Régis C. Lambert

2.6k total citations
39 papers, 1.9k citations indexed

About

Régis C. Lambert is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Régis C. Lambert has authored 39 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Cellular and Molecular Neuroscience, 18 papers in Molecular Biology and 17 papers in Cognitive Neuroscience. Recurrent topics in Régis C. Lambert's work include Neuroscience and Neuropharmacology Research (23 papers), Ion channel regulation and function (16 papers) and Neural dynamics and brain function (13 papers). Régis C. Lambert is often cited by papers focused on Neuroscience and Neuropharmacology Research (23 papers), Ion channel regulation and function (16 papers) and Neural dynamics and brain function (13 papers). Régis C. Lambert collaborates with scholars based in France, United Kingdom and United States. Régis C. Lambert's co-authors include Nathalie Leresche, Vincenzo Crunelli, F. Moos, François David, Anne Feltz, Adam C. Errington, Victor N. Uebele, John J. Renger, P Richard and Govindan Dayanithi 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

Régis C. Lambert

39 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Régis C. Lambert France 26 1.2k 749 694 317 304 39 1.9k
Jun Chul Kim Canada 21 800 0.7× 1.3k 1.7× 488 0.7× 246 0.8× 313 1.0× 36 2.5k
Georgia M. Alexander United States 19 1.1k 1.0× 537 0.7× 830 1.2× 264 0.8× 181 0.6× 30 1.8k
Frédéric Brocard France 25 866 0.8× 503 0.7× 395 0.6× 165 0.5× 413 1.4× 49 1.8k
Refik Kanjhan New Zealand 24 467 0.4× 439 0.6× 327 0.5× 289 0.9× 953 3.1× 36 1.8k
Tatiana Korotkova Germany 25 1.3k 1.2× 489 0.7× 1.6k 2.4× 165 0.5× 779 2.6× 46 2.8k
Laurens W. J. Bosman Netherlands 22 946 0.8× 440 0.6× 793 1.1× 127 0.4× 254 0.8× 42 1.9k
Silvia Pagliardini Canada 26 413 0.4× 466 0.6× 707 1.0× 457 1.4× 1.0k 3.4× 53 2.0k
Zhenyu Gao Netherlands 23 1.3k 1.2× 627 0.8× 1.1k 1.6× 96 0.3× 331 1.1× 40 2.9k
Jens C. Rekling Denmark 18 716 0.6× 599 0.8× 878 1.3× 893 2.8× 1.6k 5.4× 38 2.7k
Martine Hamann United Kingdom 26 1.7k 1.5× 1.2k 1.6× 731 1.1× 64 0.2× 139 0.5× 35 2.6k

Countries citing papers authored by Régis C. Lambert

Since Specialization
Citations

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

Fields of papers citing papers by Régis C. Lambert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Régis C. Lambert. 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 Régis C. Lambert. The network helps show where Régis C. Lambert may publish in the future.

