Pantaleo M.A.; Urbini M.; Schipani A.; Nannini M.; Indio V.; De Leo A.; Vincenzi B.; Brunello A.; Grignani G.; Casagrande M.; Fumagalli E.; Conca E.; Saponara M.; Gruppioni E.; Altimari A.; De Biase D.; Tallini G.; Ravegnini G.; Turchetti D.; Seri M.; Ardizzoni A.; Secchiero P.; Astolfi A., SDHA Germline Variants in Adult Patients With SDHA-Mutant Gastrointestinal Stromal Tumor, «FRONTIERS IN ONCOLOGY», 2022, 11, Article number: 778461, pp. 1 - 7 [articolo]Open Access
De Leo, A.; de Biase, D.; Lenzi, J.; Barbero, G.; Turchetti, D.; Grillini, M.; Ravegnini, G.; Angelini, S.; Zamagni, C.; Coluccelli, S.; Dondi, G.; De Iaco, P.; Perrone, A. M.; Tallini, G.; Santini, D.; Ceccarelli, C., Arid1a and ctnnb1/β-catenin molecular status affects the clinicopathologic features and prognosis of endometrial carcinoma: Implications for an improved surrogate molecular classification, «CANCERS», 2021, 13, Article number: 950, pp. 1 - 22 [articolo]Open Access
Dika E.; Patrizi A.; Rossi C.; Turchetti D.; Miccoli S.; Ferracin M.; Veronesi G.; Scarfi F.; Lambertini M., Clinical histopathological features and CDKN2A/CDK4/MITF mutational status of patients with multiple primary melanomas from Bologna: Italy is a fascinating but complex mosaic, «ITALIAN JOURNAL OF DERMATOLOGY AND VENEREOLOGY», 2021, 156, pp. 599 - 605 [articolo]
Innella G.; Miccoli S.; Colussi D.; Pradella L.M.; Amato L.B.; Zuntini R.; Salfi N.C.M.; Collina G.; Ferrara F.; Ricciardiello L.; Turchetti D., Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review, «PATHOLOGY RESEARCH AND PRACTICE», 2021, 218, Article number: 153339, pp. 1 - 7 [articolo]
Di Pietro M.L.; Zace D.; Orfino A.; Di Raimo F.R.; Poscia A.; de Matteis E.; Turchetti D.; Godino L.; Bertonazzi B.; Franiuk M.; Bruzzone C.; Varesco L.; Lucci-Cordisco E.; Genuardi M., Correction: Intrafamilial communication of hereditary breast and ovarian cancer genetic information in Italian women: towards a personalised approach, «EUROPEAN JOURNAL OF HUMAN GENETICS», 2021, 29, Article number: 362, pp. 1 - 1 [articolo]
Urso E.D.L.; Ponz de Leon M.; Vitellaro M.; Piozzi G.N.; Bao Q.R.; Martayan A.; Remo A.; Stigliano V.; Oliani C.; Lucci Cordisco E.; Pucciarelli S.; Ranzani G.N.; Viel A.; Adami F.; Alducci E.; Amadori L.; Arcangeli V.; Balestrino L.; Barana D.; Bertario L.; Bonanni B.; Boni S.; Bullian P.; Carbonardi F.; Carnevali I.; Castelli P.; Celotto F.; Cini G.; Crivellari G.; Libera D.D.; Dell'elice A.; Digennaro M.; D'urso A.; Fabretto A.; Fanale D.; Feroce I.; Furlan D.; Ghiorzo P.; Giacche M.; Gusella M.; Liserre B.; Mammi I.; Massuras S.; Mazza D.; Mollica E.; Morabito A.; Nardo G.; Palermo F.; Panizza E.; Patruno M.; Pedroni M.; Pensotti V.G.M.; Piozzi G.N.; Pozzi S.; Presi S.; Puzzono M.; Ravegnani M.; Ricci M.T.; Roncucci L.; Rossi G.B.; Sala E.M.; Mete L.S.; Sandona D.; Sciallero S.; Serrano D.; Signoroni S.; Spina F.; Taborelli M.; Tedaldi G.; Tibiletti M.G.; Tognazzo S.; Tolva G.; Trovato C.M.C.; Turchetti D.; Varvara D.; Vivanet C.; Zovato S.; Zuppardo R.A., Definition and management of colorectal polyposis not associated with APC/MUTYH germline pathogenic variants: AIFEG consensus statement, «DIGESTIVE AND LIVER DISEASE», 2021, 53, pp. 409 - 417 [articolo]
