Items where authors include "Pharoah, P.D."

Article

Buas, M.F., He, Q., Johnson, L.G. et al. (37 more authors) (2017) Germline variation in inflammation-related pathways and risk of Barrett's oesophagus and oesophageal adenocarcinoma. Gut, 66 (10). pp. 1739-1747. ISSN 0017-5749

Darabi, H., Beesley, J., Droit, A. et al. (111 more authors) (2016) Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs). Scientific Reports, 6. p. 32512. ISSN 2045-2322

Wyszynski, A., Hong, C.C., Lam, K. et al. (107 more authors) (2016) An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression. Human Molecular Genetics , 25 (17). pp. 3863-3876. ISSN 0964-6906

Hollestelle, A., van der Baan, F.H., Berchuck, A. et al. (355 more authors) (2016) No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer. Gynecologic Oncology, 141 (2). pp. 386-401. ISSN 0090-8258

Dunning, A.M., Michailidou, K., Kuchenbaecker, K.B. et al. (245 more authors) (2016) Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170. Nature Genetics. ISSN 1061-4036

Easton, D.F., Lesueur, F., Decker, B. et al. (126 more authors) (2016) No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing. Journal of Medical Genetics . ISSN 0022-2593

Petridis, C., Brook, M.N., Shah, V. et al. (92 more authors) (2016) Genetic predisposition to ductal carcinoma in situ of the breast. Breast Cancer Research, 18 (1). 22. ISSN 1465-542X

Jamshidi, M., Fagerholm, R., Khan, S. et al. (55 more authors) (2015) SNP-SNP interaction analysis of NF-κB signaling pathway on breast cancer survival. Oncotarget, 6 (35). pp. 37979-37994. ISSN 1949-2553

Howat, W.J., Blows, F.M., Provenzano, E. et al. (49 more authors) (2015) Performance of automated scoring of ER, PR, HER2, CK5/6 and EGFR in breast cancer tissue microarrays in the Breast Cancer Association Consortium. Journal of Pathology: Clinical Research, 1 (1). pp. 18-32. ISSN 2056-4538

Levine, D.M., Ek, W.E., Zhang, R. et al. (31 more authors) (2013) A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. Nature Genetics, 45 (12). pp. 1487-1493. ISSN 1061-4036

Wishart, G.C., Bajdik, C.D., Dicks, E. et al. (34 more authors) (2012) PREDICT Plus: development and validation of a prognostic model for early breast cancer that includes HER2. British Journal of Cancer, 107. pp. 800-807. ISSN 0007-0920

Lin, W.Y., Camp, N.J., Cannon-Albright, L.A. et al. (28 more authors) (2011) A role for XRCC2 gene polymorphisms in breast cancer risk and survival. Journal of Medical Genetics, 48 (7). pp. 477-484. ISSN 0022-2593

Milne, R.L., Gaudet, M.M., Spurdle, A.B. et al. (82 more authors) (2010) Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study. Breast Cancer Research, 12. R110. ISSN 1465-5411

Blows, F.M., Driver, K.E., Schmidt, M.K. et al. (40 more authors) (2010) Subtyping of Breast Cancer by Immunohistochemistry to Investigate a Relationship between Subtype and Short and Long Term Survival: A Collaborative Analysis of Data for 10,159 Cases from 12 Studies. PLoS Medicine, 7 (5). e1000279. ISSN 1549-1277

Garcia-Closas, M., Hall, P., Nevanlinna, H. et al. (110 more authors) (2008) Heterogeneity of Breast Cancer Associations with Five Susceptibility Loci by Clinical and Pathological Characteristics. PLoS Genetics, 4 (4). e1000054. ISSN 1553-7404