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1.
Flannick, J.* et al.: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Sci. Data 5:180002 (2018)
2.
Flannick, J.* et al.: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Sci. Data 4:170179 (2017)
3.
Scott, R.A.* et al.: An expanded genome-wide association study of type 2 diabetes in Europeans. Diabetes 66, 2888-2902 (2017)
4.
Ehret, G.B.* et al.: The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nat. Genet. 48, 1171-1184 (2016)
5.
Fuchsberger, C.* et al.: The genetic architecture of type 2 diabetes. Nature 536, 41-47 (2016)
6.
Keenan, T.* et al.: Causal assessment of serum urate levels in cardiometabolic diseases through a mendelian randomization study. J. Am. Coll. Cardiol. 67, 407-416 (2016)
7.
Gaulton, K.J.* et al.: Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci. Nat. Genet. 47, 1415-1425 (2015)
8.
Jansen, H.* et al.: Genetic variants primarily associated with type 2 diabetes are related to coronary artery disease risk. Atherosclerosis 241, 419-426 (2015)
9.
Flannick, J.* et al.: Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. Nat. Genet. 46, 357-363 (2014)
10.
Kraja, A.T.* et al.: Pleiotropic genes for metabolic syndrome and inflammation. Mol. Genet. Metab. 112, 317-338 (2014)
11.
Global Lipids Genetics Consortium et al.: Discovery and refinement of loci associated with lipid levels. Nat. Genet. 45, 1274-1283 (2013)
12.
Deloukas, P.* et al.: Large-scale association analysis identifies new risk loci for coronary artery disease. Nat. Genet. 45, 25-35 (2013)
13.
Do, R.* et al.: Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat. Genet. 45, 1345-1352 (2013)
14.
Billings, L.K.* et al.: Impact of common variation in bone-related genes on type 2 diabetes and related traits. Diabetes 61, 2176-2186 (2012)
15.
Ellinor, P.T.* et al.: Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat. Genet. 44, 670-675 (2012)
16.
Manning, A.K.* et al.: A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Nat. Genet. 44, 659-669 (2012)
17.
Morris, A.P.* et al.: Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat. Genet. 44, 981-990 (2012)
18.
O'Donnell, C.J.* et al.: Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction. Circulation 124, 2855-2864 (2012)
19.
Perry, J.R.* et al.: Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases. PLoS Genet. 8:e1002741 (2012)
20.
Saxena, R.* et al.: Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. Am. J. Hum. Genet. 90, 410-425 (2012)