Detalhe da pesquisa
1.
Targeted molecular profiling of epithelial ovarian cancer from Italian BRCA wild-type patients with a BRCA and PARP pathways gene panel.
Exp Mol Pathol
; 128: 104833, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36165864
2.
Detection of Germline Variants in 450 Breast/Ovarian Cancer Families with a Multi-Gene Panel Including Coding and Regulatory Regions.
Int J Mol Sci
; 22(14)2021 Jul 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-34299313
3.
Lynch syndrome-related non-endometrioid endometrial cancer: analysis of outcomes.
Int J Gynecol Cancer
; 30(1): 56-61, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31780564
4.
STELO: a new tool for family physicians for the correct identification of inherited cancer syndromes.
Fam Pract
; 37(1): 43-48, 2020 02 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-31536618
5.
BRCA Methylation Testing Identifies a Subset of Ovarian Carcinomas without Germline Variants That Can Benefit from PARP Inhibitor.
Int J Mol Sci
; 21(24)2020 Dec 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-33352687
6.
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification.
Hum Mutat
; 40(9): 1557-1578, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31131967
7.
Two Cases of Carcinosarcomas of the Ovary Involved in Hereditary Cancer Syndromes.
Int J Gynecol Pathol
; 36(1): 64-70, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27167672
8.
Somatic Testing on Gynecological Cancers Improve the Identification of Lynch Syndrome.
Int J Gynecol Cancer
; 27(7): 1543-1549, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28471861
9.
Concomitant mutation and epimutation of the MLH1 gene in a Lynch syndrome family.
Carcinogenesis
; 36(4): 452-8, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25742745
10.
Immunohistochemical and molecular pattern of p53 in epithelial ovarian cancers negative for germline BRCA1/2 variants.
Pathol Res Pract
; 255: 155183, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38364651
11.
MUTYH c.933+3A>C, associated with a severely impaired gene expression, is the first Italian founder mutation in MUTYH-Associated Polyposis.
Int J Cancer
; 132(5): 1060-9, 2013 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22865608
12.
MLH1 Promoter Methylation Could Be the Second Hit in Lynch Syndrome Carcinogenesis.
Genes (Basel)
; 14(11)2023 Nov 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38003003
13.
Similarities and differences in gene expression profiles of BRCA1 methylated and mutated epithelial ovarian cancers.
Front Oncol
; 13: 1268127, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37854675
14.
Pyrosequencing Assay for BRCA1 Methylation Analysis: Results from a Cross-Validation Study.
J Mol Diagn
; 25(4): 217-226, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36739964
15.
Strategies for Lynch syndrome identification in selected and unselected gynecological cancers.
Eur J Cancer Prev
; 31(4): 369-376, 2022 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34519692
16.
Case Report: Male Lobular Breast Cancer in Hereditary Cancer Syndromes.
Front Oncol
; 12: 891426, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35686104
17.
Mixed Neuroendocrine/Non-neuroendocrine Neoplasm (MiNEN) of the Ovary Arising from Endometriosis: Molecular Pathology Analysis in Support of a Pathogenetic Paradigm.
Endocr Pathol
; 33(3): 400-410, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34342838
18.
OncoPan®: An NGS-Based Screening Methodology to Identify Molecular Markers for Therapy and Risk Assessment in Pancreatic Ductal Adenocarcinoma.
Biomedicines
; 10(5)2022 May 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-35625944
19.
Hierarchical clustering analysis of pathologic and molecular data identifies prognostically and biologically distinct groups of colorectal carcinomas.
Mod Pathol
; 24(1): 126-37, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20852594
20.
Lynch syndrome and Muir-Torre phenotype associated with a recurrent variant in the 3'UTR of the MSH6 gene.
Cancer Genet
; 254-255: 1-10, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33516942