Marta Cortón

5.0k total citations
92 papers, 2.3k citations indexed

About

Marta Cortón is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Marta Cortón has authored 92 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Molecular Biology, 34 papers in Ophthalmology and 32 papers in Genetics. Recurrent topics in Marta Cortón's work include Retinal Development and Disorders (43 papers), Retinal Diseases and Treatments (24 papers) and Ocular Disorders and Treatments (17 papers). Marta Cortón is often cited by papers focused on Retinal Development and Disorders (43 papers), Retinal Diseases and Treatments (24 papers) and Ocular Disorders and Treatments (17 papers). Marta Cortón collaborates with scholars based in Spain, United States and United Kingdom. Marta Cortón's co-authors include Carmen Ayuso, Almudena Ávila‐Fernández, Fiona Blanco‐Kelly, Belén Peral, Héctor F. Escobar‐Morreale, Rosa Riveiro-Álvarez, José L. San Millán, Gemma Villuendas, Blanca Garcı́a-Sandoval and José I. Botella‐Carretero and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Scientific Reports.

In The Last Decade

Marta Cortón

89 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marta Cortón Spain	28	1.6k	615	494	308	233	92	2.3k
Rauf Latif United States	33	1.2k 0.7×	86 0.1×	511 1.0×	137 0.4×	49 0.2×	84	3.1k
Ritu Malhotra United States	10	981 0.6×	195 0.3×	106 0.2×	66 0.2×	80 0.3×	19	1.4k
Nitin Udar United States	25	1.1k 0.7×	526 0.9×	235 0.5×	22 0.1×	190 0.8×	58	1.8k
A Churchill United Kingdom	23	1.0k 0.6×	674 1.1×	263 0.5×	24 0.1×	54 0.2×	53	1.8k
Tarja Lamminen Finland	19	821 0.5×	183 0.3×	184 0.4×	145 0.5×	87 0.4×	35	1.3k
Sigrid Swagemakers Netherlands	26	1.9k 1.2×	102 0.2×	299 0.6×	33 0.1×	107 0.5×	61	2.6k
Koichiro Higasa Japan	20	794 0.5×	120 0.2×	229 0.5×	102 0.3×	37 0.2×	72	1.4k
Mais Hashem Saudi Arabia	23	1.1k 0.7×	192 0.3×	544 1.1×	18 0.1×	58 0.2×	51	1.8k
Michael P. Fautsch United States	32	1.3k 0.8×	2.3k 3.7×	185 0.4×	26 0.1×	334 1.4×	122	3.5k
Louise Ocaka United Kingdom	19	729 0.5×	357 0.6×	420 0.9×	24 0.1×	58 0.2×	30	1.2k

Countries citing papers authored by Marta Cortón

Since Specialization

Citations

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

Fields of papers citing papers by Marta Cortón

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marta Cortón

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

Cortón, Marta, Erika Maka, Achim Langenbucher, et al.. (2024). Examination of the Corneal Endothelium in Patients With Congenital Aniridia With a PAX6 Mutation Using In Vivo Confocal Laser Scanning Microscopy. Cornea. 44(3). 324–331. 1 indexed citations

Cortón, Marta, et al.. (2023). VIsoQLR: an interactive tool for the detection, quantification and fine-tuning of isoforms in selected genes using long-read sequencing. Human Genetics. 142(4). 495–506. 1 indexed citations

Ruiz, Carolina, Julie Plaisancié, Nicolas Chassaing, et al.. (2023). Minigene Splicing Assays and Long-Read Sequencing to Unravel Pathogenic Deep-Intronic Variants in PAX6 in Congenital Aniridia. International Journal of Molecular Sciences. 24(2). 1562–1562. 6 indexed citations

Kesim, Yeşim, Fabiola Ceroni, Fiona Blanco‐Kelly, et al.. (2023). Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1A3-related anophthalmia and microphthalmia. European Journal of Human Genetics. 31(10). 1175–1180. 2 indexed citations

Jubin, Claire, Marta Rodríguez de Alba, Cristina Villaverde, et al.. (2023). Long-read genome sequencing identifies cryptic structural variants in congenital aniridia cases. Human Genomics. 17(1). 45–45. 13 indexed citations

Arteche‐López, Ana, et al.. (2022). New Cerebellar Ataxia, Neuropathy, Vestibular Areflexia Syndrome cases are caused by the presence of a nonsense variant in compound heterozygosity with the pathogenic repeat expansion in the RFC1 gene. Clinical Genetics. 103(2). 236–241. 15 indexed citations

