Isabelle Audo

11.0k total citations · 1 hit paper
184 papers, 4.0k citations indexed

About

Isabelle Audo is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Isabelle Audo has authored 184 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 146 papers in Molecular Biology, 116 papers in Ophthalmology and 32 papers in Cellular and Molecular Neuroscience. Recurrent topics in Isabelle Audo's work include Retinal Development and Disorders (133 papers), Retinal Diseases and Treatments (95 papers) and Photoreceptor and optogenetics research (30 papers). Isabelle Audo is often cited by papers focused on Retinal Development and Disorders (133 papers), Retinal Diseases and Treatments (95 papers) and Photoreceptor and optogenetics research (30 papers). Isabelle Audo collaborates with scholars based in France, United States and United Kingdom. Isabelle Audo's co-authors include José‐Alain Sahel, Christina Zeitz, Saddek Mohand‐Saïd, Anthony G. Robson, Aline Antonio, Katia Marazova, Marie‐Elise Lancelot, Shomi S. Bhattacharya, Christelle Michiels and Christel Condroyer and has published in prestigious journals such as Nature Medicine, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Isabelle Audo

175 papers receiving 4.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Partial recovery of visual function in a blind patient after optogenetic therapy

2021 424 citations José‐Alain Sahel, Élise Boulanger-Scemama et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Isabelle Audo France	32	3.1k	2.1k	1.0k	601	465	184	4.0k
Steven Nusinowitz United States	38	4.1k 1.3×	2.2k 1.1×	1.3k 1.3×	823 1.4×	417 0.9×	99	5.2k
Jijing Pang United States	32	3.6k 1.1×	1.7k 0.8×	978 1.0×	483 0.8×	1.2k 2.6×	78	4.0k
Alison J. Hardcastle United Kingdom	39	3.0k 1.0×	1.6k 0.8×	703 0.7×	1.1k 1.9×	763 1.6×	127	4.2k
Radouil Tzekov United States	28	2.6k 0.8×	2.4k 1.1×	694 0.7×	941 1.6×	175 0.4×	84	3.9k
Ronald A. Bush United States	42	4.7k 1.5×	1.8k 0.9×	2.0k 2.0×	893 1.5×	545 1.2×	76	5.4k
Christian Hamel France	28	3.9k 1.3×	984 0.5×	751 0.7×	246 0.4×	313 0.7×	46	4.4k
Michael T. Matthes United States	34	3.9k 1.2×	1.7k 0.8×	1.5k 1.5×	667 1.1×	374 0.8×	66	4.9k
Thierry Léveillard France	36	3.4k 1.1×	1.2k 0.6×	1.3k 1.3×	354 0.6×	311 0.7×	113	3.9k
Daniel E. Possin United States	27	2.3k 0.7×	1.1k 0.5×	995 1.0×	501 0.8×	140 0.3×	40	2.8k
M. Dominik Fischer Germany	30	2.2k 0.7×	1.0k 0.5×	378 0.4×	383 0.6×	513 1.1×	99	2.8k

Countries citing papers authored by Isabelle Audo

Since Specialization

Citations

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

Fields of papers citing papers by Isabelle Audo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabelle Audo

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

All Works

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20 of 20 papers shown

Michiels, Christelle, Jacques Callebert, José‐Alain Sahel, et al.. (2024). Loss of ON-Pathway Function in Mice Lacking Lrit3 Decreases Recovery From Lens-Induced Myopia. Investigative Ophthalmology & Visual Science. 65(11). 18–18. 3 indexed citations

Bianco, Lorenzo, Alessio Antropoli, Christel Condroyer, et al.. (2024). RDH5 and RLBP1-Associated Inherited Retinal Diseases: Refining the Spectrum of Stationary and Progressive Phenotypes. American Journal of Ophthalmology. 267. 160–171. 2 indexed citations

Dhaenens, Claire‐Marie, Isabelle Audo, A. Lecleire–Collet, et al.. (2024). The phenotypic spectrum of CEP250 gene variants. Ophthalmic Genetics. 46(4). 354–361. 1 indexed citations

Wohlschlegel, James A., et al.. (2023). CRISPR/Cas9 : de la recherche à l’application thérapeutique. Journal Français d Ophtalmologie. 46(4). 398–407.

