Fabienne Barbet

1.1k total citations
13 papers, 743 citations indexed

About

Fabienne Barbet is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Fabienne Barbet has authored 13 papers receiving a total of 743 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Ophthalmology and 2 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Fabienne Barbet's work include Retinal Development and Disorders (7 papers), Retinal Diseases and Treatments (5 papers) and RNA regulation and disease (2 papers). Fabienne Barbet is often cited by papers focused on Retinal Development and Disorders (7 papers), Retinal Diseases and Treatments (5 papers) and RNA regulation and disease (2 papers). Fabienne Barbet collaborates with scholars based in France, Finland and United Kingdom. Fabienne Barbet's co-authors include Isabelle Perrault, Jean‐Michel Rozet, Dominique Ducroq, S. Gerber, Sylvain Hanein, Josseline Kaplan, Jean‐Louis Dufier, Arnold Munnich, Hélène Dollfus and Gaëlle Tanguy and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Neuropathology & Experimental Neurology and Advances in experimental medicine and biology.

In The Last Decade

Fabienne Barbet

13 papers receiving 729 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fabienne Barbet France 9 664 408 176 98 89 13 743
E. Fahl Germany 10 529 0.8× 354 0.9× 45 0.3× 40 0.4× 158 1.8× 15 726
Jeffrey Toy Canada 11 325 0.5× 103 0.3× 166 0.9× 39 0.4× 59 0.7× 18 519
Jacob Nellissery United States 14 518 0.8× 170 0.4× 83 0.5× 52 0.5× 95 1.1× 25 657
Seok Hong Min United States 11 709 1.1× 263 0.6× 272 1.5× 50 0.5× 166 1.9× 14 763
Yanrong Shi United States 10 485 0.7× 104 0.3× 97 0.6× 90 0.9× 53 0.6× 14 594
Corinne Leowski France 7 806 1.2× 500 1.2× 182 1.0× 104 1.1× 165 1.9× 7 858
Munefumí Sameshima Japan 13 304 0.5× 144 0.4× 51 0.3× 39 0.4× 86 1.0× 25 490
Robert R. German United States 9 531 0.8× 263 0.6× 82 0.5× 85 0.9× 164 1.8× 15 632
F Uehara Japan 14 454 0.7× 165 0.4× 32 0.2× 93 0.9× 102 1.1× 58 682
Jessica S. Rowlan United States 11 357 0.5× 167 0.4× 147 0.8× 46 0.5× 80 0.9× 16 479

Countries citing papers authored by Fabienne Barbet

Since Specialization
Citations

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

Fields of papers citing papers by Fabienne Barbet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fabienne Barbet

This figure shows the co-authorship network connecting the top 25 collaborators of Fabienne Barbet. A scholar is included among the top collaborators of Fabienne Barbet 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 Fabienne Barbet. Fabienne Barbet is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

13 of 13 papers shown
1.
Ohta, Takashi, Young Ho Kim, Jieun Oh, et al.. (2014). Alterations of theRRASandERCC1Genes at 19q13 in Gemistocytic Astrocytomas. Journal of Neuropathology & Experimental Neurology. 73(10). 908–915. 5 indexed citations
2.
Pounder, Kieran C., Florence Ayral, Maria-Halima Laaberki, et al.. (2014). Detection and genetic characterization of Seoul Virus from commensal brown rats in France. Virology Journal. 11(1). 32–32. 42 indexed citations
3.
Galizzi, Jean‐Pierre, Nolwen Guigal-Stéphan, Marianne Rodriguez, et al.. (2011). Molecular characterization of the AMPA-receptor potentiator S70340 in rat primary cortical culture: Whole-genome expression profiling. Neuroscience Research. 70(4). 349–360. 3 indexed citations
4.
Supiot, S., F. Thillays, E. Rio, et al.. (2007). Le point sur les avancées récentes de la radio-immunothérapie alpha. Cancer/Radiothérapie. 11(5). 252–259. 4 indexed citations
5.
Barbet, Fabienne, S. Gerber, Isabelle Perrault, et al.. (2007). A First Locus for Isolated Autosomal Recessive Optic Atrophy (ROA1) Maps to Chromosome 8q21-q22. Advances in experimental medicine and biology. 572. 21–27. 1 indexed citations
6.
Perrault, Isabelle, Sylvain Hanein, S. Gerber, et al.. (2005). A novel mutation in the GUCY2D gene responsible for an early onset severe RP different from the usual GUCY2D‐LCA phenotype. Human Mutation. 25(2). 222–222. 18 indexed citations
7.
8.
Perrault, Isabelle, Sylvain Hanein, S. Gerber, et al.. (2004). Retinal Dehydrogenase 12 (RDH12) Mutations in Leber Congenital Amaurosis. The American Journal of Human Genetics. 75(4). 639–646. 151 indexed citations
9.
Barbet, Fabienne, S. Gerber, Isabelle Perrault, et al.. (2003). A first locus for isolated autosomal recessive optic atrophy (ROA1) maps to chromosome 8q. European Journal of Human Genetics. 11(12). 966–971. 31 indexed citations
10.
Gerber, S., Isabelle Perrault, Sylvain Hanein, et al.. (2002). A novel mutation disrupting the cytoplasmic domain of CRB1 in a large consanguineous family of Palestinian origin affected with Leber congenital amaurosis. Ophthalmic Genetics. 23(4). 225–235. 26 indexed citations
11.
Hanein, Sylvain, Isabelle Perrault, Tuija Löppönen, et al.. (2002). Evidence of a founder effect for the RETGC1 (GUCY2D) 2943DelG mutation in Leber congenital amaurosis pedigrees of Finnish origin. Human Mutation. 20(4). 322–323. 21 indexed citations
12.
Gerber, S., Isabelle Perrault, Sylvain Hanein, et al.. (2001). Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis. European Journal of Human Genetics. 9(8). 561–571. 124 indexed citations
13.
Rozet, Jean‐Michel, Isabelle Perrault, S. Gerber, et al.. (2001). Complete abolition of the retinal-specific guanylyl cyclase (retGC-1) catalytic ability consistently leads to leber congenital amaurosis (LCA).. PubMed. 42(6). 1190–2. 41 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 E. Fahl Breakdown of academic impact, for papers by Jeffrey Toy Breakdown of academic impact, for papers by Jacob Nellissery Breakdown of academic impact, for papers by Seok Hong Min Breakdown of academic impact, for papers by Yanrong Shi Breakdown of academic impact, for papers by Corinne Leowski Breakdown of academic impact, for papers by Munefumí Sameshima Breakdown of academic impact, for papers by Robert R. German Breakdown of academic impact, for papers by F Uehara Breakdown of academic impact, for papers by Jessica S. Rowlan
Rankless by CCL
2026