrew D, Group, BioBank Japan Cooperative Hospital, Consortium, COMPASS, Consortium, EPIC-CVD, Consortium, EPIC-InterAct, Consortium, International Stroke Genetics, Consortium, METASTROKE, Consortium, Neurology Working Group of the CHARGE, Ay, Hakan, Network, NINDS Stroke Genetics, Study, UK Young Lacunar DNA, Consortium, MEGASTROKE, Sanghera, Dharambir K, Melander, Olle, Jern, Christina, Strbian, Daniel, Fernandez-Cadenas, Israel, Longstreth, W. T., Rolfs, Arndt, Bartz, Traci M, Hata, Jun, Woo, Daniel, Rosand, Jonathan, Pare, Guillaume, Hopewell, Jemma C, Saleheen, Danish, Stefansson, Kari, Worrall, Bradford B, Kittner, Steven J, Seshadri, Sudha, Benavente, Oscar R, Fornage, Myriam, Markus, Hugh S, Howson, Joanna M M, Kamatani, Yoichiro, Debette, Stephanie, Dichgans, Martin, Traylor, Matthew, Sargurupremraj, Muralidharan, Bevan, Steve, Okada, Yukinori, Mishra, Aniket, Rutten-Jacobs, Loes, Giese, Anne-Katrin, van der Laan, Sander W, Gretarsdottir, Solveig, 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 I W, DeStefano, Anita L, Hoed, Marcel den, 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, Amin, Najaf, Aparicio, Hugo S, Arnett, Donna K, Attia, John, Beiser, Alexa S, Berr, Claudine, Buring, Julie E, Bustamante, Mariana, Caso, Valeria, Cheng, Yu-Ching, Choi, Seung Hoan, Chowhan, Ayesha, Cullell, Natalia, Dartigues, Jean-François, Delavaran, Hossein, Delgado, Pilar, Dörr, Marcus, Engström, Gunnar, Ford, Ian, Gurpreet, Wander S, Hamsten, Anders, Heitsch, Laura, Hozawa, Atsushi, Ibanez, Laura, Ilinca, Andreea, Ingelsson, Martin, Iwasaki, Motoki, Jackson, Rebecca D, Jood, Katarina, den Hoed, Marcel, Jousilahti, Pekka, Kaffashian, Sara, Kalra, Lalit, Kamouchi, Masahiro, Kitazono, Takanari, Kjartansson, Olafur, Kloss, Manja, Koudstaal, Peter J, Krupinski, Jerzy, Labovitz, Daniel L, Laurie, Cathy C, Levi, Christopher R, Li, Linxin, Lind, Lars, Lindgren, Cecilia M, Lioutas, Vasileios, Liu, Yong Mei, Lopez, Oscar L, Makoto, Hirata, Martinez-Majander, Nicolas, Matsuda, Koichi, Minegishi, Naoko, Montaner, Joan, Morris, Andrew P, Muiño, Elena, Müller-Nurasyid, Martina, Norrving, Bo, Ogishima, Soichi, Parati, Eugenio A, Peddareddygari, Leema Reddy, Pedersen, Nancy L, Pera, Joanna, Perola, Markus, Pezzini, Alessandro, Pileggi, Silvana, Rabionet, Raquel, Riba-Llena, Iolanda, Ribasés, Marta, Romero, Jose R, Roquer, Jaume, Rudd, Anthony G, Sarin, Antti-Pekka, Sarju, Ralhan, Sarnowski, Chloe, Sasaki, Makoto, Satizabal, Claudia L, Satoh, Mamoru, Sattar, Naveed, Sawada, Norie, Sibolt, Gerli, Sigurdsson, Ásgeir, Smith, Albert, Sobue, Kenji, Soriano-Tárraga, Carolina, Stanne, Tara, Stine, O Colin, Stott, David J, Strauch, Konstantin, Takai, Takako, Tanaka, Hideo, Tanno, Kozo, Teumer, Alexander, Tomppo, Liisa, Torres-Aguila, Nuria P, Touze, Emmanuel, Tsugane, Shoichiro, Uitterlinden, Andre G, Valdimarsson, Einar M, van der Lee, Sven J, Völzke, Henry, Wakai, Kenji, Weir, David, Williams, Stephen R, Wolfe, Charles D A, Wong, Quenna, Xu, Huichun, Yamaji, Taiki

