Recent Advances in the Genetics of Autism Spectrum Disorder

被引:43
|
作者
De Rubeis, Silvia [1 ,2 ]
Buxbaum, Joseph D. [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Icahn Sch Med Mt Sinai, Seaver Autism Ctr Res & Treatment, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA
[4] Icahn Sch Med Mt Sinai, Dept Neurosci, New York, NY 10029 USA
[5] Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA
[6] Icahn Sch Med Mt Sinai, Mindich Child Hlth & Dev Inst, New York, NY 10029 USA
关键词
Autism spectrum disorder; Autism risk genes; Exome sequencing; Copy number variation; De novo variation; Heritability; DE-NOVO MUTATIONS; COPY-NUMBER VARIATION; NEURODEVELOPMENTAL DISORDERS; INTELLECTUAL DISABILITY; SYNAPTIC DEFECTS; PATERNAL ORIGIN; HUMAN BRAIN; RISK; VARIANTS; GENES;
D O I
10.1007/s11910-015-0553-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Autism spectrum disorder (ASD) is a devastating neurodevelopmental disorder with high prevalence in the population and a pronounced male preponderance. ASD has a strong genetic basis, but until recently, a large fraction of the genetic factors contributing to liability was still unknown. Over the past 3 years, high-throughput next-generation sequencing on large cohorts has exposed a heterogeneous and complex genetic landscape and has revealed novel risk genes. Here, we provide an overview of the recent advances on the ASD genetic architecture, with an emphasis on the estimates of heritability, the contribution of common variants, and the role of inherited and de novo rare variation. We also examine the genetic components of the reported gender bias. Finally, we discuss the emerging findings from sequencing studies and how they illuminate crucial aspects of ASD pathophysiology.
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页数:9
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