自闭症谱系障碍
自闭症遗传率
外显子组测序
遗传学
神经发育障碍
基因分型
自闭症
生物
鉴定(生物学)
外显子组
遗传建筑学
候选基因
遗传连锁
拷贝数变化
基因
基因组
心理学
发展心理学
基因型
数量性状位点
突变
植物
作者
Gokul Ramaswami,Daniel H. Geschwind
出处
期刊:Handbook of Clinical Neurology
[Elsevier BV]
日期:2018-01-01
卷期号:: 321-329
被引量:126
标识
DOI:10.1016/b978-0-444-63233-3.00021-x
摘要
Autism spectrum disorder (ASD) is a prevalent neurodevelopmental disorder characterized by impaired social interaction and stereotyped behaviors. ASD has a strong and complex genetic component, with multiple familial inheritance patterns and an estimate of up to 1000 genes potentially implicated. Over the past decade, genomic technologies have enabled rapid progress in the identification of risk genes for ASD. In this chapter, we review the delineation of ASD disease genes starting from traditional genetic studies such as linkage and association, and then focusing on more recent studies utilizing genomic technologies, such as high-throughput genotyping and exome sequencing.
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