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Page 1
Temporal correlation between the first melanoma and the first noncutaneous tumor in CKDN2A genotyped patients.
Gironi LC, Esposto E, Zottarelli F, Giorgione R, Farinelli P, Zavattaro E, Cammarata E, Di Cristo N, Ogliara P, Camillo L, Giordano M, Mellone S, Pasini B, Ambrosi A, Savoia P. Gironi LC, et al. Among authors: ogliara p. Melanoma Res. 2023 Oct 1;33(5):425-430. doi: 10.1097/CMR.0000000000000906. Epub 2023 Jun 21. Melanoma Res. 2023. PMID: 37352544
BRCA1-associated protein 1 c.368delG mutation leads to the development of multiple BAPomas and cutaneous melanomas: a novel pathogenic variant in BRCA1-associated protein tumor predisposition syndrome.
Cavallo F, Roccuzzo G, Merli M, Avallone G, Zocchi L, Ogliara P, Pasini B, Quaglino P, Ribero S. Cavallo F, et al. Among authors: ogliara p. Melanoma Res. 2022 Oct 1;32(5):390-392. doi: 10.1097/CMR.0000000000000846. Epub 2022 Aug 31. Melanoma Res. 2022. PMID: 36045597 No abstract available.
Analysis of Italian BRCA1/2 Pathogenic Variants Identifies a Private Spectrum in the Population from the Bergamo Province in Northern Italy.
Figlioli G, De Nicolo A, Catucci I, Manoukian S, Peissel B, Azzollini J, Beltrami B, Bonanni B, Calvello M, Bondavalli D, Pasini B, Vignolo Lutati F, Ogliara P, Zuradelli M, Pensotti V, De Vecchi G, Volorio S, Verderio P, Pizzamiglio S, Matullo G, Aneli S, Birolo G, Zanardi F, Tondini C, Zambelli A, Livraghi L, Franchi M, Radice P, Peterlongo P. Figlioli G, et al. Among authors: ogliara p. Cancers (Basel). 2021 Jan 30;13(3):532. doi: 10.3390/cancers13030532. Cancers (Basel). 2021. PMID: 33573335 Free PMC article.
Sensitivity to asbestos is increased in patients with mesothelioma and pathogenic germline variants in BAP1 or other DNA repair genes.
Betti M, Aspesi A, Ferrante D, Sculco M, Righi L, Mirabelli D, Napoli F, Rondón-Lagos M, Casalone E, Vignolo Lutati F, Ogliara P, Bironzo P, Gironi CL, Savoia P, Maffè A, Ungari S, Grosso F, Libener R, Boldorini R, Valiante M, Pasini B, Matullo G, Scagliotti G, Magnani C, Dianzani I. Betti M, et al. Among authors: ogliara p. Genes Chromosomes Cancer. 2018 Nov;57(11):573-583. doi: 10.1002/gcc.22670. Genes Chromosomes Cancer. 2018. PMID: 30338612
A founder MLH1 mutation in Lynch syndrome families from Piedmont, Italy, is associated with an increased risk of pancreatic tumours and diverse immunohistochemical patterns.
Borelli I, Casalis Cavalchini GC, Del Peschio S, Micheletti M, Venesio T, Sarotto I, Allavena A, Delsedime L, Barberis MA, Mandrile G, Berchialla P, Ogliara P, Bracco C, Pasini B. Borelli I, et al. Among authors: ogliara p. Fam Cancer. 2014 Sep;13(3):401-13. doi: 10.1007/s10689-014-9726-3. Fam Cancer. 2014. PMID: 24802709 Free article.