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PLoS genetics, ISSN 1553-7404, 2009, Volume 5, Issue 6, pp. e1000504 - e1000504
Journal Article
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2017, Volume 69, Issue 11, pp. 74 - 74
Results: In the ACS cohort, rs656843 (C-allele) was significantly associated with a higher incidence of PAD during the follow-up (multivariable adjusted hazard... 
Cardiovascular | Internal Medicine | Care and treatment | Cardiac patients | Heart attack | Cardiovascular disease | Heart attacks | Acute coronary syndromes | Health risk assessment
Journal Article
Statistical applications in genetics and molecular biology, ISSN 1544-6115, 2019, Volume 18, Issue 2
Journal Article
Circulation. Cardiovascular genetics, ISSN 1942-325X, 12/2017, Volume 10, Issue 6, pp. e001713 - e001713
Journal Article
by Codd, Veryan and Nelson, Christopher P and Albrecht, Eva and Mangino, Massimo and Deelen, Joris and Buxton, Jessica L and Hottenga, Jouke Jan and Fischer, Krista and Esko, Tõnu and Surakka, Ida and Broer, Linda and Nyholt, Dale R and Leach, Irene Mateo and Salo, Perttu and Hägg, Sara and Matthews, Mary K and Palmen, Jutta and Norata, Giuseppe D and O'Reilly, Paul F and Saleheen, Danish and Amin, Najaf and Balmforth, Anthony J and Beekman, Marian and de Boer, Rudolf A and Böhringer, Stefan and Braund, Peter S and Burton, Paul R and Craen, Anton J Mde and Denniff, Matthew and Dong, Yanbin and Douroudis, Konstantinos and Dubinina, Elena and Eriksson, Johan G and Garlaschelli, Katia and Guo, Dehuang and Hartikainen, Anna-Liisa and Henders, Anjali K and Houwing-Duistermaat, Jeanine J and Kananen, Laura and Karssen, Lennart C and Kettunen, Johannes and Klopp, Norman and Lagou, Vasiliki and van Leeuwen, Elisabeth M and Madden, Pamela A and Mägi, Reedik and Magnusson, Patrik K E and Männistö, Satu and McCarthy, Mark I and Medland, Sarah E and Mihailov, Evelin and Montgomery, Grant W and Oostra, Ben A and Palotie, Aarno and Peters, Annette and Pollard, Helen and Pouta, Anneli and Prokopenko, Inga and Ripatti, Samuli and Salomaa, Veikko and Suchiman, H Eka D and Valdes, Ana M and Verweij, Niek and Viñuela, Ana and Wang, Xiaoling and Wichmann, H-Erich and Widen, Elisabeth and Willemsen, Gonneke and Wright, Margaret J and Xia, Kai and Xiao, Xiangjun and van Veldhuisen, Dirk J and Catapano, Alberico L and Tobin, Martin D and Hall, Alistair S and Blakemore, Alexandra I F and van Gilst, Wiek H and Zhu, Haidong and Erdmann, Jeanette and Reilly, Muredach P and Kathiresan, Sekar and Schunkert, Heribert and Talmud, Philippa J and Pedersen, Nancy L and Perola, Markus and Ouwehand, Willem and Kaprio, Jaakko and Martin, Nicholas G and van Duijn, Cornelia M and Hovatta, Iiris and Gieger, Christian and Metspalu, Andres and Boomsma, Dorret I and Jarvelin, Marjo-Riitta and Slagboom, P Eline and Thompson, John R and Spector, Tim D and van der Harst, Pim and Samani, Nilesh J and CARDIoGRAM consortium and CARDIoGRAM Consortium
Nature genetics, ISSN 1546-1718, 2013, Volume 45, Issue 4, pp. 422 - 427
Journal Article
