Dilliott, Allison A.

Association of plasma biomarkers with cognition, cognitive decline, and daily function across and within neurodegenerative diseases: Results from the Ontario Neurodegenerative Disease Research Initiative

Sanchez, E., Wilkinson, T., Coughlan, G., Mirza, S., Baril, A., Ramirez, J., Binns, M. A., Black, S. E., Borrie, M., Dilliott, A. A., et al. (2024) · Alzheimer's & Dementia

Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatments

Cited by 62

Characterizing proteomic and transcriptomic features of missense variants in amyotrophic lateral sclerosis genes

Dilliott, A. A., Rouleau, G. A., Iqbal, S., & Farhan, S. M. K. (2022) · Brain

Amyotrophic Lateral Sclerosis ResearchGenomics and Rare Diseases

Cited by 8

Characterizing proteomic and transcriptomic features of missense variants in amyotrophic lateral sclerosis genes

Dilliott, A. A., Kwon, S., Rouleau, G. A., Iqbal, S., & Farhan, S. M. K. (2023) · Brain

Amyotrophic Lateral Sclerosis ResearchGenomics and Rare Diseases

Cited by 8

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

Cited by 5

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

Cited by 5