المساهمون: Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), Pathology, Epidemiology, Radiology & Nuclear Medicine, Cardiovascular Centre (CVC), Universitat de Barcelona, Traylor, Matthew [0000-0001-6624-8621], Okada, Yukinori [0000-0002-0311-8472], Rutten-Jacobs, Loes [0000-0003-3223-885X], van der Laan, Sander W [0000-0001-6888-1404], Adams, Hieab HH [0000-0003-3687-2508], Almgren, Peter [0000-0002-0473-0241], Amouyel, Philippe [0000-0001-9088-234X], Correa, Adolfo [0000-0002-9501-600X], Cruchaga, Carlos [0000-0002-0276-2899], den Hoed, Marcel [0000-0001-8081-428X], Gustafsson, Stefan [0000-0001-5894-0351], Havulinna, Aki S [0000-0002-4787-8959], Ikram, M Arfan [0000-0003-0372-8585], Jukema, J Wouter [0000-0002-3246-8359], Kanai, Masahiro [0000-0001-5165-4408], Lewis, Cathryn M [0000-0002-8249-8476], Lin, Wei-Yu [0000-0002-9267-7988], Magnusson, Patrik K [0000-0002-7315-7899], Pulit, Sara L [0000-0002-2502-3669], Wiggins, Kerri L [0000-0003-2749-1279], Yang, Qiong [0000-0002-3658-1375], Schadt, Eric E [0000-0002-7892-8808], Koplev, Simon [0000-0002-8586-5614], Civelek, Mete [0000-0002-8141-0284], Trégouët, David A [0000-0001-9084-7800], Christophersen, Ingrid E [0000-0002-6141-4712], Roselli, Carolina [0000-0001-5267-6756], Ellinor, Patrick T [0000-0002-2067-0533], van der Harst, Pim [0000-0002-2713-686X], Elliott, Paul [0000-0002-7511-5684], Takeuchi, Fumihiko [0000-0003-3185-5661], Jern, Christina [0000-0002-7531-2354], Saleheen, Danish [0000-0001-6193-020X], Kamatani, Yoichiro [0000-0001-8748-5597], Dichgans, Martin [0000-0002-0654-387X], Apollo - University of Cambridge Repository

