Eduardo Silva

3.5k total citations
60 papers, 1.5k citations indexed

About

Eduardo Silva is a scholar working on Molecular Biology, Ophthalmology and Epidemiology. According to data from OpenAlex, Eduardo Silva has authored 60 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 21 papers in Ophthalmology and 8 papers in Epidemiology. Recurrent topics in Eduardo Silva's work include Retinal Development and Disorders (18 papers), Retinal Diseases and Treatments (15 papers) and Visual perception and processing mechanisms (7 papers). Eduardo Silva is often cited by papers focused on Retinal Development and Disorders (18 papers), Retinal Diseases and Treatments (15 papers) and Visual perception and processing mechanisms (7 papers). Eduardo Silva collaborates with scholars based in Portugal, United States and Chile. Eduardo Silva's co-authors include Miguel Castelo‐Branco, Irene H. Maumenee, Olof Sundin, Danping Zhu, Sharola Dharmaraj, Maria José Ribeiro, Gabriela Viteri, Yingying Li, Inês R. Violante and Aldina Reis and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Eduardo Silva

56 papers receiving 1.5k citations

Peers

Eduardo Silva

OPHTH

GENET

RNMI

CMN

Arnold Munnich France

Omar A. Mahroo United Kingdom

Zheng Qin Yin China

Christian P. Hamel France

Ulrike Orth Germany

Tobias Goldmann Germany

Leah C. Byrne United States

Pete Humphries Ireland

Chiara Criscuolo Italy

Takeshi Yoshitomi Japan

Arnold Munnich France

Eduardo Silva

1.6k ×1.8

237 ×0.5

OPHTH

580 ×2.2

GENET

88 ×0.4

RNMI

341 ×1.9

CMN

Citations per year, relative to Eduardo Silva Eduardo Silva (= 1×) peers Arnold Munnich

Countries citing papers authored by Eduardo Silva

Since Specialization

Citations

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

Fields of papers citing papers by Eduardo Silva

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eduardo Silva

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

Ferreira, Sónia, et al.. (2025). Long term adult visual plasticity after the developmental critical period in genetically determined peripheral visual loss. Heliyon. 11(4). e41970–e41970.

Nunes, Alexandra, Eduardo Silva, Onésia Cristina Oliveira‐Lima, et al.. (2024). GlyT1 inhibition promotes neuroprotection in the middle cerebral artery occlusion model through the activation of GluN2A-containing NMDAR. Experimental Neurology. 383. 115006–115006. 1 indexed citations

Silva, Eduardo, et al.. (2024). Vestibulo-ocular reflex dynamics with head-impulses discriminates Usher patients type 1 and 2. Scientific Reports. 14(1). 3701–3701. 2 indexed citations

Oliveiros, Bárbara, et al.. (2023). Myopia control: short-term effect of 0.01% atropine vs. defocus incorporated multiple segment lenses—a retrospective study in European children. International Ophthalmology. 43(10). 3777–3784. 3 indexed citations

Duarte, Ana Filipa, et al.. (2022). Horizontal Gaze Palsy and Progressive Scoliosis in Dizygotic Twins.. PubMed. 72(2). 105–110. 1 indexed citations

Veiga, Paula, et al.. (2021). Prediction and cost-effectiveness comparison of amblyopia screening methods at ages 3–4 years. European Journal of Ophthalmology. 32(4). 2034–2040. 2 indexed citations

Costa, Patrício, et al.. (2021). Amblyopia screening effectiveness at 3–4 years old: a cohort study. BMJ Open Ophthalmology. 6(1). e000599–e000599. 5 indexed citations

Ferreira, Sónia, Isabel Catarina Duarte, Andreia C. Pereira, et al.. (2021). Decreased activity of piriform cortex and orbitofrontal hyperactivation in Usher Syndrome, a human disorder of ciliary dysfunction. Brain Imaging and Behavior. 16(3). 1176–1185. 2 indexed citations

Ribeiro, João Carlos, et al.. (2016). Cross-cultural validation of a taste test with paper strips. European Archives of Oto-Rhino-Laryngology. 273(10). 3407–3411. 15 indexed citations

10.

Ribeiro, Maria José, et al.. (2014). Abnormal late visual responses and alpha oscillations in neurofibromatosis type 1: a link to visual and attention deficits. Journal of Neurodevelopmental Disorders. 6(1). 4–4. 22 indexed citations

11.

Silva, Eduardo, et al.. (2013). Optic Pit. Retina. 33(8). 1708–1714. 41 indexed citations

12.

Bernardino, Inês, João Castelhano, Reza Farivar, Eduardo Silva, & Miguel Castelo‐Branco. (2013). Neural correlates of visual integration in Williams syndrome: Gamma oscillation patterns in a model of impaired coherence. Neuropsychologia. 51(7). 1287–1295. 12 indexed citations

13.

Prasov, Lev, Tehmina Masud, Shagufta Khaliq, et al.. (2012). ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous. Human Molecular Genetics. 21(16). 3681–3694. 51 indexed citations

14.

Reis, Aldina, et al.. (2012). Physiological evidence for impairment in autosomal dominant optic atrophy at the pre-ganglion level. Graefe s Archive for Clinical and Experimental Ophthalmology. 251(1). 221–234. 11 indexed citations

15.

Vásquez, Rodrigo A., et al.. (2011). Oxidative Damage of Lysozyme and Human Serum Albumin and Their Mixtures. A Comparison of Photosensitized and Peroxyl Radical Promoted Processes. The Protein Journal. 30(5). 359–365. 7 indexed citations

16.

Grazina, Manuela, et al.. (2007). Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation—A case report. European Journal of Paediatric Neurology. 11(2). 115–118. 26 indexed citations

17.

Castelo‐Branco, Miguel, Raquel Sebastião, Aldina Reis, et al.. (2007). Visual phenotype in Williams-Beuren syndrome challenges magnocellular theories explaining human neurodevelopmental visual cortical disorders. Journal of Clinical Investigation. 117(12). 3720–9. 36 indexed citations

18.

Silva, Eduardo, Sharola Dharmaraj, Ying Ying Li, et al.. (2004). A missense mutation in GUCY2D acts as a genetic modifier in RPE65 -related Leber Congenital Amaurosis. Ophthalmic Genetics. 25(3). 205–217. 17 indexed citations

19.

Viteri, Gabriela, Géraldine Carrard, Inès Birlouez‐Aragon, Eduardo Silva, & Bertrand Friguet. (2004). Age-dependent protein modifications and declining proteasome activity in the human lens. Archives of Biochemistry and Biophysics. 427(2). 197–203. 70 indexed citations

20.

Silva, Eduardo, et al.. (1995). VISIBLE LIGHT ANAEROBIC PHOTOCONVERSION OF TYROSINE SENSITIZED BY RIBOFLAVIN. CYTOTOXICITY ON MOUSE TUMORAL CELLS. Photochemistry and Photobiology. 62(6). 1041–1045. 16 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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