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The autism risk factor CHD8 is a chromatin activator in human neurons and functionally dependent on the ERK-MAPK pathway effector ELK1 | Scientific Reports
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Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder | Scientific Reports
A general framework for estimating the relative pathogenicity of human genetic variants | Nature Genetics
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CHD8 haploinsufficiency results in autistic-like phenotypes in mice | Nature
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Pten loss results in inappropriate excitatory connectivity | Molecular Psychiatry
Frontiers | Common CHD8 Genomic Targets Contrast With Model-Specific Transcriptional Impacts of CHD8 Haploinsufficiency
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Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants | Nature Communications
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![PDF] Efficient facial representations for age, gender and identity recognition in organizing photo albums using multi-output ConvNet | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/629d5af2878f79d4503a177e3bbc166a127f9e40/15-Table8-1.png "PDF] Efficient facial representations for age, gender and identity recognition in organizing photo albums using multi-output ConvNet | Semantic Scholar")
PDF] Efficient facial representations for age, gender and identity recognition in organizing photo albums using multi-output ConvNet | Semantic Scholar
Autism-linked Cullin3 germline haploinsufficiency impacts cytoskeletal dynamics and cortical neurogenesis through RhoA signaling | Molecular Psychiatry
Demographic characteristics of healthy controls | Download Table
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IJMS | Free Full-Text | Knockout of Katnal2 Leads to Autism-like Behaviors and Developmental Delay in Zebrafish
