Selective genetic overlap between amyotrophic lateral sclerosis and diseases of the frontotemporal dementia spectrum

Keyphrases

• Amyotrophic Lateral Sclerosis 100%
• Frontotemporal Dementia 100%
• Genetic Overlap 100%
• Arbitrary Units 38%
• Progressive Supranuclear Palsy 28%
• Neurodegenerative Diseases 14%
• BNIP1 14%
• Alzheimer's Disease 9%
• Mouse Model 9%
• Parkinson's Disease 9%
• Risk Genes 9%
• Corticobasal Degeneration 9%
• Functional Pathways 9%
• H1 Haplotype 9%
• Genetic Variants 4%
• Human Brain 4%
• Common Genetic Variants 4%
• Superoxide Dismutase 1 (SOD1) 4%
• Polymorphism 4%
• C9orf72 4%
• Dementia with 4%
• Lower Motor Neuron 4%
• SOD1G93A Mice 4%
• Spinal Motor Neurons 4%
• Anti-apoptotic Proteins 4%
• Neuronal Function 4%
• Means of Control 4%
• Mitophagy 4%
• Neuronal Development 4%
• WT Mice 4%
• Shared Genetic Risk 4%
• Novel Locus 4%
• Consensus Criteria 4%
• Polygenic Disorder 4%
• Upper Motor Neuron 4%
• Shared Risk 4%
• Conjunction Analysis 4%
• TDP-43 Inclusions 4%
• UNC13A 4%
• ERGIC1 4%
• Conditional FDR 4%

Neuroscience

• Amyotrophic Lateral Sclerosis 100%
• Frontotemporal Dementia 100%
• Progressive Supranuclear Palsy 28%
• Neurodegenerative Disorder 14%
• Alzheimer's Disease 9%
• Parkinson's Disease 9%
• SOD1 9%
• Corticobasal Degeneration 9%
• Haplotype 9%
• Lower Motor Neuron 4%
• Mitophagy 4%
• Upper Motor Neuron 4%
• Human Brain 4%