Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families

The effect of body mass index on endometrial cancer: a meta-analysis

(2015) E. Jenabi et al.   PUBLIC HEALTH

NGSANE: a lightweight production informatics framework for high-throughput data analysis

(2014) Fabian A. Buske et al.   BIOINFORMATICS

Clinical Evaluation of a Multiple-Gene Sequencing Panel for Hereditary Cancer Risk Assessment

(2014) Allison W. Kurian et al.   JOURNAL OF CLINICAL ONCOLOGY

The dual nature of mismatch repair as antimutator and mutator: for better or for worse

(2014) Sara Thornby Bak et al.   Frontiers in Genetics

A massive parallel sequencing workflow for diagnostic genetic testing of mismatch repair genes

(2014) Maren F. Hansen et al.   Molecular Genetics & Genomic Medicine

Mismatch repair deficiency in ovarian cancer — Molecular characteristics and clinical implications

(2013) Xue Xiao et al.   GYNECOLOGIC ONCOLOGY

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

Comprehensive comparison of three commercial human whole-exome capture platforms

(2011) Asan et al.   GENOME BIOLOGY

Cancer Statistics, 2010

(2010) A. Jemal et al.   CA-A CANCER JOURNAL FOR CLINICIANS

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

(2010) A. McKenna et al.   GENOME RESEARCH

Mismatch repair status and outcomes after adjuvant therapy in patients with surgically staged endometrial cancer

(2010) Kimberly E. Resnick et al.   GYNECOLOGIC ONCOLOGY

Methylation Analysis of MLH1 Improves the Selection of Patients for Genetic Testing in Lynch Syndrome

(2010) Lucía Pérez-Carbonell et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH

Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads

(2009) K. Ye et al.   BIOINFORMATICS

The Sequence Alignment/Map format and SAMtools

(2009) H. Li et al.   BIOINFORMATICS

Cancer Statistics, 2009

(2009) A. Jemal et al.   CA-A CANCER JOURNAL FOR CLINICIANS

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

(2009) HT Lynch et al.   CLINICAL GENETICS

Endometrial Cancer as a Familial Tumor: Pathology and Molecular Carcinogenesis (Review)

(2009) Kouji Banno et al.   CURRENT GENOMICS

DNA Mismatch Repair Deficiency in Endometrial Carcinoma

(2009) Yevgeniy Karamurzin et al.   INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY

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