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Vincent Timmerman

Active 1991–2026

105
Papers
17,962
Citations
76
h-index
101
i10-index

Citations

Citations per year for Vincent Timmerman1951: 1 citations1990: 1 citations1992: 17 citations1993: 28 citations1994: 18 citations1995: 14 citations1996: 31 citations1997: 15 citations1998: 36 citations1999: 62 citations2000: 57 citations2001: 35 citations2002: 55 citations2003: 56 citations2004: 78 citations2005: 113 citations2006: 182 citations2007: 126 citations2008: 146 citations2009: 170 citations2010: 179 citations2011: 220 citations2012: 220 citations2013: 177 citations2014: 230 citations2015: 208 citations2016: 128 citations2017: 167 citations2018: 108 citations2019: 572 citations2020: 600 citations2021: 579 citations2022: 423 citations2023: 334 citations2024: 589 citations2025: 232 citations2026: 12 citations1952–1989: no citations, so these years are not shown1991: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 1,958 citing papers, 25.7% of this breakdownChina: 659 citing papers, 8.6% of this breakdownUnited Kingdom: 590 citing papers, 7.7% of this breakdownGermany: 511 citing papers, 6.7% of this breakdownItaly: 459 citing papers, 6% of this breakdownFrance: 341 citing papers, 4.5% of this breakdownCanada: 295 citing papers, 3.9% of this breakdownBelgium: 248 citing papers, 3.3% of this breakdownAustralia: 216 citing papers, 2.8% of this breakdownNetherlands: 203 citing papers, 2.7% of this breakdownJapan: 199 citing papers, 2.6% of this breakdownSwitzerland: 193 citing papers, 2.5% of this breakdown
0%25.7%Other 23%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology49.1%
  • Medicine24.3%
  • Neuroscience22%
  • Immunology and Microbiology2%
  • Nursing0.9%
  • Agricultural and Biological Sciences0.6%
  • Other1.1%

Topics

  • Mitochondrial Function and Pathology6.1%
  • Hereditary Neurological Disorders6.1%
  • RNA Research and Splicing3.7%
  • Genetic Neurodegenerative Diseases3.6%
  • Amyotrophic Lateral Sclerosis Research3.3%
  • Endoplasmic Reticulum Stress and Disease2.7%
  • Other74.5%

Coauthors

All papers

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  1. The hnRNP family: insights into their role in health and disease

    Authors: Thomas Geuens, Delphine Bouhy, Vincent Timmerman - Human Genetics 2016 cited by 1,147

  2. A reference human induced pluripotent stem cell line for large-scale collaborative studies

    Authors: Caroline B. Pantazis, Andrian Yang, Erika Lara, Justin A. McDonough, Cornelis Blauwendraat, Lirong Peng, Hideyuki Oguro, Jitendra Kumar Kanaujiya, Jizhong Zou, David P. Sebesta, Gretchen Pratt, Erin Cross, Jeffrey Blockwick, Philip Buxton, Lauren Kinner-Bibeau, Constance Medura, Christopher Tompkins, Stephen H. Hughes, Marianita Santiana, Faraz Faghri, Mike A. Nalls, Dan Vitale, Shannon Ballard, Yue Qi, Daniel M. Ramos, Kailyn Anderson, Julia T. Stadler, Priyanka Narayan, Jason Papademetriou, Luke Reilly, Matthew P. Nelson, Sanya Aggarwal, Leah U. Rosen, Peter Kirwan, Venkat Pisupati, Steven L. Coon, Sonja W. Scholz, Theresa Priebe, Miriam Öttl, Jian Dong, Marieke Meijer, Lara J.M. Janssen, Vanessa S. Lourenco, Rik van der Kant, Dennis Crusius, Dominik Paquet, Ana‐Caroline Raulin, Guojun Bu, Aaron Held, Brian J. Wainger, Rebecca Gabriele, Jackie M. Casey, Selina Wray, Dad Abu-Bonsrah, Clare L. Parish, Melinda S. Beccari, Don W. Cleveland, Emmy Li, Indigo V.L. Rose, Martin Kampmann, Carles Calatayud, Patrik Verstreken, Laurin Heinrich, Max Y. Chen, Birgitt Schüle, Dan Dou, Erika L.F. Holzbaur, Maria Clara Zanellati, Richa Basundra, Mohanish Deshmukh, Sarah Cohen, Richa Khanna, Malavika Raman, Zachary S. Nevin, Madeline Matia, Jonas Van Lent, Vincent Timmerman, Bruce R. Conklin, Katherine Johnson Chase, Ke Zhang, Salome Funes, Daryl A. Bosco, Lena Erlebach, Marc Welzer, Deborah Kronenberg‐Versteeg, Guochang Lyu, Ernest Arenas, Elena Coccia, Lily Sarrafha, Tim Ahfeldt, John C. Marioni, William C. Skarnes, Mark Cookson, Michael E. Ward, Florian T. Merkle - Cell stem cell 2022 cited by 304

