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

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

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

http://www.wikidata.org/entity/Q35112916

about

Known glioma risk loci are associated with glioma with a family history of brain tumours--a case-control gene association study Genome-wide association study of glioma and meta-analysis A subset-based approach improves power and interpretation for the combined analysis of genetic association studies of heterogeneous traits Molecular functions and cellular roles of the ChlR1 (DDX11) helicase defective in the rare cohesinopathy Warsaw breakage syndrome RTEL1 (regulator of telomere elongation helicase 1), a DNA helicase essential for genome stability The MGMT promoter SNP rs16906252 is a risk factor for MGMT methylation in glioblastoma and is predictive of response to temozolomide Telomerase reverse transcriptase locus polymorphisms and cancer risk: a field synopsis and meta-analysis Molecular Markers in Low-Grade Glioma-Toward Tumor Reclassification The Glioma International Case-Control Study: A Report From the Genetic Epidemiology of Glioma International Consortium Association between RTEL1, PHLDB1, and TREH Polymorphisms and Glioblastoma Risk: A Case-Control Study Understanding inherited genetic risk of adult glioma - a review TERT promoter mutations and polymorphisms as prognostic factors in primary glioblastoma Adult brain cancer in the U.S. black population: a Surveillance, Epidemiology, and End Results (SEER) analysis of incidence, survival, and trends CCDC26 rs4295627 polymorphism and glioma risk: a meta-analysis Functional analysis of the 11q23.3 glioma susceptibility locus implicates PHLDB1 and DDX6 in glioma susceptibility SSBP2 variants are associated with survival in glioblastoma patients Survival and low-grade glioma: the emergence of genetic information Demographic variation in incidence of adult glioma by subtype, United States, 1992-2007.Genome-wide testing of putative functional exonic variants in relationship with breast and prostate cancer risk in a multiethnic population.Brain tumor risk according to germ-line variation in the MLLT10 locus.A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome.Biomarker Detection in Association Studies: Modeling SNPs Simultaneously via Logistic ANOVA.A functional polymorphism in the pre-miR-146a gene is associated with risk and prognosis in adult glioma.Association between the TERT Genetic Polymorphism rs2853676 and Cancer Risk: Meta-Analysis of 76,108 Cases and 134,215 Controls.DNA helicases involved in DNA repair and their roles in cancer An exploratory analysis of common genetic variants in the vitamin D pathway including genome-wide associated variants in relation to glioma risk and outcome.Rare TP53 genetic variant associated with glioma risk and outcome.Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita.Inherited variant on chromosome 11q23 increases susceptibility to IDH-mutated but not IDH-normal gliomas regardless of grade or histology.Prediagnostic body weight and survival in high grade glioma.Circadian pathway genes in relation to glioma risk and outcome.The PHLDB1 rs498872 (11q23.3) polymorphism and glioma risk: A meta-analysis.The role of the RTEL1 rs2297440 polymorphism in the risk of glioma development: a meta-analysis.An Updated and Comprehensive Meta-Analysis of Association Between Seven Hot Loci Polymorphisms from Eight GWAS and Glioma Risk.Assessment of glioma risk associated with an inherited variant at chromosome 11q23.Effect of CDKN2A/B rs4977756 polymorphism on glioma risk: a meta-analysis of 16 studies including 24077 participants.Performance of adjuvant treatment correlates with survival in reoperated glioblastomas.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.Rare and uncommon genetic variants may hold key to the 'missing heritability' in glioma.Telomerase Reverse Transcriptase Polymorphism rs2736100: A Balancing Act between Cancer and Non-Cancer Disease, a Meta-Analysis.

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

http://www.wikidata.org/entity/Q35112916

description

2011 nî lūn-bûn

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2011 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2011 թվականի հունվարին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

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

@ast

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

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type

label

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

@ast

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

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prefLabel

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

@ast

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

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S11060-010-0506-0

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Journal of Neuro-Oncology

P1476

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

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P2093

Daniel J Brat

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James E Browning

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Jeffrey J Olson

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Kathleen M Egan

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Melissa H Madden

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Paul L Moots

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Reid C Thompson

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Renato V Larocca

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Steven Brem

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Y Ann Chen

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P2860

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

The INTERPHONE study: design, epidemiological methods, and description of the study population

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

Lung cancer susceptibility locus at 5p15.33

Comprehensive genomic characterization defines human glioblastoma genes and core pathways

A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma

The 2007 WHO classification of tumours of the central nervous system

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer

Genome-wide association study identifies five susceptibility loci for glioma

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s11060-010-0506-0

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535-542

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10.1007/S11060-010-0506-0

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2

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21203894

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3138895

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