Biochemistry, Genetics and Molecular Biology
Genetics
41%
Whole Genome Sequencing
37%
Exome Sequencing
37%
Gene Network
22%
Promoter Region
19%
Intellectual Disability
16%
Genetic Variation
16%
Pribnow Box
14%
RNA
14%
Carcinogenesis
14%
Gene Expression
14%
Transcriptomics
14%
Mouse
14%
Binding Site
12%
RNA Sequence
12%
Genome Sequencing
12%
Transcription Factors
12%
Genetic Risk
12%
Genetic Heterogeneity
12%
Candidate Gene
12%
CNTNAP2
11%
Medium Spiny Neuron
9%
Gene Ontology
9%
Genetic Architecture
9%
Synapse
9%
Cell Proliferation
9%
Chromothripsis
9%
Signal Transduction
9%
Molecular Genetics
9%
Regulatory Element
9%
Expression Quantitative Trait Loci
9%
Epidermal Growth Factor Receptor
9%
Subtyping
9%
Stem Cell
9%
Survival Prediction
9%
Neurexin
9%
Coding Region
9%
Molecular Network
9%
Microarrays
9%
Prenatal Development
8%
MicroRNA
6%
Genetic Determinism
6%
Knockout Mouse
6%
Genetic Divergence
6%
Next Generation Sequencing
6%
Proband
5%
Neuroscience
Pervasive Developmental Disorder
100%
Exome Sequencing
31%
Nerve Cell Differentiation
16%
Cell Signaling
15%
Whole Genome Sequencing
13%
Genetic Variation
12%
Dementia Praecox
12%
Attention Deficit Hyperactivity Disorder
12%
Neurodevelopmental Disorder
11%
In Vivo
11%
Promoter Region
10%
Catenin
9%
Brain Development
9%
Neuroscience
9%
Stem Cell
9%
Central Nervous System
9%
Nav1.2
9%
Anoctamin 1
9%
Ferroptosis
9%
Short Tandem Repeat
9%
Transcriptomics
9%
MicroRNA
9%
Valproic Acid
9%
Developmental Disability
9%
Epidermal Growth Factor Receptor
9%
Hippocampus
9%
Mental Disorder
8%
Transcription Factors
7%
Binding Site
7%
Transcriptome
6%
Microglia
6%
Synaptic Transmission
6%
Social Behavior
5%
Prefrontal Cortex
5%
Keyphrases
Autism Spectrum Disorder
19%
Exome Sequencing Analysis
10%
Children with Developmental Disabilities
9%
KDM3B
9%
Genetic Research
9%
CFEOM3
9%
Congenital Fibrosis of the Extraocular muscles
9%
RNA m6A
9%
RNF146
9%
Microglial Dysfunction
9%
Exome Sequencing
9%
Systems Approach
9%
Glioma Stem Cells
9%
CRISPR Interference (CRISPRi)
9%
EGFRvIII
9%
Sequence Method
9%
Chromosome Doubling
9%
Heterogeneous Roles
9%
T Cell Exclusion
9%
Ferroptosis-related Genes
9%
Nav1.2
9%
Sodium Channel Subtypes
9%
Infantile Epilepsy
9%
SCN2A
9%
ANO1
9%
Chromothripsis
9%
Complex Structural Variation
9%
High-throughput Characterization
9%
Genomic Studies
9%
3D Chromatin Structure
9%
Stemness
9%
Tandem Repeat Expansion
9%
Layer-specific Genes
9%
Molecular Characterization
9%
Expression Quantitative Trait Loci (eQTL)
9%
Human Prefrontal Cortex
9%
Fetal Structural Anomalies
9%
Genetic Architecture
9%
ABT-263
8%
SCN8A
8%
Neuroimmune Response
6%
Gene Network Model
6%
E-signature
5%
