Philippe Lory

6.4k total citations
105 papers, 4.9k citations indexed

About

Philippe Lory is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Philippe Lory has authored 105 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 91 papers in Molecular Biology, 62 papers in Cellular and Molecular Neuroscience and 43 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Philippe Lory's work include Ion channel regulation and function (82 papers), Cardiac electrophysiology and arrhythmias (40 papers) and Neuroscience and Neuropharmacology Research (38 papers). Philippe Lory is often cited by papers focused on Ion channel regulation and function (82 papers), Cardiac electrophysiology and arrhythmias (40 papers) and Neuroscience and Neuropharmacology Research (38 papers). Philippe Lory collaborates with scholars based in France, United States and Canada. Philippe Lory's co-authors include Joël Nargeot, Jean Chemin, Arnaud Monteil, Emmanuel Bourinet, Isabelle Bidaud, Edward Perez‐Reyes, Gyula Váradi, Arnold Schwartz, Alexandre Mezghrani and Gerald W. Zamponi and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Philippe Lory

104 papers receiving 4.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philippe Lory France 43 3.8k 2.5k 1.4k 563 326 105 4.9k
Leanne L. Cribbs United States 40 5.4k 1.4× 3.3k 1.3× 2.4k 1.7× 888 1.6× 522 1.6× 71 6.5k
Atsushi Inanobe Japan 32 3.4k 0.9× 2.0k 0.8× 1.1k 0.7× 287 0.5× 283 0.9× 68 4.4k
Aaron P. Fox United States 31 4.2k 1.1× 3.5k 1.4× 671 0.5× 597 1.1× 222 0.7× 66 5.6k
Andreas Karschin Germany 45 4.9k 1.3× 3.9k 1.5× 1.1k 0.8× 428 0.8× 321 1.0× 80 6.2k
Jean Chemin France 35 2.6k 0.7× 1.7k 0.7× 764 0.5× 755 1.3× 630 1.9× 56 3.7k
Stephen R. Ikeda United States 40 4.0k 1.1× 3.3k 1.3× 656 0.5× 659 1.2× 168 0.5× 103 5.3k
Jürgen Daut Germany 37 3.1k 0.8× 1.3k 0.5× 1.4k 1.0× 521 0.9× 249 0.8× 68 4.3k
Michel Fink France 24 4.7k 1.2× 2.5k 1.0× 2.4k 1.7× 415 0.7× 466 1.4× 27 5.5k
Michel Fosset France 45 4.6k 1.2× 2.7k 1.1× 1.4k 1.0× 662 1.2× 185 0.6× 79 5.9k
Morten Grunnet Denmark 43 4.8k 1.3× 1.7k 0.7× 3.5k 2.5× 351 0.6× 205 0.6× 146 6.4k

