Houlden, Henry

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Association of common genetic variants with brain microbleeds: a genome-wide association study

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Analysis of Mutations in AARS2 in a Series of CSF1R-Negative Patients With Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia

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Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21–22

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Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research

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Modeling late-onset Alzheimer’s disease neuropathology via direct neuronal reprogramming

Sun, Z., Kwon, J.-S., Ren, Y., Chen, S., Walker, C. K., Lu, X., Cates, K., Karahan, H., Sviben, S., Fitzpatrick, J. A. J., et al. (2024) · Science

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Recapitulation of Endogenous 4R Tau Expression and Formation of Insoluble Tau in Directly Reprogrammed Human Neurons

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c-Jun expression in human neuropathies: a pilot study

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Mutation in FAM134B causing severe hereditary sensory neuropathy: Figure 1

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A novel human pain insensitivity disorder caused by a point mutation in ZFHX2

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Confirmation that familial clustering and age of onset in late onset Alzheimer's disease are determined at the apolipoprotein E locus

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The annotation of GBA1 has been concealed by its protein-coding pseudogene GBAP1

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Mutations in XRCC1 cause cerebellar ataxia and peripheral neuropathy

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Assessment of APOE in atypical parkinsonism syndromes

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Concomitant progressive supranuclear palsy and chronic traumatic encephalopathy in a boxer

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