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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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Ligthart, Symen, Vaez, Ahmad, Vosa, Urmo, Stathopoulou, Maria G, de Vries, Paul S, Prins, Bram P, Van der Most, Peter J, Tanaka, Toshiko, Naderi, Elnaz, Rose, Lynda M et al (show 276 more authors) , Wu, Ying, Karlsson, Robert, Barbalic, Maja, Lin, Honghuang, Pool, Rene, Zhu, Gu, Mace, Aurelien, Sidore, Carlo, Trompet, Stella, Mangino, Massimo, Sabater-Lleal, Maria, Kemp, John P, Abbasi, Ali, Kacprowski, Tim, Verweij, Niek, Smith, Albert V, Huang, Tao, Marzi, Carola, Feitosa, Mary F, Lohman, Kurt K, Kleber, Marcus E, Milaneschi, Yuri, Mueller, Christian, Huq, Mahmudul, Vlachopoulou, Efthymia, Lyytikainen, Leo-Pekka, Oldmeadow, Christopher, Deelen, Joris, Perola, Markus, Zhao, Jing Hua, Feenstra, Bjarke, Amini, Marzyeh, Lahti, Jari, Schraut, Katharina E, Fornage, Myriam, Suktitipat, Bhoom, Chen, Wei-Min, Li, Xiaohui, Nutile, Teresa, Malerba, Giovanni, Luan, Jian'an, Bak, Tom, Schork, Nicholas, Del Greco, Fabiola M, Thiering, Elisabeth, Mahajan, Anubha, Marioni, Riccardo E, Mihailov, 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Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.
AMERICAN JOURNAL OF HUMAN GENETICS, 103 (5).
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Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies <i>BCL2</i> and <i>FAM19A2</i> as Novel Insulin Sensitivity Loci.
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Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.
Nature Communications, 11 (1).
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A catalog of genetic loci associated with kidney function from analyses of a million individuals.
NATURE GENETICS, 51 (6).
957-+.
Collapse authors list.
Zeng, Lingyao, Moser, Sylvain, Mirza-Schreiber, Nazanin, Lamina, Claudia, Coassin, Stefan, Nelson, Christopher P, Annilo, Tarmo, Franzen, Oscar, Kleber, Marcus E, Mack, Salome et al (show 25 more authors) , Andlauer, Till FM, Jiang, Beibei, Stiller, Barbara, Li, Ling, Willenborg, Christina, Munz, Matthias, Kessler, Thorsten, Kastrati, Adnan, Laugwitz, Karl-Ludwig, Erdmann, Jeanette, Moebus, Susanne, Noethen, Markus M, Peters, Annette, Strauch, Konstantin, Mueller-Nurasyid, Martina, Gieger, Christian, Meitinger, Thomas, Steinhagen-Thiessen, Elisabeth, Maerz, Winfried, Metspalu, Andres, Bjoerkegren, Johan LM, Samani, Nilesh J, Kronenberg, Florian, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X and Schunkert, Heribert
(2022)
<i>Cis</i>-epistasis at the <i>LPA</i> locus and risk of cardiovascular diseases.
CARDIOVASCULAR RESEARCH, 118 (4).
pp. 1088-1102.