المصدر: Nature Genetics
Nat. Genet. 50, 524-537 (2018)
Nature Genetics, Nature Publishing Group, 2018, 50 (4), pp.524-537. ⟨10.1038/s41588-018-0058-3⟩
Nature Genetics, 50(4), 524-+. Nature Publishing Group
NATURE GENETICS
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Nature genetics
CORE (RIOXX-UK Aggregator)
Apollo
PubMed Central
Nature Genetics, 50(4), 524-537. Nature Publishing Group
Malik, R, Chauhan, G, Traylor, M, Sargurupremraj, M, Okada, Y, Mishra, A, Rutten-Jacobs, L, Giese, A-K, van der Laan, S W, Gretarsdottir, S, Anderson, C D, Chong, M, Adams, H H H, Ago, T, Almgren, P, Amouyel, P, Ay, H, Bartz, T M, Benavente, O R, Bevan, S, Boncoraglio, G B, Brown Jnr, R D, Butterworth, A S, Carrera, C, Carty, C L, Chasman, D I, Chen, W M, Cole, J W, Correa, A, Cotlarciuc, I, Cruchaga, C, Danesh, J, de Bakker, P IW, DeStefano, A L, den Hoed, M, Duan, Q, Engelter, S T, Falcone, G J, Gottesman, R F, Grewal, R P, Guðnason, V, Gustafsson, S, Haessler, J, Harris, T B, Hassan, A, Havulinna, A S, Heckbert, S R, Holliday, E G, Howard, G, Hsu, F-C, Hyacinth, H I, Arfan Ikram, M, Ingelsson, E, Irvin, M R, Jian, X, Jiménez-Conde, J, Johnson, J A, Jukema, J W, Kanai, M, Keene, K L, Kissela, B M, Kleindorfer, D O, Kooperberg, C, Kubo, M, Lange, L A, Langefeld, C D, Langenberg, C, Launer, L J, Lee, J-M, Lemmens, R, Leys, D, Lewis, C M, Lin, W-Y, Lindgren, A G, Lorentzen, E, Magnusson, P K, Maguire, J, Manichaikul, A, McArdle, P F, Meschia, J F, Mitchell, B D, Mosley, T H, Nalls, M A, Ninomiya, T, O'Donnell, M J, Psaty, B M, Pulit, S L, Rannikmäe, K, Reiner, A P, Rexrode, K M, Rice, K M, Rich, S S, Ridker, P M, Rost, N S, Rothwell, P M, Rotter, J I, Rundek, T, Sacco, R L, Sakaue, S, Sale, M M, Salomaa, V, Sapkota, B R, Schmidt, R, Oliver Schmidt, C, Schminke, U, Sharma, P, Slowik, A, Sudlow, C L M, Tatlisumak, T, Tanislav, C, Taylor, K D, Thijs, V NS, Thorleifsson, G, Thorsteinsdottir, U, Tiedt, S, Trompet, S, Tzourio, C, van Duijn, C M, Walters, M, Wareham, N J, Wassertheil-Smoller, S, Wilson, J G, Wiggins, K L, Yang, Q, Yusuf, S, Bis, J C, Pastinen, T, Ruusalepp, A, Schadt, E E, Koplev, S, Björkegren, J LM, Codoni, V, Civelek, M, Smith, N L, Trégouët, D A, Christophersen, I E, Roselli, C, Lubitz, S A, Ellinor, P T, Shyong Tai, E, Kooner, J S, Kato, N, He, J, van der Harst, P, Elliott, P, Chambers, J C, Takeuchi, F, Johnson, A D, Sanghera, D K, Melander, O, Jern, C, Strbian, D, Fernandez-Cadenas, I, Longstreth Jr, W T, Rolfs, A & Hata, J & Woo, D & Rosand, J & Pare, G & Hopewell, J C & Saleheen, D & Stefansson, K & Worrall, B B & Kittner, S J & Seshadri, S & Fornage, M & Markus, H S & Howson, J M M & Kamatani, Y & Debette, S & Dichgans, M 2018, ' Multi-ancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes ', Nature Genetics, vol. 50, no. 4, pp. 524–537 . https://doi.org/10.1038/s41588-018-0058-3Test
Recercat. Dipósit de la Recerca de Catalunya
Nature Genetics, 50(4), 524
Nature genetics 50(4), 524-537 (2018). doi:10.1038/s41588-018-0058-3
Dipòsit Digital de la UB
Universidad de Barcelona
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu

مصطلحات موضوعية: Male, 0301 basic medicine, COMPASS Consortium, Linkage disequilibrium, Candidate gene, UK Young Lacunar DNA Study, Genome-wide association study, SEPIA, Linkage Disequilibrium, Epigenesis, Genetic, classification [Stroke], International Stroke Genetics Consortium (ISGC), 0302 clinical medicine, INDEL Mutation, HEMORRHAGIC STROKE, Risk Factors, Pleiotropy, Databases, Genetic, Neurology Working Group of the CHARGE Consortium, WHITE-MATTER HYPERINTENSITIES, Gene Regulatory Networks, Stroke, Genetics & Heredity, Genetics, International Genomics of Blood Pressure (iGEN-BP) Consortium, physiopathology [Stroke], AFGen Consortium, 11 Medical And Health Sciences, Genomics, 3. Good health, [MEGASTROKE Consortium], ISCHEMIC-STROKE, VINTAGE, genetics [Stroke], CORONARY-ARTERY-DISEASE, Medical genetics, Female, EPIC-InterAct Consortium, MEGASTROKE Consortium, Life Sciences & Biomedicine, Gens, medicine.medical_specialty, SUSCEPTIBILITY LOCI, STARNET, INVENT Consortium, SMALL-VESSEL DISEASE, Biology, Polymorphism, Single Nucleotide, EPIC-CVD Consortium, Article, Chromosomes, HUMAN GENETIC-VARIATION, NINDS Stroke Genetics Network (SiGN), 03 medical and health sciences, ddc:570, Genetic variation, medicine, Humans, Genetic Predisposition to Disease, Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, Science & Technology, Models, Genetic, COMPLEX TRAITS, Computational Biology, 06 Biological Sciences, medicine.disease, METASTROKE Consortium, Human genetics, Cromosomes, BioBank Japan Cooperative Hospital Group, Genòmica, 030104 developmental biology, Genes, Genetic Loci, ATRIAL-FIBRILLATION, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, SUDDEN CARDIAC DEATH, 030217 neurology & neurosurgery, Developmental Biology, Genome-Wide Association Study