Zuntini, Roberta; Bonora, Elena; Pradella, Laura Maria; Amato, Laura Benedetta; Vidone, Michele; De Fanti, Sara; Catucci, Irene; Cortesi, Laura; Medici, Veronica; Ferrari, Simona; Gasparre, Giuseppe; Peterlongo, Paolo; Sazzini, Marco; Turchetti, Daniela, Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next?, «INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES», 2021, 22, Article number: 5832, pp. 1 - 15 [articolo]Open Access
Franiuk M.; Molinari E.; Battistuzzi L.; Razzaboni E.; De Matteis E.; Turchetti D.; Godino L.; Chiorri C.; Varesco L., Development and Validation of an Italian Adaptation of the Psychosocial Aspects of Hereditary Cancer Questionnaire, «FRONTIERS IN PSYCHOLOGY», 2021, 12, Article number: 697300, pp. 1 - 8 [articolo]Open Access
Godino L.; Turchetti D.; Jackson L.; Hennessy C.; Skirton H., Genetic counselling as a route to enhanced autonomy: using a sequential mixed methods research approach to develop a theory regarding presymptomatic genetic testing for young adults at risk of inherited cancer syndromes, «JOURNAL OF COMMUNITY GENETICS», 2021, aug 20, pp. 0 - 0 [articolo]
G. Frega, O. Kepp, D. Turchetti, A. Rizzo, M.A. Pantaleo, G. Brandi, Hypothesis on the possible relevance of the immunogenic cell death in the treatment of gestational trophoblastic neoplasms, «TRANSLATIONAL ONCOLOGY», 2021, 14, Article number: 101224, pp. 1 - 3 [articolo]Open Access
Giacomo Santandrea, Claudio Ceccarelli, Donatella Santini, Daniela Turchetti, Claudio Zamagni, Anna Myriam Perrone, Pierandrea De Iaco, Antonio De Leo, Integrated Molecular and Clinicopathologic Study of Tubo-Ovarian High-Grade Serous Carcinoma, in: Modern Pathology, 2021, pp. 744 - 744 (atti di: United States & Canadian Academy of Pathology 110th Annual Meeting, Virtual congress, 13/03/2021) [Contributo in Atti di convegno]
Di Pietro M.L.; Zace D.; Orfino A.; Di Raimo F.R.; Poscia A.; de Matteis E.; Turchetti D.; Godino L.; Beronazzi B.; Franiuk M.; Bruzzone C.; Varesco L.; Lucci-Cordisco E.; Genuardi M., Intrafamilial communication of hereditary breast and ovarian cancer genetic information in Italian women: towards a personalised approach, «EUROPEAN JOURNAL OF HUMAN GENETICS», 2021, 29, pp. 250 - 261 [articolo]
Innella G.; Bonora E.; Neri I.; Virdi A.; Guglielmo A.; Pradella L.M.; Ceccarelli C.; Amato L.B.; Lanzoni A.; Miccoli S.; Gasparre G.; Zuntini R.; Turchetti D., PTEN Hamartoma Tumor Syndrome: Skin Manifestations and Insights Into Their Molecular Pathogenesis, «FRONTIERS IN MEDICINE», 2021, 8, Article number: 688105, pp. 1 - 11 [articolo]Open Access
De Luise, Monica; Iommarini, Luisa; Marchio, Lorena; Tedesco, Greta; Coadă, Camelia Alexandra; Repaci, Andrea; Turchetti, Daniela; Tardio, Maria Lucia; Salfi, Nunzio; Pagotto, Uberto; Kurelac, Ivana; Porcelli, Anna Maria; Gasparre, Giuseppe, Pathogenic Mitochondrial DNA Mutation Load Inversely Correlates with Malignant Features in Familial Oncocytic Parathyroid Tumors Associated with Hyperparathyroidism-Jaw Tumor Syndrome, «CELLS», 2021, 10, Article number: 2920, pp. 1 - 16 [articolo]Open Access
Godino L.; Varesco L.; Bruno W.; Bruzzone C.; Battistuzzi L.; Franiuk M.; Miccoli S.; Bertonazzi B.; Graziano C.; Seri M.; Turchetti D., Preferences of Italian patients for return of secondary findings from clinical genome/exome sequencing, «JOURNAL OF GENETIC COUNSELING», 2021, 30, pp. 665 - 675 [articolo]
