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Number of items: 12.

Article

Jiang, X, Finucane, HK orcid.org/0000-0003-3864-9828, Schumacher, FR orcid.org/0000-0002-3073-7463 et al. (330 more authors) (2019) Shared heritability and functional enrichment across six solid cancers. Nature Communications, 10. 431. ISSN 2041-1723

Mavaddat, N, Michailidou, K, Dennis, J et al. (266 more authors) (2019) Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes. The American Journal of Human Genetics, 104 (1). pp. 21-34. ISSN 0002-9297

Huyghe, JR, Bien, SA, Harrison, TA et al. (196 more authors) (2019) Discovery of common and rare genetic risk variants for colorectal cancer. Nature Genetics, 51 (1). pp. 76-87. ISSN 1061-4036

Kageyama, M, Albani, S, Braconnot, P et al. (32 more authors) (2017) The PMIP4 contribution to CMIP6 – Part 4: Scientific objectives and experimental design of the PMIP4-CMIP6 Last Glacial Maximum experiments and PMIP4 sensitivity experiments. Geoscientific Model Development, 10 (11). pp. 4035-4055. ISSN 1991-959X

Telomeres Mendelian Randomization Collaboration, , Haycock, PC, Burgess, S et al. (196 more authors) (2017) Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study. JAMA Oncology, 3 (5). pp. 636-651. ISSN 2374-2437

Liu, J, Lončar, I, Collée, JM et al. (97 more authors) (2016) rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk. Scientific Reports, 6. p. 36874. ISSN 2045-2322

Gusev, A, Shi, H, Kichaev, G et al. (205 more authors) (2016) Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation. NATURE COMMUNICATIONS, 7. ARTN 10979. ISSN 2041-1723

Day, FR, Ruth, KS, Thompson, DJ et al. (240 more authors) (2015) Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nature Genetics, 47 (11). ISSN 1061-4036

Darabi, H, McCue, K, Beesley, J et al. (126 more authors) (2015) Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression. American Journal of Human Genetics .

Garcia-Closas, M, Couch, FJ, Lindstrom, S et al. (271 more authors) (2013) Genome-wide association studies identify four ER negative-specific breast cancer risk loci. Nature Genetics, 45 (4). pp. 392-398. ISSN 1061-4036

Bojesen, SE, Pooley, KA, Johnatty, SE et al. (442 more authors) (2013) Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer. Nature Genetics, 45 (4). pp. 371-384. ISSN 1061-4036

Silva, IS, De Stavola, B, McCormack, V et al. (56 more authors) (2008) Birth size and breast cancer risk: re-analysis of individual participant data from 32 studies. PLoS Medicine, 5 (9). 1372 - 1386 . ISSN 1549-1277

This list was generated on Sun Oct 13 05:02:02 2019 BST.