Rosa Rademakers, Ph.D.
Affiliations: | Neuroscience | Mayo Clinic Jacksonville, Jacksonville, FL, United States |
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Sign in to add trainee| Thomas A Ravenscroft | research assistant | 2012-2016 | Mayo Clinic Jacksonville |
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Publications
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| Vandebergh M, Ramos EM, Corriveau-Lecavalier N, et al. (2024) Gene specific effects on brain volume and cognition of in frontotemporal lobar degeneration. Medrxiv : the Preprint Server For Health Sciences |
| Valentino RR, Scotton WJ, Roemer SF, et al. (2024) MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study. The Lancet. Neurology. 23: 487-499 |
| Wang H, Chang TS, Dombroski BA, et al. (2023) Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy. Medrxiv : the Preprint Server For Health Sciences |
| Badihian N, Ali F, Botha H, et al. (2023) The MAPT P.G324L and P.A406G mutations are associated with progressive supranuclear palsy with atypical features. Parkinsonism & Related Disorders. 119: 105962 |
| Grossman M, Seeley WW, Boxer AL, et al. (2023) Frontotemporal lobar degeneration. Nature Reviews. Disease Primers. 9: 40 |
| Matchett BJ, Lincoln SJ, Baker M, et al. (2023) The SERPINA5 coding variant E228Q does not contribute to clinicopathologic characteristics in Alzheimer's disease: A cross-sectional study. Medicine. 102: e34017 |
| Valentino RR, Scotton WJ, Roemer SF, et al. (2023) Creating the Pick's disease International Consortium: Association study of H2 haplotype with risk of Pick's disease. Medrxiv : the Preprint Server For Health Sciences |
| T Vicente C, Perneel J, Wynants S, et al. (2023) C-terminal TMEM106B fragments in human brain correlate with disease-associated TMEM106B haplotypes. Brain : a Journal of Neurology |
| Perneel J, Manoochehri M, Huey ED, et al. (2023) Case report: TMEM106B haplotype alters penetrance of GRN mutation in frontotemporal dementia family. Frontiers in Neurology. 14: 1160248 |
| Lee H, Mackenzie IRA, Beg MF, et al. (2022) White-matter abnormalities in presymptomatic and mutation carriers. Brain Communications. 5: fcac333 |