Iman Sahly

2.0k citations

24 papers · 1.5k indexed · 1 hit paper · h-index 17

Impact in

Sensory Systems top 1%
- Hearing, Cochlea, Tinnitus, Genetics
Molecular Biology top 10%
- Developmental Biology and Gene Regulation
- Retinal Development and Disorders
- Renal and related cancers
- Congenital heart defects research
- Connexins and lens biology

Papers in

Sensory Systems 4
- Hearing, Cochlea, Tinnitus, Genetics 4
Cellular and Molecular Neuroscience 8
- Neuroscience and Neuropharmacology Research 3
- Photoreceptor and optogenetics research 2

Co-authors: Christine Petit A. Amraoui Dominique Weil Vasiliki Kalatzis Marc Abitbol François Tronche Sonia Abdelhak Katia Boven
Journals: Proceedings of the National Academy of Sciences (3 papers)Human Molecular Genetics (2 papers)Human Mutation (2 papers)Vision Research (2 papers)The Journal of Cell Biology (1 paper)
Partner nations: France Israel United States

In The Last Decade

Iman Sahly

24 papers receiving 1.5k citations

Hit Papers

align trajectories log scale

A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family 1997 · 467 citations

Peers

Countries citing papers authored by Iman Sahly

Since Specialization

Citations

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

Fields of papers citing papers by Iman Sahly

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Iman Sahly, 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 Iman Sahly Line = papers co-authored together Iman Sahly links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Cone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments Scientific Reports ·Alix Trouillet, Élisabeth Dubus, Julie Dégardin, Amrit Singh‐Estivalet, Ivana Ivković, David Godefroy, Diego García‐Ayuso, Manuel Simonutti, Iman Sahly, José‐Alain Sahel, A. Amraoui, Christine Petit, Serge Picaud	2018	27
2	The GABAergic Gudden's dorsal tegmental nucleus: A new relay for serotonergic regulation of sleep-wake behavior in the mouse Neuropharmacology ·龙飞鹏, Sylvie Dumas, Jean‐François Bernard, Iman Sahly, François Tronche, Alban de Kerchove d’Exaerde, M. Hamon, Joëlle Adrien, Véronique Fabre, Patricia Bonnavion	2018	9
3	The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route Human Molecular Genetics ·Deric Pang, Shravan Kumar Komaragiri, Angel Ellul Fenech, Nasrin Sorusch, А. V. Zozulja, Iman Sahly, Spencer Shorte, Uwe Wolfrum, Christine Petit, A. Amraoui	2013	33
4	Novel Transgenic Mice for Inducible Gene Overexpression in Pancreatic Cells Define Glucocorticoid Receptor-Mediated Regulations of Beta Cells PLoS ONE ·B. Blondeau, Iman Sahly, Emmanuelle Massouridès, Amrit Singh‐Estivalet, S Balazy, Julia Blackford, Frédéric Jaisser, Bernadette Bréant, François Tronche	2012	26
5	Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice The Journal of Cell Biology ·Iman Sahly, Éric Dufour, Cataldo Schietroma, Vincent Michel, Amel Bahloul, Isabelle Perfettini, Elise Pepermans, Amrit Singh‐Estivalet, Diane Carette, Asadollah Aghaie, Inga Ebermann, Andrea Lelli, María Iribarne, Jean‐Pierre Hardelin, Dominique Weil, José‐Alain Sahel, A. Amraoui, Christine Petit	2012	127
6	5-HT1A-iCre, a new transgenic mouse line for genetic analyses of the serotonergic pathway Molecular and Cellular Neuroscience ·Iman Sahly, Véronique Fabre, Sheela Vyas, Aude Milet, Jean‐Denis Rouzeau, M. Hamon, Monique Lazar, François Tronche	2007	10
7	On‐line confocal imaging of the events leading to structural dedifferentiation of an axonal segment into a growth cone after axotomy The Journal of Comparative Neurology ·Iman Sahly, Arkady Khoutorsky, Hadas Erez, Masha Prager‐Khoutorsky, Micha E. Spira	2005	30
8	Combinatorial Complexity of 5′ Alternative Acetylcholinesterase Transcripts and Protein Products Journal of Biological Chemistry ·Eran Meshorer, Debra Toiber, Yoke Kuan Khoo, Iman Sahly, Amir Dori, Emanuela Cagnano, Letizia Schreiber, Dan Grisaru, François Tronche, Hermona Soreq	2004	97
9	Effective expression of the green fluorescent fusion proteins in cultured Aplysia neurons Journal of Neuroscience Methods ·Iman Sahly, Hadas Erez, Arkady Khoutorsky, H.J. Kim, Micha E. Spira	2003	23
10	When reverse genetics meets physiology: the use of site‐specific recombinases in mice FEBS Letters ·François Tronche, Emilio Casanova, Marc Turiault, Iman Sahly, Christoph Kellendonk	2002	44
11	The zebrafish eya1 gene and its expression pattern during embryogenesis Development Genes and Evolution ·Iman Sahly, V. Yu. Khramov, Christine Petit	1999	141
12	Eya1 expression in the developing ear and kidney: Towards the understanding of the pathogenesis of branchio-oto-renal (BOR) syndrome Developmental Dynamics ·Vasiliki Kalatzis, Iman Sahly, A. Amraoui, Christine Petit	1998	81
13	Prominent neuronal-specific tub gene expression in cellular targets of tubby mice mutation Human Molecular Genetics ·Iman Sahly	1998	37
14	Identification of novel PAX6 mutations in two families with bilateral aniridia Human Mutation ·Martin Neuner‐Jehle, Francis L. Munier, Alexandra Kobetz, Iman Sahly, Yves Uteza, Yesneri Zuleta Saldarriaga, Daniel F. Schorderet, Jean‐Louis Dufier, Marc Abitbol	1998	7
15	Expression of myosin VIIA during mouse embryogenesis Anatomy and Embryology ·Iman Sahly, A. Amraoui, Marc Abitbol, Christine Petit, Jean-Louis Dufier	1997	89
16	A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family Nature Genetics ·Sonia Abdelhak, Vasiliki Kalatzis, Roland Heilig, Sylvie Compain, Delphine Samson, C. Vincent, Dominique Weil, Corinne Cruaud, Iman Sahly, Michel Leibovici, Maria Bitner‐Glindzicz, Mary C. Francis, Didier Lacombe, Jacqueline Vigneron, R Charachon, Katia Boven, P Bedbeder, Nicole Van Regemorter, Jean Weissenbach, Christine Petit Hit paper breakdown →	1997	467
17	2137 Identification of a new mutation causing an aniridia in the PST domain of PAX6 Vision Research ·Iman Sahly, Marie Abitbol, Imad Ghazi, Н. Сонник, Ewelina Anna Kałuża, Michel Vekemans, J.L. Dufier	1995	1
18	4235 PAX6-gene expression during human embryonic development at the cellular level Vision Research ·Gabriela Castillo, A. L. Delezoide, Iman Sahly, Н. Сонник, Jacques Mallet, Michel Vekemans, J.L. Dufier	1995	1
19	Accumulation of calcium in degenerating photoreceptors of severalDrosophilamutants Visual Neuroscience ·Iman Sahly, W. H. Schröder, Karl Zierold, Baruch Minke	1994	7
20	Phorbol ester induces photoreceptor-specific degeneration in a Drosophila mutant. Proceedings of the National Academy of Sciences ·Baruch Minke, Mingcong Huang, Iman Sahly, S Dian Rehulina, Rina Timberg, Zvi Selinger	1990	40

