Hans A. Kretzschmar

Affiliations: 
1992-2002 Neuropathology Georg-August-Universität Göttingen, Göttingen, Niedersachsen, Germany 
 2002-2014 Neuropathology and Prion Diseases Ludwig Maximilian University Munich, München, Bayern, Germany 
Area:
neurodegeneration, prions, neuropathology
Website:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8029091/
Google:
"Hans Kretzschmar"
Bio:

MD

UNIVERSITY MUNICH
NEUROPATHOLOGY DEPT
FEODOR-LYNEN STR 23
MUNICH, 81377
Germany

Mean distance: 17.87 (cluster 17)
 
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Publications

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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
Durrenberger PF, Fernando FS, Kashefi SN, et al. (2015) Common mechanisms in neurodegeneration and neuroinflammation: a BrainNet Europe gene expression microarray study. Journal of Neural Transmission (Vienna, Austria : 1996). 122: 1055-68
Tian C, Liu D, Xiang W, et al. (2014) Analyses of the similarity and difference of global gene expression profiles in cortex regions of three neurodegenerative diseases: sporadic Creutzfeldt-Jakob disease (sCJD), fatal familial insomnia (FFI), and Alzheimer's disease (AD). Molecular Neurobiology. 50: 473-81
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
Arzberger T, Mori K, Mackenzie I, et al. (2014) EPA-1718 - Neuropathological alterations in FTD cases with C9ORF72 mutation - new insights European Psychiatry. 29: 1
Mackenzie IR, Arzberger T, Kremmer E, et al. (2013) Dipeptide repeat protein pathology in C9ORF72 mutation cases: clinico-pathological correlations. Acta Neuropathologica. 126: 859-79
Schelzke G, Stoeck K, Eigenbrod S, et al. (2013) Report about four novel mutations in the prion protein gene. Dementia and Geriatric Cognitive Disorders. 35: 229-37
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