(Q47236669)

English

Fine-mapping of a region of chromosome 5p15.33 (TERT-CLPTM1L) suggests a novel locus in TERT and a CLPTM1L haplotype are associated with glioma susceptibility in a Chinese population

scientific article published on 2 March 2012

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/22213090

Fine-mapping of a region of chromosome 5p15.33 (TERT-CLPTM1L) suggests a novel locus in TERT and a CLPTM1L haplotype are associated with glioma susceptibility in a Chinese population (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/22213090

author name string

Yingjie Zhao

1

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/22213090

Gong Chen

2

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/22213090

Yao Zhao

3

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/22213090

Xiao Song

4

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/22213090

Hongyan Chen

5

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/22213090

Ying Mao

6

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/22213090

Daru Lu

7

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/22213090

language of work or name

0 references

publication date

2 March 2012

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/22213090

International Journal of Cancer

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/22213090

131

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/22213090

7

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/22213090

1569-1576

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/22213090

New insights into susceptibility to glioma

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Genome-wide association study identifies five susceptibility loci for glioma

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Association of sequence variants on chromosomes 20, 11, and 5 (20q13.33, 11q23.3, and 5p15.33) with glioma susceptibility in a Chinese population

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Variation at the TERT locus and predisposition for cancer

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Telomere dysfunction, genome instability and cancer

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Proteomic studies coupled with RNAi methodologies can shed further light on the downstream effects of telomerase in glioma

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

In situ detection of telomerase catalytic subunit mRNA in glioblastoma multiforme.

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Survival prediction in patients with glioblastoma multiforme by human telomerase genetic variation.

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Interpretation of association signals and identification of causal variants from genome-wide association studies

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Cancer susceptibility variants and the risk of adult glioma in a US case-control study.

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Tagging SNPs in non-homologous end-joining pathway genes and risk of glioma

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Polymorphisms of LIG4 and XRCC4 involved in the NHEJ pathway interact to modify risk of glioma

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Score tests for association between traits and haplotypes when linkage phase is ambiguous

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genes

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

A comprehensive evaluation of SNP genotype imputation

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Analyses and comparison of accuracy of different genotype imputation methods

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Telomerase activity-independent function of TERT allows glioma cells to attain cancer stem cell characteristics by inducing EGFR expression

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Common 5p15.33 and 6p21.33 variants influence lung cancer risk

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Lung cancer susceptibility locus at 5p15.33

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

New common variants affecting susceptibility to basal cell carcinoma

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Genetic variations in TERT-CLPTM1L genes and risk of squamous cell carcinoma of the head and neck

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Chromosome 5p Region SNPs Are Associated with Risk of NSCLC among Women

1 reference

https://api.crossref.org/works/10.1002%2FIJC.27417

21 January 2018

Identifiers

10.1002/IJC.27417

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/22213090

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 January 2018

http://europepmc.org/abstract/MED/22213090

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q47236669&oldid=2147592961"