共 161 条
- [1] Levy SE(2009)Autism Lancet 374 1627-1638
- [2] Mandell DS(2014)Most genetic risk for autism resides with common variation Nat Genet 46 881-885
- [3] Schultz RT(2015)Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci Neuron 87 1215-1233
- [4] Gaugler T(2014)Convergence of genes and cellular pathways dysregulated in autism spectrum disorders Am J Hum Genet 94 677-694
- [5] Klei L(2018)Comparative analyses of copy-number variation in autism spectrum disorder and schizophrenia reveal etiological overlap and biological insights Cell Rep 24 2838-2856
- [6] Sanders SJ(2010)Clinical genetic testing for patients with autism spectrum disorders Pediatrics 125 e727-e735
- [7] Bodea CA(2013)Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder Am J Hum Genet 93 607-619
- [8] Goldberg AP(2010)Functional impact of global rare copy number variation in autism spectrum disorders Nature 466 368-372
- [9] Lee AB(2019)Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder Transl Psychiatry 9 258-1965
- [10] Sanders SJ(2019)Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants Nat Neurosci 22 1961-84.e23