Items where authors include "Synofzik, M."

Article

Mengel, D. orcid.org/0000-0002-4133-7182, Soter, E., Ott, J.M. et al. (42 more authors) (2025) Blood biomarkers confirm subjective cognitive decline (SCD) as a distinct molecular and clinical stage within the NIA-AA framework of Alzheimer´s disease. Molecular Psychiatry, 30 (7). pp. 3150-3159. ISSN 1359-4184

Baumeister, H., Gellersen, H.M., Polk, S.E. et al. (48 more authors) (2025) Disease stage–specific atrophy markers in Alzheimer's disease. Alzheimer's & Dementia, 21 (7). e70482. ISSN 1552-5260

Chelban, V. orcid.org/0000-0002-7797-0756, Pellerin, D., Vijiaratnam, N. orcid.org/0000-0002-9671-0212 et al. (50 more authors) (2025) Intronic FGF14 GAA repeat expansions impact progression and survival in multiple system atrophy. Brain. ISSN 0006-8950

Rudolph, J. orcid.org/0000-0002-4849-8034, Rueckel, J., Döpfert, J. et al. (35 more authors) (2024) Artificial intelligence–based rapid brain volumetry substantially improves differential diagnosis in dementia. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring, 16 (4). e70037. ISSN 2352-8729

Chatterjee, M., Özdemir, S., Fritz, C. et al. (82 more authors) (2024) Plasma extracellular vesicle tau and TDP-43 as diagnostic biomarkers in FTD and ALS. Nature Medicine, 30. pp. 1771-1783. ISSN 1078-8956

Currò, R., Dominik, N., Facchini, S. et al. (155 more authors) (2024) Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease. Brain, 147 (5). pp. 1887-1898. ISSN 0006-8950

Hayek, D., Ziegler, G., Kleineidam, L. et al. (55 more authors) (2024) Different inflammatory signatures based on CSF biomarkers relate to preserved or diminished brain structure and cognition. Molecular Psychiatry, 29 (4). pp. 992-1004. ISSN 1359-4184

Brosseron, F., Maass, A., Kleineidam, L. et al. (49 more authors) (2023) Serum IL-6, sAXL, and YKL-40 as systemic correlates of reduced brain structure and function in Alzheimer’s disease: results from the DELCODE study. Alzheimer's Research & Therapy, 15. 13. ISSN 1758-9193

Souche, E., Beltran, S., Brosens, E. et al. (28 more authors) (2022) Recommendations for whole genome sequencing in diagnostics for rare diseases. European Journal of Human Genetics, 30 (9). pp. 1017-1021. ISSN 1018-4813