Biochemistry, Genetics and Molecular Biology
Haploinsufficiency
100%
Chromodomain
75%
Circular RNA
75%
DNA Binding
75%
Helicase
75%
Allele
50%
RNA Splicing
50%
Non-Coding RNA
50%
Alternative Splicing
50%
Overlapping Gene
25%
Exon
25%
Biogenesis
25%
Transcriptomics
25%
Transcription
25%
Synapse
25%
Loss of Function Mutation
25%
Exome Sequencing
25%
Brain Development
25%
Epigenetics
25%
Keyphrases
Autism Spectrum Disorder
100%
Haploinsufficiency
36%
SINEUP
36%
Circular RNA
27%
Chromodomain Helicase DNA-binding Proteins
27%
Molecular Convergence
27%
DNA Binding
27%
Risk Factors
27%
Back-splicing
18%
Non-coding RNA (ncRNA)
18%
RNA Splicing
18%
Risk Genes
18%
Circularization
9%
Alternative Splicing Regulation
9%
Neurodevelopmental Syndrome
9%
Exome Sequencing Analysis
9%
Brain Physiology
9%
Overlapping Genes
9%
Abnormal Pattern
9%
Postmortem Tissue
9%
Therapeutic Avenues
9%
Modular Structure
9%
Non-overlapping
9%
Unveiling
9%
Functional Class
9%
Protein Level
9%
Neurodevelopmental Disorders
9%
Potential Therapeutics
9%
New Drug Targets
9%
Brain Development
9%
Modular Architecture
9%
Significant Risk Factors
9%
Biogenesis
9%
Molecular Phenotype
9%
Susceptibility Genes
9%
Protein Production
9%
Physiological Level
9%
Mutant Alleles
9%
Biological Pathways
9%
Neurological Diseases
9%
Transcriptomics
9%
Epigenetics
9%
Gain-of-function mutation
9%
De-novo mutations
9%
Synapse
9%
Exon
9%
Complex Scenarios
9%
Alternative Splicing
9%
Neuroscience
Pervasive Developmental Disorder
100%
Haploinsufficiency
36%
Circular RNA
27%
DNA Binding
27%
Helicase
27%
Non-Coding RNA
18%
Alternative Splicing
18%
RNA Splicing
18%
Overlapping Gene
9%
Exome Sequencing
9%
In Vivo
9%
Exon
9%
Neurodevelopmental Disorder
9%
Loss of Function Mutation
9%
Synapse
9%
Transcriptomics
9%
Brain Development
9%
In Vitro
9%
Nervous System Disorder
9%