(Q37968220)

English

Identification of individuals at risk for Lynch syndrome using targeted evaluations and genetic testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer joint practice guideline

scientific article published on 14 December 2011

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scholarly article

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Europe PubMed Central

PubMed publication ID

26 August 2017

Identification of individuals at risk for Lynch syndrome using targeted evaluations and genetic testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer joint practice guideline (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

colorectal cancer

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colorectal carcinoma

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3

object named as

James Church

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Europe PubMed Central

PubMed publication ID

26 August 2017

author name string

Scott M Weissman

1

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Europe PubMed Central

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26 August 2017

Randall Burt

2

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Europe PubMed Central

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26 August 2017

Steve Erdman

4

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Europe PubMed Central

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26 August 2017

Heather Hampel

5

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Europe PubMed Central

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26 August 2017

Spring Holter

6

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Europe PubMed Central

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26 August 2017

Kory Jasperson

7

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Europe PubMed Central

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26 August 2017

Matt F Kalady

8

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Europe PubMed Central

PubMed publication ID

26 August 2017

Joy Larsen Haidle

9

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Europe PubMed Central

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26 August 2017

Henry T Lynch

10

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Europe PubMed Central

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26 August 2017

Selvi Palaniappan

11

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Europe PubMed Central

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26 August 2017

Paul E Wise

12

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Europe PubMed Central

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26 August 2017

Leigha Senter

13

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Europe PubMed Central

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26 August 2017

publication date

14 December 2011

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Europe PubMed Central

PubMed publication ID

26 August 2017

Journal of Genetic Counseling

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Europe PubMed Central

PubMed publication ID

26 August 2017

21

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26 August 2017

4

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Europe PubMed Central

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26 August 2017

484-493

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Europe PubMed Central

PubMed publication ID

26 August 2017

The International Collaborative Group on HNPCC

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microsatellite instability is frequently observed in rectal cancer and influenced by neoadjuvant chemoradiation

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MLH1 promoter methylation and gene silencing is the primary cause of microsatellite instability in sporadic endometrial cancers

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PMS2 involvement in patients suspected of Lynch syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg?

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microsatellites in the eukaryotic DNA mismatch repair genes as modulators of evolutionary mutation rate

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Point: justification for Lynch syndrome screening among all patients with newly diagnosed colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: later age of onset.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Utility of immunohistochemistry in predicting microsatellite instability in endometrial carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neoadjuvant Therapy Induces Loss of MSH6 Expression in Colorectal Carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrence and variability of germline EPCAM deletions in Lynch syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prospective evaluation of DNA mismatch repair protein expression in primary endometrial cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comment on: Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Accurate classification of MLH1/MSH2 missense variants with multivariate analysis of protein polymorphisms-mismatch repair (MAPP-MMR).

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proximal adenomas in hereditary non-polyposis colorectal cancer are prone to rapid malignant transformation

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Calculation of risk of colorectal and endometrial cancer among patients with Lynch syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epitope-positive truncating MLH1 mutation and loss of PMS2: implications for IHC-directed genetic testing for Lynch syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Selection of endometrial carcinomas for DNA mismatch repair protein immunohistochemistry using patient age and tumor morphology enhances detection of mismatch repair abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Challenges and pitfalls in HNPCC screening by microsatellite analysis and immunohistochemistry

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microsatellite instability, immunohistochemistry, and additional PMS2 staining in suspected hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial colorectal cancer type X: the other half of hereditary nonpolyposis colon cancer syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Feasibility of screening for Lynch syndrome among patients with colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risks of Lynch syndrome cancers for MSH6 mutation carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk and epidemiological time trends of gastric cancer in Lynch syndrome carriers in the Netherlands

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunohistochemistry as first-line screening for detecting colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome: a 2-antibody panel may be as predictive as a 4-antibody panel

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Colorectal cancer in HNPCC: cumulative lifetime incidence, survival and tumour distribution. A report of 121 families with proven mutations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BRAF mutations in colon cancer are not likely attributable to defective DNA mismatch repair

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

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/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic counseling considerations in the evaluation of families for Lynch syndrome--a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evolution of the nomenclature for the hereditary colorectal cancer syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Strategies to identify the Lynch syndrome among patients with colorectal cancer: a cost-effectiveness analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations associated with HNPCC predisposition -- Update of ICG-HNPCC/INSiGHT mutation database

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dominantly Inherited Constitutional Epigenetic Silencing of MLH1 in a Cancer-Affected Family Is Linked to a Single Nucleotide Variant within the 5′UTR

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incorporation of somatic BRAF mutation testing into an algorithm for the investigation of hereditary non-polyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical analysis of PMS2: mutation detection and avoidance of pseudogenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Constitutional (germline) MLH1 epimutation as an aetiological mechanism for hereditary non-polyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22167527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10897-011-9465-7

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 August 2017

ResearchGate publication ID

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