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.
First estimates of diffuse gastric cancer risks for carriers of CTNNA1 germline pathogenic variants.
J Med Genet;
59(12): 1189-1195, 2022 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36038258
3.
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
4.
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
5.
Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study.
Am J Obstet Gynecol;
225(1): 51.e1-51.e17, 2021 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33493488
6.
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
7.
Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers.
Br J Cancer;
121(2): 180-192, 2019 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31213659
8.
BRCA1/BRCA2 germline mutations and chemotherapy-related hematological toxicity in breast cancer patients.
Breast Cancer Res Treat;
174(3): 775-783, 2019 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30635808
9.
Clinical factors associated with prolonged response and survival under olaparib as maintenance therapy in BRCA mutated ovarian cancers.
Gynecol Oncol;
155(2): 262-269, 2019 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31604666
10.
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
Hum Mutat;
39(5): 593-620, 2018 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29446198
11.
Mutiple DICER1-related lesions associated with a germline deep intronic mutation.
Pediatr Blood Cancer;
65(6): e27005, 2018 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29469200
12.
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.
Breast Cancer Res Treat;
161(1): 117-134, 2017 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27796716
13.
GATA2 gene analysis in several forms of hematological malignancies including familial aggregations.
Ann Hematol;
96(10): 1635-1639, 2017 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28752392
14.
Germline BAP1 mutations predispose to renal cell carcinomas.
Am J Hum Genet;
92(6): 974-80, 2013 Jun 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23684012
15.
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
16.
Mutational analysis of JAK2, CBL, RUNX1, and NPM1 genes in familial aggregation of hematological malignancies.
Ann Hematol;
95(7): 1043-50, 2016 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27106701
17.
Familial hematological malignancies: new IDH2 mutation.
Ann Hematol;
95(12): 1943-1947, 2016 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27591990
18.
Mutation analysis of PALB2 gene in French breast cancer families.
Breast Cancer Res Treat;
154(3): 463-71, 2015 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26564480
19.
A new scoring system in cancer genetics: application to criteria for BRCA1 and BRCA2 mutation screening.
J Med Genet;
51(2): 114-21, 2014 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24343917
20.
An Integrated Cancer Prevention Strategy: the Viewpoint of the Leon Berard Comprehensive Cancer Center Lyon, France.
Cancer Prev Res (Phila);
17(4): 133-140, 2024 Apr 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38562091