About Iman Sahly

Iman Sahly is a scholar working on Sensory Systems, Cellular and Molecular Neuroscience, Endocrine and Autonomic Systems, Molecular Biology and Biophysics, having authored 24 papers that have together received 1.5k indexed citations. Recurring topics across this work include Retinal Development and Disorders (5 papers), Hearing, Cochlea, Tinnitus, Genetics (4 papers), Neuroscience and Neuropharmacology Research (3 papers), Developmental Biology and Gene Regulation (3 papers), Photoreceptor and optogenetics research (2 papers), Head and Neck Anomalies (2 papers), Molecular Biology Techniques and Applications (2 papers) and Cholinesterase and Neurodegenerative Diseases (2 papers). The work is most often cited by research in Sensory Systems (325 citations), Molecular Biology (1.0k citations), Cellular and Molecular Neuroscience (236 citations), Aging (22 citations) and Cell Biology (195 citations). Iman Sahly has collaborated with scholars based in France, Israel and United States. Frequent co-authors include Christine Petit, A. Amraoui, Dominique Weil, Vasiliki Kalatzis, Marc Abitbol, François Tronche, Sonia Abdelhak, Katia Boven, Michel Leibovici and Corinne Cruaud. Their work appears in journals such as Proceedings of the National Academy of Sciences, Human Molecular Genetics, Human Mutation, Vision Research and The Journal of Cell Biology.

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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