Keyphrases
Frontotemporal Dementia
100%
Huntington's Disease
92%
Induced Pluripotent Stem Cells (iPSCs)
69%
Stem Cell Lines
40%
CHMP2B
34%
Neurodegenerative Diseases
33%
Gene Expansion
29%
Hereditary Spastic Paraplegia
28%
Alzheimer's Disease
24%
Spinocerebellar Ataxia Type 2
23%
Age of Onset
22%
Disease Genes
21%
Cerebrospinal Fluid
19%
Alzheimer's Disease Patient
17%
Amyotrophic Lateral Sclerosis
17%
Isogenic
15%
Mutation Carriers
15%
Novel mutation
14%
Autosomal Dominant
14%
CAG Repeat Expansion
14%
Dementia with
13%
Ataxia
13%
Microtubule-associated Protein tau
13%
Microtubule-associated Protein tau Gene
13%
FTDP-17
12%
Charged multivesicular Body Protein 2B
12%
Stem Cell-derived
12%
Cognitive Impairment
12%
Early Onset
11%
Neurodegeneration
11%
Genome-wide Association Study
10%
Control Cell
10%
Psychiatric Symptoms
10%
Human Induced Pluripotent Stem Cell-derived Neurons
10%
Presenilin
10%
Spinocerebellar Ataxia
10%
CAG Repeat
9%
Social Cognition
9%
Familial Alzheimer's Disease
9%
Dementia
9%
Executive Function
9%
Huntingtin
8%
Neurofilament Light (NF-L)
8%
Cerebrospinal Fluid Biomarkers
8%
Disease Progression
8%
Cerebellar Ataxia
8%
Asymptomatic Carriers
8%
Disease Mechanisms
7%
Cas9 Protein
7%
Presenilin 1 mutation
7%
Neuroscience
Frontotemporal Dementia
81%
Huntington's Disease
72%
Stem Cell
49%
Spinocerebellar Ataxia
34%
Cell Line
33%
Neurodegenerative Disorder
32%
Alzheimer's Disease
23%
Tau Protein
20%
Ataxia
20%
Hereditary Spastic Paraplegia
18%
CAG Repeat
17%
Cognitive Disorders
13%
Paraplegia
12%
Parkinsonism
12%
Amyotrophic Lateral Sclerosis
12%
Neurodegeneration
11%
Genome-Wide Association Study
11%
Huntingtin
9%
Metabolic Pathway
8%
In Vitro
8%
Positron Emission Tomography
8%
Multiple Sclerosis
8%
Gene Mutation
7%
Cerebellum
6%
Proteomics
6%
Haplotype
6%
Social Cognition
6%
Intrathecal
6%
Magnetic Resonance Imaging
6%
CRISPR
6%
Executive Functions
6%
Amyloid
6%
Dementia with Lewy Bodies
6%
T Cell
6%
Magnetic Resonance Imaging
6%
Parkinson's Disease
5%
Gene Expression
5%
Fluorine-18
5%
Astrocyte
5%
Autophagy
5%
Fibroblast
5%
Dystonia
5%
TATA-binding Protein
5%
Biochemistry, Genetics and Molecular Biology
Induced Pluripotent Stem Cell
73%
Stem Cell Line
41%
Genetics
22%
Allele
21%
Tau Protein
21%
Autosomal Dominant Inheritance
18%
CAG Repeat
18%
CHMP2B
16%
Presenilin
16%
Tau
12%
Genome-Wide Association Study
10%
Metabolic Pathway
10%
Fibroblast
9%
Neurofilament
9%
Haplotype
8%
Autophagy
8%
Liquid
8%
CRISPR/Cas9
8%
Amyloid
7%
Genetic Divergence
7%
Motor Neuron
6%
Penetrance
6%
Genetic Counseling
6%
Lysosome
6%
Magnetism
6%
Germ Layer
5%
Gene Mutation
5%
Karyotype
5%
Autosomal Recessive Inheritance
5%
Positron Emission Tomography
5%
Proband
5%
Exon
5%
Chromosome 3
5%
Gene Expression
5%
Amyloid Precursor Protein
5%
Leukocyte
5%
TATA-binding Protein
5%
Single Nucleotide Polymorphism
5%
Genetic Architecture
5%
Metachromatic Leukodystrophy
5%
Astrocyte
5%
Episome
5%
