Sylvie Nouaille

1.4k total citations
14 papers, 982 citations indexed

About

Sylvie Nouaille is a scholar working on Sensory Systems, Molecular Biology and Neurology. According to data from OpenAlex, Sylvie Nouaille has authored 14 papers receiving a total of 982 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Sensory Systems, 9 papers in Molecular Biology and 3 papers in Neurology. Recurrent topics in Sylvie Nouaille's work include Hearing, Cochlea, Tinnitus, Genetics (13 papers), Connexins and lens biology (4 papers) and RNA regulation and disease (3 papers). Sylvie Nouaille is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (13 papers), Connexins and lens biology (4 papers) and RNA regulation and disease (3 papers). Sylvie Nouaille collaborates with scholars based in France, United States and United Kingdom. Sylvie Nouaille's co-authors include Christine Petit, Jean‐Pierre Hardelin, Saaïd Safieddine, Paul Avan, Jacques Boutet de Monvel, Amel Bahloul, Alice Emptoz, Ghizlène Lahlou, Lawrence R. Lustig and Omar Akil and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Sylvie Nouaille

14 papers receiving 971 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sylvie Nouaille France	12	711	548	202	191	97	14	982
Hideki Mutai Japan	20	626 0.9×	663 1.2×	195 1.0×	125 0.7×	91 0.9×	63	1.2k
Matthew R. Avenarius United States	15	494 0.7×	499 0.9×	176 0.9×	116 0.6×	102 1.1×	35	1.1k
Heping Yu United States	19	518 0.7×	376 0.7×	220 1.1×	123 0.6×	82 0.8×	37	909
Mirna Mustapha United States	17	944 1.3×	621 1.1×	383 1.9×	296 1.5×	82 0.8×	34	1.3k
Erich T. Boger United States	17	752 1.1×	723 1.3×	301 1.5×	130 0.7×	80 0.8×	24	1.3k
Andrea Lelli United States	16	893 1.3×	672 1.2×	227 1.1×	221 1.2×	76 0.8×	19	1.2k
Déborah Scheffer United States	13	548 0.8×	532 1.0×	97 0.5×	149 0.8×	130 1.3×	14	960
Charles Askew United States	13	747 1.1×	610 1.1×	188 0.9×	250 1.3×	174 1.8×	16	1.1k
Jaap Oostrik Netherlands	19	684 1.0×	521 1.0×	274 1.4×	174 0.9×	79 0.8×	34	964
Lisa A. Beyer United States	23	899 1.3×	431 0.8×	245 1.2×	325 1.7×	70 0.7×	41	1.3k

Countries citing papers authored by Sylvie Nouaille

Since Specialization

Citations

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

Fields of papers citing papers by Sylvie Nouaille

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sylvie Nouaille

This figure shows the co-authorship network connecting the top 25 collaborators of Sylvie Nouaille. A scholar is included among the top collaborators of Sylvie Nouaille 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 Sylvie Nouaille. Sylvie Nouaille is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

Zamani, Mina, Audrey Maudoux, Reza Maroofian, et al.. (2024). Clarin-2 gene supplementation durably preserves hearing in a model of progressive hearing loss. Molecular Therapy. 32(3). 800–817. 10 indexed citations

Calvet, Charlotte, Najate Benamer, Andrea Lelli, et al.. (2022). The SNARE protein SNAP-25 is required for normal exocytosis at auditory hair cell ribbon synapses. iScience. 25(12). 105628–105628. 16 indexed citations

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

Akil, Omar, Frank M. Dyka, Charlotte Calvet, et al.. (2019). Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model. Proceedings of the National Academy of Sciences. 116(10). 4496–4501. 195 indexed citations

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

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

Emptoz, Alice, Vincent Michel, Andrea Lelli, et al.. (2017). Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G. Proceedings of the National Academy of Sciences. 114(36). 9695–9700. 103 indexed citations

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

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

10.

Bahloul, Amel, Marie‐Christine Simmler, Vincent Michel, et al.. (2009). Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells. EMBO Molecular Medicine. 1(2). 125–138. 31 indexed citations

11.

Mustapha, Mirna, Éliane Chouery, Sylvie Nouaille, et al.. (2002). A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24–25. Human Genetics. 110(4). 348–350. 45 indexed citations

12.

Zwaenepoel, Ingrid, Mirna Mustapha, Michel Leibovici, et al.. (2002). Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22. Proceedings of the National Academy of Sciences. 99(9). 6240–6245. 130 indexed citations

13.

Verpy, Elisabeth, Saber Masmoudi, Ingrid Zwaenepoel, et al.. (2001). Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus. Nature Genetics. 29(3). 345–349. 132 indexed citations

14.

Amraoui, A., Saaïd Safieddine, Jean‐Pierre Hardelin, et al.. (2000). Unconventional Myosin VIIA Is a Novel A-kinase-anchoring Protein. Journal of Biological Chemistry. 275(38). 29654–29659. 51 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.

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