Jean Paul Vonsattel

Active 1982–2025

Also published as
Jean‐Paul Vonsattel
115
Papers
31,914
Citations
79
h-index
110
i10-index

Citations

Citations per year for Jean Paul Vonsattel1967: 1 citations1983: 1 citations1984: 1 citations1985: 1 citations1986: 6 citations1987: 11 citations1988: 10 citations1989: 10 citations1990: 20 citations1991: 21 citations1992: 21 citations1993: 31 citations1994: 39 citations1995: 106 citations1996: 116 citations1997: 163 citations1998: 148 citations1999: 194 citations2000: 266 citations2001: 262 citations2002: 250 citations2003: 267 citations2004: 281 citations2005: 274 citations2006: 324 citations2007: 275 citations2008: 279 citations2009: 330 citations2010: 390 citations2011: 404 citations2012: 328 citations2013: 280 citations2014: 311 citations2015: 282 citations2016: 308 citations2017: 354 citations2018: 308 citations2019: 875 citations2020: 966 citations2021: 1,012 citations2022: 910 citations2023: 695 citations2024: 1,085 citations2025: 522 citations2026: 11 citations1968–1982: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 5,347 citing papers, 33.1% of this breakdownUnited Kingdom: 1,356 citing papers, 8.4% of this breakdownGermany: 901 citing papers, 5.6% of this breakdownCanada: 837 citing papers, 5.2% of this breakdownChina: 781 citing papers, 4.8% of this breakdownItaly: 629 citing papers, 3.9% of this breakdownAustralia: 555 citing papers, 3.4% of this breakdownFrance: 529 citing papers, 3.3% of this breakdownSpain: 483 citing papers, 3% of this breakdownNetherlands: 459 citing papers, 2.8% of this breakdownSweden: 428 citing papers, 2.7% of this breakdownJapan: 418 citing papers, 2.6% of this breakdown
0%33.1%Other 21.2%

Fields

  • Medicine46.1%
  • Neuroscience33.6%
  • Biochemistry, Genetics and Molecular Biology15.9%
  • Nursing1.5%
  • Psychology0.5%
  • Chemistry0.5%
  • Other1.9%

Topics

  • Alzheimer's disease research and treatments11.2%
  • Genetic Neurodegenerative Diseases9.3%
  • Mitochondrial Function and Pathology6.2%
  • Parkinson's Disease Mechanisms and Treatments5%
  • Neurological disorders and treatments4.7%
  • Dementia and Cognitive Impairment Research3.4%
  • Other60.2%

Coauthors

All papers

Open in search
  1. Single cell RNA sequencing of human microglia uncovers a subset associated with Alzheimer’s disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Communications 2020 cited by 772

  2. Primary age-related tauopathy (PART): a common pathology associated with human aging

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alberto Serrano‐Pozo, Michael L. Shelanski, Thor D. Stein, Masaki Takao, Dietmar Rudolf Thal, Jon B. Toledo, Juan C. Troncoso, Jean Paul Vonsattel, Charles L. White, Thomas Wısnıewskı, Randall L. Woltjer, Masahito Yamada, Peter T. Nelson - Acta Neuropathologica 2014 cited by 1,507

  3. Plasma p‐tau181, p‐tau217, and other blood‐based Alzheimer's disease biomarkers in a multi‐ethnic, community study

    Authors: , , , , , , , , , , , , , - Alzheimer s & Dementia 2021 cited by 381

  4. CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Afroditi Chatzi, Darren G. Monckton, Michael Orth, G. Bernhard Landwehrmeyer, Jane S. Paulsen, E. Ray Dorsey, Ira Shoulson, Richard H. Myers - Cell 2019 cited by 576

  5. Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Tatiana M. Foroud, Jonathan L. Haines, Richard Mayeux, Margaret A. Pericak‐Vance, Julie A. Schneider, John Q. Trojanowski, Lindsay A. Farrer, Gerard D. Schellenberg, Gary W. Beecham, Thomas J. Montine, Gyungah Jun, Erin L. Abner, Perrie M. Adams, Marilyn S. Albert, Roger L. Albin, Liana G. Apostolova, Steven E. Arnold, Sanjay Asthana, Craig Atwood, Clinton T. Baldwin, Robert C. Barber, Lisa L. Barnes, Sandra Barral, James T. Becker, Duane Beekly, Eileen H. Bigio, Thomas D. Bird, Deborah Blacker, Bradley F. Boeve, James D. Bowen, Adam Boxer, James R. Burke, Jeffrey M. Burns, Nigel J. Cairns, Laura B. Cantwell, Chuanhai Cao, Chris Carlson, Cynthia M. Carlsson, Regina M. Carney, Minerva M. Carrasquillo, Helena C. Chui, David H. Cribbs, Elizabeth Crocco, Carlos Cruchaga, Charles DeCarli, Malcolm Dick, Rachelle S. Doody, Ranjan Duara, Nilüfer Ertekin‐Taner, Denis A. Evans, Kelley Faber, Thomas Fairchild, Kenneth B. Fallon, David W. Fardo, Martin R. Farlow, Steven H. Ferris, Douglas Galasko, Marla Gearing, Daniel H. Geschwind, Valentina Ghisays, Alison Goate, Neill R. Graff‐Radford, Robert C. Green, John H. Growdon, Håkon Håkonarson, Ronald L. Hamilton, Kara L. Hamilton‐Nelson, Lindy E. Harrell, Lawrence S. Honig, Ryan M. Huebinger and 92 more - Nature Communications 2020 cited by 490

  6. Identification of Genetic Factors that Modify Clinical Onset of Huntington’s Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - Cell 2015 cited by 684

