Saı̈d Bendahhou

6.2k total citations · 1 hit paper
56 papers, 3.3k citations indexed

About

Saı̈d Bendahhou is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Saı̈d Bendahhou has authored 56 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 29 papers in Cardiology and Cardiovascular Medicine and 22 papers in Cellular and Molecular Neuroscience. Recurrent topics in Saı̈d Bendahhou's work include Ion channel regulation and function (41 papers), Cardiac electrophysiology and arrhythmias (28 papers) and Neuroscience and Neuropharmacology Research (14 papers). Saı̈d Bendahhou is often cited by papers focused on Ion channel regulation and function (41 papers), Cardiac electrophysiology and arrhythmias (28 papers) and Neuroscience and Neuropharmacology Research (14 papers). Saı̈d Bendahhou collaborates with scholars based in France, United States and Germany. Saı̈d Bendahhou's co-authors include Louis J. Ptáček, Jacques Barhanin, Theodore Cummins, Matthew R. Donaldson, Martin Tristani‐Firouzi, Ying‐Hui Fu, Richard Warth, Rabi Tawil, Florian Lesage and Nikki Plaster and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Saı̈d Bendahhou

55 papers receiving 3.2k citations

Hit Papers

KCNQ1 Gain-of-Function Mutation in Familial Atrial Fibril... 2003 2026 2010 2018 2003 200 400 600

Peers

Saı̈d Bendahhou
Saı̈d Bendahhou
Citations per year, relative to Saı̈d Bendahhou Saı̈d Bendahhou (= 1×) peers Andrew P. Braun

Countries citing papers authored by Saı̈d Bendahhou

Since Specialization
Citations

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

Fields of papers citing papers by Saı̈d Bendahhou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Saı̈d Bendahhou

This figure shows the co-authorship network connecting the top 25 collaborators of Saı̈d Bendahhou. A scholar is included among the top collaborators of Saı̈d Bendahhou 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 Saı̈d Bendahhou. Saı̈d Bendahhou 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.
Poët, Mallorie, Nathalie Vigier, Yann Bouret, et al.. (2023). Biological fractionation of lithium isotopes by cellular Na+/H+ exchangers unravels fundamental transport mechanisms. iScience. 26(6). 106887–106887. 10 indexed citations
2.
Forest, Éric, et al.. (2020). New Structural insights into Kir channel gating from molecular simulations, HDX-MS and functional studies. Scientific Reports. 10(1). 8392–8392. 12 indexed citations
3.
Rouleau, Matthieu, et al.. (2015). Modeling Andersen's Syndrome in Human Induced Pluripotent Stem Cells. Stem Cells and Development. 25(2). 151–159. 7 indexed citations
4.
Bendahhou, Saı̈d, et al.. (2014). Defining a Mutational Panel and Predicting the Prevalence of Cystic Fibrosis in Oman. SHILAP Revista de lepidopterología. 3 indexed citations
5.
Sacco, Stefano Da, Serena Giuliano, Sabrina Sacconi, et al.. (2014). The inward rectifier potassium channel Kir2.1 is required for osteoblastogenesis. Human Molecular Genetics. 24(2). 471–479. 21 indexed citations
6.
Chatelain, Franck C., Delphine Bichet, Dominique Douguet, et al.. (2012). TWIK1, a unique background channel with variable ion selectivity. Proceedings of the National Academy of Sciences. 109(14). 5499–5504. 78 indexed citations
7.
Sacconi, Sabrina, et al.. (2012). The Potassium Channel Kir2.1 Activity is Required for Osteoblastogenesis. Biophysical Journal. 102(3). 538a–538a. 1 indexed citations
8.
Simkin, Dina, Isabelle Léna, P. Landrieu, et al.. (2011). Mechanisms underlying a life‐threatening skeletal muscle Na+ channel disorder. The Journal of Physiology. 589(13). 3115–3124. 12 indexed citations
9.
Féliciangéli, Sylvain, Magalie P. Tardy, Guillaume Sandoz, et al.. (2009). Potassium Channel Silencing by Constitutive Endocytosis and Intracellular Sequestration. Journal of Biological Chemistry. 285(7). 4798–4805. 54 indexed citations
10.
Féliciangéli, Sylvain, Saı̈d Bendahhou, Guillaume Sandoz, et al.. (2007). Does Sumoylation Control K2P1/TWIK1 Background K+ Channels?. Cell. 130(3). 563–569. 70 indexed citations
11.
Heitzmann, Dirk, Renaud Dérand, Sascha Bandulik, et al.. (2007). Invalidation of TASK1 potassium channels disrupts adrenal gland zonation and mineralocorticoid homeostasis. The EMBO Journal. 27(1). 179–187. 149 indexed citations
12.
Bendahhou, Saı̈d, et al.. (2007). Corticosteroid-exacerbated symptoms in an Andersen's syndrome kindred. Human Molecular Genetics. 16(8). 900–906. 13 indexed citations
13.
Fodstad, Heidi, Saı̈d Bendahhou, Jean‐Sébastien Rougier, et al.. (2006). Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients. Annals of Medicine. 38(4). 294–304. 32 indexed citations
14.
Bendahhou, Saı̈d, Céline Marionneau, Renaud Dérand, et al.. (2005). In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart. Cardiovascular Research. 67(3). 529–538. 112 indexed citations
15.
Franco, Michel, Saı̈d Bendahhou, Richard Warth, et al.. (2004). ARF6‐dependent interaction of the TWIK1 K + channel with EFA6, a GDP/GTP exchange factor for ARF6. EMBO Reports. 5(12). 1171–1175. 63 indexed citations
16.
Chen, Yi-Han, Shi-Jie Xu, Saı̈d Bendahhou, et al.. (2003). KCNQ1 Gain-of-Function Mutation in Familial Atrial Fibrillation. Science. 299(5604). 251–254. 702 indexed citations breakdown →
17.
Donaldson, Michael, Jeffrey L. Jensen, Martin Tristani‐Firouzi, et al.. (2003). PIP(2) binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome. HAL (Le Centre pour la Communication Scientifique Directe). 1 indexed citations
18.
Tristani‐Firouzi, Martin, Judy L. Jensen, Matthew R. Donaldson, et al.. (2002). Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome). Journal of Clinical Investigation. 110(3). 381–388. 376 indexed citations
19.
Abbott, Geoffrey W., Margaret H. Butler, Saı̈d Bendahhou, et al.. (2001). MiRP2 Forms Potassium Channels in Skeletal Muscle with Kv3.4 and Is Associated with Periodic Paralysis. Cell. 104(2). 217–231. 240 indexed citations
20.
Bendahhou, Saı̈d, T.R. Cummins, Robert C. Griggs, Yinghui Fu, & Louis J. Ptáček. (2001). Sodium channel inactivation defects are associated with acetazolamide‐exacerbated hypokalemic periodic paralysis. Annals of Neurology. 50(3). 417–420. 57 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

Rankless by CCL
2026