Detalhe da pesquisa
1.
GENESIS: a French national resource to study the missing heritability of breast cancer.
BMC Cancer
; 16: 13, 2016 Jan 12.
Artigo
Inglês
| MEDLINE | ID: mdl-26758370
2.
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers.
Hum Mol Genet
; 20(23): 4732-47, 2011 Dec 01.
Artigo
Inglês
| MEDLINE | ID: mdl-21890493
3.
The rs2910164:G>C SNP in the MIR146A gene is not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers.
Hum Mutat
; 32(9): 1004-7, 2011 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-21591024
4.
Mutation screening of MIR146A/B and BRCA1/2 3'-UTRs in the GENESIS study.
Eur J Hum Genet
; 24(9): 1324-9, 2016 08.
Artigo
Inglês
| MEDLINE | ID: mdl-26785832
5.
Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers.
Cancer Epidemiol Biomarkers Prev
; 20(5): 1032-8, 2011 May.
Artigo
Inglês
| MEDLINE | ID: mdl-21393566