Biochemistry, Genetics and Molecular Biology
Genetics
53%
DNA Methylation
48%
Genetic Divergence
30%
Exome Sequencing
27%
C9orf72
21%
Epigenetics
21%
Haploinsufficiency
21%
Mental Retardation
18%
SIN3A
16%
PSEN1
16%
Phosphatase
16%
Transport Protein
16%
Autosomal Recessive Inheritance
16%
Genetic Variation
16%
Enzyme Active Site
16%
SNP Array
16%
Mitochondrial Membrane Transport Protein
16%
Beta Oxidation
16%
Mitochondrial Trifunctional Protein Deficiency
16%
Tubulin
16%
Methylation
13%
Enzyme Activity
12%
Subcellular Localization
10%
Quantitative Reverse Transcription Polymerase Chain Reaction
10%
Dephosphorylation
10%
Induced Pluripotent Stem Cell
10%
Enzyme
9%
Genetic Screening
9%
Thiolase
8%
Mitochondrial Trifunctional Protein
8%
Brain Function
6%
Brain Development
6%
Fibroblast
6%
TARDBP
5%
Genetic Determinism
5%
Genetic Evaluation
5%
Serine
5%
Threonine
5%
Protein Phosphorylation
5%
Aggression
5%
Pedigree
5%
Phosphoprotein Phosphatase
5%
Executive Function
5%
Gene Mutation
5%
Working Memory
5%
Homozygosity
5%
Gene Expression
5%
Synapse
5%
SORL1
5%
Pleckstrin Homology Domain
5%
Neuroscience
Frontotemporal Dementia
100%
Frontal Variant Frontotemporal Dementia
35%
Primary Progressive Aphasia
19%
Neuropsychological Assessment
16%
Neurodevelopmental Disorder
16%
Magnetic Resonance Imaging
16%
Gray Matter
16%
Carrier Protein
16%
Transport Protein
16%
Mindfulness
16%
Spectrum Disorder
16%
Alpha Tubulin
16%
Executive Functions
13%
Tau Protein
13%
Corpus Callosum
9%
Neurofilament Light Chain
8%
Uncinate Fasciculus
8%
Progranulin
6%
Microtubules
6%
Social Cognition
5%
Fractional Anisotropy
5%
Phonology
5%
Medicine and Dentistry
Frontotemporal Lobar Degeneration
32%
Neurodevelopmental Disorder
18%
Diagnosis
17%
Spectrum Disorder
16%
Mitochondrial Membrane Transport Protein
16%
Rare Disease
16%
DNA Methylation
16%
Neuropsychiatric Inventory
16%
Alpha Tubulin
16%
Promoter Region
8%
Microtubule
6%
Diseases
5%
