PuSH - Publication Server of Helmholtz Zentrum München

360 Records found.
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21.
Aumann, N.* et al.: Regional variation of chronic kidney disease in Germany: Results from two population-based surveys. Kidney Blood Press. Res. 40, 231-243 (2015)
22.
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)
23.
Hägg, S.* et al.: Adiposity as a cause of cardiovascular disease: A Mendelian randomization study. Int. J. Epidemiol. 44, 578-586 (2015)
24.
Horikoshi, M.* et al.: Discovery and fine-mapping of glycaemic and obesity-related trait loci using high-density imputation. PLoS Genet. 11:e1005230 (2015)
25.
Huffman, J.E.* et al.: Modulation of genetic associations with serum urate levels by body-mass-index in humans. PLoS ONE 10:e0119752 (2015)
26.
Jansen, H.* et al.: Genetic variants primarily associated with type 2 diabetes are related to coronary artery disease risk. Atherosclerosis 241, 419-426 (2015)
27.
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)
28.
Vogt, S. et al.: Neighborhood and healthy aging in a German city: Distances to green space and senior service centers and their associations with physical constitution, disability, and health-related quality of life. Eur. J. Ageing 12, 273-283 (2015)
29.
Winkler, T.W.* et al.: The influence of age and sex on genetic associations with adult body size and shape: A large-scale genome-wide interaction study. PLoS Genet. 11:e1005378 (2015)
30.
Albrecht, E. et al.: Metabolite profiling reveals new insights into the regulation of serum urate in humans. Metabolomics 10, 141-151 (2014)
31.
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)
32.
Bidlingmaier, M. et al.: Reference intervals for Insulin-like Growth Factor-1 (IGF-1) from birth to senescence: Results from a multicenter study using a new automated chemiluminescence IGF-1 immunoassay conforming to recent international recommendations. J. Clin. Endocrinol. Metab. 9, 1712-1721 (2014)
33.
Budin-Ljosne, I.* et al.: Data sharing in large research consortia: Experiences and recommendations from ENGAGE. Eur. J. Hum. Genet. 22, 317-321 (2014)
34.
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)
35.
Ferrario, M.M.* et al.: The contribution of educational class in improving accuracy of cardiovascular risk prediction across European regions: The MORGAM Project Cohort Component. Heart 100, 1179-1187 (2014)
36.
Friedrich, N.* et al.: Age- and sex-specific reference intervals across life span for Insulin-like Growth Factor Binding Protein 3 (IGFBP-3) and the IGF-i to IGFBP-3 ratio measured by new automated chemiluminescence assays. J. Clin. Endocrinol. Metab. 99, 1675-1686 (2014)
37.
Ganesh, S.K.* et al.: Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations. Am. J. Hum. Genet. 95, 49-65 (2014)
38.
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)
39.
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)
40.
Kraja, A.T.* et al.: Pleiotropic genes for metabolic syndrome and inflammation. Mol. Genet. Metab. 112, 317-338 (2014)