PuSH - Publication Server of Helmholtz Zentrum München

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1.
Liu, J.* et al.: An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis. Nat. Commun. 10:2581 (2019)
2.
Ma, J.* et al.: A peripheral blood DNA methylation signature of hepatic fat reveals a potential causal pathway for non-alcoholic fatty liver disease. Diabetes 68, 1073-1083 (2019)
3.
Sung, Y.J.* et al.: A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure. Hum. Mol. Genet., accepted (2019)
4.
Aslibekyan, S.* et al.: Association of methylation signals with incident coronary heart disease in an epigenome-wide assessment of circulating tumor necrosis factor. JAMA Cardiol. 3, 463-472 (2018)
5.
Eismann, S.* ; Levy, D.* ; Shu, R.* & Bartzsch, S.: Bayesian optimization and attribute adjustment. In: (34th Conference on Uncertainty in Artificial Intelligence 2018, UAI 2018, 6-10 August 2018, Monterey, United States). 2018. 1042-1052 ( ; 2)
6.
Evangelou, E.* et al.: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nat. Genet. 50, 1412-1425 (2018)
7.
Evangelou, E.* et al.: Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x). Nat. Genet., accepted (2018)
8.
Feitosa, M.F.* et al.: Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. PLoS ONE 13:e0198166 (2018)
9.
Jovanova, O.S.* et al.: DNA methylation signatures of depressive symptoms in middle-aged and elderly persons meta-analysis of multiethnic epigenome-wide studies. JAMA psychiatry 75, 949-959 (2018)
10.
Liu, C.* et al.: A DNA methylation biomarker of alcohol consumption. Mol. Psychiatry 23, 422-433 (2018)
11.
Sung, Y.J.* et al.: A large-scale multi-ancestry genome-wide study accounting for smoking behavior identifies multiple significant loci for blood pressure. Am. J. Hum. Genet. 102, 375-400 (2018)
12.
Ward-Caviness, C.K. et al.: DNA methylation age is associated with an altered hemostatic profile in a multiethnic meta-analysis. Blood 132, 1842-1850 (2018)
13.
Yao, C.* et al.: Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease. Nat. Commun. 9:3268 (2018)
14.
Yao, C.* et al.: Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease (vol 9, 3268, 2018). Nat. Commun. 9:3853 (2018)
15.
Li, M.* et al.: SOS2 and ACP1 loci identified through large-scale exome chip analysis regulate kidney development and function. J. Am. Soc. Nephrol. 28, 981-994 (2017)
16.
Mandaviya, P.R.* et al.: Genetically defined elevated homocysteine levels do not result in widespread changes of DNA methylation in leukocytes. PLoS ONE 12:e0182472 (2017)
17.
Wain, L.V.* et al.: Novel blood pressure locus and gene discovery using genome-wide association study and expression data sets from blood and the kidney. Hypertension 70, e4-e19 (2017)
18.
Warren, H.R.* et al.: Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. Nat. Genet. 49, 403-415 (2017)
19.
Chen, B.H.* et al.: DNA methylation-based measures of biological age: Meta-analysis predicting time to death. Aging 8, 1844-1865 (2016)
20.
Ehret, G.B.* et al.: The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nat. Genet. 48, 1171-1184 (2016)