Genetic advances in autism: heterogeneity and convergence on shared pathways

被引:123
作者
Bill, Brent R. [1 ,2 ]
Geschwind, Daniel H. [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Psychiat, Semel Inst Neurosci & Human Behav,Ctr Autism Res, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Psychiat, Semel Inst Neurosci & Human Behav,Program Neurobe, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Program Neurogenet, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA
关键词
QUANTITATIVE TRAIT LOCUS; SPECTRUM DISORDERS; LINKAGE; RISK; INDIVIDUALS; ASSOCIATION; PREVALENCE; MUTATIONS; 16P11.2; BRAIN;
D O I
10.1016/j.gde.2009.04.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The autism spectrum disorders (ASD) are a heterogeneous set of developmental disorders characterized at their core by deficits in social interaction and communication. Current psychiatric nosology groups this broad set of disorders with strong genetic liability and multiple etiologies into the same diagnostic category. This heterogeneity has challenged genetic analyses. But shared patient resources, genomic technologies, more refined phenotypes, and novel computational approaches have begun to yield dividends in defining the genetic mechanisms at work. Over the last five years, a large number of autism susceptibility loci have emerged, redefining our notion of autism's etiologies, and reframing how we think about ASD.
引用
收藏
页码:271 / 278
页数:8
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