Bertrand Joseph

Active 1999–2025

62
Papers
23,044
Citations
47
h-index
61
i10-index

Citations

Citations per year for Bertrand Joseph1992: 1 citations1993: 2 citations1994: 1 citations1999: 4 citations2000: 9 citations2001: 14 citations2002: 12 citations2003: 26 citations2004: 35 citations2005: 35 citations2006: 49 citations2007: 41 citations2008: 48 citations2009: 42 citations2010: 72 citations2011: 76 citations2012: 85 citations2013: 114 citations2014: 129 citations2015: 219 citations2016: 283 citations2017: 317 citations2018: 356 citations2019: 1,050 citations2020: 1,317 citations2021: 1,440 citations2022: 1,380 citations2023: 1,135 citations2024: 1,582 citations2025: 792 citations2026: 25 citations1995–1998: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorChina: 3,100 citing papers, 19.5% of this breakdownUnited States: 3,045 citing papers, 19.2% of this breakdownUnited Kingdom: 771 citing papers, 4.9% of this breakdownItaly: 734 citing papers, 4.6% of this breakdownGermany: 716 citing papers, 4.5% of this breakdownCanada: 540 citing papers, 3.4% of this breakdownFrance: 524 citing papers, 3.3% of this breakdownSpain: 442 citing papers, 2.8% of this breakdownAustralia: 383 citing papers, 2.4% of this breakdownSweden: 378 citing papers, 2.4% of this breakdownSouth Korea: 367 citing papers, 2.3% of this breakdownJapan: 365 citing papers, 2.3% of this breakdown
0%19.5%Other 28.4%

Fields

  • Medicine43.4%
  • Biochemistry, Genetics and Molecular Biology29.9%
  • Neuroscience16%
  • Immunology and Microbiology5.5%
  • Agricultural and Biological Sciences0.9%
  • Nursing0.9%
  • Other3.4%

Topics

  • Neuroinflammation and Neurodegeneration Mechanisms6.8%
  • Alzheimer's disease research and treatments5.9%
  • Autophagy in Disease and Therapy3.6%
  • Ferroptosis and cancer prognosis2.8%
  • Inflammasome and immune disorders2.7%
  • Mitochondrial Function and Pathology2.6%
  • Other75.6%

Coauthors

All papers

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  1. Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Emily H. Cheng, Jerry E. Chipuk, John A. Cidlowski, Aaron Ciechanover, Gerald M. Cohen, Marcus Conrad, Juan R. Cubillos‐Ruiz, Peter E. Czabotar, Vincenzo D’Angiolella, Ted M. Dawson, Valina L. Dawson, Vincenzo De Laurenzi, Ruggero De Maria, Klaus‐Michael Debatin, Ralph J. DeBerardinis, Mohanish Deshmukh, Nicola Di Daniele, Francesco Di Virgilio, Vishva M. Dixit, Scott J. Dixon, Colin S. Duckett, Brian David Dynlacht, Wafik S. El‐Deiry, John W. Elrod, Gian María Fimia, Simone Fulda, Ana J. García‐Sáez, Abhishek D. Garg, Carmen Garrido, Evripidis Gavathiotis, Pierre Golstein, Eyal Gottlieb, Douglas R. Green, Lloyd A. Greene, Hinrich Gronemeyer, Atan Gross, György Hajnóczky, J. Marie Hardwick, Isaac S. Harris, Michael O. Hengartner, Claudio Hetz, Hidenori Ichijo, Marja Jäättelä, Bertrand Joseph, Philipp J. Jost, Philippe Juin, William J. Kaiser, Michael Karin, Thomas Kaufmann, Oliver Kepp, Adi Kimchi, Richard N. Kitsis, Daniel J. Klionsky, Richard A. Knight, Sharad Kumar, Sam W. Lee, John J. Lemasters, Beth Levine, Andreas Linkermann, Stuart A. Lipton, Richard A. Lockshin, Carlos López-Otı́n, Scott W. Lowe, Tom Luedde, Enrico Lugli, Marion MacFarlane, Frank Madeo, Michal Malewicz, Walter Malorni, Gwenola Manic and 69 more - Cell Death and Differentiation 2018 cited by 6,498

