Fortuno, Cristina; Feng, Bing-Jian; Carroll, Courtney; Innella, Giovanni; Kohlmann, Wendy; Lázaro, Conxi; Brunet, Joan; Feliubadaló, Lidia; Iglesias, Silvia; Menéndez, Mireia; Teulé, Alex; Ballinger, Mandy L; Thomas, David M; Campbell, Ainsley; Field, Mike; Harris, Marion; Kirk, Judy; Pachter, Nicholas; Poplawski, Nicola; Susman, Rachel; Tucker, Kathy; Wallis, Mathew; Williams, Rachel; Cops, Elisa; Goldgar, David; James, Paul A; Spurdle, Amanda B, Cancer Risks Associated With TP53 Pathogenic Variants: Maximum Likelihood Analysis of Extended Pedigrees for Diagnosis of First Cancers Beyond the Li-Fraumeni Syndrome Spectrum, «JCO PRECISION ONCOLOGY», 2024, 8, Article number: e2300453 , pp. 1 - 18 [Scientific article]
Olivucci, Giulia; Iovino, Emanuela; Innella, Giovanni; Turchetti, Daniela; Pippucci, Tommaso; Magini, Pamela, Long read sequencing on its way to the routine diagnostics of genetic diseases, «FRONTIERS IN GENETICS», 2024, 15, pp. - - - [Scientific article]
Hendricks, Linda A J; Hoogerbrugge, Nicoline; Mensenkamp, Arjen R; Brunet, Joan; Lleuger-Pujol, Roser; Høberg-Vetti, Hildegunn; Haavind, Marianne Tveit; Innella, Giovanni; Turchetti, Daniela; Aretz, Stefan; Spier, Isabel; Tischkowitz, Marc; Jahn, Arne; Links, Thera P; Olderode-Berends, Maran J W; Blatnik, Ana; Leter, Edward M; Evans, D Gareth; Woodward, Emma R; Steinke-Lange, Verena; Anastasiadou, Violetta C; Colas, Chrystelle; Villy, Marie-Charlotte; Benusiglio, Patrick R; Gerasimenko, Anna; Barili, Valeria; Branchaud, Maud; Houdayer, Claude; Tesi, Bianca; Yazicioglu, M Omer; van der Post, Rachel S; Schuurs-Hoeijmakers, Janneke H M; van Hest, Liselotte P; Adank, Muriel A; Duijkers, Floor; Nielsen, Maartje; Verbeek, Katja C J; van Ierland, Yvette; Giltay, Jacques C; Vos, Janet R, Cancer risks by sex and variant type in PTEN Hamartoma Tumor Syndrome, «JOURNAL OF THE NATIONAL CANCER INSTITUTE», 2023, 115, pp. 93 - 103 [Scientific article]Open Access
Trevisan, Lucia; Godino, Lea; Battistuzzi, Linda; Innella, Giovanni; Luppi, Elena; Buzzatti, Giulia; Gismondi, Viviana; Blondeaux, Eva; Bonelli, Luigina Ada; Turchetti, Daniela; Varesco, Liliana, Cascade testing in Italian Hereditary Breast Ovarian Cancer families: a missed opportunity for cancer prevention?, «FAMILIAL CANCER», 2023, ?, pp. ? - ? [Scientific article]
Barbero, Giovanna; Zuntini, Roberta; Magini, Pamela; Desiderio, Laura; Bonaguro, Michela; Perrone, Anna Myriam; Rubino, Daniela; Grippa, Mina; De Leo, Antonio; Ceccarelli, Claudio; Godino, Lea; Miccoli, Sara; Ferrari, Simona; Santini, Donatella; De Iaco, Pierandrea; Zamagni, Claudio; Innella, Giovanni; Turchetti, Daniela, Characterization of BRCA Deficiency in Ovarian Cancer, «CANCERS», 2023, 15, Article number: 1530 , pp. 1 - 18 [Scientific article]Open Access
Innella, Giovanni; Ferrari, Simona; Miccoli, Sara; Luppi, Elena; Fortuno, Cristina; Parsons, Michael T; Spurdle, Amanda B; Turchetti, Daniela, Clinical implications of VUS reclassification in a single-centre series from application of ACMG/AMP classification rules specified for BRCA1/2, «JOURNAL OF MEDICAL GENETICS», 2023, ?, pp. ? - ?? [Scientific article]
Innella, Giovanni; Godino, Lea; Erini, Giulia; De Leo, Antonio; Santini, Donatella; Perrone, Anna Myriam; De Iaco, Pierandrea; Zamagni, Claudio; Turchetti, Daniela, Factors predicting BRCA1/2 pathogenic variants in patients with ovarian cancer: a systematic review with meta-analysis, «JOURNAL OF CLINICAL PATHOLOGY», 2023, 208753, pp. 510 - 517 [Scientific article]
Innella, Giovanni; Scarano, Emanuela; Palumbo, Pietro; Carella, Massimo; Severi, Giulia, New clinical features in an adult patient with Skraban-Deardorff syndrome, «AMERICAN JOURNAL OF MEDICAL GENETICS. PART A», 2022, N/A, pp. N/A - N/A [Scientific article]
Innella G.; Greco D.; Carli D.; Magini P.; Giorgio E.; Galesi O.; Ferrero G.B.; Romano C.; Brusco A.; Graziano C., Clinical spectrum and follow-up in six individuals with Lamb–Shaffer syndrome (SOX5), «AMERICAN JOURNAL OF MEDICAL GENETICS. PART A», 2021, 185, pp. 608 - 613 [Scientific article]
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 [Scientific article]
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 [Scientific article]Open Access
Isidori F.; Bozzarelli I.; Ferrari S.; Godino L.; Innella G.; Turchetti D.; Bonora E., Rasal1 and ros1 gene variants in hereditary breast cancer, «CANCERS», 2020, 12, Article number: 2539 , pp. 1 - 19 [Scientific article]Open Access
Innella G.; Rossi C.; Romagnoli M.; Repaci A.; Bianchi D.; Cantarini M.E.; Martorana D.; Godino L.; Pession A.; Percesepe A.; Pagotto U.; Turchetti D., Results and clinical interpretation of germline RET analysis in a series of patients with medullary thyroid carcinoma: The challenge of the variants of uncertain significance, «CANCERS», 2020, 12, Article number: 3268 , pp. 1 - 12 [Scientific article]Open Access
