Jean‐Louis Dufier

4.9k total citations
106 papers, 3.3k citations indexed

About

Jean‐Louis Dufier is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Jean‐Louis Dufier has authored 106 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 41 papers in Ophthalmology and 23 papers in Genetics. Recurrent topics in Jean‐Louis Dufier's work include Retinal Development and Disorders (33 papers), Retinal Diseases and Treatments (19 papers) and Glaucoma and retinal disorders (12 papers). Jean‐Louis Dufier is often cited by papers focused on Retinal Development and Disorders (33 papers), Retinal Diseases and Treatments (19 papers) and Glaucoma and retinal disorders (12 papers). Jean‐Louis Dufier collaborates with scholars based in France, Switzerland and United States. Jean‐Louis Dufier's co-authors include Josseline Kaplan, Jean‐Michel Rozet, S. Gerber, Isabelle Perrault, Arnold Münnich, Hélène Dollfus, Arnold Munnich, Dominique Ducroq, Sylvain Hanein and Corinne Leowski and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and PLoS ONE.

In The Last Decade

Jean‐Louis Dufier

99 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jean‐Louis Dufier France 30 2.3k 1.5k 666 389 385 106 3.3k
Arnold Munnich France 25 1.9k 0.8× 860 0.6× 724 1.1× 254 0.7× 285 0.7× 54 3.2k
Jean‐Michel Rozet France 34 3.8k 1.6× 1.8k 1.2× 1.2k 1.8× 654 1.7× 471 1.2× 120 4.5k
Patrick Calvas France 31 2.1k 0.9× 915 0.6× 1.4k 2.1× 346 0.9× 721 1.9× 104 3.9k
Nurten Akarsu Türkiye 27 1.4k 0.6× 530 0.3× 817 1.2× 197 0.5× 300 0.8× 67 2.8k
Hanno J. Bolz Germany 32 2.6k 1.1× 568 0.4× 940 1.4× 366 0.9× 214 0.6× 100 3.5k
Bart P. Leroy Belgium 37 3.6k 1.6× 2.0k 1.3× 1.5k 2.2× 484 1.2× 579 1.5× 157 4.8k
Isabelle Perrault France 30 2.7k 1.2× 1.5k 1.0× 628 0.9× 452 1.2× 329 0.9× 71 3.0k
Kevin Gregory-Evans United Kingdom 27 1.6k 0.7× 682 0.4× 384 0.6× 367 0.9× 356 0.9× 55 2.3k
Irene H. Maumenee United States 47 3.4k 1.5× 2.3k 1.5× 1.9k 2.8× 522 1.3× 1.1k 3.0× 143 6.3k
Klaus Rohrschneider Germany 41 2.8k 1.2× 3.1k 2.1× 748 1.1× 327 0.8× 2.0k 5.2× 130 5.3k

Countries citing papers authored by Jean‐Louis Dufier

Since Specialization
Citations

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

Fields of papers citing papers by Jean‐Louis Dufier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jean‐Louis Dufier. 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 Jean‐Louis Dufier. The network helps show where Jean‐Louis Dufier may publish in the future.

