Panel-based testing for inherited colorectal cancer: a descriptive study of clinical testing performed by a US laboratory. (Q34022144)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24506336%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

title

Panel-based testing for inherited colorectal cancer: a descriptive study of clinical testing performed by a US laboratory (English)

1 reference

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7 March 2020

1 reference

1 reference

1

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7 March 2020

author name string

C Radford

2

1 reference

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7 March 2020

J S Dolinsky

3

1 reference

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7 March 2020

M Caldwell

4

1 reference

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7 March 2020

E Chao

5

1 reference

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7 March 2020

T Pal

6

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7 March 2020

publication date

20 March 2014

1 reference

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7 March 2020

1 reference

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7 March 2020

volume

86

1 reference

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7 March 2020

issue

6

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7 March 2020

page(s)

510-520

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Translating genomics in cancer care

7 March 2020

cites work

1 reference

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The integration of next-generation sequencing panels in the clinical cancer genetics practice: an institutional experience

5 July 2018

1 reference

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Germline deletions in the EPCAM gene as a cause of Lynch syndrome - literature review

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127163

A statewide survey of practitioners to assess knowledge and clinical practices regarding hereditary breast and ovarian cancer

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127163

ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127163

Genetic testing and cancer risk management recommendations by physicians for at-risk relatives

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127163

Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127163

Hereditary diffuse gastric cancer: updated consensus guidelines for clinical management and directions for future research

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127163

Massively parallel sequencing: the next big thing in genetic medicine

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127163

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127163

Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127163

Keeping up with the next generation: massively parallel sequencing in clinical diagnostics

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127163

Extensive gene conversion at the PMS2 DNA mismatch repair locus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127163

Hereditary breast/ovarian and colorectal cancer genetics knowledge in a national sample of US physicians

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127163

CHEK2 is a multiorgan cancer susceptibility gene

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127163

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127163

5 July 2018

Colon cancer screening

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127163

The growing complexity of the intestinal polyposis syndromes.

5 July 2018

1 reference

Colorectal cancer risk in monoallelic carriers of MYH variants

21 January 2018

1 reference

Multiplex Genetic Testing for Cancer Susceptibility: Out on the High Wire Without a Net?

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24506336

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Evidence for accelerated colorectal adenoma–carcinoma progression inMUTYH-associated polyposis?

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24506336

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/CGE.12359

1 reference

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7 March 2020

1 reference

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7 March 2020

PubMed publication ID

24506336

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24506336%20AND%20SRC:MED&resulttype=core&format=json