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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 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 Article
by Bentley, Amy R and Sung, Yun J and Brown, Michael R and Winkler, Thomas W and Kraja, Aldi T and Ntalla, Ioanna and Schwander, Karen and Chasman, Daniel I and Lim, Elise and Deng, Xuan and Guo, Xiuqing and Liu, Jingmin and Lu, Yingchang and Cheng, Ching-Yu and Sim, Xueling and Vojinovic, Dina and Huffman, Jennifer E and Musani, Solomon K and Li, Changwei and Feitosa, Mary F and Richard, Melissa A and Noordam, Raymond and Baker, Jenna and Chen, Guanjie and Aschard, Hugues and Bartz, Traci M and Ding, Jingzhong and Dorajoo, Rajkumar and Manning, Alisa K and Rankinen, Tuomo and Smith, Albert V and Tajuddin, Salman M and Zhao, Wei and Graff, Mariaelisa and Alver, Maris and Boissel, Mathilde and Chai, Jin Fang and Chen, Xu and Divers, Jasmin and Evangelou, Evangelos and Gao, Chuan and Goel, Anuj and Hagemeijer, Yanick and Harris, Sarah E and Hartwig, Fernando P and He, Meian and Horimoto, Andrea R. V. R and Hsu, Fang-Chi and Hung, Yi-Jen and Jackson, Anne U and Kasturiratne, Anuradhani and Komulainen, Pirjo and Kühnel, Brigitte and Leander, Karin and Lin, Keng-Hung and Luan, Jian’an and Lyytikäinen, Leo-Pekka and Matoba, Nana and Nolte, Ilja M and Pietzner, Maik and Prins, Bram and Riaz, Muhammad and Robino, Antonietta and Said, M. Abdullah and Schupf, Nicole and Scott, Robert A and Sofer, Tamar and Stancáková, Alena and Takeuchi, Fumihiko and Tayo, Bamidele O and van der Most, Peter J and Varga, Tibor V and Wang, Tzung-Dau and Wang, Yajuan and Ware, Erin B and Wen, Wanqing and Xiang, Yong-Bing and Yanek, Lisa R and Zhang, Weihua and Zhao, Jing Hua and Adeyemo, Adebowale and Afaq, Saima and Amin, Najaf and Amini, Marzyeh and Arking, Dan E and Arzumanyan, Zorayr and Aung, Tin and Ballantyne, Christie and Barr, R. Graham and Bielak, Lawrence F and Boerwinkle, Eric and Bottinger, Erwin P and Broeckel, Ulrich and Brown, Morris and Cade, Brian E and Campbell, Archie and Canouil, Mickaël and Charumathi, Sabanayagam and Chen, Yii-Der Ida and Christensen, Kaare and ... and COGENT-Kidney Consortium and EPIC-InterAct Consortium and Understanding Society Scientific Group and Lifelines Cohort and Understanding Soc Sci Grp and et al
Nature genetics, ISSN 1546-1718, 2019, Volume 51, Issue 4, pp. 636 - 648
Journal Article
by Surendran, Praveen and Drenos, Fotios and Young, Robin and Warren, Helen and Cook, James P and Manning, Alisa K and Grarup, Niels and Sim, Xueling and Barnes, Daniel R and Witkowska, Kate and Staley, James R and Tragante, Vinicius and Tukiainen, Taru and Yaghootkar, Hanieh and Masca, Nicholas and Freitag, Daniel F and Ferreira, Teresa and Giannakopoulou, Olga and Tinker, Andrew and Harakalova, Magdalena and Mihailov, Evelin and Liu, Chunyu and Kraja, Aldi T and Nielsen, Sune Fallgaard and Rasheed, Asif and Samuel, Maria and Zhao, Wei and Bonnycastle, Lori L and Jackson, Anne U and Narisu, Narisu and Swift, Amy J and Southam, Lorraine and Marten, Jonathan and Huyghe, Jeroen R and Stančáková, Alena and Fava, Cristiano and Ohlsson, Therese and Matchan, Angela and Stirrups, Kathleen E and Bork-Jensen, Jette and Gjesing, Anette P and Kontto, Jukka and Perola, Markus and Shaw-Hawkins, Susan and Havulinna, Aki S and Zhang, He and Donnelly, Louise A and Groves, Christopher J and Rayner, N William and Neville, Matt J and Robertson, Neil R and Yiorkas, Andrianos M and Herzig, Karl-Heinz and Kajantie, Eero and Zhang, Weihua and Willems, Sara M and Lannfelt, Lars and Malerba, Giovanni and Soranzo, Nicole and Trabetti, Elisabetta and Verweij, Niek and Evangelou, Evangelos and Moayyeri, Alireza and Vergnaud, Anne-Claire and Nelson, Christopher P and Poveda, Alaitz and Varga, Tibor V and Caslake, Muriel and de Craen, Anton J M and Trompet, Stella and Luan, Jian’an and Scott, Robert A and Harris, Sarah E and Liewald, David C M