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Sapkota, Yadav, De Vivo, Immaculata, Steinthorsdottir, Valgerdur, Fassbender, Amelie, Bowdler, Lisa, Buring, Julie E, Edwards, Todd L, Jones, Sarah, Dorien, O, Peterse, Danielle et al (show 15 more authors) , Rexrode, Kathryn M, Ridker, Paul M, Schork, Andrew J, Thorleifsson, Gudmar, Wallace, Leanne M, Kraft, Peter, Morris, Andrew P, Nyholt, Dale R, Edwards, Digna R Velez, Nyegaard, Mette, D'Hooghe, Thomas, Chasman, Daniel I, Stefansson, Kari, Missmer, Stacey A and Montgomery, Grant W
(2017)
Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry.
SCIENTIFIC REPORTS, 7 (1).
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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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Surendran, Praveen, Feofanova, Elena V, Lahrouchi, Najim, Ntalla, Ioanna, Karthikeyan, Savita, Cook, James, Chen, Lingyan, Mifsud, Borbala, Yao, Chen, Kraja, Aldi T et al (show 271 more authors) , Cartwright, James H, Hellwege, Jacklyn N, Giri, Ayush, Tragante, Vinicius, Thorleifsson, Gudmar, Liu, Dajiang J, Prins, Bram P, Stewart, Isobel D, Cabrera, Claudia P, Eales, James M, Akbarov, Artur, Auer, Paul L, Bielak, Lawrence F, Bis, Joshua C, Braithwaite, Vickie S, Brody, Jennifer A, Daw, E Warwick, Warren, Helen R, Drenos, Fotios, Nielsen, Sune Fallgaard, Faul, Jessica D, Fauman, Eric B, Fava, Cristiano, Ferreira, Teresa, Foley, Christopher N, Franceschini, Nora, Gao, He, Giannakopoulou, Olga, Giulianini, Franco, Gudbjartsson, Daniel F, Guo, Xiuqing, Harris, Sarah E, Havulinna, Aki S, Helgadottir, Anna, Huffman, Jennifer E, Hwang, Shih-Jen, Kanoni, Stavroula, Kontto, Jukka, Larson, Martin G, Li-Gao, Ruifang, Lindstrom, Jaana, Lotta, Luca A, Lu, Yingchang, Luan, Jian'an, Mahajan, Anubha, 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NATURE GENETICS, 52 (12).
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Exome-wide association study of plasma lipids in >300,000 individuals.
NATURE GENETICS, 49 (12).
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Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Nature Genetics, 50 (10).
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Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.
NATURE COMMUNICATIONS, 8 (1).
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Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.
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AMERICAN JOURNAL OF HUMAN GENETICS, 102 (3).
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Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.
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Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism.
NATURE COMMUNICATIONS, 8 (1).
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Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.
NATURE GENETICS, 51 (4).
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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.
NATURE GENETICS, 50 (4).
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Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.
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A catalog of genetic loci associated with kidney function from analyses of a million individuals.
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(2017)
A common missense variant of LILRB5 is associated with statin intolerance and myalgia.
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The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions.
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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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A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape.
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