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1.
Baumeister, S. et al.: Physical activity and Parkinson's disease: A two-sample Mendelian randomisation study. J. Neurol. Neurosurg. Psychiatr. 92, 334-335 (2021)
2.
Müller, K.* et al.: Comprehensive analysis of the mutation spectrum in 301 German ALS families. J. Neurol. Neurosurg. Psychiatr. 89, 817-827 (2018)
3.
Obayashi, M.* et al.: Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion. J. Neurol. Neurosurg. Psychiatr. 86, 986-995 (2015)
4.
Synofzik, M.* ; Kernstock, C.* ; Haack, T.B. & Schöls, L.*: Ataxia meets chorioretinal dystrophy and hypogonadism: Boucher-Neuhäuser syndrome due to PNPLA6 mutations. J. Neurol. Neurosurg. Psychiatr. 86, 580-581 (2015)
5.
Klebe, S.* et al.: The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism. J. Neurol. Neurosurg. Psychiatr. 84, 666-673 (2013)
6.
Horvath, R.* et al.: Leigh syndrome caused by mutations in the flavoprotein (Fp) subunit of succinate dehydrogenase (SDHA). J. Neurol. Neurosurg. Psychiatr. 77, 74-76 (2006)
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