The nonsense-mediated mRNA decay pathway triggers degradation of most BRCA1 mRNAs bearing premature termination codonsPERRIN-VIDOZ, Laure; SINILNIKOVA, Olga M; STOPPA-LYONNET, Dominique et al.Human molecular genetics (Print). 2002, Vol 11, Num 23, pp 2805-2814, issn 0964-6906Article

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

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor―negative breast cancer in the general populationANTONIOU, Antonis C; XIANSHU WANG; GHOUSSAINI, Maya et al.Nature genetics. 2010, Vol 42, Num 10, pp 885-892, issn 1061-4036, 8 p.Article

No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a multi-center cohort studyREBBECK, Timothy R; ANTONIOU, Antonis C; GREENE, Mark H et al.Breast cancer research and treatment. 2009, Vol 115, Num 1, pp 185-192, issn 0167-6806, 8 p.Article

Prognosis of early-onset breast cancer based on BRCA1/2 mutation status in a French population-based cohort and reviewBONADONA, Valérie; DUSSART-MOSER, Sophie; RAUDRANT, Daniel et al.Breast cancer research and treatment. 2007, Vol 101, Num 2, pp 233-245, issn 0167-6806, 13 p.Article

Common BRCA2 variants and modification of breast and ovarian cancer risk in BRCA1 mutation carriersHUGHES, David J; GINOLHAC, Sophie M; HARDOUIN, Agnès et al.Cancer epidemiology, biomarkers & prevention. 2005, Vol 14, Num 1, pp 265-267, issn 1055-9965, 3 p.Article

BRCA2 Deep Intronic Mutation Causing Activation of a Cryptic Exon: Opening toward a New Preventive Therapeutic StrategyANCZUKOW, Olga; BUISSON, Monique; LEONE, Melanie et al.Clinical cancer research (Print). 2012, Vol 18, Num 18, pp 4903-4909, issn 1078-0432, 7 p.Article

Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)MAVADDAT, Nasim; BARROWDALE, Daniel; MULLIGAN, Anna Marie et al.Cancer epidemiology, biomarkers & prevention. 2012, Vol 21, Num 1, pp 134-147, issn 1055-9965, 14 p.Article

RAD51 135G→C Modifies Breast Cancer Risk among BRCA2 Mutation Carriers : Results from a Combined Analysis of 19 StudiesANTONIOU, Antonis C; SINILNIKOVA, Olga M; COUPIER, Isabelle et al.American journal of human genetics. 2007, Vol 81, Num 6, pp 1186-1200, issn 0002-9297, 15 p.Article

Prevalence of BRCA1 and BRCA2 germline mutations in young breast cancer patients: A population-based studyDE SANJOSE, Silvia; LEONE, Mélanie; BOSCH, F. Xavier et al.International journal of cancer. 2003, Vol 106, Num 4, pp 588-593, issn 0020-7136, 6 p.Article

A Nonsynonymous Polymorphism in IRS1 Modifies Risk of Developing Breast and Ovarian Cancers in BRCA1 and Ovarian Cancer in BRCA2 Mutation CarriersDING, Yuan C; MCGUFFOG, Lesley; KRISTOFFERSSON, Ulf et al.Cancer epidemiology, biomarkers & prevention. 2012, Vol 21, Num 8, pp 1362-1370, issn 1055-9965, 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

Haplotype-based analysis of common variation in the Acetyl-CoA Carboxylase α gene and breast cancer risk : A case-control study nested within the european prospective investigation into cancer and nutritionSINILNIKOVA, Olga M; MCKAY, James D; HUGHES, David J et al.Cancer epidemiology, biomarkers & prevention. 2007, Vol 16, Num 3, pp 409-415, issn 1055-9965, 7 p.Article

Breast cancer risk in BRCA1 and BRCA2 mutation carriers and polyglutamine repeat length in the AIB1 geneHUGHES, David J; GINOLHAC, Sophie M; GIRAUD, Sophie et al.International journal of cancer. 2005, Vol 117, Num 2, pp 230-233, issn 0020-7136, 4 p.Article

BRCA1 wild-type allele modifies risk of ovarian cancer in carriers of BRCA1 germ-line mutationsGINOLHAC, Sophie M; GAD, Sophie; MULLER, Danièle et al.Cancer epidemiology, biomarkers & prevention. 2003, Vol 12, Num 2, pp 90-95, issn 1055-9965, 6 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

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

Association of the Variants CASP8 D302H and CASP10 V410I with Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation CarriersENGEL, Christoph; VERSMOLD, Beatrix; GARETH EVANS, D et al.Cancer epidemiology, biomarkers & prevention. 2010, Vol 19, Num 11, pp 2859-2868, issn 1055-9965, 10 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

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

Distinct BRCA1 rearrangements involving the BRCA1 pseudogene suggest the existence of a recombination hot spotPUGET, Nadine; GAD, Sophie; PERRIN-VIDOZ, Laure et al.American journal of human genetics. 2002, Vol 70, Num 4, pp 858-865, issn 0002-9297Article

BRCA1 R 1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer riskSPURDLE, Amanda B; WHILEY, Phillip J; KATTENTIDT-MOURAVIEVA, Anna A et al.Journal of medical genetics. 2012, Vol 49, Num 8, pp 525-532, issn 0022-2593, 8 p.Article

Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation CarriersSPURDLE, Amanda B; MARQUART, Louise; GSCHWANTLER-KAULICH, Daphne et al.Cancer epidemiology, biomarkers & prevention. 2011, Vol 20, Num 5, pp 1032-1038, issn 1055-9965, 7 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

FAN1 variants identified in multiple-case early-onset breast cancer families via exome sequencing: no evidence for association with risk for breast cancerPARK, Daniel J; ODEFREY, Fabrice A; SINILNIKOVA, Olga M et al.Breast cancer research and treatment. 2011, Vol 130, Num 3, pp 1043-1049, issn 0167-6806, 7 p.Article