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PLoS genetics, ISSN 1553-7390, 2014, Volume 10, Issue 7, pp. e1004469 - e1004469
Genome-wide association studies (GWAS) have begun to identify the common genetic component to ischaemic stroke (IS). However, IS has considerable phenotypic... 
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genome-wide association studies | Ischemia | Atherosclerosis | Genetic aspects | Research | Diagnosis | Risk factors | Index Medicus | Heart | Medical research | Stroke | Genealogy | Biomedical research | Genomes | Grants | Design | Womens health | Risk assessment | Genetics | Age | Veins & arteries | Siblings
Journal Article
European journal of human genetics : EJHG, ISSN 1018-4813, 06/2015, Volume 23, Issue 6, pp. 863 - 869
Journal Article
by Traylor, Matthew and Farrall, Martin and Holliday, Elizabeth G and Sudlow, Cathie and Hopewell, Jemma C and Cheng, Yu-Ching and Fornage, Myriam and Ikram, M Arfan and Malik, Rainer and Bevan, Steve and Thorsteinsdottir, Unnur and Nalls, Mike A and Longstreth, WT and Wiggins, Kerri L and Yadav, Sunaina and Parati, Eugenio A and DeStefano, Anita L and Worrall, Bradford B and Kittner, Steven J and Khan, Muhammad Saleem and Reiner, Alex P and Helgadottir, Anna and Achterberg, Sefanja and Fernandez-Cadenas, Israel and Abboud, Sherine and Schmidt, Reinhold and Walters, Matthew and Chen, Wei-Min and Ringelstein, E Bernd and O'Donnell, Martin and Ho, Weang Kee and Pera, Joanna and Lemmens, Robin and Norrving, Bo and Higgins, Peter and Benn, Marianne and Sale, Michele and Kuhlenbäumer, Gregor and Doney, Alexander S F and Vicente, Astrid M and Delavaran, Hossein and Algra, Ale and Davies, Gail and Oliveira, Sofia A and Palmer, Colin N A and Deary, Ian and Schmidt, Helena and Pandolfo, Massimo and Montaner, Joan and Carty, Cara and de Bakker, Paul I W and Kostulas, Konstantinos and Ferro, Jose M and van Zuydam, Natalie R and Valdimarsson, Einar and Nordestgaard, Børge G and Lindgren, Arne and Thijs, Vincent and Slowik, Agnieszka and Saleheen, Danish and Paré, Guillaume and Berger, Klaus and Thorleifsson, Gudmar and Hofman, Albert and Mosley, Thomas H and Mitchell, Braxton D and Furie, Karen and Clarke, Robert and Levi, Christopher and Seshadri, Sudha and Gschwendtner, Andreas and Boncoraglio, Giorgio B and Sharma, Pankaj and Bis, Joshua C and Gretarsdottir, Solveig and Psaty, Bruce M and Rothwell, Peter M and Rosand, Jonathan and Meschia, James F and Stefansson, Kari and Dichgans, Martin and Markus, Hugh S and The Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) and on behalf of the International Stroke Genetics Consortium and WTCCC 2 and Australian Stroke Genetics Collabo and Int Stroke Genetics Consortium and International Stroke Genetics Consortium and Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2)
Lancet neurology, ISSN 1474-4422, 11/2012, Volume 11, Issue 11, pp. 951 - 962
Journal Article
Nature (London), ISSN 0028-0836, 2020, Volume 583, Issue 7814, pp. 90 - 95
Primary immunodeficiency (PID) is characterized by recurrent and often life-threatening infections, autoimmunity and cancer, and it poses major diagnostic and... 
General | Phenotypes | Disease | Genes | Hypersensitivity | Immunodeficiency | Causation | Antibodies | Genomes | Regulatory sequences | Family medical history | Loci | Genetic screening | Gene sequencing | Genotype & phenotype | Genetics | Diagnostic systems | Mutation | Diagnosis | Children | Autoimmune diseases | Bayesian analysis | Methods | PTPN2 protein | Index Medicus | Klinisk medicin | Clinical Medicine
Journal Article
by Cole, John W and Xu, Huichun and Ryan, Kathleen and Jaworek, Thomas and Dueker, Nicole and McArdle, Patrick and Gaynor, Brady and Cheng, Yu-Ching and O'Connell, Jeffrey and Bevan, Steve and Malik, Rainer and Ahmed, Naveed Uddin and Amouyel, Philippe and Anjum, Sheraz and Bis, Joshua C and Crosslin, David and Danesh, John and Engelter, Stefan T and Fornage, Myriam and Frossard, Philippe and Gieger, Christian and Giese, Anne-Katrin and Grond-Ginsbach, Caspar and Ho, Weang Kee and Holliday, Elizabeth and Hopewell, Jemma and Hussain, M and Iqbal, W and Jabeen, S and Jannes, Jim and Kamal, Ayeesha and Kamatani, Yoichiro and Kanse, Sandip and Kloss, Manja and Lathrop, Mark and Leys, Didier and Lindgren, Arne and Longstreth, W. T and Mahmood, Khalid and Meisinger, Christa and Metso, Tiina M and Mosley, Thomas and Müller-Nurasyid, Martina and