(Q36666308)

15 August 2017

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title

Genetic testing for colon cancer (English)

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15 August 2017

Andrew M Kaz

1

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15 August 2017

Teresa A Brentnall

series ordinal

2

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15 August 2017

language of work or name

English

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publication date

1 December 2006

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Nature Reviews Gastroenterology & Hepatology

15 August 2017

published in

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15 August 2017

volume

3

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15 August 2017

issue

12

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15 August 2017

page(s)

670-679

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https://scigraph.springernature.com/pub.10.1038/ncpgasthep0663

15 August 2017

exact match

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cites work

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21 January 2018

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Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors

21 January 2018

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Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C-->T:A mutations

21 January 2018

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Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH

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21 January 2018

Colon cancer screening

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Genetic testing for inherited colon cancer

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Review article: genetic testing and counselling for hereditary colorectal cancer

21 January 2018

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Germ-line and somatic mutations of the APC gene in patients with Turcot syndrome and analysis of APC mutations in brain tumors.

21 January 2018

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Genetic and epigenetic alterations in colon cancer

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Alleles of the APC gene: an attenuated form of familial polyposis

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The clinical correlates of a 3' truncating mutation (codons 1982-1983) in the adenomatous polyposis coli gene.

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MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps

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Rare mutations predisposing to familial adenomatous polyposis in Greek FAP patients

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Different familial adenomatous polyposis phenotypes resulting from deletions of the entire APC exon 15.

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Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH

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Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas.

21 January 2018

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High frequency of MYH gene mutations in a subset of patients with familial adenomatous polyposis

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The multiple colorectal adenoma phenotype and MYH, a base excision repair gene

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Immunohistochemical expression of MYH protein can be used to identify patients with MYH-associated polyposis.

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Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria

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Challenges and pitfalls in HNPCC screening by microsatellite analysis and immunohistochemistry

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Familial juvenile polyposis coli; increased risk of colorectal cancer

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The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2, BMPR1B, and ACVR1 mutations

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Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase

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21 January 2018

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21 January 2018

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

21 January 2018

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A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22.2-31.2

21 January 2018

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Mapping of hereditary mixed polyposis syndrome (HMPS) to chromosome 10q23 by genomewide high-density single nucleotide polymorphism (SNP) scan and identification of BMPR1A loss of function

21 January 2018

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Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease

21 January 2018

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Genetic testing is important in families with a history suggestive of hereditary non-polyposis colorectal cancer even if the Amsterdam criteria are not fulfilled

21 January 2018

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21 January 2018

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21 January 2018

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7 January 2021

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7 January 2021

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7 January 2021

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0663

7 January 2021

Microsatellite instability in human colonic cancer is not a useful clinical indicator of familial colorectal cancer

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0663

7 January 2021

Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors

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7 January 2021

The risk of gastrointestinal carcinoma in familial juvenile polyposis

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7 January 2021

Germline SMAD4 or BMPR1A mutations and phenotype of juvenile polyposis

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7 January 2021

SMAD genes in juvenile polyposis

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0663

7 January 2021

Frequent 4-bp deletion in exon 9 of the SMAD4/MADH4 gene in familial juvenile polyposis patients

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0663

7 January 2021

American Society of Clinical Oncology Policy Statement Update: Genetic Testing for Cancer Susceptibility

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0663

7 January 2021

Physician assessment of family cancer history and referral for genetic evaluation in colorectal cancer patients

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0663

7 January 2021

Identifiers

DOI

10.1038/NCPGASTHEP0663

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Dimensions Publication ID

15 August 2017

1026211725

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1 reference