Implications of polygenic risk for personalised colorectal cancer screening.
about
Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer.Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease.Modeling the prevention of colorectal cancer from the combined impact of host and behavioral risk factors.Risk Model for Colorectal Cancer in Spanish Population Using Environmental and Genetic Factors: Results from the MCC-Spain study.Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci.Genome-wide association studies of cancer: current insights and future perspectives.Strongly enhanced colorectal cancer risk stratification by combining family history and genetic risk score.Telomere length and genetics are independent colorectal tumour risk factors in an evaluation of biomarkers in normal bowel.Genetic Risk Score is Associated With Prevalence of Advanced Neoplasms in a Colorectal Cancer Screening Population.Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma
P2860
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P2860
Implications of polygenic risk for personalised colorectal cancer screening.
description
2015 nî lūn-bûn
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2015年の論文
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2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
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2015年论文
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2015年论文
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2015年论文
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name
Implications of polygenic risk for personalised colorectal cancer screening.
@en
type
label
Implications of polygenic risk for personalised colorectal cancer screening.
@en
prefLabel
Implications of polygenic risk for personalised colorectal cancer screening.
@en
P2093
P2860
P356
P1433
P1476
Implications of polygenic risk for personalised colorectal cancer screening.
@en
P2093
E J Morris
I P Tomlinson
K Litchfield
M J E Frampton
P2860
P304
P356
10.1093/ANNONC/MDV540
P577
2015-11-16T00:00:00Z