Detalhe da pesquisa
1.
Mosaic BRCA1 promoter methylation contribution in hereditary breast/ovarian cancer pedigrees.
J Med Genet
; 61(3): 284-288, 2024 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37748860
2.
Hereditary cancer predispositions: Comparison of multigene panel sequencing on fresh-frozen breast/ovarian tumor versus blood.
Clin Genet
; 104(1): 107-113, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36974006
3.
Enhancing the BOADICEA cancer risk prediction model to incorporate new data on RAD51C, RAD51D, BARD1 updates to tumour pathology and cancer incidence.
J Med Genet
; 59(12): 1206-1218, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36162851
4.
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
5.
Genetic clinicians' confidence in BOADICEA comprehensive breast cancer risk estimates and counselees' psychosocial outcomes: A prospective study.
Clin Genet
; 102(1): 30-39, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35508697
6.
How to facilitate psychosocial adjustment in women tested for hereditary breast or ovarian cancer susceptibility? Insights from network analysis.
Psychooncology
; 29(3): 550-556, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31823434
7.
The "Psychosocial Aspects in Hereditary Cancer" questionnaire in women attending breast cancer genetic clinics: Psychometric validation across French-, German- and Spanish-language versions.
Eur J Cancer Care (Engl)
; 29(1): e13173, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31571365
8.
Familial disclosure by genetic healthcare professionals: a useful but sparingly used legal provision in France.
J Med Ethics
; 45(12): 811-816, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31462451
9.
Clinicopathologic Characteristics of Endometrial Cancer in Lynch Syndrome: A French Multicenter Study.
Int J Gynecol Cancer
; 27(5): 953-960, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28525912
10.
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
11.
Prevalence of Pathogenic Variants of FAN1 in More Than 5000 Patients Assessed for Genetic Predisposition to Colorectal, Breast, Ovarian, or Other Cancers.
Gastroenterology
; 156(6): 1919-1920, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30639725
12.
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
13.
CDH1 germline mutations and the hereditary diffuse gastric and lobular breast cancer syndrome: a multicentre study.
J Med Genet
; 50(7): 486-9, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23709761
14.
Clinical implications of incorporating genetic and non-genetic risk factors in CanRisk-based breast cancer risk prediction.
Breast
; 73: 103615, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38061307
15.
Male breast cancer: No evidence for mosaic BRCA1 promoter methylation involvement.
Breast
; 73: 103620, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38096711
16.
Association and performance of polygenic risk scores for breast cancer among French women presenting or not a familial predisposition to the disease.
Eur J Cancer
; 179: 76-86, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36509001
17.
Assessment of psychosocial difficulties by genetic clinicians and distress in women at high risk of breast cancer: a prospective study.
Eur J Hum Genet
; 30(9): 1067-1075, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35399119
18.
Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants.
J Clin Oncol
; 40(14): 1529-1541, 2022 05 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35077220
19.
EMMA, a cost- and time-effective diagnostic method for simultaneous detection of point mutations and large-scale genomic rearrangements: application to BRCA1 and BRCA2 in 1,525 patients.
Hum Mutat
; 32(3): 325-34, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21120943
20.
Hereditary diffuse gastric cancer syndrome: improved performances of the 2015 testing criteria for the identification of probands with a CDH1 germline mutation.
J Med Genet
; 52(8): 563-5, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26025002