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Pulit, Sara L, Weng, Lu-Chen, McArdle, Patrick F, Trinquart, Ludovic, Choi, Seung Hoan, Mitchell, Braxton D, Rosand, Jonathan, de Bakker, Paul IW, Benjamin, Emelia J, Ellinor, Patrick T et al (show 351 more authors) , Kittner, Steven J, Lubitz, Steven A, Anderson, Christopher D, Christophersen, Ingrid E, Rienstra, Michiel, Roselli, Carolina, Yin, Xiaoyan, Geelhoed, Bastiaan, Barnard, John, Lin, Honghuang, Arking, Dan E, Smith, Albert V, Albert, Christine M, Chaffin, Mark, Tucker, Nathan R, Li, Molong, Klarin, Derek, Bihlmeyer, Nathan A, Low, Siew-Kee, Weeke, Peter E, Mueller-Nurasyid, Martina, Smith, J Gustav, Brody, Jennifer A, Niemeijer, Maartje N, Doerr, Marcus, Trompet, Stella, Huffman, Jennifer, Gustafsson, Stefan, Schurmann, Claudia, Kleber, Marcus E, Lyytikainen, Leo-Pekka, Seppala, Ilkka, Malik, Rainer, Horimoto, Andrea RVR, Perez, Marco, Sinisalo, Juha, Aeschbacher, Stefanie, Theriault, Sebastien, Yao, Jie, Radmanesh, Farid, Weiss, Stefan, Teumer, Alexander, Clauss, Sebastian, 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(2018)
Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes.
NEUROLOGY-GENETICS, 4 (6).
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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, De Bunt, Martijn Van, Pearson, Richard D, Kumar, Ashish, Muller-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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(2017)
Data Descriptor: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
SCIENTIFIC DATA, 4 (1).
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Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
NATURE GENETICS, 52 (12).
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An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.
DIABETES, 66 (11).
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Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.
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(2016)
The genetic architecture of type 2 diabetes.
NATURE, 536 (7614).
41-+.