(Q36507457)

English

Accuracy of MSI testing in predicting germline mutations of MSH2 and MLH1: a case study in Bayesian meta-analysis of diagnostic tests without a gold standard

scientific article published on 14 April 2005

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

0 references

Accuracy of MSI testing in predicting germline mutations of MSH2 and MLH1: a case study in Bayesian meta-analysis of diagnostic tests without a gold standard (English)

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

author name string

Sining Chen

1

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Patrice Watson

2

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Giovanni Parmigiani

3

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

publication date

14 April 2005

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

6

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

3

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

450-464

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

describes a project that uses

1 reference

Europe PubMed Central

18 June 2022

https://europepmc.org/article/PMC/2274000

based on heuristic

inferred from PubMed Central ID database lookup

maintained by WikiProject

WikiProject Mathematics

0 references

BayesMendel: an R environment for Mendelian risk prediction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

Identification and characterization of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

Cost-effectiveness of microsatellite instability screening as a method for detecting hereditary nonpolyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

Value of pedigree/clinical data, immunohistochemistry and microsatellite instability analyses in reducing the cost of determining hMLH1 and hMSH2 gene mutations in patients with colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

Extensive molecular screening for hereditary non-polyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

Conversion of diploidy to haploidy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

Microsatellite instability in adenomas as a marker for hereditary nonpolyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

Strategies for screening for hereditary non-polyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

Genetic susceptibility to non-polyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

Microsatellite instability in sporadic colorectal cancer is not an independent prognostic factor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

Microsatellite instability-a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

Microsatellite instability in cancer of the proximal colon

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

30 September 2017

Complex germline rearrangement of BRCA1 associated with breast and ovarian cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

28 June 2018

Cumulative incidence of colorectal and extracolonic cancers in MLH1 and MSH2 mutation carriers of hereditary nonpolyposis colorectal cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

28 June 2018

Diagnostic microsatellite instability: definition and correlation with mismatch repair protein expression.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

28 June 2018

Comparison of selection strategies for genetic testing of patients with hereditary nonpolyposis colorectal carcinoma: effectiveness and cost-effectiveness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

21 September 2018

Hereditary nonpolyposis colorectal cancer in young colorectal cancer patients: high-risk clinic versus population-based registry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

21 September 2018

MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

21 September 2018

Screening without a "gold standard": the Hui-Walter paradigm revisited

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

21 September 2018

Efficient detection of hereditary nonpolyposis colorectal cancer gene carriers by screening for tumor microsatellite instability before germline genetic testing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

21 September 2018

Population-based molecular detection of hereditary nonpolyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

21 September 2018

Molecular Screening for Hereditary Nonpolyposis Colorectal Cancer: A Prospective, Population-Based Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

4 December 2018

Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2274000

4 December 2018

Microsatellite instability in colorectal-cancer patients with suspected genetic predisposition

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered Expression of MLH1, MSH2, and MSH6 in Predisposition to Hereditary Nonpolyposis Colorectal Cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Color bar coding the BRCA1 gene on combed DNA: a useful strategy for detecting large gene rearrangements

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correlation of mismatch repair genes immunohistochemistry and microsatellite instability status in HNPCC-associated tumours

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of hMLH1 and hMSH2 in patients with suspected hereditary nonpolyposis colorectal cancer: correlation with microsatellite instability and abnormalities of mismatch repair protein expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allele separation facilitates interpretation of potential splicing alterations and genomic rearrangements

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of microsatellite instability and immunohistochemistry for the prediction of germ-line MSH2 and MLH1 mutations in hereditary nonpolyposis colon cancer families

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of Alu-PCR, microsatellite instability, and immunohistochemical analyses in finding features characteristic for hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimating the error rates of diagnostic tests

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic instability in colorectal cancer: relationship to clinicopathological variables and family history

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunohistochemistry for hMLH1 and hMSH2: a practical test for DNA mismatch repair-deficient tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A deletion/insertion mutation in the BRCA2 gene in a breast cancer family: a possible role of the Alu-polyA tail in the evolution of the deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of germline MSH2 gene mutations in endometrial cancer not fulfilling the new clinical criteria for hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A population based cohort study of patients with multiple colon and endometrial cancer: Correlation of microsatellite instability (msi) status, age at diagnosis and cancer risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microsatellite instability as a predictor of a mutation in a DNA mismatch repair gene in familial colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel approach to estimate the proportion of hereditary nonpolyposis colorectal cancer of total colorectal cancer burden

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831578

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/BIOSTATISTICS/KXI021

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

ResearchGate publication ID

0 references

zbMATH Open document ID

0 references

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