Arianna Nicolussi | Ricerc@Sapienza

Pubblicazioni

Titolo	Pubblicato in	Anno
Molecular profiling of male breast cancer by multigene panel testing: Implications for precision oncology	FRONTIERS IN ONCOLOGY	2023
NSD1 mutations and pediatric high-grade gliomas: a comparative genomic study in primary and recurrent tumors	DIAGNOSTICS	2022
Clinical Multigene Panel Sequencing Identifies Distinct Mutational Association Patterns in Metastatic Colorectal Cancer	FRONTIERS IN ONCOLOGY	2020
CTNNB1 p.L31P mutation in an ovarian endometrioid carcinoma with synchronous uterine endometrioid carcinoma	PATHOLOGY RESEARCH AND PRACTICE	2020
A novel BRCA2 splice variant identified in a young woman	MOLECULAR GENETICS & GENOMIC MEDICINE	2020
A simplified genomic profiling approach predicts outcome in metastatic colorectal cancer	CANCERS	2019
Next-generation sequencing of BRCA1 and BRCA2 genes for rapid detection of germline mutations in hereditary breast/ovarian cancer	PEERJ	2019
Identification of novel BRCA1 large genomic rearrangements by a computational algorithm of amplicon-based Next-Generation Sequencing data	PEERJ	2019
The role of peroxiredoxins in cancer	MOLECULAR AND CLINICAL ONCOLOGY	2017
Optimizing the identification of risk-relevant mutations by multigene panel testing in selected hereditary breast/ovarian cancer families	CANCER MEDICINE	2017
Detection of ATM germline variants by the p53 mitotic centrosomal localization test in BRCA1/2-negative patients with early-onset breast cancer	JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH	2016
Validation of the Ion Torrent PGM sequencing for the prospective routine molecular diagnostic of colorectal cancer.	CLINICAL BIOCHEMISTRY	2015