Arianna Nicolussi

Rome, 00161, Italy

Last Updated: 09/26/2026

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Found 20 publications

NSD1 Mutations and Pediatric High-Grade Gliomas: A Comparative Genomic Study in Primary and Recurrent Tumors.

NSD1 Mutations and Pediatric High-Grade Gliomas: A Comparative Genomic Study in Primary and Recurrent Tumors.

Journal: Diagnostics (Basel, Switzerland)

Published: November 13, 2022

Molecular profiling of male breast cancer by multigene panel testing: Implications for precision oncology.

Molecular profiling of male breast cancer by multigene panel testing: Implications for precision oncology.

Journal: Frontiers in oncology

Published: November 07, 2022

CTNNB1 p.L31P mutation in an ovarian endometrioid carcinoma with synchronous uterine endometrioid carcinoma.

CTNNB1 p.L31P mutation in an ovarian endometrioid carcinoma with synchronous uterine endometrioid carcinoma.

Journal: Pathology, research and practice

Published: August 24, 2020

A novel BRCA2 splice variant identified in a young woman.

A novel BRCA2 splice variant identified in a young woman.

Journal: Molecular genetics & genomic medicine

Published: June 21, 2020

Clinical Multigene Panel Sequencing Identifies Distinct Mutational Association Patterns in Metastatic Colorectal Cancer.

Clinical Multigene Panel Sequencing Identifies Distinct Mutational Association Patterns in Metastatic Colorectal Cancer.

Journal: Frontiers in oncology

Published: October 02, 2019

Identification of novel BRCA1 large genomic rearrangements by a computational algorithm of amplicon-based Next-Generation Sequencing data.

Identification of novel BRCA1 large genomic rearrangements by a computational algorithm of amplicon-based Next-Generation Sequencing data.

Journal: PeerJ

Published: August 29, 2019

A Simplified Genomic Profiling Approach Predicts Outcome in Metastatic Colorectal Cancer.

A Simplified Genomic Profiling Approach Predicts Outcome in Metastatic Colorectal Cancer.

Journal: Cancers

Published: December 24, 2018

Next-generation sequencing of BRCA1 and BRCA2 genes for rapid detection of germline mutations in hereditary breast/ovarian cancer.

Next-generation sequencing of BRCA1 and BRCA2 genes for rapid detection of germline mutations in hereditary breast/ovarian cancer.

Journal: PeerJ

Published: December 07, 2018

Optimizing the identification of risk-relevant mutations by multigene panel testing in selected hereditary breast/ovarian cancer families.

Optimizing the identification of risk-relevant mutations by multigene panel testing in selected hereditary breast/ovarian cancer families.

Journal: Cancer medicine

Published: August 31, 2017

Erratum to: Detection of ATM germline variants by the p53 mitotic centrosomal localization test in BRCA1/2-negative patients with early-onset breast cancer.

Erratum to: Detection of ATM germline variants by the p53 mitotic centrosomal localization test in BRCA1/2-negative patients with early-onset breast cancer.

Journal: Journal of experimental & clinical cancer research : CR

Published: November 14, 2016

Detection of ATM germline variants by the p53 mitotic centrosomal localization test in BRCA1/2-negative patients with early-onset breast cancer.

Detection of ATM germline variants by the p53 mitotic centrosomal localization test in BRCA1/2-negative patients with early-onset breast cancer.

Journal: Journal of experimental & clinical cancer research : CR

Published: July 28, 2016

The role of peroxiredoxins in cancer.

The role of peroxiredoxins in cancer.

Journal: Molecular and clinical oncology

Published: July 01, 2016

Showing 1-12 of 20

Last Updated: 09/26/2026