De Leo, G. Santandrea, R. Zuntini, G. Barbero, D. Turchetti, B. Corti, D. Rubino, G. Dondi, G. Borghese, A.N. Della Gatta, A.M. Perrone, P. De Iaco, C. Ceccarelli, D. Santini., BRCA and High-Grade Serous Carcinoma: a Morphological, Immunohistochemical and Genetic Study., in: Modern Pathology, «MODERN PATHOLOGY», 2019, pp. 27 - 28 (atti di: Annual Meeting of United States and Canadian Academy of Pathology (USCAP) 2019, National Harbor, Maryland, USA., MARCH 16-21, 2019) [Contribution to conference proceedings]
Turchetti, Daniela; Zuntini, Roberta; Tricarico, Rossella; Bellacosa, Alfonso, BRCA2 in Ovarian Development and Function, «THE NEW ENGLAND JOURNAL OF MEDICINE», 2019, 380, pp. 1086 - 1087 [Comment or similar]
G. Santandrea, A. De Leo, C. Ceccarelli, G. Barbero, S. Ferrari, D. Turchetti, D. Rubino, C. Zamagni, G. Dondi, A.M. Perrone, P. De Iaco, D. Santini., High-grade serous carcinoma: a comprehensive genetic and clinico-pathologic study of a heterogeneous neoplasm., in: Pathologica, «PATHOLOGICA», 2019, pp. 256 - 257 (atti di: Congress of the Italian Society of Anatomic Pathology (SIAPEC) 2019, Torino, 16/10/2019) [Contribution to conference proceedings]
A. De Leo, C. Ceccarelli, D. Turchetti, D. Santini, A.M. Perrone, P. De Iaco., Pathologic findings in risk-reducing salpingo-oophorectomy (RRSO) in women with BRCA1 or BRCA2 mutations: a single center experience., in: International Journal of Gynecologic Cancer, 2019, pp. 455 - 456 (atti di: 21st European Congress on Gynaecological Oncology, Athens, 2 - 5 November 2019) [Contribution to conference proceedings]
Godino, Lea; Turchetti, Daniela; Jackson, Leigh; Hennessy, Catherine; Skirton, Heather, Presymptomatic genetic testing for hereditary cancer in young adults: a survey of young adults and parents, «EUROPEAN JOURNAL OF HUMAN GENETICS», 2019, 27, pp. 291 - 299 [Scientific article]
De Leo, G. Santandrea, C. Ceccarelli, G. Barbero, S. Ferrari, D. Turchetti, D. Rubino, A. M. Perrone, P. De Iaco, D. Santini., Supporting the hypothesis of a dualistic model for high-grade serous carcinoma: a genetic and pathological study., in: Virchows Archiv, 2019, pp. 55 - 55 (atti di: 31st European Congress of Pathology, Nice, 7 - 11 September 2019) [Contribution to conference proceedings]
Jackson, Leigh; O’Connor, Anita; Paneque, Milena; Curtisova, Vaclava; Lunt, Peter W.; Pourova, Radka Kremlíková; Macek, Milan; Stefansdottir, Vigdis; Turchetti, Daniela; Campos, Mariana; Henneman, Lidewij; Godino, Lea; Skirton, Heather; Cornel, Martina C.*, The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages, «GENETICS IN MEDICINE», 2019, 21, pp. 718 - 726 [Scientific article]Open Access
Zuntini, Roberta; Ferrari, Simona; Bonora, Elena; Buscherini, Francesco; Bertonazzi, Benedetta; Grippa, Mina; Godino, Lea; Miccoli, Sara; Turchetti, Daniela*, Dealing With BRCA1/2 unclassified variants in a cancer genetics clinic: Does cosegregation analysis help?, «FRONTIERS IN GENETICS», 2018, 9, Article number: 378 , pp. 1 - 15 [Scientific article]Open Access
