Biochemistry, Genetics and Molecular Biology
Nested Gene
92%
Mutation
77%
Association
68%
Desmin
34%
Survival
33%
Genetics
27%
C9orf72
25%
Phenotype
23%
Sample
23%
Genome-Wide Association Study
22%
Whole Genome Sequencing
20%
Age
19%
Protein
17%
Haplotype
16%
Chromosome
16%
Single-Nucleotide Polymorphism
15%
Genotyping
13%
DNA Methylation
12%
Genetic Architecture
11%
Length
11%
Expression Quantitative Trait Loci
10%
Next Generation Sequencing
10%
Development
9%
Chromosome 9
9%
Allele
9%
Genetic Divergence
8%
Genetic Linkage
8%
Telomere Length
8%
DNA
7%
Prion
7%
Introspection
7%
Heritability
7%
Single Nucleotide Polymorphism
7%
Mutant
7%
Mendelian Randomization
7%
SOD1
6%
Trinucleotide Repeat Expansion
6%
FUS
6%
Exome Sequencing
6%
Motor Neuron
5%
Genetic Determinism
5%
Probe
5%
Electric Potential
5%
Screening
5%
Genetic Disorder
5%
Kinesin
5%
Clinical Trial
5%
Weight
5%
Untranslated Region
5%
DNA Sequencing
5%
Medicine and Dentistry
Patient
43%
Desmin
42%
Amyotrophic Lateral Sclerosis
35%
Gene
30%
Myopathy
28%
Muscle
22%
Family
21%
Disease
17%
Association
17%
Phenotype
17%
Tail
9%
Analysis
9%
Age
9%
Muscle Biopsy
8%
Inclusion Body Myositis
8%
Progressive Supranuclear Palsy
8%
Mendelian Randomization Analysis
8%
Protein
7%
Genome Wide Association Study
7%
Inpatient
7%
Cardiomyopathy
7%
Restrictive Cardiomyopathy
6%
Blood
6%
T Cell
6%
Muscle Weakness
5%
Muscular Dystrophy
5%
Autosomal Dominant Inheritance
5%
Degenerative Disease
5%
Nerve Block
5%
Neuroscience
Amyotrophic Lateral Sclerosis
100%
Gene
35%
Desmin
25%
Muscle Disorder
19%
Meta-Analysis
18%
Neurodegenerative Disorder
17%
Frontotemporal Dementia
16%
Phenotype
16%
Genome-Wide Association Study
13%
Genetic Variation
11%
SOD1
10%
Single-Nucleotide Polymorphism
9%
Chromosome
7%
Genotype
6%
Protein
6%
Motor Neuron
6%
Parkinson's Disease
5%
Haplotype
5%
Whole Genome Sequencing
5%
Chromosome 9
5%
Alzheimer's Disease
5%
Untranslated Region
5%