Norrving, Bo and Parati, Eugenio and Peters, Annette and Pezzini, Alessandro and Quereshi, I and Rasheed, Asif and Rauf, A and Salam, T and Shen, Jess and Słowik, Agnieszka and Stanne, Tara and Strauch, Konstantin and Tatlisumak, Turgut and Thijs, Vincent N and Tiedt, Steffen and Traylor, Matthew and Waldenberger, Melanie and Walters, Matthew and Zhao, Wei and Boncoraglio, Giorgio and Debette, Stéphanie and Jern, Christina and Levi, Christopher and Markus, Hugh and Meschia, James and Rolfs, Arndt and Rothwell, Peter and Saleheen, Danish and Seshadri, Sudha and Sharma, Pankaj and Sudlow, Cathie and Worrall, Bradford and Stine, O. Colin and Kittner, Steven J and Mitchell, Braxton D and WTCCC-2 Consortium and METASTROKE Consortium of the ISGC and METASTROKE Consortium ISGC and Institutionen för biomedicin and Sahlgrenska akademin and Institute of Biomedicine and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy
PloS one, ISSN 1932-6203, 11/2018, Volume 13, Issue 11, pp. e0206554 - e0206554
Journal Article
Journal Article
by Malik, Rainer and Chauhan, Ganesh and Traylor, Matthew and Sargurupremraj, Muralidharan and Okada, Yukinori and Mishra, Aniket and Rutten-Jacobs, Loes and Giese, Anne-Katrin and van der Laan, Sander W and Gretarsdottir, Solveig and Anderson, Christopher D and Chong, Michael and Adams, Hieab H. H and Ago, Tetsuro and Almgren, Peter and Amouyel, Philippe and Ay, Hakan and Bartz, Traci M and Benavente, Oscar R and Bevan, Steve and Boncoraglio, Giorgio B and Brown, Robert D and Butterworth, Adam S and Carrera, Caty and Carty, Cara L and Chasman, Daniel I and Chen, Wei-Min and Cole, John W and Correa, Adolfo and Cotlarciuc, Ioana and Cruchaga, Carlos and Danesh, John and de Bakker, Paul I. W and DeStefano, Anita L and den Hoed, Marcel and Duan, Qing and Engelter, Stefan T and Falcone, Guido J and Gottesman, Rebecca F and Grewal, Raji P and Gudnason, Vilmundur and Gustafsson, Stefan and Haessler, Jeffrey and Harris, Tamara B and Hassan, Ahamad and Havulinna, Aki S and Heckbert, Susan R and Holliday, Elizabeth G and Howard, George and Hsu, Fang-Chi and Hyacinth, Hyacinth I and Ikram, M. Arfan and Ingelsson, Erik and Irvin, Marguerite R and Jian, Xueqiu and Jiménez-Conde, Jordi and Johnson, Julie A and Jukema, J. Wouter and Kanai, Masahiro and Keene, Keith L and Kissela, Brett M and Kleindorfer, Dawn O and Kooperberg, Charles and Kubo, Michiaki and Lange, Leslie A and Langefeld, Carl D and Langenberg, Claudia and Launer, Lenore J and Lee, Jin-Moo and Lemmens, Robin and Leys, Didier and Lewis, Cathryn M and Lin, Wei-Yu and Lindgren, Arne G and Lorentzen, Erik and Magnusson, Patrik K and Maguire, Jane and Manichaikul, Ani and McArdle, Patrick F and Meschia, James F and Mitchell, Braxton D and Mosley, Thomas H and Nalls, Michael A and Ninomiya, Toshiharu and O’Donnell, Martin J and Psaty, Bruce M and Pulit, Sara L and Rannikmäe, Kristiina and Reiner, Alexander P and Rexrode, Kathryn M and Rice, Kenneth and Rich, Stephen S and Ridker, Paul M and Rost, Natalia S and Rothwell, Peter M and Rotter, Jerome I and Rundek, Tatjana and Sacco, Ralph L and Sakaue, Saori and Sale, Michele M and ... and Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and International Stroke Genetics Consortium (ISGC) and AFGen Consortium and NINDS Stroke Genetics Network (SiGN) and UK Young Lacunar DNA Study and EPIC-CVD Consortium and INVENT Consortium and International Genomics of Blood Pressure (iGEN-BP) Consortium and MEGASTROKE Consortium and BioBank Japan Cooperative Hospital Group and COMPASS Consortium and METASTROKE Consortium and EPIC-InterAct Consortium and Neurology Working Group of the CHARGE Consortium and STARNET and Int Stroke Genetics Consortium ISG and Int Genomics Blood Pressure iGEN and Cohorts Heart Aging Res Genomic and BioBank Japan Cooperative Hosp Grp and NINDS Stroke Genetics Network Si and Neurology Working Grp Charge Con
Nature genetics, ISSN 1546-1718, 03/2018, Volume 50, Issue 4, pp. 524 - 537
Stroke has multiple etiologies, but the underlying genes and pathways are largely unknown. We conducted a multiancestry genome-wide-association meta-analysis... 
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Stroke | Genes | Health risks | Risk | Cardiovascular disease | Genomes | Genetic diversity | Regression analysis | Loci | Meta-analysis | Consortia | Pleiotropy | Etiology | Blood pressure | Thromboembolism | Bioinformatics | Asians | Index Medicus
Journal Article