Evaluation of the current knowledge limitations in breast cancer research: a gap analysis-Reference-Cited by-同舟云学术

Evaluation of the current knowledge limitations in breast cancer research: a gap analysis

Published:2008-03-27 Issue:2 Volume:10 Page:
ISSN:1465-542X
Container-title:Breast Cancer Research
language:en
Short-container-title:Breast Cancer Res

Author:

Thompson Alastair, ,Brennan Keith,Cox Angela,Gee Julia,Harcourt Diana,Harris Adrian,Harvie Michelle,Holen Ingunn,Howell Anthony,Nicholson Robert,Steel Michael,Streuli Charles

Publisher

Springer Science and Business Media LLC

Link

http://link.springer.com/content/pdf/10.1186/bcr1983.pdf

Reference125 articles.

1. The CHEK2 Breast Cancer Case-Control Consortium: CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies. Am J Hum Genet. 2004, 74: 1175-1182. 10.1086/421251.

2. Renwick A, Thompson D, Seal S, Kelly P, Chagtai T, Ahmed M, North B, Jayatilake H, Barfoot R, Spanova K, McGuffog L, Evans DG, Eccles D, Breast Cancer Susceptibility Collaboration (UK), Easton DF, Stratton MR, Rahman N: ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles. Nat Genet. 2006, 38: 873-875. 10.1038/ng1837.

3. Seal S, Thompson D, Renwick A, Elliott A, Kelly P, Barfoot R, Chagtai T, Jayatilake H, Ahmed M, Spanova K, North B, McGuffog L, Evans DG, Eccles D, Breast Cancer Susceptibility Collaboration (UK), Easton DF, Stratton MR, Rahman N: Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. Nat Genet. 2006, 38: 1239-10.1038/ng1902.

4. The Breast Cancer Association Consortium: Commonly studied SNPs and breast cancer: negative results from 12,000–32,000 cases and controls from the Breast Cancer Association Consortium. J Natl Cancer Inst. 2006, 98: 1382-1396.

5. Cox A, Dunning AM, Garcia-Closas M, Balasubramanian S, Reed MW, Pooley KA, Scollen S, Baynes C, Ponder BA, Chanock S, Lissowska J, Brinton L, Peplonska B, Southey MC, Hopper JL, McCredie MR, Giles GG, Fletcher O, Johnson N, dos Santos Silva I, Gibson L, Bojesen SE, Nordestgaard BG, Axelsson CK, Torres D, Hamann U, Justenhoven C, Brauch H, Chang-Claude J, Kropp S, et al: A common coding variant in CASP8 is associated with breast cancer risk. Nat Genet. 2007, 39: 352-358. 10.1038/ng1981. [Erratum: Nat Genet 2007, 39:688.]

Cited by 83 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Dietary behaviours of individuals with lynch syndrome at high risk of colorectal cancer: Results from the AAS-lynch study;Clinical Nutrition ESPEN;2023-10

2. Bridging the “Know-Do” Gaps in Five Non-Communicable Diseases Using a Common Framework Driven by Implementation Science;Journal of Healthcare Leadership;2023-07

3. Exploring the prognostic significance of FOXM1 gene expression in human breast cancer by bioinformatics analysis;Gene Reports;2022-12

4. Quantitative mapping of human hair greying and reversal in relation to life stress;eLife;2021-06-22

5. Comprehensive Network Analysis of the Molecular Regulation Mechanism for Breast Cancer Metastasis;Oncologie;2021