Prion Diseases

Prion disease is a transmissible neurodegenerative disorder caused by pathogenic isoforms of prion protein that propagate through neural tissue by inducing conformational misfolding of normal cellular prion protein, resulting in progressive neuronal degeneration and death.

6.5K

Publications

469.5K

Citations

16.3K

Authors

3.1K

Institutions

Publications per year

2017–2026

833

Authors

16.3K

  1. SB
    Stanley B. Prusiner

    University of California, San Francisco, United States

    268 publications · 53.9K citations

    124

    h-index

  2. BC
    Byron Caughey

    National Institute of Allergy and Infectious Diseases, United States

    136 publications · 17.9K citations

    72

    h-index

  3. AA
    Adriano Aguzzi

    University Hospital of Zurich, Switzerland

    154 publications · 18.4K citations

    69

    h-index

  4. JC
    John Collinge

    University College London, United Kingdom

    166 publications · 18.8K citations

    69

    h-index

  5. SJ
    Stephen J. DeArmond

    University of California, San Francisco, United States

    102 publications · 17.2K citations

    61

    h-index

1–5 of 16.3K

Venues

  1. Proceedings of the National Academy of Sciences

    PNAS · 243 publications · 43.6K citations

    123

    h-index

  2. Journal of Biological Chemistry

    JBC · 296 publications · 26.2K citations

    94

    h-index

  3. Journal of General Virology

    304 publications · 22.9K citations

    87

    h-index

  4. Journal of Virology

    JVI · 280 publications · 23.2K citations

    85

    h-index

  5. PLoS Pathogens

    134 publications · 9.4K citations

    59

    h-index

1–5

See also

Prion Diseases

Molecular Mechanisms

Diagnosis

Transmission Routes

Clinical Variants

Therapeutic Strategies