Prevalence of Lynch syndrome and Lynch-like syndrome among patients with colorectal cancer in a Japanese hospital-based population

Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts

(2017) Daniel D Buchanan et al.   JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY

Prevalence of Lynch syndrome in a Middle Eastern population with colorectal cancer

(2015) Abdul K. Siraj et al.   CANCER

Identification of a Japanese Lynch syndrome patient with large deletion in the 3′ region of theEPCAMgene

(2015) Hidetaka Eguchi et al.   JAPANESE JOURNAL OF CLINICAL ONCOLOGY

Prevalence ofMLH1constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancer

(2015) Adela Castillejo et al.   JOURNAL OF MEDICAL GENETICS

Lynch syndrome in the 21st century: clinical perspectives

(2015) A.K. Tiwari et al.   QJM-AN INTERNATIONAL JOURNAL OF MEDICINE

Lower prevalence of Lynch syndrome in colorectal cancer patients in a Japanese hospital-based population

(2015) Kensuke Kumamoto et al.   SURGERY TODAY

DNA hypermethylation appears early and shows increased frequency with dysplasia in Lynch syndrome-associated colorectal adenomas and carcinomas

(2015) Satu Valo et al.   Clinical Epigenetics

Prevalence of somatic mutl homolog 1 promoter hypermethylation in Lynch syndrome colorectal cancer

(2014) Leticia Moreira et al.   CANCER

Biallelic MUTYH mutations can mimic Lynch syndrome

(2014) Monika Morak et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Colon and Endometrial Cancers With Mismatch Repair Deficiency Can Arise From Somatic, Rather Than Germline, Mutations

(2014) Sigurdis Haraldsdottir et al.   GASTROENTEROLOGY

Lynch-like syndrome: Characterization and comparison with EPCAM deletion carriers

(2014) So Young Kang et al.   INTERNATIONAL JOURNAL OF CANCER

Comparison of clinical features between suspected familial colorectal cancer type X and Lynch syndrome in Japanese patients with colorectal cancer: a cross-sectional study conducted by the Japanese Society for Cancer of the Colon and Rectum

(2014) Tatsuro Yamaguchi et al.   JAPANESE JOURNAL OF CLINICAL ONCOLOGY

Somatic aberrations of mismatch repair genes as a cause of microsatellite-unstable cancers

(2014) Willemina RR Geurts-Giele et al.   JOURNAL OF PATHOLOGY

The role of epigenetics in Lynch syndrome

(2013) Megan P. Hitchins   Familial Cancer

Do lifestyle factors influence colorectal cancer risk in Lynch syndrome?

(2013) Fränzel J. B. van Duijnhoven et al.   Familial Cancer

Risk of Cancer in Cases of Suspected Lynch Syndrome Without Germline Mutation

(2013) María Rodríguez–Soler et al.   GASTROENTEROLOGY

Somatic Mutations in MLH1 and MSH2 Are a Frequent Cause of Mismatch-Repair Deficiency in Lynch Syndrome-Like Tumors

(2013) Arjen R. Mensenkamp et al.   GASTROENTEROLOGY

Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts

(2013) Hans F A Vasen et al.   GUT

Oncogene abnormalities in a series of primary melanomas of the sinonasal tract: NRAS mutations and cyclin D1 amplification are more frequent than KIT or BRAF mutations

(2013) Meriem Chraybi et al.   HUMAN PATHOLOGY

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

(2013) Bryony A Thompson et al.   NATURE GENETICS

Regulation of MLH1 mRNA and protein expression by promoter methylation in primary colorectal cancer: a descriptive and prognostic cancer marker study

(2013) Lars Henrik Jensen et al.   CELLULAR ONCOLOGY

MLH1 methylation screening is effective in identifying epimutation carriers

(2012) Marta Pineda et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

EPCAM deletion carriers constitute a unique subgroup of Lynch syndrome patients

(2012) Marjolijn J. L. Ligtenberg et al.   Familial Cancer

Somatic mosaicism and double somatic hits can lead to MSI colorectal tumors

(2012) Isabelle Sourrouille et al.   Familial Cancer

Identification of Lynch Syndrome Among Patients With Colorectal Cancer

(2012) Leticia Moreira et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Screening for Lynch Syndrome in Colorectal Cancer: Are We Doing Enough?

(2011) Guillaume Canard et al.   ANNALS OF SURGICAL ONCOLOGY

Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer

(2011) Lucía Pérez-Carbonell et al.   GUT

Smoking and Colorectal Cancer in Lynch Syndrome: Results from the Colon Cancer Family Registry and The University of Texas M.D. Anderson Cancer Center

(2010) M. Pande et al.   CLINICAL CANCER RESEARCH

Screening for germline mutations of MLH1, MSH2, MSH6 and PMS2 genes in Slovenian colorectal cancer patients: implications for a population specific detection strategy of Lynch syndrome

(2009) Gašper Berginc et al.   Familial Cancer

Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members

(2009) Heikki J. Järvinen et al.   JOURNAL OF CLINICAL ONCOLOGY

Identification in Daily Practice of Patients With Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer): Revised Bethesda Guidelines-Based ApproachVersusMolecular Screening

(2008) Catherine Julié et al.   AMERICAN JOURNAL OF GASTROENTEROLOGY

Feasibility of Screening for Lynch Syndrome Among Patients With Colorectal Cancer

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