Detalhe da pesquisa
1.
Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element.
Am J Hum Genet
; 108(7): 1190-1203, 2021 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34146516
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.
Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study.
Br J Sports Med
; 56(20): 1157-1170, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36328784
4.
Mendelian randomisation study of smoking exposure in relation to breast cancer risk.
Br J Cancer
; 125(8): 1135-1145, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34341517
5.
CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers.
Br J Cancer
; 124(4): 842-854, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33495599
6.
Inherited mutations in BRCA1 and BRCA2 in an unselected multiethnic cohort of Asian patients with breast cancer and healthy controls from Malaysia.
J Med Genet
; 55(2): 97-103, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28993434
7.
The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity.
Hum Mutat
; 39(5): 729-741, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29460995
8.
Rare, protein-truncating variants in ATM, CHEK2 and PALB2, but not XRCC2, are associated with increased breast cancer risks.
J Med Genet
; 54(11): 732-741, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28779002
9.
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.
J Med Genet
; 53(5): 298-309, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26921362
10.
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
11.
Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
Nat Commun
; 12(1): 2986, 2021 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-33990587
12.
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
Nat Commun
; 12(1): 1078, 2021 02 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33597508
13.
Targeted Resequencing of the Coding Sequence of 38 Genes Near Breast Cancer GWAS Loci in a Large Case-Control Study.
Cancer Epidemiol Biomarkers Prev
; 28(4): 822-825, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30642840
14.
The functional ALDH2 polymorphism is associated with breast cancer risk: A pooled analysis from the Breast Cancer Association Consortium.
Mol Genet Genomic Med
; 7(6): e707, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31066241
15.
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).
Sci Rep
; 6: 32512, 2016 09 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27600471