Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer. - Wikidata - awgldk - TriplyDB

Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.

Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.

http://www.wikidata.org/entity/Q40423712

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Findings in young adults at colonoscopy from a hospital service database audit The Role of PALB2 in the DNA Damage Response and Cancer Predisposition.MicroRNA-449a deficiency promotes colon carcinogenesis.Epigenetic silencing of MLH1 in endometrial cancers is associated with larger tumor volume, increased rate of lymph node positivity and reduced recurrence-free survival.Germline Genetic Features of Young Individuals with Colorectal Cancer.Low Prevalence of Criteria for Early Screening in Young-Onset Colorectal Cancer.Lower gastrointestinal neuroendocrine neoplasms associated with hereditary cancer syndromes: a case series.Nine primary malignant neoplasms-involving the esophagus, stomach, colon, rectum, prostate, and external ear canal-without microsatellite instability: a case report.Expanding the spectrum of germline variants in cancer.Sporadic endometrial adenocarcinoma with MMR deficiency due to biallelic MSH2 somatic mutations.In Silico Systems Biology Analysis of Variants of Uncertain Significance in Lynch Syndrome Supports the Prioritization of Functional Molecular Validation.Reply to 'Comment on 'Distinct clinical outcomes of two CIMP-positive colorectal cancer subtypes based on a revised CIMP classification system".Identification of genetic variants for clinical management of familial colorectal tumors.Validation of CZECANCA (CZEch CAncer paNel for Clinical Application) for targeted NGS-based analysis of hereditary cancer syndromes.Inherited DNA-Repair Defects in Colorectal Cancer.Recent progress in Lynch syndrome and other familial colorectal cancer syndromes.Advantages and Some Remaining Challenges in Hereditary Gastrointestinal Cancer Panel Testing.Establishing a research agenda for early-onset colorectal cancer.Colorectal cancer: genetic abnormalities, tumor progression, tumor heterogeneity, clonal evolution and tumor-initiating cells.Gene promoter and exon DNA methylation changes in colon cancer development - mRNA expression and tumor mutation alterations.Recent advances in colorectal cancer screening Using Somatic Mutations from Tumors to Classify Variants in Mismatch Repair Genes Barriers to Lynch Syndrome Testing and Preoperative Result Availability in Early-onset Colorectal Cancer: A National Physician Survey Study Frequent basal cell cancer development is a clinical marker for inherited cancer susceptibility Defining Early-Onset Colon and Rectal Cancers

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Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.

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JAMAONCOL.2016.5194

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Prevalence and Spectrum of Ger ...... Early-Onset Colorectal Cancer.

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Ahmet Yilmaz

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Amy A Shaper

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Angela Jacobson

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P2860

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

PD-1 Blockade in Tumors with Mismatch-Repair Deficiency

Accurate and exact CNV identification from targeted high-throughput sequence data.

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

Colon and endometrial cancers with mismatch repair deficiency can arise from somatic, rather than germline, mutations.

Development and analytical validation of a 25-gene next generation sequencing panel that includes the BRCA1 and BRCA2 genes to assess hereditary cancer risk.

Next-Generation Sequencing Panels for the Diagnosis of Colorectal Cancer and Polyposis Syndromes: A Cost-Effectiveness Analysis

Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.

ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing.

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