Biochemistry, Genetics and Molecular Biology
Mutation
94%
Nested Gene
89%
Phenotype
63%
Mental Retardation
46%
Genetics
34%
SOD1
24%
Haploinsufficiency
24%
Chromosome
16%
FUS
16%
Sequencing
16%
Survival
15%
Spectrum
12%
Upper Motor Neuron
11%
TCF4
11%
Association
11%
Wolf-Hirschhorn Syndrome
10%
TARDBP
10%
TAR DNA Binding Protein
9%
Induced Pluripotent Stem Cell
9%
SYNGAP1
9%
Glutamate
9%
Exome Sequencing
8%
Autosomal Recessive Inheritance
8%
Array Comparative Genomic Hybridization
8%
Genotype Phenotype Correlation
8%
ATXN2
7%
Length
7%
Loss of Function Mutation
7%
Allele
6%
Fibroblast
6%
Chromosome Regions
6%
Candidate Gene
6%
Magnetic Resonance Imaging
6%
CHRNA4
5%
Age
5%
Speech
5%
Microdeletion Syndrome
5%
Modulation
5%
Electric Potential
5%
Medical Genetics
5%
Genome-Wide Association Study
5%
Medicine and Dentistry
Patient
56%
Amyotrophic Lateral Sclerosis
45%
Gene
42%
Syndrome
37%
Diseases
24%
Intellectual Disability
23%
Epileptic Seizure
21%
Diagnosis
14%
Phenotype
14%
Neuron
14%
Combination Therapy
13%
Induced Pluripotent Stem Cell
12%
Haploinsufficiency
11%
Wolf-Hirschhorn Syndrome
10%
Epilepsy
10%
Glutamic Acid
9%
Motor Neuron
6%
Analysis
6%
Association
6%
Pluripotent Stem Cell Line
6%
Craniofacial Synostosis
6%
Girl
6%
Family
5%
Microcephaly
5%
Facies
5%
Clinical Genetics
5%
Neuroscience
Amyotrophic Lateral Sclerosis
100%
Gene
45%
SOD1
23%
Phenotype
22%
Intellectual Disability
20%
Upper Motor Neuron
13%
Kinesin
9%
Lower Motor Neuron
8%
Neurodegenerative Disorder
8%
Exon
7%
Polyglutamine
6%
Frontotemporal Dementia
6%
CHRNA4
5%
Genome-Wide Association Study
5%
