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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
De novo variants in ATP2B1 lead to neurodevelopmental delay
No difference in penetrance between truncating and missense/aberrant splicing pathogenic variants in MLH1 and MSH2
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants
Associations of pathogenic variants in MLH1, MSH2, and MSH6 with risk of colorectal adenomas and tumors and with somatic mutations in patients with Lynch syndrome
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants
The Apparent Genetic Anticipation in PMS2-Associated Lynch Syndrome Families Is Explained by Birth-cohort Effect
The Apparent Genetic Anticipation in PMS2-Associated Lynch Syndrome Families Is Explained by Birth-cohort Effect
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report
No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies
Cancer Risks for PMS2-Associated Lynch Syndrome
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers
Lynch Syndrome Caused by Germline PMS2 Mutations: Delineating the Cancer Risk
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome
Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors
Recurrence and Variability of Germline EPCAM Deletions in Lynch Syndrome
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study
Recommendations to improve identification of hereditary and familial colorectal cancer in Europe