PuSH - Publication Server of Helmholtz Zentrum München

25 Records found.
Zum Exportieren der Ergebnisse bitte einloggen.
Lay all publications on this page into basket
Nicolas, A.* et al.: Genome-wide analyses identify KIF5A as a novel ALS gene. Neuron 97, 1268-1283.e6 (2018)
Ward-Caviness, C.K. et al.: Analysis of repeated leukocyte DNA methylation assessments reveals persistent epigenetic alterations after an incident myocardial infarction. Clin. Epigenet. 10:161 (2018)
Jansen, I.E.* et al.: Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing. Genome Biol. 18:22 (2017)
Witoelar, A.W.* et al.: Genome-wide pleiotropy between Parkinson disease and autoimmune diseases. JAMA Neurol. 74, 780-792 (2017)
Chen, B.H.* et al.: DNA methylation-based measures of biological age: Meta-analysis predicting time to death. Aging 8, 1844-1865 (2016)
de Vries, P.S.* et al.: A meta-analysis of 120,246 individuals identifies 18 new loci for fibrinogen concentration. Hum. Mol. Genet. 25, 358-370 (2016)
Guerreiro, R.* et al.: Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases. Neurobiol. Aging 38, 214.e7-214.e10 (2016)
Huan, T.* et al.: A whole-blood transcriptome meta-analysis identifies gene expression signatures of cigarette smoking. Hum. Mol. Genet. 25, 4611-4623 (2016)
Joehanes, R.* et al.: Epigenetic signatures of cigarette smoking. Circ. Cardiovasc. Genet. 9, 436-447 (2016)
Lesage, S.* et al.: Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy. Am. J. Hum. Genet. 98, 500-513 (2016)
Ligthart, S.* et al.: DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases. Genome Biol. 17:255 (2016)
van der Harst, P.* et al.: 52 Genetic loci influencing myocardial mass. J. Am. Coll. Cardiol. 68, 1435-1448 (2016)
Huan, T.* et al.: A meta-analysis of gene expression signatures of blood pressure and hypertension. PLoS Genet. 11:e1005035 (2015)
Pfeiffer, L. et al.: DNA methylation of lipid-related genes affects blood lipid levels. Circ. Cardiovasc. Genet. 8, 334-342 (2015)
Westra, H.J.* et al.: Cell specific eQTL analysis without sorting cells. PLoS Genet. 11:e1005223 (2015)
Nalls, M.A.* et al.: Genetic comorbidities in Parkinson's disease. Hum. Mol. Genet. 23, 831-841 (2014)
Vimaleswaran, K.S.* et al.: Association of vitamin D status with arterial blood pressure and hypertension risk: A mendelian randomisation study. Lancet Diabet. Endocrinol. 2, 719-729 (2014)
Rietveld, C.A.* et al.: GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science 340, 1467-1471 (2013)
Westra, H.J.* et al.: Systematic identification of trans eQTLs as putative drivers of known disease associations. Nat. Genet. 45, 1238-1243 (2013)
Keller, M.F.* et al.: Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. Hum. Mol. Genet. 21, 4996-5009 (2012)