Detalhe da pesquisa
1.
Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2.
Br J Cancer
; 128(12): 2283-2294, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37076566
2.
Colorectal cancer early methylation alterations affect the crosstalk between cell and surrounding environment, tracing a biomarker signature specific for this tumor.
Int J Cancer
; 143(4): 907-920, 2018 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29542109
3.
A novel APC promoter 1B deletion shows a founder effect in Italian patients with classical familial adenomatous polyposis phenotype.
Genes Chromosomes Cancer
; 56(12): 846-854, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28791770
4.
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.
Hum Mol Genet
; 24(18): 5345-55, 2015 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26130695
5.
Type and frequency of MUTYH variants in Italian patients with suspected MAP: a retrospective multicenter study.
J Hum Genet
; 62(2): 309-315, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27829682
6.
Genetic instability in lymphoblastoid cell lines expressing biallelic and monoallelic variants in the human MUTYH gene.
Hum Mol Genet
; 23(14): 3843-52, 2014 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24569162
7.
Streamlining the diagnostic pathway for Lynch syndrome in colorectal cancer patients: a 10-year experience in a single Italian Cancer Center.
Eur J Cancer Prev
; 33(4): 355-362, 2024 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38190337
8.
Cascade testing in Italian Hereditary Breast Ovarian Cancer families: a missed opportunity for cancer prevention?
Fam Cancer
; 2023 Nov 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-37968543
9.
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
10.
The Advantages of Next-Generation Sequencing Molecular Classification in Endometrial Cancer Diagnosis.
J Clin Med
; 12(23)2023 Nov 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38068290
11.
Male breast cancer risk associated with pathogenic variants in genes other than BRCA1/2: an Italian case-control study.
Eur J Cancer
; 188: 183-191, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37262986
12.
Implementing NGS-based BRCA tumour tissue testing in FFPE ovarian carcinoma specimens: hints from a real-life experience within the framework of expert recommendations.
J Clin Pathol
; 74(9): 596-603, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32895300
13.
Clustered protocadherins methylation alterations in cancer.
Clin Epigenetics
; 11(1): 100, 2019 07 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31288858
14.
Leucocytes telomere length and breast cancer risk/ susceptibility: A case-control study.
PLoS One
; 13(5): e0197522, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29782524
15.
Increased risk of colorectal adenomas in Italian subjects carrying the p53 PIN3 A2-Pro72 haplotype.
Digestion
; 74(3-4): 228-35, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-17374954
16.
Cyclooxygenase-2 expression in FAP patients carrying germ line MYH mutations.
Cancer Epidemiol Biomarkers Prev
; 14(8): 2049-52, 2005 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-16103460
17.
Referral of Ovarian Cancer Patients for Genetic Counselling by Oncologists: Need for Improvement.
Public Health Genomics
; 18(4): 225-32, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26111740
18.
APC rearrangements in familial adenomatous polyposis: heterogeneity of deletion lengths and breakpoint sequences underlies similar phenotypes.
Fam Cancer
; 14(1): 41-9, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25159889
19.
Clinical application of micronucleus test: a case-control study on the prediction of breast cancer risk/susceptibility.
PLoS One
; 9(11): e112354, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25415331
20.
The FMR1 CGG repeat test is not a candidate prescreening tool for identifying women with a high probability of being carriers of BRCA mutations.
Eur J Hum Genet
; 22(2): 280-2, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24065114