Muriel Bozon

1.5k total citations
36 papers, 1.1k citations indexed

About

Muriel Bozon is a scholar working on Cellular and Molecular Neuroscience, Cell Biology and Molecular Biology. According to data from OpenAlex, Muriel Bozon has authored 36 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cellular and Molecular Neuroscience, 12 papers in Cell Biology and 11 papers in Molecular Biology. Recurrent topics in Muriel Bozon's work include Axon Guidance and Neuronal Signaling (14 papers), Erythrocyte Function and Pathophysiology (10 papers) and Neurogenesis and neuroplasticity mechanisms (8 papers). Muriel Bozon is often cited by papers focused on Axon Guidance and Neuronal Signaling (14 papers), Erythrocyte Function and Pathophysiology (10 papers) and Neurogenesis and neuroplasticity mechanisms (8 papers). Muriel Bozon collaborates with scholars based in France, United States and United Kingdom. Muriel Bozon's co-authors include Valérie Castellani, Frédéric Moret, Homaira Nawabi, Laurette Morlé, Julien Falk, Ahmad Bechara, Nicole Alloisio, J. Delaunay, Karine Kindbeiter and Karima Abouzid and has published in prestigious journals such as Nature Communications, Neuron and Genes & Development.

In The Last Decade

Muriel Bozon

36 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Muriel Bozon France 19 564 407 313 254 184 36 1.1k
Anna Wade United States 10 310 0.5× 482 1.2× 139 0.4× 555 2.2× 80 0.4× 18 1.1k
Scott M. Gianino United States 21 298 0.5× 483 1.2× 156 0.5× 195 0.8× 91 0.5× 23 1.8k
Nithin Karanth United States 2 320 0.6× 597 1.5× 114 0.4× 555 2.2× 43 0.2× 4 1.2k
Suzana Atanasoski Switzerland 19 456 0.8× 614 1.5× 179 0.6× 318 1.3× 76 0.4× 26 1.2k
Sachiko Aono Japan 17 286 0.5× 556 1.4× 489 1.6× 135 0.5× 59 0.3× 36 996
Monique Jouet United Kingdom 13 490 0.9× 453 1.1× 158 0.5× 170 0.7× 42 0.2× 16 976
Laurence Goutebroze France 19 579 1.0× 610 1.5× 520 1.7× 224 0.9× 91 0.5× 36 1.5k
Yvette Zarb Switzerland 8 187 0.3× 608 1.5× 131 0.4× 94 0.4× 131 0.7× 10 1.3k
Kyoji Ohyama Japan 14 364 0.6× 890 2.2× 193 0.6× 335 1.3× 43 0.2× 29 1.3k

Countries citing papers authored by Muriel Bozon

Since Specialization
Citations

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

Fields of papers citing papers by Muriel Bozon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Muriel Bozon

