Feasibility of screening for Lynch syndrome among patients with colorectal cancer (Q37103121)

18 August 2017

Feasibility of screening for Lynch syndrome among patients with colorectal cancer (English)

1 reference

18 August 2017

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1 reference

1 reference

Albert de la Chapelle

16

object named as

Albert de la Chapelle

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Mark Arnold

object named as

Mark Arnold

4

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author name string

Heather Hampel

1

1 reference

18 August 2017

Wendy L Frankel

2

1 reference

18 August 2017

Edward Martin

3

1 reference

18 August 2017

Karamjit Khanduja

5

1 reference

18 August 2017

Philip Kuebler

6

1 reference

18 August 2017

Mark Clendenning

7

1 reference

18 August 2017

Kaisa Sotamaa

8

1 reference

18 August 2017

Thomas Prior

9

1 reference

18 August 2017

Judith A Westman

10

1 reference

18 August 2017

Jenny Panescu

11

1 reference

18 August 2017

Dan Fix

12

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18 August 2017

Janet Lockman

13

1 reference

18 August 2017

Jennifer LaJeunesse

14

1 reference

18 August 2017

Ilene Comeras

15

1 reference

18 August 2017

language of work or name

English

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publication date

22 September 2008

1 reference

Journal of Clinical Oncology

18 August 2017

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18 August 2017

26

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18 August 2017

35

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18 August 2017

5783-5788

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Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Family history assessment to detect increased risk for colorectal cancer: conceptual considerations and a preliminary economic analysis

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Use of microsatellite instability and immunohistochemistry testing for the identification of individuals at risk for Lynch syndrome

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Immunohistochemical analysis of adenocarcinoma of the small intestine: a tissue microarray study

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Conventional and tissue microarray immunohistochemical expression analysis of mismatch repair in hereditary colorectal tumors

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Recurrent germline mutation in MSH2 arises frequently de novo

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Two-sided confidence intervals for the single proportion: comparison of seven methods

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Diagnostic tests 2: Predictive values

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Diagnostic tests. 1: Sensitivity and specificity

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Recommendations for follow-up care of individuals with an inherited predisposition to cancer. I. Hereditary nonpolyposis colon cancer. Cancer Genetics Studies Consortium

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Methylation of CpG in a small region of the hMLH1 promoter invariably correlates with the absence of gene expression.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Clues to the pathogenesis of familial colorectal cancer

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

Long-range PCR facilitates the identification of PMS2-specific mutations.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

The reliability of immunohistochemistry as a prescreening method for the diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC)--results of an international collaborative study

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

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

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2645108

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

3 September 2018

1 reference

12 December 2020

1 reference

12 December 2020

The family history--more important than ever

1 reference

12 December 2020

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

1 reference

12 December 2020

Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients

1 reference

12 December 2020

An Evidence-Based Review on Surveillance for Lynch Syndrome

1 reference

12 December 2020

Hereditary colorectal cancer

1 reference

12 December 2020

Pathogenicity of the hereditary colorectal cancer mutation hMLH1 del616 linked to shortage of the functional protein

1 reference

12 December 2020

Tissue Microarray Immunohistochemical Expression Analysis of Mismatch Repair (hMLH1 and hMSH2 Genes) in Endometrial Carcinoma and Atypical Endometrial Hyperplasia: Relationship with Microsatellite Instability

1 reference

12 December 2020

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

1 reference

12 December 2020

Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients

1 reference

12 December 2020

Altered expression of hMSH2 and hMLH1 in tumors with microsatellite instability and genetic alterations in mismatch repair genes

1 reference

12 December 2020

A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting Highlights and Bethesda Guidelines

1 reference

12 December 2020

Identifiers

DOI

10.1200/JCO.2008.17.5950

1 reference

release_wrfowtjcbrbnthypkkzslcgv2q

18 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/wrfowtjcbrbnthypkkzslcgv2q

24 November 2022

mapped directly with Wikidata item

1 reference

18 August 2017

PubMed publication ID

18809606

1 reference