Thomas Voets

29.8k total citations · 6 hit papers
251 papers, 22.8k citations indexed

About

Thomas Voets is a scholar working on Sensory Systems, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Thomas Voets has authored 251 papers receiving a total of 22.8k indexed citations (citations by other indexed papers that have themselves been cited), including 165 papers in Sensory Systems, 97 papers in Molecular Biology and 69 papers in Cellular and Molecular Neuroscience. Recurrent topics in Thomas Voets's work include Ion Channels and Receptors (160 papers), Ion channel regulation and function (72 papers) and Neurobiology and Insect Physiology Research (47 papers). Thomas Voets is often cited by papers focused on Ion Channels and Receptors (160 papers), Ion channel regulation and function (72 papers) and Neurobiology and Insect Physiology Research (47 papers). Thomas Voets collaborates with scholars based in Belgium, Germany and United States. Thomas Voets's co-authors include Bernd Nilius, Guy Droogmans, Grzegorz Owsianik, Joris Vriens, Annelies Janssens, Karel Talavera, Jean Prenen, Rudi Vennekens, Jan Eggermont and Hiroyuki Watanabe and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Thomas Voets

246 papers receiving 22.6k citations

Hit Papers

Transient Receptor Potent... 2003 2026 2010 2018 2007 2003 2004 2003 2014 250 500 750 1000

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Thomas Voets 13.3k 9.4k 6.1k 4.4k 3.9k 251 22.8k
Makoto Tominaga 17.0k 1.3× 7.8k 0.8× 7.8k 1.3× 4.4k 1.0× 10.3k 2.7× 402 30.8k
Reinhold Penner 10.2k 0.8× 9.1k 1.0× 5.1k 0.8× 4.3k 1.0× 1.6k 0.4× 129 18.5k
Bernd Nilius 19.8k 1.5× 16.3k 1.7× 9.1k 1.5× 6.8k 1.5× 6.3k 1.6× 412 36.5k
Michael J. Caterina 15.3k 1.2× 6.0k 0.6× 7.3k 1.2× 3.0k 0.7× 9.6k 2.5× 94 24.2k
Thomas Gudermann 6.3k 0.5× 7.6k 0.8× 4.1k 0.7× 4.2k 1.0× 2.0k 0.5× 317 17.2k
James W. Putney 11.4k 0.9× 17.5k 1.9× 9.4k 1.5× 2.5k 0.6× 3.8k 1.0× 292 28.1k
Veit Flockerzi 8.8k 0.7× 13.3k 1.4× 8.6k 1.4× 2.6k 0.6× 2.2k 0.6× 252 20.9k
Lutz Birnbaumer 9.7k 0.7× 27.5k 2.9× 14.5k 2.4× 3.2k 0.7× 4.6k 1.2× 556 42.8k
Stuart Bevan 8.5k 0.6× 5.2k 0.6× 6.2k 1.0× 1.8k 0.4× 6.7k 1.7× 135 17.5k
Michael X. Zhu 6.5k 0.5× 6.2k 0.7× 3.2k 0.5× 1.3k 0.3× 1.5k 0.4× 232 13.5k

Countries citing papers authored by Thomas Voets

Since Specialization
Citations

This map shows the geographic impact of Thomas Voets's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Thomas Voets with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas Voets more than expected).

Fields of papers citing papers by Thomas Voets

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas Voets. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Thomas Voets. The network helps show where Thomas Voets may publish in the future.

