Joris Vriens

13.5k total citations · 4 hit papers
109 papers, 9.1k citations indexed

About

Joris Vriens is a scholar working on Sensory Systems, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Joris Vriens has authored 109 papers receiving a total of 9.1k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Sensory Systems, 25 papers in Molecular Biology and 23 papers in Cellular and Molecular Neuroscience. Recurrent topics in Joris Vriens's work include Ion Channels and Receptors (63 papers), Neurobiology and Insect Physiology Research (21 papers) and Ion channel regulation and function (15 papers). Joris Vriens is often cited by papers focused on Ion Channels and Receptors (63 papers), Neurobiology and Insect Physiology Research (21 papers) and Ion channel regulation and function (15 papers). Joris Vriens collaborates with scholars based in Belgium, United Kingdom and Germany. Joris Vriens's co-authors include Bernd Nilius, Thomas Voets, Hiroyuki Watanabe, Guy Droogmans, Jean Prenen, Annelies Janssens, Grzegorz Owsianik, Rudi Vennekens, B. Nilius and Giovanni Appendino 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

Joris Vriens

104 papers receiving 9.0k citations

Hit Papers

Anandamide and arachidoni... 2002 2026 2010 2018 2003 2002 2003 2018 250 500 750

Author Peers

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

Author Last Decade Papers Cites
Joris Vriens 6.0k 2.8k 2.1k 1.9k 1.6k 109 9.1k
Grzegorz Owsianik 6.5k 1.1× 3.6k 1.3× 1.5k 0.7× 2.0k 1.1× 1.9k 1.2× 63 9.6k
Rudi Vennekens 5.4k 0.9× 3.2k 1.1× 1.2k 0.6× 1.7k 0.9× 2.0k 1.3× 106 8.0k
Christian Harteneck 4.7k 0.8× 4.3k 1.5× 1.9k 0.9× 2.0k 1.0× 1.3k 0.9× 82 8.9k
Jean Prenen 5.3k 0.9× 3.4k 1.2× 1.2k 0.6× 1.7k 0.9× 1.8k 1.1× 55 7.8k
Marc Freichel 4.2k 0.7× 3.9k 1.4× 1.0k 0.5× 2.4k 1.3× 1.4k 0.9× 145 8.2k
Guy Droogmans 5.9k 1.0× 6.0k 2.1× 1.9k 0.9× 3.0k 1.6× 2.4k 1.6× 86 11.4k
David J. Beech 4.1k 0.7× 5.4k 1.9× 2.2k 1.0× 2.8k 1.5× 1.0k 0.7× 208 9.8k
Indu S. Ambudkar 5.0k 0.8× 4.7k 1.7× 1.6k 0.8× 2.4k 1.3× 1.1k 0.7× 172 9.3k
Uhtaek Oh 3.7k 0.6× 3.3k 1.2× 2.7k 1.3× 2.1k 1.1× 632 0.4× 104 7.6k
David D. McKemy 4.8k 0.8× 1.4k 0.5× 2.1k 1.0× 2.5k 1.4× 1.2k 0.8× 47 6.9k

Countries citing papers authored by Joris Vriens

Since Specialization
Citations

This map shows the geographic impact of Joris Vriens'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 Joris Vriens with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Joris Vriens more than expected).

Fields of papers citing papers by Joris Vriens

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joris Vriens. 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 Joris Vriens. The network helps show where Joris Vriens may publish in the future.

Co-authorship network of co-authors of Joris Vriens

This figure shows the co-authorship network connecting the top 25 collaborators of Joris Vriens. A scholar is included among the top collaborators of Joris Vriens 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 Joris Vriens. Joris Vriens 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
2.
Saarela, Ulla, Riikka K. Arffman, Sharon Lie Fong, et al.. (2025). PCOS endometrium-derived epithelial organoids as a novel model to study endometrial dysfunction. Human Reproduction. 40(8). 1535–1549. 1 indexed citations
3.
Saarela, Ulla, Noah Ollikainen, Matti Poutanen, et al.. (2025). Prenatally androgenized PCOS mice have ovary-independent uterine dysfunction and placental inflammation aggravated by high-fat diet. Science Advances. 11(19). eadu3699–eadu3699.
4.
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
5.
Boon, Ruben, Joris Vriens, Leo A. van Grunsven, et al.. (2023). Osmolar Modulation Drives Reversible Cell Cycle Exit and Human Pluripotent Cell Differentiation via NF‐κВ and WNT Signaling. Advanced Science. 11(7). e2307554–e2307554. 5 indexed citations
6.
Pinto, Sílvia, et al.. (2023). TRPM3 as a novel target to alleviate acute oxaliplatin-induced peripheral neuropathic pain. Pain. 164(9). 2060–2069. 22 indexed citations
7.
Peeraer, Karen, Thomas D’Hooghe, Jacky Boivin, et al.. (2022). Great expectations of IVF patients: the role of gender, dispositional optimism and shared IVF prognoses. Human Reproduction. 37(5). 997–1006. 12 indexed citations
8.
Philippaert, Koenraad, et al.. (2020). Horizontal Hippocampal Slices of the Mouse Brain. Journal of Visualized Experiments. 1 indexed citations
10.
Mulier, Marie, Nele Van Ranst, Nikky Corthout, et al.. (2020). Upregulation of TRPM3 in nociceptors innervating inflamed tissue. eLife. 9. 30 indexed citations
11.
Clercq, Katrien De, Marie Mulier, Katharina Held, et al.. (2018). A TRP channel trio mediates acute noxious heat sensing. Nature. 555(7698). 662–666. 326 indexed citations breakdown →
12.
Tóth, Balázs István, Maik Konrad, Debapriya Ghosh, et al.. (2015). Regulation of the transient receptor potential channel TRPM3 by phosphoinositides. The Journal of General Physiology. 146(1). 51–63. 52 indexed citations
13.
Tóth, Balázs István, Joris Vriens, Debapriya Ghosh, & Thomas Voets. (2014). Cellular Regulation of Transient Receptor Potential Melastatin 3 (TRPM3) Channel Activity. Biophysical Journal. 106(2). 334a–334a. 1 indexed citations
14.
Rath, Géraldine, Julie Saliez, Miguel Romero, et al.. (2012). Vascular Hypoxic Preconditioning Relies on TRPV4-Dependent Calcium Influx and Proper Intercellular Gap Junctions Communication. Arteriosclerosis Thrombosis and Vascular Biology. 32(9). 2241–2249. 48 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, Grzegorz Owsianik, Joris Vriens, et al.. (2009). Functional characterisation of trip channels in mouse urothelium: a major role for trpv4. Neurourology and Urodynamics. 28(7). 709–710. 1 indexed citations
17.
Masuyama, Ritsuko, Joris Vriens, Thomas Voets, et al.. (2008). TRPV4-Mediated Calcium Influx Regulates Terminal Differentiation of Osteoclasts. Cell Metabolism. 8(3). 257–265. 285 indexed citations
18.
Masuyama, Ritsuko, Joris Vriens, Sophie Torrekens, et al.. (2007). TRPV4 affects bone remodeling by regulating calcium signaling required for osteoclast activity. Journal of Bone and Mineral Research. 22. 1 indexed citations
19.
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
20.
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 →

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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