Authié, Colas, et al.. (2023). Development and Validation of a Novel Mobility Test for Rod-Cone Dystrophies: From Reality to Virtual Reality. American Journal of Ophthalmology. 258. 43–54. 7 indexed citations

Audo, Isabelle, Marco Nassisi, Christina Zeitz, & José‐Alain Sahel. (2023). The Extraordinary Phenotypic and Genetic Variability of Retinal and Macular Degenerations: The Relevance to Therapeutic Developments. Cold Spring Harbor Perspectives in Medicine. 14(6). a041652–a041652. 2 indexed citations

Strauß, Rupert W., Alexander Ho, Anamika Jha, et al.. (2023). Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 24-Month Period (ProgStar Report No. 17). American Journal of Ophthalmology. 250. 157–170. 9 indexed citations

Nassisi, Marco, Christel Condroyer, Aline Antonio, et al.. (2022). Large Benefit from Simple Things: High-Dose Vitamin A Improves RBP4-Related Retinal Dystrophy. International Journal of Molecular Sciences. 23(12). 6590–6590. 6 indexed citations

Nanteau, Céline, Angélique Terray, Yvrick Zagar, et al.. (2022). Modeling PRPF31 retinitis pigmentosa using retinal pigment epithelium and organoids combined with gene augmentation rescue. npj Regenerative Medicine. 7(1). 39–39. 31 indexed citations

10.

Callebert, Jacques, Robert M. Duvoisin, Christelle Michiels, et al.. (2022). Mice Lacking Gpr179 with Complete Congenital Stationary Night Blindness Are a Good Model for Myopia. International Journal of Molecular Sciences. 24(1). 219–219. 7 indexed citations

11.

Kong, Xiangrong, Millena Bittencourt, Rupert W. Strauß, et al.. (2021). Longitudinal Changes in Scotopic and Mesopic Macular Function as Assessed with Microperimetry in Patients With Stargardt Disease: SMART Study Report No. 2. American Journal of Ophthalmology. 236. 32–44. 6 indexed citations

12.

Muller, Jean, Christina Zeitz, Carolin D. Obermaier, et al.. (2021). Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal Dystrophy. International Journal of Molecular Sciences. 22(12). 6410–6410. 10 indexed citations

13.

Kay, Christine N., Nicola Williamson, Rob Arbuckle, et al.. (2021). Qualitative interviews with patients and caregivers regarding visual function impairments and impacts on vision-dependent activities of daily living and health-related quality of life in RPE65-related Retinitis Pigmentosa and Leber Congenital Amaurosis. Investigative Ophthalmology & Visual Science. 62(8). 3589–3589. 6 indexed citations

14.

Tavares, Erika, Shriya Deshmukh, Isabelle Audo, et al.. (2020). Phenotype Driven Analysis of Whole Genome Sequencing Identifies Deep Intronic Variants that Cause Retinal Dystrophies by Aberrant Exonization. Investigative Ophthalmology & Visual Science. 61(10). 36–36. 16 indexed citations

15.

Joumaa, Wissam H., George Cherfan, Kazem Zibara, et al.. (2019). Next Generation Sequencing Identifies Five Novel Mutations in Lebanese Patients with Bardet–Biedl and Usher Syndromes. Genes. 10(12). 1047–1047. 7 indexed citations

16.

Štingl, Katarína, Anne Kurtenbach, Christoph Kernstock, et al.. (2019). Full-field electroretinography, visual acuity and visual fields in Usher syndrome: a multicentre European study. Documenta Ophthalmologica. 139(2). 151–160. 8 indexed citations

17.

Matet, Alexandre, Susanne Kohl, Britta Baumann, et al.. (2018). Multimodal imaging including semiquantitative short-wavelength and near-infrared autofluorescence in achromatopsia. Scientific Reports. 8(1). 5665–5665. 8 indexed citations

18.

Habeler, Walter, Olivier Goureau, Pierre de la Grange, et al.. (2013). Human Induced Pluripotent Stem Cells As a Tool to Model a Form of Leber Congenital Amaurosis. Cellular Reprogramming. 15(3). 233–246. 25 indexed citations

19.

Bujakowska, Kinga M., Isabelle Audo, Saddek Mohand‐Saïd, et al.. (2011). CRB1 mutations in inherited retinal dystrophies. Human Mutation. 33(2). 306–315. 149 indexed citations

20.

Audo, Isabelle, José‐Alain Sahel, Saddek Mohand‐Saïd, et al.. (2010). EYS is a major gene for rod-cone dystrophies in France. Human Mutation. 31(5). E1406–E1435. 84 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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