Cécile Méjécase

498 total citations
24 papers, 299 citations indexed

About

Cécile Méjécase is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Cécile Méjécase has authored 24 papers receiving a total of 299 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 9 papers in Ophthalmology and 7 papers in Genetics. Recurrent topics in Cécile Méjécase's work include Retinal Development and Disorders (19 papers), Retinal Diseases and Treatments (9 papers) and Photoreceptor and optogenetics research (5 papers). Cécile Méjécase is often cited by papers focused on Retinal Development and Disorders (19 papers), Retinal Diseases and Treatments (9 papers) and Photoreceptor and optogenetics research (5 papers). Cécile Méjécase collaborates with scholars based in United Kingdom, France and United States. Cécile Méjécase's co-authors include Mariya Moosajee, Isabelle Audo, Christina Zeitz, José‐Alain Sahel, Christel Condroyer, Saddek Mohand‐Saïd, Aline Antonio, Saïd El Shamieh, Marco Nassisi and Fiona Boyard and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Cécile Méjécase

21 papers receiving 295 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cécile Méjécase United Kingdom 11 247 140 72 47 46 24 299
Neringa Jurkutė United Kingdom 11 362 1.5× 159 1.1× 57 0.8× 37 0.8× 43 0.9× 23 400
Muhammad Asif Naeem Pakistan 12 271 1.1× 152 1.1× 76 1.1× 41 0.9× 35 0.8× 30 325
María Isabel López-Molina Spain 12 287 1.2× 130 0.9× 70 1.0× 45 1.0× 21 0.5× 18 351
Galuh Astuti Netherlands 12 340 1.4× 142 1.0× 106 1.5× 56 1.2× 42 0.9× 23 423
Aurore Germain France 5 317 1.3× 193 1.4× 68 0.9× 38 0.8× 56 1.2× 5 372
Adrian Dockery Ireland 9 248 1.0× 101 0.7× 115 1.6× 17 0.4× 37 0.8× 19 302
Jeremy M. Hoffmann United States 7 356 1.4× 134 1.0× 84 1.2× 71 1.5× 68 1.5× 10 409
Dikla Bandah‐Rozenfeld Israel 8 372 1.5× 194 1.4× 99 1.4× 64 1.4× 46 1.0× 10 401
Aaron Black United States 5 209 0.8× 107 0.8× 83 1.2× 32 0.7× 37 0.8× 10 264
Frans P.M. Cremers Netherlands 9 375 1.5× 190 1.4× 78 1.1× 31 0.7× 39 0.8× 13 428

Countries citing papers authored by Cécile Méjécase

Since Specialization
Citations

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

Fields of papers citing papers by Cécile Méjécase

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cécile Méjécase

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

All Works

20 of 20 papers shown
1.
Méjécase, Cécile, et al.. (2025). Dominant RDH12-retinitis pigmentosa impairs photoreceptor development and implicates cone involvement in retinal organoids. Frontiers in Cell and Developmental Biology. 13. 1511066–1511066.
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Méjécase, Cécile, et al.. (2021). Ocular Phenotype Associated with DYRK1A Variants. Genes. 12(2). 234–234. 7 indexed citations
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Nassisi, Marco, Cécile Méjécase, Saïd El Shamieh, et al.. (2021). Retinal Phenotype of Patients With Isolated Retinal Degeneration Due toCLN3Pathogenic Variants in a French Retinitis Pigmentosa Cohort. JAMA Ophthalmology. 139(3). 278–278. 22 indexed citations
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Méjécase, Cécile, et al.. (2020). The genetic landscape of inherited eye disorders in 74 consecutive families from the United Arab Emirates. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(3). 762–772. 12 indexed citations
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Méjécase, Cécile, et al.. (2020). Generation of two human control iPS cell lines (UCLi016-A and UCLi017-A) from healthy donors with no known ocular conditions. Stem Cell Research. 49. 102113–102113. 6 indexed citations
10.
Méjécase, Cécile, et al.. (2020). Practical guide to genetic screening for inherited eye diseases. SHILAP Revista de lepidopterología. 12. 4197780448–4197780448. 32 indexed citations
11.
Liu, Bingqian, Cécile Méjécase, Christel Condroyer, et al.. (2019). Generation of human induced pluripotent stem cell lines from a patient with ITM2B-related retinal dystrophy and a non mutated brother. Stem Cell Research. 41. 101625–101625. 3 indexed citations
12.
Nassisi, Marco, Saddek Mohand‐Saïd, Camille Andrieu, et al.. (2019). Prevalence of ABCA4 Deep-Intronic Variants and Related Phenotype in An Unsolved “One-Hit” Cohort with Stargardt Disease. International Journal of Molecular Sciences. 20(20). 5053–5053. 24 indexed citations
13.
Khateb, Samer, Marco Nassisi, Kinga M. Bujakowska, et al.. (2019). Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations inPDE6AandPDE6B. JAMA Ophthalmology. 137(6). 669–669. 25 indexed citations
14.
Nassisi, Marco, Saddek Mohand‐Saïd, Camille Andrieu, et al.. (2019). Peripapillary Sparing With Near Infrared Autofluorescence Correlates With Electroretinographic Findings in Patients With Stargardt Disease. Investigative Ophthalmology & Visual Science. 60(15). 4951–4951. 8 indexed citations
15.
Audo, Isabelle, Saddek Mohand‐Saïd, Élise Boulanger-Scemama, et al.. (2018). MERTK mutation update in inherited retinal diseases. Human Mutation. 39(7). 887–913. 44 indexed citations
16.
Zeitz, Christina, et al.. (2018). A Novel Heterozygous Missense Mutation inGNAT1Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night Blindness. BioMed Research International. 2018. 1–10. 8 indexed citations
17.
Nassisi, Marco, Saddek Mohand‐Saïd, Claire‐Marie Dhaenens, et al.. (2018). Expanding the Mutation Spectrum in ABCA4: Sixty Novel Disease Causing Variants and Their Associated Phenotype in a Large French Stargardt Cohort. International Journal of Molecular Sciences. 19(8). 2196–2196. 24 indexed citations
18.
Méjécase, Cécile, Aurélie Hummel, Saddek Mohand‐Saïd, et al.. (2018). Whole exome sequencing resolves complex phenotype and identifies CC2D2A mutations underlying non‐syndromic rod‐cone dystrophy. Clinical Genetics. 95(2). 329–333. 18 indexed citations
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Méjécase, Cécile, Saddek Mohand‐Saïd, Aurélie Hummel, et al.. (2017). CC2D2A mutations lead to variable phenotypes in a family with retinal dystrophy. Investigative Ophthalmology & Visual Science. 58(8). 573–573. 2 indexed citations
20.
Méjécase, Cécile, Claudine Mayer, Olivier Poch, et al.. (2016). Identification of a Novel Homozygous Nonsense Mutation Confirms the Implication of GNAT1 in Rod-Cone Dystrophy. PLoS ONE. 11(12). e0168271–e0168271. 17 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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