Keyphrases
Restless Legs Syndrome
100%
Dystonia
29%
Genome-wide Association Study
19%
Parkinson's Disease
19%
MEIS1
12%
Movement Disorders
10%
Meta-analysis
10%
Whole Exome Sequencing
10%
Exome Sequencing
10%
Multiple Sclerosis
9%
Narcolepsy
9%
Genetic Risk
9%
DNA Methylation (DNAm)
9%
Neurodevelopmental Disorders
9%
Pathophysiology
8%
Age of Onset
8%
Rare Variants
8%
Isolated Dystonia
8%
Common Variants
8%
Intellectual Disability
7%
Autosomal Dominant
7%
Exome
7%
Genetic Factors
7%
Epigenome-wide Association Study
7%
Susceptibility Loci
7%
Early Onset
7%
Gain-of-function mutation
7%
Huntington's Disease
6%
European Ancestry
6%
Generalized Dystonia
6%
Pergolide
6%
KMT2B
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%
Disease Risk
5%
Biochemistry, Genetics and Molecular Biology
Genetics
50%
Genome-Wide Association Study
26%
Exome Sequencing
25%
Allele
16%
Missense
15%
MEIS1
15%
Exome
14%
Genomics
13%
Autosomal Dominant Inheritance
12%
Genetic Risk
12%
Genetic Determinism
11%
Candidate Gene
10%
Rare Variant
10%
Mental Retardation
10%
DNA Methylation
10%
Genetic Divergence
9%
Single Nucleotide Polymorphism
9%
Gene Linkage
9%
Single-Nucleotide Polymorphism
9%
Immunity
8%
Prevalence
8%
Genetic Architecture
8%
Exon
8%
Epigenome
7%
Epigenetics
7%
Comorbidity
6%
Genotyping
6%
Fibroblast
6%
BTBD9
6%
Genome Wide Association Study
6%
Next Generation Sequencing
5%
Dopaminergic
5%
Transcription Factors
5%
Gene Mutation
5%
Linkage Analysis
5%
Limb Movement
5%
Methylation
5%
Autosomal Recessive Inheritance
5%
