1. A Targeted Approach to Genetic Counseling in Breast Cancer Patients: The Experience of an Italian Local Project. Issue 1 (January 2016) Authors: La Verde, Nicla; Corsi, Fabio; Moretti, Anna; Peissel, Bernard; Dalu, Davide; Girelli, Serena; Fasola, Cinzia; Gambaro, Anna; Roversi, Gaia; Azzollini, Jacopo; Radice, Paolo; Pensotti, Valeria; Farina, Gabriella; Manoukian, Siranoush Journal: Tumori Issue: Volume 102:Issue 1(2016) Page Start: 45 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores. (28th July 2021) Authors: Barnes, Daniel R; Silvestri, Valentina; Leslie, Goska; McGuffog, Lesley; Dennis, Joe; Yang, Xin; Adlard, Julian; Agnarsson, Bjarni A; Ahmed, Munaza; Aittomäki, Kristiina; Andrulis, Irene L; Arason, Adalgeir; Arnold, Norbert; Auber, Bernd; Azzollini, Jacopo; Balmaña, Judith; Barkardottir, Rosa B; ... Journal: Journal of the National Cancer Institute Issue: Volume 114:Number 1(2022) Page Start: 109 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical heterogeneity and reduced penetrance in DICER1 syndrome: a report of three families. Issue 6 (December 2021) Authors: Azzollini, Jacopo; Ferrari, Andrea; Stracuzzi, Alessandra; Chiaravalli, Stefano; Terenziani, Monica; Spreafico, Filippo; Grasso, Maurizia; Collini, Paola; Pensotti, Valeria; Massimino, Maura; Arbustini, Eloisa; Manoukian, Siranoush Journal: Tumori Issue: Volume 107:Issue 6(2021) Page Start: NP144 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium. (18th June 2014) Authors: Milne, Roger L.; Burwinkel, Barbara; Michailidou, Kyriaki; Arias-Perez, Jose-Ignacio; Zamora, M. Pilar; Menéndez-Rodríguez, Primitiva; Hardisson, David; Mendiola, Marta; González-Neira, Anna; Pita, Guillermo; Alonso, M. Rosario; Dennis, Joe; Wang, Qin; Bolla, Manjeet K.; Swerdlow, Anthony; Ashwor... Other Names: Berchuck Andrew author non-byline.; Eeles Rosalind A. author non-byline.; Olama Ali Amin Al author non-byline.; Kote-Jarai Zsofia author non-byline.; Benlloch Sara author non-byline.; Antoniou Antonis author non-byline.; McGuffog Lesley author non-byline.; Offit Ken author non-byline.; Lee Andrew... Journal: Human molecular genetics Issue: Volume 23:Number 22(2014:Nov. 15) Page Start: 6096 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Cornelia de Lange individuals with new and recurrent SMC1A mutations enhance delineation of mutation repertoire and phenotypic spectrum. Issue 11 (2nd October 2013) Authors: Gervasini, Cristina; Russo, Silvia; Cereda, Anna; Parenti, Ilaria; Masciadri, Maura; Azzollini, Jacopo; Melis, Daniela; Aravena, Teresa; Doray, Bérénice; Ferrarini, Alessandra; Garavelli, Livia; Selicorni, Angelo; Larizza, Lidia Journal: American journal of medical genetics Issue: Volume 161:Issue 11(2013:Nov.) Page Start: 2909 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Evaluation of CYP17A1 and CYP1B1 polymorphisms in male breast cancer risk. Issue 8 (August 2019) Authors: Rizzolo, Piera; Silvestri, Valentina; Valentini, Virginia; Zelli, Veronica; Bucalo, Agostino; Zanna, Ines; Bianchi, Simonetta; Tibiletti, Maria Grazia; Russo, Antonio; Varesco, Liliana; Tedaldi, Gianluca; Bonanni, Bernardo; Azzollini, Jacopo; Manoukian, Siranoush; Coppa, Anna; Giannini, Giuseppe;... Journal: Endocrine connections Issue: Volume 8:Issue 8(2019) Page Start: 1224 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study. (12th October 2018) Authors: Qian, Frank; Wang, Shengfeng; Mitchell, Jonathan; McGuffog, Lesley; Barrowdale, Daniel; Leslie, Goska; Oosterwijk, Jan C; Chung, Wendy K; Evans, D Gareth; Engel, Christoph; Kast, Karin; Aalfs, Cora M; Adank, Muriel A; Adlard, Julian; Agnarsson, Bjarni A; Aittomäki, Kristiina; Alducci, Elisa; Andr... Journal: Journal of the National Cancer Institute Issue: Volume 111:Number 4(2019) Page Start: 350 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Insight into genetic susceptibility to male breast cancer by multigene panel testing: Results from a multicenter study in Italy. Issue 2 (24th January 2019) Authors: Rizzolo, Piera; Zelli, Veronica; Silvestri, Valentina; Valentini, Virginia; Zanna, Ines; Bianchi, Simonetta; Masala, Giovanna; Spinelli, Alessandro Mauro; Tibiletti, Maria Grazia; Russo, Antonio; Varesco, Liliana; Giannini, Giuseppe; Capalbo, Carlo; Calistri, Daniele; Cortesi, Laura; Viel, Alessa... Journal: International journal of cancer Issue: Volume 145:Issue 2(2019) Page Start: 390 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. 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) ↗
10. Mutational spectrum in a worldwide study of 29, 700 families with BRCA1 or BRCA2 mutations. Issue 5 (12th March 2018) Authors: Rebbeck, Timothy R.; Friebel, Tara M.; Friedman, Eitan; Hamann, Ute; Huo, Dezheng; Kwong, Ava; Olah, Edith; Olopade, Olufunmilayo I.; Solano, Angela R.; Teo, Soo‐Hwang; Thomassen, Mads; Weitzel, Jeffrey N.; Chan, TL; Couch, Fergus J.; Goldgar, David E.; Kruse, Torben A.; Palmero, Edenir Inêz; Par... Journal: Human mutation Issue: Volume 39:Issue 5(2018) Page Start: 593 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