Crystel Bonnet

2.6k total citations
70 papers, 1.6k citations indexed

About

Crystel Bonnet is a scholar working on Molecular Biology, Sensory Systems and Neurology. According to data from OpenAlex, Crystel Bonnet has authored 70 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 35 papers in Sensory Systems and 18 papers in Neurology. Recurrent topics in Crystel Bonnet's work include Hearing, Cochlea, Tinnitus, Genetics (35 papers), Vestibular and auditory disorders (16 papers) and Connexins and lens biology (14 papers). Crystel Bonnet is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (35 papers), Vestibular and auditory disorders (16 papers) and Connexins and lens biology (14 papers). Crystel Bonnet collaborates with scholars based in France, Morocco and Algeria. Crystel Bonnet's co-authors include Christine Petit, José‐Alain Sahel, A. Amraoui, Marisol Corral‐Debrinski, Sami Ellouze, Valérie Forster, Sébastien Augustin, Aïcha Bouaita, Sylvie Lazereg and Philippe Denoulet and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Crystel Bonnet

66 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Crystel Bonnet France 20 1.1k 525 213 208 154 70 1.6k
Tarja Joensuu Finland 19 670 0.6× 252 0.5× 261 1.2× 134 0.6× 24 0.2× 31 1.3k
Asadollah Aghaie France 13 641 0.6× 403 0.8× 80 0.4× 153 0.7× 20 0.1× 16 904
Hans‐Henrik M. Dahl Australia 23 1.2k 1.0× 392 0.7× 73 0.3× 95 0.5× 490 3.2× 51 1.9k
Christian P. Hamel France 26 2.0k 1.8× 109 0.2× 216 1.0× 150 0.7× 144 0.9× 71 2.4k
Michael Gonzalez United States 26 1.0k 0.9× 127 0.2× 371 1.7× 365 1.8× 69 0.4× 47 1.9k
Ayala Lagziel Israel 18 611 0.5× 515 1.0× 80 0.4× 310 1.5× 40 0.3× 22 1.2k
Hideki Mutai Japan 20 663 0.6× 626 1.2× 132 0.6× 195 0.9× 12 0.1× 63 1.2k
Kumar N. Alagramam United States 24 1.1k 1.0× 1.3k 2.4× 156 0.7× 477 2.3× 3 0.0× 56 1.9k
Tina Märker Germany 13 1.0k 0.9× 490 0.9× 248 1.2× 160 0.8× 3 0.0× 17 1.3k
S. M. Slapnick United States 12 220 0.2× 420 0.8× 51 0.2× 120 0.6× 15 0.1× 16 606

Countries citing papers authored by Crystel Bonnet

Since Specialization
Citations

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

Fields of papers citing papers by Crystel Bonnet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Crystel Bonnet

This figure shows the co-authorship network connecting the top 25 collaborators of Crystel Bonnet. A scholar is included among the top collaborators of Crystel Bonnet 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 Crystel Bonnet. Crystel Bonnet 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.
Bouzid, Amal, Amal Souissi, Fakher Frikha, et al.. (2025). Whole exome sequencing identifies ABHD14A and MRNIP as novel candidate genes for developmental language disorder. Scientific Reports. 15(1). 367–367.
2.
Bonnet, Crystel, et al.. (2024). Splice-altering variant of PJVK gene in a Mauritanian family with non-syndromic hearing impairment. Journal of Applied Genetics. 66(4). 925–932.
3.
4.
Petit, Christine, Crystel Bonnet, & Saaïd Safieddine. (2023). Deafness: from genetic architecture to gene therapy. Nature Reviews Genetics. 24(10). 665–686. 57 indexed citations
5.
Jean, Philippe, Fabienne Wong Jun Tai, Amrit Singh‐Estivalet, et al.. (2023). Single-cell transcriptomic profiling of the mouse cochlea: An atlas for targeted therapies. Proceedings of the National Academy of Sciences. 120(26). e2221744120–e2221744120. 34 indexed citations
6.
Abdelghaffar, Houria, et al.. (2023). Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families. Biochemical Genetics. 62(3). 1914–1924. 1 indexed citations
7.
Fakin, Ana, Crystel Bonnet, Anne Kurtenbach, et al.. (2021). Characteristics of Retinitis Pigmentosa Associated with ADGRV1 and Comparison with USH2A in Patients from a Multicentric Usher Syndrome Study Treatrush. International Journal of Molecular Sciences. 22(19). 10352–10352. 5 indexed citations
8.
Bonnet, Crystel, Majida Charif, Mostafa Kandil, et al.. (2020). A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family. International Journal of Pediatric Otorhinolaryngology. 140. 110481–110481. 6 indexed citations
9.
Štingl, Katarína, Anne Kurtenbach, Christoph Kernstock, et al.. (2019). Full-field electroretinography, visual acuity and visual fields in Usher syndrome: a multicentre European study. Documenta Ophthalmologica. 139(2). 151–160. 8 indexed citations
10.
Charoute, Hicham, et al.. (2019). Further Evidence for the Implication of the <b><i>MET</i></b> Gene in Non-Syndromic Autosomal Recessive Deafness. Human Heredity. 84(3). 109–116. 3 indexed citations
11.
Lerat, Justine, Crystel Bonnet, François Cartault, et al.. (2018). High prevalence of congenital deafness on Reunion Island is due to a founder variant of LHFPL5. Clinical Genetics. 95(1). 177–181. 3 indexed citations
12.
Charoute, Hicham, Hassan Rouba, Mostafa Kabine, et al.. (2018). A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family. Gene. 659. 89–92. 3 indexed citations
13.
Bonnet, Crystel, Malek Louha, Yosra Bouyacoub, et al.. (2014). Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness. PLoS ONE. 9(6). e99797–e99797. 21 indexed citations
14.
Marlin, Sandrine, Sandra Chantot‐Bastaraud, Albert David, et al.. (2013). Discovery of a Large Deletion of KAL1 in 2 Deaf Brothers. Otology & Neurotology. 34(9). 1590–1594. 8 indexed citations
15.
Fakin, Ana, Martina Jarc-Vidmar, Damjan Glavač, et al.. (2012). Fundus autofluorescence and optical coherence tomography in relation to visual function in Usher syndrome type 1 and 2. Vision Research. 75. 60–70. 49 indexed citations
16.
Bonnet, Crystel & A. Amraoui. (2011). Usher syndrome (sensorineural deafness and retinitis pigmentosa). Current Opinion in Neurology. 25(1). 42–49. 102 indexed citations
17.
Bonnet, Crystel, Sébastien Augustin, Sami Ellouze, et al.. (2008). The optimized allotopic expression of ND1 or ND4 genes restores respiratory chain complex I activity in fibroblasts harboring mutations in these genes. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1783(10). 1707–1717. 93 indexed citations
18.
Bonnet, Crystel, et al.. (2006). The peroxisomal import proteins PEX2, PEX5 and PEX7 are differently involved in Podospora anserina sexual cycle. Molecular Microbiology. 62(1). 157–169. 51 indexed citations
19.
Bonnet, Crystel, Dominique Boucher, Sylvie Lazereg, et al.. (2001). Differential Binding Regulation of Microtubule-associated Proteins MAP1A, MAP1B, and MAP2 by Tubulin Polyglutamylation. Journal of Biological Chemistry. 276(16). 12839–12848. 173 indexed citations
20.
Cherbut, Christine, et al.. (1993). Sugar composition of dietary fibre and short-chain fatty acid production during in vitro fermentation by human bacteria. HAL (Le Centre pour la Communication Scientifique Directe). 1 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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