(Q37248283)

19 August 2017

Lynch syndrome-associated extracolonic tumors are rare in two extended families with the same EPCAM deletion (English)

1 reference

19 August 2017

Nicoline Hoogerbrugge

12

object named as

Nicoline Hoogerbrugge

1 reference

19 August 2017

Marjolijn J L Ligtenberg

13

object named as

Marjolijn J L Ligtenberg

1 reference

19 August 2017

Henry T Lynch

1

1 reference

19 August 2017

Douglas L Riegert-Johnson

2

1 reference

19 August 2017

Carrie Snyder

3

1 reference

19 August 2017

Jane F Lynch

4

1 reference

19 August 2017

Jill Hagenkord

5

1 reference

19 August 2017

C Richard Boland

6

1 reference

19 August 2017

Jennifer Rhees

7

1 reference

19 August 2017

Stephen N Thibodeau

8

1 reference

19 August 2017

Lisa A Boardman

9

1 reference

19 August 2017

Janine Davies

10

1 reference

19 August 2017

Roland P Kuiper

11

1 reference

19 August 2017

language of work or name

English

0 references

publication date

19 July 2011

1 reference

The American Journal of Gastroenterology

19 August 2017

1 reference

19 August 2017

106

1 reference

19 August 2017

10

1 reference

19 August 2017

1829-1836

1 reference

https://scigraph.springernature.com/pub.10.1038/ajg.2011.203

19 August 2017

0 references

cites work

Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

EPCAM germ line deletions as causes of Lynch syndrome in Spanish patients

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

Extending comprehensive cancer center expertise in clinical cancer genetics and genomics to diverse communities: the power of partnership

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

Electronic reminders for pathologists promote recognition of patients at risk for Lynch syndrome: cluster-randomised controlled trial

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

Underdiagnosis of Lynch syndrome involves more than family history criteria

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

Feasibility of screening for Lynch syndrome among patients with colorectal cancer

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

Genetic mapping of a locus predisposing to human colorectal cancer

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

Mutation of a mutL homolog in hereditary colon cancer

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

Management of hereditary site-specific colon cancer

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

Recurrence and variability of germline EPCAM deletions in Lynch syndrome.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

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

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

Family information service and hereditary cancer

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

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

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3805505

Genetic mapping of a second locus predisposing to hereditary non–polyposis colon cancer

3 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FAJG.2011.203

Familial colonic cancer without antecedent polyposis

21 January 2018

1 reference

12 December 2020

Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). I. Clinical description of resource

1 reference

12 December 2020

Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). II. Biomarker studies

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Hereditary colorectal cancer

1 reference

12 December 2020

Identifiers

DOI

10.1038/AJG.2011.203

1 reference

Dimensions Publication ID

19 August 2017

0 references

1 reference

19 August 2017

1 reference