Effect of the overexpression of BRCA2 unclassified missense variants on spontaneous homologous recombination in human cellsBALIA, Cristina; GALLI, Alvaro; CALIGO, Maria Adelaide et al.Breast cancer research and treatment. 2011, Vol 129, Num 3, pp 1001-1009, issn 0167-6806, 9 p.Article

Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriersSTEVENS, Kristen N; XIANSHU WANG; OSORIO, Ana et al.Breast cancer research and treatment. 2012, Vol 136, Num 1, pp 295-302, issn 0167-6806, 8 p.Article

Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk PredictionANTONIOU, Antonis C; BEESLEY, Jonathan; ISAACS, Claudine et al.Cancer research (Chicago, Ill.). 2010, Vol 70, Num 23, pp 9742-9754, issn 0008-5472, 13 p.Article

Mutational analysis of the NM23.H1 gene in human breast cancerCIPOLLINI, Giovanna; MORETTI, Angela; GHIMENTI, Chiara et al.Cancer genetics and cytogenetics. 2000, Vol 121, Num 2, pp 181-185, issn 0165-4608Article

A recombination-based method to characterize human BRCA1 missense variantsGUIDUGLI, Lucia; RUGANI, Chiara; LOMBARDI, Grazia et al.Breast cancer research and treatment. 2011, Vol 125, Num 1, pp 265-272, issn 0167-6806, 8 p.Article

p53 inactivation is a rare event in familial breast tumors negative for BRCA1 and BRCA2 mutationsSENSI, Elisa; TANCREDI, Mariella; ARETINI, Paolo et al.Breast cancer research and treatment. 2003, Vol 82, Num 1, pp 1-9, issn 0167-6806, 9 p.Article

Microsatellite alterations and K-ras, TGFssRII, IGFRII and bax mutations in sporadic cancers of the gastrointestinal tractCALIGO, Maria A; GHIMENTI, Chiara; SENSI, Elisa et al.Oncology reports. 2000, Vol 7, Num 6, pp 1371-1375, issn 1021-335XArticle

Identification of two novel BRCA1-partner genes in the DNA double-strand break repair pathwayGUGLIELMI, Chiara; CERRI, Iacopo; EVANGELISTA, Monica et al.Breast cancer research and treatment. 2013, Vol 141, Num 3, pp 515-522, issn 0167-6806, 8 p.Article

Clinicopathological significance of GADD45 gene alterations in human familial breast carcinomaSENSI, Elisa; TANCREDI, Mariella; ARETINI, Paolo et al.Breast cancer research and treatment. 2004, Vol 87, Num 2, pp 197-201, issn 0167-6806, 5 p.Article

Haplotype analysis of BRCA 1 gene reveals a new gene rearrangement: characterization of a 19.9 KBP deletionTANCREDI, Mariella; SENSI, Elisa; CIPOLLINI, Giovanna et al.European journal of human genetics. 2004, Vol 12, Num 9, pp 775-777, issn 1018-4813, 3 p.Article

Multimodal Assessment of Protein Functional Deficiency Supports Pathogenicity of BRCA1 p.V1688de1DE NICOLO, Arcangela; PARISINI, Emilio; GARBER, Judy E et al.Cancer research (Chicago, Ill.). 2009, Vol 69, Num 17, pp 7030-7037, issn 0008-5472, 8 p.Article

Characterisation of gene expression profiles of yeast cells expressing BRCA1 missense variantsDI CECCO, Leontina; MELISSARI, Erika; MARIOTTI, Veronica et al.European journal of cancer (1990). 2009, Vol 45, Num 12, pp 2187-2196, issn 0959-8049, 10 p.Article

Aberrant expression of BARD1 in breast and ovarian cancers with poor prognosisWU, Jian-Yu; VLASTOS, Anne-Therese; PELTE, Marie-Francoise et al.International journal of cancer. 2006, Vol 118, Num 5, pp 1215-1226, issn 0020-7136, 12 p.Article

High level of messenger RNA for BRMS1 in primary breast carcinomas is associated with poor prognosisLOMBARDI, Grazia; DI CRISTOFANO, Claudio; BEVILACQUA, Generoso et al.International journal of cancer. 2007, Vol 120, Num 6, pp 1169-1178, issn 0020-7136, 10 p.Article

Penetrances of breast and ovarian cancer in a large series of families tested for BRCA1/2 mutationsMARRONI, Fabio; ARETINI, Paolo; SANTAROSA, Manuela et al.European journal of human genetics. 2004, Vol 12, Num 11, pp 899-906, issn 1018-4813, 8 p.Article

The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriersLAITMAN, Yael; KUCHENBAECKER, Karoline B; SCHMUTZLER, Rita K et al.Breast cancer research and treatment. 2012, Vol 132, Num 3, pp 1119-1126, issn 0167-6806, 8 p.Article

Different expressivity of BRCA1 and BRCA2: analysis of 179 Italian pedigrees with identified mutationARETINI, Paolo; D'ANDREA, Emma; CALIGO, Maria Adelaide et al.Breast cancer research and treatment. 2003, Vol 81, Num 1, pp 71-79, issn 0167-6806, 9 p.Article

Common alleles at 6q25.1 and 1 p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriersANTONIOU, Antonis C; KARTSONAKI, Christiana; ZAFFARONI, Daniela et al.Human molecular genetics (Print). 2011, Vol 20, Num 16, pp 3304-3321, issn 0964-6906, 18 p.Article

The Role of KRAS rs61764370 in Invasive Epithelial Ovarian Cancer: Implications for Clinical TestingPHAROAH, Paul D. P; PALMIERI, Rachel T; BECKMANN, Matthias W et al.Clinical cancer research (Print). 2011, Vol 17, Num 11, pp 3742-3750, issn 1078-0432, 9 p.Article

No evidence that GATA3 rs570613 SNP modifies breast cancer riskJOHNATTY, Sharon E; COUCH, Fergus J; FINK-RETTER, Anneliese et al.Breast cancer research and treatment. 2009, Vol 117, Num 2, pp 371-379, issn 0167-6806, 9 p.Article

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 CarriersCOUCH, Fergus J; GAUDET, Mia M; MCGUFFOG, Lesley et al.Cancer epidemiology, biomarkers & prevention. 2012, Vol 21, Num 4, pp 645-657, issn 1055-9965, 13 p.Article

Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriersCOX, David G; SIMARD, Jacques; SZABO, Csilla et al.Human molecular genetics (Print). 2011, Vol 20, Num 23, pp 4732-4747, issn 0964-6906, 16 p.Article

Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation CarriersRAMUS, Susan J; KARTSONAKI, Christiana; XIANSHU WANG et al.Journal of the National Cancer Institute. 2011, Vol 103, Num 2, pp 105-116, issn 0027-8874, 12 p.Article

Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation CarriersANTONIOU, Antonis C; SPURDLE, Amanda B; HOFMANN, Wera et al.American journal of human genetics. 2008, Vol 82, Num 4, pp 937-948, issn 0002-9297, 12 p.Article

Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriersIM, Kate M; KIRCHHOFF, Tomas; GUIDUCCI, Candace et al.Human genetics. 2011, Vol 130, Num 5, pp 685-699, issn 0340-6717, 15 p.Article