Detalhe da pesquisa
1.
Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.
Am J Hum Genet
; 108(10): 1907-1923, 2021 10 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34597585
2.
Novel germline MET pathogenic variants in French patients with papillary renal cell carcinomas type I.
Hum Mutat
; 43(3): 316-327, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34882875
3.
Health management of patients with COVID-19: is there a room for hydrotherapeutic approaches?
Int J Biometeorol
; 66(5): 1031-1038, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35079866
4.
Analysis of 11 candidate genes in 849 adult patients with suspected hereditary cancer predisposition.
Genes Chromosomes Cancer
; 60(2): 73-78, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33099839
5.
Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation.
Breast Cancer Res
; 23(1): 79, 2021 08 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34344426
6.
Gene- and pathway-level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility.
Int J Cancer
; 148(8): 1895-1909, 2021 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33368296
7.
Feedback of extended panel sequencing in 1530 patients referred for suspicion of hereditary predisposition to adult cancers.
Clin Genet
; 99(1): 166-175, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33047316
8.
The Functions of the Demethylase JMJD3 in Cancer.
Int J Mol Sci
; 22(2)2021 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-33478063
9.
Is BRCA2 involved in early onset colorectal cancer risk?
Clin Genet
; 97(4): 668-669, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31875949
10.
A high expression ratio of RhoA/RhoB is associated with the migratory and invasive properties of basal-like Breast Tumors.
Int J Med Sci
; 17(17): 2799-2808, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33162807
11.
Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing.
Int J Cancer
; 144(8): 1962-1974, 2019 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30303537
12.
Psychosocial and clinical factors of probands impacting intrafamilial disclosure and uptake of genetic testing among families with BRCA1/2 or MMR gene mutations.
Psychooncology
; 28(8): 1679-1686, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31152683
13.
BRACAVENIR: an observational study of expectations and coping in young women with high hereditary risk of breast and ovarian cancer.
Hered Cancer Clin Pract
; 17: 7, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30858899
14.
Antioxydation And Cell Migration Genes Are Identified as Potential Therapeutic Targets in Basal-Like and BRCA1 Mutated Breast Cancer Cell Lines.
Int J Med Sci
; 15(1): 46-58, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29333087
15.
Long-term improvement of breast cancer survivors' quality of life by a 2-week group physical and educational intervention: 5-year update of the 'PACThe' trial.
Br J Cancer
; 116(11): 1389-1393, 2017 May 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-28427084
16.
Anti-EGFR monoclonal antibodies enhance sensitivity to DNA-damaging agents in BRCA1-mutated and PTEN-wild-type triple-negative breast cancer cells.
Mol Carcinog
; 56(5): 1383-1394, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27864890
17.
Global analysis of H3K27me3 as an epigenetic marker in prostate cancer progression.
BMC Cancer
; 17(1): 261, 2017 04 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28403887
18.
BRCA Share: A Collection of Clinical BRCA Gene Variants.
Hum Mutat
; 37(12): 1318-1328, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27633797
19.
GENESIS: a French national resource to study the missing heritability of breast cancer.
BMC Cancer
; 16: 13, 2016 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-26758370
20.
BRCA1 and BRCA2 mutations in ethnic Lebanese Arab women with high hereditary risk breast cancer.
Oncologist
; 20(4): 357-64, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25777348