(Q33605565)

28 July 2017

Universal molecular screening does not effectively detect Lynch syndrome in clinical practice (English)

1 reference

28 July 2017

1 reference

Desmond Yip

4

0 references

author name string

Beatrice Brennan

1

1 reference

28 July 2017

Christine T Hemmings

2

1 reference

28 July 2017

Ian Clark

3

1 reference

28 July 2017

Mitali Fadia

5

1 reference

28 July 2017

Douglas R Taupin

6

1 reference

28 July 2017

9 February 2017

1 reference

Therapeutic Advances in Gastroenterology

28 July 2017

1 reference

28 July 2017

10

1 reference

28 July 2017

4

1 reference

28 July 2017

361-371

1 reference

Findings made in gene panel to whole genome sequencing: data, knowledge, ethics - and consequences?

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

Achieving behaviour change for detection of Lynch syndrome using the Theoretical Domains Framework Implementation (TDFI) approach: a study protocol

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk Management

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

Universal tumor screening for Lynch syndrome: Assessment of the perspectives of patients with colorectal cancer regarding benefits and barriers

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

Familial colorectal cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

A model-based assessment of the cost-utility of strategies to identify Lynch syndrome in early-onset colorectal cancer patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

Creation of a network to promote universal screening for Lynch syndrome: the LynchSyndrome Screening Network

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

A systematic review of factors that act as barriers to patient referral to genetic services

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

Comparing universal Lynch syndrome tumor-screening programs to evaluate associations between implementation strategies and patient follow-through

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

Improving identification of lynch syndrome patients: a comparison of research data with clinical records

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

Identification of Lynch syndrome among patients with colorectal cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

Current and emerging trends in Lynch syndrome identification in women with endometrial cancer.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

Feasibility of screening for Lynch syndrome among patients with colorectal cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

The incidentalome: a threat to genomic medicine

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

Lynch syndrome (HNPCC) and microsatellite instability

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

Strategies for screening for hereditary non-polyposis colorectal cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5405883

Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.

21 June 2018

1 reference

https://api.crossref.org/works/10.1177%2F1756283X17690990

Economic evaluation of genetic screening for Lynch syndrome in Germany.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1756283X17690990

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1756283X17690990

Population-based molecular detection of hereditary nonpolyposis colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1756283X17690990

Comparison of predictive models, clinical criteria and molecular tumour screening for the identification of patients with Lynch syndrome in a population-based cohort of colorectal cancer patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1756283X17690990

The increasing incidence of young-onset colorectal cancer: a call to action

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1756283X17690990

Yield of routine molecular analyses in colorectal cancer patients ≤70 years to detect underlying Lynch syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1756283X17690990

The InSiGHT database: utilizing 100 years of insights into Lynch syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1756283X17690990

Population-based molecular screening for Lynch syndrome: implications for personalized medicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1756283X17690990

Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1756283X17690990

Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic tests

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1756283X17690990

Ten Years After Mutation Testing for Lynch Syndrome: Cancer Incidence and Outcome in Mutation-Positive and Mutation-Negative Family Members

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1756283X17690990

Identification in Daily Practice of Patients With Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer): Revised Bethesda Guidelines-Based ApproachVersusMolecular Screening

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1756283X17690990

Genetic/Familial High-Risk Assessment: Colorectal Version 1.2016, NCCN Clinical Practice Guidelines in Oncology

21 January 2018

1 reference

12 December 2020

Value of database linkage: are patients at risk of familial colorectal cancer being referred for genetic counselling and testing?

1 reference

12 December 2020

Microsatellite instability is associated with tumors that characterize the hereditary non-polyposis colorectal carcinoma syndrome

1 reference

12 December 2020

The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)

1 reference

12 December 2020

Hereditary colorectal cancer

1 reference

12 December 2020

Screening for Lynch syndrome in colorectal cancer: are we doing enough?

1 reference

12 December 2020

Screening reduces colorectal cancer rate in families with hereditary nonpolyposis colorectal cancer

1 reference

12 December 2020

Identifiers

DOI

10.1177/1756283X17690990

1 reference

28 July 2017

1 reference

28 July 2017

1 reference