وصف الملف: application/pdf; Print-Electronic; application/vnd.openxmlformats-officedocument.wordprocessingml.document

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e62d8d0fa25dfb6be411c3a18bccb356Test
https://doi.org/10.1038/s41588-018-0058-3Test

المؤلفون: Simona Barlera, Giovanni Birolo, Simon Myers, Viola Grugni, Vincenzo Lorenzo Pascali, Andrea Angius, Mait Metspalu, Francesca Brisighelli, Antonio Torroni, Francesco Montinaro, Hovirag Lancioni, Luísa Pereira, Antonella Mulas, Mohammed Melhaoui, Alessandro Achilli, Serena Aneli, Mohammed Cherkaoui, Peristera Paschou, M. Peyret-Guzzon, Pilar Galan, Giorgio B. Boncoraglio, A. M. Di Blasio, Stéphane Mazières, C. Di Gaetano, Garrett Hellenthal, Giuseppe Matullo, George Stamatoyannopoulos, Joanna Giemza, J. Di Cristofaro, Magdalena Zoledziewska, Irene Cardinali, Georgios Athanasiadis, Cristian Capelli, François-Xavier Ricaut, Jacques Chiaroni, Anna Olivieri, Alessandro Raveane, Luca Pagani, Toomas Kivisild, Abdellatif Baali, Nicolas Brucato, Christian Dina, Jean-Michel Dugoujon, Clare Bycroft, Alberto Piazza, Silvia Parolo, Francesco Cucca, Ornella Semino

