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Works
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Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-BRCA1/2 breast cancer families
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer
One to 2-year surveillance intervals reduce risk of colorectal cancer in families with Lynch syndrome
Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors
Enrichment of low penetrance susceptibility loci in a Dutch familial colorectal cancer cohort
A cell-free assay for the functional analysis of variants of the mismatch repair protein MLH1.
Cancer Risks for PMS2-Associated Lynch Syndrome
The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families
