Marisol Cano

3.9k total citations · 1 hit paper
53 papers, 3.2k citations indexed

About

Marisol Cano is a scholar working on Ophthalmology, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Marisol Cano has authored 53 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Ophthalmology, 22 papers in Molecular Biology and 12 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Marisol Cano's work include Retinal Diseases and Treatments (23 papers), Retinal Development and Disorders (9 papers) and Genomics, phytochemicals, and oxidative stress (6 papers). Marisol Cano is often cited by papers focused on Retinal Diseases and Treatments (23 papers), Retinal Development and Disorders (9 papers) and Genomics, phytochemicals, and oxidative stress (6 papers). Marisol Cano collaborates with scholars based in United States, United Kingdom and Spain. Marisol Cano's co-authors include James T. Handa, Lei Wang, Katayoon B. Ebrahimi, Sayantan Datta, Mira M. Sachdeva, Natalia Fijalkowski, Masashi Fujihara, Shyam Biswal, Peter Gehlbach and Ashley Behrens and has published in prestigious journals such as Nature, Nature Communications and PLoS ONE.

In The Last Decade

Marisol Cano

52 papers receiving 3.1k citations

Hit Papers

The impact of oxidative stress and inflammation on RPE de... 2017 2026 2020 2023 2017 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marisol Cano United States 27 1.7k 1.6k 774 459 288 53 3.2k
Puran S. Bora United States 30 1.2k 0.7× 807 0.5× 481 0.6× 683 1.5× 259 0.9× 89 2.5k
Haydee E. P. Bazán United States 39 874 0.5× 1.3k 0.8× 1.6k 2.0× 349 0.8× 133 0.5× 143 4.2k
Julio Escribano Spain 30 1.2k 0.7× 1.8k 1.1× 476 0.6× 128 0.3× 176 0.6× 116 3.6k
Eri Kubo Japan 30 459 0.3× 1.7k 1.1× 356 0.5× 156 0.3× 152 0.5× 111 2.6k
Giovanna Angelini Italy 27 275 0.2× 847 0.5× 164 0.2× 1.3k 2.8× 164 0.6× 57 2.9k
Megan E. Cavet United States 22 380 0.2× 467 0.3× 228 0.3× 193 0.4× 37 0.1× 47 1.5k
Aramati B. M. Reddy India 24 441 0.3× 831 0.5× 247 0.3× 166 0.4× 69 0.2× 47 1.7k
P. Bhattacherjee United States 27 864 0.5× 593 0.4× 210 0.3× 330 0.7× 43 0.1× 76 2.1k
Daniel A. Cunha Belgium 32 123 0.1× 1.3k 0.8× 162 0.2× 339 0.7× 545 1.9× 50 3.6k
Xiang Lin China 24 86 0.0× 826 0.5× 164 0.2× 552 1.2× 124 0.4× 108 2.4k