المساهمون: Dipartimento di Biologia e Biotecnologie ‘Lazzaro Spallanzani’, University of Pavia, University of Pavia, University of Oxford [Oxford], Aarhus University [Aarhus], Istituto di Ricerche Farmacologiche Mario Negri, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Fondazione 'Istituto Neurologico Nazionale C. Mondino'-Fondazione 'Istituto Neurologico Nazionale C. Mondino', University of Turin, Fondazione IRCCS Istituto Neurologico 'Carlo Besta', Dipartimento di Genetica, Biologica e Biochimica, Università degli studi di Torino (UNITO), Laboratoire d'Etude du Rayonnement et de la Matière en Astrophysique (LERMA), École normale supérieure - Paris (ENS Paris)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut national des sciences de l'Univers (INSU - CNRS)-Observatoire de Paris, PSL Research University (PSL)-PSL Research University (PSL)-Université de Cergy Pontoise (UCP), Université Paris-Seine-Université Paris-Seine-Centre National de la Recherche Scientifique (CNRS), Georgia Tech - CNRS [Metz] (UMI2958), Ecole Nationale Supérieure des Arts et Metiers Metz-SUPELEC-Georgia Institute of Technology [Atlanta]-Georgia Institute of Technology [Lorraine, France]-CentraleSupélec-Centre National de la Recherche Scientifique (CNRS)-Université de Franche-Comté (UFC), Etablissement Français du Sang - Alpes-Méditerranée (EFS - Alpes-Méditerranée), Etablissement Français du Sang, Anthropologie bio-culturelle, Droit, Ethique et Santé (ADES), Aix Marseille Université (AMU)-EFS ALPES MEDITERRANEE-Centre National de la Recherche Scientifique (CNRS), Génétique des maladies multifactorielles (GMM), Université de Lille, Droit et Santé-Centre National de la Recherche Scientifique (CNRS), Unité de Recherche en Epidémiologie Nutritionnelle (UREN), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Sorbonne Paris Cité (USPC)-Université Paris 13 (UP13)-Conservatoire National des Arts et Métiers [CNAM] (CNAM)-Institut National de la Recherche Agronomique (INRA), Equipe 3: EREN- Equipe de Recherche en Epidémiologie Nutritionnelle (CRESS - U1153), Université Paris 13 (UP13)-Institut National de la Recherche Agronomique (INRA)-Conservatoire National des Arts et Métiers [CNAM] (CNAM)-Centre de Recherche Épidémiologie et Statistique Sorbonne Paris Cité (CRESS (U1153 / UMR_A_1125 / UMR_S_1153)), Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de la Recherche Agronomique (INRA)-Université Paris Descartes - Paris 5 (UPD5)-Université Sorbonne Paris Cité (USPC)-Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de la Recherche Agronomique (INRA)-Université Paris Descartes - Paris 5 (UPD5)-Université Sorbonne Paris Cité (USPC), Centre National de la Recherche Scientifique (CNRS), Dipartimento di Genetica e Microbiologica, Università di Pavia, Dipartimento di Genetica e Microbiologia, Instituto de Investigação e Inovação em Saúde, Raveane, A, Aneli, S, Montinaro, F, Athanasiadis, G, Barlera, S, Birolo, G, Boncoraglio, G, Di Blasio, A, Di Gaetano, C, Pagani, L, Parolo, S, Paschou, P, Piazza, A, Stamatoyannopoulos, G, Angius, A, Brucato, N, Cucca, F, Hellenthal, G, Mulas, A, Peyret-Guzzon, M, Zoledziewska, M, Baali, A, Bycroft, C, Cherkaoui, M, Chiaroni, J, Di Cristofaro, J, Dina, C, Dugoujon, J, Galan, P, Giemza, J, Kivisild, T, Mazieres, S, Melhaoui, M, Metspalu, M, Myers, S, Pereira, L, Ricaut, F, Brisighelli, F, Cardinali, I, Grugni, V, Lancioni, H, Pascali, V, Torroni, A, Semino, O, Matullo, G, Achilli, A, Olivieri, A, Capelli, C, Mazières, Stéphane, Dipartimento di Biologia e Biotecnologie 'Lazzaro Spallanzani' = Department of Biology and Biotechnology [Univ di Pavia] (DBB UNIPV), Università degli Studi di Pavia = University of Pavia (UNIPV), University of Oxford, Università degli studi di Torino = University of Turin (UNITO), École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut national des sciences de l'Univers (INSU - CNRS)-Observatoire de Paris, Université Paris sciences et lettres (PSL)-Université de Cergy Pontoise (UCP), Georgia Tech Lorraine [Metz], Ecole Nationale Supérieure des Arts et Metiers Metz-Georgia Institute of Technology [Atlanta]-Ecole Supérieure d'Electricité - SUPELEC (FRANCE)-CentraleSupélec-Centre National de la Recherche Scientifique (CNRS)-Université de Franche-Comté (UFC), Université Bourgogne Franche-Comté [COMUE] (UBFC)-Université Bourgogne Franche-Comté [COMUE] (UBFC), Université Paris 13 (UP13)-Institut National de la Recherche Agronomique (INRA)-Conservatoire National des Arts et Métiers [CNAM] (CNAM), HESAM Université - Communauté d'universités et d'établissements Hautes écoles Sorbonne Arts et métiers université (HESAM)-HESAM Université - Communauté d'universités et d'établissements Hautes écoles Sorbonne Arts et métiers université (HESAM)-Université Sorbonne Paris Cité (USPC)-Institut National de la Santé et de la Recherche Médicale (INSERM), HESAM Université - Communauté d'universités et d'établissements Hautes écoles Sorbonne Arts et métiers université (HESAM)-HESAM Université - Communauté d'universités et d'établissements Hautes écoles Sorbonne Arts et métiers université (HESAM)-Centre de Recherche Épidémiologie et Statistique Sorbonne Paris Cité (CRESS (U1153 / UMR_A_1125 / UMR_S_1153)), Institut National de la Recherche Agronomique (INRA)-Université Paris Diderot - Paris 7 (UPD7)-Université Paris Descartes - Paris 5 (UPD5)-Université Sorbonne Paris Cité (USPC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de la Recherche Agronomique (INRA)-Université Paris Diderot - Paris 7 (UPD7)-Université Paris Descartes - Paris 5 (UPD5)-Université Sorbonne Paris Cité (USPC)-Institut National de la Santé et de la Recherche Médicale (INSERM), École normale supérieure - Paris (ENS Paris), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Sorbonne Paris Cité (USPC)-Université Paris 13 (UP13)-Conservatoire National des Arts et Métiers [CNAM] (CNAM), HESAM Université (HESAM)-HESAM Université (HESAM)-Institut National de la Recherche Agronomique (INRA), HESAM Université (HESAM)-HESAM Université (HESAM)-Centre de Recherche Épidémiologie et Statistique Sorbonne Paris Cité (CRESS (U1153 / UMR_A_1125 / UMR_S_1153)), Université Paris Diderot - Paris 7 (UPD7)-Université Sorbonne Paris Cité (USPC)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de la Recherche Agronomique (INRA)-Université Paris Diderot - Paris 7 (UPD7)-Université Sorbonne Paris Cité (USPC)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de la Recherche Agronomique (INRA), Università degli Studi di Pavia, Institut National de la Recherche Agronomique (INRA)-Conservatoire National des Arts et Métiers [CNAM] (CNAM)-Université Paris 13 (UP13)-Centre de Recherche Épidémiologie et Statistique Sorbonne Paris Cité (CRESS (U1153 / UMR_A_1125 / UMR_S_1153)), Université Paris 13 (UP13)-Institut National de la Recherche Agronomique (INRA)-Conservatoire National des Arts et Métiers [CNAM] (CNAM)-Université Sorbonne Paris Cité (USPC)-Institut National de la Santé et de la Recherche Médicale (INSERM)

