Pubblicazioni

Characterization of human frataxin missense variants in cancer tissues

2019 - HUMAN MUTATION

Petrosino, Maria; Pasquo, Alessandra; Novak, Leonore; Toto, Angelo; Gianni, Stefano; Mantuano, Elide; Veneziano, Liana; Minicozzi, Velia; Pastore, Annalisa; Puglisi, Rita; Capriotti, Emidio; Chiaraluce, Roberta; Consalvi, Valerio

Targeted next generation sequencing of breast implant-associated anaplastic large cell lymphoma reveals mutations in JAK/STAT signalling pathway genes, TP53 and DNMT3A

2018 - BRITISH JOURNAL OF HAEMATOLOGY

DI NAPOLI, Arianna; Jain, Preti; Duranti, Enrico; Margolskee, Elizabeth; Arancio, Walter; Facchetti, Fabio; Alobeid, Bachir; SANTANELLI DI POMPEO, Fabio; Mansukhani, Mahesh; Bhagat, Govind

Genomic and Molecular Landscape of DNA Damage Repair Deficiency across The Cancer Genome Atlas

2018 - CELL REPORTS

Theo A, Knijnenburg; Linghua, Wang; Michael T, Zimmermann; Nyasha, Chambwe; Galen F, Gao; Andrew D, Cherniack; Huihui, Fan; Hui, Shen; Gregory P, Way; Casey S, Greene; Yuexin, Liu; Rehan, Akbani; Bin, Feng; Lawrence A, Donehower; Chase, Miller; Yang, Shen; Mostafa, Karimi; Haoran, Chen; Pora, Kim; Peilin, Jia; Eve, Shinbrot; Shaojun, Zhang; Jianfang, Liu; Hai, Hu; Matthew H, Bailey; Christina, Yau; Denise, Wolf; Zhongming, Zhao; John N, Weinstein; Lei, Li; Li, Ding; Gordon B, Mills; Peter W, Laird; David A, Wheeler; Ilya, Shmulevich; Alvaro, Domenico; Bragazzi, MARIA CONSIGLIA; Cardinale, Vincenzo; Gaudio, Eugenio; Raymond J, Monnat; Yonghong, Xiao; Chen, Wang

Pediatric non-Down syndrome acute megakaryoblastic leukemia is characterized by distinct genomic subsets with varying outcomes

2017 - NATURE GENETICS

De Rooij, J. D. E.; Branstetter, C.; Ma, J.; Li, Y.; Walsh, M. P.; Cheng, J.; Obulkasim, A.; Dang, J.; Easton, J.; Verboon, L. J.; Mulder, H. L.; Zimmermann, M.; Koss, C.; Gupta, P.; Edmonson, M.; Rusch, M.; Lim, J. Y. S.; Reinhardt, K.; Pigazzi, M.; Song, G.; Yeoh, A. E. J.; Shih, L. -Y.; Liang, D. -C.; Halene, S.; Krause, D. S.; Zhang, J.; Downing, J. R.; Locatelli, F.; Reinhardt, D.; Van Den Heuvel-Eibrink, M. M.; Zwaan, C. M.; Fornerod, M.; Gruber, T. A.

Somatic alterations of targetable oncogenes are frequently observed in BRCA1/2 mutation negative male breast cancers

2016 - ONCOTARGET

Rizzolo, Piera; Navazio, ANNA SARA; Silvestri, Valentina; Valentini, Virginia; Zelli, Veronica; Zanna, Ines; Masala, Giovanna; Bianchi, Simonetta; ScarnÃ², Marco; Tommasi, Stefania; Palli, Domenico; Ottini, Laura

Recommendations for the implementation of BRCA testing in the care and treatment pathways of ovarian cancer patients

2016 - FUTURE ONCOLOGY

Pinto, Carmine; Bella, Maria Angela; Capoluongo, Ettore; Carrera, Paola; Clemente, Claudio; Colombo, Nicoletta; Cortesi, Laura; De Rosa, Gaetano; Fenizia, Francesca; Genuardi, Maurizio; Gori, Stefania; Guarneri, Valentina; Marchetti, Antonio; Marchetti, Paolo; Normanno, Nicola; Pasini, Barbara; Pignata, Sandro; Radice, Paolo; Ricevuto, Enrico; Russo, Antonio; Tagliaferri, Pierosandro; Tassone, Pierfrancesco; Truini, Mauro; Varesco, Liliana

Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents

2016 - BLOOD

Wlodarski, M. W.; Hirabayashi, S.; Pastor, V.; Stary, J.; Hasle, H.; Masetti, R.; Dworzak, M.; Schmugge, M.; Van Den Heuvel-Eibrink, M.; Ussowicz, M.; De Moerloose, B.; Catala, A.; Smith, O. P.; Sedlacek, P.; Lankester, A. C.; Zecca, M.; Bordon, V.; Matthes-Martin, S.; Abrahamsson, J.; Kuhl, J. S.; Sykora, K. -W.; Albert, M. H.; Przychodzien, B.; Maciejewski, J. P.; Schwarz, S.; Gohring, G.; Schlegelberger, B.; Cseh, A.; Noellke, P.; Yoshimi, A.; Locatelli, F.; Baumann, I.; Strahm, B.; Niemeyer, C. M.