Elise Orhan

725 total citations
12 papers, 284 citations indexed

About

Elise Orhan is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Ophthalmology. According to data from OpenAlex, Elise Orhan has authored 12 papers receiving a total of 284 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 5 papers in Ophthalmology. Recurrent topics in Elise Orhan's work include Retinal Development and Disorders (9 papers), Photoreceptor and optogenetics research (6 papers) and Retinal Diseases and Treatments (5 papers). Elise Orhan is often cited by papers focused on Retinal Development and Disorders (9 papers), Photoreceptor and optogenetics research (6 papers) and Retinal Diseases and Treatments (5 papers). Elise Orhan collaborates with scholars based in United Kingdom, France and United States. Elise Orhan's co-authors include Christina Zeitz, Isabelle Audo, José‐Alain Sahel, Christelle Michiels, Marion Neuillé, Aline Antonio, Saïd El Shamieh, Jane P. Hughes, Marie‐Elise Lancelot and Thierry Léveillard and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Elise Orhan

12 papers receiving 279 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elise Orhan United Kingdom 8 244 122 117 36 29 12 284
Marina França Dias Brazil 3 290 1.2× 125 1.0× 77 0.7× 34 0.9× 51 1.8× 6 337
Cécile Méjécase United Kingdom 11 247 1.0× 140 1.1× 47 0.4× 46 1.3× 72 2.5× 24 299
Bhubanananda Sahu United States 13 276 1.1× 122 1.0× 60 0.5× 36 1.0× 40 1.4× 21 344
Rasa Valiauga United States 5 277 1.1× 46 0.4× 112 1.0× 29 0.8× 31 1.1× 6 329
Barrett Leehy United States 8 145 0.6× 102 0.8× 30 0.3× 34 0.9× 23 0.8× 10 214
Neringa Jurkutė United Kingdom 11 362 1.5× 159 1.3× 37 0.3× 43 1.2× 57 2.0× 23 400
S. J. Bowne United States 3 436 1.8× 209 1.7× 121 1.0× 54 1.5× 57 2.0× 4 466
L.S. Sullivan United States 3 431 1.8× 210 1.7× 120 1.0× 56 1.6× 59 2.0× 6 463
P. O'Rourke United States 2 243 1.0× 127 1.0× 116 1.0× 105 2.9× 35 1.2× 4 314
Regine Mühlfriedel Germany 12 393 1.6× 215 1.8× 150 1.3× 73 2.0× 52 1.8× 24 468

Countries citing papers authored by Elise Orhan

Since Specialization
Citations

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

Fields of papers citing papers by Elise Orhan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elise Orhan

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

All Works

12 of 12 papers shown
1.
McClements, Michelle E., Alun R. Barnard, Elise Orhan, et al.. (2021). Functional expression of complement factor I following AAV-mediated gene delivery in the retina of mice and human cells. Gene Therapy. 28(5). 265–276. 41 indexed citations
2.
Orhan, Elise, Marion Neuillé, Miguel Dias, et al.. (2021). A New Mouse Model for Complete Congenital Stationary Night Blindness Due to Gpr179 Deficiency. International Journal of Molecular Sciences. 22(9). 4424–4424. 5 indexed citations
3.
Ellis, Scott, et al.. (2020). GT005, a gene therapy for the treatment of dry age-related macular degeneration (AMD). Investigative Ophthalmology & Visual Science. 61(7). 2295–2295. 19 indexed citations
4.
Orhan, Elise, Deniz Dalkara, Marion Neuillé, et al.. (2015). Genotypic and Phenotypic Characterization of P23H Line 1 Rat Model. PLoS ONE. 10(5). e0127319–e0127319. 41 indexed citations
5.
Orhan, Elise, Deniz Dalkara, Christophe Lechauve, et al.. (2015). Genotypic and Phenotypic Characterization of the P23H Line 1 Rat Model. 56(7). 5391–5391. 1 indexed citations
6.
Neuillé, Marion, Catherine W. Morgans, Elise Orhan, et al.. (2015). LRIT3 is essential to localize TRPM1 to the dendritic tips of ON-bipolar cells and may play a role in cone synapse formation. 56(7). 2612–2612. 1 indexed citations
7.
Neuillé, Marion, Catherine W. Morgans, Yan Cao, et al.. (2015). LRIT3 is essential to localize TRPM1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation. European Journal of Neuroscience. 42(3). 1966–1975. 42 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.
Neuillé, Marion, Saïd El Shamieh, Elise Orhan, et al.. (2014). Lrit3 Deficient Mouse (nob6): A Novel Model of Complete Congenital Stationary Night Blindness (cCSNB). PLoS ONE. 9(3). e90342–e90342. 45 indexed citations
10.
Zeitz, Christina, Samuel G. Jacobson, Christian Hamel, et al.. (2013). Whole exome sequencing identifies mutations in LRIT3 as a cause for autosomal recessive complete congenital stationary night blindness. Investigative Ophthalmology & Visual Science. 54(15). 3350–3350. 2 indexed citations
11.
Orhan, Elise, Laurent Prézeau, Saïd El Shamieh, et al.. (2013). Further Insights Into GPR179: Expression, Localization, and Associated Pathogenic Mechanisms Leading to Complete Congenital Stationary Night Blindness. Investigative Ophthalmology & Visual Science. 54(13). 8041–8041. 17 indexed citations
12.
Audo, Isabelle, Saddek Mohand‐Saïd, Claire‐Marie Dhaenens, et al.. (2011). RP1 and autosomal dominant rod-cone dystrophy: Novel mutations, a review of published variants, and genotype-phenotype correlation. Human Mutation. 33(1). 73–80. 31 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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