Keyphrases
Amyotrophic Lateral Sclerosis
100%
Multi-ethnic
100%
Rare Variant Analysis
100%
Primary Lateral Sclerosis
100%
ANTXR2
100%
Intolerant
18%
Gene-based
18%
TARDBP
18%
ALKBH3
18%
Collapse Analysis
18%
Genetic Variants
9%
Nervous System
9%
Neurodegenerative Diseases
9%
Gain-of-function mutation
9%
Superoxide Dismutase 1 (SOD1)
9%
Physical Function
9%
Novel Pathways
9%
Antisense Oligonucleotides
9%
Novel Genes
9%
First-ever
9%
Disease Manifestations
9%
Protective Allele
9%
Intolerance
9%
Domain-independent
9%
Rare Variant Association Study
9%
TANK-binding Kinase 1 (TBK1)
9%
Novel Control
9%
Rare Variant Burden
9%
Protein-truncating Variants
9%
Residual Variation
9%
Biochemistry, Genetics and Molecular Biology
Rare Variant
100%
TARDBP
66%
Genetic Divergence
33%
Oligonucleotide
33%
Loss of Function Mutation
33%
Antisense
33%
SOD1
33%
Medicine and Dentistry
Amyotrophic Lateral Sclerosis
100%
Primary Lateral Sclerosis
100%
Diseases
18%
Genetic Variability
9%
Loss of Function Mutation
9%
Degenerative Disease
9%
Antisense Oligonucleotide
9%
Nervous System
9%
Neuroscience
Amyotrophic Lateral Sclerosis
100%
Primary Lateral Sclerosis
100%
Neurodegenerative Disorder
9%
Antisense Oligonucleotide
9%
Nervous System
9%
SOD1
9%
Loss of Function Mutation
9%