Elisabeth Verpy

2.1k citations

22 papers · 1.6k indexed · h-index 17

Co-authors: Christine Petit Michel Leibovici Mario Tosi Ingrid Zwaenepoel Stéphane Blanchard Andreas Gal Richard J. Goodyear Guy P. Richardson
Topics: Hearing, Cochlea, Tinnitus, Genetics (15 papers)Connexins and lens biology (6 papers)Coagulation, Bradykinin, Polyphosphates, and Angioedema (5 papers)
Cited by: Sensory Systems Neurology Otorhinolaryngology
Journals: Nature Proceedings of the National Academy of Sciences Journal of Biological Chemistry
Partner nations: France United States United Kingdom

In The Last Decade

Elisabeth Verpy

22 papers receiving 1.6k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane 2019 ·Proceedings of the National Academy of Sciences ·Paul Avan,(unknown),Vincent Michel,Typhaine Dupont,Jean‐Pierre Hardelin,Christine Petit,Elisabeth Verpy	35
2	Cochlear outer hair cell horizontal top connectors mediate mature stereocilia bundle mechanics 2019 ·Science Advances ·Alexander X. Cartagena‐Rivera,(unknown),(unknown),Elisabeth Verpy,Richard S. Chadwick	15
3	An unusually powerful mode of low-frequency sound interference due to defective hair bundles of the auditory outer hair cells 2014 ·Proceedings of the National Academy of Sciences ·Kazusaku Kamiya,Vincent Michel,Fabrice Giraudet,(unknown),Isabelle Foucher,(unknown),Isabelle Perfettini,(unknown),Elisabeth Verpy,(unknown),Ursula Seidler,Maria-Magdalena Georgescu,Paul Avan,A. Amraoui,Christine Petit	15
4	Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairment 2013 ·Gene ·Crystel Bonnet,Malek Louha,Natalie Loundon,Nicolas Michalski,Elisabeth Verpy,(unknown),Jean‐Pierre Hardelin,Isabelle Rouillon,Laurence Jonard,R. Couderc,Souad Gherbi,E.N. Garabédian,Françoise Denoyelle,Christine Petit,Sandrine Marlin	19
5	Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane 2010 ·The Journal of Comparative Neurology ·Elisabeth Verpy,Michel Leibovici,Nicolas Michalski,Richard J. Goodyear,(unknown),Dominique Weil,Guy P. Richardson,Christine Petit	95
6	Stereocilin-deficient mice reveal the origin of cochlear waveform distortions 2008 ·Nature ·Elisabeth Verpy,Dominique Weil,Michel Leibovici,Richard J. Goodyear,Ghislaine Hamard,(unknown),G. Lefèvre,Jean‐Pierre Hardelin,Guy P. Richardson,Paul Avan,Christine Petit	108
7	Inactivation of NADPH oxidase organizer 1 Results in Severe Imbalance 2006 ·Current Biology ·(unknown),Judit Knisz,Yuzhou Zhang,Jonas Baltrušaitis,Curt D. Sigmund,Ruediger Thalmann,Richard J. Smith,Elisabeth Verpy,Botond Bánfi	83
8	Initial characterization of kinocilin, a protein of the hair cell kinocilium 2005 ·Hearing Research ·Michel Leibovici,Elisabeth Verpy,Richard J. Goodyear,Ingrid Zwaenepoel,Stéphane Blanchard,(unknown),Guy P. Richardson,Christine Petit	19
9	Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness 2002 ·Human Genetics ·Xiao Ouyang,Xia Xia,Elisabeth Verpy,(unknown),Arti Pandya,Christine Petit,Thomas J. Bałkany,Walter E. Nance,Xue Liu	89
10	Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus 2001 ·Nature Genetics ·Elisabeth Verpy,Saber Masmoudi,Ingrid Zwaenepoel,Michel Leibovici,Tim Hutchin,Ignacio del Castillo,Sylvie Nouaille,Stéphane Blanchard,(unknown),Jean‐Luc Popot,Felipe Moreno,Robert F. Mueller,Christine Petit	132
11	Identification of three novel mutations in the USH1C gene and detection of thirty-one polymorphisms used for haplotype analysis 2001 ·Human Mutation ·Ingrid Zwaenepoel,Elisabeth Verpy,Stéphane Blanchard,Moritz Meins,Eckart Apfelstedt-Sylla,Andreas Gal,Christine Petit	5
12	Twister mutant mice are defective for otogelin, a component specific to inner ear acellular membranes 2000 ·Mammalian Genome ·Marie‐Christine Simmler,Ingrid Zwaenepoel,Elisabeth Verpy,Laurent Guillaud,(unknown),Christine Petit,Jean‐Jacques Panthier	36
13	A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C 2000 ·Nature Genetics ·Elisabeth Verpy,Michel Leibovici,Ingrid Zwaenepoel,Xue-Zhong Liu,Andreas Gal,Nabiha Salem,Ahmad M. Mansour,Stéphane Blanchard,Ichiro Kobayashi,Bronya J.B. Keats,Rima Slim,Christine Petit	357
14	Identification of three novel mutations in the USH1C gene and detection of thirty-one polymorphisms used for haplotype analysis 2000 ·Human Mutation ·Ingrid Zwaenepoel,Elisabeth Verpy,S Blanchard,Moritz Meins,Eckart Apfelstedt-Sylla,Andreas Gal,Christine Petit	33
15	Novel Variants of Human IFN-α Detected in Tumor Cell Lines and Biopsy Specimens 1997 ·Journal of Interferon & Cytokine Research ·Irina Golovleva,Matteo Biasotto,Elisabeth Verpy,Göran Roos,T Meo,Mario Tosi,Erik Lundgren	2
16	Exhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angiodema. 1996 ·PubMed ·Elisabeth Verpy,(unknown),M. Brai,Gabriella Misiano,T Meo,Mario Tosi	90
17	COOH-terminal Substitutions in the Serpin C1 Inhibitor That Cause Loop Overinsertion and Subsequent Multimerization 1995 ·Journal of Biological Chemistry ·Dorina Roem,Eric Eldering,Elisabeth Verpy,Tommaso Meo,Mario Tosi	88
18	Crucial residues in the carboxy-terminal end of C1 inhibitor revealed by pathogenic mutants impaired in secretion or function. 1995 ·Journal of Clinical Investigation ·Elisabeth Verpy,Evelyne Couture‐Tosi,Eric Eldering,Margarita López‐Trascasa,Peter Späth,T Meo,Mario Tosi	58
19	Efficient detection of point mutations on color-codedstrands of target DNA. 1994 ·Proceedings of the National Academy of Sciences ·Elisabeth Verpy,(unknown),T Meo,Mario Tosi	61
20	C1 inhibitor mutations which affect intracellular transport and secretion in type I hereditary angioedema. 1993 ·PubMed ·Elisabeth Verpy,Evelyne Couture‐Tosi,Mario Tosi	16

About Elisabeth Verpy

Elisabeth Verpy is a scholar working on Sensory Systems, Otorhinolaryngology and Neurology, having authored 22 papers that have together received 1.6k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (15 papers), Connexins and lens biology (6 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (5 papers). The work is most often cited by research in Sensory Systems (895 citations), Neurology (328 citations) and Otorhinolaryngology (145 citations). Elisabeth Verpy has collaborated with scholars based in France, United States and United Kingdom. Frequent 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. Their work appears in journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

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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