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2020
Mark Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis
Vujkovic, Marijana ; Melander, Olle ^LU and Saleheen, Danish (2020) In Nature Genetics 52(7). p.680-691
- Contribution to journal › Article
2017
Mark Exome-wide association study of plasma lipids in >300,000 individuals
Liu, Dajiang J ; Peloso, Gina M. ; Yu, Haojie ; Butterworth, Adam S. ; Mahajan, Anubha ; Saleheen, Danish ; Franks, Paul ^LU ; Renström, Frida ^LU ; V Varga, Tibor ^LU and Groop, Leif ^LU , et al. (2017) In Nature Genetics 49(12). p.1758-1766
- Contribution to journal › Article
Mark Genetic variation at 16q24.2 is associated with small vessel stroke
Traylor, Matthew ; Malik, Rainer ; Nalls, Mike A. ; Cotlarciuc, Ioana ; Radmanesh, Farid ; Thorleifsson, Gudmar ; Hanscombe, Ken B. ; Langefeld, Carl D. ; Saleheen, Danish and Rost, Natalia S. , et al. (2017) In Annals of Neurology 81(3). p.383-394
- Contribution to journal › Article
Mark New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals
Kraja, Aldi T. ; Cook, James P. ; Warren, Helen R. ; Surendran, Praveen ; Liu, Chunyu ; Evangelou, Evangelos ; Manning, Alisa K. ; Grarup, Niels ; Drenos, Fotios and Sim, Xueling , et al. (2017) In Circulation: Cardiovascular Genetics 10(5).
- 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 Low-frequency and common genetic variation in ischemic stroke : The METASTROKE collaboration
Malik, Rainer ; Traylor, Matthew ; Pulit, Sara L ; Bevan, Steve ; Hopewell, Jemma C ; Holliday, Elizabeth G ; Zhao, Wei ; Abrantes, Patricia ; Amouyel, Philippe and Attia, John R , et al. (2016) In Neurology 86(13). p.26-1217
- Contribution to journal › Article
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 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
Mark A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease
Scott, Robert A. ; Freitag, Daniel F. ; Li, Li ^LU ; Chu, Audrey Y. ; Surendran, Praveen ; Young, Robin ; Grarup, Niels ; Stancáková, Alena ; Chen, Yuning and Varga, Tibor V. ^LU , et al. (2016) In Science Translational Medicine 8(341).
- Contribution to journal › Article
Mark Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Surendran, Praveen ; Drenos, Fotios ; Young, Robin ; Warren, Helen ; Cook, James P. ; Manning, Alisa K. ; Grarup, Niels ; Sim, Xueling ; Barnes, Daniel R. and Witkowska, Kate , et al. (2016) In Nature Genetics 48(10). p.1151-1161
- Contribution to journal › Article

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