Biochemistry, Genetics and Molecular Biology
Gene
100%
Genetics
42%
Genomics
21%
Protein
17%
Epigenetics
16%
C9orf72
14%
Exome Sequencing
14%
Genetic Divergence
14%
Exome
13%
PDGFRA
12%
Proteinopathy
11%
ANK1
8%
Spectrum
8%
Differentially Methylated Regions
8%
PSEN1
8%
Tau
7%
Genome Wide Association Study
7%
Genetic Correlation
7%
Epigenome
7%
Motor Neuron
6%
Heritability
6%
PSEN2
6%
Signal Transduction
6%
Histone Modification
6%
Posttranslational Modification
6%
Genetic Architecture
6%
Methylation
6%
Genotyping
6%
Transactive Response Dna Binding Protein-43
5%
Epidermolysis bullosa
5%
Loss of Heterozygosity
5%
Gene Inactivation
5%
Profilin 1
5%
TARDBP
5%
Acetylation
5%
Collagen
5%
O-6-Methylguanine-DNA Methyltransferase
5%
Klinefelter Syndrome
5%
CRYAB
5%
Methylome
5%
Metabolic Pathway
5%
Isocitrate Dehydrogenase
5%
FUS
5%
ABCA7
5%
Leucine-Rich Repeat
5%
PRNP
5%
ATRX
5%
DNA Isolation
5%
Mitochondrial Genetics
5%
Lipocortin
5%
Medicine and Dentistry
Pathology
30%
Patient
28%
Glioblastoma
25%
Diagnosis
25%
Frontotemporal Lobar Degeneration
25%
Alzheimer's Disease
22%
Brain
21%
Neoplasm
19%
Gene
19%
Disease
17%
Myopathy
14%
Traumatic Brain Injury
12%
Lesion
12%
Tau
11%
Genome Wide Association Study
11%
Ganglioglioma
9%
Therapeutic Procedure
8%
Child
7%
Dementia
7%
Degenerative Disease
7%
Neuropathology
6%
Neuron
6%
TDP 43 Proteinopathy
6%
Morphology
6%
Differentiation
6%
Heterozygosity
6%
Sarcoplasmic reticulum
6%
Mutant
6%
Family
6%
Chronic Traumatic Encephalopathy
6%
Spinal Cord
6%
Laboratory
6%
Cells
5%
Analysis
5%
Closed Head Injury
5%
Adult
5%
Onset Age
5%
Severe Acute Respiratory Syndrome Coronavirus 2
5%
Riluzole
5%
Protein Tyrosine Kinase
5%
Spinal Cord Injury
5%
Shy-Drager Syndrome
5%
Young Adult
5%
Centronuclear Myopathy
5%
Exome Sequencing
5%
Case Report
5%
Myenteric Plexus
5%
Nuclear Import
5%
Recognition
5%
Kinesin
5%
Neuroscience
Brain
79%
Frontotemporal Dementia
37%
Neurodegenerative Disorder
37%
Dementia with Lewy Bodies
34%
Glioma
24%
Neuron
21%
Spinal Cord
16%
Parkinson's Disease
14%
Cerebellum
12%
Staining Technique
11%
Multiple System Atrophy
11%
Glioblastoma Multiforme
10%
Entorhinal Cortex
9%
Dementia
9%
Neurotrauma
9%
DNA Methylation
8%
Hippocampus
8%
Central Nervous System
6%
Expression Analysis
6%
Muscle Disorder
5%
6-O-Methylguanine
5%
Peroxisome Proliferator-Activated Receptor Gamma
5%
Paraplegia
5%
Leucine Rich Repeat Kinase 2
5%
CX3CL1
5%
Signal Transduction Pathway
5%
