Angélique Terray

849 total citations
9 papers, 596 citations indexed

About

Angélique Terray is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Ophthalmology. According to data from OpenAlex, Angélique Terray has authored 9 papers receiving a total of 596 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 3 papers in Cellular and Molecular Neuroscience and 2 papers in Ophthalmology. Recurrent topics in Angélique Terray's work include Retinal Development and Disorders (8 papers), CRISPR and Genetic Engineering (4 papers) and Photoreceptor and optogenetics research (3 papers). Angélique Terray is often cited by papers focused on Retinal Development and Disorders (8 papers), CRISPR and Genetic Engineering (4 papers) and Photoreceptor and optogenetics research (3 papers). Angélique Terray collaborates with scholars based in France, United States and United Kingdom. Angélique Terray's co-authors include Olivier Goureau, José‐Alain Sahel, Céline Nanteau, Sacha Reichman, Gaël Orieux, Amélie Slembrouck, Emeline F. Nandrot, Christelle Monville, Walter Habeler and Anaïs Potey and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Development and The American Journal of Human Genetics.

In The Last Decade

Angélique Terray

9 papers receiving 593 citations

Peers

Angélique Terray
Julien Maruotti United States
Cassidy Hinman United States
Koray Dogan Kaya United States
R. L. Shearer United States
Milan Fernando United Kingdom
Julien Maruotti United States
Angélique Terray
Citations per year, relative to Angélique Terray Angélique Terray (= 1×) peers Julien Maruotti

Countries citing papers authored by Angélique Terray

Since Specialization
Citations

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

Fields of papers citing papers by Angélique Terray

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Angélique Terray

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

All Works

9 of 9 papers shown
1.
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
2.
Gribaudo, Simona, Nour Nicolas, Margot Jarrige, et al.. (2021). Dynamic extrinsic pacing of the HOX clock in human axial progenitors controls motor neuron subtype specification. Development. 148(6). 40 indexed citations
3.
Terray, Angélique, Amélie Slembrouck, Céline Nanteau, et al.. (2017). Generation of an induced pluripotent stem cell (iPSC) line from a patient with autosomal dominant retinitis pigmentosa due to a mutation in the NR2E3 gene. Stem Cell Research. 24. 1–4. 5 indexed citations
4.
Terray, Angélique, Amélie Slembrouck, Céline Nanteau, et al.. (2017). Establishment of an induced pluripotent stem (iPS) cell line from dermal fibroblasts of an asymptomatic patient with dominant PRPF31 mutation. Stem Cell Research. 25. 26–29. 7 indexed citations
5.
Reichman, Sacha, Amélie Slembrouck, Giuliana Gagliardi, et al.. (2017). Generation of Storable Retinal Organoids and Retinal Pigmented Epithelium from Adherent Human iPS Cells in Xeno-Free and Feeder-Free Conditions. Stem Cells. 35(5). 1176–1188. 162 indexed citations
6.
M’Barek, Karim Ben, Walter Habeler, Mohamed Jarraya, et al.. (2017). Human ESC–derived retinal epithelial cell sheets potentiate rescue of photoreceptor cell loss in rats with retinal degeneration. Science Translational Medicine. 9(421). 90 indexed citations
7.
Shamieh, Saïd El, Cécile Méjécase, Matteo Bertelli, et al.. (2017). Further Insights into the Ciliary Gene and Protein KIZ and Its Murine Ortholog PLK1S1 Mutated in Rod-Cone Dystrophy. Genes. 8(10). 277–277. 5 indexed citations
8.
Shamieh, Saïd El, Marion Neuillé, Angélique Terray, et al.. (2014). Whole-Exome Sequencing Identifies KIZ as a Ciliary Gene Associated with Autosomal-Recessive Rod-Cone Dystrophy. The American Journal of Human Genetics. 94(4). 625–633. 39 indexed citations
9.
Reichman, Sacha, Angélique Terray, Amélie Slembrouck, et al.. (2014). From confluent human iPS cells to self-forming neural retina and retinal pigmented epithelium. Proceedings of the National Academy of Sciences. 111(23). 8518–8523. 217 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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