Ekaterina Rogaeva
Affiliations: | Tanz Centre for Research in Neurodegenerative Disease | University of Toronto, Toronto, ON, Canada |
Google:
"Ekaterina Rogaeva"Mean distance: (not calculated yet)
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Rajabli F, Benchek P, Tosto G, et al. (2023) Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies and nominates ancestry-specific loci , , and as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. Medrxiv : the Preprint Server For Health Sciences |
| Li S, Poon CH, Zhang Z, et al. (2023) MicroRNA-128 suppresses tau phosphorylation and reduces amyloid-beta accumulation by inhibiting the expression of GSK3β, APPBP2, and mTOR in Alzheimer's disease. Cns Neuroscience & Therapeutics |
| Couto B, Martinez-Valbuena I, Lee S, et al. (2022) Protracted Course-Progressive Supranuclear Palsy (PC-PSP). European Journal of Neurology |
| Dilliott AA, Abdelhady A, Sunderland KM, et al. (2021) Contribution of rare variant associations to neurodegenerative disease presentation. Npj Genomic Medicine. 6: 80 |
| Zhang Y, Zhang Y, Aman Y, et al. (2021) Amyloid-β toxicity modulates tau phosphorylation through the PAX6 signalling pathway. Brain : a Journal of Neurology |
| Lai D, Alipanahi B, Fontanillas P, et al. (2021) Genome-wide association studies of LRRK2 modifiers of Parkinson's disease. Annals of Neurology |
| Chia R, Sabir MS, Bandres-Ciga S, et al. (2021) Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture. Nature Genetics |
| Ayodele T, Rogaeva E, Kurup JT, et al. (2021) Early-Onset Alzheimer's Disease: What Is Missing in Research? Current Neurology and Neuroscience Reports. 21: 4 |
| Reitz C, Rogaeva E, Beecham GW. (2020) Late-onset vs nonmendelian early-onset Alzheimer disease: A distinction without a difference? Neurology. Genetics. 6: e512 |
| Ramirez J, Dilliott AA, Binns MA, et al. (2020) Parkinson's Disease, NOTCH3 Genetic Variants, and White Matter Hyperintensities. Movement Disorders : Official Journal of the Movement Disorder Society |