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Browsing by Author Beesley, J.
Showing results 1 to 21 of 21
| Full Text | Issue Date | Title | Author(s) | | 2012 | Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study. | Jakubowska, A.; Rozkrut, D.; Antoniou, A.; Hamann, U.; Scott, R.J., et al |
| 2012 | Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers | Ramus, S.J.; Antoniou, A.C.; Kuchenbaecker, K.B.; Soucy, P.; Beesley, J., et al |
| 2012 | Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers | Couch, F.J.; Gaudet, M.M.; Antoniou, A.C.; Ramus, S.J.; Kuchenbaecker, K.B., et al |
| 2012 | A Nonsynonymous Polymorphism in IRS1 Modifies Risk of Developing Breast and Ovarian Cancers in BRCA1 and Ovarian Cancer in BRCA2 Mutation Carriers. | Ding, Y.C.; McGuffog, L.; Healey, S.; Friedman, E.; Laitman, Y., et al |
| 2012 | Breast Cancer Risk and 6q22.33: Combined Results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2. | Kirchhoff, T.; Gaudet, M.M.; Antoniou, A.C.; McGuffog, L.; Humphreys, M.K., et al |
| 2012 | Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers | Antoniou, A.C.; Kuchenbaecker, K.B.; Soucy, P.; Beesley, J.; Chen, X, et al |
| 2012 | Genome-wide association study for ovarian cancer susceptibility using pooled DNA. | Lu, Y.; Chen, X.; Beesley, J.; Johnatty, S.E.; Defazio, A., et al |
| 2011 | Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2 | Osorio, A.; Milne, R.L.; Alonso, R.; Pita, G.; Peterlongo, P., et al |
| 2011 | Functional polymorphisms in the TERT promoter are associated with risk of serous epithelial ovarian and breast cancers | Beesley, J.; Pickett, H.A.; Johnatty, S.E.; Dunning, A.M.; Chen, X., et al |
| 2011 | Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers | Spurdle, A.B.; Marquart, L.; McGuffog, L.; Healey, S.; Sinilnikova, O., et al |
| 2011 | Polymorphisms in stromal genes and susceptibility to serous epithelial ovarian cancer: a report from the Ovarian Cancer Association Consortium | Amankwah, E.K.; Wang, Q.; Schildkraut, J.M.; Tsai, Y.Y.; Ramus, S.J., et al |
| 2011 | Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium | Broeks, A.; Schmidt, M.K.; Sherman, M.E.; Couch, F.J.; Hopper, J.L., et al |
| 2011 | Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers. | Cox, D.G.; Simard, J.; Sinnett, D.; Hamdi, Y.; Soucy, P., et al |
| 2011 | Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers | Ramus, S.J.; Kartsonaki, C.; Gayther, S.A.; Pharoah, P.D.; Sinilnikova, O.M., et al |
| 2011 | Exploring the link between MORF4L1 and risk of breast cancer. | Martrat, G.; Maxwell, C.M.; Tominaga, E.; Porta-de-la-Riva, M.; Bonifaci, N., et al |
| 2010 | A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. | Goode, E.L.; Chenevix-Trench, G.; Song, H.; Ramus, S.J.; Notaridou, M., et al |
| 2010 | Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction. | Antoniou, A.C.; Beesley, J.; McGuffog, L.; Sinilnikova, O.M.; Healey, S., et al |
| 2009 | No evidence that GATA3 rs570613 SNP modifies breast cancer risk. | Johnatty, S.E.; Couch, F.J.; Fredericksen, Z.; Tarrell, R.; Spurdle, A.B., et al |
| 2009 | Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers. | Antoniou, A.C.; Sinilnikova, O.M.; McGuffog, L.; Healey, S.; Nevanlinna, H., et al |
| 2009 | Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA). | Osorio, A.; Milne, R.L.; Pita, G.; Peterlongo, P.; Heikkinen, T., et al |
| 2008 | Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers. | Antoniou, A.C.; Spurdle, A.B.; Sinilnikova, O.M.; Healey, S.; Pooley, K.A., et al |
Showing results 1 to 21 of 21
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