Anna Coppa | 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
Male breast cancer risk associated with pathogenic variants in genes other than BRCA1/2: an Italian case-control study	EUROPEAN JOURNAL OF CANCER	2023
ENIGMA CHEK2gether Project. A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk	CLINICAL CANCER RESEARCH	2023
A gene dosage‐dependent effect unveils NBS1 as both a haploinsufficient tumour suppressor and an essential gene for SHH‐medulloblastoma	NEUROPATHOLOGY & APPLIED NEUROBIOLOGY	2022
NSD1 mutations and pediatric high-grade gliomas: a comparative genomic study in primary and recurrent tumors	DIAGNOSTICS	2022
A combination of PARP and CHK1 inhibitors efficiently antagonizes MYCN-driven tumors	ONCOGENE	2021
A multidisciplinary approach for the differential diagnosis between multiple primary lung adenocarcinomas and intrapulmonary metastases	PATHOLOGY RESEARCH AND PRACTICE	2021
Transcriptome of male breast cancer matched with germline profiling reveals novel molecular subtypes with possible clinical relevance	CANCERS	2021
Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores	JOURNAL OF THE NATIONAL CANCER INSTITUTE	2021
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
Evaluation of CYP17A1 and CYP1B1 polymorphisms in male breast cancer risk	ENDOCRINE CONNECTIONS	2019
SMO-M2 mutation does not support cell-autonomous Hedgehog activity in cerebellar granule cell precursors	SCIENTIFIC REPORTS	2019
Identification of novel BRCA1 large genomic rearrangements by a computational algorithm of amplicon-based Next-Generation Sequencing data	PEERJ	2019
A possible role of FANCM mutations in male breast cancer susceptibility: Results from a multicenter study in Italy	THE BREAST	2018
Effective treatment of a platinum-resistant cutaneous squamous cell carcinoma case by EGFR pathway inhibition	MOLECULAR AND CLINICAL ONCOLOGY	2018
Coexistence of three EGFR mutations in an NSCLC patient: A brief report	THE INTERNATIONAL JOURNAL OF BIOLOGICAL MARKERS	2018

Laboratori di ricerca

Oncologia Molecolare