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Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment
Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study
No difference in penetrance between truncating and missense/aberrant splicing pathogenic variants in MLH1 and MSH2
Uptake of hysterectomy and bilateral salpingooophorectomy in carriers of pathogenic mismatch repair variants
Associations of height with the risks of colorectal and endometrial cancer in persons with Lynch syndrome
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants
Shared heritability and functional enrichment across six solid cancers (vol 10, 431, 2019)
Shared heritability and functional enrichment across six solid cancers
Cancer Risks for PMS2-Associated Lynch Syndrome
Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database
Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicity
Identification of a melanoma susceptibility locus and somatic mutation in TET2
A variant in FTO shows association with melanoma risk not due to BMI
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3
Genome-wide association study identifies three new melanoma susceptibility loci
Risks of Lynch Syndrome Cancers for MSH6 Mutation Carriers