Countries citing papers authored by Philippe Lory

Since Specialization
Citations

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

Fields of papers citing papers by Philippe Lory

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philippe Lory

This figure shows the co-authorship network connecting the top 25 collaborators of Philippe Lory. A scholar is included among the top collaborators of Philippe Lory 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 Philippe Lory. Philippe Lory 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.
Huang, Jian, Xiao Fan, Xueqin Jin, et al.. (2024). Structural basis for human Cav3.2 inhibition by selective antagonists. Cell Research. 34(6). 440–450. 14 indexed citations
2.
Lemmers, Céline, et al.. (2021). The sodium leak channel NALCN regulates cell excitability of pituitary endocrine cells. The FASEB Journal. 35(5). e21400–e21400. 6 indexed citations
3.
Lory, Philippe, Sophie Nicole, & Arnaud Monteil. (2020). Neuronal Cav3 channelopathies: recent progress and perspectives. Pflügers Archiv - European Journal of Physiology. 472(7). 831–844. 43 indexed citations
4.
5.
Terrasso, Ana Paula, Daniel Simão, Christina Begon‐Pescia, et al.. (2018). Lysosomal and network alterations in human mucopolysaccharidosis type VII iPSC-derived neurons. Scientific Reports. 8(1). 16644–16644. 15 indexed citations
6.
Gangarossa, Giuseppe, Dominique Françon, Jean Chemin, et al.. (2015). Blockade of T-type calcium channels prevents tonic-clonic seizures in a maximal electroshock seizure model. Neuropharmacology. 101. 320–329. 27 indexed citations
7.
Bertaso, Federica, Anne-Laure Mausset-Bonnefont, Alexandra Metz, et al.. (2014). RNAi silencing of P/Q-type calcium channels in Purkinje neurons of adult mouse leads to episodic ataxia type 2. Neurobiology of Disease. 68. 47–56. 16 indexed citations
8.
Bidaud, Isabelle, et al.. (2013). 5,6-EET potently inhibits T-type calcium channels: implication in the regulation of the vascular tone. Pflügers Archiv - European Journal of Physiology. 466(9). 1759–1768. 19 indexed citations
9.
Weiss, Norbert, Shahid Hameed, José M. Fernández‐Fernández, et al.. (2011). A Cav3.2/Syntaxin-1A Signaling Complex Controls T-type Channel Activity and Low-threshold Exocytosis. Journal of Biological Chemistry. 287(4). 2810–2818. 103 indexed citations
10.
Swayne, Leigh Anne, Alexandre Mezghrani, Philippe Lory, Joël Nargeot, & Arnaud Monteil. (2010). The NALCN ion channel is a new actor in pancreatic β-cell physiology. Islets. 2(1). 54–56. 14 indexed citations
11.
Vitko, Iuliia, Isabelle Bidaud, Juan Manuel Arias, et al.. (2007). The I–II Loop Controls Plasma Membrane Expression and Gating of Cav3.2 T-Type Ca2+Channels: A Paradigm for Childhood Absence Epilepsy Mutations. Journal of Neuroscience. 27(2). 322–330. 99 indexed citations
12.
Lory, Philippe & Jean Chemin. (2007). Towards the discovery of novel T-type calcium channel blockers. Expert Opinion on Therapeutic Targets. 11(5). 717–722. 36 indexed citations
13.
Mangoni, Matteo E., Anne‐Laure Léoni, Brigitte Couette, et al.. (2006). Bradycardia and Slowing of the Atrioventricular Conduction in Mice Lacking Ca V 3.1/α 1G T-Type Calcium Channels. Circulation Research. 98(11). 1422–1430. 228 indexed citations
14.
Lory, Philippe, et al.. (2006). T‐type Cav3.3 calcium channels produce spontaneous low‐threshold action potentials and intracellular calcium oscillations. European Journal of Neuroscience. 23(9). 2321–2329. 41 indexed citations
15.
Méchaly, Ilana, et al.. (2005). The involvement of Cav3.2/α1H T‐type calcium channels in excitability of mouse embryonic primary vestibular neurones. The Journal of Physiology. 567(1). 67–78. 23 indexed citations
16.
Berthier, Christine, Arnaud Monteil, Philippe Lory, & Caroline Strube. (2002). α1H mRNA in single skeletal muscle fibres accounts for T‐type calcium current transient expression during fetal development in mice. The Journal of Physiology. 539(3). 681–691. 47 indexed citations
17.
Bidaud, Isabelle, Philippe Lory, Pierre Nicolas, Marc Bulant, & Ali Ladram. (2002). Characterization and functional expression of cDNAs encoding thyrotropin‐releasing hormone receptor from Xenopus laevis. European Journal of Biochemistry. 269(18). 4566–4576. 24 indexed citations
18.
Lapie, P., Philippe Lory, & Bertrand Fontaine. (1997). Hypokalemic periodic paralysis: an autosomal dominant muscle disorder caused by mutations in a voltage-gated calcium channel. Neuromuscular Disorders. 7(4). 234–240. 33 indexed citations
19.
Váradi, Gyula, et al.. (1991). Acceleration of activation and inactivation by the β subunit of the skeletal muscle calcium channel. Nature. 352(6331). 159–162. 252 indexed citations
20.
Lory, Philippe, et al.. (1990). Zinc has opposite effects on NMDA and Non-NMDA receptors expressed in xenopus oocytes. Neuron. 4(5). 733–740. 144 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Leanne L. Cribbs Breakdown of academic impact, for papers by Atsushi Inanobe Breakdown of academic impact, for papers by Aaron P. Fox Breakdown of academic impact, for papers by Andreas Karschin Breakdown of academic impact, for papers by Jean Chemin Breakdown of academic impact, for papers by Stephen R. Ikeda Breakdown of academic impact, for papers by Jürgen Daut Breakdown of academic impact, for papers by Michel Fink Breakdown of academic impact, for papers by Michel Fosset Breakdown of academic impact, for papers by Morten Grunnet
Rankless by CCL
2026