Biochemistry, Genetics and Molecular Biology
Intellectual Disability
100%
Missense
66%
Genetics
59%
Glycosylphosphatidylinositol
34%
Exome Sequencing
26%
GRIA3
25%
Genetic Screening
23%
Genotype Phenotype Correlation
23%
Genotyping
22%
Exome
20%
Comorbidity
16%
GRIA1
16%
Genomics
14%
Autosomal Dominant Inheritance
14%
Candidate Gene
14%
ZEB2
13%
Fibroblast
12%
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
10%
Phosphatidylinositol
10%
Body Height
9%
Polysaccharide
9%
Infancy
9%
Diptera
9%
Brain Development
8%
Whole Cell Patch Clamp
8%
Molecular Genetics
8%
Channel Blocker
8%
Orthology
8%
Vitamin B6
8%
Pyridoxine
8%
Clinical Trial
7%
Synapse
7%
Pyridoxal Phosphate
7%
Congenital Disorder of Glycosylation
7%
Metabolomics
7%
Adaptive Behavior
7%
Prevalence
7%
Glutamate Receptor
7%
RNA Sequence
7%
Medicine and Dentistry
Epileptic Seizure
97%
Disease
60%
Brain Disease
42%
Developmental Delay
37%
Genetic Screening
31%
Congenital Malformation
23%
Glycosylphosphatidylinositol
22%
Hypotonia
22%
GRIA3
17%
Genotype Phenotype Correlation
15%
Short Stature
15%
Exome Sequencing
14%
Status Epilepticus
14%
Clinician
14%
Dysmorphic Feature
14%
Clinical Feature
14%
Partial Seizure
13%
Cerebellum Hypoplasia
13%
Clinical Finding
13%
Autosomal Recessive Inheritance
13%
Drug Resistant Epilepsy
13%
Neurologic Finding
12%
Diagnosis
12%
Neurologic Disease
12%
Comorbidity
12%
Patient with Epilepsy
12%
Hypertrichosis
11%
Wilson's Disease
11%
Molecular Diagnosis
10%
Epilepsy Syndromes
10%
GRIA1
10%
Genetic Disorder
10%
Infantile Spasm
10%
Epileptic Spasms
9%
Prevalence
9%
Receptor
9%
Central Nervous System
9%
Stereotypic Movement Disorder
8%
Skeleton Malformation
8%
Infection
8%
Autosomal Dominant Inheritance
8%
Pyridoxine
7%
Targeted Therapy
7%
Pathognomonic
7%
Pervasive Developmental Disorder
7%
Glutamate Receptor
7%
Pyridoxal 5 Phosphate
7%
Conus medullaris
7%
Bone Development
7%
Psychomotor Development
6%
Neuroscience
Brain Disease
49%
GRIA3
31%
Behavior (Neuroscience)
22%
Comorbidity
21%
Hypotonia
20%
Neurodevelopmental Disorder
19%
In Vitro
17%
Status Epilepticus
17%
Glycosylphosphatidylinositol
17%
Stereotypic Movement Disorder
14%
Exome Sequencing
13%
Electroencephalography
13%
Pervasive Developmental Disorder
13%
Tonic-Clonic Seizure
12%
Myoclonus
12%
Amitriptyline
11%
Hypoplasia
11%
Dystonia
11%
GRIA1
10%
Receptor
10%
Haploinsufficiency
10%
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
8%
In Vivo
7%
Focal Epilepsy
7%
Single-Nucleotide Polymorphism
7%
Pyridoxal Phosphate
7%
Febrile Seizure
7%
Amino Acid
7%
Motor Skills
7%
AMPA
7%
Synaptic Transmission
7%
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%