Co-authorship network of co-authors of Jean‐Louis Dufier

This figure shows the co-authorship network connecting the top 25 collaborators of Jean‐Louis Dufier. A scholar is included among the top collaborators of Jean‐Louis Dufier 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 Jean‐Louis Dufier. Jean‐Louis Dufier 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.
Dufier, Jean‐Louis, Jean‐Michel Rozet, Josseline Kaplan, & Olivier Roche. (2013). Du glaucome congénital au glaucome chronique de l’adulte : un continuum clinique et génétique. Bulletin de l Académie Nationale de Médecine. 197(1). 133–141.
2.
Stoetzel, Corinne, Laura Liebermann, Vincent Marion, et al.. (2010). Confirmation of ADAMTSL4 mutations for autosomal recessive isolated bilateral Ectopia Lentis. Ophthalmic Genetics. 31(1). 47–51. 29 indexed citations
3.
Quentien, M.-H., M Ménasche, Jean‐Louis Dufier, et al.. (2010). Truncation of PITX2 differentially affects its activity on physiological targets. Journal of Molecular Endocrinology. 46(1). 9–19. 7 indexed citations
4.
Gout, Olivier, et al.. (2010). Polymorphisme clinique de la myasthénie à point de départ oculaire ; analyse rétrospective sur cinq ans. Journal Français d Ophtalmologie. 33(10). 728–738. 2 indexed citations
5.
Vignal, Catherine, et al.. (2009). Clinical Polymorphism of Myasthenia Gravis Beginning With Isolated Ocular Symptoms. Investigative Ophthalmology & Visual Science. 50(13). 4035–4035. 1 indexed citations
6.
Orssaud, Christophe, et al.. (2008). Le rôle de la vision dans la lecture. 1(1). 28–32. 1 indexed citations
7.
Gerber, S., Sylvain Hanein, Isabelle Perrault, et al.. (2007). Mutations in LCA5 are an uncommon cause of Leber congenital amaurosis (LCA) type II. Human Mutation. 28(12). 1245–1245. 19 indexed citations
8.
Perrault, Isabelle, et al.. (2007). Spectrum of NPHP6/CEP290 mutations in Leber congenital amaurosis and delineation of the associated phenotype. Human Mutation. 28(4). 416–416. 6 indexed citations
9.
Kaplan, Josseline, et al.. (2006). Usher Syndrome Type 1a: From Myth to Reality. Investigative Ophthalmology & Visual Science. 47(13). 4605–4605. 1 indexed citations
10.
Pelletier, Valérie, Marguerite Jambou, Nathalie Delphin, et al.. (2006). Comprehensive survey of mutations in RP2 and RPGR in patients affected with distinct retinal dystrophies: genotype–phenotype correlations and impact on genetic counseling. Human Mutation. 28(1). 81–91. 104 indexed citations
11.
Bièche, Ivan, Olivier Roche, Ingrid Laurendeau, et al.. (2006). Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report. BMC Medical Genetics. 7(1). 82–82. 14 indexed citations
12.
Paycha, F., et al.. (2005). Diagnostic et traitement des glaucomes: Aide de l’informatique. Journal Français d Ophtalmologie. 28(4). 396–400.
13.
Hanein, Sylvain, Nadine Gigarel, Jean‐Michel Rozet, et al.. (2003). NDP gene mutations in 14 French families with Norrie disease. Human Mutation. 22(6). 499–499. 29 indexed citations
14.
Doz, François, Martine Peter, Gudrun Schleiermacher, et al.. (1996). N-MYC amplification, loss of heterozygosity on the short arm of chromosome 1 and DNA ploidy in retinoblastoma. European Journal of Cancer. 32(4). 645–649. 19 indexed citations
15.
Khelfaoui, Fatima, Pierre Validire, Anne Aupérin, et al.. (1996). Histopathologic risk factors in retinoblastoma: A retrospective study of 172 patients treated in a single institution. Cancer. 77(6). 1206–1213. 24 indexed citations
16.
Souied, Eric, S. Gerber, Jean‐Michel Rozet, et al.. (1995). P 367 Two novel missense mutations of peripherin/RDS gene in autosomal dominant retinitis pigmentosa (ADRP), in pedigrees from France. Vision Research. 35. S221–S221. 2 indexed citations
17.
Bonneau, Dominique, Josseline Kaplan, G. Girard, & Jean‐Louis Dufier. (1992). Autosomal inheritance of “senile” retinitis pigmentosa. A report of a family with consanguinity. Clinical Genetics. 42(4). 199–200. 2 indexed citations
18.
Orssaud, Christophe & Jean‐Louis Dufier. (1989). Objectivation par cartographie cérébrale de la neutralisation corticale au cours de l'amblyopie fonctionnelle. 84(3). 375–378.
19.
Basile, Geneviève de Saint, Alain Fischer, Jean‐Pierre Cartron, et al.. (1988). Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotype. Human Genetics. 80(1). 85–89. 52 indexed citations
20.
Turleau, C, J. de Grouchy, Jean‐Louis Dufier, et al.. (1981). Aniridia, male pseudohermaphroditism, gonadoblastoma, mental retardation, and del 11p13. Human Genetics. 57(3). 300–306. 49 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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