Loss of Heterozygosity Analysis at Different Chromosome Regions in Wilms Tumor Confirms 1p Allelic Loss as a Marker of Worse Prognosis: A Study from the Italian Association of Pediatric Hematology and OncologySPREAFICO, Filippo; GAMBA, Beatrice; MOROSI, Carlo et al.The Journal of urology. 2013, Vol 189, Num 1, pp 260-266, issn 0022-5347, 7 p.Article

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

No evidence for an association between the earwax-associated polymorphism in ABCC11 and breast cancer risk in Caucasian womenBEESLEY, Jonathan; JOHNATTY, Sharon E; CHENEVIX-TRENCH, Georgia et al.Breast cancer research and treatment. 2011, Vol 126, Num 1, pp 235-239, issn 0167-6806, 5 p.Article

Rare variants in XRCC2 as breast cancer susceptibility allelesHILBERS, Florentine S; WIJNEN, Juul T; COUCH, Fergus J et al.Journal of medical genetics. 2012, Vol 49, Num 10, pp 618-620, issn 0022-2593, 3 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

Non-chromosome 11-p syndromes in wilms tumor patients : Clinical and cytogenetic report of two down syndrome cases and one turner syndrome caseSPREAFICO, Filippo; TERENZIANI, Monica; RADICE, Paolo et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 1, pp 85-88, issn 1552-4825, 4 p.Article

A human cell-based assay to evaluate the effects of alterations in the MLH1 mismatch repair geneBLASI, Monica Francesca; VENTURA, Ilenia; AQUILINA, Gabriele et al.Cancer research (Baltimore). 2006, Vol 66, Num 18, pp 9036-9044, issn 0008-5472, 9 p.Article

Cyclooxygenase-2 expression in FAP patients carrying germ line MYH mutationsFRATTINI, Milo; CARNEVALI, Ileana; PIEROTTI, Marco A et al.Cancer epidemiology, biomarkers & prevention. 2005, Vol 14, Num 8, pp 2049-2052, issn 1055-9965, 4 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

Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysisCARVALHO, Marcelo A; MARSILLAC, Sylvia M; BAUMBACH, Lisa et al.Cancer research (Baltimore). 2007, Vol 67, Num 4, pp 1494-1501, issn 0008-5472, 8 p.Article

Bilateral preaxial polydactyly in a WAGR syndrome patientMANOUKIAN, Siranoush; CROLLA, John A; SPREAFICO, Filippo et al.American journal of medical genetics. 2005, Vol 134A, Num 4, pp 426-429, issn 0148-7299, 4 p.Article

Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cellsSIRCHIA, Silvia M; RAMOSCELLI, Lisetta; SIMONI, Giuseppe et al.Cancer research (Baltimore). 2005, Vol 65, Num 6, pp 2139-2146, issn 0008-5472, 8 p.Article

Atypical epithelial proliferation in fallopian tubes in prophylactic salpingo-oophorectomy specimens from BRCA1 and BRCA2 germline mutation carriersCARCANGIU, Maria L; RADICE, Paolo; MANOUKIAN, Siranoush et al.International journal of gynecological pathology. 2004, Vol 23, Num 1, pp 35-40, issn 0277-1691, 6 p.Article

Pathology of ovarian cancers in BRCA1 and BRCA2 carriersLAKHANI, Sunil R; MANEK, Sanjiv; MEIJERS-HEIJBOER, Hanne et al.Clinical cancer research. 2004, Vol 10, Num 7, pp 2473-2481, issn 1078-0432, 9 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

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

Confirmation of 5p12 As a Susceptibility Locus for Progesterone-Receptor―Positive, Lower Grade Breast CancerMILNE, Roger L; GOODE, Ellen L; BENITEZ, Javier et al.Cancer epidemiology, biomarkers & prevention. 2011, Vol 20, Num 10, pp 2222-2231, issn 1055-9965, 10 p.Article

Reproductive and Hormonal Factors, and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers : Results from the International BRCA1/2 Carrier Cohort StudyANTONIOU, Antonis C; ROOKUS, Matti; FAIVRE, Laurence et al.Cancer epidemiology, biomarkers & prevention. 2009, Vol 18, Num 2, pp 601-610, issn 1055-9965, 10 p.Article

Age at menarche and menopause and breast cancer risk in the international BRCA1/2 carrier cohort studyCHANG-CLAUDE, Jenny; ANDRIEU, Nadine; LUPORSI, Elisabeth et al.Cancer epidemiology, biomarkers & prevention. 2007, Vol 16, Num 4, pp 740-746, issn 1055-9965, 7 p.Article

Increased frequency of disease-causing MYH mutations in colon cancer familiesPETERLONGO, Paolo; MITRA, Nandita; OFFIT, Kenneth et al.Carcinogenesis (New York. Print). 2006, Vol 27, Num 11, pp 2243-2249, issn 0143-3334, 7 p.Article

Prediction of BRCA1 status in patients with breast cancer using estroqen receptor and basal phenotypeLAKHANI, Sunil R; REIS-FILHO, Jorge S; CHANG-CLAUDE, Jenny et al.Clinical cancer research. 2005, Vol 11, Num 14, pp 5175-5180, issn 1078-0432, 6 p.Article

Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomasGISMONDI, Viviana; META, Maurizio; DE LEON, Maurizio Ponz et al.International journal of cancer. 2004, Vol 109, Num 5, pp 680-684, issn 0020-7136, 5 p.Article

A Classification Model for BRCA2 DNA Binding Domain Missense Variants Based on Homology-Directed Repair ActivityGUIDUGLI, Lucia; PANKRATZ, Vernon S; SINGER, Christian et al.Cancer research (Chicago, Ill.). 2013, Vol 73, Num 1, pp 265-275, issn 0008-5472, 11 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

Methylation of O⁶-methylguanine-DNA methyltransferase (MGMT) promoter gene in triple-negative breast cancer patientsFUMAGALLI, Caterina; PRUNERI, Giancarlo; VIALE, Giuseppe et al.Breast cancer research and treatment. 2012, Vol 134, Num 1, pp 131-137, issn 0167-6806, 7 p.Article