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au.\*:("VIEL, Alessandra")

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Stability of BAT26 in tumours of hereditary nonpolyposis colorectal cancer patients with MSH2 intragenic deletionPASTRELLO, Chiara; BAGLIONI, Silvana; TIBILETTI, Maria Grazia et al.European journal of human genetics. 2006, Vol 14, Num 1, pp 63-68, issn 1018-4813, 6 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

Germ line mutations of mismatch repair genes in hereditary nonpolyposis colorectal cancer patients with small bowel cancer : International society for gastrointestinal hereditary tumours collaborative studyPARK, Jae-Gahb; KIM, Duck-Woo; BROWN, Gregor J et al.Clinical cancer research. 2006, Vol 12, Num 11, pp 3389-3393, issn 1078-0432, 5 p., 1Article

Two PMS2 mutations in a turcot syndrome family with small bowel cancersAGOSTINI, Marco; TIBILETTI, Maria Grazia; VIEL, Alessandra et al.The American journal of gastroenterology. 2005, Vol 100, Num 8, pp 1886-1891, issn 0002-9270, 6 p.Article

Polymorphic CAG repeat length within the androgen receptor gene: Identification of a subgroup of patients with increased risk of ovarian cancerSANTAROSA, Manuela; BIDOLI, Ettore; GALLO, Angelo et al.Oncology reports. 2002, Vol 9, Num 3, pp 639-644, issn 1021-335XArticle

Microsatellite instability and high content of activated cytotoxic lymphocytes identify colon cancer patients with a favorable prognosisGUIDOBONI, Massimo; GAFA, Hoberta; DOLCETTI, Riccardo et al.The American journal of pathology. 2001, Vol 159, Num 1, pp 297-304, issn 0002-9440Article

Association between hsa-mir-146a genotype and tumor age-of-onset in BRCA1/BRCA2-negative familial breast and ovarian cancer patientsPASTRELLO, Chiara; POLESEL, Jerry; DELLA PUPPA, Lara et al.Carcinogenesis (New York. Print). 2010, Vol 31, Num 12, pp 2124-2126, issn 0143-3334, 3 p.Article

Somatic Mosaicism in a Patient With Lynch SyndromePASTRELLO, Chiara; FORNASARIG, Mara; PIN, Elisa et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 2, pp 212-215, issn 1552-4825, 4 p.Article

Twelve years of endoscopic surveillance in a family carrying biallelic Y165C MYH defect : Report of a caseFORNASARIG, Mara; MINISINI, Alessandro M; VIEL, Alessandra et al.Diseases of the colon & rectum. 2006, Vol 49, Num 2, pp 272-275, issn 0012-3706, 4 p.Article

Early-age-at-onset colorectal cancer and microsatellite instability as markers of hereditary nonpolyposis colorectal cancerPUCCIARELLI, Salvatore; AGOSTINI, Marco; VIEL, Alessandra et al.Diseases of the colon & rectum. 2003, Vol 46, Num 3, pp 305-312, issn 0012-3706, 8 p.Conference Paper

MUTYH c.933+3A>C, associated with a severely impaired gene expression, is the first Italian founder mutation in MUTYH-Associated PolyposisPIN, Elisa; PASTRELLO, Chiara; MAESTRO, Roberta et al.International journal of cancer (Print). 2013, Vol 132, Num 5, pp 1060-1069, issn 0020-7136, 10 p.Article

An American founder mutation in MLH1TOMSIC, Jerneja; LIYANARACHCHI, Sandya; VIEL, Alessandra et al.International journal of cancer (Print). 2012, Vol 130, Num 9, pp 2088-2095, issn 0020-7136, 8 p.Article

Mutations of an intronic repeat induce impaired MRE11 expression in primary human cancer with microsatellite instabilityGIANNINI, Giuseppe; RINALDI, Christian; FRATI, Luigi et al.Oncogene (Basingstoke). 2004, Vol 23, Num 15, pp 2640-2647, issn 0950-9232, 8 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

Genotype-phenotype correlations in individuals with a founder mutation in the MLH1 gene and hereditary non-polyposis colorectal cancerPONZ DE LEON, Maurizio; BENATTI, Piero; RONCUCCI, Luca et al.Scandinavian journal of gastroenterology. 2007, Vol 42, Num 6, pp 746-753, issn 0036-5521, 8 p.Article

Identification and Classification of Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome) : Adapting Old Concepts to Recent Advancements. Report from the Italian Association for the Study of Hereditary Colorectal Tumors Consensus GroupPONZ DE LEON, Maurizio; BERTARIO, Lucio; GENUARDI, Maurizio et al.Diseases of the colon & rectum. 2007, Vol 50, Num 12, pp 2126-2134, issn 0012-3706, 9 p.Article

Assessing the pathogenicity of MLH1 missense mutations in patients with suspected hereditary nonpolyposis colorectal cancer: correlation with clinical, genetic and functional featuresBELVEDERESI, Laura; BIANCHI, Francesca; PORFIRI, Emilio et al.European journal of human genetics. 2006, Vol 14, Num 7, pp 853-859, issn 1018-4813, 7 p.Article

Clinical and biologic heterogeneity of hereditary nonpolyposis colorectal cancerBENATTI, Piero; RONCUCCI, Luca; ROSSI, Giuseppina et al.International journal of cancer. 2001, Vol 95, Num 5, pp 323-328, issn 0020-7136Article

Molecular screening for hereditary nonpolyposis colorectal cancer : a prospective, population-based studyPERCESEPE, Antonio; BORGHI, Francesca; RONCUCCI, Luca et al.Journal of clinical oncology. 2001, Vol 19, Num 19, pp 3944-3950, issn 0732-183XArticle

Clinical and pathologic characteristics of BRCA-positive and BRCA-negative male breast cancer patients: results from a collaborative multicenter study in ItalyOTTINI, Laura; SILVESTRI, Valentina; PETERLONGO, Paolo et al.Breast cancer research and treatment. 2012, Vol 134, Num 1, pp 411-418, issn 0167-6806, 8 p.Article

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

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

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