Amel Bahloul

2.4k total citations
22 papers, 1.6k citations indexed

About

Amel Bahloul is a scholar working on Sensory Systems, Molecular Biology and Cell Biology. According to data from OpenAlex, Amel Bahloul has authored 22 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Sensory Systems, 11 papers in Molecular Biology and 6 papers in Cell Biology. Recurrent topics in Amel Bahloul's work include Hearing, Cochlea, Tinnitus, Genetics (16 papers), Connexins and lens biology (4 papers) and Mass Spectrometry Techniques and Applications (3 papers). Amel Bahloul is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (16 papers), Connexins and lens biology (4 papers) and Mass Spectrometry Techniques and Applications (3 papers). Amel Bahloul collaborates with scholars based in France, United States and United Kingdom. Amel Bahloul's co-authors include Christine Petit, Isabelle Perfettini, Paul Avan, Isabelle Roux, Saaïd Safieddine, Anne Houdusse, Vincent Michel, Marie‐Christine Simmler, Jean‐Pierre Hardelin and Régis Nouvian and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Amel Bahloul

21 papers receiving 1.6k citations

Peers

Amel Bahloul
Philomena Mburu United Kingdom
Karen P. Steel United Kingdom
Martin Schwander United States
Rachel A. Dumont United States
Anabel Varela United Kingdom
Michael D. Weston United States
Philomena Mburu United Kingdom
Amel Bahloul
Citations per year, relative to Amel Bahloul Amel Bahloul (= 1×) peers Philomena Mburu

Countries citing papers authored by Amel Bahloul

Since Specialization
Citations

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

Fields of papers citing papers by Amel Bahloul

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amel Bahloul

This figure shows the co-authorship network connecting the top 25 collaborators of Amel Bahloul. A scholar is included among the top collaborators of Amel Bahloul 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 Amel Bahloul. Amel Bahloul 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
2.
Ruel, Jérôme, et al.. (2023). Current Advances in Gene Therapies of Genetic Auditory Neuropathy Spectrum Disorder. Journal of Clinical Medicine. 12(3). 738–738. 15 indexed citations
3.
Michel, Vincent, Elise Pepermans, Jacques Boutet de Monvel, et al.. (2020). Interaction of protocadherin-15 with the scaffold protein whirlin supports its anchoring of hair-bundle lateral links in cochlear hair cells. Scientific Reports. 10(1). 16430–16430. 8 indexed citations
4.
Delhommel, Florent, Florence Cordier, Ariel Méchaly, et al.. (2020). Deciphering the Unexpected Binding Capacity of the Third PDZ Domain of Whirlin to Various Cochlear Hair Cell Partners. Journal of Molecular Biology. 432(22). 5920–5937. 7 indexed citations
5.
Bahloul, Amel, Christine Petit, Sang Jin Kim, et al.. (2019). A Novel Heterozygous Missense Variant (c.667G>T;p.Gly223Cys) in USH1C That Interferes With Cadherin-Related 23 and Harmonin Interaction Causes Autosomal Dominant Nonsyndromic Hearing Loss. Annals of Laboratory Medicine. 40(3). 224–231. 4 indexed citations
6.
Michalski, Nicolas, Juan D. Goutman, Sarah M. Auclair, et al.. (2017). Otoferlin acts as a Ca2+ sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapses. eLife. 6. 87 indexed citations
7.
Delhommel, Florent, Florence Cordier, Benjamin Bardiaux, et al.. (2017). Structural Characterization of Whirlin Reveals an Unexpected and Dynamic Supramodule Conformation of Its PDZ Tandem. Structure. 25(11). 1645–1656.e5. 19 indexed citations
8.
Bahloul, Amel, Jean‐Pierre Hardelin, Mohamed Makrelouf, et al.. (2016). Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome. PLoS ONE. 11(9). e0161893–e0161893. 17 indexed citations
9.
Pepermans, Elise, Vincent Michel, Richard J. Goodyear, et al.. (2014). The CD 2 isoform of protocadherin‐15 is an essential component of the tip‐link complex in mature auditory hair cells. EMBO Molecular Medicine. 6(7). 984–992. 54 indexed citations
10.
Maréchal, Jean‐Didier, et al.. (2012). Crystal Structure of Two Anti-Porphyrin Antibodies with Peroxidase Activity. PLoS ONE. 7(12). e51128–e51128. 10 indexed citations
11.
Sahly, Iman, Éric Dufour, Cataldo Schietroma, et al.. (2012). Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice. The Journal of Cell Biology. 199(2). 381–399. 127 indexed citations
12.
Michel, Vincent, Isabelle Foucher, Amel Bahloul, et al.. (2011). Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia. Proceedings of the National Academy of Sciences. 108(14). 5825–5830. 104 indexed citations
13.
Bahloul, Amel, Vincent Michel, Jean‐Pierre Hardelin, et al.. (2010). Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipids. Human Molecular Genetics. 19(18). 3557–3565. 77 indexed citations
14.
Roux, Isabelle, Suzanne Hosie, Stuart L. Johnson, et al.. (2009). Myosin VI is required for the proper maturation and function of inner hair cell ribbon synapses. Human Molecular Genetics. 18(23). 4615–4628. 78 indexed citations
15.
Michalski, Nicolas, Vincent Michel, Amel Bahloul, et al.. (2007). Molecular Characterization of the Ankle-Link Complex in Cochlear Hair Cells and Its Role in the Hair Bundle Functioning. Journal of Neuroscience. 27(24). 6478–6488. 158 indexed citations
16.
Roux, Isabelle, Saaïd Safieddine, Régis Nouvian, et al.. (2006). Otoferlin, Defective in a Human Deafness Form, Is Essential for Exocytosis at the Auditory Ribbon Synapse. Cell. 127(2). 277–289. 499 indexed citations
17.
Ménétrey, Julie, Amel Bahloul, & Anne Houdusse. (2006). Une myosine à contre-sens. médecine/sciences. 22(2). 120–122.
18.
Ménétrey, Julie, Amel Bahloul, Amber L. Wells, et al.. (2005). The structure of the myosin VI motor reveals the mechanism of directionality reversal. Nature. 435(7043). 779–785. 181 indexed citations
19.
Chevreux, Guillaume, Noëlle Potier, Alain Van Dorsselaer, et al.. (2005). Electrospray ionization mass spectrometry studies of noncovalent myosin VI complexes reveal a new specific calmodulin binding site. Journal of the American Society for Mass Spectrometry. 16(8). 1367–1376. 16 indexed citations
20.
Bahloul, Amel, Guillaume Chevreux, Amber L. Wells, et al.. (2004). The unique insert in myosin VI is a structural calcium–calmodulin binding site. Proceedings of the National Academy of Sciences. 101(14). 4787–4792. 62 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