List of works - Hans Kretzschmar

A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the rule

scientific article published on 24 September 2007

Amyloid precursor protein intracellular domain modulates cellular calcium homeostasis and ATP content.

scientific article published in August 2007

Analyses of protease resistance and aggregation state of abnormal prion protein across the spectrum of human prions

scientific article published on 29 July 2013

Analysis of RNA Expression Profiles Identifies Dysregulated Vesicle Trafficking Pathways in Creutzfeldt-Jakob Disease

scientific article published on 16 November 2018

Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins

scientific article published on 17 October 2013

CSF amyloid-β peptides in neuropathologically diagnosed dementia with Lewy bodies and Alzheimer's disease.

scientific article published in January 2011

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

scientific article

Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA

scientific article published on 30 June 2012

Different CSF β-amyloid processing in Alzheimer’s and Creutzfeldt–Jakob disease

scientific article published on 06 January 2011

Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJD.

scientific article published on 29 January 2004

Effects of formalin fixation, paraffin embedding, and time of storage on DNA preservation in brain tissue: a BrainNet Europe study

scientific article published on 23 April 2007

Gamma-secretase inhibition reduces spine density in vivo via an amyloid precursor protein-dependent pathway.

scientific article published in August 2009

Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis

scientific article published on 27 October 2010

Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy

scientific article published on 16 June 2015

Heart fatty acid binding protein as a potential diagnostic marker for neurodegenerative diseases.

scientific article

Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification

scientific article published on 29 August 2009

Inter-laboratory comparison of neuropathological assessments of β-amyloid protein: a study of the BrainNet Europe consortium

scientific article published on 15 March 2008

Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype

scientific article published on 26 July 2012

Microglial Cx3cr1 knockout prevents neuron loss in a mouse model of Alzheimer's disease

scientific article

Mixed brain pathologies in dementia: the BrainNet Europe consortium experience

scientific article published on 10 October 2008

Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

scientific article published on 25 December 2011

R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia

scientific article

Serum heart-type fatty acid-binding protein and cerebrospinal fluid tau: marker candidates for dementia with Lewy bodies

scientific article

Staging of neurofibrillary pathology in Alzheimer's disease: a study of the BrainNet Europe Consortium

scientific article published on 26 March 2008

Tau protein, Abeta42 and S-100B protein in cerebrospinal fluid of patients with dementia with Lewy bodies

scientific article published on 5 January 2005

hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations

scientific article published on 5 February 2013

List of works by Hans Kretzschmar

A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the rule

Amyloid precursor protein intracellular domain modulates cellular calcium homeostasis and ATP content.

Analyses of protease resistance and aggregation state of abnormal prion protein across the spectrum of human prions

Analysis of RNA Expression Profiles Identifies Dysregulated Vesicle Trafficking Pathways in Creutzfeldt-Jakob Disease

Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins

CSF amyloid-β peptides in neuropathologically diagnosed dementia with Lewy bodies and Alzheimer's disease.

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA

Different CSF β-amyloid processing in Alzheimer’s and Creutzfeldt–Jakob disease

Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJD.

Effects of formalin fixation, paraffin embedding, and time of storage on DNA preservation in brain tissue: a BrainNet Europe study

Gamma-secretase inhibition reduces spine density in vivo via an amyloid precursor protein-dependent pathway.

Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis

Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy

Heart fatty acid binding protein as a potential diagnostic marker for neurodegenerative diseases.

Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification

Inter-laboratory comparison of neuropathological assessments of β-amyloid protein: a study of the BrainNet Europe consortium

Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype

Microglial Cx3cr1 knockout prevents neuron loss in a mouse model of Alzheimer's disease

Mixed brain pathologies in dementia: the BrainNet Europe consortium experience

Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia

Serum heart-type fatty acid-binding protein and cerebrospinal fluid tau: marker candidates for dementia with Lewy bodies

Staging of neurofibrillary pathology in Alzheimer's disease: a study of the BrainNet Europe Consortium

Tau protein, Abeta42 and S-100B protein in cerebrospinal fluid of patients with dementia with Lewy bodies

hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations