Autism spectrum disorder genomics: The progress and potential of genomic technologies

被引:9
|
作者
Ghralaigh, Fiana Ni [1 ,2 ]
Gallagher, Louise [1 ]
Lopez, Lorna M. [1 ,2 ]
机构
[1] Trinity Coll Dublin, Dept Psychiat, Dublin, Ireland
[2] Maynooth Univ, Dept Biol, Maynooth, Kildare, Ireland
基金
爱尔兰科学基金会;
关键词
Autism; Genomics; Rare; Variation; Whole-genome; Sequencing; ASD; COPY-NUMBER VARIATION; DE-NOVO CNVS; LARGE-SCALE; GENETIC RISK; CANDIDATE GENES; SCHIZOPHRENIA; HERITABILITY; INSIGHTS; COHORT;
D O I
10.1016/j.ygeno.2020.09.022
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Genomic technologies have accelerated research progress in autism spectrum disorder (ASD) genomics and promises to further transform our understanding of the genetic basis of this neurodevelopmental disorder. Here we review the current evidence for the genetic basis of ASD, present the progress of large-scale studies to date and highlight the potential of genomic technologies. In particular, we discuss evidence for the importance of identifying rare genetic variants in family-based studies. Genomics is a key feature of future healthcare and our review illustrates it's potential to improve our biological understanding of neurodevelopmental disorders, and to ultimately aid ASD diagnosis, inform medical decision making and establish genomics as central to personalised medicine.
引用
收藏
页码:5136 / 5142
页数:7
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