(Q34618184)

3 August 2017

title

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease (English)

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3 August 2017

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A Pollett

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3 August 2017

Albert de la Chapelle

11

object named as

A de la Chapelle

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3 August 2017

M O Woods

1

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3 August 2017

H B Younghusband

2

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3 August 2017

P S Parfrey

3

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3 August 2017

S Gallinger

4

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3 August 2017

J McLaughlin

5

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3 August 2017

E Dicks

6

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3 August 2017

S Stuckless

7

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3 August 2017

B Bapat

9

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3 August 2017

M Mrkonjic

10

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3 August 2017

M Clendenning

12

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3 August 2017

S N Thibodeau

13

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3 August 2017

M Simms

14

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3 August 2017

A Dohey

15

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3 August 2017

P Williams

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3 August 2017

D Robb

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3 August 2017

C Searle

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3 August 2017

J S Green

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3 August 2017

R C Green

20

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3 August 2017

language of work or name

English

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publication date

3 August 2010

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3 August 2017

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3 August 2017

volume

59

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3 August 2017

issue

10

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3 August 2017

page(s)

1369-1377

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MUTYH Associated Polyposis (MAP).

3 August 2017

cites work

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7 July 2018

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7 July 2018

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7 July 2018

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Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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

7 July 2018

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7 July 2018

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

7 July 2018

1 reference

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Evidence for BRAF mutation and variable levels of microsatellite instability in a syndrome of familial colorectal cancer

7 July 2018

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

7 July 2018

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7 July 2018

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The Newfoundland population: a unique resource for genetic investigation of complex diseases

7 July 2018

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Low-penetrance genes and their involvement in colorectal cancer susceptibility.

7 July 2018

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7 July 2018

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Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

7 July 2018

1 reference

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Ontario familial colon cancer registry: methods and first-year response rates.

7 July 2018

1 reference

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Recurrent germline mutation in MSH2 arises frequently de novo

7 July 2018

1 reference

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Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland

7 July 2018

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Two-sided confidence intervals for the single proportion: comparison of seven methods

7 July 2018

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Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.

7 July 2018

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Most low-level microsatellite instability in colorectal cancers can be explained without an elevated slippage rate.

26 October 2018

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Variants on 9p24 and 8q24 are associated with risk of colorectal cancer: results from the Colon Cancer Family Registry

26 October 2018

1 reference

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Colon Cancer Family Registry: an international resource for studies of the genetic epidemiology of colon cancer.

26 October 2018

1 reference

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Incorporation of somatic BRAF mutation testing into an algorithm for the investigation of hereditary non-polyposis colorectal cancer.

26 October 2018

1 reference

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Inheritance of a Cancer-AssociatedMLH1Germ-Line Epimutation

26 October 2018

1 reference

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The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3047452

Very high incidence of familial colorectal cancer in Newfoundland: a comparison with Ontario and 13 other population-based studies.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3047452

Long-range PCR facilitates the identification of PMS2-specific mutations.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3047452

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3047452

High frequency of hereditary colorectal cancer in Newfoundland likely involves novel susceptibility genes.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3047452

What is the best way to assess microsatellite instability status in colorectal cancer? Study on a population base of 462 colorectal cancers.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3047452

A hereditary nonpolyposis colorectal carcinoma case associated with hypermethylation of the MLH1 gene in normal tissue and loss of heterozygosity of the unmethylated allele in the resulting microsatellite instability-high tumor

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3047452

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

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3047452

A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3047452

The identical 5' splice-site acceptor mutation in five attenuated APC families from Newfoundland demonstrates a founder effect

9 December 2018

1 reference

12 December 2020

Effectiveness of each Bethesda marker in defining microsatellite instability when screening for Lynch syndrome

1 reference

12 December 2020

A new variant database for mismatch repair genes associated with Lynch syndrome

1 reference

12 December 2020

No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients

1 reference

12 December 2020

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

1 reference

12 December 2020

Interpretation of immunohistochemistry for mismatch repair proteins is only reliable in a specialized setting

1 reference

12 December 2020

Molecular and clinical characteristics in 32 families affected with familial adenomatous polyposis

1 reference

12 December 2020

Identifiers

DOI

10.1136/GUT.2010.208462

1 reference

3 August 2017

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3 August 2017

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