1. BRCA1/2 germline missense mutations: a systematic review. Issue 3 (May 2018) Authors: Corso, Giovanni; Feroce, Irene; Intra, Mattia; Toesca, Antonio; Magnoni, Francesca; Sargenti, Manuela; Naninato, Paola; Caldarella, Pietro; Pagani, Gianmatteo; Vento, Annarita; Veronesi, Paolo; Bonanni, Bernardo; Galimberti, Viviana Journal: European journal of cancer prevention Issue: Volume 27:Issue 3(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical criteria revision for hereditary lobular breast cancer associated with E-cadherin germline mutations. (10th May 2018) Authors: Corso, Giovanni; De Scalzi, Alessandra; Feroce, Irene; Veronesi, Paolo; Bonanni, Bernardo; Galimberti, Viviana Journal: Personalized medicine Issue: Volume 15:Number 3(2018) Page Start: 153 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Complementary molecular approaches reveal heterogeneous CDH1 germline defects in Italian patients with hereditary diffuse gastric cancer (HDGC) syndrome. Issue 5 (3rd February 2014) Authors: Molinaro, Valeria; Pensotti, Valeria; Marabelli, Monica; Feroce, Irene; Barile, Monica; Pozzi, Simonetta; Laghi, Luigi; Serrano, Davide; Bernard, Loris; Bonanni, Bernardo; Ranzani, Guglielmina Nadia Journal: Genes, chromosomes & cancer Issue: Volume 53:Issue 5(2014:May) Page Start: 432 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Definition and management of colorectal polyposis not associated with APC/MUTYH germline pathogenic variants: AIFEG consensus statement. Issue 4 (April 2021) Authors: Urso, Emanuele Damiano Luca; Ponz de Leon, Maurizio; Vitellaro, Marco; Piozzi, Guglielmo Niccolò; Bao, Quoc Riccardo; Martayan, Aline; Remo, Andrea; Stigliano, Vittoria; Oliani, Cristina; Lucci Cordisco, Emanuela; Pucciarelli, Salvatore; Ranzani, Guglielmina Nadia; Viel, Alessandra; Adami, France... Journal: Digestive and liver disease Issue: Volume 53:Issue 4(2021) Page Start: 409 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Fenretinide (4-HPR): A Preventive Chance for Women at Genetic and Familial Risk?. (5th March 2012) Authors: Cazzaniga, Massimiliano; Varricchio, Clara; Montefrancesco, Chiara; Feroce, Irene; Guerrieri-Gonzaga, Aliana Other Names: Soprano Dianne R. Academic Editor. Journal: Journal of biomedicine and biotechnology Issue: Volume 2012(2012) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Hereditary lobular breast cancer with an emphasis on E-cadherin genetic defect. Issue 7 (21st June 2018) Authors: Corso, Giovanni; Figueiredo, Joana; La Vecchia, Carlo; Veronesi, Paolo; Pravettoni, Gabriella; Macis, Debora; Karam, Rachid; Lo Gullo, Roberto; Provenzano, Elena; Toesca, Antonio; Mazzocco, Ketti; Carneiro, Fátima; Seruca, Raquel; Melo, Soraia; Schmitt, Fernando; Roviello, Franco; De Scalzi, Ales... Journal: Journal of medical genetics Issue: Volume 55:Issue 7(2018) Page Start: 431 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Is tumor testing efficiency for Lynch syndrome different in rectal and colon cancer?. Issue 12 (December 2020) Authors: Marabelli, Monica; Gandini, Sara; Rafaniello, Paola Raviele; Calvello, Mariarosaria; Tolva, Gianluca; Feroce, Irene; Lazzeroni, Matteo; Marino, Elena; Dal Molin, Matteo; Trovato, Cristina; Guerrieri-Gonzaga, Aliana; Petz, Wanda Luisa; Barberis, Massimo; Bertario, Lucio; Bonanni, Bernardo Journal: Digestive and liver disease Issue: Volume 52:Issue 12(2020) Page Start: 1503 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification. Issue 9 (13th September 2019) Authors: Parsons, Michael T.; Tudini, Emma; Li, Hongyan; Hahnen, Eric; Wappenschmidt, Barbara; Feliubadaló, Lidia; Aalfs, Cora M.; Agata, Simona; Aittomäki, Kristiina; Alducci, Elisa; Alonso‐Cerezo, María Concepción; Arnold, Norbert; Auber, Bernd; Austin, Rachel; Azzollini, Jacopo; Balmaña, Judith; Barbie... Editors: Moult, John; Brenner, Steven E. Other Names: Karchin Rachel guestEditor.; Pal Lipika R. specialEditor. Journal: Human mutation Issue: Volume 40:Issue 9(2019) Page Start: 1557 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Prognostic impact of germline mutations in inherited cancer syndromes. (October 2017) Authors: Corso, Giovanni; Feroce, Irene; Intra, Mattia; Veronesi, Paolo; Sacchini, Virgilio; Bonanni, Bernardo; Galimberti, Viviana Journal: Future oncology Issue: Volume 13:Number 24(2017) Page Start: 2125 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Rare variants in XRCC2 as breast cancer susceptibility alleles. Issue 10 (10th October 2012) Authors: Hilbers, Florentine S; Wijnen, Juul T; Hoogerbrugge, Nicoline; Oosterwijk, Jan C; Collee, Margriet J; Peterlongo, Paolo; Radice, Paolo; Manoukian, Siranoush; Feroce, Irene; Capra, Fabio; Couch, Fergus J; Wang, Xianshu; Guidugli, Lucia; Offit, Kenneth; Shah, Sohela; Campbell, Ian G; Thompson, Ella... Journal: Journal of medical genetics Issue: Volume 49:Issue 10(2012) Page Start: 618 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