Biochemistry, Genetics and Molecular Biology
Rolandic Epilepsy
100%
GRIN2A
68%
Genetics
68%
Spike
54%
Gene Linkage
38%
PAX6
30%
NMDA Receptor
24%
Single-Nucleotide Polymorphism
23%
Speech and Language
23%
Proband
22%
Copy-Number Variation
20%
Sex Chromosome Aneuploidies
20%
Agonist
20%
MicroRNA
20%
CNTNAP2
20%
Cholinergic
20%
Binding Site
20%
Gene Locus
20%
Prevalence
20%
Synapse
20%
Slow-Wave Sleep
17%
Genotyping
17%
Comorbidity
15%
Genetic Risk
14%
Glutamic Acid
13%
Aspartic Acid
13%
Written Language
13%
Single Nucleotide Polymorphism
12%
Bioinformatics
10%
Case-Control Study
10%
Minor Allele Frequency
10%
Rare Variant
10%
Gene Frequency
10%
Language Ability
10%
Pedigree
9%
Allele
8%
Linkage Analysis
7%
Patch Clamp Technique
6%
Binding Domain
6%
Confocal Microscopy
6%
C-Terminus
6%
Patient Coding
6%
HEK 293 Cells
6%
Calcium Transport
6%
Missense Mutation
6%
Receptor Gene
6%
Western Blot
6%
Glutamate Receptor
6%
Major Gene
6%
Inherited Mutation
6%
Neuroscience
Rolandic Epilepsy
75%
GRIN2A
68%
Copy Number Variation
41%
Focal Epilepsy
41%
Pervasive Developmental Disorder
30%
Autism
25%
Landau Kleffner Syndrome
25%
Brain Disease
25%
Single-Nucleotide Polymorphism
22%
Synapse
22%
Language Disorders
20%
Allele Frequency
20%
Receptor Trafficking
20%
Dyslexia
20%
Receptor Agonist
20%
Cholinergic
20%
Epileptic Absence
20%
Migraine
20%
NMDA Receptor
20%
Gene Locus
20%
Attention Deficit Hyperactivity Disorder
20%
Glutamic Acid
13%
Agonist
13%
Childhood Absence Epilepsy
13%
Spike-and-Wave
13%
Slow-Wave Sleep
13%
Language Disorder
10%
Aspartic Acid
10%
PAX6
10%
MECP2
10%
Hyperactivity
10%
KCNB1
10%
KCNA2
10%
Seizure Types
10%
Exome Sequencing
10%
Benign Epilepsy
10%
Pediatric Epilepsy
8%
Positive Allosteric Modulator
6%
Aphasia
6%
Receptor
6%
Calcium Transport
6%
C-Terminus
6%
HEK 293 Cells
6%
Missense Mutation
6%
Western Blot
6%
Receptor Gene
6%
Patch Clamp Technique
6%
Speech Disorder
5%
N Methyl Dextro Aspartic Acid Receptor 2A
5%
Comparative Genomics
5%
Medicine and Dentistry
GRIN2A
68%
Partial Seizure
61%
Rolandic Epilepsy
56%
Landau-Kleffner Syndrome
27%
Brain Disease
27%
Benign Childhood Epilepsy
25%
Cholinergic Synapse
20%
Molecular Profiling
20%
Pediatric Epilepsy
20%
Speech and Language
20%
Genetic Analysis
20%
NMDA Receptor
20%
Disease
17%
Slow-Wave Sleep
15%
Epileptic Seizure
12%
Epilepsy Syndromes
12%
Language Disorder
10%
Specific Language Impairment
10%
Fisher Exact Test
10%
Multimodal Imaging
10%
Speech Sound Disorder
10%
Benign Epilepsy
10%
Speech Disorder
8%
N Methyl-D-Aspartate Receptor
6%
Cell Surface
6%
Glycine Receptor Agonist
6%
Allosteric Modulator
6%
Flux Assay
6%
Glutamate Receptor Agonist
6%
Carboxy Terminal Sequence
6%
Confocal Microscopy
6%
Receptor Gene
6%
Glutamic Acid
6%
Patch Clamp
6%
Calcium Transport
6%
Aphasia
6%
Receptor
6%
HEK 293 Cells
6%
Western Blot
6%
Patient-Data
6%
Missense Mutation
6%
Comorbidity
6%
Genetic Risk Factor
5%
N Methyl Dextro Aspartic Acid Receptor 2A
5%
Exon
5%
Partial Epilepsy
5%
