Keyphrases
Age of Onset
24%
Alpha-synuclein (α-syn)
13%
Alzheimer's Disease
16%
Antipsychotic-induced Parkinsonism
19%
Antipsychotics
23%
Ashkenazi Jews
16%
Cathepsin B
11%
CHRNA5
10%
Chromosomal Microarray
19%
Cognitive Decline
10%
Dopaminergic Neurons
9%
Elderly People
15%
Environmental Factors
10%
Episodic Memory
9%
Extrapyramidal Symptoms
10%
Fetus
9%
G2019S
10%
GBA mutations
9%
Gene Expression Level
9%
Genetic Variants
15%
Genome-wide Association Study
23%
Genotype
10%
Glucocerebrosidase Activity
10%
Israel
31%
Israeli
14%
Israeli Arabs
13%
Jewish
28%
Leucine-rich Repeat Kinase 2 (LRRK2)
15%
Meta-analysis
11%
Movement Disorders
9%
Neurodevelopmental Disorders
9%
Nicotine Dependence
17%
Nicotinic Cholinergic Receptors
14%
Non-associated
12%
Parkinson Patients
21%
Parkinson's Disease
100%
Parkinson's Disease Risk
15%
Pathogenic Variants
15%
Patients with Parkinson's Disease
9%
Receptor Gene
9%
RGS2
13%
Schizophrenia
29%
Schizophrenic Patients
15%
Single nucleotide Polymorphism
32%
SNP
12%
Susceptibility Genes
12%
Tardive Dyskinesia
23%
Type 2 Diabetes Mellitus (T2DM)
47%
Whole Exome Sequencing
10%
Young Women
13%
Neuroscience
Adverse Effect
5%
Alpha-Synuclein
5%
Alzheimer's Disease
23%
Antipsychotic
35%
Apolipoprotein
6%
Cathepsin B
6%
CHRNA5
9%
Cognitive Function
10%
Deep Brain Stimulation
8%
Dementia with Lewy Bodies
8%
Diabetes Mellitus
8%
Distal Hereditary Motor Neuropathies
5%
Dopamine Receptor
6%
Dopaminergic
9%
Dyskinesia
9%
Episodic Memory
10%
Executive Function
6%
Exome Sequencing
10%
Extrapyramidal Symptoms
5%
Fluorine-18
5%
Gene Expression
9%
Genetic Variation
6%
Genome-Wide Association Study
20%
Glucosylceramidase
9%
Haplotype
10%
Haptoglobin
8%
L-DOPA
11%
Magnetic Resonance Imaging
6%
Meta-Analysis
10%
Muscular Dystrophy
5%
Neuropathy
10%
Nicotinic Acetylcholine Receptor
13%
Parkinson's Disease
94%
Parkinsonism
19%
Polyneuropathy
6%
Positron Emission Tomography
5%
Receptor Gene
10%
RGS2 Protein
8%
Single-Nucleotide Polymorphism
38%
Stereotypic Movement Disorder
10%
Synuclein
5%
Tardive Dyskinesia
23%
Tobacco Dependence
12%
Untranslated Region
5%
Biochemistry, Genetics and Molecular Biology
Allele
17%
Alpha-Synuclein
5%
Amyloidosis
8%
Antipsychotic
6%
Array Comparative Genomic Hybridization
13%
Autophagy
5%
Autosomal Dominant Inheritance
11%
Autosomal Recessive Inheritance
7%
Candidate Gene
14%
Cathepsin B
8%
CHRNA3
5%
CHRNA5
11%
Dopaminergic
6%
Enzyme
6%
Enzyme Activity
5%
Episodic Memory
9%
Exome
5%
Exome Sequencing
25%
Gene Interaction
5%
Gene Linkage
5%
Genetic Determinism
5%
Genetic Disorder
7%
Genetic Divergence
15%
Genetic Risk
7%
Genetics
43%
Genome-Wide Association Study
26%
Genotyping
24%
Glucocerebrosidase
10%
Glucosylceramidase
10%
GRIA2
5%
Haplotype
9%
Intellectual Disability
6%
LRRK2
10%
Minor Allele Frequency
8%
Molecular Inversion Probe
6%
Next Generation Sequencing
6%
Nicotinic Acetylcholine Receptor
10%
Polygenic Score
8%
Positron Emission Tomography
5%
Proband
9%
Rare Variant
14%
Receptor Gene
11%
Single Nucleotide Polymorphism
25%
Single-Nucleotide Polymorphism
32%
Synuclein
5%
Transthyretin
8%
Whole Genome Sequencing
6%