  7. Neuropathological Classification of Huntingtonʼs Disease

    Authors: , , , , , - Journal of Neuropathology & Experimental Neurology 1985 cited by 2,604

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Roger N. Rosenberg, Charles L. White, Isidró Ferrer, Albert Lladó, Manuela Neumann, Hans A. Kretzschmar, Christine M. Hulette, Kathleen A. Welsh‐Bohmer, Bruce L. Miller, Ainhoa Alzualde, Adolfo López de Munain, Ann C. McKee, Marla Gearing, Allan I. Levey, James J. Lah, John Hardy, Jonathan D. Rohrer, Tammaryn Lashley, Ian R. Mackenzie, Howard Feldman, Ronald L. Hamilton, Steven T. DeKosky, Julie van der Zee, Samir Kumar‐Singh, Christine Van Broeckhoven, Richard Mayeux, Jean Paul Vonsattel, Juan C. Troncoso, Jillian J. Kril, John B. Kwok, Glenda M. Halliday, Thomas D. Bird, Paul G. Ince, Pamela J. Shaw, Nigel J. Cairns, John C. Morris, Catriona McLean, Charles DeCarli, William G. Ellis, Stefanie H. Freeman, Matthew P. Frosch, John H. Growdon, Daniel P. Perl, Mary Sano, David A. Bennett, Julie A. Schneider, Thomas G. Beach, Eric M. Reiman, Bryan K. Woodruff, Jeffrey L. Cummings, Harry V. Vinters, Carol A. Miller, Helena C. Chui, Irina Alafuzoff, Päivi Hartikainen, Danielle Seilhean, Douglas Galasko, Eliezer Masliah, Carl W. Cotman, MJ Tuñón, Mònica Martínez, David G. Muñoz, Steven L. Carroll, Daniel Marson, Peter Riederer, Nenad Bogdanović, Gerard D Schellenberg, Håkon Håkonarson, John Q. Trojanowski, Virginia M.‐Y. Lee - Nature Genetics 2010 cited by 609

  9. The Second NINDS/NIBIB Consensus Meeting to Define Neuropathological Criteria for the Diagnosis of Chronic Traumatic Encephalopathy

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , - Journal of Neuropathology & Experimental Neurology 2021 cited by 320

  10. Cyclophilin D deficiency attenuates mitochondrial and neuronal perturbation and ameliorates learning and memory in Alzheimer's disease

    Authors: , , , , , , , , , , , , , , - Nature Medicine 2008 cited by 932

  11. Cerebral amyloid angiopathy without and with cerebral hemorrhages: A comparative histological study

    Authors: , , , , , - Annals of Neurology 1991 cited by 654

  12. MHC-I expression renders catecholaminergic neurons susceptible to T-cell-mediated degeneration

    Authors: , , , , , , , , , , , , - Nature Communications 2014 cited by 338

  13. Office of Rare Diseases Neuropathologic Criteria for Corticobasal Degeneration

    Authors: , , , , , , , , , , , , , - Journal of Neuropathology & Experimental Neurology 2002 cited by 718

  14. Huntington Disease

    Authors: , - Journal of Neuropathology & Experimental Neurology 1998 cited by 1,312

  15. Trinucleotide repeat length instability and age of onset in Huntington's disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , S. Robert Snodgrass, Margot de Young, Nancy S. Wexler, Chaya Moscowitz, Graciela K. Penchaszadeh, H MacFarlane, Mark J. Anderson, Bruce G. Jenkins, Jayalakshmi Srinidhi, Glenn Barnes, James F. Gusella, Marcy E. MacDonald - Nature Genetics 1993 cited by 1,099

  16. CGG Repeat-Associated Translation Mediates Neurodegeneration in Fragile X Tremor Ataxia Syndrome

    Authors: , , , , , , , , , , , , , , , , , - Neuron 2013 cited by 493

  17. Polyamine pathway contributes to the pathogenesis of Parkinson disease

    Authors: , , , , , , , , , , , , , , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 2010 cited by 159

  18. Model‐guided microarray implicates the retromer complex in Alzheimer's disease

    Authors: , , , , , , , , - Annals of Neurology 2005 cited by 458

  19. Differential diagnosis of parkinsonism: a metabolic imaging study using pattern analysis

    Authors: , , , , , , , , , , - The Lancet Neurology 2010 cited by 352

  20. Rapid induction of Alzheimer A beta amyloid formation by zinc

    Authors: , , , , , , , , - Science 1994 cited by 1,518

  21. Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain

    Authors: , , , , , , , , , - Human Molecular Genetics 2007 cited by 231

  22. PART, a distinct tauopathy, different from classical sporadic Alzheimer disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Acta Neuropathologica 2015 cited by 173

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Steven E. Arnold, John Q. Trojanowski, Virginia M. Lee, Gregor K. Wenning, Charles L. White, Günter U. Höglinger, Ulrich Müller, Bernie Devlin, Lawrence I. Golbe, Julia E. Crook, Joseph E. Parisi, Bradley F. Boeve, Keith A. Josephs, Zbigniew K. Wszołek, Ryan J. Uitti, Neill R. Graff‐Radford, Irene Litvan, Steven G. Younkin, Li-San Wang, Nilüfer Ertekin‐Taner, Rosa Rademakers, Hakon Hakonarsen, Gerard D. Schellenberg, Dennis W. Dickson - Nature Communications 2015 cited by 241

  24. Huntington disease oligodendrocyte maturation deficits revealed by single-nucleus RNAseq are rescued by thiamine-biotin supplementation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Communications 2022 cited by 77