2021
DOI: 10.18632/aging.203428
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Glioma: interaction of acquired and germline genetics

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Cited by 2 publications
(2 citation statements)
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“…In 2016, the WHO classification included genomic analysis as a novel approach for newly diagnosed glioma patients. Therefore, an increasing number of studies [ 4 , 5 , 6 ] have attempted to identify genetic risk factors for brain cancer through genome-wide association study (GWAS) approaches in which single-nucleotide polymorphisms (SNPs) have been found to have associations with brain malignancy, especially in malignant glioma [ 7 , 8 ]. An SNP is a variation at a single base pair among individuals, which may indicate a risk locus.…”
Section: Introductionmentioning
confidence: 99%
“…In 2016, the WHO classification included genomic analysis as a novel approach for newly diagnosed glioma patients. Therefore, an increasing number of studies [ 4 , 5 , 6 ] have attempted to identify genetic risk factors for brain cancer through genome-wide association study (GWAS) approaches in which single-nucleotide polymorphisms (SNPs) have been found to have associations with brain malignancy, especially in malignant glioma [ 7 , 8 ]. An SNP is a variation at a single base pair among individuals, which may indicate a risk locus.…”
Section: Introductionmentioning
confidence: 99%
“…Gliomas are classified based on histopathological distribution into low-grade (LGG) and high-grade (HGG) gliomas. LGGs are generally well differentiated, while HGGs are characterized by low differentiation and the resulting worse prognosis [2]. However, recent studies emphasize the limitations of traditional histopathological classification that highlight the significant heterogenicity of gliomas.…”
mentioning
confidence: 99%