Imad Ghazi

1.0k citations

15 papers · 688 indexed · h-index 10

Impact in

Ophthalmology top 1%
- Retinal Diseases and Treatments
- Glaucoma and retinal disorders
Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics

Papers in ⓘ

Molecular Biology 11
- Retinal Development and Disorders 9
- Retinoids in leukemia and cellular processes 2
- RNA regulation and disease 2
Ophthalmology 7
- Retinal Diseases and Treatments 7

Co-authors: Jean‐Michel Rozet (13 shared papers)Josseline Kaplan (11 shared papers)S. Gerber (12 shared papers)Isabelle Perrault (10 shared papers)Jean‐Louis Dufier (9 shared papers)Arnold Münnich (6 shared papers)Corinne Leowski (4 shared papers)Dominique Ducroq (5 shared papers)
Journals: European Journal of Human Genetics (3 papers)Vision Research (2 papers)Journal of Medical Genetics (2 papers)Human Mutation (1 paper)Molecular Genetics and Metabolism (1 paper)
Partner nations: France United Kingdom Switzerland

In The Last Decade

Imad Ghazi

15 papers receiving 670 citations

Peers

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-authors

The 25 scholars most cited alongside Imad Ghazi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Imad Ghazi Line = papers co-authored together Imad Ghazi links everyone, so they are left out of the graph.

