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

Pyloric Gland Adenoma in Lynch Syndrome

(2014) Seung Eun Lee et al.   AMERICAN JOURNAL OF SURGICAL PATHOLOGY

Differentiating Lynch-Like From Lynch Syndrome

(2014) John M. Carethers   GASTROENTEROLOGY

The Landscape of Microsatellite Instability in Colorectal and Endometrial Cancer Genomes

(2013) Tae-Min Kim et al.   CELL

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

Genetic variants associated with colorectal cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence

(2013) Xiangyu Ma et al.   GUT

Germline and somatic polymerase ϵ and δ mutations define a new class of hypermutated colorectal and endometrial cancers

(2013) Sarah Briggs et al.   JOURNAL OF PATHOLOGY

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

(2012) Isabelle Sourrouille et al.   Familial Cancer

Usefulness of epithelial cell adhesion molecule expression in the algorithmic approach to Lynch syndrome identification

(2012) Eva Musulen et al.   HUMAN PATHOLOGY

Identification of Lynch Syndrome Among Patients With Colorectal Cancer

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

ColoSeq Provides Comprehensive Lynch and Polyposis Syndrome Mutational Analysis Using Massively Parallel Sequencing

(2012) Colin C. Pritchard et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

EBV infection and mismatch repair deficiency mediated by loss of hMLH1 expression contribute independently to the development of multiple synchronous gastric carcinomas

(2012) Ha Young Park et al.   JOURNAL OF SURGICAL ONCOLOGY

The molecular basis of EPCAM expression loss in Lynch syndrome-associated tumors

(2012) Cathrin Huth et al.   MODERN PATHOLOGY

Comprehensive molecular characterization of human colon and rectal cancer

(2012)   NATURE

Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas

(2012) Claire Palles et al.   NATURE GENETICS

Three novel germline mutations in MLH1 and MSH2 in families with Lynch syndrome living on Jeju island, Korea

(2011) Young-Mee Kim et al.   BMB Reports

Deciphering the colon cancer genes-report of the InSiGHT-Human Variome Project Workshop, UNESCO, Paris 2010

(2011) Maija R.J. Kohonen-Corish et al.   HUMAN MUTATION

Recurrence and variability of germline EPCAM deletions in Lynch syndrome

(2011) Roland P. Kuiper et al.   HUMAN MUTATION

Frequency of Deletions of EPCAM (TACSTD1) in MSH2-Associated Lynch Syndrome Cases

(2011) Kandelaria Rumilla et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Somatic Hypermethylation of MSH2 Is a Frequent Event in Lynch Syndrome Colorectal Cancers

(2010) T. Nagasaka et al.   CANCER RESEARCH

A Multicenter Study to Validate the Reproducibility of MSI Testing With a Panel of 5 Quasimonomorphic Mononucleotide Repeats

(2010) Ermanno Nardon et al.   DIAGNOSTIC MOLECULAR PATHOLOGY

Microsatellite Instability in Colorectal Cancer

(2010) C. Richard Boland et al.   GASTROENTEROLOGY

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease

(2010) M. O. Woods et al.   GUT

Analysis of EPCAM Protein Expression in Diagnostics of Lynch Syndrome

(2010) Matthias Kloor et al.   JOURNAL OF CLINICAL ONCOLOGY

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications

(2009) HT Lynch et al.   CLINICAL GENETICS

Germline hypermethylation ofMLH1andEPCAMdeletions are a frequent cause of Lynch syndrome

(2009) Renée C. Niessen et al.   GENES CHROMOSOMES & CANCER

Deletions removing the last exon ofTACSTD1constitute a distinct class of mutations predisposing to Lynch syndrome

(2009) Marietta E. Kovacs et al.   HUMAN MUTATION

ClassifyingMLH1andMSH2variants using bioinformatic prediction, splicing assays, segregation, and tumor characteristics

(2009) Sven Arnold et al.   HUMAN MUTATION

Recurring MLH1 deleterious mutations in unrelated Chinese Lynch syndrome families in Singapore

(2008) Hui-Ling Yap et al.   Familial Cancer

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1

(2008) Marjolijn J L Ligtenberg et al.   NATURE GENETICS