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Page 1
Non-Coding RNA and Tumor Development in Neurofibromatosis Type 1: ANRIL Rs2151280 Is Associated with Optic Glioma Development and a Mild Phenotype in Neurofibromatosis Type 1 Patients.
Genes (Basel). 2019 Nov 5;10(11):892. doi: 10.3390/genes10110892.
Genes (Basel). 2019.
PMID: 31694342
Free PMC article.
Review.
Simultaneous Detection of NF1, SPRED1, LZTR1, and NF2 Gene Mutations by Targeted NGS in an Italian Cohort of Suspected NF1 Patients.
Bianchessi D, Ibba MC, Saletti V, Blasa S, Langella T, Paterra R, Cagnoli GA, Melloni G, Scuvera G, Natacci F, Cesaretti C, Finocchiaro G, Eoli M.
Bianchessi D, et al.
Genes (Basel). 2020 Jun 19;11(6):671. doi: 10.3390/genes11060671.
Genes (Basel). 2020.
PMID: 32575496
Free PMC article.
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126 novel mutations in Italian patients with neurofibromatosis type 1.
Bianchessi D, Morosini S, Saletti V, Ibba MC, Natacci F, Esposito S, Cesaretti C, Riva D, Finocchiaro G, Eoli M.
Bianchessi D, et al.
Mol Genet Genomic Med. 2015 Jul 7;3(6):513-25. doi: 10.1002/mgg3.161. eCollection 2015 Nov.
Mol Genet Genomic Med. 2015.
PMID: 26740943
Free PMC article.
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Risk of Optic Pathway Glioma in Neurofibromatosis Type 1: No Evidence of Genotype-Phenotype Correlations in A Large Independent Cohort.
Melloni G, Eoli M, Cesaretti C, Bianchessi D, Ibba MC, Esposito S, Scuvera G, Morcaldi G, Micheli R, Piozzi E, Avignone S, Chiapparini L, Pantaleoni C, Natacci F, Finocchiaro G, Saletti V.
Melloni G, et al. Among authors: bianchessi d.
Cancers (Basel). 2019 Nov 21;11(12):1838. doi: 10.3390/cancers11121838.
Cancers (Basel). 2019.
PMID: 31766501
Free PMC article.
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DNA microarray analysis identifies CKS2 and LEPR as potential markers of meningioma recurrence.
Menghi F, Orzan FN, Eoli M, Farinotti M, Maderna E, Pisati F, Bianchessi D, Valletta L, Lodrini S, Galli G, Anghileri E, Pellegatta S, Pollo B, Finocchiaro G.
Menghi F, et al. Among authors: bianchessi d.
Oncologist. 2011;16(10):1440-50. doi: 10.1634/theoncologist.2010-0249. Epub 2011 Sep 23.
Oncologist. 2011.
PMID: 21948653
Free PMC article.
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Identification of an atypical microdeletion generating the RNF135-SUZ12 chimeric gene and causing a position effect in an NF1 patient with overgrowth.
Ferrari L, Scuvera G, Tucci A, Bianchessi D, Rusconi F, Menni F, Battaglioli E, Milani D, Riva P.
Ferrari L, et al. Among authors: bianchessi d.
Hum Genet. 2017 Oct;136(10):1329-1339. doi: 10.1007/s00439-017-1832-5. Epub 2017 Aug 3.
Hum Genet. 2017.
PMID: 28776093
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Methylation of O6-methylguanine DNA methyltransferase and loss of heterozygosity on 19q and/or 17p are overlapping features of secondary glioblastomas with prolonged survival.
Eoli M, Menghi F, Bruzzone MG, De Simone T, Valletta L, Pollo B, Bissola L, Silvani A, Bianchessi D, D'Incerti L, Filippini G, Broggi G, Boiardi A, Finocchiaro G.
Eoli M, et al. Among authors: bianchessi d.
Clin Cancer Res. 2007 May 1;13(9):2606-13. doi: 10.1158/1078-0432.CCR-06-2184.
Clin Cancer Res. 2007.
PMID: 17473190
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