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A general framework for estimating the relative pathogenicity of human genetic variants | Nature Genetics
Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder | Scientific Reports
CHD8 haploinsufficiency results in autistic-like phenotypes in mice | Nature
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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An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder | Nature Genetics
Pten loss results in inappropriate excitatory connectivity | Molecular Psychiatry
Frontiers | Common CHD8 Genomic Targets Contrast With Model-Specific Transcriptional Impacts of CHD8 Haploinsufficiency
Patterns of de novo tandem repeat mutations and their role in autism | Nature
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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
Frontiers | Clustered Protocadherins Emerge as Novel Susceptibility Loci for Mental Disorders
De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects | PLOS Genetics
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