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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)
Karasik, D.* et al.: Disentangling the genetics of lean mass. Am. J. Clin. Nutr. 109, 276-287 (2019)
Skaaby, T.* et al.: Association of alcohol consumption with allergic disease and asthma: A multi-centre Mendelian randomization analysis. Addiction 114, 216-225 (2019)
Varzari, A.* et al.: Genetic variation in TLR pathway and the risk of pulmonary tuberculosis in a Moldavian population. Infect. Genet. Evol. 68, 84-90 (2019)
Wittenbecher, C.* et al.: Insulin-like growth factor binding protein 2 (IGFBP-2) and the risk of developing type 2 diabetes. Diabetes 68, 188-197 (2019)
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)
Benedetti, E. et al.: Erratum: Publisher Correction: Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway (Nature communications (2017) 8 1 (1483)). Nat. Commun. 9:706 (2018)
Do, K.T. et al.: Characterization of missing values in untargeted MS-based metabolomics data and evaluation of missing data handling strategies. Metabolomics 14:128 (2018)
Elhadad, M.A. et al.: Using the plasma proteome to decipher metabolic syndrome pathophysiology and discover a diagnostic biomarker panel. Eur. Heart J. 39, 998-998 (2018)
Flannick, J.* et al.: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Sci. Data 5:180002 (2018)
Fritsche, L. et al.: Genetic variation in TCF7L2 rs7903146 and history of GDM negatively and independently impact on diabetes-associated metabolic traits. Diabetes Res. Clin. Pract. 146, 251-257 (2018)
Gerlini, R. et al.: Glucose tolerance and insulin sensitivity define adipocyte transcriptional programs in human obesity. Mol. Metab. 18, 42-50 (2018)
Giuranna, J.* et al.: The effect of SH2B1 variants on expression of leptin- and insulin-induced pathways in murine hypothalamus. Obes. Facts 11, 93-108 (2018)
Kesselmeier, M.* et al.: High-throughput DNA methylation analysis in anorexia nervosa confirms TNXB hypermethylation. World J. Biol. Psychiatry 19, 187-199 (2018)
Klarin, D.* et al.: Genetics of blood lipids among similar to 300,000 multi-ethnic participants of the Million Veteran Program. Nat. Genet. 50, 1514-1523 (2018)
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.: Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. Nat. Genet. 50, 559-571 (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)
Rivas, M.A.* et al.: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population. PLoS Genet. 14:e1007329 (2018)
Rosendahl, J.* et al.: Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis. Gut 67, 1855–186 (2018)