Pierluigi Gambetti

Active 1971–2025

132
Papers
23,702
Citations
93
h-index
130
i10-index

Citations

Citations per year for Pierluigi Gambetti1922: 1 citations1971: 1 citations1973: 4 citations1975: 2 citations1976: 3 citations1977: 3 citations1978: 2 citations1979: 2 citations1980: 4 citations1981: 11 citations1982: 11 citations1983: 19 citations1984: 26 citations1985: 31 citations1986: 41 citations1987: 27 citations1988: 31 citations1989: 46 citations1990: 42 citations1991: 36 citations1992: 57 citations1993: 58 citations1994: 87 citations1995: 83 citations1996: 82 citations1997: 132 citations1998: 168 citations1999: 184 citations2000: 177 citations2001: 233 citations2002: 214 citations2003: 227 citations2004: 224 citations2005: 197 citations2006: 202 citations2007: 143 citations2008: 174 citations2009: 194 citations2010: 220 citations2011: 124 citations2012: 129 citations2013: 71 citations2014: 94 citations2015: 94 citations2016: 145 citations2017: 116 citations2018: 150 citations2019: 371 citations2020: 387 citations2021: 382 citations2022: 261 citations2023: 151 citations2024: 205 citations2025: 66 citations2026: 7 citations1923–1970: no citations, so these years are not shown1972: no citations, so this year is not shown1974: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 1,760 citing papers, 33.1% of this breakdownUnited Kingdom: 585 citing papers, 11% of this breakdownItaly: 379 citing papers, 7.1% of this breakdownGermany: 372 citing papers, 7% of this breakdownFrance: 254 citing papers, 4.8% of this breakdownCanada: 247 citing papers, 4.6% of this breakdownJapan: 190 citing papers, 3.6% of this breakdownAustralia: 145 citing papers, 2.7% of this breakdownSpain: 140 citing papers, 2.6% of this breakdownSwitzerland: 119 citing papers, 2.2% of this breakdownChina: 118 citing papers, 2.2% of this breakdownSweden: 110 citing papers, 2.1% of this breakdown
0%33.1%Other 17%

Fields

  • Biochemistry, Genetics and Molecular Biology53.3%
  • Medicine34.5%
  • Neuroscience8.5%
  • Agricultural and Biological Sciences0.7%
  • Psychology0.7%
  • Nursing0.5%
  • Other1.8%

Topics

  • Prion Diseases and Protein Misfolding17.8%
  • Alzheimer's disease research and treatments11.2%
  • Neurological diseases and metabolism9.2%
  • Trace Elements in Health5.9%
  • Parkinson's Disease Mechanisms and Treatments2.9%
  • Amyotrophic Lateral Sclerosis Research2%
  • Other51%

Coauthors

All papers

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

    Authors: , , , , , , , , , , , , , , , , , - Annals of Neurology 1999 cited by 1,449

  2. Quantifying prion disease penetrance using large population control cohorts

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jesús de Pedro‐Cuesta, Stéphane Haı̈k, Jean Laplanche, Élodie Bouaziz-Amar, J.-P. Brandel, Sabina Capellari, Piero Parchi, Anna Poleggi, Anna Ladogana, Anne O’Donnell‐Luria, Konrad J. Karczewski, Jamie L. Marshall, Michael Boehnke, Markku Laakso, Karen L. Mohlke, Anna K. Kähler, Kimberly Chambert, Steven A. McCarroll, Patrick F. Sullivan, Christina M. Hultman, Shaun Purcell, Pamela Sklar, Sven J. van der Lee, Annemieke J.M. Rozemüller, Casper Jansen, Albert Hofman, Robert Kraaij, Jeroen van Rooij, M. Arfan Ikram, André G. Uitterlinden, Cornelia M. van Duijn, Mark J. Daly, Daniel G. MacArthur - Science Translational Medicine 2016 cited by 469

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

    Authors: , , , , , , , , , , , , , , , , , - Acta Neuropathologica 2012 cited by 232

  4. Evidence for the Conformation of the Pathologic Isoform of the Prion Protein Enciphering and Propagating Prion Diversity

