(Q50711835)

18 March 2018

title

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

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18 March 2018

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R C Green

1

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18 March 2018

J S Green

2

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18 March 2018

S K Buehler

3

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18 March 2018

J D Robb

4

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18 March 2018

D Daftary

5

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18 March 2018

S Gallinger

6

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18 March 2018

J R McLaughlin

7

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18 March 2018

P S Parfrey

8

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18 March 2018

H B Younghusband

9

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18 March 2018

publication date

1 January 2007

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18 March 2018

published in

Familial Cancer

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18 March 2018

volume

6

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18 March 2018

issue

1

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18 March 2018

page(s)

53-62

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18 March 2018

https://scigraph.springernature.com/pub.10.1007/s10689-006-9104-x

exact match

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cites work

Cancer risk in relatives of patients with common colorectal cancer.

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Crossref

https://api.crossref.org/works/10.1007%2FS10689-006-9104-X

The effect of family size on estimates of the frequency of hereditary non-polyposis colorectal cancer.

21 January 2018

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The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas

21 January 2018

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12 December 2020

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

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12 December 2020

Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients

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12 December 2020

Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis

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A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO

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12 December 2020

Frequency of hereditary non-polyposis colorectal cancer among Uruguayan patients with colorectal cancer

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12 December 2020

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

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12 December 2020

Frequency of hereditary nonpolyposis colorectal cancer. A prospective multicenter study in Finland.

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12 December 2020

Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: later age of onset.

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12 December 2020

Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from Newfoundland.

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12 December 2020

Evaluation of screening strategy for detecting hereditary nonpolyposis colorectal carcinoma

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Validation and simplification of Bethesda guidelines for identifying apparently sporadic forms of colorectal carcinoma with microsatellite instability

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12 December 2020

Frequency of hereditary non-polyposis colorectal cancer and other colorectal cancer familial forms in Spain: a multicentre, prospective, nationwide study

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12 December 2020

Clinical and genetic epidemiology of inherited renal disease in Newfoundland

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12 December 2020

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

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12 December 2020

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

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12 December 2020

A founder effect in the newfoundland population reduces the Bardet-Biedl syndrome I (BBS1) interval to 1 cM

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12 December 2020

Role of DNA mismatch repair defects in the pathogenesis of human cancer

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12 December 2020

SISE matters: the sum of information on seventy-yr-old equivalents measures pedigree information content when assessing the risk of HNPCC in a family.

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12 December 2020

Does this patient have a family history of cancer? An evidence-based analysis of the accuracy of family cancer history

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12 December 2020

A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancer

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12 December 2020

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

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12 December 2020

Hereditary colorectal cancer

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12 December 2020

Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers.

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12 December 2020

Colorectal screening is associated with reduced colorectal cancer risk: a case-control study within the population-based Ontario Familial Colorectal Cancer Registry

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12 December 2020

A founder effect in three large Newfoundland families with a novel clinically variable spastic ataxia and supranuclear gaze palsy

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12 December 2020

Incidence of hereditary non-polyposis colorectal cancer in a population-based study of 1137 consecutive cases of colorectal cancer

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12 December 2020

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

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12 December 2020

Frequency of hereditary non-polyposis colorectal cancer in Danish colorectal cancer patients

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12 December 2020

Frequency of familial colon cancer and hereditary nonpolyposis colorectal cancer (Lynch syndrome) in a large population database

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12 December 2020

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

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12 December 2020

Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma

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12 December 2020

Family history and colorectal cancer: predictors of risk

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12 December 2020

Role of APC and DNA mismatch repair genes in the development of colorectal cancers

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12 December 2020

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

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12 December 2020

Family history of colorectal cancer in a Sweden county

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12 December 2020

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

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12 December 2020

Evolution of the nomenclature for the hereditary colorectal cancer syndromes

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12 December 2020

Family cancer histories predictive of a high risk of hereditary non-polyposis colorectal cancer associate significantly with a genomic rearrangement in hMSH2 or hMLH1.

1 reference

12 December 2020

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

1 reference

12 December 2020

Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer.

1 reference

12 December 2020

Germline APC variants in patients with multiple colorectal adenomas, with evidence for the particular importance of E1317Q

1 reference

12 December 2020

10.1007/S10689-006-9104-X

Identifiers

DOI

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18 March 2018

PubMed ID

17039269

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18 March 2018