Céline Bonnet

2.2k total citations
68 papers, 907 citations indexed

About

Céline Bonnet is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Céline Bonnet has authored 68 papers receiving a total of 907 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 30 papers in Genetics and 13 papers in Cellular and Molecular Neuroscience. Recurrent topics in Céline Bonnet's work include Genomic variations and chromosomal abnormalities (16 papers), Genetic Neurodegenerative Diseases (8 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Céline Bonnet is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Genetic Neurodegenerative Diseases (8 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Céline Bonnet collaborates with scholars based in France, Canada and United States. Céline Bonnet's co-authors include Philippe Jonveaux, Bruno Leheup, Christophe Philippe, Julien Engelhardt, Hugues Loiseau, Luc Bauchet, A. Grüber, Isabelle Baldi, Émilie Berteaud and Mylène Béri and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and European Heart Journal.

In The Last Decade

Céline Bonnet

63 papers receiving 886 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Céline Bonnet France 16 380 378 116 112 103 68 907
Isabella Torrente Italy 19 414 1.1× 228 0.6× 55 0.5× 68 0.6× 155 1.5× 48 874
Dorota Monies Saudi Arabia 22 579 1.5× 507 1.3× 99 0.9× 75 0.7× 69 0.7× 48 1.3k
Boris Keren France 21 649 1.7× 515 1.4× 52 0.4× 79 0.7× 105 1.0× 70 1.1k
Sachiko Nishina Japan 20 533 1.4× 230 0.6× 100 0.9× 103 0.9× 48 0.5× 82 1.2k
Nara Sobreira United States 19 690 1.8× 671 1.8× 82 0.7× 68 0.6× 41 0.4× 61 1.3k
Arif O. Khan Saudi Arabia 24 845 2.2× 610 1.6× 161 1.4× 74 0.7× 58 0.6× 131 1.8k
Mark D. Ludman Canada 20 446 1.2× 386 1.0× 120 1.0× 52 0.5× 39 0.4× 41 1.2k
Sumita Danda India 16 489 1.3× 269 0.7× 108 0.9× 54 0.5× 49 0.5× 122 1.0k
Arto Immonen Finland 13 403 1.1× 442 1.2× 97 0.8× 213 1.9× 128 1.2× 26 960
Shamir Zenvirt Israel 16 618 1.6× 367 1.0× 59 0.5× 205 1.8× 203 2.0× 22 1.2k

Countries citing papers authored by Céline Bonnet

Since Specialization
Citations

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

Fields of papers citing papers by Céline Bonnet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Céline Bonnet

