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Jan Steyaert

Active 1989–2025

116
Papers
20,703
Citations
68
h-index
110
i10-index

Citations

Citations per year for Jan Steyaert1987: 2 citations1989: 1 citations1990: 4 citations1991: 5 citations1992: 4 citations1994: 5 citations1995: 3 citations1996: 7 citations1997: 7 citations1998: 9 citations1999: 9 citations2000: 1 citations2001: 8 citations2002: 3 citations2003: 5 citations2004: 8 citations2005: 8 citations2006: 7 citations2007: 8 citations2008: 8 citations2009: 15 citations2010: 23 citations2011: 112 citations2012: 172 citations2013: 220 citations2014: 225 citations2015: 286 citations2016: 301 citations2017: 347 citations2018: 412 citations2019: 1,010 citations2020: 1,084 citations2021: 945 citations2022: 796 citations2023: 621 citations2024: 985 citations2025: 472 citations2026: 17 citations1988: no citations, so this year is not shown1993: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,436 citing papers, 27.3% of this breakdownChina: 959 citing papers, 10.7% of this breakdownUnited Kingdom: 797 citing papers, 8.9% of this breakdownGermany: 630 citing papers, 7.1% of this breakdownFrance: 372 citing papers, 4.2% of this breakdownJapan: 303 citing papers, 3.4% of this breakdownAustralia: 279 citing papers, 3.1% of this breakdownBelgium: 278 citing papers, 3.1% of this breakdownSwitzerland: 276 citing papers, 3.1% of this breakdownCanada: 266 citing papers, 3% of this breakdownItaly: 220 citing papers, 2.5% of this breakdownNetherlands: 186 citing papers, 2.1% of this breakdown
0%27.3%Other 21.5%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology58.3%
  • Medicine24%
  • Neuroscience7%
  • Agricultural and Biological Sciences1.8%
  • Computer Science1.6%
  • Immunology and Microbiology1.3%
  • Other6%

Topics

  • Receptor Mechanisms and Signaling13.1%
  • Neuropeptides and Animal Physiology6.8%
  • Monoclonal and Polyclonal Antibodies Research4.4%
  • Neuroscience and Neuropharmacology Research2.5%
  • Computational Drug Discovery Methods2.5%
  • Protein Structure and Dynamics2.3%
  • Other68.4%

Coauthors

All papers

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  1. Crystal structure of the β2 adrenergic receptor–Gs protein complex

    Authors: Søren G. F. Rasmussen, Brian T. DeVree, Yaozhong Zou, Andrew C. Kruse, Ka Young Chung, Tong Sun Kobilka, Foon Sun Thian, Pil Seok Chae, Els Pardon, Diane Calinski, Jesper Mosolff Mathiesen, Syed Tasadaque Ali Shah, Joseph A. Lyons, Martin Caffrey, Samuel H. Gellman, Jan Steyaert, Georgios Skiniotis, William I. Weis, Roger K. Sunahara, Brian K. Kobilka - Nature 2011 cited by 3,076

  2. A general protocol for the generation of Nanobodies for structural biology

    Authors: Els Pardon, Toon Laeremans, Sarah Triest, Søren G. F. Rasmussen, Alexandre Wohlkönig, A. Ruf, Serge Muyldermans, Wim G. J. Hol, Brian K. Kobilka, Jan Steyaert - Nature Protocols 2014 cited by 812

  3. Structural insights into µ-opioid receptor activation

    Authors: Weijiao Huang, Aashish Manglik, AJ Venkatakrishnan, Toon Laeremans, Evan N. Feinberg, Adrian L. Sanborn, Hideaki Kato, Kathryn E. Livingston, Thor S. Thorsen, Ralf C. Kling, Sébastien Granier, Peter Gmeiner, Stephen M. Husbands, John R. Traynor, William I. Weis, Jan Steyaert, Ron O. Dror, Brian K. Kobilka - Nature 2015 cited by 921

  4. Structure of a nanobody-stabilized active state of the β2 adrenoceptor

    Authors: Søren G. F. Rasmussen, Hee‐Jung Choi, Juan José Fung, Els Pardon, Paola Casarosa, Pil Seok Chae, Brian T. DeVree, Daniel M. Rosenbaum, Foon Sun Thian, Tong Sun Kobilka, Andreas Schnapp, Ingo Konetzki, Roger K. Sunahara, Samuel H. Gellman, Alexander Pautsch, Jan Steyaert, William I. Weis, Brian K. Kobilka - Nature 2011 cited by 1,706

  5. Activation and allosteric modulation of a muscarinic acetylcholine receptor

    Authors: Andrew C. Kruse, Aaron M. Ring, Aashish Manglik, Jianxin Hu, Kelly Hu, Katrin Eitel, Harald Hübner, Els Pardon, Céline Valant, Patrick M. Sexton, Arthur Christopoulos, Christian C. Felder, Peter Gmeiner, Jan Steyaert, William I. Weis, K. Christopher García, Jürgen Wess, Brian K. Kobilka - Nature 2013 cited by 920

