Keywords
Dementia; Genetics; Neurodegeneration; Neurodegenerative Diseases
Selected publications
- König, T. et al. (2022) ‘C9orf72 repeat length might influence clinical sub-phenotypes in dementia patients’, Neurobiology of Disease, 175, p. 105927. Available at: http://dx.doi.org/10.1016/j.nbd.2022.105927.
- Mir, R. et al. (2018) ‘The Parkinson’s disease VPS35[D620N] mutation enhances LRRK2-mediated Rab protein phosphorylation in mouse and human’, Biochemical Journal, 475(11), pp. 1861–1883. Available at: http://dx.doi.org/10.1042/bcj20180248.
- Parvizi, T. et al. (2022) ‘Real-world applicability of glial fibrillary acidic protein and neurofilament light chain in Alzheimer’s disease’, Frontiers in Aging Neuroscience, 14. Available at: http://dx.doi.org/10.3389/fnagi.2022.887498.
- Dorninger, F. et al. (2019) ‘Disturbed neurotransmitter homeostasis in ether lipid deficiency’, Human Molecular Genetics, 28(12), pp. 2046–2061. Available at: http://dx.doi.org/10.1093/hmg/ddz040.
- Meka, D.P. et al. (2019) ‘Radial somatic F‐actin organization affects growth cone dynamics during early neuronal development’, EMBO reports, 20(12). Available at: http://dx.doi.org/10.15252/embr.201947743.