Paola Ogliara
Turin, Italy
Last Updated: 09/26/2026
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Found 9 publications
Rapid minigene workflow for functional reclassification of splicing variants in hereditary cancer diagnostics.
Journal: Journal of medical genetics
Published: April 17, 2026
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.
Journal: Melanoma research
Published: September 01, 2022
Analysis of Italian BRCA1/2 Pathogenic Variants Identifies a Private Spectrum in the Population from the Bergamo Province in Northern Italy.
Journal: Cancers
Published: December 03, 2020
Sensitivity to asbestos is increased in patients with mesothelioma and pathogenic germline variants in BAP1 or other DNA repair genes.
Journal: Genes, chromosomes & cancer
Published: February 05, 2018
Melanoma-prone families: new evidence of distinctive clinical and histological features of melanomas in CDKN2A mutation carriers.
Journal: Archives of dermatological research
Published: July 26, 2017
CDKN2A and BAP1 germline mutations predispose to melanoma and mesothelioma.
Journal: Cancer letters
Published: March 21, 2016
Germline CDKN2A mutations in childhood melanoma: a case of melanoma-pancreatic cancer syndrome.
Journal: International journal of dermatology
Published: June 19, 2014
A founder MLH1 mutation in Lynch syndrome families from Piedmont, Italy, is associated with an increased risk of pancreatic tumours and diverse immunohistochemical patterns.
Journal: Familial cancer
Published: May 08, 2014
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Last Updated: 09/26/2026