Christel Condroyer

4.4k total citations
49 papers, 1.1k citations indexed

About

Christel Condroyer is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Christel Condroyer has authored 49 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 28 papers in Ophthalmology and 11 papers in Cellular and Molecular Neuroscience. Recurrent topics in Christel Condroyer's work include Retinal Development and Disorders (35 papers), Retinal Diseases and Treatments (26 papers) and Photoreceptor and optogenetics research (10 papers). Christel Condroyer is often cited by papers focused on Retinal Development and Disorders (35 papers), Retinal Diseases and Treatments (26 papers) and Photoreceptor and optogenetics research (10 papers). Christel Condroyer collaborates with scholars based in France, United States and United Kingdom. Christel Condroyer's co-authors include Christina Zeitz, Alexis Brice, Isabelle Audo, Suzanne Lesage, José‐Alain Sahel, Aline Antonio, Alexandra Dürr, Saddek Mohand‐Saïd, Pierre Pollak and François Viallet and has published in prestigious journals such as PLoS ONE, Brain and Neurology.

In The Last Decade

Christel Condroyer

47 papers receiving 1.1k citations

Peers

Christel Condroyer

NEURO

OPHTH

CMN

PHYSI

Gaoying Ren United States

Frédéric Lebrun-Julien Switzerland

Sandrine Joly Canada

Christina S. Winborn United States

Mercedes Salvador‐Silva United States

Ericka Oglesby United States

Haoliang Huang United States

R. J. Colello United Kingdom

Henri Leinonen United States

Abigail T. Fahim United States

Gaoying Ren United States

Christel Condroyer

449 ×0.7

176 ×0.5

NEURO

213 ×0.7

OPHTH

312 ×1.3

CMN

54 ×0.2

PHYSI

Citations per year, relative to Christel Condroyer Christel Condroyer (= 1×) peers Gaoying Ren

Countries citing papers authored by Christel Condroyer

Since Specialization

Citations

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

Fields of papers citing papers by Christel Condroyer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christel Condroyer

This figure shows the co-authorship network connecting the top 25 collaborators of Christel Condroyer. A scholar is included among the top collaborators of Christel Condroyer 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 Christel Condroyer. Christel Condroyer 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

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

Antropoli, Alessio, Lorenzo Bianco, Christel Condroyer, et al.. (2024). Extensive Macular Atrophy with Pseudodrusen-like appearance. Ophthalmology. 131(10). 1175–1184. 10 indexed citations

Sangermano, Riccardo, Priya Gupta, C W Price, et al.. (2024). Coding and non-coding variants in the ciliopathy gene CFAP410 cause early-onset non-syndromic retinal degeneration. npj Genomic Medicine. 9(1). 58–58. 1 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

Cordonnier, Monique, et al.. (2021). Congenital stationary night blindness in a patient with mild learning disability due to a compound heterozygous microdeletion of 15q13 and a missense mutation in TRPM1. Ophthalmic Genetics. 42(3). 296–299. 1 indexed citations

Argentini, Manuela, Christelle Michiels, Valérie Forster, et al.. (2021). First identification of ITM2B interactome in the human retina. Scientific Reports. 11(1). 17210–17210. 4 indexed citations

Nassisi, Marco, Carlo Lavia, Saddek Mohand‐Saïd, et al.. (2021). Near-infrared fundus autofluorescence alterations correlate with swept-source optical coherence tomography angiography findings in patients with retinitis pigmentosa. Scientific Reports. 11(1). 3180–3180. 9 indexed citations

Zeitz, Christina, Marco Nassisi, Camille Andrieu, et al.. (2021). CHM mutation spectrum and disease: An update at the time of human therapeutic trials. Human Mutation. 42(4). 323–341. 10 indexed citations

Mohand‐Saïd, Saddek, Sarah Mrejen, Aline Antonio, et al.. (2019). Outer Retinal Alterations Associated With Visual Outcomes in Best Vitelliform Macular Dystrophy. American Journal of Ophthalmology. 208. 429–437. 12 indexed citations

10.

Lassot, Irina, Suzanne Lesage, Barbara A. Zieba, et al.. (2018). The E3 Ubiquitin Ligases TRIM17 and TRIM41 Modulate α-Synuclein Expression by Regulating ZSCAN21. Cell Reports. 25(9). 2484–2496.e9. 30 indexed citations

11.

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

12.

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

13.

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

14.

Lesage, Suzanne, José Brás, Florence Cormier‐Dequaire, et al.. (2015). Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease. Neurology Genetics. 1(1). e9–e9. 70 indexed citations

15.

Boulanger-Scemama, Élise, Saïd El Shamieh, Vanessa Démontant, et al.. (2015). Next-generation sequencing applied to a large French cone and cone-rod dystrophy cohort: mutation spectrum and new genotype-phenotype correlation. Orphanet Journal of Rare Diseases. 10(1). 85–85. 75 indexed citations

16.

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

17.

Lesage, Suzanne, Isabelle Le Ber, Christel Condroyer, et al.. (2013). C9orf72 repeat expansions are a rare genetic cause of parkinsonism. Brain. 136(2). 385–391. 119 indexed citations

18.

Anheim, Mathieu, Alexis Elbaz, Suzanne Lesage, et al.. (2012). Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers. Neurology. 78(6). 417–420. 183 indexed citations

19.

Lesage, Suzanne, Christel Condroyer, André R. Troiano, et al.. (2009). Follow-up study of the GIGYF2 gene in French families with Parkinson's disease. Neurobiology of Aging. 31(6). 1069–1071. 8 indexed citations

20.

Çetinkaya, Caroline Pirkevi, Suzanne Lesage, Christel Condroyer, et al.. (2009). A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype. Neurogenetics. 10(3). 271–273. 13 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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