Corinne Leowski

1.3k total citations
7 papers, 858 citations indexed

About

Corinne Leowski is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Corinne Leowski has authored 7 papers receiving a total of 858 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Ophthalmology and 2 papers in Genetics. Recurrent topics in Corinne Leowski's work include Retinal Development and Disorders (6 papers), Retinal Diseases and Treatments (5 papers) and Glaucoma and retinal disorders (2 papers). Corinne Leowski is often cited by papers focused on Retinal Development and Disorders (6 papers), Retinal Diseases and Treatments (5 papers) and Glaucoma and retinal disorders (2 papers). Corinne Leowski collaborates with scholars based in France, United Kingdom and Morocco. Corinne Leowski's co-authors include S. Gerber, Jean‐Michel Rozet, Josseline Kaplan, Isabelle Perrault, Jean‐Louis Dufier, Eric H. Souied, Arnold Munnich, Sophie Châtelin, Imad Ghazi and Arnold Münnich and has published in prestigious journals such as Nature Genetics, Human Molecular Genetics and Human Mutation.

In The Last Decade

Corinne Leowski

7 papers receiving 838 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Corinne Leowski France	7	806	500	182	165	104	7	858
F. P. M. Cremers Netherlands	7	804 1.0×	482 1.0×	130 0.7×	93 0.6×	132 1.3×	8	879
Birgit Lorenz Germany	7	588 0.7×	383 0.8×	105 0.6×	148 0.9×	65 0.6×	10	720
Sharola Dharmaraj United States	11	647 0.8×	472 0.9×	233 1.3×	93 0.6×	74 0.7×	15	791
Karin W. Littink Netherlands	12	669 0.8×	328 0.7×	142 0.8×	146 0.9×	117 1.1×	13	711
Louisa M. Affatigato United States	13	1.0k 1.3×	620 1.2×	160 0.9×	247 1.5×	117 1.1×	17	1.2k
Karina E Guziewicz United States	13	676 0.8×	354 0.7×	147 0.8×	157 1.0×	87 0.8×	26	762
Sophie Châtelin France	7	512 0.6×	316 0.6×	87 0.5×	136 0.8×	66 0.6×	8	585
Lina Zelinger Israel	15	653 0.8×	246 0.5×	183 1.0×	135 0.8×	109 1.0×	19	733
Drew Everhart United States	6	651 0.8×	248 0.5×	180 1.0×	205 1.2×	77 0.7×	8	696
Sten Kjellström United States	14	909 1.1×	416 0.8×	248 1.4×	155 0.9×	98 0.9×	23	1.0k

Countries citing papers authored by Corinne Leowski

Since Specialization

Citations

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

Fields of papers citing papers by Corinne Leowski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Corinne Leowski

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

All Works

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7 of 7 papers shown

1.

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

2.

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

3.

Perrault, Isabelle, Jean‐Michel Rozet, S. Gerber, et al.. (2000). Spectrum of retGC1 mutations in Leber's congenital amaurosis. European Journal of Human Genetics. 8(8). 578–582. 93 indexed citations

4.

Perrault, Isabelle, Jean‐Michel Rozet, S. Gerber, et al.. (1999). Leber Congenital Amaurosis. Molecular Genetics and Metabolism. 68(2). 200–208. 110 indexed citations

5.

Rozet, Jean‐Michel, S. Gerber, Eric H. Souied, et al.. (1998). Spectrum of ABCR gene mutations in autosomal recessive macular dystrophies. European Journal of Human Genetics. 6(3). 291–295. 126 indexed citations

6.

Perrault, Isabelle, Jean‐Michel Rozet, Patrick Calvas, et al.. (1996). Retinal–specific guanylate cyclase gene mutations in Leber's congenital amaurosis. Nature Genetics. 14(4). 461–464. 353 indexed citations

7.

Camuzat, Agnès, Hélène Dollfus, Jean‐Michel Rozet, et al.. (1995). A gene for Leber's congenital amaurosis maps to chromosome 17p. Human Molecular Genetics. 4(8). 1447–1452. 33 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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