Genetic testing for colon cancer (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

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15 August 2017

3

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15 August 2017

12

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15 August 2017

670-679

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

15 August 2017

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cites work

Genetic testing for high-risk colon cancer patients

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

21 January 2018

Colon cancer screening

1 reference

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

The molecular basis of Turcot's syndrome

21 January 2018

1 reference

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

Genetic testing for inherited colon cancer

21 January 2018

1 reference

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

Review article: genetic testing and counselling for hereditary colorectal cancer

21 January 2018

1 reference

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

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

1 reference

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

Biology of the adenomatous polyposis coli tumor suppressor

21 January 2018

1 reference

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

Genetic and epigenetic alterations in colon cancer

21 January 2018

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Rare mutations predisposing to familial adenomatous polyposis in Greek FAP patients

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH

21 January 2018

1 reference

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

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

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

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

The hereditary nonpolyposis colorectal cancer syndrome: genetics and clinical implications

21 January 2018

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

The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer

21 January 2018

1 reference

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

Cancer risk in mutation carriers of DNA-mismatch-repair genes

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Challenges and pitfalls in HNPCC screening by microsatellite analysis and immunohistochemistry

21 January 2018

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

Familial juvenile polyposis coli; increased risk of colorectal cancer

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Very high risk of cancer in familial Peutz-Jeghers syndrome

21 January 2018

1 reference

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

Allele loss and mutation screen at the Peutz-Jeghers (LKB1) locus (19p13.3) in sporadic ovarian tumours.

21 January 2018

1 reference

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

Genetic screening for Peutz-Jeghers syndrome

21 January 2018

1 reference

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

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

21 January 2018

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

Relative frequency and morphology of cancers in STK11 mutation carriers

21 January 2018

1 reference

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

Genetics and the common cancers

21 January 2018

1 reference

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

Colorectal cancer: molecules and populations

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

1 reference

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

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

21 January 2018

1 reference

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

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

1 reference

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

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

21 January 2018

1 reference

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

AGA technical review on hereditary colorectal cancer and genetic testing.

21 January 2018

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Microsatellite instability

1 reference

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

7 January 2021

American Gastroenterological Association medical position statement: hereditary colorectal cancer and genetic testing

1 reference

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

1 reference

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

7 January 2021

Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors

1 reference

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

7 January 2021

The risk of gastrointestinal carcinoma in familial juvenile polyposis

1 reference

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

7 January 2021

Germline SMAD4 or BMPR1A mutations and phenotype of juvenile polyposis

1 reference

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

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

1 reference

Dimensions Publication ID

15 August 2017

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