流行病学
胶质瘤
医学
入射(几何)
全基因组关联研究
肿瘤科
内科学
疾病
病理
生物
遗传学
基因型
癌症研究
基因
单核苷酸多态性
物理
光学
作者
Quinn T. Ostrom,Haley Gittleman,Lindsay Stetson,Selene Virk,Jill S. Barnholtz‐Sloan
出处
期刊:Cancer treatment and research
日期:2014-12-02
卷期号:: 1-14
被引量:348
标识
DOI:10.1007/978-3-319-12048-5_1
摘要
Gliomas are the most common type of primary intracranial tumors. Some glioma subtypes cause significant mortality and morbidity that are disproportionate to their relatively rare incidence. A very small proportion of glioma cases can be attributed to inherited genetic disorders. Many potential risk factors for glioma have been studied to date, but few provide explanation for the number of brain tumors identified. The most significant of these factors includes increased risk due to exposure to ionizing radiation, and decreased risk with history of allergy or atopic disease. The potential effect of exposure to cellular phones has been studied extensively, but the results remain inconclusive. Recent genomic analyses, using the genome-wide association study (GWAS) design, have identified several inherited risk variants that are associated with increased glioma risk. The following chapter provides an overview of the current state of research in the epidemiology of intracranial glioma.
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