Paweł P. Liberski

Research interests

Publications

• Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study

  The Lancet Neurology · 2020 · https://doi.org/10.1016/s1474-4422(20)30273-8

• Cerebrospinal fluid neurofilament light levels in neurodegenerative dementia: Evaluation of diagnostic accuracy in the differential diagnosis of prion diseases

  Alzheimer s & Dementia · 2018 · https://doi.org/10.1016/j.jalz.2017.12.008

• Germline and somatic FGFR1 abnormalities in dysembryoplastic neuroepithelial tumors

  Acta Neuropathologica · 2016 · 10.1007/s00401-016-1549-x

• The sheddase ADAM10 is a potent modulator of prion disease

  eLife · 2015 · https://doi.org/10.7554/elife.04260

• Astrocyte Depletion Impairs Redox Homeostasis and Triggers Neuronal Loss in the Adult CNS

  Cell Reports · 2015 · 10.1016/j.celrep.2015.07.051

• The toxicity of antiprion antibodies is mediated by the flexible tail of the prion protein

  Nature · 2013 · 10.1038/nature12402

• Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR

  Nature Genetics · 2013 · 10.1038/ng.2849

• Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas

  Acta Neuropathologica · 2013 · https://doi.org/10.1007/s00401-013-1095-8

• Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma

  Nature · 2012 · https://doi.org/10.1038/nature10833

• Hotspot Mutations in H3F3A and IDH1 Define Distinct Epigenetic and Biological Subgroups of Glioblastoma

  Cancer Cell · 2012 · https://doi.org/10.1016/j.ccr.2012.08.024

• Glioma cells showing IDH1 mutation cannot be propagated in standard cell culture conditions

  British Journal of Cancer · 2011 · 10.1038/bjc.2011.27

• De novo generation of a transmissible spongiform encephalopathy by mouse transgenesis

  Proceedings of the National Academy of Sciences · 2008 · 10.1073/pnas.0810680105

• Molecular Profiling Identifies Prognostic Subgroups of Pediatric Glioblastoma and Shows Increased YB-1 Expression in Tumors

  Journal of Clinical Oncology · 2007 · 10.1200/jco.2006.07.8626

• Neuronal cell death in transmissible spongiform encephalopathies (prion diseases) revisited: from apoptosis to autophagy

  The International Journal of Biochemistry & Cell Biology · 2004 · 10.1016/j.biocel.2004.04.016

• Autophagy is a part of ultrastructural synaptic pathology in Creutzfeldt–Jakob disease: a brain biopsy study

  The International Journal of Biochemistry & Cell Biology · 2004 · https://doi.org/10.1016/j.biocel.2004.04.014

• Papillary Tumor of the Pineal Region

  The American Journal of Surgical Pathology · 2003 · https://doi.org/10.1097/00000478-200304000-00011

• Coexistence of Alzheimer-type neuropathology in Creutzfeldt-Jakob disease

  Acta Neuropathologica · 1998 · 10.1007/s004010050870

• Severe, Early and Selective Loss of a Subpopulation of GABAergic Inhibitory Neurons in Experimental Transmissible Spongiform Encephalopathies

  Brain Pathology · 1998 · 10.1111/j.1750-3639.1998.tb00188.x

• Heightened expression of tumor necrosis factor alpha, interleukin 1 alpha, and glial fibrillary acidic protein in experimental Creutzfeldt-Jakob disease in mice.

  Proceedings of the National Academy of Sciences · 1996 · 10.1073/pnas.93.18.9754

• The Original Gerstmann‐Sträussler‐Scheinker Family of Austria: Divergent Clinicopathological Phenotypes but Constant PrP Genotype

  Brain Pathology · 1995 · 10.1111/j.1750-3639.1995.tb00596.x

Current projects

No projects listed.