Aline Antonio

2.3k total citations
36 papers, 990 citations indexed

About

Aline Antonio is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Aline Antonio has authored 36 papers receiving a total of 990 indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 28 papers in Ophthalmology and 9 papers in Cellular and Molecular Neuroscience. Recurrent topics in Aline Antonio's work include Retinal Development and Disorders (34 papers), Retinal Diseases and Treatments (28 papers) and Photoreceptor and optogenetics research (9 papers). Aline Antonio is often cited by papers focused on Retinal Development and Disorders (34 papers), Retinal Diseases and Treatments (28 papers) and Photoreceptor and optogenetics research (9 papers). Aline Antonio collaborates with scholars based in France, United States and United Kingdom. Aline Antonio's co-authors include Isabelle Audo, José‐Alain Sahel, Christina Zeitz, Saddek Mohand‐Saïd, Marie‐Elise Lancelot, Shomi S. Bhattacharya, Christel Condroyer, Jean‐Paul Saraiva, Mélanie Letexier and Kinga M. Bujakowska and has published in prestigious journals such as PLoS ONE, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Aline Antonio

35 papers receiving 977 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Aline Antonio France	18	897	562	182	164	142	36	990
Louisa M. Affatigato United States	13	1.0k 1.1×	620 1.1×	247 1.4×	160 1.0×	194 1.4×	17	1.2k
Nathalie M. Bax Netherlands	17	851 0.9×	544 1.0×	121 0.7×	76 0.5×	135 1.0×	24	941
Blanca Garcı́a-Sandoval Spain	21	1.0k 1.2×	549 1.0×	169 0.9×	187 1.1×	158 1.1×	56	1.2k
Sten Kjellström United States	14	909 1.0×	416 0.7×	155 0.9×	248 1.5×	320 2.3×	23	1.0k
Corinne Leowski France	7	806 0.9×	500 0.9×	165 0.9×	182 1.1×	92 0.6×	7	858
Karin W. Littink Netherlands	12	669 0.7×	328 0.6×	146 0.8×	142 0.9×	89 0.6×	13	711
Jeaneen L. Andorf United States	11	942 1.1×	363 0.6×	129 0.7×	397 2.4×	105 0.7×	17	1.0k
Genevieve Wright United Kingdom	18	1.2k 1.4×	822 1.5×	214 1.2×	214 1.3×	215 1.5×	35	1.4k
Karina E Guziewicz United States	13	676 0.8×	354 0.6×	157 0.9×	147 0.9×	99 0.7×	26	762
Christian Hamel France	9	851 0.9×	461 0.8×	283 1.6×	123 0.8×	129 0.9×	14	972

Countries citing papers authored by Aline Antonio

Since Specialization

Citations

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

Fields of papers citing papers by Aline Antonio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aline Antonio

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

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

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

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

10.

Mohand‐Saïd, Saddek, Claire‐Marie Dhaenens, Aline Antonio, et al.. (2018). Phenotypic Characteristics of a French Cohort of Patients with X-Linked Retinoschisis. Ophthalmology. 125(10). 1587–1596. 22 indexed citations

11.

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

12.

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

13.

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

14.

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

15.

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

16.

Audo, Isabelle, Kinga M. Bujakowska, Thierry Léveillard, et al.. (2012). Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases. Orphanet Journal of Rare Diseases. 7(1). 8–8. 125 indexed citations

17.

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

18.

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

19.

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

20.

Audo, Isabelle, Kinga M. Bujakowska, Saddek Mohand‐Saïd, et al.. (2010). Prevalence and novelty of PRPF31 mutations in French autosomal dominant rod-cone dystrophy patients and a review of published reports. BMC Medical Genetics. 11(1). 145–145. 42 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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