Keyphrases
Autism Spectrum Disorder
100%
Whole Genome Sequencing
29%
Autism
26%
Exome Sequencing
21%
Non-coding
18%
Type-specific
15%
Neuropsychiatric Disorders
13%
Massively Parallel Reporter Assay
12%
Dysregulation
12%
Human Brain Development
12%
Functional Impact
11%
Systems Approach
11%
Sequence Method
11%
Molecular Characterization
11%
Psychiatric Disorders
11%
Neuropsychiatric
11%
Ultraviolet Irradiation
11%
Risk Variant
11%
Cancer Types
11%
Human Brain
11%
Promoter Variants
11%
Neurodevelopmental Disorders
11%
Neurodevelopment
10%
Integrative Analysis
9%
De-novo mutations
9%
DNA Variation
9%
Non-coding Variants
8%
Genetic Variation
8%
Schizophrenia
8%
SCN2A
8%
Transcriptomics
8%
Synaptic Plasticity
8%
Signaling Pathway
8%
Gene Expression
8%
Risk Genes
7%
Human Cortex
7%
Genetic Architecture
7%
Sequencing Studies
7%
Structural Variation
7%
CNTNAP2
7%
Ultraviolet Exposure
7%
Non-coding Elements
7%
Catenin
7%
Mouse Brain
7%
Genetic Heterogeneity
7%
Genome Sequencing
7%
Central Nervous System
6%
Protein-coding Genes
6%
Neurobiology
6%
CRISPR Interference (CRISPRi)
6%
Biochemistry, Genetics and Molecular Biology
Genomics
50%
Genetics
46%
Whole Genome Sequencing
43%
Transcriptomics
26%
Promoter Region
23%
Exome Sequencing
21%
Genetic Variation
15%
Gene Expression
15%
RNA
14%
Gene Network
13%
Binding Site
12%
Signal Transduction
12%
Human Genome
11%
Tamsulosin
11%
Sex Difference
11%
Genome Sequencing
11%
Genetic Divergence
10%
Intellectual Disability
10%
Synaptic Transmission
10%
Transcription Factors
9%
RNA Sequence
9%
Brain Development
9%
Nerve Cell Differentiation
9%
Proband
8%
Pribnow Box
8%
Carcinogenesis
8%
Coding Region
8%
Upregulation
8%
N6-Methyladenosine
8%
Developmental Stage
7%
Genetic Heterogeneity
7%
Candidate Gene
7%
Functional Genomics
7%
Expression Quantitative Trait Loci
7%
Catenin
7%
Genetic Risk
6%
Genetic Architecture
6%
Single-Nucleotide Polymorphism
6%
Genetic Determinism
6%
Regulatory Element
6%
MicroRNA
6%
Epidermal Growth Factor Receptor
6%
Gene Mutation
6%
Mouse Model
6%
Subtyping
6%
Germline
5%
Germ Cell
5%
CNTNAP2
5%
Medium Spiny Neuron
5%
Gene Ontology
5%
Neuroscience
Pervasive Developmental Disorder
68%
Exome Sequencing
18%
Transcriptomics
15%
Nerve Cell Differentiation
15%
Whole Genome Sequencing
13%
Brain Development
11%
Genetic Variation
10%
Cell Signaling
9%
Gene Expression
8%
Attention Deficit Hyperactivity Disorder
7%
Central Nervous System
7%
Neurogenesis
7%
Autism
7%
Promoter Region
7%
Neurodevelopmental Disorder
6%
In Vivo
6%
Catenin
5%
Stem Cell
5%
Nav1.2
5%
Anoctamin 1
5%
Ferroptosis
5%
Short Tandem Repeat
5%
MicroRNA
5%
Valproic Acid
5%
Developmental Disability
5%
Epidermal Growth Factor Receptor
5%
Hippocampus
5%
Amnesia
5%
Neurobiology
5%
Functional Genomics
5%
Microglia
5%
Cerebellum
5%
Tamsulosin
5%
Exon
5%
Voltage Gated Sodium Channel
5%
Haploinsufficiency
5%
Brain Disease
5%
Genome Project
5%
RASopathies
5%
Binding Site
5%
