An Individual with Both MUTYH-Associated Polyposis and Lynch Syndrome Identified by Multi-Gene Hereditary Cancer Panel Testing: A Case Report (Q39020597)

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scientific article published on 16 March 2016

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Language	Label	Description	Also known as
English	An Individual with Both MUTYH-Associated Polyposis and Lynch Syndrome Identified by Multi-Gene Hereditary Cancer Panel Testing: A Case Report	scientific article published on 16 March 2016

Statements

instance of

scholarly article

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stated in

Europe PubMed Central

PMC publication ID

4792865

retrieved

8 September 2017

title

An Individual with Both MUTYH-Associated Polyposis and Lynch Syndrome Identified by Multi-Gene Hereditary Cancer Panel Testing: A Case Report (English)

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Europe PubMed Central

PMC publication ID

4792865

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8 September 2017

main subject

Lynch syndrome

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based on heuristic

inferred from title

polyposis

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based on heuristic

inferred from title

author name string

Stephanie A Cohen

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1

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Europe PubMed Central

PMC publication ID

4792865

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8 September 2017

Christopher A Tan

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2

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Europe PubMed Central

PMC publication ID

4792865

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8 September 2017

Ryan Bisson

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3

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Europe PubMed Central

PMC publication ID

4792865

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8 September 2017

publication date

16 March 2016

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stated in

Europe PubMed Central

PMC publication ID

4792865

retrieved

8 September 2017

published in

Frontiers in Genetics

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Europe PubMed Central

PMC publication ID

4792865

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8 September 2017

volume

7

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Europe PubMed Central

PMC publication ID

4792865

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8 September 2017

page(s)

36

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Europe PubMed Central

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4792865

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8 September 2017

cites work

Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4792865

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9 September 2017

High Prevalence of Hereditary Cancer Syndromes in Adolescents and Young Adults With Colorectal Cancer

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4792865

retrieved

9 September 2017

ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4792865

retrieved

9 September 2017

Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4792865

retrieved

9 September 2017

The genetic basis of Lynch syndrome and its implications for clinical practice and risk management

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4792865

retrieved

9 September 2017

Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4792865

retrieved

9 September 2017

A case of endometrial cancer in the context of a BRCA2 mutation and double heterozygosity for Lynch syndrome

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4792865

retrieved

9 September 2017

Feasibility of screening for Lynch syndrome among patients with colorectal cancer

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4792865

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9 September 2017

Characterization of mutant MUTYH proteins associated with familial colorectal cancer.

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4792865

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9 September 2017

Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4792865

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9 September 2017

Germline truncating mutations in both MSH2 and BRCA2 in a single kindred

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4792865

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9 September 2017

Genetic diagnosis of high-penetrance susceptibility for colorectal cancer (CRC) is achievable for a high proportion of familial CRC by exome sequencing.

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4792865

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21 August 2018

Prevalence of germline MUTYH mutations among Lynch-like syndrome patients

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4792865

retrieved

21 August 2018

Clinical Implications of the Colorectal Cancer Risk Associated With MUTYH Mutation

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.3389%2FFGENE.2016.00036

retrieved

21 January 2018

MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/27014339

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The natural history of a combined defect in MSH6 and MUTYH in a HNPCC family

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/27014339

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.3389/FGENE.2016.00036

1 reference

stated in

Europe PubMed Central

PMC publication ID

4792865

retrieved

8 September 2017

PMC publication ID

4792865

1 reference

stated in

Europe PubMed Central

PMC publication ID

4792865

retrieved

8 September 2017

PubMed publication ID

27014339

1 reference

stated in

Europe PubMed Central

PMC publication ID

4792865

retrieved

8 September 2017

 

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