|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
Optimization of the diagnosis of inherited colorectal cancer using NGS and capture of exonic and intronic sequences of panel genes.
|
29967336 |
2018 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
Spectrum of mismatch repair gene mutations and clinical presentation of Hispanic individuals with Lynch syndrome.
|
28449805 |
2017 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
GeneticVariation |
CLINVAR |
Targeted sequencing of established and candidate colorectal cancer genes in the Colon Cancer Family Registry Cohort.
|
29212164 |
2017 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
GeneticVariation |
CLINVAR |
Thyroid cancer in a patient with Lynch syndrome - case report and literature review.
|
28769567 |
2017 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
A molecular inversion probe-based next-generation sequencing panel to detect germline mutations in Chinese early-onset colorectal cancer patients.
|
28445943 |
2017 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
Assessment of the InSiGHT Interpretation Criteria for the Clinical Classification of 24 MLH1 and MSH2 Gene Variants.
|
27629256 |
2017 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
|
28514183 |
2017 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
GeneticVariation |
CLINVAR |
Elucidating the molecular basis of MSH2-deficient tumors by combined germline and somatic analysis.
|
28577310 |
2017 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
MSH2 Loss in Primary Prostate Cancer.
|
28790115 |
2017 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
GeneticVariation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
2016 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
MLH1 Ile219Val Polymorphism in Argentinean Families with Suspected Lynch Syndrome.
|
27606285 |
2016 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
Mutation profiles of synchronous colorectal cancers from a patient with Lynch syndrome suggest distinct oncogenic pathways.
|
27284491 |
2016 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
Multilocus Inherited Neoplasia Alleles Syndrome: A Case Series and Review.
|
26659639 |
2016 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
Analysis of Lynch Syndrome Mismatch Repair Genes in Women with Endometrial Cancer.
|
27398995 |
2016 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
Oligonucleotide-directed mutagenesis screen to identify pathogenic Lynch syndrome-associated MSH2 DNA mismatch repair gene variants.
|
26951660 |
2016 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
GeneticVariation |
CLINVAR |
Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
|
26681312 |
2016 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
The role of germline mutations in the BRCA1/2 and mismatch repair genes in men ascertained for early-onset and/or familial prostate cancer.
|
26289772 |
2016 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.
|
27064304 |
2016 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
GeneticVariation |
CLINVAR |
Oligonucleotide-directed mutagenesis screen to identify pathogenic Lynch syndrome-associated MSH2 DNA mismatch repair gene variants.
|
26951660 |
2016 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
Patients with colorectal cancer associated with Lynch syndrome and MLH1 promoter hypermethylation have similar prognoses.
|
26866578 |
2016 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
|
27601186 |
2016 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation |
CLINVAR |
Improving performance of multigene panels for genomic analysis of cancer predisposition.
|
26845104 |
2016 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
GeneticVariation |
CLINVAR |
Improving performance of multigene panels for genomic analysis of cancer predisposition.
|
26845104 |
2016 |
|
| Entrez Id: |
4436 |
| Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
Biomarker |
CLINGEN |
Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer.
|
27329137 |
2016 |