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Justice, A.E.* et al.: Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Nat. Genet. 51, 452–469 (2019)
Ligthart, S.* et al.: Genome analyses of >200,000 individuals identify 58 loci for chronic inflammation and highlight pathways that link inflammation and complex disorders. Am. J. Hum. Genet. 103, 691-706 (2018)
Mahajan, A.* et al.: Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps. Nat. Genet. 50, 1505-1513 (2018)
Turcot, V.* et al.: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nat. Genet. 50, 26-41 (2018)
Turcot, V.* et al.: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (vol 50, pg 765, 2017). Nat. Genet. 50, 764-768 (2018)
Christophersen, I.E.* et al.: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat. Genet. 49, 946-952 (2017)
Justice, A.E.* et al.: Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Nat. Commun. 8:14977 (2017)
Marouli, E.* et al.: Rare and low-frequency coding variants alter human adult height. Nature 542, 186-190 (2017)
Wain, L.V.* et al.: Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets. Nat. Genet. 49, 416-425 (2017)
Zeller, T.* et al.: Transcriptome-wide analysis identifies novel associations with blood pressure. Hypertension 70, 713-750 (2017)
Huan, T.* et al.: A whole-blood transcriptome meta-analysis identifies gene expression signatures of cigarette smoking. Hum. Mol. Genet. 25, 4611-4623 (2016)
Lessard, S.* et al.: Testing the role of predicted gene knockouts in human anthropometric trait variation. Hum. Mol. Genet. 25, 2082-2092 (2016)
Teumer, A.* et al.: Analyzing illumina gene expression microarray data obtained from human whole blood cell and blood monocyte samples. Methods Mol. Biol. 1368, 85-97 (2016)
Homuth, G.* et al.: Extensive alterations of the whole-blood transcriptome are associated with body mass index: Results of an mRNA profiling study involving two large population-based cohorts. BMC Med. Genomics 8:65 (2015)
Huan, T.* et al.: A meta-analysis of gene expression signatures of blood pressure and hypertension. PLoS Genet. 11:e1005035 (2015)
Huffman, J.E.* et al.: Modulation of genetic associations with serum urate levels by body-mass-index in humans. PLoS ONE 10:e0119752 (2015)
Joshi, P.K.* et al.: Directional dominance on stature and cognition in diverse human populations. Nature 523, 459-462 (2015)
Lal, D.* et al.: Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies. PLoS Genet. 11:e1005226 (2015)
Peters, M.J.* et al.: The transcriptional landscape of age in human peripheral blood. Nat. Commun. 6:8570 (2015)
Westra, H.J.* et al.: Cell specific eQTL analysis without sorting cells. PLoS Genet. 11:e1005223 (2015)