  2. Neuroinflammation in Alzheimer's disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Olga Garaschuk, Erik Boddeke, Charles A. Dinarello, John C.S. Breitner, Greg M. Cole, Douglas T. Golenbock, Markus P. Kummer - The Lancet Neurology 2015 cited by 6,102

  3. Apoptotic cell death in disease—Current understanding of the NCCD 2023

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Pierluigi Bove, Patricia Boya, Catherine Brenner, Petr Brož, Thomas Brunner, Rune Busk Damgaard, George A. Calin, Michelangelo Campanella, Eleonora Candi, Michele Carbone, Didac Carmona‐Gutiérrez, Francesco Cecconi, Francis Ka-Ming Chan, Guoqiang Chen, Quan Chen, Youhai H. Chen, Emily H. Cheng, Jerry E. Chipuk, John A. Cidlowski, Aaron Ciechanover, Gennaro Ciliberto, Marcus Conrad, Juan R. Cubillos‐Ruiz, Peter E. Czabotar, Vincenzo D’Angiolella, Mads Daugaard, Ted M. Dawson, Valina L. Dawson, Ruggero De Maria, Bart De Strooper, Klaus‐Michael Debatin, Ralph J. DeBerardinis, Alexei Degterev, Giannino Del Sal, Mohanish Deshmukh, Francesco Di Virgilio, Marc Diederich, Scott J. Dixon, Brian David Dynlacht, Wafik S. El‐Deiry, John W. Elrod, Kurt Engeland, Gian María Fimia, Claudia Galassi, Carlo Ganini, Ana J. García‐Sáez, Abhishek D. Garg, Carmen Garrido, Evripidis Gavathiotis, Motti Gerlic, Sourav Ghosh, Douglas R. Green, Lloyd A. Greene, Hinrich Gronemeyer, Georg Häcker, György Hajnóczky, J. Marie Hardwick, Ygal Haupt, Sudan He, David M. Heery, Michael O. Hengartner, Claudio Hetz, David A. Hildeman, Hidenori Ichijo, Satoshi Inoue, Marja Jäättelä, Ana Janic, Bertrand Joseph, Philipp J. Jost, Thirumala‐Devi Kanneganti and 128 more - Cell Death and Differentiation 2023 cited by 351

  4. Microglia: Agents of the CNS Pro-Inflammatory Response

    Authors: , , , , , , , , , - Cells 2020 cited by 356

  5. Microglial subtypes: diversity within the microglial community

    Authors: , , , - The EMBO Journal 2019 cited by 574

  6. Essential versus accessory aspects of cell death: recommendations of the NCCD 2015

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Vincenzo De Laurenzi, Ruggero De Maria, K-M Debatin, N Di Daniele, Vishva M. Dixit, Brian David Dynlacht, Wafik S. El‐Deiry, Gian María Fimia, Richard A. Flavell, Simone Fulda, Carmen Garrido, M-L Gougeon, Douglas R. Green, Hinrich Gronemeyer, György Hajnóczky, J. Marie Hardwick, Michael O. Hengartner, Hidenori Ichijo, Bertrand Joseph, Philipp J. Jost, Thomas Kaufmann, Oliver Kepp, Daniel J. Klionsky, Richard A. Knight, Sharad Kumar, John J. Lemasters, Beth Levine, Andreas Linkermann, Stuart A. Lipton, Richard A. Lockshin, Carlos López-Otı́n, Enrico Lugli, Frank Madeo, Walter Malorni, J-C Marine, Séamus J. Martin, J-C Martinou, Jan Paul Medema, Pascal Meier, Sonia Melino, Noboru Mizushima, Ute M. Moll, Cristina Muñoz‐Pinedo, Gabriel Núñez, Andrew Oberst, Theocharis Panaretakis, Josef Penninger, Marcus E. Peter, Mauro Piacentini, Paolo Pinton, Jochen H.M. Prehn, Hamsa Puthalakath, Gabriel A. Rabinovich, Kodi S. Ravichandran, Rosario Rizzuto, Cecília M. P. Rodrigues, David C. Rubinsztein, Thomas Rudel, Yufang Shi, H-U Simon, Brent R. Stockwell, György Szabadkai, Stephen W. G. Tait, Ho Lam Tang, N Tavernarakis, Yoshihide Tsujimoto, Tom Vanden Berghe, Peter Vandenabeele, Andreas Villunger, Erwin F. Wagner and 8 more - Cell Death and Differentiation 2014 cited by 1,020

