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Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC
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A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancer
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Cecconi, M., Forzano, F., Milani, D., Cavani, S., Baldo, C., Selicorni, A., Pantaleoni, C., Silengo, M., Ferrero, G.B., Scarano, G., Della Monica, M., Fischetto, R., Grammatico, P., Majore, S., Zampino, G., Memo, L., Cordisco, E. Lucci, Neri, G., Pierluigi, M., Bricarelli, F. Dagna, Grasso, M., Faravelli, Francesca
Published in American journal of medical genetics. Part A (30.04.2005)
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A founder MLH1 mutation in families from the districts of Modena and Reggio-Emilia in northern Italy with hereditary non-polyposis colorectal cancer associated with protein elongation and instability
Caluseriu, O, Di Gregorio, C, Lucci-Cordisco, E, Santarosa, M, Trojan, J, Brieger, A, Benatti, P, Pedroni, M, Colibazzi, T, Bellacosa, A, Neri, G, Ponz de Leon, M, Viel, A, Genuardi, M
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Identification of the founder BRCA1 mutation c.4117G>T (p.Glu1373) recurring in the Abruzzo and Lazio regions of Central Italy and predisposing to breast/ovarian and BRCA1-related cancers
Giacomo, D Di, Calicchia, M., Candria, S., Bruera, G., Ferella, S., Lucci Cordisco, E., Tosi, M., Genuardi, M., Ricevuto, E.
Published in Annals of oncology (01.10.2019)
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1891P - Identification of the founder BRCA1 mutation c.4117G>T (p.Glu1373) recurring in the Abruzzo and Lazio regions of Central Italy and predisposing to breast/ovarian and BRCA1-related cancers
Giacomo, D Di, Calicchia, M., Candria, S., Bruera, G., Ferella, S., Lucci Cordisco, E., Tosi, M., Genuardi, M., Ricevuto, E.
Published in Annals of oncology (01.10.2019)
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Familial microsatellite-stable non-polyposis colorectal cancer: Incidence and characteristics in a clinic-based population
Rovella, V., Carrara, S., Cogliandolo, S., Crucitti, A., Coco, C., Magistrelli, P., Lucci-Cordisco, E., Anti, M., Neri, G., Genuardi, M.
Published in Annals of oncology (01.06.2001)
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Cost-effectiveness analysis of screening programs for Lynch syndrome in Italy
Pastorino, R, Tognetto, A, Di Marco, M, Lucci-Cordisco, E, Genuardi, M, Villari, P, Basile, M, Boccia, S
Published in European journal of public health (01.11.2018)
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20P Unexpected germline pathogenic variants in gynaecologic cancers identified through a comprehensive cancer genome profiling programme
Duranti, S., Panfili, A., Nero, C., Minucci, A., Pietrosante, A., Preziosi, J., Marino, I., Giacomini, F., Pasciuto, T., Mozzetta, I., Giacò, L., Iacobelli, V., Preziosi, A., Piermattei, A., Maneri, G., Fagotti, A., Fanfani, F., Cordisco, E. Lucci, Genuardi, M., Scambia, G.
Published in ESMO open (01.06.2024)
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96P Analysis of concordance between microsatellite instability by next generation sequencing (NGS-MSI) and mismatch repair deficiency by immunohistochemistry (IHC-MMR) in endometrial cancer (EC) patients
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174P Endocrine disruptors and life STILe in patients carrying BRCA pathogenic VAriants with breast and/or ovarian CAncer and women without neoplasm: The STILVARCA study
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Identification of Muir-Torre syndrome among patients with sebaceous tumors and keratoacanthomas: Role of clinical features, microsatellite instability, and immunohistochemistry
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Published in Cancer (01.03.2005)
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