Associated Papers
Single-cell transcriptome identifies molecular subtype of autism spectrum disorder impacted by de novo loss-of-function variants regulating glial cells.
Nassir N et al.
Human Genomics, 2021
34802461 (PubMed )
Supplement: 40246_2021_368_MOESM2_ESM.xlsx › DbLOF
CNTN5-/+or EHMT2-/+human iPSC-derived neurons from individuals with autism develop hyperactive neuronal networks.
Deneault E et al.
Elife, 2019
Genome-wide characteristics of de novo mutations in autism.
Yuen RK et al.
Npj Genomic Medicine, 2016
27525107 (PubMed )
Supplement: npjgenmed201627-s3.xlsx › Table_S10
Genetic diagnosis of autism spectrum disorders: the opportunity and challenge in the genomics era.
Jiang YH et al.
Critical Reviews in Clinical Laboratory Sciences, 2014
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing.
Jiang YH et al.
American Journal of Human Genetics, 2013
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