المصدر: Science Advances
Science Advances, American Association for the Advancement of Science (AAAS), 2019, 5 (9), pp.eaaw3492. ⟨10.1126/sciadv.aaw3492⟩
Science Advances, 2019, 5 (9), pp.eaaw3492. ⟨10.1126/sciadv.aaw3492⟩
Raveane, A, Aneli, S, Montinaro, F, Athanasiadis, G, Barlera, S, Birolo, G, Boncoraglio, G, Di Blasio, A M, Di Gaetano, C, Pagani, L, Parolo, S, Paschou, P, Piazza, A, Stamatoyannopoulos, G, Angius, A, Brucato, N, Cucca, F, Hellenthal, G, Mulas, A, Peyret-Guzzon, M, Zoledziewska, M, Baali, A, Bycroft, C, Cherkaoui, M, Chiaroni, J, Di Cristofaro, J, Dina, C, Dugoujon, J M, Galan, P, Giemza, J, Kivisild, T, Mazieres, S, Melhaoui, M, Metspalu, M, Myers, S, Pereira, L, Ricaut, F X, Brisighelli, F, Cardinali, I, Grugni, V, Lancioni, H, Pascali, V L, Torroni, A, Semino, O, Matullo, G, Achilli, A, Olivieri, A & Capelli, C 2019, ' Population structure of modern-day Italians reveals patterns of ancient and archaic ancestries in Southern Europe ', Science Advances, vol. 5, no. 9, eaaw3492 . https://doi.org/10.1126/sciadv.aaw3492Test

مصطلحات موضوعية: SELECTION, [SHS.ANTHRO-BIO]Humanities and Social Sciences/Biological anthropology, Distribution (economics), Population genetics, Neanderthal genome project, 0302 clinical medicine, Peninsula, HISTORY, Databases, Genetic, ADAPTATION, Research Articles, History, Ancient, media_common, Neanderthals, MODERN HUMANS, 0303 health sciences, Multidisciplinary, geography.geographical_feature_category, POPULATION GENETICS, GENOMICS, EUROPE, Population Genetic, SciAdv r-articles, ASSOCIATION, [SHS.ANTHRO-BIO] Humanities and Social Sciences/Biological anthropology, Multidisciplinary Sciences, ADMIXTURE, Geography, Italy, Ethnology, Science & Technology - Other Topics, Neanderthals / genetics, Research Article, EUROPE, MIGRATION, media_common.quotation_subject, Pastoralism, Human Genetic, Settore BIO/08 - ANTROPOLOGIA, GENETIC-STRUCTURE, SEQUENCE, White People, 03 medical and health sciences, Bronze Age, POPULATION GENETICS, Genetic variation, Animals, Humans, DNA, Ancient, European Continental Ancestry Group / genetics, 030304 developmental biology, Science & Technology, business.industry, Genome, Human, Genetic Drift, Human Genetics, Anthropology, GENOME-WIDE PATTERNS, business, GENOMICS, 030217 neurology & neurosurgery, Diversity (politics), Genome-Wide Association Study

