Elisabeth Verpy

2.1k total citations
22 papers, 1.6k citations indexed

About

Elisabeth Verpy is a scholar working on Sensory Systems, Molecular Biology and Genetics. According to data from OpenAlex, Elisabeth Verpy has authored 22 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Sensory Systems, 7 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Elisabeth Verpy's work include Hearing, Cochlea, Tinnitus, Genetics (15 papers), Connexins and lens biology (6 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (5 papers). Elisabeth Verpy is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (15 papers), Connexins and lens biology (6 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (5 papers). Elisabeth Verpy collaborates with scholars based in France, United States and United Kingdom. Elisabeth Verpy's co-authors include Christine Petit, Michel Leibovici, Mario Tosi, Ingrid Zwaenepoel, Stéphane Blanchard, Andreas Gal, Richard J. Goodyear, Guy P. Richardson, Nabiha Salem and Ahmad M. Mansour 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

Elisabeth Verpy

22 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elisabeth Verpy France 17 895 738 328 235 180 22 1.6k
Nahid G. Robertson United States 22 1.1k 1.3× 616 0.8× 726 2.2× 242 1.0× 44 0.2× 31 1.7k
Ingrid Zwaenepoel France 11 537 0.6× 789 1.1× 198 0.6× 114 0.5× 135 0.8× 12 1.3k
Jianyong Shou United States 24 862 1.0× 1.2k 1.7× 85 0.3× 129 0.5× 75 0.4× 41 2.2k
Philomena Mburu United Kingdom 12 1.3k 1.5× 1.5k 2.0× 395 1.2× 224 1.0× 35 0.2× 19 2.2k
Karen P. Steel United Kingdom 17 1.1k 1.2× 1.1k 1.5× 293 0.9× 214 0.9× 40 0.2× 21 1.7k
Benjamin K. August United States 19 312 0.3× 717 1.0× 232 0.7× 97 0.4× 73 0.4× 40 1.5k
Michael D. Weston United States 27 1.8k 2.0× 2.2k 3.0× 397 1.2× 199 0.8× 33 0.2× 45 3.2k
Kate F. Barald United States 23 346 0.4× 1.0k 1.4× 75 0.2× 62 0.3× 88 0.5× 59 1.7k
Francine M. Jodelka United States 18 416 0.5× 883 1.2× 131 0.4× 130 0.6× 202 1.1× 23 1.2k
Sovann Kaing United States 13 224 0.3× 946 1.3× 246 0.8× 77 0.3× 103 0.6× 14 2.1k

Countries citing papers authored by Elisabeth Verpy

Since Specialization
Citations

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

Fields of papers citing papers by Elisabeth Verpy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisabeth Verpy

This figure shows the co-authorship network connecting the top 25 collaborators of Elisabeth Verpy. A scholar is included among the top collaborators of Elisabeth Verpy 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 Elisabeth Verpy. Elisabeth Verpy 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.
Avan, Paul, Vincent Michel, Typhaine Dupont, et al.. (2019). Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane. Proceedings of the National Academy of Sciences. 116(51). 25948–25957. 35 indexed citations
2.
Cartagena‐Rivera, Alexander X., et al.. (2019). Cochlear outer hair cell horizontal top connectors mediate mature stereocilia bundle mechanics. Science Advances. 5(2). eaat9934–eaat9934. 15 indexed citations
3.
Kamiya, Kazusaku, Vincent Michel, Fabrice Giraudet, et al.. (2014). An unusually powerful mode of low-frequency sound interference due to defective hair bundles of the auditory outer hair cells. Proceedings of the National Academy of Sciences. 111(25). 9307–9312. 15 indexed citations
4.
Bonnet, Crystel, Malek Louha, Natalie Loundon, et al.. (2013). Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairment. Gene. 527(2). 537–540. 19 indexed citations
5.
Verpy, Elisabeth, Michel Leibovici, Nicolas Michalski, et al.. (2010). Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane. The Journal of Comparative Neurology. 519(2). 194–210. 95 indexed citations
6.
Verpy, Elisabeth, Dominique Weil, Michel Leibovici, et al.. (2008). Stereocilin-deficient mice reveal the origin of cochlear waveform distortions. Nature. 456(7219). 255–258. 108 indexed citations
7.
Knisz, Judit, Yuzhou Zhang, Jonas Baltrušaitis, et al.. (2006). Inactivation of NADPH oxidase organizer 1 Results in Severe Imbalance. Current Biology. 16(2). 208–213. 83 indexed citations
8.
Leibovici, Michel, Elisabeth Verpy, Richard J. Goodyear, et al.. (2005). Initial characterization of kinocilin, a protein of the hair cell kinocilium. Hearing Research. 203(1-2). 144–153. 19 indexed citations
9.
Ouyang, Xiao, Xia Xia, Elisabeth Verpy, et al.. (2002). Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness. Human Genetics. 111(1). 26–30. 89 indexed citations
10.
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
11.
Zwaenepoel, Ingrid, Elisabeth Verpy, Stéphane Blanchard, et al.. (2001). Identification of three novel mutations in the USH1C gene and detection of thirty-one polymorphisms used for haplotype analysis. Human Mutation. 17(1). 34–34. 5 indexed citations
12.
Simmler, Marie‐Christine, Ingrid Zwaenepoel, Elisabeth Verpy, et al.. (2000). Twister mutant mice are defective for otogelin, a component specific to inner ear acellular membranes. Mammalian Genome. 11(11). 961–966. 36 indexed citations
13.
Verpy, Elisabeth, Michel Leibovici, Ingrid Zwaenepoel, et al.. (2000). A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C. Nature Genetics. 26(1). 51–55. 357 indexed citations
14.
Zwaenepoel, Ingrid, Elisabeth Verpy, S Blanchard, et al.. (2000). Identification of three novel mutations in the USH1C gene and detection of thirty-one polymorphisms used for haplotype analysis. Human Mutation. 17(1). 34–41. 33 indexed citations
15.
Golovleva, Irina, Matteo Biasotto, Elisabeth Verpy, et al.. (1997). Novel Variants of Human IFN-α Detected in Tumor Cell Lines and Biopsy Specimens. Journal of Interferon & Cytokine Research. 17(10). 637–645. 2 indexed citations
16.
Verpy, Elisabeth, et al.. (1996). Exhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angiodema.. PubMed. 59(2). 308–19. 90 indexed citations
17.
Roem, Dorina, Eric Eldering, Elisabeth Verpy, Tommaso Meo, & Mario Tosi. (1995). COOH-terminal Substitutions in the Serpin C1 Inhibitor That Cause Loop Overinsertion and Subsequent Multimerization. Journal of Biological Chemistry. 270(6). 2579–2587. 88 indexed citations
18.
Verpy, Elisabeth, Evelyne Couture‐Tosi, Eric Eldering, et al.. (1995). Crucial residues in the carboxy-terminal end of C1 inhibitor revealed by pathogenic mutants impaired in secretion or function.. Journal of Clinical Investigation. 95(1). 350–359. 58 indexed citations
19.
Verpy, Elisabeth, et al.. (1994). Efficient detection of point mutations on color-codedstrands of target DNA.. Proceedings of the National Academy of Sciences. 91(5). 1873–1877. 61 indexed citations
20.
Verpy, Elisabeth, Evelyne Couture‐Tosi, & Mario Tosi. (1993). C1 inhibitor mutations which affect intracellular transport and secretion in type I hereditary angioedema.. PubMed. 120–4. 16 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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