Sigrun Roeber, MD
Affiliations: | 2003- | Neuropathology | Ludwig-Maximilians-Universität München, München, Bayern, Germany |
Area:
Neural degenerationWebsite:
https://www.en.neuropathologie.med.uni-muenchen.de/publications/roeber_s/index.htmlGoogle:
"Sigrun Roeber"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Hans A. Kretzschmar | research scientist | 2014 | Ludwig Maximilian University Munich |
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Publications
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| 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 |
| 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 |
| Briel N, Ruf VC, Pratsch K, et al. (2022) Single-nucleus chromatin accessibility profiling highlights distinct astrocyte signatures in progressive supranuclear palsy and corticobasal degeneration. Acta Neuropathologica |
| Kovacs GG, Lukic MJ, Irwin DJ, et al. (2020) Distribution patterns of tau pathology in progressive supranuclear palsy. Acta Neuropathologica |
| Cali CP, Patino M, Tai YK, et al. (2019) C9orf72 intermediate repeats are associated with corticobasal degeneration, increased C9orf72 expression and disruption of autophagy. Acta Neuropathologica |
| Gasparoni G, Bultmann S, Lutsik P, et al. (2018) DNA methylation analysis on purified neurons and glia dissects age and Alzheimer's disease-specific changes in the human cortex. Epigenetics & Chromatin. 11: 41 |
| Roeber S, Müller-Sarnowski F, Kress J, et al. (2015) Three novel presenilin 1 mutations marking the wide spectrum of age at onset and clinical patterns in familial Alzheimer's disease. Journal of Neural Transmission (Vienna, Austria : 1996) |
| Kouri N, Ross OA, Dombroski B, et al. (2015) Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy. Nature Communications. 6: 7247 |
| Respondek G, Stamelou M, Kurz C, et al. (2014) The phenotypic spectrum of progressive supranuclear palsy: a retrospective multicenter study of 100 definite cases. Movement Disorders : Official Journal of the Movement Disorder Society. 29: 1758-66 |
| Craggs LJ, Yamamoto Y, Ihara M, et al. (2014) White matter pathology and disconnection in the frontal lobe in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Neuropathology and Applied Neurobiology. 40: 591-602 |