by Scott, Robert A and Lagou, Vasiliki and Welch, Ryan P and Wheeler, Eleanor and Montasser, May E and Luan, Jian'an and Mägi, Reedik and Strawbridge, Rona J and Rehnberg, Emil and Gustafsson, Stefan and Kanoni, Stavroula and Rasmussen-Torvik, Laura J and Yengo, Loïc and Lecoeur, Cecile and Shungin, Dmitry and Sanna, Serena and Sidore, Carlo and Johnson, Paul C D and Jukema, J Wouter and Johnson, Toby and Mahajan, Anubha and Verweij, Niek and Thorleifsson, Gudmar and Hottenga, Jouke-Jan and Shah, Sonia and Smith, Albert V and Sennblad, Bengt and Gieger, Christian and Salo, Perttu and Perola, Markus and Timpson, Nicholas J and Evans, David M and Pourcain, Beate St and Wu, Ying and Andrews, Jeanette S and Hui, Jennie and Bielak, Lawrence F and Zhao, Wei and Horikoshi, Momoko and Navarro, Pau and Isaacs, Aaron and O'Connell, Jeffrey R and Stirrups, Kathleen and Vitart, Veronique and Hayward, Caroline and Esko, Tõnu and Mihailov, Evelin and Fraser, Ross M and Fall, Tove and Voight, Benjamin F and Raychaudhuri, Soumya and Chen, Han and Lindgren, Cecilia M and Morris, Andrew P and Rayner, Nigel W and Robertson, Neil and Rybin, Denis and Liu, Ching-Ti and Beckmann, Jacques S and Willems, Sara M and Chines, Peter S and Jackson, Anne U and Kang, Hyun Min and Stringham, Heather M and Song, Kijoung and Tanaka, Toshiko and Peden, John F and Goel, Anuj and Hicks, Andrew A and An, Ping and Müller-Nurasyid, Martina and Franco-Cereceda, Anders and Folkersen, Lasse and Marullo, Letizia and Jansen, Hanneke and Oldehinkel, Albertine J and Bruinenberg, Marcel and Pankow, James S and North, Kari E and Forouhi, Nita G and Loos, Ruth J F and Edkins, Sarah and Varga, Tibor V and Hallmans, Göran and Oksa, Heikki and Antonella, Mulas and Nagaraja, Ramaiah and Trompet, Stella and Ford, Ian and Bakker, Stephan J L and Kong, Augustine and Kumari, Meena and Gigante, Bruna and Herder, Christian and Munroe, Patricia B and Caulfield, Mark and Antti, Jula and Mangino, Massimo and Small, Kerrin and Miljkovic, Iva and ... and DIAbetes Genetics Replication and Meta-analysis (DIAGRAM) Consortium and DIAbet Genetics Replication
Nature genetics, ISSN 1546-1718, 2012, Volume 44, Issue 9, pp. 991 - 1005
Journal Article
by Wheeler, Eleanor and Leong, Aaron and Liu, Ching-Ti and Hivert, Marie-France and Strawbridge, Rona J and Podmore, Clara and Li, Man and Yao, Jie and Sim, Xueling and Hong, Jaeyoung and Chu, Audrey Y and Zhang, Weihua and Wang, Xu and Chen, Peng and Maruthur, Nisa M and Porneala, Bianca C and Sharp, Stephen J and Jia, Yucheng and Kabagambe, Edmond K and Chang, Li-Ching and Chen, Wei-Min and Elks, Cathy E and Evans, Daniel S and Fan, Qiao and Giulianini, Franco and Go, Min Jin and Hottenga, Jouke-Jan and Hu, Yao and Jackson, Anne U and Kanoni, Stavroula and Kim, Young Jin and Kleber, Marcus E and Ladenvall, Claes and Lecoeur, Cecile and Lim, Sing-Hui and Lu, Yingchang and Mahajan, Anubha and Marzi, Carola and Nalls, Mike A and Navarro, Pau and Nolte, Ilja M and Rose, Lynda M and Rybin, Denis V and Sanna, Serena and Shi, Yuan and Stram, Daniel O and Takeuchi, Fumihiko and Tan, Shu Pei and van der Most, Peter J and Van Vliet-Ostaptchouk, Jana V and