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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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Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes.
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Common Genetic Variation in Relation to Brachial Vascular Dimensions and Flow-Mediated Vasodilation.
CIRCULATION-GENOMIC AND PRECISION MEDICINE, 12 (2).
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Cystatin C and Cardiovascular Disease A Mendelian Randomization Study.
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Data Descriptor: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
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(2020)
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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NATURE COMMUNICATIONS, 8 (1).
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(2016)
The genetic architecture of type 2 diabetes.
NATURE, 536 (7614).
41-+.
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Chen, Xu, Gustafsson, Stefan, Whitington, Thomas, Borne, Yan, Lorentzen, Erik, Sun, Jitong, Almgren, Peter, Su, Jun, Karlsson, Robert, Song, Jie et al (show 19 more authors) , Lu, Yi, Zhan, Yiqiang, Hagg, Sara, Svensson, Per, Smedby, Karin E, Slager, Susan L, Ingelsson, Erik, Lindgren, Cecilia M, Morris, Andrew P, Melander, Olle, Karlsson, Thomas, de Faire, Ulf, Caidahl, Kenneth, Engstrom, Gunnar, Lind, Lars, Karlsson, Mikael CI, Pedersen, Nancy L, Frostegard, Johan and Magnusson, Patrik KE
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A genome-wide association study of IgM antibody against phosphorylcholine: shared genetics and phenotypic relationship to chronic lymphocytic leukemia.
HUMAN MOLECULAR GENETICS, 27 (10).
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