Giovanna Scarra-Bianchi

Genoa, Italy

Last Updated: 09/26/2026

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Found 23 publications

Functional analysis of a CDKN2A 5'UTR germline variant associated with pancreatic cancer development.

Functional analysis of a CDKN2A 5'UTR germline variant associated with pancreatic cancer development.

Journal: PloS one

Published: July 20, 2017

Heterogeneity and frequency of BRAF mutations in primary melanoma: Comparison between molecular methods and immunohistochemistry.

Heterogeneity and frequency of BRAF mutations in primary melanoma: Comparison between molecular methods and immunohistochemistry.

Journal: Oncotarget

Published: September 20, 2016

Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations.

Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations.

Journal: Human genetics

Published: April 05, 2016

The CDKN2A/p16(INK) (4a) 5'UTR sequence and translational regulation: impact of novel variants predisposing to melanoma.

The CDKN2A/p16(INK) (4a) 5'UTR sequence and translational regulation: impact of novel variants predisposing to melanoma.

Journal: Pigment cell & melanoma research

Published: September 14, 2015

Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families.

Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families.

Journal: The Journal of investigative dermatology

Published: July 29, 2015

Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup.

Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup.

Journal: Journal of the American Academy of Dermatology

Published: July 28, 2015

A combination of immunohistochemistry and molecular approaches improves highly sensitive detection of BRAF mutations in papillary thyroid cancer.

A combination of immunohistochemistry and molecular approaches improves highly sensitive detection of BRAF mutations in papillary thyroid cancer.

Journal: Endocrine

Published: June 16, 2015

Histologic features of melanoma associated with CDKN2A genotype.

Histologic features of melanoma associated with CDKN2A genotype.

Journal: Journal of the American Academy of Dermatology

Published: July 15, 2014

Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions.

Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions.

Journal: International journal of cancer

Published: March 24, 2014

Brooke-Spiegler syndrome tumor spectrum beyond the skin: a patient carrying germline R936X CYLD mutation and a somatic CYLD mutation in Brenner tumor.

Brooke-Spiegler syndrome tumor spectrum beyond the skin: a patient carrying germline R936X CYLD mutation and a somatic CYLD mutation in Brenner tumor.

Journal: Future oncology (London, England)

Published: February 25, 2014

CDKN2A unclassified variants in familial malignant melanoma: combining functional and computational approaches for their assessment.

CDKN2A unclassified variants in familial malignant melanoma: combining functional and computational approaches for their assessment.

Journal: Human mutation

Published: July 03, 2013

Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families.

Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families.

Journal: The Journal of investigative dermatology

Published: May 01, 2013

Showing 1-12 of 23

Last Updated: 09/26/2026