Medicine and Dentistry
Epileptic Seizure
100%
Disease
58%
Brain Disease
40%
Developmental Delay
36%
Genetic Screening
30%
Glycosylphosphatidylinositol
22%
Hypotonia
21%
Congenital Malformation
21%
GRIA3
16%
Genotype Phenotype Correlation
15%
Diagnosis
14%
Neurologic Disease
14%
Comorbidity
14%
Exome Sequencing
14%
Status Epilepticus
14%
Clinician
14%
Dysmorphic Feature
13%
Short Stature
13%
Clinical Feature
13%
Partial Seizure
13%
Cerebellum Hypoplasia
12%
Clinical Finding
12%
Autosomal Recessive Inheritance
12%
Targeted Therapy
12%
Drug Resistant Epilepsy
12%
Neurologic Finding
12%
Patient with Epilepsy
11%
Treatment of Epilepsy
11%
Heredity
11%
Hypertrichosis
11%
Wilson's Disease
11%
Epilepsy Syndromes
10%
GRIA1
10%
Genetic Disorder
10%
Molecular Diagnosis
9%
Infantile Spasm
9%
Epileptic Spasms
9%
Receptor
8%
Central Nervous System
8%
Stereotypic Movement Disorder
8%
Skeleton Malformation
8%
Infection
8%
Autosomal Dominant Inheritance
8%
Prevalence
7%
Pyridoxine
7%
Pathognomonic
7%
Pervasive Developmental Disorder
7%
Glutamate Receptor
7%
Pyridoxal 5 Phosphate
7%
Conus medullaris
6%
Biochemistry, Genetics and Molecular Biology
Intellectual Disability
96%
Missense
63%
Genetics
61%
Glycosylphosphatidylinositol
33%
GRIA3
24%
Exome Sequencing
24%
Genotype Phenotype Correlation
22%
Genetic Screening
22%
Genotyping
22%
Comorbidity
19%
GRIA1
15%
Exome
13%
Autosomal Dominant Inheritance
13%
Candidate Gene
13%
ZEB2
12%
Genetic Determinism
11%
Penetrance
11%
Wild Type
11%
Autosomal Recessive Inheritance
11%
Decision Making
11%
DYRK1A
11%
Phenylketonuria
11%
Flow Cytometry
11%
Anabolism
10%
Ion Channel
10%
AMPA Receptor
10%
PIGA
10%
Amino Acids
9%
Phosphatidylinositol
9%
Body Height
9%
Polysaccharide
9%
Infancy
9%
Diptera
9%
Genomics
8%
Brain Development
8%
Whole Cell Patch Clamp
8%
Molecular Genetics
8%
Channel Blocker
8%
Orthology
8%
Vitamin B6
7%
Pyridoxine
7%
Clinical Trial
7%
Synapse
7%
Pyridoxal Phosphate
7%
Congenital Disorder of Glycosylation
7%
Metabolomics
6%
Adaptive Behavior
6%
Prevalence
6%
Glutamate Receptor
6%
Amino Methyl Phosphonic Acid
6%
Neuroscience
Brain Disease
48%
GRIA3
29%
Behavior (Neuroscience)
22%
Comorbidity
20%
Hypotonia
20%
Neurodevelopmental Disorder
19%
In Vitro
17%
Status Epilepticus
16%
Glycosylphosphatidylinositol
16%
Stereotypic Movement Disorder
13%
Exome Sequencing
13%
Electroencephalography
13%
Pervasive Developmental Disorder
12%
Tonic-Clonic Seizure
12%
Myoclonus
12%
Amitriptyline
11%
Hypoplasia
11%
Dystonia
11%
GRIA1
10%
Receptor
10%
Haploinsufficiency
9%
Synapse
9%
Attention Deficit Hyperactivity Disorder
9%
Glutamate Receptor
8%
Seizure Types
8%
Generalised Epilepsy
8%
Ataxia
8%
Microcephaly
8%
ZEB2
8%
Brain Development
8%
Ion Channel
8%
Pyridoxine
7%
In Vivo
7%
Focal Epilepsy
7%
Single-Nucleotide Polymorphism
7%
Pyridoxal Phosphate
7%
Febrile Seizure
6%
Amino Acid
6%
Motor Skills
6%
AMPA
6%
Synaptic Transmission
6%
Propionic Acid
6%
Isoxazole
6%
Neurological Disorder
6%
Genetic Generalized Epilepsy
6%
Cognitive Disorders
6%
Parkinson's Disease
5%
Cell Signaling
5%
Somatics
5%
AMPA Receptor
5%
