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by Webb, Thomas R and Erdmann, Jeanette and Stirrups, Kathleen E and Stitziel, Nathan O and Masca, Nicholas G.D and Jansen, Henning and Kanoni, Stavroula and Nelson, Christopher P and Ferrario, Paola G and König, Inke R and Eicher, John D and Johnson, Andrew D and Hamby, Stephen E and Betsholtz, Christer and Ruusalepp, Arno and Franzén, Oscar and Schadt, Eric E and Björkegren, Johan L.M and Weeke, Peter E and Auer, Paul L and Schick, Ursula M and Lu, Yingchang and Zhang, He and Dube, Marie-Pierre and Goel, Anuj and Farrall, Martin and Peloso, Gina M and Won, Hong-Hee and Do, Ron and van Iperen, Erik and Kruppa, Jochen and Mahajan, Anubha and Scott, Robert A and Willenborg, Christina and Braund, Peter S and van Capelleveen, Julian C and Doney, Alex S.F and Donnelly, Louise A and Asselta, Rosanna and Merlini, Pier A and Duga, Stefano and Marziliano, Nicola and Denny, Josh C and Shaffer, Christian and El-Mokhtari, Nour Eddine and Franke, Andre and Heilmann, Stefanie and Hengstenberg, Christian and Hoffmann, Per and Holmen, Oddgeir L and Hveem, Kristian and Jansson, Jan-Håkan and Jöckel, Karl-Heinz and Kessler, Thorsten and Kriebel, Jennifer and Laugwitz, Karl L and Marouli, Eirini and Martinelli, Nicola and McCarthy, Mark I and Van Zuydam, Natalie R and Meisinger, Christa and Esko, Tõnu and Mihailov, Evelin and Escher, Stefan A and Alver, Maris and Moebus, Susanne and Morris, Andrew D and Virtamo, Jarma and Nikpay, Majid and Olivieri, Oliviero and Provost, Sylvie and AlQarawi, Alaa and Robertson, Neil R and Akinsansya, Karen O and Reilly, Dermot F and Vogt, Thomas F and Yin, Wu and Asselbergs, Folkert W and Kooperberg, Charles and Jackson, Rebecca D and Stahl, Eli and Müller-Nurasyid, Martina and Strauch, Konstantin and Varga, Tibor V and Waldenberger, Melanie and Zeng, Lingyao and Chowdhury, Rajiv and Salomaa, Veikko and Ford, Ian and Jukema, J. Wouter and Amouyel, Philippe and Kontto, Jukka and Nordestgaard, Børge G and Ferrières, Jean and Saleheen, Danish and Sattar, Naveed and Surendran, Praveen and Wagner, Aline and Young, Robin and Howson, Joanna M.M and ... and Wellcome Trust Case Control Consortium and Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators and MORGAM Investigators and Wellcome Trust Case Control and Myocardial Infarction Genetics
Journal of the American College of Cardiology, ISSN 0735-1097, 2017, Volume 69, Issue 7, pp. 823 - 836
Abstract Background Genome-wide association studies have so far identified 56 loci associated with risk of coronary artery disease (CAD). Many CAD loci show... 
Cardiovascular | Internal Medicine | expression quantitative trait loci | genetics | genome-wide association | single nucleotide polymorphism | cholesteryl ester transfer protein | Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Genome-Wide Association Study | Gene Frequency | Humans | Coronary Artery Disease - genetics | Female | Male | Coronary Artery Disease - epidemiology | Genetic Pleiotropy | Polymorphism, Single Nucleotide | Genetic Loci | Odds Ratio | Case-Control Studies | Coronary heart disease | Analysis | Genealogy | Cardiovascular disease | Genomes | Metabolism | Gene expression | Blood | Risk factors | Studies | Celiac disease | Lipoproteins | Coronary vessels | Rheumatoid arthritis | Quality control | Calcification | Diabetes | Bioinformatics | Index Medicus | Abridged Index Medicus | LD, linkage disequilibrium | CETP, cholesteryl ester transfer protein | eQTL, expression quantitative trait locus | CAD, coronary artery disease | GWAS, genome-wide association study | BMI, body mass index | SNP, single nucleotide polymorphism | HDL, high-density lipoprotein | LDL, low-density lipoprotein | Original Investigation | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin
Journal Article
The New England journal of medicine, ISSN 1533-4406, 03/2016, Volume 374, Issue 12, pp. 1134 - 1144
Journal Article
Journal Article
Nature genetics, ISSN 1546-1718, 12/2010, Volume 43, Issue 2, pp. 117 - 120
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
Scientific reports, ISSN 2045-2322, 04/2019, Volume 9, Issue 1, pp. 6320 - 6320
..., Maria del C. Valdes-Hernandez1, Xin Wang1, Tom MacGillivray 1, Alex S. F. Doney6, Baljean Dhillon 1, John M. starr5,7, Mark E. Bastin5,8, Emanuele trucco 9, Ian J... 
