Patterns of de novo tandem repeat mutations and their role in autism | Nature
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A general framework for estimating the relative pathogenicity of human genetic variants | Nature Genetics
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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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De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects | PLOS Genetics
Forecasting risk gene discovery in autism with machine learning and genome-scale data | Scientific Reports
![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
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Pten loss results in inappropriate excitatory connectivity | Molecular Psychiatry
Rare variants and the oligogenic architecture of autism: Trends in Genetics
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Autism-linked Cullin3 germline haploinsufficiency impacts cytoskeletal dynamics and cortical neurogenesis through RhoA signaling | Molecular Psychiatry
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder | Nature Genetics
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Frontiers | Common CHD8 Genomic Targets Contrast With Model-Specific Transcriptional Impacts of CHD8 Haploinsufficiency