  6. Conformational biosensors reveal GPCR signalling from endosomes

    Authors: Roshanak Irannejad, Jin C. Tomshine, Jon R. Tomshine, Michael Chevalier, Jacob P. Mahoney, Jan Steyaert, Søren G. F. Rasmussen, Roger K. Sunahara, Hana El‐Samad, Bo Huang, Mark von Zastrow - Nature 2013 cited by 857

  7. Structural insights into the activation of metabotropic glutamate receptors

    Authors: Antoine Koehl, Hongli Hu, Dan Feng, Bingfa Sun, Yan Zhang, Michael J. Robertson, Matthew Chu, Tong Sun Kobilka, Toon Laeremans, Jan Steyaert, Jeffrey Tarrasch, Somnath Dutta, Rasmus Fonseca, William I. Weis, Jesper Mosolff Mathiesen, Georgios Skiniotis, Brian K. Kobilka - Nature 2019 cited by 330

  8. Structure, substrate recognition and initiation of hyaluronan synthase

    Authors: Finn P. Maloney, Jeremi Kuklewicz, Robin A. Corey, Yunchen Bi, Ruoya Ho, Łukasz Mateusiak, Els Pardon, Jan Steyaert, Phillip J. Stansfeld, Jochen Zimmer - Nature 2022 cited by 141

  9. The Molecular Mechanism of Transport by the Mitochondrial ADP/ATP Carrier

    Authors: Jonathan J. Ruprecht, Martin King, Thomas Zögg, Antoniya A. Aleksandrova, Els Pardon, Paul G. Crichton, Jan Steyaert, Edmund R.S. Kunji - Cell 2019 cited by 335

  10. Distinct conformations of GPCR–β-arrestin complexes mediate desensitization, signaling, and endocytosis

    Authors: Thomas J. Cahill, A. Thomsen, Jeffrey Tarrasch, Bianca Plouffe, Anthony H. Nguyen, Fan Yang, Li-Yin Huang, Alem W. Kahsai, Daniel L. Bassoni, Bryant J. Gavino, Jane E. Lamerdin, Sarah Triest, Arun K. Shukla, Benjamin Berger, John R. Little, Albert Antar, Adi Blanc, Chang-xiu Qu, Xin Chen, Kouki Kawakami, Asuka Inoue, Junken Aoki, Jan Steyaert, Jin‐Peng Sun, Michel Bouvier, Georgios Skiniotis, Robert J. Lefkowitz - National Academy of Sciences, Proceedings of the National Academy of Sciences 2017 cited by 385

  11. Structure of PINK1 in complex with its substrate ubiquitin

    Authors: Alexander F. Schubert, Christina Gladkova, Els Pardon, Jane L. Wagstaff, Stefan M.V. Freund, Jan Steyaert, Sarah Maslen, David Komander - Nature 2017 cited by 191

  12. A Genetically Encoded Biosensor Reveals Location Bias of Opioid Drug Action

    Authors: Miriam Stoeber, Damien Jullié, Braden T. Lobingier, Toon Laeremans, Jan Steyaert, Peter W. Schiller, Aashish Manglik, Mark von Zastrow - Neuron 2018 cited by 299

  13. Allosteric coupling from G protein to the agonist-binding pocket in GPCRs

    Authors: Brian T. DeVree, Jacob P. Mahoney, Gisselle A. Vélez-Ruiz, Søren G. F. Rasmussen, Adam J. Kuszak, Elin Edwald, Juan-Jose Fung, Aashish Manglik, Matthieu Masureel, Yang Du, Rachel A. Matt, Els Pardon, Jan Steyaert, Brian K. Kobilka, Roger K. Sunahara - Nature 2016 cited by 298

  14. Nanobodies to Study G Protein–Coupled Receptor Structure and Function

    Authors: Aashish Manglik, Brian K. Kobilka, Jan Steyaert - The Annual Review of Pharmacology and Toxicology 2016 cited by 267

  15. GABAA receptor signalling mechanisms revealed by structural pharmacology.

    Authors: Simonas Masiulis, Rooma Desai, Tomasz Uchański, Itziar Serna Martin, Duncan Laverty, Dimple Karia, Tomas Malinauskas, Jasenko Zivanov, Els Pardon, Abhay Kotecha, Jan Steyaert, Keith W. Miller, A.R. Aricescu - Nature 2018 cited by 557

  16. Cryo-EM structure of the human α1β3γ2 GABAA receptor in a lipid bilayer

    Authors: Duncan Laverty, Rooma Desai, Tomasz Uchański, Simonas Masiulis, Wojciech J. Stec, Tomas Malinauskas, Jasenko Zivanov, Els Pardon, Jan Steyaert, Keith W. Miller, A.R. Aricescu - Nature 2018 cited by 343

