Keyphrases
Dystrophin Gene
98%
Schizophrenia
93%
Duchenne muscular Dystrophy
76%
Charcot-Marie-Tooth Disease
74%
DNA Diagnosis
61%
Exon
60%
Gene Expression
57%
Dystrophin
55%
RNA Sequencing (RNA-seq)
50%
Wilson Disease
49%
Disease Genes
46%
Neural Stem Cells
45%
Autosomal Dominant
45%
Autism Spectrum Disorder
44%
Mdx Mice
44%
Single-cell RNA Sequencing (scRNA-seq)
43%
Growth Hormone Deficiency
40%
Splicing mutation
38%
Pituitary Hormone Deficiency
37%
Panic Disorder
37%
Spinal muscular Atrophy
37%
Mouse Skeletal muscle
37%
Autism
37%
Ballistic
37%
Major Depressive Disorder
37%
Prenatal Diagnosis
35%
Neuropsychiatric Disorders
34%
Single nucleotide Polymorphism
33%
Etiology
32%
Pseudogene
30%
Transcription Factor 4 (TCF4)
30%
Russian children
30%
Neurofilament Light (NF-L)
30%
Gene mutation
29%
Human Neural Stem Cells (hNSCs)
29%
Missense mutation
29%
Middle Turbinate
29%
Olfactory Neuroepithelium
28%
Y Chromosome
28%
Polymerase Chain Reaction
28%
Early Onset
26%
Russian Patients
25%
Neuronal Cells
24%
Bashkortostan
24%
Dual Signal Amplification
24%
Amplification Method
24%
Deconvolution
24%
Tyrosine Kinase
24%
Moesin
24%
Nijmegen Breakage Syndrome
24%
Biochemistry, Genetics and Molecular Biology
Exon
100%
Haplotype
99%
Genetics
73%
Gene Linkage
71%
RNA
68%
Progenitor Cell
63%
Dystrophin
49%
RNA Sequencing
48%
Gene Linkage Disequilibrium
44%
Pedigree
43%
Polymerase Chain Reaction
41%
Gene Expression
40%
Y Chromosome
40%
Isolated Growth Hormone Deficiency
37%
Pituitary Hormone
37%
Allele
36%
Single-Nucleotide Polymorphism
35%
Autosomal Dominant Inheritance
33%
Missense Mutation
31%
Genetic Divergence
31%
Molecular Genetics
30%
TCF4
30%
Neurofilament Light
30%
Pseudogene
28%
Intron
28%
RNA Sequence
28%
DNA Analysis
27%
Genomics
27%
Pituitary-Specific Positive Transcription Factor 1
27%
Receptor Tyrosine Kinase
26%
Nijmegen Breakage Syndrome
24%
Long Noncoding RNA
24%
Antisense
24%
Moesin
24%
Non-Coding RNA
24%
Gene Mutation
24%
Microsatellite
24%
Candidate Gene
24%
Tyrosine Kinase
22%
Transcriptome
22%
Multiplex Polymerase Chain Reaction
21%
B Cell
20%
Contig
18%
Transcriptomics
18%
Enhancer Region
18%
Light Chain
18%
Lod Score
17%
Nerve Cell Differentiation
17%
21-Hydroxylase
16%
Human Genome
16%
Neuroscience
Neural Stem Cell
75%
Gene Expression
73%
Haplotype
66%
RNA-Seq
61%
Dystrophin
49%
Charcot-Marie-Tooth Disease
49%
Linkage Disequilibrium
48%
Single-Nucleotide Polymorphism
48%
Transcriptome
44%
RNA Sequence
40%
Etiology of Schizophrenia
38%
Major Depressive Disorder
37%
Autism
37%
Microsatellite
36%
Transfection
32%
Genome-Wide Association Study
30%
In Vitro
27%
Skeletal Muscle
24%
Y Chromosome
24%
Oligopeptide
24%
Pseudogene
24%
Moesin
24%
Long Non-Coding RNA
24%
Rett Syndrome
24%
Panic Disorder
24%
Brain Disease
24%
Cell Line
23%
Complementary DNA
20%
Turbinate
19%
Transcriptomics
18%
Pervasive Developmental Disorder
18%
Nerve Cell Differentiation
17%
Neuropathy
16%
Autism Spectrum Disorder
16%
Meta-Analysis
16%
Temporal Lobe
15%
Brain Development
15%
Methyl CpG Binding Protein 2
14%
Neurofilament Light Chain
14%
Neurofilament
14%
Muscular Dystrophy
14%
Missense Mutation
13%
Patch Clamp
12%
Pyridoxal Phosphate
12%
GABRA5
12%
Opioid Dependence
12%
Muscle Atrophy
12%
Kinase
12%
Peripheral Myelin Protein 22
12%
Spiral Ganglion Neuron
12%
