(Q37345978)

English

Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives

scientific article published on January 2009

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Statements

scholarly article

1 reference

Europe PubMed Central

19 August 2017

Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives (English)

1 reference

Europe PubMed Central

19 August 2017

colorectal cancer

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

colorectal carcinoma

1 reference

based on heuristic

inferred from title

author name string

Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Working Group

1

1 reference

Europe PubMed Central

19 August 2017

language of work or name

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publication date

1 January 2009

1 reference

Europe PubMed Central

19 August 2017

Genetics in Medicine

1 reference

Europe PubMed Central

19 August 2017

11

1 reference

Europe PubMed Central

19 August 2017

35-41

1 reference

Europe PubMed Central

19 August 2017

1

1 reference

Europe PubMed Central

19 August 2017

https://scigraph.springernature.com/pub.10.1097/gim.0b013e31818fa2ff

0 references

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743612

6 September 2017

The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Initiative: methods of the EGAPP Working Group

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743612

6 September 2017

Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743612

6 September 2017

Hereditary Non-Polyposis Colorectal Cancer: the rise and fall of a confusing term

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743612

6 September 2017

Screening for the Lynch syndrome (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=2743612

6 September 2017

Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743612

6 September 2017

Decision analysis in the surgical treatment of colorectal cancer due to a mismatch repair gene defect

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743612

26 June 2018

Decrease in mortality in Lynch syndrome families because of surveillance.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743612

2 September 2018

Benchmark for evaluating the quality of DNA sequencing: proposal from an international external quality assessment scheme.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743612

2 September 2018

Benefits of colonoscopic surveillance and prophylactic colectomy in patients with hereditary nonpolyposis colorectal cancer mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2743612

2 September 2018

Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31818FA2FF

21 January 2018

Economic Evaluation of the Familial Cancer Programme in Western Australia: Predictive Genetic Testing for Familial Adenomatous Polyposis and Hereditary Non-Polyposis Colorectal Carcinoma

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E31818FA2FF

21 January 2018

Estimated analytic validity of HFE C282Y mutation testing in population screening: The potential value of confirmatory testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/19125126

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening and preventive behaviors one year after predictive genetic testing for hereditary nonpolyposis colorectal carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/19125126

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures

1 reference

https://pubmed.ncbi.nlm.nih.gov/19125126

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prophylactic Surgery to Reduce the Risk of Gynecologic Cancers in the Lynch Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19125126

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cost-effectiveness of surveillance programs for families at high and moderate risk of hereditary non-polyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/19125126

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

2006 Update of ASCO Recommendations for the Use of Tumor Markers in Gastrointestinal Cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/19125126

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cost-effectiveness analysis of colorectal screening of hereditary nonpolyposis colorectal carcinoma gene carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/19125126

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1097/GIM.0B013E31818FA2FF

1 reference

Europe PubMed Central

19 August 2017

Dimensions Publication ID

0 references

release_olasbmj5g5ealgqnkhyjbcwvdu

1 reference

https://api.fatcat.wiki/v0/release/olasbmj5g5ealgqnkhyjbcwvdu

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

19 August 2017

1 reference

Europe PubMed Central

19 August 2017

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