Wong, Andrew and Yengo, Loic and Zhao, Wanting and Goel, Anuj and Martinez Larrad, Maria Teresa and Radke, Dörte and Salo, Perttu and Tanaka, Toshiko and van Iperen, Erik P. A and Abecasis, Goncalo and Afaq, Saima and Alizadeh, Behrooz Z and Bertoni, Alain G and Bonnefond, Amelie and Böttcher, Yvonne and Bottinger, Erwin P and Campbell, Harry and Carlson, Olga D and Chen, Chien-Hsiun and Cho, Yoon Shin and Garvey, W. Timothy and Gieger, Christian and Goodarzi, Mark O and Grallert, Harald and Hamsten, Anders and Hartman, Catharina A and Herder, Christian and Hsiung, Chao Agnes and Huang, Jie and Igase, Michiya and Isono, Masato and Katsuya, Tomohiro and Khor, Chiea-Chuen and Kiess, Wieland and Kohara, Katsuhiko and Kovacs, Peter and Lee, Juyoung and Lee, Wen-Jane and Lehne, Benjamin and Li, Huaixing and Liu, Jianjun and Lobbens, Stephane and Luan, Jian'an and Lyssenko, Valeriya and Meitinger, Thomas and Miki, Tetsuro and Miljkovic, Iva and Moon, Sanghoon and Mulas, Antonella and Müller, Gabriele and ... and EPIC-CVD Consortium and EPIC-InterAct Consortium and Lifelines Cohort Study
PLoS medicine, ISSN 1549-1676, 2017, Volume 14, Issue 9, p. e1002383
Background Glycated hemoglobin (HbA1c) is used to diagnose type 2 diabetes (T2D) and assess glycemic control in patients with diabetes. Previous genome-wide... 
GLYCATED HEMOGLOBIN | MEDICINE, GENERAL & INTERNAL | FASTING PLASMA-GLUCOSE | US POPULATION | VARIANTS | A(1C) | GLYCEMIC TRAITS | LOCI | PREVALENCE | ETHNICITY | ASSOCIATION | Genetic Variation | Diabetes Mellitus, Type 2 - diagnosis | Genome-Wide Association Study | Phenotype | Diabetes Mellitus, Type 2 - genetics | Glycated Hemoglobin A - metabolism | Humans | Risk | Glycated Hemoglobin A - genetics | Diabetes Mellitus, Type 2 - epidemiology | Type 2 diabetes | Analysis | African Americans | Genotype | Diagnosis | Research | Health aspects | Risk factors | Health care | Pediatrics | Dehydrogenases | Populations | Laboratories | Genomics | Genomes | Biology | Glucose | Epidemiology | Medical schools | Incidence | Very large scale | Hemoglobin | Population | Genetics | Glucosephosphate dehydrogenase | Public health | Internal medicine | Diabetes mellitus | Health risks | Preventive medicine | Metabolism | Minority & ethnic groups | Disease control | Disease prevention | Genetic variance | Screening | Hospitals | Gene frequency | Womens health | Alleles | Adults | Diagnostic systems | Diabetes | Clinical medicine | VDP | Klinisk medisinske fag: 750 | Hematologi: 775 | Hematology: 775 | Medisinske Fag: 700 | Clinical medical disciplines: 750 | Medical disciplines: 700 | phenotype | Basic Medicine | Medical and Health Sciences | meta analysis | Medicin och hälsovetenskap | Hemoglobin A, Glycosylated | genetic variation | Klinisk medicin | Medicinsk genetik | Medical Genetics | Clinical Medicine | genetics | Endokrinologi och diabetes | genome-wide association study | Medicinska och farmaceutiska grundvetenskaper | hemoglobin A1c protein, human | Diabetes Mellitus, Type 2 | metabolism | risk | glycosylated hemoglobin | human | Endocrinology and Diabetes
Journal Article