and Marioni, Riccardo and Menni, Cristina and Farmaki, Aliki-Eleni and Hallmans, Göran and Renström, Frida and Huffman, Jennifer E and Hassinen, Maija and Burgess, Stephen and Vasan, Ramachandran S and Felix, Janine F and Uria-Nickelsen, Maria and Malarstig, Anders and Reilly, Dermot F and Hoek, Maarten and Vogt, Thomas F and Lin, Honghuang and Lieb, Wolfgang and Traylor, Matthew and Markus, Hugh S and Highland, Heather M and Justice, Anne E and Marouli, Eirini and Lindström, Jaana and Uusitupa, Matti and Komulainen, Pirjo and Lakka, Timo A and ... and Wellcome Trust Case Control Consortium and Understanding Society Scientific Group and EchoGen Consortium and GoT2DGenes Consortium and ExomeBP Consortium and EPIC-CVD Consortium and CHD Exome+ Consortium and CHARGE+ Exome Chip Blood Pressure Consortium and CHARGE-Heart Failure Consortium and METASTROKE Consortium and EPIC-InterAct Consortium and Lifelines Cohort Study and GIANT Consortium and T2D-GENES Consortium and Understanding Soc Sci Grp and Wellcome Trust Case Control Consor and CHD Exome Consortium and Giant Consortiumm and CHARGE Exome Chip Blood Pressure C and CHARGE Heart Failure Consortiumm and EchoGen Consortiumm and Metastroke Consortiumm
Nature genetics, ISSN 1546-1718, 2016, Volume 48, Issue 10, pp. 1151 - 1161
Journal Article
by Turcot, Valérie and Lu, Yingchang and Highland, Heather M and Schurmann, Claudia and Justice, Anne E and Fine, Rebecca S and Bradfield, Jonathan P and Esko, Tõnu and Giri, Ayush and Graff, Mariaelisa and Guo, Xiuqing and Hendricks, Audrey E and Karaderi, Tugce and Lempradl, Adelheid and Locke, Adam E and Mahajan, Anubha and Marouli, Eirini and Sivapalaratnam, Suthesh and Young, Kristin L and Alfred, Tamuno and Feitosa, Mary F and Masca, Nicholas G. D and Manning, Alisa K and Medina-Gomez, Carolina and Mudgal, Poorva and Ng, Maggie C. Y and Reiner, Alex P and Vedantam, Sailaja and Willems, Sara M and Winkler, Thomas W and Abecasis, Gonçalo and Aben, Katja K and Alam, Dewan S and Alharthi, Sameer E and Allison, Matthew and Amouyel, Philippe and Asselbergs, Folkert W and Auer, Paul L and Balkau, Beverley and Bang, Lia E and Barroso, Inês and Bastarache, Lisa and Benn, Marianne and Bergmann, Sven and Bielak, Lawrence F and Blüher, Matthias and Boehnke, Michael and Boeing, Heiner and Boerwinkle, Eric and Böger, Carsten A and Bork-Jensen, Jette and Bots, Michiel L and Bottinger, Erwin P and Bowden, Donald W and Brandslund, Ivan and Breen, Gerome and Brilliant, Murray H and Broer, Linda and Brumat, Marco and Burt, Amber A and Butterworth, Adam S and Campbell, Peter T and Cappellani, Stefania and Carey, David J and Catamo, Eulalia and Caulfield, Mark J and Chambers, John C and Chasman, Daniel I and Chen, Yii-Der I and Chowdhury, Rajiv and Christensen, Cramer and Chu, Audrey Y and Cocca, Massimiliano and Collins, Francis S and Cook, James P and Corley, Janie and Corominas Galbany, Jordi and Cox, Amanda J and Crosslin, David S and Cuellar-Partida, Gabriel and D’Eustacchio, Angela and Danesh, John and Davies, Gail and Bakker, Paul I. W and Groot, Mark C. H and Mutsert, Renée and Deary, Ian J and Dedoussis, George and Demerath, Ellen W and Heijer, Martin and Hollander, Anneke I and Ruijter, Hester M and Dennis, Joe G and Denny, Josh C and Di Angelantonio, Emanuele and Drenos, Fotios and Du, Mengmeng and Dubé, Marie-Pierre and Dunning, Alison M and Easton, Douglas F and ... and Chd Exome Consortium and EPIC InterAct Consortium and Global Lipids Genetic Consortium and GoT2D Genes Consortium and MAGIC Investigators and Understanding Soc Sci Grp and ReproGen Consortium and Interval Study and Epic-Cvd Consortium and ExomeBP Consortium and T2D-Genes Consortium and INTERVAL Study and EPIC-CVD Consortium and EPIC InterAct Consortium and CHD Exome+ Consortium and Understanding Society Scientific Group and The MAGIC Investigators
Nature genetics, ISSN 1546-1718, 2017, Volume 50, Issue 1, pp. 26 - 41
Journal Article