وصف الملف: application/pdf; Electronic-eCollection

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7040fa6e38d12d3609b2454624b55ea3Test
http://hdl.handle.net/11577/3308038Test

المؤلفون: Vincenzo Lorenzo Pascali, Francesca Brisighelli, Simona Barlera, Luca Pagani, Nicolas Brucato, Joanna Giemza, Hovirag Lancioni, Clare Bycroft, Alberto Piazza, Jean-Michel Dugoujon, Antonella Mulas, Mohammed Cherkaoui, Francesco Cucca, Giovanni Birolo, Alessandro Achilli, Serena Aneli, C. Di Gaetano, M. Peyret-Guzzon, Garrett Hellenthal, Pilar Galan, A. M. Di Blasio, Giuseppe Matullo, Christian Dina, Antonio Torroni, George Stamatoyannopoulos, Irene Cardinali, Viola Grugni, Luísa Pereira, Mait Metspalu, Georgios Athanasiadis, Peristera Paschou, Abdellatif Baali, Cristian Capelli, Mohammed Melhaoui, François-Xavier Ricaut, Simon Myers, Andrea Angius, Francesco Montinaro, Ornella Semino, Anna Olivieri, Toomas Kivisild, Magdalena Zoledziewska, Giorgio B. Boncoraglio, Silvia Parolo, Alessandro Raveane

مصطلحات موضوعية: 0303 health sciences, Genetic diversity, Neanderthal, geography.geographical_feature_category, biology, Pastoralism, Neanderthal genome project, 03 medical and health sciences, 0302 clinical medicine, Geography, Bronze Age, Peninsula, biology.animal, Genetic variation, Genetic structure, Ethnology, 030217 neurology & neurosurgery, 030304 developmental biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d56eec24a71a3aa925555b955e5b1c1Test

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: Reinhold Schmidt, Cathie Sudlow, Matthew Traylor, Ranjan Deka, Will Longstreth, Rainer Malik, William J. Devan, Bradford B. Worrall, John Attia, Magdy Selim, Bruce M. Psaty, Jessica G. Woo, Kristiina Rannikmäe, Farid Radmanesh, Devin L. Brown, Joshua C. Bis, D Poole, Steven J. Kittner, Elizabeth G. Holliday, Natalia S. Rost, Agnieszka Slowik, Cathy R. Zhang, Stéphanie Debette, Giorgio B. Boncoraglio, Jonathan Rosand, Pankaj Sharma, Chelsea S. Kidwell, Scott Silliman, Thomas W.K. Battey, Tom Van Agtmael, Hugh S. Markus, Daniel Woo, James F. Meschia, Peter M. Rothwell, Lisa J. Martin, Joan Montaner, Carl D. Langefeld, Guido J. Falcone, Christopher D. Anderson, Pippa A. Thomson, Braxton D. Mitchell, Jordi Jimenez-Conde, Mohammad Arfan Ikram, Gail Davies, Myriam Fornage, Sudha Seshadri, Qiong Yang, Arne Lindgren, Martin Dichgans, Christopher R Levi, Björn M. Hansen, Steve Bevan

