Contact information
Olaf Ansorge
Associate Professor
Recent publications
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Isolated homozygous R217X OPTN mutation causes knock-out of functional C-terminal optineurin domains and associated oligodendrogliopathy-dominant ALS-TDP.
Journal article
Nolan M. et al, (2021), J Neurol Neurosurg Psychiatry
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Detection and Quantification of Novel C-terminal TDP-43 Fragments in ALS-TDP.
Journal article
Feneberg E. et al, (2020), Brain Pathol
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Amyotrophic lateral sclerosis with a heterozygous D91A SOD1 variant and classical ALS-TDP neuropathology.
Journal article
Feneberg E. et al, (2020), Neurology, 95, 595 - 596
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Quantitative patterns of motor cortex proteinopathy across ALS genotypes.
Journal article
Nolan M. et al, (2020), Acta Neuropathol Commun, 8
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A Noninvasive Comparison Study between Human Gliomas with IDH1 and IDH2 Mutations by MR Spectroscopy.
Journal article
Shen X. et al, (2019), Metabolites, 9