PuSH - Publication Server of Helmholtz Zentrum München

18 Records found.
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1.
Abe, K.* et al.: Gain-of-function mutations in a member of the Src family kinases cause autoinflammatory bone disease in mice and humans. Proc. Natl. Acad. Sci. U.S.A. 116, 11872-11877 (2019)
2.
Jiang, X.* et al.: Shared heritability and functional enrichment across six solid cancers. Nat. Commun. 10:431 (2019)
3.
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)
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.
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)
6.
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)
7.
Day, F.R.* et al.: Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. Nat. Genet. 49, 834-841 (2017)
8.
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)
9.
Day, F.R.* et al.: Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nat. Genet. 47, 1294-1303 (2015)
10.
Day, F.R.* et al.: Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility, and BRCA1-mediated DNA repair. Obstet. Gynecol. 70, 758-762 (2015)
11.
Khan, S.* et al.: MicroRNA related polymorphisms and breast cancer risk. PLoS ONE 9:e109973 (2014)
12.
Perry, J.R.* et al.: DNA mismatch repair gene MSH6 implicated in determining age at natural menopause. Hum. Mol. Genet. 23, 2490-2497 (2014)
13.
Perry, J.R.B.* et al.: Parent-of-origin specific allelic associations among 106 genomic1 loci for age at menarche. Nature 514, 92-97 (2014)
14.
French, J.D.* et al.: Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers. Am. J. Hum. Genet. 92, 489-503 (2013)
15.
Garcia-Closas, M.* et al.: Genome-wide association studies identify four ER negative-specific breast cancer risk loci. Nat. Genet. 45, 392-398 (2013)
16.
Michailidou, K.* et al.: Large-scale genotyping identifies 41 new loci associated with breast cancer risk. Nat. Genet. 45, 353-361 (2013)
17.
Ghoussaini, M.* et al.: Genome-wide association analysis identifies three new breast cancer susceptibility loci. Nat. Genet. 44, 312-319 (2012)
18.
Siddiq, A.* et al.: A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. Hum. Mol. Genet. 21, 5373-5384 (2012)