    Authors: , , , , , , , , , - Science 1996 cited by 872

  5. Prions in the Urine of Patients with Variant Creutzfeldt–Jakob Disease

    Authors: , , , , , , , , , , , , , - New England Journal of Medicine 2014 cited by 215

  6. Bank Vole Prion Protein As an Apparently Universal Substrate for RT-QuIC-Based Detection and Discrimination of Prion Strains

    Authors: , , , , , , , , - PLoS Pathogens 2015 cited by 173

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Alzheimer s & Dementia 2014 cited by 118

  8. Diagnostic and prognostic value of human prion detection in cerebrospinal fluid

    Authors: , , , , , , , , , , , , , , , , , - Annals of Neurology 2016 cited by 225

  9. Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Beata Sikorska, Ewa Golańska, Paweł P. Liberski, Miguel Calero, Olga Calero, Pascual Sánchez‐Juan, Antonio Salas, Federico Martinón‐Torres, Élodie Bouaziz-Amar, Stéphane Haı̈k, Jean Laplanche, Jean-Phillipe Brandel, Phillipe Amouyel, Jean‐Charles Lambert, Piero Parchi, Anna Bartoletti‐Stella, Sabina Capellari, Anna Poleggi, Anna Ladogana, Maurizio Pocchiari, Serena Aneli, Giuseppe Matullo, Richard Knight, Saima Zafar, Inga Zerr, Stephanie A. Booth, Michael B. Coulthart, Gerard H. Jansen, Katie Glisic, Janis Blevins, Pierluigi Gambetti, Jiri Safar, Brian S. Appleby, John Collinge, Simon Mead - The Lancet Neurology 2020 cited by 77

  10. Treatable neurological disorders misdiagnosed as Creutzfeldt‐Jakob disease

    Authors: , , , , , , - Annals of Neurology 2011 cited by 214

  11. Early preclinical detection of prions in the skin of prion-infected animals

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , - Nature Communications 2019 cited by 66

  12. Hirano Body Filaments Contain Actin and Actin-Associated Proteins

    Authors: , , - Journal of Neuropathology & Experimental Neurology 1987 cited by 143

  13. Evaluation of a New Criterion for Detecting Prion Disease With Diffusion Magnetic Resonance Imaging

    Authors: , , , , , , , , , , , , - JAMA Neurology 2020 cited by 77

  14. Molecular basis of phenotypic variability in sporadc creudeldt‐jakob disease

    Authors: , , , , , , , , , , , - Annals of Neurology 1996 cited by 877

  15. Sporadic human prion diseases: molecular insights and diagnosis

    Authors: , , , , , - The Lancet Neurology 2012 cited by 378

  16. Chronic Wasting Disease of Elk: Transmissibility to Humans Examined by Transgenic Mouse Models

    Authors: , , , , , , , , , , , , , , , , , , - Journal of Neuroscience 2005 cited by 268

  17. Cell‐free propagation of prion strains

    Authors: , , , , , - The EMBO Journal 2008 cited by 191

  18. Astrocytes in the developing human brain

    Authors: , - Acta Neuropathologica 1986 cited by 97

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

    Authors: , , , , , , , , , , , , , , , , , , - Acta Neuropathologica 2021 cited by 55

  20. Fatal Familial Insomnia and Dysautonomia with Selective Degeneration of Thalamic Nuclei

    Authors: , , , , , , , , - New England Journal of Medicine 1986 cited by 636

  21. Genetic influence on the structural variations of the abnormal prion protein

    Authors: , , , , , , , , , , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 2000 cited by 341

  22. A novel human disease with abnormal prion protein sensitive to protease

    Authors: , , , , , , , , , , , , , , , , , , , , , , - Annals of Neurology 2008 cited by 311

  23. Variably protease‐sensitive prionopathy: A new sporadic disease of the prion protein

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Annals of Neurology 2010 cited by 287

  24. Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt–Jakob disease: its effect on the phenotype and prion-type characteristics

    Authors: , , , , , , , , , , - Brain 2009 cited by 183