NETWORK ALTERATIONS | VASCULAR RISK-FACTORS | COGNITIVE-ABILITY | ASSOCIATIONS | DEMENTIA | ABNORMALITIES | MRI | RATIONALE | IMAGE-ANALYSIS | BRAIN | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Neuroimaging | Stroke | Vascular diseases | Magnetic resonance imaging | Retina | Fractals | Microvasculature | Substantia alba | Index Medicus
Journal Article
by Prokopenko, Inga and Langenberg, Claudia and Florez, Jose C and Saxena, Richa and Soranzo, Nicole and Thorleifsson, Gudmar and Loos, Ruth J F and Manning, Alisa K and Jackson, Anne U and Aulchenko, Yurii and Potter, Simon C and Erdos, Michael R and Sanna, Serena and Hottenga, Jouke-Jan and Wheeler, Eleanor and Kaakinen, Marika and Lyssenko, Valeriya and Chen, Wei-Min and Ahmadi, Kourosh and Beckmann, Jacques S and Bergman, Richard N and Bochud, Murielle and Bonnycastle, Lori L and Buchanan, Thomas A and Cao, Antonio and Cervino, Alessandra and Coin, Lachlan and Collins, Francis S and Crisponi, Laura and de Geus, Eco J C and Dehghan, Abbas and Deloukas, Panos and Doney, Alex S F and Elliott, Paul and Freimer, Nelson and Gateva, Vesela and Herder, Christian and Hofman, Albert and Hughes, Thomas E and Hunt, Sarah and Illig, Thomas and Inouye, Michael and Isomaa, Bo and Johnson, Toby and Kong, Augustine and Krestyaninova, Maria and Kuusisto, Johanna and Laakso, Markku and Lim, Noha and Lindblad, Ulf and Lindgren, Cecilia M and McCann, Owen T and Mohlke, Karen L and Morris, Andrew D and Naitza, Silvia and Orrù, Marco and Palmer, Colin N A and Pouta, Anneli and Randall, Joshua and Rathmann, Wolfgang and Saramies, Jouko and Scheet, Paul and Scott, Laura J and Scuteri, Angelo and Sharp, Stephen and Sijbrands, Eric and Smit, Jan H and Song, Kijoung and Steinthorsdottir, Valgerdur and Stringham, Heather M and Tuomi, Tiinamaija and Tuomilehto, Jaakko and Uitterlinden, André G and Voight, Benjamin F and Waterworth, Dawn and Wichmann, H-Erich and Willemsen, Gonneke and Witteman, Jacqueline C M and Yuan, Xin and Zhao, Jing Hua and Zeggini, Eleftheria and Schlessinger, David and Sandhu, Manjinder and Boomsma, Dorret I and Uda, Manuela and Spector, Tim D and Penninx, Brenda WJH and Altshuler, David and Vollenweider, Peter and Jarvelin, Marjo Riitta and Lakatta, Edward and Waeber, Gerard and Fox, Caroline S and Peltonen, Leena and Groop, Leif C and Mooser, Vincent and Cupples, L Adrienne and Thorsteinsdottir, Unnur and Boehnke, Michael and Barroso, Inês and ... and Institutionen för medicin, avdelningen för samhällsmedicin och folkhälsa and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Institute of Medicine, School of Public Health and Community Medicine and Sahlgrenska Academy
Nature genetics, ISSN 1546-1718, 12/2008, Volume 41, Issue 1, pp. 77 - 81
Journal Article