(Q38873936)

English

Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors

scientific article published on 27 March 2017

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scholarly article

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Europe PubMed Central

7 September 2017

Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors (English)

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7 September 2017

genome-wide association study

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based on heuristic

inferred from title

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Yanwen Chen

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Georgina Armstrong

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Yanhong Liu

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Marc Sanson

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Ulrika Andersson

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GliomaScan Consortium

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Helen Hansen

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Faith Davis

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Ching Lau

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27 March 2017

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Nature Genetics

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789-794

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describes a project that uses

genome-wide association study

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https://scigraph.springernature.com/pub.10.1038/ng.3823

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Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets

1 reference

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FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic data

1 reference

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9 September 2017

Molecular Profiling Reveals Biologically Discrete Subsets and Pathways of Progression in Diffuse Glioma

1 reference

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The Glioma International Case-Control Study: A Report From the Genetic Epidemiology of Glioma International Consortium

1 reference

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9 September 2017

Longer genotypically-estimated leukocyte telomere length is associated with increased adult glioma risk

1 reference

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9 September 2017

Quantifying the heritability of glioma using genome-wide complex trait analysis

1 reference

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9 September 2017

CBTRUS Statistical Report: Primary Brain and Central Nervous System Tumors Diagnosed in the United States in 2008-2012.

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9 September 2017

Genome-wide association study identifies multiple susceptibility loci for glioma

1 reference

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Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study

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LRIG1 enhances the radiosensitivity of radioresistant human glioblastoma U251 cells via attenuation of the EGFR/Akt signaling pathway.

1 reference

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Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors

1 reference

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Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas

1 reference

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Telomere maintenance and the etiology of adult glioma

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9 September 2017

miR-20a mediates temozolomide-resistance in glioblastoma cells via negatively regulating LRIG1 expression

1 reference

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Genomically amplified Akt3 activates DNA repair pathway and promotes glioma progression

1 reference

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9 September 2017

Integrative analysis of 111 reference human epigenomes

1 reference

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9 September 2017

Germline mutations in shelterin complex genes are associated with familial glioma

1 reference

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CBTRUS statistical report: primary brain and central nervous system tumors diagnosed in the United States in 2007-2011.

1 reference

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visPIG--a web tool for producing multi-region, multi-track, multi-scale plots of genetic data.

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9 September 2017

Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk

1 reference

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9 September 2017

The epidemiology of glioma in adults: a "state of the science" review

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An atlas of active enhancers across human cell types and tissues

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Super-enhancers in the control of cell identity and disease

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The role of JAK-STAT signaling within the CNS.

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Systematic identification of trans eQTLs as putative drivers of known disease associations

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The Genotype-Tissue Expression (GTEx) project

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Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14

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Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions

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A low-frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and astrocytomas with IDH1 or IDH2 mutation

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Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

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HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants

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A germline variant in the TP53 polyadenylation signal confers cancer susceptibility

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Chromosome 7p11.2 (EGFR) variation influences glioma risk

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Distinct germ line polymorphisms underlie glioma morphologic heterogeneity

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GCTA: a tool for genome-wide complex trait analysis

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DNA methylation, isocitrate dehydrogenase mutation, and survival in glioma

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Meta-analysis and imputation refines the association of 15q25 with smoking quantity

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Identification of a CpG island methylator phenotype that defines a distinct subgroup of glioma

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RPA-like mammalian Ctc1-Stn1-Ten1 complex binds to single-stranded DNA and protects telomeres independently of the Pot1 pathway

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Targeted capture and massively parallel sequencing of 12 human exomes

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Genome-wide association study identifies five susceptibility loci for glioma

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5558246

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

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A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

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IDH1 mutations are early events in the development of astrocytomas and oligodendrogliomas

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IDH1 and IDH2 mutations in gliomas

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Brain tumor epidemiology: consensus from the Brain Tumor Epidemiology Consortium

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Reproductive factors and hormone use and risk of adult gliomas

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PLINK: a tool set for whole-genome association and population-based linkage analyses

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9 September 2017

Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum

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9 September 2017

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9 September 2017

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9 September 2017

A new multipoint method for genome-wide association studies by imputation of genotypes

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9 September 2017

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

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9 September 2017

Genome-wide association study of prostate cancer identifies a second risk locus at 8q24

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9 September 2017

Population structure and eigenanalysis

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9 September 2017

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9 September 2017

Mobile phone use and risk of glioma in adults: case-control study

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9 September 2017

KORA-gen--resource for population genetics, controls and a broad spectrum of disease phenotypes

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9 September 2017

The SU.VI.MAX Study: a randomized, placebo-controlled trial of the health effects of antioxidant vitamins and minerals

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9 September 2017

LRIG1 restricts growth factor signaling by enhancing receptor ubiquitylation and degradation

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9 September 2017

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9 September 2017

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9 September 2017

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9 September 2017

Assessment of clinically silent atherosclerotic disease and established and novel risk factors for predicting myocardial infarction and cardiac death in healthy middle-aged subjects: rationale and design of the Heinz Nixdorf RECALL Study. Risk Facto

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14 September 2017

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14 September 2017

Endoplasmic reticulum stress-inducing drugs sensitize glioma cells to temozolomide through downregulation of MGMT, MPG, and Rad51

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5558246

17 June 2018

Isocitrate dehydrogenase 1 codon 132 mutation is an important prognostic biomarker in gliomas.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5558246

17 June 2018

Familial risks in nervous-system tumours: a histology-specific analysis from Sweden and Norway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5558246

22 August 2018

Amplification and overexpression of the MDM4 (MDMX) gene from 1q32 in a subset of malignant gliomas without TP53 mutation or MDM2 amplification.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5558246

22 August 2018

Polygenes, risk prediction, and targeted prevention of breast cancer

1 reference

https://api.crossref.org/works/10.1038%2FNG.3823

7 January 2021

based on heuristic

inferred from DOI database lookup

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10.1038/NG.3823

1 reference

Europe PubMed Central

7 September 2017

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0 references

1 reference

Europe PubMed Central

7 September 2017

1 reference

Europe PubMed Central

7 September 2017

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