Ability of known susceptibility SNPs to predict colorectal cancer risk for persons with and without a family history
Author:
Funder
National Institutes of Health
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Genetics(clinical),Oncology,Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10689-019-00136-6.pdf
Reference27 articles.
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2. Hopper JL (2011) Disease-specific prospective family study cohorts enriched for familial risk. Epidemiol Perspect Innov 8(1):2. https://doi.org/10.1186/1742-5573-8-2
3. Dunlop MG, Tenesa A, Farrington SM, Ballereau S, Brewster DH, Koessler T et al (2013) Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42,103 individuals. Gut 62(6):871–881. https://doi.org/10.1136/gutjnl-2011-300537
4. Huyghe JR, Bien SA, Harrison TA, Kang HM, Chen S, Schmit SL et al (2019) Discovery of common and rare genetic risk variants for colorectal cancer. Nat Genet 51(1):76–87. https://doi.org/10.1038/s41588-018-0286-6
5. Jenkins MA, Makalic E, Dowty JG, Schmidt DF, Dite GS, MacInnis RJ et al (2016) Quantifying the utility of single nucleotide polymorphisms to guide colorectal cancer screening. Future Oncol 12(4):503–513. https://doi.org/10.2217/fon.15.303
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