Alejandro Garanto

3.2k total citations
62 papers, 1.7k citations indexed

About

Alejandro Garanto is a scholar working on Molecular Biology, Ophthalmology and Cell Biology. According to data from OpenAlex, Alejandro Garanto has authored 62 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Molecular Biology, 16 papers in Ophthalmology and 9 papers in Cell Biology. Recurrent topics in Alejandro Garanto's work include Retinal Development and Disorders (40 papers), CRISPR and Genetic Engineering (22 papers) and Retinal Diseases and Treatments (16 papers). Alejandro Garanto is often cited by papers focused on Retinal Development and Disorders (40 papers), CRISPR and Genetic Engineering (22 papers) and Retinal Diseases and Treatments (16 papers). Alejandro Garanto collaborates with scholars based in Netherlands, United States and Spain. Alejandro Garanto's co-authors include Rob W.J. Collin, Frans P.M. Cremers, Lonneke Duijkers, Gemma Marfany, Sílvia Albert, Riccardo Sangermano, Roser Gonzàlez‐Duarte, Mubeen Khan, Nathalie M. Bax and Carel B. Hoyng and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Scientific Reports.

In The Last Decade

Alejandro Garanto

60 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alejandro Garanto Netherlands	24	1.5k	453	241	214	178	62	1.7k
Nicole Weisschuh Germany	27	1.3k 0.9×	964 2.1×	377 1.6×	124 0.6×	251 1.4×	73	1.8k
Christian Hamel France	20	1.2k 0.8×	323 0.7×	265 1.1×	158 0.7×	203 1.1×	39	1.5k
Panagiotis I. Sergouniotis United Kingdom	30	1.8k 1.2×	1.1k 2.5×	579 2.4×	279 1.3×	273 1.5×	83	2.3k
Andrew F.X. Goldberg United States	24	1.4k 0.9×	373 0.8×	213 0.9×	378 1.8×	548 3.1×	41	1.7k
Rinki Ratnapriya United States	24	890 0.6×	748 1.7×	243 1.0×	171 0.8×	86 0.5×	46	1.5k
Marcia Lloyd United States	15	987 0.6×	620 1.4×	66 0.3×	182 0.9×	154 0.9×	18	1.2k
C.F. Inglehearn United Kingdom	19	1.2k 0.8×	410 0.9×	167 0.7×	363 1.7×	216 1.2×	34	1.3k
Alexander B. Quiambao United States	16	924 0.6×	338 0.7×	125 0.5×	282 1.3×	117 0.7×	26	1.1k
Sassan M. Azarian United States	10	1.1k 0.7×	575 1.3×	102 0.4×	237 1.1×	206 1.2×	16	1.3k
Minghao Jin United States	20	1.0k 0.7×	475 1.0×	60 0.2×	244 1.1×	189 1.1×	37	1.3k

Countries citing papers authored by Alejandro Garanto

Since Specialization

Citations

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

Fields of papers citing papers by Alejandro Garanto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alejandro Garanto

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

Karjosukarso, Dyah W., Lonneke Duijkers, Sander Bervoets, et al.. (2025). Preclinical assessment of splicing modulation therapy for ABCA4 variant c.768G>T in Stargardt disease. Communications Medicine. 5(1). 25–25. 2 indexed citations

Engelke, Udo F. H., Astrid Oudakker, Dirk J. Lefeber, et al.. (2025). Targeting AASS alleviates neurotoxicity and improves mitochondrial function in astrocyte models for pyridoxine-dependent epilepsy. Molecular Therapy — Nucleic Acids. 36(4). 102728–102728.

Anido, Alejandro Allo, et al.. (2024). Efficacy, biodistribution and safety comparison of chemically modified antisense oligonucleotides in the retina. Nucleic Acids Research. 52(17). 10447–10463. 5 indexed citations

Karjosukarso, Dyah W., Lonneke Duijkers, Frans P.M. Cremers, et al.. (2024). Preclinical Development of Antisense Oligonucleotides to Rescue Aberrant Splicing Caused by an Ultrarare ABCA4 Variant in a Child with Early-Onset Stargardt Disease. Cells. 13(7). 601–601. 3 indexed citations

Karnebeek, Clara D.M. van, et al.. (2024). Generation of hiPSC lines from four pyridoxine-dependent epilepsy (PDE) patients carrying the variant c.1279G>C in ALDH7A1 in homozygosis. Stem Cell Research. 79. 103480–103480. 2 indexed citations

