Biochemistry, Genetics and Molecular Biology
Adaptive Behavior
7%
Amino Acids
10%
AMPA Receptor
10%
Anabolism
13%
Autosomal Dominant Inheritance
14%
Autosomal Recessive Inheritance
11%
Body Height
9%
Brain Development
8%
Candidate Gene
14%
Channel Blocker
8%
Clinical Trial
7%
Cohort Study
11%
Comorbidity
16%
Congenital Disorder of Glycosylation
9%
Decision Making
11%
Diptera
9%
DYRK1A
11%
Electroencephalogram
7%
Exome
19%
Exome Sequencing
26%
Fibroblast
11%
Flow Cytometry
11%
Genetic Screening
23%
Genetics
61%
Genomics
20%
Genotype Phenotype Correlation
23%
Genotyping
22%
Glycosylphosphatidylinositol
36%
GRIA1
16%
GRIA3
24%
Infancy
9%
Intellectual Disability
97%
Ion Channel
10%
Metabolomics
7%
Missense
64%
Molecular Genetics
8%
Orthology
8%
Penetrance
11%
Phenylketonuria
11%
Phosphatidylinositol
9%
PIGA
10%
Polysaccharide
9%
Prevalence
7%
Pyridoxal Phosphate
7%
Pyridoxine
7%
Synapse
7%
Vitamin B6
7%
Whole Cell Patch Clamp
8%
Wild Type
11%
ZEB2
13%
Medicine and Dentistry
Amitriptyline
11%
Autosomal Dominant Inheritance
8%
Autosomal Recessive Inheritance
13%
Brain Disease
46%
Central Nervous System
8%
Cerebellum Hypoplasia
13%
Clinical Feature
13%
Clinical Finding
13%
Clinician
14%
Comorbidity
12%
Congenital Malformation
24%
Conus medullaris
7%
Developmental Delay
37%
Diagnosis
12%
Disease
59%
Disease
8%
Drug Resistant Epilepsy
12%
Dysmorphic Feature
14%
Epilepsy Syndromes
10%
Epileptic Seizure
100%
Epileptic Spasms
9%
Exome Sequencing
14%
Genetic Disorder
10%
Genetic Screening
31%
Genotype Phenotype Correlation
15%
Glutamate Receptor
7%
Glycosylphosphatidylinositol
23%
GRIA1
10%
GRIA3
16%
Hypertrichosis
11%
Hypotonia
22%
Infantile Spasm
9%
Infection
8%
Molecular Diagnosis
10%
Neurologic Disease
12%
Neurologic Finding
12%
Partial Seizure
13%
Pathognomonic
7%
Patient with Epilepsy
11%
Pervasive Developmental Disorder
7%
Prevalence
9%
Pyridoxal 5 Phosphate
7%
Pyridoxine
7%
Receptor
8%
Short Stature
14%
Skeleton Malformation
8%
Status Epilepticus
14%
Stereotypic Movement Disorder
8%
Targeted Therapy
7%
Wilson's Disease
11%
Neuroscience
Amino Acid
7%
Amitriptyline
16%
AMPA
6%
Antiseizure Medication
6%
Ataxia
8%
Attention Deficit Hyperactivity Disorder
9%
Automutilation
8%
Behavior (Neuroscience)
23%
Brain Development
8%
Brain Disease
54%
Cognitive Disorders
6%
Communication Disorder
7%
Comorbidity
21%
Dystonia
11%
Electroencephalography
13%
Exome Sequencing
13%
Exon
6%
Febrile Seizure
7%
Focal Epilepsy
7%
Generalised Epilepsy
8%
Genetic Generalized Epilepsy
6%
Glutamate Receptor
8%
Glycosylphosphatidylinositol
16%
GRIA1
10%
GRIA3
30%
Haploinsufficiency
9%
Hypoplasia
11%
Hypotonia
20%
In Vitro
17%
In Vivo
7%
Ion Channel
8%
Isoxazole
6%
Microcephaly
8%
Motor Skills
7%
Myoclonus
12%
Neurodevelopmental Disorder
19%
Neurological Disorder
6%
Pervasive Developmental Disorder
13%
Propionic Acid
6%
Pyridoxal Phosphate
7%
Pyridoxine
7%
Receptor
10%
Seizure Types
8%
Single-Nucleotide Polymorphism
8%
Status Epilepticus
16%
Stereotypic Movement Disorder
13%
Synapse
9%
Synaptic Transmission
6%
Tonic-Clonic Seizure
12%
ZEB2
8%
