Biochemistry, Genetics and Molecular Biology
Genetics
48%
DNA Methylation
32%
Genetic Divergence
28%
C9orf72
25%
Exome Sequencing
20%
Genetic Screening
16%
Epigenetics
14%
Haploinsufficiency
14%
Mental Retardation
12%
Haplotype
11%
SIN3A
10%
Transport Protein
10%
Autosomal Recessive Inheritance
10%
Genetic Variation
10%
Enzyme Active Site
10%
Mitochondrial Membrane Transport Protein
10%
Beta Oxidation
10%
Mitochondrial Trifunctional Protein Deficiency
10%
Tubulin
10%
Phosphatase
10%
Polygenic Score
10%
Carrier Protein
10%
DSM-5
10%
Clinical Trial
10%
Methylation
9%
PSEN1
9%
Proband
8%
SNP Array
8%
Enzyme Activity
8%
Subcellular Localization
7%
Quantitative Reverse Transcription Polymerase Chain Reaction
7%
Dephosphorylation
7%
Induced Pluripotent Stem Cell
7%
Enzyme
6%
Thiolase
5%
Mitochondrial Trifunctional Protein
5%
Rare Variant
5%
TAR DNA Binding Protein
5%
Neuroscience
Frontotemporal Dementia
100%
Frontal Variant Frontotemporal Dementia
24%
Primary Progressive Aphasia
13%
Neurodevelopmental Disorder
10%
Magnetic Resonance Imaging
10%
Carrier Protein
10%
Transport Protein
10%
Mindfulness
10%
Spectrum Disorder
10%
Alpha Tubulin
10%
Neuropsychological Assessment
10%
Disinhibition
10%
Big Five Personality Trait
10%
Personality Test
10%
Whole Genome Sequencing
10%
Executive Function
9%
Tau Protein
9%
Gray Matter Volume
9%
Amyotrophic Lateral Sclerosis
8%
Corpus Callosum
6%
Neurofilament Light Chain
5%
Uncinate Fasciculus
5%
Personality Traits
5%
Medicine and Dentistry
Frontotemporal Lobar Degeneration
21%
Neurodevelopmental Disorder
10%
Spectrum Disorder
10%
Mitochondrial Membrane Transport Protein
10%
Rare Disease
10%
DNA Methylation
10%
Neuropsychiatric Inventory
10%
Alpha Tubulin
10%
Promoter Region
5%