  3. Profiling peripheral nerve macrophages reveals two macrophage subsets with distinct localization, transcriptome and response to injury

    Authors: Elke Ydens, Lukas Amann, Bob Asselbergh, Charlotte L. Scott, Liesbet Martens, Dorine Sichien, Omar Mossad, Thomas Blank, Sofie De Prijck, Donovan Low, Takahiro Masuda, Yvan Saeys, Vincent Timmerman, Ralf Stumm, Florent Ginhoux, Marco Prinz, Sophie Janssens, Martin Guilliams - Nature Neuroscience 2020 cited by 241

  4. Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

    Authors: Stephan Züchner, Irina Mersiyanova, M. Muglia, Nisrine Bissar‐Tadmouri, Julie M. Rochelle, Е. Л. Дадали, Mario Zappia, Eva Nelis, A. Patitucci, Jan Senderek, Yeşim Parman, Oleg V. Evgrafov, Peter De Jonghe, Yuji Takahashi, Shoij Tsuji, Margaret A. Pericak‐Vance, Aldo Quattrone, Esra Battologlu, A. V. Polyakov, Vincent Timmerman, J. M. Schröder, Jeffery M. Vance - Nature Genetics 2004 cited by 1,562

  5. Small heat shock proteins operate as molecular chaperones in the mitochondrial intermembrane space

    Authors: Elias Adriaenssens, Bob Asselbergh, Pablo Rivera-Mejías, Sven Bervoets, Leen Vendredy, Vicky De Winter, Katrien Spaas, Riet De Rycke, Gert Van Isterdael, Francis Impens, Thomas Langer, Vincent Timmerman - Nature Cell Biology 2023 cited by 76

  6. HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1–induced Charcot-Marie-Tooth disease

    Authors: Constantin d’Ydewalle, Jyothsna Krishnan, Driss M Chiheb, Philip Van Damme, Joy Irobi, Alan P. Kozikowski, Pieter Vanden Berghe, Vincent Timmerman, Wim Robberecht, Ludo Van Den Bosch - Nature Medicine 2011 cited by 461

  7. The chaperone-assisted selective autophagy complex dynamics and dysfunctions

    Authors: B. Tedesco, Leen Vendredy, Vincent Timmerman, Angelo Poletti - Autophagy 2023 cited by 113

  8. DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)

    Authors: Ying-Zhang Chen, Craig L. Bennett, Huy M. Huynh, Ian P. Blair, Imke Puls, Joy Irobi, Ines Dierick, Annette Abel, Marina Kennerson, Bruce A. Rabin, Garth A. Nicholson, Michaela Auer‐Grumbach, Klaus Wagner, Peter De Jonghe, John W. Griffin, Kenneth H. Fischbeck, Vincent Timmerman, David R. Cornblath, Phillip F. Chance - The American Journal of Human Genetics 2004 cited by 812

  9. Mitochondria-associated membranes as hubs for neurodegeneration

    Authors: Michiel Krols, Gert Van Isterdael, Bob Asselbergh, Anna Kremer, Saskia Lippens, Vincent Timmerman, Sophie Janssens - Acta Neuropathologica 2016 cited by 199

  10. Partial Inhibition of Glycolysis Reduces Atherogenesis Independent of Intraplaque Neovascularization in Mice

    Authors: Paola Perrotta, Bieke Van der Veken, Pieter Van der Veken, Isabel Pintelon, Laurence Roosens, Elias Adriaenssens, Vincent Timmerman, Pieter‐Jan Guns, Guido R.Y. De Meyer, Wim Martinet - Arteriosclerosis Thrombosis and Vascular Biology 2020 cited by 67