Co-authorship network of co-authors of Thomas Voets

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Voets. A scholar is included among the top collaborators of Thomas Voets based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Thomas Voets. Thomas Voets is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Janssen, A.J.M., Sofie Kessels, Yanyan Wang, et al.. (2025). APOE deficiency inhibits amyloid-facilitated (A) tau pathology (T) and neurodegeneration (N), halting progressive ATN pathology in a preclinical model. Molecular Psychiatry. 30(10). 4512–4528. 1 indexed citations
2.
Boonen, Brett & Thomas Voets. (2024). A frozen portrait of a warm channel. Cell Calcium. 123. 102927–102927.
3.
Becker, Lena‐Luise, Denise Horn, Felix Boschann, et al.. (2023). Primidone improves symptoms in TRPM3‐linked developmental and epileptic encephalopathy with spike‐and‐wave activation in sleep. Epilepsia. 64(5). e61–e68. 9 indexed citations
4.
Janssens, Annelies, et al.. (2023). Inhibition of TRPM8 by the urinary tract analgesic drug phenazopyridine. European Journal of Pharmacology. 942. 175512–175512. 3 indexed citations
5.
Voets, Thomas, et al.. (2023). pH‐dependent modulation of TRPV1 by modality‐selective antagonists. British Journal of Pharmacology. 180(21). 2750–2761. 6 indexed citations
6.
Startek, Justyna B., et al.. (2021). The Agonist Action of Alkylphenols on TRPA1 Relates to Their Effects on Membrane Lipid Order: Implications for TRPA1-Mediated Chemosensation. International Journal of Molecular Sciences. 22(7). 3368–3368. 10 indexed citations
7.
Mulier, Marie, Nele Van Ranst, Nikky Corthout, et al.. (2020). Upregulation of TRPM3 in nociceptors innervating inflamed tissue. eLife. 9. 30 indexed citations
8.
Startek, Justyna B., Brett Boonen, Alejandro López‐Requena, et al.. (2019). Mouse TRPA1 function and membrane localization are modulated by direct interactions with cholesterol. eLife. 8. 45 indexed citations
9.
López‐Requena, Alejandro, et al.. (2019). Expression and Functional Role of TRPV4 in Bone Marrow-Derived CD11c+ Cells. International Journal of Molecular Sciences. 20(14). 3378–3378. 16 indexed citations
10.
Menigoz, Aurélie, Sílvia Pinto, Tim Tambuyzer, et al.. (2018). Disentangling the role of TRPM4 in hippocampus-dependent plasticity and learning: an electrophysiological, behavioral and FMRI approach. Brain Structure and Function. 223(8). 3557–3576. 18 indexed citations
11.
Uvin, Pieter, Jan Franken, Mathieu Boudes, et al.. (2013). The bladder-cooling reflex is a local phenomenon, mediated by TRPA1. Neurourology and Urodynamics. 32(6). 572–573. 1 indexed citations
12.
Mathar, Ilka, Rudi Vennekens, Marcel Meissner, et al.. (2011). Increased catecholamine secretion contributes to hypertension in TRPM4-deficient mice. Naunyn-Schmiedeberg s Archives of Pharmacology. 383. 6–7. 2 indexed citations
13.
Colsoul, Barbara, Anica Schraenen, Katleen Lemaire, et al.. (2010). Loss of high-frequency glucose-induced Ca 2+ oscillations in pancreatic islets correlates with impaired glucose tolerance in Trpm5 −/− mice. Proceedings of the National Academy of Sciences. 107(11). 5208–5213. 163 indexed citations
14.
Karashima, Yuji, Karel Talavera, Wouter Everaerts, et al.. (2009). TRPA1 acts as a cold sensor in vitro and in vivo. Proceedings of the National Academy of Sciences. 106(4). 1273–1278. 473 indexed citations
15.
Krakow, Deborah, Joris Vriens, Natalia Camacho, et al.. (2009). Mutations in the Gene Encoding the Calcium-Permeable Ion Channel TRPV4 Produce Spondylometaphyseal Dysplasia, Kozlowski Type and Metatropic Dysplasia. The American Journal of Human Genetics. 84(3). 307–315. 148 indexed citations
16.
Everaerts, Wouter, Karel Talavera, Maarten Gees, et al.. (2009). Allyl isothyocynate induces bladder overactivity via direct activation of both trpa1 and trpv1. Neurourology and Urodynamics. 28(7). 865–865. 1 indexed citations
17.
Everaerts, Wouter, et al.. (2009). App441-1, a novel trpv4 agonist is able to induce bladder overactivity in rats and mice. Neurourology and Urodynamics. 28(7). 701–702. 3 indexed citations
18.
Vriens, Joris, Makoto Suzuki, Thomas Voets, & Bernd Nilius. (2005). Modulation of the Ca2+ permeable cation channel TRPV4 by cytochrome P450 epoxygenases in vascular endothelium. Biophysical Journal. 88(1). 14 indexed citations
19.
Vriens, Joris, Hiroyuki Watanabe, Annelies Janssens, et al.. (2003). Cell swelling, heat, and chemical agonists use distinct pathways for the activation of the cation channel TRPV4. Proceedings of the National Academy of Sciences. 101(1). 396–401. 505 indexed citations breakdown →
20.
Dinkelacker, Vera, Thomas Voets, Erwin Neher, & Tobias Moser. (2000). The readily releasable pool of vesicles in chromaffin cells is replenished in a temperature-dependent manner and transiently overfills at 37 degrees C.. PubMed Central. 20(22). 8377–83. 49 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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