  7. ARG1-expressing microglia show a distinct molecular signature and modulate postnatal development and function of the mouse brain

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , José L. Venero, Bertrand Joseph - Nature Neuroscience 2023 cited by 94

  8. The impact of aging on mitochondrial function and biogenesis pathways in skeletal muscle of sedentary high‐ and low‐functioning elderly individuals

    Authors: , , , , , , , , , , , - Aging Cell 2012 cited by 398

  9. The return of the nucleus: transcriptional and epigenetic control of autophagy

    Authors: , , - Nature Reviews Molecular Cell Biology 2013 cited by 463

  10. Caspase signalling controls microglia activation and neurotoxicity

    Authors: , , , , , , , , , , - Nature 2011 cited by 592

  11. Microglia-Secreted Galectin-3 Acts as a Toll-like Receptor 4 Ligand and Contributes to Microglial Activation

    Authors: , , , , , , , , , , , , , , , , , , , - Cell Reports 2015 cited by 357

  12. The histone H4 lysine 16 acetyltransferase hMOF regulates the outcome of autophagy

    Authors: , , , , , , , , , - Nature 2013 cited by 327

  13. Epigenetics Control Microglia Plasticity

    Authors: , - Frontiers in Cellular Neuroscience 2018 cited by 157

  14. New insights into the role of mitochondria in aging: mitochondrial dynamics and more

    Authors: , , , , , - Journal of Cell Science 2010 cited by 514

  15. Mitochondrial pathways in sarcopenia of aging and disuse muscle atrophy

    Authors: , , , , , , , - Biological Chemistry 2012 cited by 320

  16. Autophagy regulation by RNA alternative splicing and implications in human diseases

    Authors: , , - Nature Communications 2022 cited by 47

  17. The mitochondrial death pathway: a promising therapeutic target in diseases

    Authors: , , , - Journal of Cellular and Molecular Medicine 2009 cited by 269

  18. Beneficial effects of exercise on age‐related mitochondrial dysfunction and oxidative stress in skeletal muscle

    Authors: , , - The Journal of Physiology 2015 cited by 194

  19. Multifaceted microglia — key players in primary brain tumour heterogeneity

    Authors: , , , - Nature Reviews Neurology 2021 cited by 54

  20. Expression of mitochondrial fission and fusion regulatory proteins in skeletal muscle during chronic use and disuse

    Authors: , , , , - Muscle & Nerve 2013 cited by 165

  21. Dysregulation of Mitochondrial Quality Control Processes Contribute to Sarcopenia in a Mouse Model of Premature Aging

    Authors: , , , , , , , - PLoS ONE 2013 cited by 159

  22. TET2 Regulates the Neuroinflammatory Response in Microglia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , - Cell Reports 2019 cited by 101

  23. The hunger strikes back: an epigenetic memory for autophagy

    Authors: , , - Cell Death and Differentiation 2023 cited by 38

  24. Histone onco-modifications

    Authors: , , - Oncogene 2011 cited by 308