PuSH - Publication Server of Helmholtz Zentrum München

14 Records found.
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1.
Laaksonen, J.* et al.: Discovery of mitochondrial DNA variants associated with genome-wide blood cell gene expression: A population-based mtDNA sequencing study. Hum. Mol. Genet. 28, 1381-1391 (2019)
2.
Mononen, N.* et al.: Whole blood microRNA levels associate with glycemic status and correlate with target mRNAs in pathways important to type 2 diabetes. Sci. Rep. 9:8887 (2019)
3.
Wuttke, M.* et al.: A catalog of genetic loci associated with kidney function from analyses of a million individuals. Nat. Genet. 51, 957-972 (2019)
4.
Bihlmeyer, N.A.* et al.: ExomeChip-wide analysis of 95 626 individuals identifies 10 novel loci associated with QT and JT intervals. Circ. Genom. Precis. Med. 11:e001758 (2018)
5.
Taipale, T.* et al.: Fatty liver is associated with blood pathways of inflammatory response, immune system activation and prothrombotic state in Young Finns Study. Sci. Rep. 8, 10358:10358 (2018)
6.
Laaksonen, J.* et al.: Blood pathway analyses reveal differences between prediabetic subjects with or without dyslipidaemia. The Cardiovascular Risk in Young Finns Study. Diabetes Metab. Res. Rev. 33:e2914 (2017)
7.
Nolte, I.M.* et al.: Genetic loci associated with heart rate variability and their effects on cardiac disease risk. Nat. Commun. 8:15805 (2017)
8.
Sulkava, M.* et al.: Differentially expressed genes and canonical pathway expression in human atherosclerotic plaques-Tampere Vascular Study. Sci. Rep. 7:41483 (2017)
9.
Sulkava, M.* et al.: Differentially expressed genes and canonical pathways in the ascending thoracic aortic aneurysm - The Tampere Vascular Study. Sci. Rep. 7:12127 (2017)
10.
Elovainio, M.* et al.: Activated immune-inflammatory pathways are associated with long-standing depressive symptoms: Evidence from gene-set enrichment analyses in the Young Finns Study. J. Psychiatr. Res. 71, 120-125 (2015)
11.
Hernesniemi, J.A.* et al.: Predicting sudden cardiac death using common genetic risk variants for coronary artery disease. Eur. Heart J. 36, 1669-1675 (2015)
12.
Kato, N.* et al.: Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. Nat. Genet. 47, 1282-1293 (2015)
13.
Turpeinen, H.* et al.: A genome-wide expression quantitative trait loci analysis of proprotein convertase subtilisin/kexin enzymes identifies a novel regulatory gene variant for FURIN expression and blood pressure. Hum. Genet. 134, 627-636 (2015)
14.
Arking, D.E.* et al.: Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nat. Genet. 46, 826-836 (2014)