Medicine & Life Sciences
Whole Exome Sequencing
100%
Parkinson Disease, Familial, Type 1
66%
Trinucleotide Repeat Expansion
63%
Dystonia
61%
Dystonic Disorders
57%
Spinocerebellar Ataxias
56%
Ataxia
55%
Sweden
54%
Whole Genome Sequencing
53%
Homeobox Genes
48%
Zinc Fingers
47%
Tremor
45%
Genetic Testing
43%
Glycine
42%
Cognitive Dysfunction
40%
Phenotype
37%
Parkinson Disease
35%
Movement Disorders
35%
Dementia
35%
Genes
29%
Stroke
28%
Mutation
23%
Idiopathic basal ganglia calcification 1
19%
Gait
16%
Ataxia, Sensory, Autosomal Dominant
16%
Primary Dysautonomias
15%
Cerebral Small Vessel Diseases
15%
Genetic Databases
13%
Tandem Repeat Sequences
13%
Paraplegia
12%
Neuropathology
12%
Arterioles
11%
Cerebral Hemorrhage
11%
Genetic Association Studies
11%
Cerebrovascular Disorders
10%
Basal Ganglia
10%
Central Nervous System
10%
White Matter
9%
Intranuclear Inclusion Bodies
9%
Enteric Nervous System
9%
Patient Selection
9%
Virulence
9%
Vascular Endothelial Growth Factor A
9%
Autopsy
8%
alpha-Synuclein
8%
Saccades
8%
Communication
7%
Arteries
7%
Peripheral Nervous System
7%
Genotype
7%