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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 Genomic correlates of glatiramer acetate adverse cardiovascular effects lead to a novel locus mediating coronary risk
Brænne, Ingrid ; Zeng, Lingyao ; Willenborg, Christina ; Tragante, Vinicius ; Kessler, Thorsten ; Willer, Cristen J ; Laakso, Markku ; Wallentin, Lars ^LU ; Franks, Paul W ^LU and Salomaa, Veikko , et al. (2017) In PLoS ONE 12(8). p.0182999-0182999
- Contribution to journal › Article
Mark A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors
Brænne, Ingrid ; Willenborg, Christina ; Tragante, Vinicius ; Kessler, Thorsten ; Zeng, Lingyao ; Reiz, Benedikt ; Kleinecke, Mariana ; Von Ameln, Simon ; Willer, Cristen J and Laakso, Markku , 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 NEK1 mutations in familial amyotrophic lateral sclerosis.
Brenner, David ; Müller, Kathrin ; Wieland, Thomas ; Weydt, Patrick ; Böhm, Sarah ; Lulé, Dorothée ; Hübers, Annemarie ; Neuwirth, Christoph ; Weber, Markus and Borck, Guntram , et al. (2016) In Brain 139(5).
- Contribution to journal › Letter
Mark A reference panel of 64,976 haplotypes for genotype imputation
McCarthy, Shane ; Das, Sayantan ; Kretzschmar, Warren ; Delaneau, Olivier ; Wood, Andrew R. ; Teumer, Alexander ; Kang, Hyun Min ; Fuchsberger, Christian ; Danecek, Petr and Sharp, Kevin , et al. (2016) In Nature Genetics 48(10). p.1279-1283
- 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 A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease
Nikpay, Majid ; Goel, Anuj ; Won, Hong-Hee ; Hall, Leanne M. ; Willenborg, Christina ; Kanoni, Stavroula ; Saleheen, Danish ; Kyriakou, Theodosios ; Nelson, Christopher P. and Hopewell, Jemma C. , et al. (2015) In Nature Genetics 47(10). p.1121-1121
- 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
2014
Mark Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.
Flannick, Jason ; Thorleifsson, Gudmar ; Beer, Nicola L ; Jacobs, Suzanne B R ; Grarup, Niels ; Burtt, Noël P ; Mahajan, Anubha ; Fuchsberger, Christian ; Atzmon, Gil and Benediktsson, Rafn , et al. (2014) In Nature Genetics 46(4). p.357-357
- Contribution to journal › Article

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