Godino, Lea; Jackson, Leigh; Turchetti, Daniela; Hennessy, Catherine; Skirton, Heather, Decision making and experiences of young adults undergoing presymptomatic genetic testing for familial cancer: A longitudinal grounded theory study, «EUROPEAN JOURNAL OF HUMAN GENETICS», 2018, 26, pp. 44 - 53 [Scientific article]Open Access
Muscarella, Lucia Anna; Turchetti, Daniela; Fontana, Andrea; Baorda, Filomena; Palumbo, Orazio; la Torre, Annamaria; de Martino, Danilo; Franco, Renato; Losito, Nunzia Simona; Repaci, Andrea; Pagotto, Uberto; Cinque, Luigia; Copetti, Massimiliano; Chiofalo, Maria Grazia; Pezzullo, Luciano; Graziano, Paolo; Scillitani, Alfredo; Guarnieri, Vito*, Large deletion at the CDC73 gene locus and search for predictive markers of the presence of a CDC73 genetic lesion, «ONCOTARGET», 2018, 9, pp. 20721 - 20733 [Scientific article]Open Access
Prossomariti, Anna; Piazzi, Giulia; D'Angelo, Leonarda; Miccoli, Sara; Turchetti, Daniela; Alquati, Chiara; Montagna, Claudio; Bazzoli, Franco; Ricciardiello, Luigi, miR-155 Is Downregulated in Familial Adenomatous Polyposis and Modulates WNT Signaling by Targeting AXIN1 and TCF4, «MOLECULAR CANCER RESEARCH», 2018, 16, pp. 1965 - 1976 [Scientific article]
Dámaso, Estela; Castillejo, Adela; Arias, María del Mar; Canet-Hermida, Julia; Navarro, Matilde; del Valle, Jesús; Campos, Olga; Fernández, Anna; Marín, Fátima; Turchetti, Daniela; García-Díaz, Juan de Dios; Lázaro, Conxi; Genuardi, Maurizio; Rueda, Daniel; Alonso, Ángel; Soto, Jose Luis; Hitchins, Megan; Pineda, Marta*; Capellá, Gabriel, Primary constitutional MLH1 epimutations: a focal epigenetic event, «BRITISH JOURNAL OF CANCER», 2018, 119, pp. 978 - 987 [Scientific article]Open Access
Ciavarella, Michele; Miccoli, Sara; Prossomariti, Anna; Pippucci, Tommaso; Bonora, Elena; Buscherini, Francesco; Palombo, Flavia; Zuntini, Roberta; Balbi, Tiziana; Ceccarelli, Claudio; Bazzoli, Franco; Ricciardiello, Luigi; Turchetti, Daniela; Piazzi, Giulia, Somatic APC mosaicism and oligogenic inheritance in genetically unsolved colorectal adenomatous polyposis patients, «EUROPEAN JOURNAL OF HUMAN GENETICS», 2018, --, pp. 1 - 9 [Scientific article]Open Access
Tricarico, Rossella; Kasela, Mariann; Mareni, Cristina; Thompson, Bryony A.; Drouet, Aurélie; Staderini, Lucia; Gorelli, Greta; Crucianelli, Francesca; Ingrosso, Valentina; Kantelinen, Jukka; Papi, Laura; De Angioletti, Maria; Berardi, Margherita; Gaildrat, Pascaline; Soukarieh, Omar; Turchetti, Daniela; Martins, Alexandra; Spurdle, Amanda B.; Nyström, Minna; Genuardi, Maurizio, Assessment of the InSiGHT Interpretation Criteria for the Clinical Classification of 24 MLH1 and MSH2 Gene Variants, «HUMAN MUTATION», 2017, 38, pp. 64 - 77 [Scientific article]
Zuntini, Roberta; Cortesi, Laura; Calistri, Daniele; Pippucci, Tommaso; Martelli, Pier Luigi; Casadio, Rita; Capizzi, Elisa; Santini, Donatella; Miccoli, Sara; Medici, Veronica; Danesi, Rita; Marchi, Isabella; Zampiga, Valentina; Fiorentino, Michelangelo; Ferrari, Simona; Turchetti, Daniela, BRCA1 p.His1673del is a pathogenic mutation associated with a predominant ovarian cancer phenotype, «ONCOTARGET», 2017, 8, pp. 22640 - 22648 [Scientific article]
