108 research outputs found

    Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes

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    Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis

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    Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia

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    Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis

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    Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

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    Protein network analysis reveals selectively vulnerable regions and biological processes in FTD

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    CXCR4 involvement in neurodegenerative diseases

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    Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies

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

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    A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

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