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2019
Mark Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Teumer, Alexander ; Li, Yong ; Ghasemi, Sahar ; Prins, Bram P. ; Wuttke, Matthias ; Hermle, Tobias ; Giri, Ayush ; Sieber, Karsten B. ; Qiu, Chengxiang and Kirsten, Holger , et al. (2019) In Nature Communications 10(1).
- Contribution to journal › Article
2017
Mark Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation : The AFGen Consortium
Weng, Lu Chen ; Lunetta, Kathryn L ; Müller-Nurasyid, Martina ; Smith, Albert Vernon ; Thériault, Sébastien ; Weeke, Peter E. ; Barnard, John ; Bis, Joshua C. ; Lyytikäinen, Leo-Pekka and Kleber, Marcus E , et al. (2017) In Scientific Reports 7(1).
- Contribution to journal › Article
Mark Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
Webb, Thomas R. ; Erdmann, Jeanette ; Stirrups, Kathleen E. ; Stitziel, Nathan O. ; Masca, Nicholas G D ; Jansen, Henning ; Kanoni, Stavroula ; Nelson, Christopher P ; Ferrario, Paola G. and König, Inke R. , et al. (2017) In Journal of the American College of Cardiology 69(7). p.823-836
- Contribution to journal › Article
2016
Mark Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2.
Cheng, Yu-Ching ; Stanne, Tara M ; Giese, Anne-Katrin ; Ho, Weang Kee ; Traylor, Matthew ; Amouyel, Philippe ; Holliday, Elizabeth G ; Malik, Rainer ; Xu, Huichun and Kittner, Steven J , et al. (2016) In Stroke: a journal of cerebral circulation 47(2). p.307-316
- Contribution to journal › Article
Mark Analysis with the exome array identifies multiple new independent variants in lipid loci
Kanoni, Stavroula ; Masca, Nicholas G D ; Stirrups, Kathleen E. ; Varga, Tibor V. ^LU ; Warren, Helen R ; Scott, Robert A. ; Southam, Lorraine ; Zhang, Weihua ; Yaghootkar, Hanieh and Müller-Nurasyid, Martina , et al. (2016) In Human Molecular Genetics 25(18). p.4094-4106
- Contribution to journal › Article
Mark Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease
Stitziel, Nathan O. ; Stirrups, Kathleen E. ; Masca, Nicholas G D ; Erdmann, Jeanette ; Ferrario, Paola G. ; König, Inke R. ; Weeke, Peter E. ; Webb, Thomas R. ; Auer, Paul L. and Schick, Ursula M. , et al. (2016) In New England Journal of Medicine 374(12). p.1134-1144
- Contribution to journal › Article
2015
Mark Harmonising and linking biomedical and clinical data across disparate data archives to enable integrative cross-biobank research.
Spjuth, Ola ; Krestyaninova, Maria ; Hastings, Janna ; Shen, Huei-Yi ; Heikkinen, Jani ; Waldenberger, Melanie ; Langhammer, Arnulf ; Ladenvall, Claes ^LU ; Esko, Tõnu and Persson, Mats-Åke ^LU , et al. (2015) In European Journal of Human Genetics
- Contribution to journal › Article
Mark Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.
Kato, Norihiro ; Loh, Marie ; Takeuchi, Fumihiko ; Verweij, Niek ; Wang, Xu ; Zhang, Weihua ; Kelly, Tanika N ; Saleheen, Danish ; Lehne, Benjamin and Leach, Irene Mateo , et al. (2015) In Nature Genetics 47(11). p.93-1282
- Contribution to journal › Article
Mark The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.
Winkler, Thomas W ; Justice, Anne E ; Graff, Mariaelisa ; Barata, Llilda ; Feitosa, Mary F ; Chu, Su ; Czajkowski, Jacek ; Esko, Tõnu ; Fall, Tove and Kilpeläinen, Tuomas O , et al. (2015) In PLoS Genetics 11(10).
- Contribution to journal › Article
2014
Mark Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
Arking, Dan E ; Pulit, Sara L ; Crotti, Lia ; van der Harst, Pim ; Munroe, Patricia B ; Koopmann, Tamara T ; Sotoodehnia, Nona ; Rossin, Elizabeth J ; Morley, Michael and Wang, Xinchen , et al. (2014) In Nature Genetics 46(8). p.826-836
- Contribution to journal › Article

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