Co-authorship network of co-authors of Régis C. Lambert

This figure shows the co-authorship network connecting the top 25 collaborators of Régis C. Lambert. A scholar is included among the top collaborators of Régis C. Lambert 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 Régis C. Lambert. Régis C. Lambert 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.
McCafferty, Cian, François David, Magor L. Lörincz, et al.. (2018). Cortical drive and thalamic feed-forward inhibition control thalamic output synchrony during absence seizures. Nature Neuroscience. 21(5). 744–756. 78 indexed citations
2.
Crunelli, Vincenzo, Magor L. Lörincz, William M. Connelly, et al.. (2018). Dual function of thalamic low-vigilance state oscillations: rhythm-regulation and plasticity. Nature reviews. Neuroscience. 19(2). 107–118. 82 indexed citations
3.
Boutourlinsky, Katia, et al.. (2018). Layer 2/3 Pyramidal Neurons Control the Gain of Cortical Output. Cell Reports. 24(11). 2799–2807.e4. 48 indexed citations
4.
Leresche, Nathalie & Régis C. Lambert. (2017). GABA receptors and T-type Ca2+ channels crosstalk in thalamic networks. Neuropharmacology. 136(Pt A). 37–45. 5 indexed citations
5.
Lambert, Régis C., Christine Tuleau-Malot, Thomas Bessaïh, et al.. (2017). Reconstructing the functional connectivity of multiple spike trains using Hawkes models. Journal of Neuroscience Methods. 297. 9–21. 17 indexed citations
6.
David, François, Vincenzo Crunelli, Nathalie Leresche, & Régis C. Lambert. (2016). Dynamic Analysis of the Conditional Oscillator Underlying Slow Waves in Thalamocortical Neurons. Frontiers in Neural Circuits. 10. 10–10. 5 indexed citations
7.
Taylor, Hannah, Joscha T. Schmiedt, Nihan Çarçak, et al.. (2014). Investigating local and long-range neuronal network dynamics by simultaneous optogenetics, reverse microdialysis and silicon probe recordings in vivo. Journal of Neuroscience Methods. 235. 83–91. 14 indexed citations
8.
Crunelli, Vincenzo, François David, Nathalie Leresche, & Régis C. Lambert. (2014). Role for T-type Ca2+ channels in sleep waves. Pflügers Archiv - European Journal of Physiology. 466(4). 735–745. 29 indexed citations
9.
Leresche, Nathalie, et al.. (2013). Dynamics of Intrinsic Dendritic Calcium Signaling during Tonic Firing of Thalamic Reticular Neurons. PLoS ONE. 8(8). e72275–e72275. 16 indexed citations
10.
Deleuze, Charlotte, François David, Hee‐Sup Shin, et al.. (2012). T-Type Calcium Channels Consolidate Tonic Action Potential Output of Thalamic Neurons to Neocortex. Journal of Neuroscience. 32(35). 12228–12236. 58 indexed citations
11.
Leresche, Nathalie, Régis C. Lambert, Adam C. Errington, & Vincenzo Crunelli. (2011). From sleep spindles of natural sleep to spike and wave discharges of typical absence seizures: is the hypothesis still valid?. Pflügers Archiv - European Journal of Physiology. 463(1). 201–212. 70 indexed citations
12.
Lambert, Régis C., Thomas Bessaïh, & Nathalie Leresche. (2006). Modulation of Neuronal T-Type Calcium Channels. CNS & Neurological Disorders - Drug Targets. 5(6). 611–627. 25 indexed citations
13.
Vincent, Pierre, Uwe Maskos, Laurence Bourgeais, et al.. (2006). Live imaging of neural structure and function by fibred fluorescence microscopy. EMBO Reports. 7(11). 1154–1161. 59 indexed citations
14.
Leresche, Nathalie, et al.. (2004). Paradoxical Potentiation of Neuronal T-Type Ca2+Current by ATP at Resting Membrane Potential. Journal of Neuroscience. 24(24). 5592–5602. 36 indexed citations
15.
Kozlov, Andreï S., Jung‐Ha Lee, Leanne L. Cribbs, et al.. (1999). Distinct kinetics of cloned T‐type Ca2 +  channels lead to differential Ca2 +  entry and frequency‐dependence during mock action potentials. European Journal of Neuroscience. 11(12). 4149–4158. 72 indexed citations
16.
Tamura, Richard N., Dolphine Oda, Vito Quaranta, et al.. (1997). Coating of titanium alloy with soluble laminin‐5 promotes cell attachment and hemidesmosome assembly in gingival epithelial cells: potential application to dental implants. Journal of Periodontal Research. 32(3). 287–294. 68 indexed citations
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19.
Lambert, Régis C., Govindan Dayanithi, F. Moos, & P Richard. (1994). A rise in the intracellular Ca2+ concentration of isolated rat supraoptic cells in response to oxytocin.. The Journal of Physiology. 478(2). 275–287. 165 indexed citations
20.

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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