1
None of the SNPs tested were significantly associated with CRC risk in the replication study.
2
Height was not associated with CRC-specific or all-cause death.
3
Results: None of the 172 SNPs analysed in our study could be formally associated with CRC risk.
4
Results: None of the 28 SNPs analyzed in our study was found to be associated with CRC risk.
5
Frequency of bowel movement, stool quantity, feeling discomfort and laxative use was not overall associated with CRC risk.
6
Multiple factors are causally associated with CRC development, such as genetic and epigenetic alterations, inflammatory bowel disease, lifestyle and dietary factors.
7
Logistic regression models were used to investigate a range of adverse outcomes independently associated with CRC and its surgical and adjunctive treatments.
8
These NCCN Guidelines Insights focus on genes newly associated with CRC risk on multigene panels, the associated evidence, and currently recommended management strategies.
9
ATP8B1 was found to be the novel gene associated with CRC that shows changes at cytogenetic, gene and exon levels.