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Data Descriptor: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
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Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
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NATURE GENETICS, 50 (1).
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Rare and low-frequency coding variants alter human adult height.
NATURE, 542 (7640).
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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.
NATURE GENETICS, 50 (4).
559-571+.
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Flannick, Jason, Fuchsberger, Christian, Mahajan, Anubha, Teslovich, Tanya M, Agarwala, Vineeta, Gaulton, Kyle J, Caulkins, Lizz, Koesterer, Ryan, Ma, Clement, Moutsianas, Loukas et al (show 291 more authors) , McCarthy, Davis J, Rivas, Manuel A, Perry, John RB, Sim, Xueling, Blackwell, Thomas W, Robertson, Neil R, Rayner, N William, Cingolani, Pablo, Locke, Adam E, Tajes, Juan Fernandez, Highland, Heather M, Dupuis, Josee, Chines, Peter S, Lindgren, Cecilia M, Hartl, Christopher, Jackson, Anne U, Chen, Han, Huyghe, Jeroen R, van de Bunt, Martijn, Pearson, Richard D, Kumar, Ashish, Mueller-Nurasyid, Martina, Grarup, Niels, Stringham, Heather M, Gamazon, Eric R, Lee, Jaehoon, Chen, Yuhui, Scott, Robert A, Below, Jennifer E, Chen, Peng, Huang, Jinyan, Go, Min Jin, Stitzel, Michael L, Pasko, Dorota, Parker, Stephen CJ, Varga, Tibor V, Green, Todd, Beer, Nicola L, Day-Williams, Aaron G, Ferreira, Teresa, Fingerlin, Tasha, Horikoshi, Momoko, Hu, Cheng, Huh, Iksoo, Ikram, Mohammad Kamran, 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SCIENTIFIC DATA, 5 (1).
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Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.
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A common missense variant of LILRB5 is associated with statin intolerance and myalgia.
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3569-3U31.
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The genetic architecture of type 2 diabetes.
NATURE, 536 (7614).
41-+.
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Siddiqui, Moneeza Kalhan, Veluchamy, Abirami, Maroteau, Cyrielle, Tavendale, Roger, Carr, Fiona, Pearson, Ewan, Colhoun, Helen, Morris, Andrew D, George, Jacob, Doney, Alexander et al (show 7 more authors) , Pirmohamed, Munir ORCID: 0000-0002-7534-7266, Alfirevic, Ana ORCID: 0000-0002-2801-9817, Wadelius, Mia, van der Zee, Anke H Maitland, Ridker, Paul M, Chasman, Daniel I and Palmer, Colin NA
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<i>CKM</i> Glu83Gly Is Associated With Blunted Creatine Kinase Variation, but Not With Myalgia.
CIRCULATION-CARDIOVASCULAR GENETICS, 10 (4).
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