Standout Papers

Prions 1982 2026 1996 2011 4.5k
  1. Prions (1998)
    Stanley B. Prusiner Proceedings of the National Academy of Sciences
  2. Novel Proteinaceous Infectious Particles Cause Scrapie (1982)
    Stanley B. Prusiner Science
  3. Molecular Biology of Prion Diseases (1991)
    Stanley B. Prusiner Science
  4. Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein (1992)
    Hansruedi Büeler, Marek Fischer et al. Nature
  5. A cellular gene encodes scrapie PrP 27-30 protein (1985)
    Bruno Oesch, David Westaway et al. Cell
  6. Eight prion strains have PrPSc molecules with different conformations (1998)
    Jiri Safar, Holger Wille et al. Nature Medicine
  7. Identification of a Protein That Purifies with the Scrapie Prion (1982)
    David C. Bolton, Michael P. McKinley et al. Science
  8. Scrapie prions aggregate to form amyloid-like birefringent rods (1983)
    Stanley B. Prusiner, Michael P. McKinley et al. Cell
  9. Synthetic Mammalian Prions (2004)
    Giuseppe Legname, Ilia V. Baskakov et al. Science
  10. Prion Protein Biology (1998)
    Stanley B. Prusiner, Michael R. Scott et al. Cell
  11. A protease-resistant protein is a structural component of the Scrapie prion (1983)
    Michael P. McKinley, David C. Bolton et al. Cell
  12. Prion Diseases and the BSE Crisis (1997)
    Stanley B. Prusiner Science
  13. Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication (1990)
    Stanley B. Prusiner, Michael Scott et al. Cell
  14. Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion Diversity (1996)
    Glenn C. Telling, Piero Parchi et al. Science
  15. Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein (1995)
    Glenn C. Telling, Michael Scott et al. Cell
  16. Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene (1986)
    Konrad Basler, Bruno Oesch et al. Cell
  17. Linkage of a prion protein missense variant to Gerstmann–Sträussler syndrome (1989)
    Karen Hsiao, Harry F. Baker et al. Nature
  18. A Transmembrane Form of the Prion Protein in Neurodegenerative Disease (1998)
    Ramanujan S. Hegde, James A. Mastrianni et al. Science
  19. Structure of the recombinant full-length hamster prion protein PrP(29–231): The N terminus is highly flexible (1997)
    David G. Donne, John H. Viles et al. Proceedings of the National Academy of Sciences
  20. Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques (1989)
    Michael Scott, Dallas Foster et al. Cell
  21. Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonism (2015)
    Stanley B. Prusiner, Amanda L. Woerman et al. Proceedings of the National Academy of Sciences
  22. Neurodegenerative Diseases and Prions (2001)
    Stanley B. Prusiner New England Journal of Medicine
  23. Separation and properties of cellular and scrapie prion proteins. (1986)
    R. Meyer, Michael P. McKinley et al. Proceedings of the National Academy of Sciences
  24. Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains (1996)
    Martin Vey, Holger Wille et al. Proceedings of the National Academy of Sciences
  25. Formic acid pretreatment enhances immunostaining of cerebral and systemic amyloids. (1987)
    Tetsuyuki Kitamoto, Koji Ogomori et al. PubMed
  26. Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation (1997)
    Kiyotoshi Kaneko, Laurence Zulianello et al. Proceedings of the National Academy of Sciences
  27. Evidence for synthesis of scrapie prion proteins in the endocytic pathway. (1992)
    David Borchelt, Albert Taraboulos et al. Journal of Biological Chemistry
  28. Spontaneous Neurodegeneration in Transgenic Mice with Mutant Prion Protein (1990)
    Karen Hsiao, Michael Scott et al. Science
  29. Slow transmissible diseases of the nervous system (1979)
    Stanley B. Prusiner, W. J. Hadlow Academic Press eBooks
  30. Distinct prion proteins in short and long scrapie incubation period mice (1987)
    David Westaway, Patricia A. Goodman et al. Cell
  31. Purification and structural studies of a major scrapie prion protein (1984)
    Stanley B. Prusiner, Darlene Groth et al. Cell
  32. Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform (1997)
    Thomas Leroy James, He Liu et al. Proceedings of the National Academy of Sciences
  33. Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies. (1993)
    Stanley B. Prusiner, Darlene Groth et al. Proceedings of the National Academy of Sciences
  34. Further purification and characterization of scrapie prions (1982)
    Stanley B. Prusiner, David C. Bolton et al. Biochemistry
  35. Structural Clues to Prion Replication (1994)
    Fred E. Cohen, Keh‐Ming Pan et al. Science
  36. Scrapie prion proteins are synthesized in neurons. (1986)
    H. A. Kretzschmar, Stanley B. Prusiner et al. PubMed
  37. Linkage of prion protein and scrapie incubation time genes (1986)
    George A. Carlson, David T. Kingsbury et al. Cell
  38. Characterization of cloned cDNA representing rat myelin basic protein: Absence of expression in brain of shiverer mutant mice (1983)
    Arthur Roach, Khrista Boylan et al. Cell
  39. Scrapie-infected murine neuroblastoma cells produce protease-resistant prion proteins (1988)
    Michael R. Scott, Jeffrey M. Bockman et al. Journal of Virology
  40. Measurement of the scrapie agent using an incubation time interval assay (1982)
    Stanley B. Prusiner, S. Patricia Cochran et al. Annals of Neurology
  41. Predicted alpha-helical regions of the prion protein when synthesized as peptides form amyloid. (1992)
    Marı́a Gasset, M. A. Baldwin et al. Proceedings of the National Academy of Sciences
  42. Molecular Cloning of a Human Prion Protein cDNA (1986)
    Hans A. Kretzschmar, Linda Stowring et al. DNA

Immediate Impact

25 by Nobel laureates 120 from Science/Nature 167 standout
Sub-graph 1 of 13

Citing Papers

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84 intermediate papers

Works of Stanley B. Prusiner being referenced

Evidence for assembly of prions with left-handed β-helices into trimers
2004
Novel Proteinaceous Infectious Particles Cause Scrapie
1982 StandoutScience
and 107 more

Author Peers

Author Last Decade Papers Cites
Stanley B. Prusiner 61621 31101 25393 523 67.7k
Adriano Aguzzi 27961 12474 7268 544 41.2k
Susan Lindquist 44333 5612 3486 295 55.7k
Konrad Beyreuther 20903 4041 4970 436 40.5k
Hans A. Kretzschmar 18635 9078 4312 288 31.8k
Fred E. Cohen 22452 7382 6903 180 25.9k
John Collinge 19563 10479 6961 332 21.6k
William M. Pardridge 16947 5860 1960 491 39.5k
Roland Riek 16991 3107 2652 278 24.8k
Peter T. Lansbury 17957 4630 2031 222 34.8k
Bart De Strooper 26248 6072 1671 382 50.4k

All Works

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