Laurence Ris

2.8k total citations
74 papers, 2.2k citations indexed

About

Laurence Ris is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Laurence Ris has authored 74 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Cellular and Molecular Neuroscience, 31 papers in Neurology and 25 papers in Molecular Biology. Recurrent topics in Laurence Ris's work include Neuroscience and Neuropharmacology Research (32 papers), Vestibular and auditory disorders (18 papers) and Neuroinflammation and Neurodegeneration Mechanisms (12 papers). Laurence Ris is often cited by papers focused on Neuroscience and Neuropharmacology Research (32 papers), Vestibular and auditory disorders (18 papers) and Neuroinflammation and Neurodegeneration Mechanisms (12 papers). Laurence Ris collaborates with scholars based in Belgium, France and United Kingdom. Laurence Ris's co-authors include Emile Godaux, Pierre‐Paul Vidal, Ilse Dewachter, Karl-Peter Giese, Arnauld Villers, Catherine de Waele, Mauro Serafin, Fred Van Leuven, Keiko Mizuno and Delphine Reversé and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neuroscience.

In The Last Decade

Laurence Ris

70 papers receiving 2.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Laurence Ris Belgium 27 885 745 729 633 374 74 2.2k
Derya R. Shimshek Switzerland 30 924 1.0× 572 0.8× 1.0k 1.4× 949 1.5× 257 0.7× 54 3.0k
Zhenghua Xiang China 32 459 0.5× 601 0.8× 760 1.0× 434 0.7× 163 0.4× 84 2.9k
Joao Bráz United States 23 1.4k 1.6× 341 0.5× 660 0.9× 2.1k 3.3× 300 0.8× 39 3.0k
M. R. Luquín Spain 38 1.9k 2.1× 398 0.5× 566 0.8× 369 0.6× 340 0.9× 148 4.0k
Shan‐Xue Jin United States 15 1.6k 1.8× 290 0.4× 1.0k 1.4× 1.7k 2.6× 268 0.7× 24 3.1k
Maria Vittoria Podda Italy 24 572 0.6× 681 0.9× 461 0.6× 313 0.5× 357 1.0× 69 1.8k
Gian Battista Azzena Italy 24 566 0.6× 434 0.6× 591 0.8× 515 0.8× 252 0.7× 49 2.0k
Masaki Sakurai Japan 20 1.0k 1.2× 889 1.2× 524 0.7× 171 0.3× 551 1.5× 49 2.1k
François S. Roman France 26 988 1.1× 216 0.3× 572 0.8× 372 0.6× 548 1.5× 66 2.0k
Mohammed Filali Canada 29 1.2k 1.4× 996 1.3× 1.2k 1.6× 1.1k 1.8× 254 0.7× 47 3.5k