  11. A de novo gain-of-function mutation in SCN11A causes loss of pain perception

    Authors: Enrico Leipold, Lutz Liebmann, Georg Christoph Korenke, Theresa Heinrich, Sebastian Gießelmann, Jonathan Baets, Matthias Ebbinghaus, R. Oliver Goral, Tommy Stödberg, J. Christopher Hennings, Markus Bergmann, Janine Altmüller, Hölger Thiele, Andrea Wetzel, Peter Nürnberg, Vincent Timmerman, Peter De Jonghe, Robert Blum, Hans‐Georg Schaible, Joachim Weis, Stefan H. Heinemann, Christian A. Hübner, Ingo Kurth - Nature Genetics 2013 cited by 304

  12. Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy

    Authors: Ingo Kurth, Torsten Pamminger, J. Christopher Hennings, Désirée Soehendra, Antje K. Huebner, Annelies Rotthier, Jonathan Baets, Jan Senderek, Haluk Topaloğlu, Sandra A. Farrell, Gudrun Nürnberg, Peter Nürnberg, Peter De Jonghe, Andreas Gal, Christoph Kaether, Vincent Timmerman, Christian A. Hübner - Nature Genetics 2009 cited by 256

  13. Microglial derived extracellular vesicles activate autophagy and mediate multi‐target signaling to maintain cellular homeostasis

    Authors: Bram van den Broek, Isabel Pintelon, Ibrahim Hamad, Sofie Kessels, Mansour Haidar, Niels Hellings, Jerome J. A. Hendriks, Markus Kleinewietfeld, Bert Brône, Vincent Timmerman, Jean‐Pierre Timmermans, Veerle Somers, L. Michiels, Joy Irobi - Journal of Extracellular Vesicles 2020 cited by 58

  14. Neuropathy-causing mutations in HSPB1 impair autophagy by disturbing the formation of SQSTM1/p62 bodies

    Authors: Mansour Haidar, Bob Asselbergh, Elias Adriaenssens, Vicky De Winter, Jean‐Pierre Timmermans, Michaela Auer‐Grumbach, Manisha Juneja, Vincent Timmerman - Autophagy 2019 cited by 71

  15. Induced pluripotent stem cell-derived motor neurons of CMT type 2 patients reveal progressive mitochondrial dysfunction

    Authors: Jonas Van Lent, Peter Verstraelen, Bob Asselbergh, Elias Adriaenssens, Ligia Mateiu, Christophe Verbist, Vicky De Winter, Kristel Eggermont, Ludo Van Den Bosch, Winnok H. De Vos, Vincent Timmerman - Brain 2021 cited by 56

  16. Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy

    Authors: Albena Jordanova, Joy Irobi, Florian P. Thomas, Patrick Van Dijck, Kris Meerschaert, Maarten Dewil, Ines Dierick, An Jacobs, Els De Vriendt, Velina Guergueltcheva, Chitharanjan V. Rao, Ivailo Tournev, Francisco A A Gondim, Marc D’Hooghe, Veerle Van Gerwen, Patrick Callaerts, Ludo Van Den Bosch, Jean‐Pierre Timmermans, Wim Robberecht, Jan Gettemans, Johan M. Thevelein, Peter De Jonghe, Ivo Kremensky, Vincent Timmerman - Nature Genetics 2006 cited by 376

  17. Small heat shock proteins in neurodegenerative diseases

    Authors: Leen Vendredy, Elias Adriaenssens, Vincent Timmerman - Cell Stress and Chaperones 2020 cited by 93

  18. Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome

    Authors: Christian Windpassinger, Michaela Auer‐Grumbach, Joy Irobi, Heema Patel, Erwin Petek, Gerd Hörl, Roland Malli, Johanna A. Reed, Ines Dierick, Nathalie Verpoorten, Thomas T. Warner, Christos Proukakis, Peter Van den Bergh, Christine Verellen, Lionel Van Maldergem, Luciano Merlini, Peter De Jonghe, Vincent Timmerman, Andrew H. Crosby, Klaus Wagner - Nature Genetics 2004 cited by 380