المساهمون: Epidemiology

المصدر: Neurology, 84(9), 918-926. Lippincott Williams & Wilkins

مصطلحات موضوعية: Collagen Type IV, medicine.medical_specialty, Linkage disequilibrium, Pathology, Neurology, Population, Col·lagen -- Malalties, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, Gastroenterology, Article, Internal medicine, medicine, Humans, SNP, education, Genetic Association Studies, Intracerebral hemorrhage, education.field_of_study, business.industry, Polimorfisme genètic, Genetic Variation, Odds ratio, medicine.disease, Hyperintensity, Cerebral Small Vessel Diseases, Neurology (clinical), B990 Subjects Allied to Medicine not elsewhere classified, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3fe92dfdebfd987e4afdac5d0f853abTest
https://doi.org/10.1212/wnl.0000000000001309Test

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: 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: Boukje de Vries, Matthew Traylor, Lynn Cherkas, Kristiina Rannikmäe, Jaakko Kaprio, Jonathan Rosand, Rainer Malik, Gisela M. Terwindt, Martin Farrall, Daniel I. Chasman, Robert Clarke, Tobias Kurth, Braxton D. Mitchell, Verneri Anttila, Tobias Freilinger, Markus Schürks, George Davey Smith, Maija Wessman, Jonathan Sturm, Catherine Sudlow, David P. Strachan, Lydia Quaye, Martin Dichgans, Bradford B. Worrall, Arn M. J. M. van den Maagdenberg, Kari Stefansson, Cornelia M. van Duijn, Lannie Ligthart, Terho Lehtimäki, James F. Meschia, Joshua C. Bis, Christian Kubisch, Pankaj Sharma, Jane Maguire, Chris Cotsapas, Bendik S. Winsvold, W. T. Longstreth, Hugh S. Markus, Peter M. Rothwell, Mikko Kallela, Jason A. Vander Heiden, Aarno Palotie, M. Arfan Ikram, Michel D. Ferrari, Jemma C. Hopewell, Giorgio B. Boncoraglio, Myriam Fornage, Sudha Seshadri, Dale R. Nyholt, Olli T. Raitakari, Alexander P. Reiner, Elizabeth G. Holliday, J.A. Zwart

المساهمون: Epidemiology, Internal Medicine, Neuroscience Campus Amsterdam - Neurobiology of Mental Health, Biological Psychology

المصدر: Neurology, 84(21), 2132-2145. Lippincott Williams & Wilkins
Neurology, 84(21), 2132-2145
Malik, R, Freilinger, T, Winsvold, B S, Anttila, V, van der Heiden, J, Traylor, M, de Vries, B, Holliday, E G, Terwindt, G M, Sturm, J, Bis, J C, Hopewell, J C, Ferrari, M D, Rannikmae, K, Wessman, M, Kallela, M, Kubisch, C, Fornage, M, Meschia, J F, Lehtimäki, T, Sudlow, C, Clarke, R, Chasman, D I, Mitchell, B D, Maguire, J, Kaprio, J, Farrall, M, Raitakari, O T, Kurth, T, Arfan Ikram, M, Reiner, A P, Longstreth, J W T, Rothwell, P M, Strachan, D P, Sharma, P, Seshadri, S, Quaye, L, Cherkas, L, Schürks, M, Rosand, J, Ligthart, L, Boncoraglio, G B, Davey Smith, G, van Duijn, C M, Stefansson, K, Worrall, B B, Nyholt, DR, Markus, H S, van den Maagdenberg, A M J M, Cotsapas, C, Zwart, J A & Palotie, A 2015, ' Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants ', Neurology, vol. 84, no. 21, pp. 2132-2145 . https://doi.org/10.1212/WNL.0000000000001606Test
Neurology, 84(21), 2132-2145. American Academy of Neurology

مصطلحات موضوعية: Migraine without Aura, Candidate gene, Migraine with Aura, Genome-wide association study, Biology, Genetic correlation, Article, Brain Ischemia, 03 medical and health sciences, 0302 clinical medicine, SDG 3 - Good Health and Well-being, Genetic variation, medicine, Genetic predisposition, Humans, 030304 developmental biology, Genetics, 0303 health sciences, ta3121, medicine.disease, Migraine with aura, 3. Good health, Genetic load, Stroke, Migraine, Neurology (clinical), medicine.symptom, 030217 neurology & neurosurgery, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ffc4160ddf923fc37dbf90c9b4f5af2Test
https://pure.eur.nl/en/publications/466f463c-baf0-409d-9a3c-c4e10c488030Test

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