Imad Ghazi

1.0k total citations
15 papers, 688 citations indexed

About

Imad Ghazi is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Imad Ghazi has authored 15 papers receiving a total of 688 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Ophthalmology and 4 papers in Genetics. Recurrent topics in Imad Ghazi's work include Retinal Development and Disorders (9 papers), Retinal Diseases and Treatments (7 papers) and RNA regulation and disease (2 papers). Imad Ghazi is often cited by papers focused on Retinal Development and Disorders (9 papers), Retinal Diseases and Treatments (7 papers) and RNA regulation and disease (2 papers). Imad Ghazi collaborates with scholars based in France, United Kingdom and Switzerland. Imad Ghazi's co-authors include Jean‐Michel Rozet, Josseline Kaplan, S. Gerber, Isabelle Perrault, Jean‐Louis Dufier, Arnold Münnich, Corinne Leowski, Dominique Ducroq, Eric H. Souied and Sophie Châtelin and has published in prestigious journals such as Human Molecular Genetics, Vision Research and American Journal of Ophthalmology.

In The Last Decade

Imad Ghazi

15 papers receiving 670 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Imad Ghazi France 10 618 366 120 93 87 15 688
F. P. M. Cremers Netherlands 7 804 1.3× 482 1.3× 130 1.1× 119 1.3× 53 0.6× 8 879
Corinne Leowski France 7 806 1.3× 500 1.4× 182 1.5× 92 1.0× 21 0.2× 7 858
Blanca Garcı́a-Sandoval Spain 21 1.0k 1.7× 549 1.5× 187 1.6× 158 1.7× 118 1.4× 56 1.2k
Birgit Lorenz Germany 7 588 1.0× 383 1.0× 105 0.9× 68 0.7× 15 0.2× 10 720
David Bessant United Kingdom 14 292 0.5× 345 0.9× 99 0.8× 279 3.0× 37 0.4× 21 639
Antje Bernd Germany 11 601 1.0× 420 1.1× 167 1.4× 174 1.9× 122 1.4× 22 821
Katsuhiro Hosono Japan 13 407 0.7× 197 0.5× 132 1.1× 64 0.7× 22 0.3× 45 507
Béatrice Bocquet France 16 527 0.9× 264 0.7× 80 0.7× 53 0.6× 13 0.1× 37 607
Samer Khateb Israel 16 525 0.8× 178 0.5× 147 1.2× 56 0.6× 67 0.8× 43 662
Xunlun Sheng China 14 386 0.6× 249 0.7× 118 1.0× 121 1.3× 36 0.4× 48 598

Countries citing papers authored by Imad Ghazi

Since Specialization
Citations

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

Fields of papers citing papers by Imad Ghazi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Imad Ghazi

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

All Works

15 of 15 papers shown
1.
Perrault, Isabelle, Nicolas Goudin, Sabine Defoort‐Dhellemmes, et al.. (2019). AON-Mediated Exon Skipping to Bypass Protein Truncation in Retinal Dystrophies Due to the Recurrent CEP290 c.4723A > T Mutation. Fact or Fiction?. Genes. 10(5). 368–368. 18 indexed citations
2.
Rozet, Jean‐Michel, Isabelle Perrault, Nadine Gigarel, et al.. (2002). Dominant X-linked RP is Frequently Accounted for by Truncating Mutations in the Exon ORF15 of the RPGR Gene. 43(13). 788–788. 1 indexed citations
3.
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
4.
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
5.
Souied, Eric H., Dominique Ducroq, S. Gerber, et al.. (1999). Age-related macular degeneration in grandparents of patients with Stargardt disease: genetic study. American Journal of Ophthalmology. 128(2). 173–178. 37 indexed citations
6.
Rozet, Jean‐Michel, S. Gerber, Eric Souied, et al.. (1999). The ABCR Gene: A Major Disease Gene in Macular and Peripheral Retinal Degenerations with Onset from Early Childhood to the Elderly. Molecular Genetics and Metabolism. 68(2). 310–315. 28 indexed citations
7.
8.
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
9.
Perrault, Isabelle, Sophie Châtelin, Jean‐Michel Rozet, et al.. (1998). Exclusion of five subunits of cGMP phosphodiesterase in Leber's congenital amaurosis. Human Genetics. 102(3). 322–326. 3 indexed citations
10.
Ghazi, Imad, Jean‐Michel Rozet, Sophie Châtelin, et al.. (1997). Severe manifestations in carrier females in X linked retinitis pigmentosa.. Journal of Medical Genetics. 34(10). 793–797. 36 indexed citations
11.
Sahly, Iman, Marc Abitbol, Claudine Laurent, et al.. (1996). Identification of a novel PAX6 gene mutation in an Aniridia patient. Human Mutation. 7(4). 377–377. 3 indexed citations
12.
Sahly, Iman, et al.. (1995). 2137 Identification of a new mutation causing an aniridia in the PST domain of PAX6. Vision Research. 35. S88–S88. 1 indexed citations
13.
Kaplan, Josseline, A. Camuzat, Hélène Dollfus, et al.. (1995). 3235 A gene for Leber's congenital amaurosis maps to chromosome 17p. Vision Research. 35. S132–S132. 1 indexed citations
14.
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
15.
Kaplan, Josseline, S. Gerber, Dominique Bonneau, et al.. (1992). A gene for usher syndrome type I (USH1A) maps to chromosome 14q. Genomics. 14(4). 979–987. 110 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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