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BMC bioinformatics, ISSN 1471-2105, 2017, Volume 18, Issue 1, pp. 429 - 8
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
Journal of the American College of Cardiology, ISSN 0735-1097, 2014, Volume 63, Issue 12, pp. 1200 - 1210
Journal Article
by Graff, Mariaelisa and Scott, Robert A and Justice, Anne E and Young, Kristin L and Feitosa, Mary F and Barata, Llilda and Winkler, Thomas W and Chu, Audrey Y and Mahajan, Anubha and Hadley, David and Xue, Luting and Workalemahu, Tsegaselassie and Heard-Costa, Nancy L and den Hoed, Marcel and Ahluwalia, Tarunveer S and Qi, Qibin and Ngwa, Julius S and Renström, Frida and Quaye, Lydia and Eicher, John D and Hayes, James E and Cornelis, Marilyn and Kutalik, Zoltan and Lim, Elise and Luan, Jian’an and Huffman, Jennifer E and Zhang, Weihua and Zhao, Wei and Griffin, Paula J and Haller, Toomas and Ahmad, Shafqat and Marques-Vidal, Pedro M and Bien, Stephanie and Yengo, Loic and Teumer, Alexander and Smith, Albert Vernon and Kumari, Meena and Harder, Marie Neergaard and Justesen, Johanne Marie and Kleber, Marcus E and Hollensted, Mette and Lohman, Kurt and Rivera, Natalia V and Whitfield, John B and Zhao, Jing Hua and Stringham, Heather M and Lyytikäinen, Leo-Pekka and Huppertz, Charlotte and Willemsen, Gonneke and Peyrot, Wouter J and Wu, Ying and Kristiansson, Kati and Demirkan, Ayse and Fornage, Myriam and Hassinen, Maija and Bielak, Lawrence F and Cadby, Gemma and Tanaka, Toshiko and Mägi, Reedik and van der Most, Peter J and Jackson, Anne U and Bragg-Gresham, Jennifer L and Vitart, Veronique and Marten, Jonathan and Navarro, Pau and Bellis, Claire and Pasko, Dorota and Johansson, Åsa and Snitker, Søren and Cheng, Yu-Ching and Eriksson, Joel and Lim, Unhee and Aadahl, Mette and Adair, Linda S and Amin, Najaf and Balkau, Beverley and Auvinen, Juha and Beilby, John and Bergman, Richard N and Bergmann, Sven and Bertoni, Alain G and Blangero, John and Bonnefond, Amélie and Bonnycastle, Lori L and Borja, Judith B and Brage, Søren and Busonero, Fabio and Buyske, Steve and Campbell, Harry and Chines, Peter S and Collins, Francis S and Corre, Tanguy and Smith, George Davey and Delgado, Graciela E and Dueker, Nicole and Dörr, Marcus and Ebeling, Tapani and Eiriksdottir, Gudny and Esko, Tõnu and Faul, Jessica D and ... and PAGE Consortium and EPIC-InterAct Consortium and CHARGE Consortium and Institute of Neuroscience and Physiology and Göteborgs universitet and Gothenburg University and Institutionen för medicin, avdelningen för invärtesmedicin och klinisk nutrition and Sahlgrenska Academy and Centre for Bone and Arthritis Research and Sahlgrenska akademin and Institute of Medicine, Department of Internal Medicine and Clinical Nutrition and Institutionen för neurovetenskap och fysiologi
PLoS genetics, ISSN 1553-7404, 2017, Volume 13, Issue 4, p. e1006528
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, 2018, Volume 13, Issue 11, p. e0206554
Background and purpose Polymorphisms in coagulation genes have been associated with early-onset ischemic stroke. Here we pursue an a priori hypothesis that... 
YOUNG-ADULTS | MORTALITY | POPULATION | FACTOR-V-LEIDEN | POLYMORPHISMS | METAANALYSIS | MYOCARDIAL-INFARCTION | MULTIDISCIPLINARY SCIENCES | CLASSIFICATION | MECHANISMS | GENOME-WIDE ASSOCIATION | Brain Ischemia - epidemiology | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Genetic Association Studies | Humans | Middle Aged | Brain Ischemia - genetics | African Americans - genetics | Male | Endothelial Protein C Receptor - genetics | Case-Control Studies | Stroke - genetics | Young Adult | Adolescent | Age of Onset | Adult | Female | Stroke - epidemiology | Polymorphism, Single Nucleotide | Thrombomodulin - genetics | Stroke (Disease) | Genetic variation | African Americans | Genetic aspects | Research | Health aspects | Endothelium | Membrane proteins | Heart attacks | Coagulation | Population studies | Cardiovascular disease | Genomes | Single-nucleotide polymorphism | Risk factors | Proteins | Receptors | Ischemia | Pruning | Genetics | Thrombomodulin | Age | Stroke | Health risks | Protein C | Genetic diversity | Risk analysis | Minority & ethnic groups | Endothelial cells | Medicine | Hospitals | Replication | Health risk assessment | Age composition | Neurologi | Endothelial Protein C Receptor | Brain Ischemia | European Continental Ancestry Group | Single Nucleotide | Neurology | epidemiology | genetics | Polymorphism
Journal Article
Journal Article