Genetic variants within the hTERT gene and the risk of colorectal cancer in Lynch syndrome (Q26775022)

12

John L Hopper

0 references

Melissa C. Southey

6

Melissa C Southey

0 references

Christophe Rosty

Christophe Rosty

4

1 reference

ORCID Public Data File 2021

Mark Jenkins

13

Mark A Jenkins

0 references

Ingrid Winship

10

Ingrid M Winship

0 references

Daniel D Buchanan

14

Daniel D Buchanan

0 references

Susan Parry

7

Susan Parry

0 references

Finlay Macrae

9

Finlay A Macrae

0 references

Mark Clendenning

2

Mark Clendenning

0 references

Susan Preston-Martin

5

Susan G Preston

0 references

John A Baron

11

John A Baron

0 references

author name string

Aung Ko Win

1

0 references

William Crawford

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

3

0 references

language of work or name

English

0 references

publication date

November 2015

0 references

1 reference

6

0 references

issue

11-12

0 references

page(s)

445-51

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

Variation at the TERT locus and predisposition for cancer

7 April 2017

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

Do lifestyle factors influence colorectal cancer risk in Lynch syndrome?

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

Genetic variant in the telomerase gene modifies cancer risk in Lynch syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

The TERT variant rs2736100 is associated with colorectal cancer risk

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

TERT's role in colorectal carcinogenesis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

Meta-analysis of new genome-wide association studies of colorectal cancer risk

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

Evaluation of Lynch syndrome modifier genes in 748 MMR mutation carriers

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

Smoking and colorectal cancer in Lynch syndrome: results from the Colon Cancer Family Registry and the University of Texas M.D. Anderson Cancer Center

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

Analysis of case-control studies of genetic and environmental factors with missing genetic information and haplotype-phase ambiguity

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

A note on robust variance estimation for cluster-correlated data

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndrome.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4701223

A weighted cohort approach for analysing factors modifying disease risks in carriers of high-risk susceptibility genes

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26807197

12 December 2020

inferred from PubMed ID database lookup

The Australasian Colorectal Cancer Family Registry

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26807197

12 December 2020

inferred from PubMed ID database lookup

Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26807197

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.18632/GENESANDCANCER.85

0 references

Fatcat ID

release_6vim3wpi6zbxzfixfmpmntviya

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/6vim3wpi6zbxzfixfmpmntviya

24 November 2022