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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
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No difference in penetrance between truncating and missense/aberrant splicing pathogenic variants in MLH1 and MSH2
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Uptake of hysterectomy and bilateral salpingooophorectomy in carriers of pathogenic mismatch repair variants
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Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants
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The "unnatural" history of colorectal cancer in Lynch syndrome: lessons from colonoscopy surveillance
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Risk-reducing gynecological surgery in Lynch syndrome
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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
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Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants
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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
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No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies
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Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility
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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
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Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing
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Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report
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Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database
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Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database
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A pooled analysis of the outcome of prospective colonoscopic surveillance for familial colorectal cancer
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Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database
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Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome
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Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors
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Deciphering the Colon Cancer Genes-Report of the InSiGHT-Human Variome Project Workshop, UNESCO, Paris 2010
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Recurrence and Variability of Germline EPCAM Deletions in Lynch Syndrome
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Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study
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Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study
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