PuSH - Publication Server of Helmholtz Zentrum München

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1.
Jiang, X.* et al.: Shared heritability and functional enrichment across six solid cancers. Nat. Commun. 10:431 (2019)
2.
Li, Y.* et al.: Genetic interaction analysis among oncogenesis-related genes revealed novel genes and networks in lung cancer development. Oncotarget 10, 1760-1774 (2019)
3.
Yu, B.* et al.: The consortium of metabolomics studies (COMETS): Metabolomics in 47 prospective cohort studies. Am. J. Epidemiol. 188, 991-1012 (2019)
4.
Zhu, Y.* et al.: Elevated platelet count appears to be causally associated with increased risk of lung cancer: A Mendelian randomization analysis. Cancer Epidemiol. Biomarkers Prev. 28, 935-942 (2019)
5.
Ferreiro-Iglesias, A.* et al.: Fine mapping of MHC region in lung cancer highlights independent susceptibility loci by ethnicity. Nat. Commun. 9:3927 (2018)
6.
Ji, X.* et al.: Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk. Nat. Commun. 9:3221 (2018)
7.
Jiang, X.* et al.: Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels. Nat. Commun. 9:260 (2018)
8.
Kachuri, L.* et al.: Mendelian Randomization and mediation analysis of leukocyte telomere length and risk of lung and head and neck cancers. Int. J. Epidemiol., accepted (2018)
9.
Li, Y.* et al.: Genome-wide interaction study of smoking behavior and non-small cell lung cancer risk in Caucasian population. Carcinogenesis 39, 336-346 (2018)
10.
Rosenberger, A.* et al.: Genetic modifiers of radon-induced lung cancer risk: A genome-wide interaction study in former uranium miners. Int. Arch. Occup. Environ. Health 91, 937-950 (2018)
11.
Carreras-Torres, R.* et al.: Obesity, metabolic factors and risk of different histological types of lung cancer: A Mendelian randomization study. PLoS ONE 12:e0177875 (2017)
12.
Dimitrakopoulou, V.I.* et al.: Circulating vitamin D concentration and risk of seven cancers: Mendelian randomisation study. BMJ:Br. Med. J. 359:j4761 (2017)
13.
McKay, J.D.* et al.: Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. Nat. Genet. 49, 1126-1132 (2017)
14.
Allen, N.E.* et al.: Selenium and prostate cancer: Analysis of individual participant data from fifteen prospective studies. J. Natl. Cancer Inst. 108:djw153 (2016)
15.
Brenner, D.R.* et al.: Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia. Carcinogenesis 36, 1314-1326 (2015)
16.
Park, S.L.* et al.: Pleiotropic associations of risk variants identified for other cancers with lung cancer risk: The PAGE and TRICL consortia. J. Natl. Cancer Inst. 106:dju061 (2014)
17.
den Hoed, M.* et al.: Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat. Genet. 45, 621-631 (2013)
18.
Timofeeva, M.N.* et al.: Influence of common genetic variation on lung cancer risk: Meta-analysis of 14900 cases and 29485 controls. Hum. Mol. Genet. 21, 4980-4995 (2012)
19.
Wu, X.* et al.: A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23. Hum. Mol. Genet. 21, 456-462 (2012)
20.
Purdue, M.P.* et al.: Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3. Nat. Genet. 43, 60-65 (2011)