Ilaria Cangini
Meldola, Italy
Last Updated: 09/26/2026
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Found 20 publications
Mutational and low-coverage whole genome sequencing identifies actionable DNA repair alterations in prostate cancer plasma DNA.
Journal: Scientific reports
Published: December 05, 2024
Comprehensive genetic and epigenetic characterization of Lynch-like syndrome patients.
Journal: International journal of cancer
Published: October 28, 2024
Olaparib as a rescue treatment in platinum-refractory germ-cell tumors: the IGG-02 phase II trial.
Journal: ESMO open
Published: September 11, 2024
Exploring the promoter regions of cancer predisposition genes in patients with triple-negative breast cancer reveals the presence of rare germline variants.
Journal: The oncologist
Published: April 12, 2024
A Novel FLCN Variant in a Suspected Birt-Hogg-Dubè Syndrome Patient.
Journal: International journal of molecular sciences
Published: July 13, 2023
Clinical Impact of Next-Generation Sequencing Multi-Gene Panel Highlighting the Landscape of Germline Alterations in Ovarian Cancer Patients.
Journal: International journal of molecular sciences
Published: October 18, 2022
Case Report: A BRCA2 Mutation Identified Through Next-Generation Sequencing in a Birt-Hogg-Dubè Syndrome Family.
Journal: Frontiers in oncology
Published: December 14, 2021
Comprehensive analysis of DNA damage repair genes reveals pathogenic variants beyond BRCA and suggests the need for extensive genetic testing in pancreatic cancer.
Journal: BMC cancer
Published: January 13, 2021
Male Breast Cancer: Results of the Application of Multigene Panel Testing to an Italian Cohort of Patients.
Journal: Diagnostics (Basel, Switzerland)
Published: March 31, 2020
Identification of a novel large EPCAM-MSH2 duplication, concurrently with LOHs in chromosome 20 and X, in a family with Lynch syndrome.
Journal: International journal of colorectal disease
Published: September 23, 2019
Last Updated: 09/26/2026