An integrative analysis of non-coding regulatory DNA variations associated with autism spectrum disorder

Keyphrases

• Analysis pipeline 16%
• Autism Spectrum Disorder 100%
• Binding Affinity 16%
• CNTNAP2 33%
• Coding DNA Sequence 16%
• Coding mutation 16%
• Complex Disorders 16%
• Computational Prediction 16%
• DNA Variation 100%
• Dysregulation 16%
• Evolutionary Conservation 16%
• Fetal Neurodevelopment 16%
• Function Code 16%
• Genetic Etiology 33%
• Genetic Heterogeneity 16%
• Genetic Liability 16%
• Genetic Studies 16%
• Genetic Variation 16%
• Genome-wide Analysis 16%
• Idiopathic Autism 16%
• Integrative Analysis 100%
• Loss Function 33%
• Maternally Inherited 16%
• MicroRNA 16%
• MicroRNA Genes 16%
• MiR-873-5p 16%
• Neurodevelopmental 16%
• Neurodevelopmental Disorders 16%
• New Resources 16%
• Non-coding 100%
• Non-coding Region 16%
• Non-protein 16%
• NRXN1 16%
• NRXN2 16%
• Protein-coding Genes 33%
• Publicly Available Dataset 16%
• Regulatory DNA 100%
• Regulatory Function 16%
• Regulatory Region 16%
• Regulatory Variants 33%
• Risk Genes 50%
• Signaling Pathway 16%
• Single nucleotide Variant 50%
• Synaptic Signaling 16%
• Transcription Factor Binding Sites 16%

Biochemistry, Genetics and Molecular Biology

• Binding Affinity 25%
• Binding Site 25%
• CNTNAP2 50%
• Coding Region 50%
• Genetic Conservation 25%
• Genetic Variation 25%
• Genetics 100%
• Genome Wide Association Study 25%
• MicroRNA 50%
• Nerve Cell Differentiation 25%
• NRXN1 25%
• Promoter Region 25%
• Regulatory Region 25%
• Signal Transduction 25%
• Single-Nucleotide Polymorphism 75%
• Transcription Factors 25%