(Q30492977)

14 October 2017

Risks of Lynch syndrome cancers for MSH6 mutation carriers (English)

1 reference

14 October 2017

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3

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14 October 2017

21

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14 October 2017

22

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14 October 2017

38

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14 October 2017

Albert de la Chapelle

36

Albert de la Chapelle

0 references

Jenny N. Poynter

Jenny N Poynter

29

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Daniel D Buchanan

Daniel Buchanan

14

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Mark Jenkins

Mark A Jenkins

40

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Hans Vasen

Hans F Vasen

37

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John Potter

John Potter

35

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John Hopper

34

John L Hopper

1 reference

14 October 2017

1

Laura Baglietto

1 reference

14 October 2017

39

Stephen N Thibodeau

1 reference

14 October 2017

2

Noralane M Lindor

1 reference

14 October 2017

10

Rebecca A Barnetson

1 reference

14 October 2017

11

Susan M Farrington

1 reference

14 October 2017

24

Susan Parry

1 reference

14 October 2017

19

Finlay Macrae

1 reference

14 October 2017

26

Barbara Leggett

1 reference

14 October 2017

18

Jeremy Jass

1 reference

14 October 2017

33

Steve Gallinger

1 reference

14 October 2017

20

Yoland Antill

1 reference

14 October 2017

23

Jack Goldblatt

1 reference

14 October 2017

25

Graeme Suthers

1 reference

14 October 2017

16

Joanne Young

1 reference

14 October 2017

30

John A Baron

1 reference

14 October 2017

32

Robert Haile

1 reference

14 October 2017

13

Heather Hampel

1 reference

14 October 2017

Darren M White

4

1 reference

14 October 2017

Anja Wagner

5

1 reference

14 October 2017

Encarna B Gomez Garcia

6

1 reference

14 October 2017

Annette H J T Vriends

7

1 reference

14 October 2017

Dutch Lynch Syndrome Study Group

8

1 reference

14 October 2017

Nicola R Cartwright

9

1 reference

14 October 2017

Albert Tenesa

12

1 reference

14 October 2017

Sven Arnold

15

1 reference

14 October 2017

Michael D Walsh

17

1 reference

14 October 2017

Malinda Butz

27

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14 October 2017

Melyssa Aronson

28

1 reference

14 October 2017

language of work or name

English

0 references

publication date

22 December 2009

1 reference

Journal of the National Cancer Institute

14 October 2017

1 reference

14 October 2017

102

1 reference

14 October 2017

3

1 reference

14 October 2017

193-201

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Screening for colorectal cancer: U.S. Preventive Services Task Force recommendation statement

14 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

Feasibility of screening for Lynch syndrome among patients with colorectal cancer

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

Germline MSH6 mutations are more prevalent in endometrial cancer patient cohorts than hereditary non polyposis colorectal cancer cohorts

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

Prediction of germline mutations and cancer risk in the Lynch syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

Hereditary Non-Polyposis Colorectal Cancer: the rise and fall of a confusing term

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

Diagnostic approach and management of Lynch syndrome (hereditary nonpolyposis colorectal carcinoma): a guide for clinicians

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

Analysis of hMLH1 and hMSH2 gene dosage alterations in hereditary nonpolyposis colorectal cancer patients by novel methods

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

Evidence for autosomal dominant inheritance of prostate cancer

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

14 July 2018

Remarks on ascertainment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

Cancer Risks For Mismatch Repair Gene Mutation Carriers: A Population-Based Early Onset Case-Family Study

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

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

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

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

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

Toward new strategies to select young endometrial cancer patients for mismatch repair gene mutation analysis.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

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

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

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

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2815724

Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors

26 November 2018

1 reference

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

1 reference

12 December 2020

Two Swedish founder MSH6 mutations, one nonsense and one missense, conferring high cumulative risk of Lynch syndrome.

1 reference

12 December 2020

Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients

1 reference

12 December 2020

Surveillance for endometrial cancer in hereditary nonpolyposis colorectal cancer syndrome

1 reference

12 December 2020

Comment on: Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients

1 reference

12 December 2020

Prospective Determination of Prevalence of Lynch Syndrome in Young Women With Endometrial Cancer

1 reference

12 December 2020

Diagnostic markers for early detection of ovarian cancer

1 reference

12 December 2020

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

1 reference

12 December 2020

Cancer risk associated with germline DNA mismatch repair gene mutations

1 reference

12 December 2020

Identifiers

DOI

10.1093/JNCI/DJP473

1 reference

14 October 2017

1 reference

14 October 2017

1 reference