Keyphrases
Restless Legs Syndrome
100%
Dystonia
28%
Parkinson's Disease
19%
Genome-wide Association Study
18%
MEIS1
13%
Movement Disorders
10%
Meta-analysis
10%
DNA Methylation (DNAm)
10%
Whole Exome Sequencing
10%
Exome Sequencing
10%
Multiple Sclerosis
9%
Narcolepsy
9%
Neurodevelopmental Disorders
9%
Pathophysiology
8%
KMT2B
8%
Genetic Risk
8%
Age of Onset
8%
Rare Variants
8%
Intellectual Disability
7%
Common Variants
7%
Autosomal Dominant
7%
Exome
7%
Genetic Factors
7%
Epigenome-wide Association Study
7%
Susceptibility Loci
7%
Early Onset
6%
Isolated Dystonia
6%
Gain-of-function mutation
6%
Huntington's Disease
6%
Generalized Dystonia
6%
European Ancestry
6%
Pergolide
6%
Risk Loci
6%
Genetic Architecture
6%
Neurodegenerative Diseases
5%
Single nucleotide Polymorphism
5%
Missense Variants
5%
BTBD9
5%
Parkinson Patients
5%
Frontotemporal Lobar Degeneration
5%
SNP
5%
Biochemistry, Genetics and Molecular Biology
Genetics
52%
Genome-Wide Association Study
27%
Exome Sequencing
25%
Exome
17%
Allele
16%
MEIS1
16%
Missense
15%
Genomics
13%
Autosomal Dominant Inheritance
13%
Candidate Gene
12%
DNA Methylation
12%
Genetic Risk
11%
Genetic Determinism
11%
Mental Retardation
11%
Rare Variant
10%
Single Nucleotide Polymorphism
10%
Genetic Divergence
9%
Gene Linkage
9%
Single-Nucleotide Polymorphism
9%
Genetic Architecture
9%
Exon
8%
Prevalence
8%
Epigenome
7%
Comorbidity
7%
Methylation
7%
BTBD9
7%
Epigenetics
7%
Dopaminergic
6%
Fibroblast
6%
Genotyping
6%
Transcription Factors
6%
Genome Wide Association Study
6%
Next Generation Sequencing
5%
Limb Movement
5%
Gene Mutation
5%
Linkage Analysis
5%
Genome Sequencing
5%
Animal Model
5%