Countries citing papers authored by Laurence Ris

Since Specialization
Citations

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

Fields of papers citing papers by Laurence Ris

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laurence Ris

This figure shows the co-authorship network connecting the top 25 collaborators of Laurence Ris. A scholar is included among the top collaborators of Laurence Ris 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 Laurence Ris. Laurence Ris 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.
2.
Chéron, Guy, et al.. (2025). Beyond Vision: Response of the Mouse Visual Cortex to Multimodal Stimulation. European Journal of Neuroscience. 62(3). e70225–e70225.
3.
Azouz, Abdulkader, Maren Sitte, Gabriela Salinas, et al.. (2025). Temporal refinement of Dach1 expression contributes to the development of somatosensory neurons. The EMBO Journal. 44(10). 2882–2905.
4.
Ris, Laurence, Hilde Bastiaens, Jozef Michielsen, et al.. (2023). Management of Low Back Pain: Do Physiotherapists Know the Evidence-Based Guidelines?. International Journal of Environmental Research and Public Health. 20(9). 5611–5611. 8 indexed citations
5.
6.
Shetty, Mahesh Shivarama, Laurence Ris, R. Schindler, et al.. (2021). Mice lacking the cAMP effector protein POPDC1 show enhanced hippocampal synaptic plasticity. Cerebral Cortex. 32(16). 3457–3471. 4 indexed citations
7.
Vermeiren, Simon, Roberta Gualdani, Sampurna Chakrabarti, et al.. (2021). Prdm12 modulates pain-related behavior by remodeling gene expression in mature nociceptors. Pain. 163(8). e927–e941. 5 indexed citations
8.
Michielsen, Jozef, et al.. (2021). An interactive e-learning module to promote bio-psycho-social management of low back pain in healthcare professionals: a pilot study. Journal of Manual & Manipulative Therapy. 30(2). 105–115. 8 indexed citations
9.
Pierrot, Nathalie, Laurence Ris, Ilie‐Cosmin Stancu, et al.. (2019). Sex-regulated gene dosage effect of PPARα on synaptic plasticity. Life Science Alliance. 2(2). e201800262–e201800262. 19 indexed citations
10.
Jensen, Cathy, Ron Kooijman, Ann Massie, et al.. (2016). Astrocytic β2 Adrenergic Receptor Gene Deletion Affects Memory in Aged Mice. PLoS ONE. 11(10). e0164721–e0164721. 27 indexed citations
11.
Grevesse, Thomas, Arnauld Villers, Marie Versaevel, et al.. (2016). Matrix stiffness modulates formation and activity of neuronal networks of controlled architectures. Biomaterials. 89. 14–24. 69 indexed citations
12.
Stancu, Ilie‐Cosmin, Bruno Vasconcelos, Laurence Ris, et al.. (2015). Templated misfolding of Tau by prion-like seeding along neuronal connections impairs neuronal network function and associated behavioral outcomes in Tau transgenic mice. Acta Neuropathologica. 129(6). 875–894. 119 indexed citations
13.
Ris, Laurence, Arnauld Villers, & Emile Godaux. (2009). Synaptic capture-mediated long-lasting long-term potentiation is strongly dependent on mRNA translation. Neuroreport. 20(17). 1572–1576. 7 indexed citations
14.
Dewachter, Ilse, Laurence Ris, Tomasz Jaworski, et al.. (2009). GSK3ß, a centre-staged kinase in neuropsychiatric disorders, modulates long term memory by inhibitory phosphorylation at Serine-9. Neurobiology of Disease. 35(2). 193–200. 82 indexed citations
15.
Godaux, Emile, et al.. (2007). Involvement of hyperpolarization-activated cation channels in synaptic modulation. Neuroreport. 18(12). 1231–1235. 7 indexed citations
16.
Ris, Laurence, Marco Angelo, Florian Plattner, et al.. (2005). Sexual dimorphisms in the effect of low‐level p25 expression on synaptic plasticity and memory. European Journal of Neuroscience. 21(11). 3023–3033. 33 indexed citations
17.
Ris, Laurence, Denis Nonclercq, Henri Alexandre, et al.. (2003). Labyrinthectomy changes T-type calcium channels in vestibular neurones of the guinea pig. Neuroreport. 14(12). 1585–1589. 8 indexed citations
18.
Nonclercq, Denis, et al.. (2003). Properties of neurons from the rat medial vestibular nucleus in microexplant culture. Neuroscience Letters. 338(1). 45–48. 1 indexed citations
19.
Ris, Laurence, et al.. (2001). Increase in dynamic excitability of vestibular neurons in guinea pig brainstem slices during vestibular compensation. The Society for Neuroscience Abstracts. 27(1). 784. 2 indexed citations
20.
Schneider, Ilka, Delphine Reversé, Ilse Dewachter, et al.. (2001). Mutant Presenilins Disturb Neuronal Calcium Homeostasis in the Brain of Transgenic Mice, Decreasing the Threshold for Excitotoxicity and Facilitating Long-term Potentiation. Journal of Biological Chemistry. 276(15). 11539–11544. 115 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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