Keyphrases
Restless Legs Syndrome
100%
Dystonia
28%
Parkinson's Disease
19%
Genome-wide Association Study
18%
MEIS1
12%
Meta-analysis
10%
Whole Exome Sequencing
10%
Multiple Sclerosis
9%
Movement Disorders
9%
Narcolepsy
9%
DNA Methylation (DNAm)
9%
Exome Sequencing
9%
Pathophysiology
8%
Neurodevelopmental Disorders
8%
Genetic Risk
8%
Age of Onset
8%
Rare Variants
8%
Common Variants
7%
Autosomal Dominant
7%
Intellectual Disability
7%
Genetic Factors
7%
Epigenome-wide Association Study
7%
Susceptibility Loci
7%
Early Onset
7%
Isolated Dystonia
7%
Exome
7%
Huntington's Disease
6%
Generalized Dystonia
6%
European Ancestry
6%
Pergolide
6%
KMT2B
6%
Risk Loci
6%
Genetic Architecture
6%
Neurodegenerative Diseases
5%
Single nucleotide Polymorphism
5%
Gain-of-function mutation
5%
Missense Variants
5%
BTBD9
5%
Parkinson Patients
5%
Frontotemporal Lobar Degeneration
5%
SNP
5%
Disease Risk
5%
Biochemistry, Genetics and Molecular Biology
Genetics
51%
Genome-Wide Association Study
27%
Exome Sequencing
24%
Allele
15%
Missense
15%
MEIS1
15%
Autosomal Dominant Inheritance
13%
Exome
13%
Genomics
13%
Candidate Gene
12%
Genetic Determinism
11%
Genetic Risk
10%
Mental Retardation
10%
Genetic Divergence
10%
Gene Linkage
9%
DNA Methylation
9%
Single Nucleotide Polymorphism
9%
Single-Nucleotide Polymorphism
9%
Exon
8%
Immunity
8%
Genetic Architecture
8%
Prevalence
8%
BTBD9
7%
Comorbidity
7%
Epigenetics
7%
Fibroblast
7%
Genotyping
6%
Dopaminergic
6%
Epigenome
6%
Next Generation Sequencing
6%
Genome Wide Association Study
6%
Linkage Analysis
6%
Limb Movement
5%
Gene Mutation
5%
Methylation
5%
Autosomal Recessive Inheritance
5%
