Biochemistry, Genetics and Molecular Biology
Actin
12%
ATP1A2
18%
ATP1A3
18%
Autosomal Dominant Inheritance
18%
Autosomal Recessive Inheritance
18%
Brain Development
17%
BRCA1
18%
C-Terminus
12%
Cell Membrane
15%
Centrosome
22%
Childhood
11%
Consensus
18%
Cytoskeleton
13%
Dendrite
18%
Development
38%
DNA
12%
DNA Replication
14%
Dynamics
22%
Electric Potential
25%
Exome Sequencing
36%
Fibroblast
46%
Genetic Code
81%
Genetics
24%
Germline
18%
Glycosylphosphatidylinositol
18%
GRIN1
18%
GRIN2B
18%
Growth
17%
Language
13%
Mediator
18%
Mental Retardation
39%
Microarray
11%
Missense Mutation
18%
Mutation
44%
Nerve Cell Differentiation
18%
Nested Gene
81%
Nuclear Membrane
20%
Phenotype
96%
Pregnancy
37%
Proband
18%
Protein
72%
Regulatory Mechanism
29%
RNA Sequence
22%
Spectrum
73%
Surface Property
18%
Tubulin
32%
Ubiquitin Ligase
12%
Ultrasound
18%
Wild Type
27%
Zebra Fish
16%
Medicine and Dentistry
Analysis
28%
Brain Malformation
42%
Brainstem
18%
Capillary
12%
Cardiomyocyte
14%
Cell Damage
18%
Channelopathy
18%
Cohen Syndrome
18%
Congenital Malformation
33%
Consensus
18%
Corpus Callosum Agenesis
21%
Cortical Malformation
18%
Craniofacial Malformation
18%
Dendrite
18%
Developmental Delay
23%
Diagnosis
30%
Dilated Cardiomyopathy
18%
Diseases
26%
Dysplasia
18%
Exome Sequencing
24%
Family
24%
Fetus
16%
Fetus Echography
21%
Fibroblast
18%
Gene
38%
Gene Discovery
18%
Giant Cell
18%
Hypospadias
18%
Inpatient
23%
Jaw
18%
Macrocephaly
12%
Maculopathy
18%
Microarray
15%
Microtubule
11%
Missense Mutation
18%
Neurodevelopmental Disorder
18%
Patient
100%
Phenotype
13%
Polyneuropathy
18%
Pregnancy
18%
Protein
20%
Retinopathy
18%
Skeleton Malformation
18%
Skull
18%
Spectrum Disorder
18%
Syndrome
21%
Therapeutic Procedure
11%
Tissues
12%
Tubulin
20%
Vanilloid Receptor 4
18%
Neuroscience
Agenesis
18%
Aspartic Acid
8%
Ataxia
18%
Autoimmune Disorder
9%
Autophagy
9%
Brain
49%
Brain Development
15%
C-Terminus
18%
Cell Nucleus Membrane
18%
Corpus Callosum
28%
Dendrite
12%
Diabetes
18%
Eicosanoid Receptor
8%
Epilepsy
21%
Exome Sequencing
9%
F Actin
18%
Gene
36%
Generalised Epilepsy
6%
GRIN1
18%
GRIN2B
18%
In Vitro
9%
Intellectual Disability
18%
Intractable Epilepsy
6%
Mass Spectrometry
9%
Microcephaly
30%
Microglia
9%
Microtubules
6%
Missense Mutation
12%
Mitochondrion
9%
Mitophagy
18%
Multiple Sclerosis
9%
Mutagenesis
9%
Nerve Cell Differentiation
18%
Nervous System Disorder
9%
Neurodegeneration
18%
Neurodevelopmental Disorder
34%
Neuron
9%
Neuronal Migration
11%
Oligomer
6%
Parkinson's Disease
9%
Phenotype
37%
Posterior Cranial Fossa
6%
Protein
24%
Protein Family
6%
Seizure
18%
Spinocerebellar Ataxia
18%
Status Epilepticus
6%
Tubulin
18%
Ubiquitin Protein Ligase
9%
Ubiquitin Protein Ligase E3
9%