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PALB2 sequencing in Italian familial breast cancer cases reveals a high-risk mutation recurrent in the province of Bergamo.
Catucci I, Peterlongo P, Ciceri S, Colombo M, Pasquini G, Barile M, Bonanni B, Verderio P, Pizzamiglio S, Foglia C, Falanga A, Marchetti M, Galastri L, Bianchi T, Corna C, Ravagnani F, Bernard L, Fortuzzi S, Sardella D, Scuvera G, Peissel B, Manoukian S, Tondini C, Radice P. Catucci I, et al. Among authors: ciceri s. Genet Med. 2014 Sep;16(9):688-94. doi: 10.1038/gim.2014.13. Epub 2014 Feb 20. Genet Med. 2014. PMID: 24556926 Free article.
Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors.
Roversi G, Picinelli C, Bestetti I, Crippa M, Perotti D, Ciceri S, Saccheri F, Collini P, Poliani PL, Catania S, Peissel B, Pagni F, Russo S, Peterlongo P, Manoukian S, Finelli P. Roversi G, et al. Among authors: ciceri s. Sci Rep. 2015 Oct 20;5:15454. doi: 10.1038/srep15454. Sci Rep. 2015. PMID: 26482194 Free PMC article.
Genetic and epigenetic analyses guided by high resolution whole-genome SNP array reveals a possible role of CHEK2 in Wilms tumour susceptibility.
Ciceri S, Gamba B, Corbetta P, Mondini P, Terenziani M, Catania S, Nantron M, Bianchi M, D'Angelo P, Torri F, Macciardi F, Collini P, Di Martino M, Melchionda F, Di Cataldo A, Spreafico F, Radice P, Perotti D; AIEOP study group. Ciceri S, et al. Oncotarget. 2018 Sep 25;9(75):34079-34089. doi: 10.18632/oncotarget.26123. eCollection 2018 Sep 25. Oncotarget. 2018. PMID: 30344923 Free PMC article.
Analysis of the mutational status of SIX1/2 and microRNA processing genes in paired primary and relapsed Wilms tumors and association with relapse.
Ciceri S, Montalvão-de-Azevedo R, Tajbakhsh A, Bertolotti A, Spagnuolo RD, Boschetti L, Capasso M, D'Angelo P, Serra A, Diomedi-Camassei F, Meli M, Nantron M, Quarello P, Buccoliero AM, Tamburini A, Ciniselli CM, Verderio P, Collini P, Radice P, Spreafico F, Perotti D. Ciceri S, et al. Cancer Gene Ther. 2021 Sep;28(9):1016-1024. doi: 10.1038/s41417-020-00268-3. Epub 2020 Dec 6. Cancer Gene Ther. 2021. PMID: 33281191
A novel WT1 mutation in familial wilms tumor.
Melchionda F, Spreafico F, Ciceri S, Lima M, Collini P, Pession A, Massimino M, Radice P, Perotti D. Melchionda F, et al. Among authors: ciceri s. Pediatr Blood Cancer. 2013 Aug;60(8):1388-9. doi: 10.1002/pbc.24539. Epub 2013 Mar 28. Pediatr Blood Cancer. 2013. PMID: 23554000 No abstract available.
29 results