The rs12975333 variant in the miR-125a and breast cancer risk in Germany, Italy, Australia and SpainPETERLONGO, Paolo; CALECA, Laura; LANGHEINZ, Anne et al.Journal of medical genetics. 2011, Vol 48, Num 10, pp 703-704, issn 0022-2593, 2 p.Article

Incidental carcinomas in prophylactic specimens in BRCA1 and BRCA2 germ-line mutation carriers, with emphasis on fallopian tube lesions : Report of 6 cases and review of the literatureCARCANGIU, Maria L; PEISSEL, Bernard; PASINI, Barbara et al.The American journal of surgical pathology. 2006, Vol 30, Num 10, pp 1222-1230, issn 0147-5185, 9 p.Article

Four new cases of double heterozygosity for BRCA1 and BRCA2 gene mutations: clinical, pathological, and family characteristicsZURADELLI, Monica; PEISSEL, Bernard; SANTORO, Armando et al.Breast cancer research and treatment. 2010, Vol 124, Num 1, pp 251-258, issn 0167-6806, 8 p.Article

Mapping of melanoma modifier loci in RET transgenic miceDRAGANI, Tommaso A; PEISSEL, Bernard; ZANESI, Nicola et al.Japanese journal of cancer research. 2000, Vol 91, Num 11, pp 1142-1147, issn 0910-5050Article

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

Allele-specific patterns of the mouse parathyroid hormone-related protein: influences on cell adhesion and migrationBENELLI, Roberto; PEISSEL, Bernard; MANENTI, Giacomo et al.Oncogene (Basingstoke). 2003, Vol 22, Num 49, pp 7711-7715, issn 0950-9232, 5 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

Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriersANTONIOU, Antonis C; SINILNIKOVA, Olga M; NEUHAUSEN, Susan L et al.Human molecular genetics (Print). 2009, Vol 18, Num 22, pp 4442-4456, issn 0964-6906, 15 p.Article

Loss of tyrosinase activity confers increased skin tumor susceptibility in miceSARAN, Anna; SPINOLA, Monica; PIGNATIELLO, Carmen et al.Oncogene (Basingstoke). 2004, Vol 23, Num 23, pp 4130-4135, issn 0950-9232, 6 p.Article

Inhibition of both skin and lung tumorigenesis by CAR-R mouse-derived cancer modifier lociSARAN, Anna; ZAFFARONI, Daniela; COVELLI, Vincenzo et al.International journal of cancer. 2002, Vol 97, Num 5, pp 580-583, issn 0020-7136Article

A cancer modifier role for parathyroid hormone-related proteinMANENTI, Giacomo; PEISSEL, Bernard; DRAGANI, Tommaso A et al.Oncogene (Basingstoke). 2000, Vol 19, Num 47, pp 5324-5328, issn 0950-9232Article

Evidence for a link between TNFRSF11A and risk of breast cancerBONIFACI, Núria; PALAFOX, Marta; BARILE, Monica et al.Breast cancer research and treatment. 2011, Vol 129, Num 3, pp 947-954, 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

The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriersCATUCCI, Irene; VERDERIO, Paolo; VIEL, Alessandra et al.Breast cancer research and treatment. 2011, Vol 125, Num 3, pp 855-860, issn 0167-6806, 6 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

SCCA2-like serpins mediate genetic predisposition to skin tumorsGARIBOLDI, Manuela; PEISSEL, Bernard; MAURICHI, Andrea et al.Cancer research (Baltimore). 2003, Vol 63, Num 8, pp 1871-1875, issn 0008-5472, 5 p.Article

X chromosome inactivation pattern in BRCA gene mutation carriersMANOUKIAN, Siranoush; VERDERIO, Paolo; ALLEMANI, Claudia et al.European journal of cancer (1990). 2013, Vol 49, Num 5, pp 1136-1141, issn 0959-8049, 6 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

Two new CHEK2 germ-line variants detected in breast cancer/sarcoma families negative for BRCA1, BRCA2, and TP53 gene mutationsMANOUKIAN, Siranoush; PEISSEL, Bernard; FRIGERIO, Simona et al.Breast cancer research and treatment. 2011, Vol 130, Num 1, pp 207-215, issn 0167-6806, 9 p.Article

Clinical genetic testing for familial melanoma in Italy: A cooperative studyBRUNO, William; GHIORZO, Paola; MANOUKIAN, Siranoush et al.Journal of the American Academy of Dermatology. 2009, Vol 61, Num 5, pp 775-782, issn 0190-9622, 8 p.Article

Cutaneous Melanoma in Childhood and Adolescence Shows Frequent Loss of INK4A and Gain of KITDANIOTTI, Maria; FERRARI, Andrea; BONO, Aldo et al.Journal of investigative dermatology. 2009, Vol 129, Num 7, pp 1759-1768, issn 0022-202X, 10 p.Article

Germline mutations of TP53 and BRCA2 genes in breast cancer/sarcoma familiesMANOUKIAN, Siranoush; PEISSEL, Bernard; PIEROTTI, Marco A et al.European journal of cancer (1990). 2007, Vol 43, Num 3, pp 601-606, issn 0959-8049, 6 p.Article