Detalhe da pesquisa
1.
The impact of coding germline variants on contralateral breast cancer risk and survival.
Am J Hum Genet
; 110(3): 475-486, 2023 03 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36827971
2.
Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women.
N Engl J Med
; 384(5): 428-439, 2021 02 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33471991
3.
FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women.
Eur J Hum Genet
; 31(5): 578-587, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36707629
4.
Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival.
Res Sq
; 2023 Feb 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36824750
5.
Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival.
Cancer Med
; 12(15): 16142-16162, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37401034
6.
Gene-Environment Interactions Relevant to Estrogen and Risk of Breast Cancer: Can Gene-Environment Interactions Be Detected Only among Candidate SNPs from Genome-Wide Association Studies?
Cancers (Basel)
; 13(10)2021 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-34069208
7.
No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a multi-center cohort study.
Breast Cancer Res Treat
; 115(1): 185-92, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18523885
8.
Contribution of BRCA1 and BRCA2 mutations to inherited ovarian cancer.
Hum Mutat
; 28(12): 1207-15, 2007 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17688236
9.
Screening for the BRCA1-ins6kbEx13 mutation: potential for misdiagnosis. Mutation in brief #964. Online.
Hum Mutat
; 28(5): 525-6, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17397054