Detalhe da pesquisa
1.
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
2.
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
3.
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
4.
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
5.
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
6.
French college of gynecologists and obstetricians (CNGOF) recommendations for clinical practice: Place of breast self-examination in screening strategies.
Breast
; 75: 103619, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38547580
7.
[Place of breast self-examination in screening strategies. French College of Gynecologists and Obstetricians (CNGOF) recommendations for clinical practice]. / Recommandations pour la pratique clinique du CNGOF. Place de l'auto-examen des seins dans les stratégies de dépistage.
Gynecol Obstet Fertil Senol
; 51(10): 437-447, 2023 Oct.
Artigo
em Francês
| MEDLINE | ID: mdl-37652173
8.
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
9.
[Non-genetic indications for risk reducing mastectomies: Guidelines of the National College of French Gynecologists and Obstetricians (CNGOF)]. / Indications des mastectomies de réduction de risque en dehors du risque avéré de prédisposition héréditaire : recommandations du Collège national des gynécologues et obstétriciens français (CNGOF).
Gynecol Obstet Fertil Senol
; 50(2): 107-120, 2022 Feb.
Artigo
em Francês
| MEDLINE | ID: mdl-34920167
10.
TUMOSPEC: A Nation-Wide Study of Hereditary Breast and Ovarian Cancer Families with a Predicted Pathogenic Variant Identified through Multigene Panel Testing.
Cancers (Basel)
; 13(15)2021 Jul 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34359559
11.
A review of histopathological subtypes of ovarian cancer in BRCA-related French Canadian cancer families.
Fam Cancer
; 6(4): 491-7, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17636423
12.
Discrimination between serous low malignant potential and invasive epithelial ovarian tumors using molecular profiling.
Oncogene
; 24(29): 4672-87, 2005 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-15940270
13.
[Multidisciplinary team meetings settings on the management of women at high risk of inherited breast cancer. A French study]. / Mise en place des modalités de réunions de concertation pluridisciplinaire pour la prise en charge des patientes prédisposées héréditairement au cancer du sein. Une étude française.
Bull Cancer
; 103(6): 571-83, 2016 Jun.
Artigo
em Francês
| MEDLINE | ID: mdl-27178881
14.
First case report of an adrenocortical carcinoma caused by a BRCA2 mutation.
Medicine (Baltimore)
; 95(36): e4756, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27603373
15.
Breast Cancer Risk Associated with Estrogen Exposure and Truncating Mutation Location in BRCA1/2 Carriers.
Cancer Epidemiol Biomarkers Prev
; 24(4): 698-707, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25613119
16.
Signature of a silent killer: expression profiling in epithelial ovarian cancer.
Expert Rev Mol Diagn
; 4(2): 157-67, 2004 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-14995903
17.
A focus group study on breast cancer risk presentation: one format does not fit all.
Eur J Hum Genet
; 21(7): 719-24, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23169493
18.
Allelic transcripts dosage effect in morphologically normal ovarian cells from heterozygous carriers of a BRCA1/2 French Canadian founder mutation.
Cancer Prev Res (Phila)
; 5(5): 765-77, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22401979
19.
Comprehensive BRCA1 and BRCA2 mutation analyses and review of French Canadian families with at least three cases of breast cancer.
Fam Cancer
; 9(4): 507-17, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20694749
20.
Germ-line exon 21 EGFR mutations, V843I and P848L, in nonsmall cell lung cancer patients.
Eur Respir Rev
; 23(133): 390-2, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25176975