  17. Structure of the Nanobody-Stabilized Active State of the Kappa Opioid Receptor

    Authors: Tao Che, Susruta Majumdar, Saheem A. Zaidi, Pauline W. Ondachi, John D. McCorvy, Sheng Wang, Philip D. Mosier, Rajendra Uprety, Eyal Vardy, B. Krumm, Gye Won Han, Ming-Yue Lee, Els Pardon, Jan Steyaert, Xi‐Ping Huang, Ryan T. Strachan, Alexandra R. Tribo, Gavril W. Pasternak, F. Ivy Carroll, Raymond C. Stevens, Vadim Cherezov, Vsevolod Katritch, Daniel Wacker, Bryan L. Roth - Cell 2018 cited by 377

  18. Structures of influenza A virus RNA polymerase offer insight into viral genome replication

    Authors: Haitian Fan, Alexander P. Walker, Loïc Carrique, J.R. Keown, Itziar Serna Martin, Dimple Karia, Jane Sharps, Narin Hengrung, Els Pardon, Jan Steyaert, Jonathan M. Grimes, Ervin Fodor - Nature 2019 cited by 242

  19. Allosteric nanobodies reveal the dynamic range and diverse mechanisms of G-protein-coupled receptor activation

    Authors: Dean P. Staus, Ryan T. Strachan, Aashish Manglik, Biswaranjan Pani, Alem W. Kahsai, Tae Hun Kim, Laura M. Wingler, Seungkirl Ahn, Arnab K. Chatterjee, Ali Masoudi, Andrew C. Kruse, Els Pardon, Jan Steyaert, William I. Weis, R. Scott Prosser, Brian K. Kobilka, Tommaso Costa, Robert J. Lefkowitz - Nature 2016 cited by 328

  20. Megabodies expand the nanobody toolkit for protein structure determination by single-particle cryo-EM

    Authors: Tomasz Uchański, Simonas Masiulis, Baptiste Fischer, Valentina Kalichuk, Uriel López-Sánchez, Eleftherios Zarkadas, Miriam Weckener, Andrija Sente, Philip N. Ward, Alexandre Wohlkönig, Thomas Zögg, Han Remaut, James H. Naismith, Hugues Nury, Wim Vranken, A.R. Aricescu, Els Pardon, Jan Steyaert - Nature Methods 2021 cited by 153

  21. Structural basis of purine nucleotide inhibition of human uncoupling protein 1

    Authors: Scott A. Jones, Prerana Gogoi, Jonathan J. Ruprecht, Martin King, Yang Lee, Thomas Zögg, Els Pardon, Deepak Chand, Stefan Steimle, Danielle M. Copeman, Camila A. Cotrim, Jan Steyaert, Paul G. Crichton, Vera Y. Moiseenkova‐Bell, Edmund R.S. Kunji - Science Advances 2023 cited by 70

  22. Structure-based design of nanobodies that inhibit seeding of Alzheimer’s patient–extracted tau fibrils

    Authors: Romany Abskharon, Hope Pan, M.R. Sawaya, Paul M. Seidler, E. Olivares, Yu Chen, Kevin A. Murray, Jeffrey Zhang, Carter Lantz, Megan Bentzel, David R. Boyer, Duilio Cascio, Binh A. Nguyen, Ke Hou, Xinyi Cheng, Els Pardon, Christopher Kazu Williams, Alissa L. Nana, Harry V. Vinters, Salvatore Spina, Lea T. Grinberg, William W. Seeley, Jan Steyaert, Charles Glabe, Rachel R. Ogorzalek Loo, Joseph A. Loo, David Eisenberg - National Academy of Sciences, Proceedings of the National Academy of Sciences 2023 cited by 47

  23. Structure of an endosomal signaling GPCR–G protein–β-arrestin megacomplex

    Authors: Anthony H. Nguyen, A. Thomsen, Thomas J. Cahill, Rick Huang, Li-Yin Huang, Tara C. Marcink, Oliver B. Clarke, Søren Heissel, Ali Masoudi, Danya Ben-Hail, Fadi Samaan, Venkata P. Dandey, Yong Zi Tan, Chuan Hong, Jacob P. Mahoney, Sarah Triest, John R. Little, Xin Chen, Roger K. Sunahara, Jan Steyaert, Henrik Molina, Zhiheng Yu, Amédée des Georges, Robert J. Lefkowitz - Nature Structural & Molecular Biology 2019 cited by 227

  24. Development of a universal nanobody-binding Fab module for fiducial-assisted cryo-EM studies of membrane proteins

    Authors: Joël S. Bloch, Somnath Mukherjee, Julia Kowal, E.V. Filippova, Martina Niederer, Els Pardon, Jan Steyaert, Anthony A. Kossiakoff, Kaspar P. Locher - National Academy of Sciences, Proceedings of the National Academy of Sciences 2021 cited by 117