Keyphrases
Parkinson's Disease
98%
Type 2 Diabetes Mellitus (T2DM)
50%
Single nucleotide Polymorphism
34%
Schizophrenia
30%
Israel
28%
Jewish
28%
Age of Onset
26%
Tardive Dyskinesia
25%
Genome-wide Association Study
24%
Antipsychotics
24%
Parkinson Patients
22%
Chromosomal Microarray
20%
Antipsychotic-induced Parkinsonism
20%
Nicotine Dependence
18%
Alzheimer's Disease
17%
Ashkenazi Jews
17%
Elderly People
16%
Leucine-rich Repeat Kinase 2 (LRRK2)
16%
Schizophrenic Patients
16%
Genetic Variants
16%
Pathogenic Variants
15%
Nicotinic Cholinergic Receptors
14%
Israeli
14%
RGS2
14%
Israeli Arabs
14%
Young Women
13%
Susceptibility Genes
13%
Non-associated
12%
SNP
12%
Parkinson's Disease Risk
12%
CHRNA5
11%
Extrapyramidal Symptoms
11%
Environmental Factors
11%
Cognitive Decline
11%
Meta-analysis
10%
Genotype
10%
G2019S
10%
Whole Exome Sequencing
10%
Patients with Parkinson's Disease
10%
GBA mutations
10%
Episodic Memory
10%
Fetus
10%
Neurodevelopmental Disorders
10%
Movement Disorders
10%
Receptor Gene
9%
Gene Expression Level
9%
Cognitively Normal
9%
Alpha-synuclein (α-syn)
9%
LRRK2 mutation
9%
Phenotypic Spectrum
9%
Neuroscience
Parkinson's Disease
100%
Dementia Praecox
48%
Single-Nucleotide Polymorphism
39%
Antipsychotic
35%
Alzheimer's Disease
25%
Tardive Dyskinesia
24%
Parkinsonism
21%
Genome-Wide Association Study
18%
Nicotinic Acetylcholine Receptor
14%
Tobacco Dependence
13%
Typical Antipsychotic
11%
L-DOPA
11%
Stereotypic Movement Disorder
11%
Episodic Memory
11%
Cognitive Function
11%
Receptor Gene
10%
Haplotype
10%
Meta-Analysis
10%
Peripheral Neuropathy
10%
CHRNA5
10%
Glucosylceramidase
10%
Dopaminergic
10%
Gene Expression
10%
Exome Sequencing
10%
Dyskinesia
9%
Haptoglobin
9%
RGS2 Protein
9%
Diabetes Mellitus
9%
Dementia with Lewy Bodies
9%
Electrical Brain Stimulation
8%
Genetic Variation
7%
Magnetic Resonance Imaging
7%
Executive Functions
6%
Dopamine Receptor
6%
Cathepsin B
6%
Psychosis
6%
Extrapyramidal Symptoms
6%
Polyneuropathy
6%
Apolipoprotein
6%
Untranslated Region
6%
Distal Hereditary Motor Neuropathies
6%
Alpha-Synuclein
5%
Synuclein
5%
Pervasive Developmental Disorder
5%
Fluorine-18
5%
Elevated Plus Maze
5%
Positron Emission Tomography
5%
Amygdala
5%
Adverse Effect
5%
Individual Differences
5%
Biochemistry, Genetics and Molecular Biology
Genetics
45%
Single-Nucleotide Polymorphism
32%
Genome-Wide Association Study
27%
Exome Sequencing
26%
Single Nucleotide Polymorphism
25%
Genotyping
24%
Allele
17%
Candidate Gene
15%
Genetic Divergence
14%
Array Comparative Genomic Hybridization
14%
Episodic Memory
14%
Autosomal Dominant Inheritance
11%
LRRK2
11%
Receptor Gene
10%
Glucocerebrosidase
10%
Glucosylceramidase
10%
Nicotinic Acetylcholine Receptor
10%
CHRNA5
9%
Smoking
9%
Haplotype
9%
Proband
9%
Molecular Inversion Probe
9%
Positron Emission Tomography
9%
Microarrays
9%
Cathepsin B
9%
Amyloidosis
9%
Transthyretin
9%
Minor Allele Frequency
8%
Executive Function
8%
Genetic Risk
7%
Genetic Disorder
7%
Autosomal Recessive Inheritance
7%
Working Memory
7%
Intellectual Disability
7%
Whole Genome Sequencing
7%
Classification
6%
Next Generation Sequencing
6%
Enzyme
6%
Dopaminergic
6%
Genetic Determinism
5%
Alpha-Synuclein
5%
GRIA2
5%
Gene Linkage
5%
Gene Interaction
5%
Enzyme Activity
5%
Autophagy
5%
Exome
5%
Missense
5%
Cognition
5%