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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, 2012, Volume 11, Issue 11, pp. 951 - 962
Journal Article
Nature genetics, ISSN 1546-1718, 2017, Volume 49, Issue 10, pp. 1511 - 1516
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by Nalls, Mike A and Pankratz, Nathan and Lill, Christina M and Do, Chuong B and Hernandez, Dena G and Saad, Mohamad and DeStefano, Anita L and Kara, Eleanna and Bras, Jose and Sharma, Manu and Schulte, Claudia and Keller, Margaux F and Arepalli, Sampath and Letson, Christopher and Edsall, Connor and Stefansson, Hreinn and Liu, Xinmin and Pliner, Hannah and Lee, Joseph H and Cheng, Rong and Ikram, M Arfan and Ioannidis, John P A and Hadjigeorgiou, Georgios M and Bis, Joshua C and Martinez, Maria and Perlmutter, Joel S and Goate, Alison and Marder, Karen and Fiske, Brian and Sutherland, Margaret and Xiromerisiou, Georgia and Myers, Richard H and Clark, Lorraine N and Stefansson, Kari and Hardy, John A and Heutink, Peter and Chen, Honglei and Wood, Nicholas W and Houlden, Henry and Payami, Haydeh and Brice, Alexis and Scott, William K and Gasser, Thomas and Bertram, Lars and Eriksson, Nicholas and Foroud, Tatiana and Singleton, Andrew B and Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI) and GenePD and Hussman Institute of Human Genomics (HIHG) and 23andMe and Greek Parkinson's Disease Consortium and International Parkinson's Disease Genomics Consortium (IPDGC) and Cohorts for Health and Aging Research in Genetic Epidemiology (CHARGE) and United Kingdom Brain Expression Consortium (UKBEC) and NeuroGenetics Research Consortium (NGRC) and The Ashkenazi Jewish Dataset Investigator and North American Brain Expression Consortium (NABEC) and Alzheimer Genetic Analysis Group and IPDG and Ashkenazi Jewish Dataset Investiga and 23AndMe and NABEC and HIHG and Greek Parkinson's Dis Consortium and GParkinson's Study Grp PSG Parkins and NGRC and Alzheimer Genetic Analysis Gr and CHARGE and UKBEC and Ashkenazi Jewish Dataset Investigator
Nature genetics, ISSN 1546-1718, 2014, Volume 46, Issue 9, pp. 989 - 993
Journal Article
Lancet neurology, ISSN 1474-4422, 2015, Volume 14, Issue 10, pp. 1002 - 1009
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
..., Cecile Lecoeur 40, Sing-Hui Lim 41, Yingchang Lu 42,43, Anubha Mahajan 44, Carola Marzi 45,46, Mike A. Nalls 47,48, Pau Navarro 49, Ilja M. Nolte 50, Lynda M. Rose... 
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
by Stewart, S E and Yu, D and Scharf, J M and Neale, B M and Fagerness, J A and Mathews, C A and Arnold, P D and Evans, P D and Gamazon, E R and Osiecki, L and McGrath, L and Haddad, S and Crane, J and Hezel, D and Illman, C and Mayerfeld, C and Konkashbaev, A and Liu, C and Pluzhnikov, A and Tikhomirov, A and Edlund, C K and Rauch, S L and Moessner, R and Falkai, P and Maier, W and Ruhrmann, S and Grabe, H-J and Lennertz, L and Wagner, M and Bellodi, L and Cavallini, M C and Richter, M A and Cook, E H and Kennedy, J L and Rosenberg, D and Stein, D J and Hemmings, S M J and Lochner, C and Azzam, A and Chavira, D A and Fournier, E and Garrido, H and Sheppard, B and Umaña, P and Murphy, D L and Wendland, J R and Veenstra-VanderWeele, J and Denys, D and Blom, R and Deforce, D and Van Nieuwerburgh, F and Westenberg, H G M and Walitza, S and Egberts, K and Renner, T and Miguel, E C and Cappi, C and Hounie, A G and Conceição do Rosário, M and Sampaio, A S and Vallada, H and Nicolini, H and Lanzagorta, N and Camarena, B and Delorme, R and Leboyer, M and Pato, C N and Pato, M T and Voyiaziakis, E and Heutink, P and Cath, D C and Posthuma, D and Smit, J H and Samuels, J and Bienvenu, O J and Cullen, B and Fyer, A J and Grados, M A and Greenberg, B D and McCracken, J T and Riddle, M A and Wang, Y and Coric, V and Leckman, J F and Bloch, M and Pittenger, C and Eapen, V and Black, D W and Ophoff, R A and Strengman, E and Cusi, D and Turiel, M and Frau, F and Macciardi, F and Gibbs, J R and Cookson, M R and Singleton, A and Hardy, J and Crenshaw, A T and Parkin, M A and ... and UK Brain Expression Database and North American Brain Expression Consortium and North Amer Brain Expression Consor
Molecular psychiatry, ISSN 1476-5578, 2012, Volume 18, Issue 7, pp. 788 - 798
Journal Article
Journal Article