(Q43248924)

17 November 2017

Colorectal cancer risk in monoallelic carriers of MYH variants (English)

1 reference

17 November 2017

1 reference

1 reference

1

1 reference

17 November 2017

3

1 reference

17 November 2017

Mathew F Rudd

2

1 reference

PMC publication ID

1592556

17 November 2017

language of work or name

English

0 references

publication date

1 October 2006

1 reference

American Journal of Human Genetics

17 November 2017

1 reference

17 November 2017

79

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17 November 2017

4

1 reference

17 November 2017

768-71; author reply 771-2

1 reference

Germline mutations in the MYH gene in Swedish familial and sporadic colorectal cancer

17 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592556

Germline susceptibility to colorectal cancer due to base-excision repair gene defects

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592556

Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592556

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592556

Role of inherited defects of MYH in the development of sporadic colorectal cancer

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592556

Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592556

Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592556

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592556

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592556

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592556

A marginal likelihood approach for estimating penetrance from kin-cohort designs

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592556

An exact method for meta-analysis of case-control and follow-up studies.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592556

Colorectal cancer risk in individuals with biallelic or monoallelic mutations of MYH

15 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16960817

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/507912

1 reference

17 November 2017

1 reference

PMC publication ID

1592556

17 November 2017

PubMed publication ID

16960817

1 reference

PMC publication ID

1592556