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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.
Böger, C.A.* et al.: NFAT5 and SLC4A10 loci associate with plasma osmolality. J. Am. Soc. Nephrol. 28, 2311-2321 (2017)
3.
Flannick, J.* et al.: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Sci. Data 4:170179 (2017)
4.
Manning, A.* et al.: A low-frequency inactivating Akt2 variant enriched in the Finnish population is associated with fasting insulin levels and type 2 diabetes risk. Diabetes 66, 2019-2032 (2017)
5.
Fuchsberger, C.* et al.: The genetic architecture of type 2 diabetes. Nature 536, 41-47 (2016)
6.
Lange, L.A.* et al.: Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. Am. J. Hum. Genet. 94, 233-245 (2014)
7.
Ng, M.C.Y.* et al.: Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes. PLoS Genet. 10:e100451 (2014)
8.
Ganesh, S.K.* et al.: Loci influencing blood pressure identified using a cardiovascular gene-centric array. Hum. Mol. Genet. 22, 1663-1678 (2013)
9.
Asselbergs, F.W.* et al.: Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. Am. J. Hum. Genet. 91, 823-838 (2012)
10.
Wassel, C.L.* et al.: Genetic determinants of the ankle-brachial index: A meta-analysis of a cardiovascular candidate gene 50K SNP panel in the Candidate gene Association Resource (CARe) consortium. Atherosclerosis 222, 138-147 (2012)
11.
Fox, E.R.* et al.: Association of genetic variation with systolic and diastolic blood pressure among African Americans: The Candidate Gene Association Resource study. Hum. Mol. Genet. 20, 2273-2284 (2011)
12.
Teslovich, T.M.* et al.: Biological, clinical and population relevance of 95 loci for blood lipids. Nature 466, 707-713 (2010)