(Q35925149)

English

Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study

scientific article published on 13 February 2012

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scholarly article

1 reference

Europe PubMed Central

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11 August 2017

Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study (English)

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

DNA mismatch repair

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based on heuristic

inferred from title

9

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11 August 2017

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Aung Ko Win

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Daniel D Buchanan

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Daniel D Buchanan

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Ingrid Winship

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Mark A Jenkins

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Melissa C. Southey

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Melissa C Southey

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object named as

John L Hopper

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11 August 2017

Loic Le Marchand

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Loïc Le Marchand

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11 August 2017

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Stephen N Thibodeau

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Stephen N Thibodeau

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Europe PubMed Central

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11 August 2017

Steven Gallinger

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object named as

Steven Gallinger

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Europe PubMed Central

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11 August 2017

Polly A Newcomb

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Polly A Newcomb

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11 August 2017

Noralane Lindor

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Noralane M Lindor

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11 August 2017

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object named as

Finlay A Macrae

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11 August 2017

Mark Clendenning

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object named as

Mark Clendenning

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11 August 2017

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object named as

Dennis J Ahnen

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11 August 2017

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object named as

Jack Goldblatt

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11 August 2017

Shanaka R Gunawardena

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object named as

Shanaka R Gunawardena

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11 August 2017

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object named as

Joanne P Young

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11 August 2017

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object named as

John A Baron

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11 August 2017

Robert W. Haile

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object named as

Robert W Haile

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11 August 2017

Katherine L. Tucker

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object named as

Katherine M Tucker

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11 August 2017

author name string

Graeme P Young

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11 August 2017

Julie Arnold

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11 August 2017

Bharati Bapat

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11 August 2017

Graham Casey

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11 August 2017

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publication date

13 February 2012

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11 August 2017

Journal of Clinical Oncology

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Europe PubMed Central

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11 August 2017

30

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11 August 2017

9

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11 August 2017

958-964

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Europe PubMed Central

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11 August 2017

The search for unaffected individuals with Lynch syndrome: do the ends justify the means?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

2 October 2017

No evidence of excess breast cancer risk among mutation-negative women from BRCA mutation-positive families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

2 October 2017

Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

2 October 2017

Risks of Lynch syndrome cancers for MSH6 mutation carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

2 October 2017

Population-based family history-specific risks for colorectal cancer: a constellation approach

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

2 October 2017

Risk of pancreatic cancer in families with Lynch syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

2 October 2017

Genetic variation in genes for the xenobiotic-metabolizing enzymes CYP1A1, EPHX1, GSTM1, GSTT1, and GSTP1 and susceptibility to colorectal cancer in Lynch syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

2 October 2017

The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

2 October 2017

Cytochrome P450 17A1 and catechol O-methyltransferase polymorphisms and age at Lynch syndrome colon cancer onset in Newfoundland

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

2 October 2017

Prediction of germline mutations and cancer risk in the Lynch syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

2 October 2017

Hereditary nonpolyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutation-negative kindreds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

2 October 2017

Population carrier frequency of hMSH2 and hMLH1 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

2 October 2017

Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

2 October 2017

Life-time risk of different cancers in hereditary non-polyposis colorectal cancer (HNPCC) syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

11 July 2018

Differential diagnosis of hereditary nonpolyposis colorectal cancer (Lynch syndrome I and Lynch syndrome II)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

11 July 2018

Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in Lynch syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

24 September 2018

Breast cancer risks in individuals testing negative for a known family mutation in BRCA1 or BRCA2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

24 September 2018

Mismatch repair defective breast cancer in the hereditary nonpolyposis colorectal cancer syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

24 September 2018

Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

24 September 2018

IGF1 is a modifier of disease risk in hereditary non-polyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

24 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

24 September 2018

Decrease in mortality in Lynch syndrome families because of surveillance.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

24 September 2018

Screening for pancreatic neoplasia in high-risk individuals: an EUS-based approach

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

24 September 2018

Hereditary non-polyposis colorectal cancer: current risks of colorectal cancer largely overestimated.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

24 September 2018

MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

24 September 2018

A database to support the interpretation of human mismatch repair gene variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

14 November 2018

GSTM1 and GSTT1 polymorphisms as modifiers of age at diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC) in a homogeneous cohort of individuals carrying a single predisposing mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

14 November 2018

Large genomic alterations in hMSH2 and hMLH1 in early-onset colorectal cancer: identification of a large complex de novo hMLH1 alteration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

14 November 2018

Risk of Ovarian Cancer in BRCA1 and BRCA2 Mutation-Negative Hereditary Breast Cancer Families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

14 November 2018

Use of Molecular Tumor Characteristics to Prioritize Mismatch Repair Gene Testing in Early-Onset Colorectal Cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3341109

14 November 2018

Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22331944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extracolonic cancer in hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22331944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic polymorphisms in carcinogen metabolism and their association to hereditary nonpolyposis colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22331944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Male breast cancer in the hereditary nonpolyposis colorectal cancer syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22331944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prophylactic Surgery to Reduce the Risk of Gynecologic Cancers in the Lynch Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22331944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The additive effect of p53 Arg72Pro and RNASEL Arg462Gln genotypes on age of disease onset in Lynch syndrome patients with pathogenic germline mutations in MSH2 or MLH1

1 reference

https://pubmed.ncbi.nlm.nih.gov/22331944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22331944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Breast cancer immunohistochemistry can be useful in triage of some HNPCC families

1 reference

https://pubmed.ncbi.nlm.nih.gov/22331944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1200/JCO.2011.39.5590

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

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