  19. Mutations in the SPTLC2 Subunit of Serine Palmitoyltransferase Cause Hereditary Sensory and Autonomic Neuropathy Type I

    Authors: Annelies Rotthier, Michaela Auer‐Grumbach, Katrien Janssens, Jonathan Baets, Anke Penno, Le­onardo Almeida-Souza, Kim van Hoof, An Jacobs, Els De Vriendt, Beate Schlotter‐Weigel, Wolfgang N. Löscher, Petr Vondráček, Pavel Seeman, Peter De Jonghe, Patrick Van Dijck, Albena Jordanova, Thorsten Hornemann, Vincent Timmerman - The American Journal of Human Genetics 2010 cited by 189

  20. Altered interplay between endoplasmic reticulum and mitochondria in Charcot–Marie–Tooth type 2A neuropathy

    Authors: Nathalie Bernard‐Marissal, Gerben van Hameren, Manisha Juneja, Christophe Pellegrino, Lauri Louhivuori, Luca Bartesaghi, Cylia Rochat, Omar El Mansour, Jean‐Jacques Médard, Marie Croisier, Catherine Maclachlan, Olivier Poirot, Per Uhlén, Vincent Timmerman, Nicolas Tricaud, Bernard L. Schneider, Roman Chrast - National Academy of Sciences, Proceedings of the National Academy of Sciences 2019 cited by 100

  21. Loss of Neurological Disease HSAN-I-Associated Gene SPTLC2 Impairs CD8+ T Cell Responses to Infection by Inhibiting T Cell Metabolic Fitness

    Authors: Jingxia Wu, Sicong Ma, Roger Sandhoff, Yanan Ming, Agnes Hotz‐Wagenblatt, Vincent Timmerman, Nathalie Bonello‐Palot, Beate Schlotter‐Weigel, Michaela Auer‐Grumbach, Pavel Seeman, Wolfgang N. Löscher, Markus Reindl, Florian Weiß, Eric Y. Mah, Nina Weisshaar, Alaa Madi, Kerstin Möhr, Tilo Schlimbach, Rubí M.-H. Velasco Cárdenas, Jonas Koeppel, Florian Grünschläger, Lisann Müller, Maren Baumeister, Britta Brügger, Michael Schmitt, Guido Wabnitz, Yvonne Samstag, Guoliang Cui - Immunity 2019 cited by 55

  22. NCAM1 and GDF15 are biomarkers of Charcot-Marie-Tooth disease in patients and mice

    Authors: Matthew J Jennings, Alexia Kagiava, Leen Vendredy, Emily L. Spaulding, Marina Stavrou, Denisa Hathazi, Anika Grüneboom, Vicky De Winter, Burkhard Gess, Ulrike Schara, Oksana Pogoryelova, Hanns Lochmüller, Christoph H. Borchers, Andreas Roos, Robert W. Burgess, Vincent Timmerman, Kleopas A. Kleopa, Rita Horváth - Brain 2022 cited by 37

  23. Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy

    Authors: Oleg V. Evgrafov, Irina Mersiyanova, Joy Irobi, Ludo Van Den Bosch, Ines Dierick, Conrad L. Leung, O. A. Schagina, Nathalie Verpoorten, Katrien Van Impe, В. П. Федотов, Е. Л. Дадали, Michaela Auer‐Grumbach, Christian Windpassinger, Klaus Wagner, Zoran D‎. Mitrović, David Hilton‐Jones, Kevin Talbot, Jean‐Jacques Martin, Natalia Vasserman, Svetlana Tverskaya, A. V. Polyakov, Ronald K.H. Liem, Jan Gettemans, Wim Robberecht, Peter De Jonghe, Vincent Timmerman - Nature Genetics 2004 cited by 584

  24. Mutations in the Small GTP-ase Late Endosomal Protein RAB7 Cause Charcot-Marie-Tooth Type 2B Neuropathy

    Authors: Kristien Verhoeven, Peter De Jonghe, Katrien Coen, Nathalie Verpoorten, Michaela Auer‐Grumbach, Jennifer M. Kwon, David Fitzpatrick, Eric Schmedding, Els De Vriendt, An Jacobs, Veerle Van Gerwen, Klaus Wagner, Hans‐Peter Hartung, Vincent Timmerman - The American Journal of Human Genetics 2003 cited by 453