Sara Volorio

Milan, Italy

Last Updated: 09/26/2026

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Found 23 publications

From Therapy to Cancer Prevention Using HRD Testing on Patients with High-grade Ovarian Cancer.

From Therapy to Cancer Prevention Using HRD Testing on Patients with High-grade Ovarian Cancer.

Journal: Cancer prevention research (Philadelphia, Pa.)

Published: October 14, 2024

De novo germline pathogenic variant in Lynch Syndrome: A rare event or the tip of the iceberg?

De novo germline pathogenic variant in Lynch Syndrome: A rare event or the tip of the iceberg?

Journal: Tumori

Published: September 11, 2023

OncoPan®: An NGS-Based Screening Methodology to Identify Molecular Markers for Therapy and Risk Assessment in Pancreatic Ductal Adenocarcinoma.

OncoPan®: An NGS-Based Screening Methodology to Identify Molecular Markers for Therapy and Risk Assessment in Pancreatic Ductal Adenocarcinoma.

Journal: Biomedicines

Published: April 27, 2022

Analysis of Italian BRCA1/2 Pathogenic Variants Identifies a Private Spectrum in the Population from the Bergamo Province in Northern Italy.

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

Development, technical validation, and clinical application of a multigene panel for hereditary gastrointestinal cancer and polyposis.

Development, technical validation, and clinical application of a multigene panel for hereditary gastrointestinal cancer and polyposis.

Journal: Tumori

Published: May 10, 2019

Two Missense Variants Detected in Breast Cancer Probands Preventing BRCA2-PALB2 Protein Interaction.

Two Missense Variants Detected in Breast Cancer Probands Preventing BRCA2-PALB2 Protein Interaction.

Journal: Frontiers in oncology

Published: August 03, 2018

Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.

Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.

Journal: Nature communications

Published: April 11, 2018

Haplotype analyses of the c.1027C>T and c.2167_2168delAT recurrent truncating mutations in the breast cancer-predisposing gene PALB2.

Haplotype analyses of the c.1027C>T and c.2167_2168delAT recurrent truncating mutations in the breast cancer-predisposing gene PALB2.

Journal: Breast cancer research and treatment

Published: August 31, 2016

The hidden genomic landscape of acute myeloid leukemia: subclonal structure revealed by undetected mutations.

The hidden genomic landscape of acute myeloid leukemia: subclonal structure revealed by undetected mutations.

Journal: Blood

Published: December 16, 2014

FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.

FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.

Journal: Human molecular genetics

Published: December 01, 2014

Whole exome sequencing identifies driver mutations in asymptomatic computed tomography-detected lung cancers with normal karyotype.

Whole exome sequencing identifies driver mutations in asymptomatic computed tomography-detected lung cancers with normal karyotype.

Journal: Cancer genetics

Published: August 29, 2014

Deep sequencing of the X chromosome reveals the proliferation history of colorectal adenomas.

Deep sequencing of the X chromosome reveals the proliferation history of colorectal adenomas.

Journal: Genome biology

Published: April 29, 2014

Showing 1-12 of 23

Last Updated: 09/26/2026