This figure shows the co-authorship network connecting the top 25 collaborators of Céline Bonnet. A scholar is included among the top collaborators of Céline 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 Céline Bonnet. Céline 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.
2.
Bastos, Paulo, Anne Pavy‐Le Traon, Fabrice Bonneville, et al.. (2024). How to distinguish spinocerebellar ataxia 27B from late onset cerebellar ataxia: insights from a case–control study. Journal of Neurology. 272(1). 45–45. 3 indexed citations
3.
Pellerin, David, Matt C. Danzi, Céline Bonnet, et al.. (2024). Oculomotor Findings in Spinocerebellar Ataxia 27B: A Case Series. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 52(5). 868–870. 1 indexed citations
4.
Bonnet, Céline, et al.. (2024). Megalencephaly secondary to a novel germline missense variant p.Asp322Tyr in AKT3 associated with growth hormone deficiency and central hypothyroidism: A case report. American Journal of Medical Genetics Part A. 194(7). e63585–e63585. 1 indexed citations
5.
Bonnet, Céline, Virginie Roth, Yannis Duffourd, et al.. (2024). Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur–Chung neurodevelopmental syndrome. American Journal of Medical Genetics Part A. 194(9). e63642–e63642. 1 indexed citations
6.
Bronner, Myriam, et al.. (2023). ENPP1 homozygous stop-loss variant causing generalized arterial calcifications of infancy: About a severe neonatal clinical case. European Journal of Medical Genetics. 66(8). 104803–104803.
7.
Indelicato, Elisabetta, David Pellerin, Matt C. Danzi, et al.. (2023). Spinocerebellar ataxia 27B: episodic symptoms and acetazolamide response in 34 patients. Brain Communications. 5(5). fcad239–fcad239. 12 indexed citations
8.
Gauthier, Mélanie, Céline Bonnet, Alain Lozniewski, et al.. (2023). Scale-Up of Academic Mesenchymal Stromal Cell Production. Journal of Clinical Medicine. 12(13). 4414–4414. 1 indexed citations
9.
Ravel, Jean‐Marie, M. Renaud, Jean Muller, et al.. (2023). Clinical utility of periodic reinterpretation of CNVs of uncertain significance: an 8-year retrospective study. Genome Medicine. 15(1). 39–39. 7 indexed citations
10.
Lambert, Laëtitia, Ange‐Line Bruel, Frédéric Tran Mau‐Them, et al.. (2022). Atypical phenotype of a patient with Bardet–Biedl syndrome type 4. Molecular Genetics & Genomic Medicine. 10(5). e1869–e1869. 1 indexed citations
11.
Cholet, Sophie, Bertrand Isidor, Benjamin Cogné, et al.. (2021). MAN1B1-CDG: Three new individuals and associated biochemical profiles. Molecular Genetics and Metabolism Reports. 28. 100775–100775. 9 indexed citations
12.
Agopiantz, Mikaël, Patricia Forgez, Stéphanie Lacomme, et al.. (2017). Expression of neurotensin receptor 1 in endometrial adenocarcinoma is correlated with histological grade and clinical outcome. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 471(4). 521–530. 14 indexed citations
13.
Bonnet, Céline, Asma Ali Khan, Emmanuel Bresso, et al.. (2013). Extended spectrum of MBD5 mutations in neurodevelopmental disorders. European Journal of Human Genetics. 21(12). 1457–1461. 30 indexed citations
14.
Maldergem, Lionel Van, Qingming Hou, Vera M. Kalscheuer, et al.. (2013). Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth. Human Molecular Genetics. 22(16). 3306–3314. 55 indexed citations
15.
Bonnet, Céline, et al.. (2009). Aberrant GRIA3 transcripts with multi‐exon duplications in a family with X‐linked mental retardation. American Journal of Medical Genetics Part A. 149A(6). 1280–1289. 30 indexed citations
16.
Bonnet, Céline, Sophie Krieger, Myriam Vézain, et al.. (2008). Screening BRCA1 and BRCA2 unclassified variants for splicing mutations using reverse transcription PCR on patient RNA and an ex vivo assay based on a splicing reporter minigene. Journal of Medical Genetics. 45(7). 438–446. 89 indexed citations
17.
Echaniz‐Laguna, Andoni, Bertrand Degos, Céline Bonnet, et al.. (2006). NDRG1-linked Charcot-Marie-Tooth disease (CMT4D) with central nervous system involvement. Neuromuscular Disorders. 17(2). 163–168. 36 indexed citations
18.
Bonnet, Céline, et al.. (2006). Characterization of mosaic supernumerary ring chromosomes by array‐CGH: Segmental aneusomy for proximal 4q in a child with tall stature and obesity. American Journal of Medical Genetics Part A. 140A(3). 233–237. 30 indexed citations
19.
Bonnet, Céline, et al.. (2006). Pure de-novo 5 Mb duplication at Xp11.22–p11.23 in a male: phenotypic and molecular characterization. Journal of Human Genetics. 51(9). 815–821. 29 indexed citations
20.
Bonnet, Céline. (1995). [Cognitive processes in perception: perceptive knowledge].. PubMed. 151(8-9). 442–50. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Isabella Torrente Breakdown of academic impact, for papers by Dorota Monies Breakdown of academic impact, for papers by Boris Keren Breakdown of academic impact, for papers by Sachiko Nishina Breakdown of academic impact, for papers by Nara Sobreira Breakdown of academic impact, for papers by Arif O. Khan Breakdown of academic impact, for papers by Mark D. Ludman Breakdown of academic impact, for papers by Sumita Danda Breakdown of academic impact, for papers by Arto Immonen Breakdown of academic impact, for papers by Shamir Zenvirt
Rankless by CCL
2026