López‐Rodríguez, Rosario, Javier Ruiz‐Hornillos, Marta Cortón, et al.. (2022). Androgen receptor polyQ alleles and COVID‐19 severity in men: A replication study. Andrology. 11(1). 24–31. 3 indexed citations

Perea‐Romero, Irene, Lorena de la Fuente, Raquel Escutia Romero, et al.. (2022). Aggregated Genomic Data as Cohort-Specific Allelic Frequencies can Boost Variants and Genes Prioritization in Non-Solved Cases of Inherited Retinal Dystrophies. International Journal of Molecular Sciences. 23(15). 8431–8431. 3 indexed citations

Alba, Marta Rodríguez de, María José Trujillo-Tiebas, Cristina Villaverde, et al.. (2021). Fine Breakpoint Mapping by Genome Sequencing Reveals the First Large X Inversion Disrupting the NHS Gene in a Patient with Syndromic Cataracts. International Journal of Molecular Sciences. 22(23). 12713–12713. 7 indexed citations

10.

Perea‐Romero, Irene, Fiona Blanco‐Kelly, Iker Sánchez‐Navarro, et al.. (2021). NGS and phenotypic ontology-based approaches increase the diagnostic yield in syndromic retinal diseases. Human Genetics. 140(12). 1665–1678. 12 indexed citations

11.

Pozo‐Valero, Marta Del, Rosa Riveiro-Álvarez, Fiona Blanco‐Kelly, et al.. (2020). Genotype–Phenotype Correlations in a Spanish Cohort of 506 Families With Biallelic ABCA4 Pathogenic Variants. American Journal of Ophthalmology. 219. 195–204. 22 indexed citations

12.

Roman‐Rodriguez, Francisco J, Lara Álvarez, Begoña Díez, et al.. (2019). NHEJ-Mediated Repair of CRISPR-Cas9-Induced DNA Breaks Efficiently Corrects Mutations in HSPCs from Patients with Fanconi Anemia. Cell stem cell. 25(5). 607–621.e7. 69 indexed citations

13.

Plaisancié, Julie, Patrícia Locosque Ramos, Véronique Gaston, et al.. (2018). Implication of non-coding PAX6 mutations in aniridia. Human Genetics. 137(10). 831–846. 34 indexed citations

14.

Martín-Mérida, Inmaculada, Rocío Sánchez-Alcudia, Patrícia José, et al.. (2017). Analysis of the PRPF31 Gene in Spanish Autosomal Dominant Retinitis Pigmentosa Patients: A Novel Genomic Rearrangement. Investigative Ophthalmology & Visual Science. 58(2). 1045–1045. 20 indexed citations

15.

Cortón, Marta, Laura Campello, Mayka Sánchez, et al.. (2016). Identification of the Photoreceptor Transcriptional Co-Repressor SAMD11 as Novel Cause of Autosomal Recessive Retinitis Pigmentosa. Scientific Reports. 6(1). 35370–35370. 14 indexed citations

16.

Bocquet, Béatrice, Vincent Daïen, Almudena Ávila‐Fernández, et al.. (2015). Autosomal recessive retinitis pigmentosa withRP1mutations is associated with myopia. British Journal of Ophthalmology. 99(10). 1360–1365. 15 indexed citations

17.

Nikopoulos, Konstantinos, Almudena Ávila‐Fernández, Marta Cortón, et al.. (2015). Identification of two novel mutations in CDHR1 in consanguineous Spanish families with autosomal recessive retinal dystrophy. Scientific Reports. 5(1). 13902–13902. 23 indexed citations

18.

Ávila‐Fernández, Almudena, Marta Cortón, Koji M. Nishiguchi, et al.. (2012). Identification of an RP1 Prevalent Founder Mutation and Related Phenotype in Spanish Patients with Early-Onset Autosomal Recessive Retinitis. Ophthalmology. 119(12). 2616–2621. 41 indexed citations

19.

Acosta, Manuel Barreiro‐de, Ana Echarri, Daniel Carpio, et al.. (2011). A pharmacogenetics study of TPMT and ITPA genes detects a relationship with side effects and clinical response in patients with inflammatory bowel disease receiving Azathioprine.. PubMed. 20(3). 247–53. 37 indexed citations

20.

Cortón, Marta, José I. Botella‐Carretero, Juan Antonio López, et al.. (2007). Proteomic analysis of human omental adipose tissue in the polycystic ovary syndrome using two-dimensional difference gel electrophoresis and mass spectrometry. Human Reproduction. 23(3). 651–661. 96 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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