This figure shows the co-authorship network connecting the top 25 collaborators of Muriel Bozon. A scholar is included among the top collaborators of Muriel Bozon 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 Muriel Bozon. Muriel Bozon 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.
Kindbeiter, Karine, Muriel Bozon, Olivier Thoumine, et al.. (2020). SlitC-PlexinA1 mediates iterative inhibition for orderly passage of spinal commissural axons through the floor plate. eLife. 9. 8 indexed citations
2.
Boubakar, Leïla, Karine Kindbeiter, Muriel Bozon, et al.. (2019). A Spatiotemporal Sequence of Sensitization to Slits and Semaphorins Orchestrates Commissural Axon Navigation. Cell Reports. 29(2). 347–362.e5. 22 indexed citations
3.
Ménard, Marie, Juliana M. Coelho‐Aguiar, Loraine Jarrosson-Wuillème, et al.. (2018). The dependence receptor TrkC regulates the number of sensory neurons during DRG development. Developmental Biology. 442(2). 249–261. 4 indexed citations
4.
Delloye‐Bourgeois, Céline, Karine Kindbeiter, Servane Tauszig-Delamasure, et al.. (2017). Microenvironment-Driven Shift of Cohesion/Detachment Balance within Tumors Induces a Switch toward Metastasis in Neuroblastoma. Cancer Cell. 32(4). 427–443.e8. 55 indexed citations
5.
Reynaud, Florie, Muriel Bozon, Karine Kindbeiter, et al.. (2015). Cerebrospinal fluid-derived Semaphorin3B orients neuroepithelial cell divisions in the apicobasal axis. Nature Communications. 6(1). 6366–6366. 30 indexed citations
6.
Nawabi, Homaira, Florie Reynaud, Edmund Derrington, et al.. (2012). gdnf Activates Midline Repulsion by Semaphorin3B via NCAM during Commissural Axon Guidance. Neuron. 75(6). 1051–1066. 77 indexed citations
7.
Nawabi, Homaira, Anne Briançon‐Marjollet, Christopher Clark, et al.. (2010). A midline switch of receptor processing regulates commissural axon guidance in vertebrates. Genes & Development. 24(4). 396–410. 113 indexed citations
8.
Lesca, Gaëtan, Virginie Bernard, Muriel Bozon, et al.. (2007). Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardation. European Journal of Medical Genetics. 50(3). 200–208. 5 indexed citations
9.
Morlé, Laurette, Muriel Bozon, Laurent Duret, et al.. (2004). Physical and transcript map of the autosomal dominant colobomatous microphthalmia locus on chromosome 15q12–q15 and refinement to a 4.4 Mb region. European Journal of Human Genetics. 12(7). 574–578. 6 indexed citations
10.
Vérot, Lucie, Nicole Alloisio, Laurette Morlé, et al.. (2003). Localization of a non‐syndromic X‐linked mental retardation gene (MRX80) to Xq22‐q24. American Journal of Medical Genetics Part A. 122A(1). 37–41. 5 indexed citations
11.
Morlé, Laurette, Muriel Bozon, Jean‐Christophe Zech, et al.. (2000). A Locus for Autosomal Dominant Colobomatous Microphthalmia Maps to Chromosome 15q12-q15. The American Journal of Human Genetics. 67(6). 1592–1597. 35 indexed citations
12.
Alloisio, Nicole, Laurette Morlé, Muriel Bozon, et al.. (1999). Mutation in the zonadhesin-like domain of α-tectorin associated with autosomal dominant non-syndromic hearing loss. European Journal of Human Genetics. 7(2). 255–258. 39 indexed citations
13.
Maillet, Philippe, et al.. (1999). A premature termination codon within an alternative exon affecting only the metabolism of transcripts that retain this exon. Human Mutation. 14(2). 145–155. 9 indexed citations
14.
Zech, Jean‐Christophe, Laurette Morlé, Nicole Alloisio, et al.. (1999). Wagner vitreoretinal degeneration with genetic linkage refinement on chromosome 5q13-q14. Graefe s Archive for Clinical and Experimental Ophthalmology. 237(5). 387–393. 13 indexed citations
15.
Hayette, Sandrine, Muriel Bozon, Nicole Alloisio, et al.. (1998). Two distinct truncated variants of ankyrin associated with hereditary spherocytosis. American Journal of Hematology. 58(1). 36–41. 16 indexed citations
16.
Morlé, Laurette, Muriel Bozon, Nicole Alloisio, et al.. (1997). Ankyrin Bugey: A de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosis. American Journal of Hematology. 54(3). 242–248. 17 indexed citations
17.
Randon, Jacques, Emanuele Miraglia del Giudice, Muriel Bozon, et al.. (1997). Frequent de novo mutations of the ANK1 gene mimic a recessive mode of transmission in hereditary spherocytosis: three new ANK1 variants: ankyrins Bari, Napoli II and Anzio. British Journal of Haematology. 96(3). 500–506. 21 indexed citations
18.
Alloisio, Nicole, Pascale Texier, Agnès Vallier, et al.. (1997). Modulation of Clinical Expression and Band 3 Deficiency in Hereditary Spherocytosis. Blood. 90(1). 414–420. 36 indexed citations
19.
Delgado, Julio C., Muriel Bozon, Marcela Salazar, et al.. (1996). MHC class II alleles and haplotypes in patients with pemphigus vulgaris from India. Tissue Antigens. 48(6). 668–672. 47 indexed citations
20.
Hayette, Sandrine, Laurette Morlé, Muriel Bozon, et al.. (1995). A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemia. British Journal of Haematology. 89(4). 762–770. 25 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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