Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia

Keyphrases

• Frontotemporal Dementia 100%
• Progressive Supranuclear Palsy 100%
• Corticobasal Degeneration 100%
• Shared Genetic Risk 100%
• SNP 30%
• Genetic Overlap 30%
• Tauopathy 20%
• Overlapping Genes 20%
• Transcript Level 10%
• Gene Locus 10%
• Odds Ratio 10%
• Genome-wide Association Study 10%
• Risk Allele 10%
• Protein-protein Interaction 10%
• Neurodegenerative Diseases 10%
• Glia 10%
• Protein-coding Genes 10%
• Risk Genes 10%
• Genetic Risk 10%
• Clinical Evidence 10%
• Neurodevelopmental 10%
• C-X-C Chemokine Receptor Type 4 (CXCR4) 10%
• Pathobiology 10%
• Expression Change 10%
• Adult Brain 10%
• Gene Signature 10%
• Genetic Method 10%
• Omnibus 10%
• Strong Ties 10%
• Genetic Evidence 10%
• Large Genome 10%
• In Cis 10%
• Regional Vulnerability 10%
• Fold Enrichment 10%
• Gene Co-expression Network 10%
• H1 Haplotype 10%
• Shared Risk 10%
• Pathological Evidence 10%
• MAPT Haplotype 10%
• Neuronal Vulnerability 10%

Biochemistry, Genetics and Molecular Biology

• Genetics 100%
• Genetic Risk 100%
• Single Nucleotide Polymorphism 60%
• Haplotype 40%
• Overlapping Gene 40%
• Gene Locus 20%
• Gene Expression Profiling 20%
• Allele 20%
• Genome-Wide Association Study 20%
• Epidermal Growth Factor Receptor 20%
• Tau 20%
• Protein Interaction 20%
• CXCR4 20%
• Cladistics 20%
• Transcriptome 20%

Neuroscience

• Frontotemporal Dementia 100%
• Corticobasal Degeneration 100%
• Progressive Supranuclear Palsy 100%
• Haplotype 20%
• Overlapping Gene 20%
• Tauopathy 20%
• Gene Expression 10%
• Neurodegenerative Disorder 10%
• Epidermal Growth Factor Receptor 10%
• Glia 10%
• CXCR4 10%
• Genome-Wide Association Study 10%
• Gene Locus 10%
• Protein Interaction 10%
• Transcriptome 10%