All Works

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15 of 15 papers shown

#	Work
1	Spectrum of ABCR gene mutations in autosomal recessive macular dystrophies European Journal of Human Genetics ·Jean‐Michel Rozet, S. Gerber, Eric H. Souied, Isabelle Perrault, Sophie Châtelin, Imad Ghazi, Corinne Leowski, Jean‐Louis Dufier, Arnold Munnich, Josseline Kaplan	1998	126
2	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 ·S. Gerber, Isabelle Perrault, Sylvain Hanein, Fabienne Barbet, Dominique Ducroq, Imad Ghazi, Dominique Martin‐Coignard, Corinne Leowski, Tessa Homfray, Jean‐Louis Dufier, Arnold Münnich, Josseline Kaplan, Jean‐Michel Rozet	2001	124
3	A gene for usher syndrome type I (USH1A) maps to chromosome 14q Genomics ·Josseline Kaplan, S. Gerber, Dominique Bonneau, Jean‐Michel Rozet, O. Delrieu, Marie‐Louise Briard, Hélène Dollfus, Imad Ghazi, Jean‐Louis Dufier, J Frézal, Arnold Münnich	1992	110
4	Spectrum of retGC1 mutations in Leber's congenital amaurosis European Journal of Human Genetics ·Isabelle Perrault, Jean‐Michel Rozet, S. Gerber, Imad Ghazi, Dominique Ducroq, Eric H. Souied, Corinne Leowski, Michèle Bonnemaison, Jean‐Louis Dufier, Arnold Münnich, Josseline Kaplan	2000	93
5	Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evidence of clinical heterogeneity at this locus Journal of Medical Genetics ·Jean‐Michel Rozet, S. Gerber, Imad Ghazi, Isabelle Perrault, Dominique Ducroq, Eric Souied, Annick Cabot, J.L. Dufier, A Munnich, Josseline Kaplan	1999	74
6	Age-related macular degeneration in grandparents of patients with Stargardt disease: genetic study American Journal of Ophthalmology ·Eric H. Souied, Dominique Ducroq, S. Gerber, Imad Ghazi, Jean‐Michel Rozet, Isabelle Perrault, Arnold Münnich, J.L. Dufier, G. Coscas, G. Soubrane, Josseline Kaplan	1999	37
7	Severe manifestations in carrier females in X linked retinitis pigmentosa. Journal of Medical Genetics ·E. Souied, Bertrand Ségues, Imad Ghazi, Jean‐Michel Rozet, Sophie Châtelin, S. Gerber, Isabelle Perrault, A Michel-Awad, Marie‐Louise Briard, Ghislaine Plessis, Jean‐Louis Dufier, A Munnich, Josseline Kaplan	1997	36
8	A gene for Leber's congenital amaurosis maps to chromosome 17p Human Molecular Genetics ·Agnès Camuzat, Hélène Dollfus, Jean‐Michel Rozet, S. Gerber, Dominique Bonneau, Michèle Bonnemaison, Marie‐Louise Briard, Jean-Louis Dufier, Imad Ghazi, Corinne Leowski, Jean Weissenbach, J Frézal, Susanne Arnold, Josseline Kaplan	1995	33
9	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 ·Jean‐Michel Rozet, S. Gerber, Eric Souied, Dominique Ducroq, Isabelle Perrault, Imad Ghazi, G. Soubrane, G. Coscas, Jean‐Louis Dufier, Arnold Münnich, Josseline Kaplan	1999	28
10	AON-Mediated Exon Skipping to Bypass Protein Truncation in Retinal Dystrophies Due to the Recurrent CEP290 c.4723A > T Mutation. Fact or Fiction? Genes ·Iris Barny, Isabelle Perrault, Christel Michel, Nicolas Goudin, Sabine Defoort‐Dhellemmes, Imad Ghazi, Josseline Kaplan, Jean‐Michel Rozet, Xavier Gérard	2019	18
11	Exclusion of five subunits of cGMP phosphodiesterase in Leber's congenital amaurosis Human Genetics ·Isabelle Perrault, Sophie Châtelin, Vanessa Nancy, Jean‐Michel Rozet, S. Gerber, Imad Ghazi, Eric H. Souied, Jean‐Louis Dufier, Arnold Munnich, Jean de Gunzburg, Josseline Kaplan	1998	3
12	Identification of a novel PAX6 gene mutation in an Aniridia patient Human Mutation ·Iman Sahly, Marc Abitbol, Claudine Laurent, Imad Ghazi, Florence Ribeaudeau, Michel Vekemans, Jean‐Louis Dufier	1996	3
13	2137 Identification of a new mutation causing an aniridia in the PST domain of PAX6 Vision Research ·Iman Sahly, Marie Abitbol, Imad Ghazi, Florence Ribeaudeau, M. Gérard, Michel Vekemans, J.L. Dufier	1995	1
14	3235 A gene for Leber's congenital amaurosis maps to chromosome 17p Vision Research ·Josseline Kaplan, A. Camuzat, Hélène Dollfus, Jean‐Michel Rozet, S. Gerber, D Bonneau, Imad Ghazi, Jean‐Louis Dufier, Arnold Münnich	1995	1
15	Dominant X-linked RP is Frequently Accounted for by Truncating Mutations in the Exon ORF15 of the RPGR Gene Jean‐Michel Rozet, Isabelle Perrault, Nadine Gigarel, Eric H. Souied, Imad Ghazi, S. Gerber, J-Ll Dufier, A Munnich, Kaplan Jc	2002	1

About Imad Ghazi

Imad Ghazi is a scholar working on Molecular Biology, Ophthalmology, Genetics, Radiology, Nuclear Medicine and Imaging and Cellular and Molecular Neuroscience, having authored 15 papers that have together received 688 indexed citations. Recurring topics across this work include Retinal Development and Disorders (9 papers), Retinal Diseases and Treatments (7 papers), Retinopathy of Prematurity Studies (2 papers), Retinoids in leukemia and cellular processes (2 papers), RNA regulation and disease (2 papers), Ocular Disorders and Treatments (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and interferon and immune responses (1 paper). The work is most often cited by research in Ophthalmology (366 citations), Sensory Systems (87 citations), Molecular Biology (618 citations), Cell Biology (86 citations) and Cellular and Molecular Neuroscience (81 citations). Imad Ghazi has collaborated with scholars based in France, United Kingdom and Switzerland. Frequent co-authors include Jean‐Michel Rozet, Josseline Kaplan, S. Gerber, Isabelle Perrault, Jean‐Louis Dufier, Arnold Münnich, Corinne Leowski, Dominique Ducroq, Sophie Châtelin and Eric H. Souied. Their work appears in journals such as European Journal of Human Genetics, Vision Research, Journal of Medical Genetics, Human Mutation and Molecular Genetics and Metabolism.

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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