Dwosh, Emily

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

Baker, M., Mackenzie, I. R., Pickering-Brown, S. M., Gass, J., Rademakers, R., Lindholm, C., Snowden, J., Adamson, J., Sadovnick, A. D., Rollinson, S., et al. (2006) · Nature

Alzheimer's disease research and treatmentsAmyotrophic Lateral Sclerosis Research

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Enhancing variant of uncertain significance (VUS) interpretation in neurogenetics: collaborative experiences from a tertiary care centre

Horowitz, K., Fotopoulos, N. H., Mistry, A. J., Simo, J., Medeiros, M., Bucco, I. D., Ginsberg, M., Dwosh, E., La Piana, R., Rouleau, G. A., et al. (2025) · Journal of Medical Genetics

Genomics and Rare DiseasesGenetic Neurodegenerative Diseases

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Enhancing Variant of Uncertain Significance (VUS) Interpretation in Neurogenetics: Collaborative Experiences from a Tertiary Care Centre

Horowitz, K., Fotopoulos, N. H., Mistry, A. J., Simo, J., Medeiros, M., Bucco, I. D., Ginsberg, M., Dwosh, E., La Piana, R., Rouleau, G. A., et al. (2024) · Journal of Medical Genetics

Genomics and Rare DiseasesGenetic Neurodegenerative Diseases

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