Detalhe da pesquisa
1.
Segregation analysis of 17,425 population-based breast cancer families: Evidence for genetic susceptibility and risk prediction.
Am J Hum Genet
; 109(10): 1777-1788, 2022 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36206742
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.
Characterisation of protein-truncating and missense variants in PALB2 in 15 768 women from Malaysia and Singapore.
J Med Genet
; 59(5): 481-491, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33811135
4.
A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis.
Br J Cancer
; 126(7): 1082-1090, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35039627
5.
Prevalence of BRCA1 and BRCA2 pathogenic variants in a large, unselected breast cancer cohort.
Int J Cancer
; 144(5): 1195-1204, 2019 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30175445
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.
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
8.
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
9.
Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers.
Am J Hum Genet
; 92(4): 489-503, 2013 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-23540573
10.
Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression.
Hum Mol Genet
; 22(12): 2520-8, 2013 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23535824
11.
Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants - an Asian study of 572 families.
Lancet Reg Health West Pac
; 44: 101017, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38333895
12.
Independent validation of genes and polymorphisms reported to be associated with radiation toxicity: a prospective analysis study.
Lancet Oncol
; 13(1): 65-77, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22169268
13.
Genome-wide association study of treatment-related toxicity two years following radiotherapy for breast cancer.
Radiother Oncol
; 187: 109806, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37437607
14.
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk.
Nat Genet
; 55(9): 1435-1439, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37592023
15.
Breast Cancer Risk in Women from Ghana Carrying Rare Germline Pathogenic Mutations.
Cancer Epidemiol Biomarkers Prev
; 31(8): 1593-1601, 2022 08 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35654374
16.
Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry.
Cancers (Basel)
; 14(14)2022 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35884425
17.
CYP2D6 gene variants: association with breast cancer specific survival in a cohort of breast cancer patients from the United Kingdom treated with adjuvant tamoxifen.
Breast Cancer Res
; 12(4): R64, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20731819
18.
Population Study of Ovarian Cancer Risk Prediction for Targeted Screening and Prevention.
Cancers (Basel)
; 12(5)2020 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32429029
19.
Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families.
J Clin Oncol
; 38(7): 674-685, 2020 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31841383
20.
Seq4SNPs: new software for retrieval of multiple, accurately annotated DNA sequences, ready formatted for SNP assay design.
BMC Bioinformatics
; 10: 180, 2009 Jun 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-19523221