Biochemistry, Genetics and Molecular Biology
Phenotype
77%
Nested Gene
59%
Protein
50%
Spectrum
48%
Mutation
46%
Exome Sequencing
35%
Development
27%
Regulatory Mechanism
27%
Pregnancy
26%
Genetics
24%
Fibroblast
24%
BRCA1
22%
RNA Sequence
22%
Glycosylphosphatidylinositol
22%
Autosomal Recessive Inheritance
22%
GRIN1
22%
Proband
22%
Wild Type
21%
Cell Membrane
18%
Ultrasound
17%
Surface Property
16%
Language
15%
ATP1A2
15%
Electric Potential
14%
Nerve Cell Differentiation
14%
C-Terminus
14%
Zebra Fish
14%
C-Type Lectin
14%
Germline
13%
Childhood
13%
Consensus
13%
Microarray
13%
Brain Development
12%
Western Blot
12%
Cell Survival
12%
Growth
11%
Transcription
11%
Missense Mutation
11%
Dendrite
11%
Phenotypic Heterogeneity
11%
Motor Performance
11%
Tubulin
11%
Penetrance
11%
Ultrasonography
11%
Magnetic Resonance Imaging
11%
Speech
11%
Synaptogenesis
11%
ATPase
11%
Structural Protein
11%
Protein Modeling
11%
Medicine and Dentistry
Patient
100%
Brain Malformation
39%
Diagnosis
31%
Analysis
29%
Gene
22%
Congenital Malformation
22%
Exome Sequencing
22%
Vanilloid Receptor 4
22%
Syndrome
19%
Fetus
19%
Microarray
18%
Cohen Syndrome
16%
Maculopathy
16%
Phenotype
16%
Family
15%
Corpus Callosum Agenesis
14%
Spectrum Disorder
13%
Consensus
13%
Therapeutic Procedure
13%
Tubulin
13%
Cortical Dysplasia
12%
Fetus Echography
11%
Diseases
11%
Gene Discovery
11%
Protein
11%
Missense Mutation
11%
Dendrite
11%
Screening
11%
Giant Cell
11%
Jaw
11%
Genetic Disorder
9%
Exome
9%
Dysplasia
9%
N Methyl-D-Aspartate Receptor
9%
Comprehension
9%
Capillary
8%
Tissues
8%
Cell Damage
8%
Genetic Prenatal Diagnosis
8%
Retrospective Cohort Study
8%
Channelopathy
8%
Macrocephaly
8%
Mosaicism
8%
Child
8%
Inpatient
8%
Carbonate Dehydratase Inhibitor
8%
Age
7%
Intellectual Disability
7%
Woman
6%
Lesion
6%
Neuroscience
Brain
35%
Gene
28%
Epilepsy
25%
Phenotype
24%
Protein
21%
Corpus Callosum
18%
Neurodevelopmental Disorder
18%
Seizure
16%
Spinocerebellar Ataxia
16%
Intellectual Disability
14%
Nerve Cell Differentiation
14%
Mitophagy
14%
C-Terminus
14%
F Actin
14%
Neurodegeneration
14%
Tubulin
13%
Neuronal Migration
11%
Missense Mutation
11%
Agenesis
11%
Ataxia
11%
Microcephaly
10%
Eicosanoid Receptor
9%
In Vitro
7%
Exome Sequencing
7%
Ubiquitin Protein Ligase E3
7%
Autoimmune Disorder
7%
Ubiquitin Protein Ligase
7%
Mass Spectrometry
7%
Mutagenesis
7%
Multiple Sclerosis
7%
Autophagy
7%
Mitochondrion
7%
Nervous System Disorder
7%
Parkinson's Disease
7%
Microglia
7%
Neuron
7%
Status Epilepticus
7%
Intractable Epilepsy
7%
Generalised Epilepsy
7%
Basal Ganglia
6%
Hippocampus
6%
Cortical Malformation
6%
Protein Family
5%
Oligomer
5%
Microtubules
5%
Posterior Cranial Fossa
5%
Neurite
5%
Collapsin Response Mediator Protein
5%
Synapse Formation
5%
Psychopathology
5%