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Browsing by Author Chenevix-Trench, G.

Full Text	Issue Date	Title	Author(s)
	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	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	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
	2011	The role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing	Pharoah, P.D.; Palmieri, R.T.; Ramus, S.J.; Gayther, S.A.; Andrulis, I.L., 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
	2010	Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers.	Wang, X.; Pankratz, V.S.; Fredericksen, Z.; Tarrell, R.; Karaus, M., 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
	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	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