Diane Ritchie

University of Edinburgh — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

34h-index4.3kcitations100works1.22yr avg

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Research Topics

Prion Diseases and Protein Misfolding(81), Neurological diseases and metabolism(31), Trace Elements in Health(16), Alzheimer's disease research and treatments(5), Fibromyalgia and Chronic Fatigue Syndrome Research(5)

Publications99 total

The Phenotypic Spectrum of Sporadic Creutzfeldt‐Jakob Disease Cortical Subtype

Annals of Neurology·2025Open Access

Inherited prion disease caused by a novel frameshift mutation of <i>PRNP</i> resulting in protein truncation at codon 157

1 cited

Journal of Alzheimer s Disease·2025· 1 citedOpen Access

Characterization of variably protease-sensitive prionopathy by capillary electrophoresis

1 cited

Scientific Reports·2024· 1 citedOpen Access

Pathological spectrum of sporadic Creutzfeldt–Jakob disease

4 cited

Pathology·2024· 4 citedOpen Access

Characterization of Variably Protease-Sensitive Prionopathy by Capillary Electrophoresis

2024Open Access

Enhanced <scp>Creutzfeldt‐Jakob</scp> disease surveillance in the older population: Assessment of a protocol for screening brain tissue donations for prion disease

4 cited

Brain Pathology·2023· 4 citedOpen Access

Conservation of vCJD Strain Properties After Extraction and In Vitro Propagation of PrPSc from Archived Formalin-Fixed Brain and Appendix Tissues Using Highly Sensitive Protein Misfolding Cyclic Amplification

Molecular Neurobiology·2023Open Access

Prion diseases

1 cited

Elsevier eBooks·2022· 1 cited

Variant CJD: Reflections a Quarter of a Century on

33 cited

Pathogens·2021· 33 citedOpen Access

Prion strains associated with iatrogenic CJD in French and UK human growth hormone recipients

12 cited

Acta Neuropathologica Communications·2021· 12 citedOpen Access

Phenotypic diversity of genetic Creutzfeldt–Jakob disease: a histo-molecular-based classification

50 cited

Acta Neuropathologica·2021· 50 citedOpen Access

Fatal insomnia: the elusive prion disease

1 cited

BMJ Case Reports·2021· 1 citedOpen Access

Novel Morphological Glial Alterations in the Spectrum of Prion Disease Types: A Focus on Common Findings

3 cited

Pathogens·2021· 3 citedOpen Access

Prion Diseases: A Unique Transmissible Agent or a Model for Neurodegenerative Diseases?

33 cited

Biomolecules·2021· 33 citedOpen Access

Transmission characteristics of heterozygous cases of Creutzfeldt-Jakob disease with variable abnormal prion protein allotypes

37 cited

Acta Neuropathologica Communications·2020· 37 citedOpen Access

Study protocol for enhanced CJD surveillance in the 65+ years population group in Scotland: an observational neuropathological screening study of banked brain tissue donations for evidence of prion disease

5 cited

BMJ Open·2019· 5 citedOpen Access

Renewed assessment of the risk of emergent advanced cell therapies to transmit neuroproteinopathies

8 cited

Acta Neuropathologica·2018· 8 citedOpen Access

Issue Information

Annals of Neurology·2018Open Access

Sporadic Fatal Insomnia in Europe: Phenotypic Features and Diagnostic Challenges

65 cited

Annals of Neurology·2018· 65 citedOpen Access

Detection of alpha‐synuclein conformational variants from gastro‐intestinal biopsy tissue as a potential biomarker for Parkinson's disease

54 cited

Neuropathology and Applied Neurobiology·2018· 54 citedOpen Access

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Frequent Co-authors

James W. Ironside(34), Mark Head(20), Alexander Peden(9), Linda McCardle(6), Steven Williams(6), Matthew Bishop(6), Robert Will(6), Marcelo A. Barria(6), Helen Yull(5), David A. Hilton(4), Karen Brown(4), M. E. Bruce(4), Jean Manson(4), P. G. Edwards(3), Moira E. Bruce(3), Abigail B. Diack(3), Pedro Piccardo(3), Ellen Gelpí(3), Jeanne E. Bell(2), Lisa Conyers(2)