Alexandre Benmerah

7.1k total citations
87 papers, 5.3k citations indexed

About

Alexandre Benmerah is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Alexandre Benmerah has authored 87 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 49 papers in Cell Biology and 28 papers in Genetics. Recurrent topics in Alexandre Benmerah's work include Cellular transport and secretion (35 papers), Genetic and Kidney Cyst Diseases (26 papers) and Microtubule and mitosis dynamics (17 papers). Alexandre Benmerah is often cited by papers focused on Cellular transport and secretion (35 papers), Genetic and Kidney Cyst Diseases (26 papers) and Microtubule and mitosis dynamics (17 papers). Alexandre Benmerah collaborates with scholars based in France, United States and United Kingdom. Alexandre Benmerah's co-authors include Alice Dautry‐Varsat, Nadine Cerf–Bensussan, Christophe Lamaze, Bernadette Bègue, Mark G. H. Scott, Stéfano Marullo, Sanford M. Simon, Joshua Z. Rappoport, Annick Dujeancourt and Charles G. Lo 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

Alexandre Benmerah

86 papers receiving 5.3k citations

Peers

Alexandre Benmerah
Masatoshi Maki Japan
Angela Wandinger‐Ness United States
Jack Fransen Netherlands
James E. Casanova United States
Marcelo Ehrlich Israel
Roland Wedlich‐Söldner Germany
George Banting United Kingdom
Franck Perez France
Rohan D. Teasdale Australia
Emmanuel Boucrot United Kingdom
Masatoshi Maki Japan
Alexandre Benmerah
Citations per year, relative to Alexandre Benmerah Alexandre Benmerah (= 1×) peers Masatoshi Maki

Countries citing papers authored by Alexandre Benmerah

Since Specialization
Citations

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

Fields of papers citing papers by Alexandre Benmerah

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexandre Benmerah

This figure shows the co-authorship network connecting the top 25 collaborators of Alexandre Benmerah. A scholar is included among the top collaborators of Alexandre Benmerah 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 Alexandre Benmerah. Alexandre Benmerah 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.
Garfa‐Traoré, Meriem, Federica Roccio, Caterina Miceli, et al.. (2023). Fluid shear stress triggers cholesterol biosynthesis and uptake in inner medullary collecting duct cells, independently of nephrocystin-1 and nephrocystin-4. Frontiers in Molecular Biosciences. 10. 1254691–1254691. 3 indexed citations
2.
Stokman, Marijn F., Sophie Saunier, & Alexandre Benmerah. (2021). Renal Ciliopathies: Sorting Out Therapeutic Approaches for Nephronophthisis. Frontiers in Cell and Developmental Biology. 9. 653138–653138. 21 indexed citations
3.
Reilly, Madeline Louise, Noor Ul Ain, Céline Huber, et al.. (2020). Biallelic KIF24 Variants Are Responsible for a Spectrum of Skeletal Disorders Ranging From Lethal Skeletal Ciliopathy to Severe Acromesomelic Dysplasia. Journal of Bone and Mineral Research. 37(9). 1642–1652. 7 indexed citations
4.
Reilly, Madeline Louise, Lucia Binó, Ondřej Bernatík, et al.. (2020). KIF14 controls ciliogenesis via regulation of Aurora A and is important for Hedgehog signaling. The Journal of Cell Biology. 219(6). 17 indexed citations
5.
Schönauer, Ria, Daniela A. Braun, Shirlee Shril, et al.. (2020). Novel nephronophthisis-associated variants reveal functional importance of MAPKBP1 dimerization for centriolar recruitment. Kidney International. 98(4). 958–969. 6 indexed citations
6.
Molla‐Herman, Anahi, et al.. (2019). Monitoring β-Arrestin 2 Targeting to the Centrosome, Basal Body, and Primary Cilium by Fluorescence Microscopy. Methods in molecular biology. 1957. 271–289. 4 indexed citations
7.
Stráner, Pál, Christelle Arrondel, Alexandre Benmerah, et al.. (2018). C-terminal oligomerization of podocin mediates interallelic interactions. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1864(7). 2448–2457. 12 indexed citations
8.
Freywald, Tanya, Darrell D. Mousseau, Deborah H. Anderson, et al.. (2014). Ligand stimulation induces clathrin- and Rab5-dependent downregulation of the kinase-dead EphB6 receptor preceded by the disruption of EphB6-Hsp90 interaction. Cellular Signalling. 26(12). 2645–2657. 7 indexed citations
9.
Marion, Sabrina, Julie Mazzolini, Floriane Herit, et al.. (2012). The NF-κB Signaling Protein Bcl10 Regulates Actin Dynamics by Controlling AP1 and OCRL-Bearing Vesicles. Developmental Cell. 23(5). 954–967. 65 indexed citations
10.
Lima‐Fernandes, Evelyne, Hervé Enslen, Emeline Camand, et al.. (2011). Distinct functional outputs of PTEN signalling are controlled by dynamic association with β‐arrestins. The EMBO Journal. 30(13). 2557–2568. 55 indexed citations
11.
Gibert, Maryse, Marie‐Noëlle Monier, Richard Ruez, et al.. (2010). Endocytosis and toxicity of clostridial binary toxins depend on a clathrin-independent pathway regulated by Rho-GDI. Cellular Microbiology. 13(1). 154–170. 36 indexed citations
12.
Borck, Guntram, Anahi Molla‐Herman, Nathalie Boddaert, et al.. (2008). Clinical, cellular, and neuropathological consequences ofAP1S2mutations: further delineation of a recognizable X-linked mental retardation syndrome. Human Mutation. 29(7). 966–974. 36 indexed citations
13.
Burtey, Anne, Joshua Z. Rappoport, Jérôme Bouchet, et al.. (2006). Dynamic Interaction of HIV‐1 Nef with the Clathrin‐Mediated Endocytic Pathway at the Plasma Membrane. Traffic. 8(1). 61–76. 42 indexed citations
14.
Montagnac, Guillaume, Anahi Molla‐Herman, Jérôme Bouchet, et al.. (2005). Intracellular Trafficking of CD23: Differential Regulation in Humans and Mice by Both Extracellular and Intracellular Exons. The Journal of Immunology. 174(9). 5562–5572. 20 indexed citations
15.
Montagnac, Guillaume, Linda Chia‐Hui Yu, Claudia Bevilacqua, et al.. (2005). Differential Role for CD23 Splice Forms in Apical to Basolateral Transcytosis of IgE/Allergen Complexes. Traffic. 6(3). 230–242. 30 indexed citations
16.
Scott, Mark G. H., Hassan Issafras, Anne Burtey, et al.. (2005). Homo- and Hetero-oligomerization of β-Arrestins in Living Cells. Journal of Biological Chemistry. 280(48). 40210–40215. 84 indexed citations
17.
Rappoport, Joshua Z., Sanford M. Simon, & Alexandre Benmerah. (2004). Understanding Living Clathrin-Coated Pits. Traffic. 5(5). 327–337. 73 indexed citations
18.
Kent, Helen M., Harvey T. McMahon, Philip R. Evans, Alexandre Benmerah, & David J. Owen. (2002). γ-Adaptin Appendage Domain. Structure. 10(8). 1139–1148. 69 indexed citations
19.
Lamaze, Christophe, Annick Dujeancourt, Takeshi Baba, et al.. (2001). Interleukin 2 Receptors and Detergent-Resistant Membrane Domains Define a Clathrin-Independent Endocytic Pathway. Molecular Cell. 7(3). 661–671. 424 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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