Keyphrases
Parkinson's Disease
100%
Dystonia
54%
Idiopathic Parkinson's Disease
24%
Movement Disorders
19%
Chorea
19%
Early Onset
16%
Gain-of-function mutation
14%
Genome-wide Association Study
14%
Age of Onset
12%
Childhood-onset
12%
Biallelic
11%
Missense Variants
11%
Nkx2.1
11%
Deep Brain Stimulation
11%
Monogenic
10%
Myoclonus-dystonia
10%
Parkinson Genetics
10%
Genetic Program
10%
Basal Ganglia
10%
Pathogenic Variants
9%
Generalized Dystonia
9%
Myoclonus
9%
Phosphodiesterase 10A (PDE10A)
9%
Parkin
9%
Genetic Testing
9%
Hyperkinetic Movement Disorders
9%
Leucine-rich Repeat Kinase 2 (LRRK2)
9%
ADCY5
8%
KMT2B
8%
Neurodegenerative Diseases
8%
Huntington's Disease
7%
Isolated Dystonia
7%
Parkinson's Disease Risk
7%
Genetic Causes
7%
Developmental Delay
7%
Parkinson Patients
6%
Related Disorders
6%
Causative Gene
6%
Amyotrophic Lateral Sclerosis
6%
Neurological Diseases
6%
Intellectual Disability
6%
Phenotypic Spectrum
6%
Autosomal Dominant
6%
Late-onset
6%
Mendelian Randomization
6%
Gene Variants
6%
MED27
6%
Restless Legs Syndrome
6%
Early-onset Dystonia
6%
Psychiatric Disorders
6%
Biochemistry, Genetics and Molecular Biology
Genetics
70%
Genetic Divergence
22%
Exome Sequencing
17%
Genome-Wide Association Study
17%
Missense
14%
Genetic Program
13%
Mental Retardation
12%
LRRK2
12%
Dopaminergic
11%
Genetic Screening
11%
Penetrance
11%
Genotyping
10%
Glucocerebrosidase
10%
Glucosylceramidase
10%
Genetic Risk
9%
SGCE
9%
Autosomal Dominant Inheritance
8%
Mendelian Randomization
7%
Exome
7%
Brain Development
7%
Missense Mutation
7%
Kinase
7%
Phosphotransferase
7%
Proband
7%
Autosomal Recessive Inheritance
7%
Magnetism
6%
Genetic Variation
6%
Genomics
6%
Single-Nucleotide Polymorphism
6%
Genetic Architecture
6%
Allele
6%
Genome Wide Association Study
6%
Initiation Factor
6%
Polygenic Score
6%
Complex Genomic Disorder
6%
Artificial Neural Network
5%
Cyclic Adenosine Monophosphate
5%
Methylation
5%
Eukaryotic Translation
5%
Gene Mutation
5%
Mitochondrion
5%
PINK1
5%
Whole Genome Sequencing
5%
Fibroblast
5%
Dideoxynucleotide Sequencing
5%
Neuroscience
Dystonia
63%
Parkinson's Disease
53%
Stereotypic Movement Disorder
25%
Chorea
15%
Basal Ganglia
13%
Parkin
10%
Huntington's Disease
9%
Myoclonus
9%
Glucosylceramidase
8%
Dopaminergic
8%
Exome Sequencing
8%
Genome-Wide Association Study
7%
Electrical Brain Stimulation
7%
Phosphodiesterase
6%
Cyclic Adenosine Monophosphate
6%
Ataxia
6%
Restless Legs Syndrome
6%
Amyotrophic Lateral Sclerosis
6%
Adenylyl Cyclase
6%
Hypoplasia
6%
Neurobiology
6%
Cerebellum
5%
Mitochondrion
5%