PuSH - Publication Server of Helmholtz Zentrum München

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1.
Braenne, I.* et al.: Genomic correlates of glatiramer acetate adverse cardiovascular effects lead to a novel locus mediating coronary risk. PLoS ONE 12:e0182999 (2017)
2.
Power, R.A.* et al.: Genome-wide association for major depression through age at onset stratification: Major depressive disorder working group of the Psychiatric Genomics Consortium. Biol. Psychiatry 81, 325-335 (2017)
3.
LeBlanc, M.* et al.: Identifying novel gene variants in coronary artery disease and shared genes with several cardiovascular risk factors. Circ. Res. 118, 83-94 (2016)
4.
Pattaro, C.* et al.: Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat. Commun. 7:10023 (2016)
5.
Zhao, Y.* et al.: Network-based identification and prioritization of key regulators of coronary artery disease loci. Arterioscler. Thromb. Vasc. Biol. 36, 928-941 (2016)
6.
Asl, H.F.* et al.: Expression quantitative trait loci acting across multiple tissues are enriched in inherited risk for coronary artery disease. Circ. Cardiovasc. Genet. 8, 305-315 (2015)
7.
Ghosh, S.* et al.: Systems genetics analysis of genome-wide association study reveals novel associations between key biological processes and coronary artery disease. Arterioscler. Thromb. Vasc. Biol. 35, 1712-1722 (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.
Kaess, B.M.* et al.: Circulating brain-derived neurotrophic factor concentrations and the risk of cardiovascular disease in the community. J. Am. Heart Assoc. 4:e001544 (2015)
10.
Almontashiri, N.* et al.: SPG7 variant escapes phosphorylation-regulated processing by AFG3L2, elevates mitochondrial ROS, and is associated with multiple clinical phenotypes. Cell Rep. 7, 834-847 (2014)
11.
Dichgans, M.* et al.: Shared genetic susceptibility to ischemic stroke and coronary artery disease: A genome-wide analysis of common variants. Stroke 45, 24-36 (2014)
12.
Hartiala, J.* et al.: Comparative genome-wide association studies in mice and humans for trimethylamine N-oxide, a proatherogenic metabolite of choline and l-carnitine. Arterioscler. Thromb. Vasc. Biol. 34, 1307-1313 (2014)
13.
Holmes, M.V.* et al.: Novel genetic approach to investigate the role of plasma secretory phospholipase A2 (sPLA(2))-V isoenzyme in coronary heart disease modified mendelian randomization analysis using PLA2G5 expression levels. Circ. Cardiovasc. Genet. 7, 144-150 (2014)
14.
Codd, V.* et al.: Identification of seven loci affecting mean telomere length and their association with disease. Nat. Genet. 45, 422-427 (2013)
15.
Dastani, Z.* et al.: The shared allelic architecture of adiponectin levels and coronary artery disease. Atherosclerosis 229, 145-148 (2013)
16.
den Hoed, M.* et al.: Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat. Genet. 45, 621-631 (2013)
17.
Erdmann, J.* et al.: Dysfunctional nitric oxide signalling increases risk of myocardial infarction. Nature 504, 432-436 (2013)
18.
Ganesh, S.K.* et al.: Loci influencing blood pressure identified using a cardiovascular gene-centric array. Hum. Mol. Genet. 22, 1663-1678 (2013)
19.
Ho, J.E.* et al.: Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling. J. Clin. Invest. 123, 4208-4218 (2013)
20.
Köttgen, A.* et al.: Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nat. Genet. 45, 145-154 (2013)