(Q34346668)

1 August 2017

title

Risk of urothelial bladder cancer in Lynch syndrome is increased, in particular among MSH2 mutation carriers (English)

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1 August 2017

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Nicoline Hoogerbrugge

object named as

N Hoogerbrugge

10

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author name string

R S van der Post

1

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1 August 2017

L A Kiemeney

2

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1 August 2017

M J L Ligtenberg

3

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1 August 2017

J A Witjes

4

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1 August 2017

C A Hulsbergen-van de Kaa

5

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1 August 2017

D Bodmer

6

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1 August 2017

L Schaap

7

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1 August 2017

C M Kets

8

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1 August 2017

J H J M van Krieken

9

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1 August 2017

language of work or name

English

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publication date

1 July 2010

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Journal of Medical Genetics

1 August 2017

published in

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1 August 2017

volume

47

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1 August 2017

issue

7

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1 August 2017

page(s)

464-470

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Risks of Lynch syndrome cancers for MSH6 mutation carriers

1 August 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

Management of extracolonic tumours in patients with Lynch syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

EAU guidelines on non-muscle-invasive urothelial carcinoma of the bladder

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instability

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

Bladder tumor markers beyond cytology: International Consensus Panel on bladder tumor markers

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

Risk of colorectal and endometrial cancer for carriers of mutations of the hMLH1 and hMSH2 gene: correction for ascertainment

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

Cumulative incidence of colorectal and extracolonic cancers in MLH1 and MSH2 mutation carriers of hereditary nonpolyposis colorectal cancer.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

Extracolonic cancers associated with hereditary nonpolyposis colorectal cancer in the Utah Population Database.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

Microsatellite instability, immunohistochemistry, and additional PMS2 staining in suspected hereditary nonpolyposis colorectal cancer

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

Cancer risk in 348 French MSH2 or MLH1 gene carriers

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

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

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

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

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

Urinary tract cancer and hereditary nonpolyposis colorectal cancer: risks and screening options.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

Cancer Characteristics in Swedish Families Fulfilling Criteria for Hereditary Nonpolyposis Colorectal Cancer

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2991077

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

27 October 2018

1 reference

12 December 2020

Urinary tract cancer screening through analysis of urinary red blood cell volume distribution

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12 December 2020

Frequent microsatellite instability in sporadic tumors of the upper urinary tract

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12 December 2020

Multiple primary cancer, including transitional cell carcinoma of the upper uroepithelial tract in a multigeneration HNPCC family: molecular genetic, diagnostic, and management implications

1 reference

12 December 2020

Extracolonic cancer in hereditary nonpolyposis colorectal cancer

1 reference

12 December 2020

Cancer risk associated with germline DNA mismatch repair gene mutations

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12 December 2020

Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium

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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

A novel germline mutation of MSH2 in a hereditary nonpolyposis colorectal cancer patient with liposarcoma

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12 December 2020

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

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12 December 2020

Differential cancer predisposition in Lynch syndrome: insights from molecular analysis of brain and urinary tract tumors

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12 December 2020

Screening for urinary tract cancer with urine cytology in Lynch syndrome and familial colorectal cancer

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12 December 2020

[The risk of cancer in the Netherlands]

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12 December 2020

Identifiers

DOI

10.1136/JMG.2010.076992

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1 August 2017

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1 August 2017

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