Biochemistry, Genetics and Molecular Biology
Nested Gene
92%
Association
84%
Mutation
64%
Genetics
49%
Survival
24%
Genome-Wide Association Study
23%
Protein
22%
Phenotype
20%
Age
19%
Sample
19%
Genotyping
15%
Heritability
15%
Genetic Risk
15%
Motor Neuron
15%
Genetic Architecture
14%
Mendelian Randomization
14%
Chromosome
13%
Single-Nucleotide Polymorphism
13%
C9orf72
13%
DNA
12%
Exome Sequencing
12%
Transactive Response Dna Binding Protein-43
12%
Genome Sequencing
12%
Genetic Divergence
11%
Iron
11%
Single Nucleotide Polymorphism
10%
LRRK2
10%
Autosomal Recessive Inheritance
10%
Haplotype
10%
DNA Methylation
9%
Allele
9%
Smoking
9%
Childhood
8%
Kinase
8%
Candidate Gene
8%
Microsatellite Marker
8%
Type IV Collagen
8%
Complex Genomic Disorder
8%
Exon
7%
Gene Linkage Disequilibrium
7%
Basement Membrane
6%
Time
6%
PINK1
6%
C-Terminus
6%
Position
6%
Leucine-Rich Repeat
6%
Case-Control Study
6%
Penetrance
5%
Telomere Length
5%
Antibody
5%
Neuroscience
Amyotrophic Lateral Sclerosis
100%
Parkinson's Disease
63%
Gene
62%
Frontotemporal Dementia
19%
Neurodegenerative Disorder
16%
Motor Neurone Disease
14%
Meta-Analysis
14%
Phenotype
14%
Motor Neuron
12%
Polymorphism
12%
Protein
12%
Genotype
11%
Spinal Muscular Atrophy
10%
Brain
10%
Genome-Wide Association Study
9%
Genetic Variation
8%
Alzheimer's Disease
7%
Exon
7%
Single-Nucleotide Polymorphism
7%
DNA Methylation
5%
Parkin
5%
Genetics of Parkinson's Disease
5%
Medicine and Dentistry
Amyotrophic Lateral Sclerosis
34%
Patient
29%
Parkinson's Disease
25%
Gene
21%
Degenerative Motor System Disorder
14%
Diseases
14%
Association
11%
Survival
9%
Inpatient
9%
Therapeutic Procedure
9%
Genome Wide Association Study
8%
Gastrostomy
8%
Analysis
8%
Phenotype
8%
Heritability
6%
Clinician
5%
Assessment
5%
Placebo
5%
Smoking
5%
Amaurosis
5%
Symptom
5%
Family
5%
