Jerry E. Chipuk

Active 2001–2025

64
Papers
23,251
Citations
50
h-index
60
i10-index

Citations

Citations per year for Jerry E. Chipuk1985: 3 citations1990: 1 citations1991: 1 citations2001: 1 citations2002: 9 citations2003: 8 citations2004: 52 citations2005: 125 citations2006: 209 citations2007: 148 citations2008: 195 citations2009: 218 citations2010: 226 citations2011: 201 citations2012: 182 citations2013: 246 citations2014: 222 citations2015: 249 citations2016: 264 citations2017: 267 citations2018: 251 citations2019: 935 citations2020: 1,069 citations2021: 1,134 citations2022: 987 citations2023: 821 citations2024: 1,215 citations2025: 626 citations2026: 15 citations1986–1989: no citations, so these years are not shown1992–2000: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,890 citing papers, 22.3% of this breakdownChina: 2,823 citing papers, 21.7% of this breakdownGermany: 602 citing papers, 4.6% of this breakdownUnited Kingdom: 518 citing papers, 4% of this breakdownFrance: 493 citing papers, 3.8% of this breakdownItaly: 484 citing papers, 3.7% of this breakdownAustralia: 386 citing papers, 3% of this breakdownCanada: 334 citing papers, 2.6% of this breakdownJapan: 313 citing papers, 2.4% of this breakdownIndia: 292 citing papers, 2.2% of this breakdownSpain: 277 citing papers, 2.1% of this breakdownSouth Korea: 268 citing papers, 2.1% of this breakdown
0%22.3%Other 25.5%

Fields

  • Biochemistry, Genetics and Molecular Biology46.1%
  • Medicine37.6%
  • Immunology and Microbiology7.9%
  • Neuroscience2.1%
  • Agricultural and Biological Sciences1.3%
  • Engineering1.1%
  • Other3.9%

Topics

  • Cell death mechanisms and regulation5.7%
  • Mitochondrial Function and Pathology5.4%
  • Autophagy in Disease and Therapy4.3%
  • Ferroptosis and cancer prognosis3.3%
  • Inflammasome and immune disorders2.8%
  • ATP Synthase and ATPases Research2.3%
  • Other76.2%

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. 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

  3. Chemical Inhibition of the Mitochondrial Division Dynamin Reveals Its Role in Bax/Bak-Dependent Mitochondrial Outer Membrane Permeabilization

    Authors: , , , , , , , , , , - Developmental Cell 2008 cited by 1,196

  4. 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

  5. Dietary Intake Regulates the Circulating Inflammatory Monocyte Pool

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - Cell 2019 cited by 449

  6. Mitochondrial Division Is Requisite to RAS-Induced Transformation and Targeted by Oncogenic MAPK Pathway Inhibitors

    Authors: , , , , , , , , , , - Molecular Cell 2015 cited by 395

  7. Direct Activation of Bax by p53 Mediates Mitochondrial Membrane Permeabilization and Apoptosis

    Authors: , , , , , , - Science 2004 cited by 2,048

  8. The BCL-2 Family Reunion

    Authors: , , , , - Molecular Cell 2010 cited by 1,413

  9. PPARdelta activation induces metabolic and contractile maturation of human pluripotent stem cell-derived cardiomyocytes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Cell stem cell 2022 cited by 94

  10. Mitochondrial outer membrane permeabilization during apoptosis: the innocent bystander scenario

    Authors: , , - Cell Death and Differentiation 2006 cited by 612

  11. Mitochondrial dynamics as regulators of cancer biology

    Authors: , - Cellular and Molecular Life Sciences 2017 cited by 230

  12. Sustained CD28 costimulation is required for self-renewal and differentiation of TCF-1 + PD-1 + CD8 T cells

    Authors: , , , , , , , , , , , , , , , , , - Science Immunology 2023 cited by 73

  13. Mitochondrial Fission in Human Diseases

    Authors: , - Handbook of experimental pharmacology 2016 cited by 176

  14. BH3 Domains of BH3-Only Proteins Differentially Regulate Bax-Mediated Mitochondrial Membrane Permeabilization Both Directly and Indirectly

    Authors: , , , , , , - Molecular Cell 2005 cited by 1,158

  15. How do BCL-2 proteins induce mitochondrial outer membrane permeabilization?

    Authors: , - Trends in Cell Biology 2008 cited by 976

  16. Sphingolipid Metabolism Cooperates with BAK and BAX to Promote the Mitochondrial Pathway of Apoptosis

    Authors: , , , , , , , - Cell 2012 cited by 433

  17. GM-CSF Controls Nonlymphoid Tissue Dendritic Cell Homeostasis but Is Dispensable for the Differentiation of Inflammatory Dendritic Cells

    Authors: , , , , , , , , , , , , , , , , , , - Immunity 2012 cited by 413

  18. A local tumor microenvironment acquired super-enhancer induces an oncogenic driver in colorectal carcinoma

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Communications 2022 cited by 45

  19. Lymphatic endothelial S1P promotes mitochondrial function and survival in naive T cells

    Authors: , , , , , , , , , , , - Nature 2017 cited by 183

  20. The deadly landscape of pro‐apoptotic BCL‐2 proteins in the outer mitochondrial membrane

    Authors: , - FEBS Journal 2015 cited by 138

  21. Mechanistic connections between mitochondrial biology and regulated cell death

    Authors: , , , - Developmental Cell 2021 cited by 65

  22. Dynamic death decisions: How mitochondrial dynamics shape cellular commitment to apoptosis and ferroptosis

    Authors: , , - Developmental Cell 2024 cited by 58

  23. Disruption of mitochondrial electron transport chain function potentiates the pro-apoptotic effects of MAPK inhibition

    Authors: , , , , , - Journal of Biological Chemistry 2017 cited by 88

  24. MDM2 Integrates Cellular Respiration and Apoptotic Signaling through NDUFS1 and the Mitochondrial Network

    Authors: , , , , , , , , , , , , , - Molecular Cell 2019 cited by 78