Garanto, Alejandro, et al.. (2024). Antisense Oligonucleotide-Based Rescue of Complex Intronic Splicing Defects in ABCA4. Nucleic Acid Therapeutics. 34(3). 125–133. 1 indexed citations

Schröter, Julian, et al.. (2023). Exploring genotype–phenotype correlations in glutaric aciduria type 1. Journal of Inherited Metabolic Disease. 46(3). 371–390. 8 indexed citations

Mercey, Olivier, Katrin Junger, Alejandro Garanto, et al.. (2023). Gene augmentation of LCA5-associated Leber congenital amaurosis ameliorates bulge region defects of the photoreceptor ciliary axoneme. JCI Insight. 8(10). 13 indexed citations

Conte, Federica, Angel Ashikov, Monique van Scherpenzeel, et al.. (2023). In Vitro Skeletal Muscle Model of PGM1 Deficiency Reveals Altered Energy Homeostasis. International Journal of Molecular Sciences. 24(9). 8247–8247. 6 indexed citations

10.

Albert, Sílvia, Nathalie M. Bax, Carel B. Hoyng, et al.. (2023). Generation of an iPSC line (RMCGENi020-A) from a patient with Stargardt disease harboring the recurrent intronic ABCA4 variant c.4253+43G>A. Stem Cell Research. 73. 103252–103252.

11.

Garanto, Alejandro, Geert‐Jan van Gemert, Alfredo Cabrera‐Orefice, et al.. (2023). Comparative Clustering (CompaCt) of eukaryote complexomes identifies novel interactions and sheds light on protein complex evolution. PLoS Computational Biology. 19(8). e1011090–e1011090. 1 indexed citations

12.

Duijkers, Lonneke, Michael Kwint, Hester Y. Kroes, et al.. (2022). The Predicted Splicing Variant c.11+5G>A in RPE65 Leads to a Reduction in mRNA Expression in a Cell-Specific Manner. Cells. 11(22). 3640–3640. 8 indexed citations

13.

Aartsma‐Rus, Annemieke, Alejandro Garanto, Willeke van Roon‐Mom, et al.. (2022). Consensus Guidelines for the Design and In Vitro Preclinical Efficacy Testing N-of-1 Exon Skipping Antisense Oligonucleotides. Nucleic Acid Therapeutics. 33(1). 17–25. 35 indexed citations

14.

Corral-Serrano, Julio C., et al.. (2021). A look into retinal organoids: methods, analytical techniques, and applications. Cellular and Molecular Life Sciences. 78(19-20). 6505–6532. 63 indexed citations

15.

Khan, Mubeen, Stéphanie S. Cornelis, Riccardo Sangermano, et al.. (2020). In or Out? New Insights on Exon Recognition through Splice-Site Interdependency. International Journal of Molecular Sciences. 21(7). 2300–2300. 9 indexed citations

16.

Abril, Josep F., Sokol V. Todi, Naheed W. Khan, et al.. (2020). The Deubiquitinating Enzyme Ataxin-3 Regulates Ciliogenesis and Phagocytosis in the Retina. Cell Reports. 33(6). 108360–108360. 21 indexed citations

17.

Garanto, Alejandro, et al.. (2019). Molecular Therapies for Inherited Retinal Diseases—Current Standing, Opportunities and Challenges. Genes. 10(9). 654–654. 62 indexed citations

18.

Haas, Ria de, Devashish Das, Alejandro Garanto, et al.. (2017). Therapeutic effects of the mitochondrial ROS-redox modulator KH176 in a mammalian model of Leigh Disease. Scientific Reports. 7(1). 11733–11733. 34 indexed citations

19.

Ávila‐Fernández, Almudena, Raquel Pérez-Carro, Marta Cortón, et al.. (2015). Whole-exome sequencing reveals ZNF408 as a new gene associated with autosomal recessive retinitis pigmentosa with vitreal alterations. Human Molecular Genetics. 24(14). 4037–4048. 37 indexed citations

20.

Garanto, Alejandro, et al.. (2012). Targeted knockdown of Cerkl, a retinal dystrophy gene, causes mild affectation of the retinal ganglion cell layer. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822(8). 1258–1269. 26 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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