Amplicon-based NGS test for assessing MLH1 promoter methylation and its correlation with BRAF mutation in colorectal cancer patients

Universal Immunohistochemistry for Lynch Syndrome: A Systematic Review and Meta-Analysis of 58,580 Colorectal Carcinomas

(2021) E.L. Eikenboom et al.   Clinical Gastroenterology and Hepatology

A modified screening strategy for Lynch syndrome among MLH1-deficient CRCs: Analysis from consecutive Chinese patients in a single center

(2021) Wenmiao Wang et al.   Translational Oncology

Clinicopathological and molecular characterization of Brazilian families at risk for Lynch syndrome

(2021) André Escremim de Paula et al.   Cancer Genetics

Distinct clinical phenotype and genetic testing strategy for Lynch syndrome in China based on a large colorectal cancer cohort

(2020) Lin Dong et al.   INTERNATIONAL JOURNAL OF CANCER

Universal endometrial cancer tumor typing: How much has immunohistochemistry, microsatellite instability, and MLH1 methylation improved the diagnosis of Lynch syndrome across the population?

(2019) Ryan M. Kahn et al.   CANCER

Genetic and genomic basis of the mismatch repair system involved in Lynch syndrome

(2019) Kazuo Tamura et al.   International Journal of Clinical Oncology

Reliable Clinical MLH1 Promoter Hypermethylation Assessment Using a High-Throughput Genome-Wide Methylation Array Platform

(2019) Jamal K. Benhamida et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

A tailored approach to BRAF and MLH1 methylation testing in a universal screening program for Lynch syndrome

(2017) Tomer Adar et al.   MODERN PATHOLOGY

Genetic/Familial High-Risk Assessment: Colorectal Version 1.2016, NCCN Clinical Practice Guidelines in Oncology

(2016) Dawn Provenzale et al.   Journal of the National Comprehensive Cancer Network

Deficient mismatch repair: Read all about it (Review)

(2015) SUSAN RICHMAN   INTERNATIONAL JOURNAL OF ONCOLOGY

Guidelines on Genetic Evaluation and Management of Lynch Syndrome: A Consensus Statement by the US Multi-Society Task Force on Colorectal Cancer

(2014) Francis M. Giardiello et al.   GASTROENTEROLOGY

TumourMLH1promoter region methylation testing is an effective prescreen for Lynch Syndrome (HNPCC)

(2014) K Newton et al.   JOURNAL OF MEDICAL GENETICS

B-Raf mutation: A key player in molecular biology of cancer

(2013) M.A. Rahman et al.   EXPERIMENTAL AND MOLECULAR PATHOLOGY

Correlation of tumour BRAF mutations andMLH1methylation with germline mismatch repair (MMR) gene mutation status: a literature review assessing utility of tumour features for MMR variant classification

(2012) Michael T Parsons et al.   JOURNAL OF MEDICAL GENETICS

EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome

(2009) Glenn E Palomaki et al.   GENETICS IN MEDICINE

Feasibility of Screening for Lynch Syndrome Among Patients With Colorectal Cancer

(2008) Heather Hampel et al.   JOURNAL OF CLINICAL ONCOLOGY