Countries citing papers authored by Marisol Cano

Since Specialization
Citations

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

Fields of papers citing papers by Marisol Cano

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marisol Cano

This figure shows the co-authorship network connecting the top 25 collaborators of Marisol Cano. A scholar is included among the top collaborators of Marisol Cano 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 Marisol Cano. Marisol Cano is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Sforza, Daniel, Marisol Cano, Cornelia Peterson, et al.. (2025). A Feasibility Study of Preclinical Ocular X-Ray FLASH Radiation Therapy. International Journal of Radiation Oncology*Biology*Physics. 123(4). 1165–1175. 2 indexed citations
2.
Datta, Sayantan, et al.. (2018). The impact of lipids, lipid oxidation, and inflammation on AMD, and the potential role of miRNAs on lipid metabolism in the RPE. Experimental Eye Research. 181. 346–355. 84 indexed citations
3.
Wang, Jie, Cristina Zibetti, Peng Shang, et al.. (2018). ATAC-Seq analysis reveals a widespread decrease of chromatin accessibility in age-related macular degeneration. Nature Communications. 9(1). 1364–1364. 111 indexed citations
4.
Handa, James T., Marisol Cano, Lei Wang, Sayantan Datta, & Tongyun Liu. (2016). Lipids, oxidized lipids, oxidation-specific epitopes, and Age-related Macular Degeneration. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1862(4). 430–440. 89 indexed citations
5.
Cruz‐Guilloty, Fernando, Ali Saeed, Stéphanie Duffort, et al.. (2014). T Cells and Macrophages Responding to Oxidative Damage Cooperate in Pathogenesis of a Mouse Model of Age-Related Macular Degeneration. PLoS ONE. 9(2). e88201–e88201. 53 indexed citations
6.
Wang, Lei, Marisol Cano, & James T. Handa. (2014). p62 provides dual cytoprotection against oxidative stress in the retinal pigment epithelium. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1843(7). 1248–1258. 77 indexed citations
7.
Cano, Marisol, Brad P. Barnett, Lei Wang, Sonny Dike, & James T. Handa. (2013). Cigarette Smoke (CS) and Nrf2 Deficiency Induce Mitochondrial Dysfunction in Retinal Pigment Epithelial (RPE) Cells. Investigative Ophthalmology & Visual Science. 54(15). 1800–1800. 1 indexed citations
8.
Chen, Chen, Marisol Cano, Joshua J. Wang, et al.. (2013). Role of Unfolded Protein Response Dysregulation in Oxidative Injury of Retinal Pigment Epithelial Cells. Antioxidants and Redox Signaling. 20(14). 2091–2106. 60 indexed citations
9.
Sachdeva, Mira M., Marisol Cano, & James T. Handa. (2013). Nrf2 signaling is impaired in the aging RPE given an oxidative insult. Experimental Eye Research. 119. 111–114. 169 indexed citations
10.
Sinha, Debasish, Mallika Valapala, Imran Ahmed Bhutto, et al.. (2012). βA3/A1-crystallin is required for proper astrocyte template formation and vascular remodeling in the retina. Transgenic Research. 21(5). 1033–1042. 21 indexed citations
11.
Sunshine, Sarah B., Joel Sunshine, Marisol Cano, Jordan J. Green, & James T. Handa. (2011). Nitric Oxide Induces Nrf2 Signaling In RPE Cells In Vitro. Investigative Ophthalmology & Visual Science. 52(14). 2345–2345. 1 indexed citations
12.
Weismann, David, Karsten Hartvigsen, Nadine Lauer, et al.. (2011). Complement factor H binds malondialdehyde epitopes and protects from oxidative stress. Nature. 478(7367). 76–81. 444 indexed citations
13.
Kondo, Naoshi, Marisol Cano, Katayoon B. Ebrahimi, & James T. Handa. (2010). Nrf2 Signaling is Activated After Cigarette Smoke Extract Exposure in Rpe Cells in vitro and in vivo. Investigative Ophthalmology & Visual Science. 51(13). 4104–4104. 1 indexed citations
14.
Cano, Marisol, et al.. (2010). Advanced Glycation Endproducts (AGEs) Favor LDL Retention in the Fundus. Investigative Ophthalmology & Visual Science. 51(13). 6162–6162. 1 indexed citations
15.
Wu, Tinghuai, Masashi Fujihara, Jane Tian, et al.. (2010). Apolipoprotein B100 secretion by cultured ARPE‐19 cells is modulated by alteration of cholesterol levels. Journal of Neurochemistry. 114(6). 1734–1744. 28 indexed citations
16.
Nishi, Yutaro, Christoph Engler, Renata T. Kashiwabuchi, et al.. (2010). Evaluation of phacoemulsification‐induced oxidative stress and damage of cultured human corneal endothelial cells in different solutions using redox fluorometry microscopy. Acta Ophthalmologica. 88(8). e323–7. 6 indexed citations
17.
Cano, Marisol, Masashi Fujihara, Norihiro Nagai, et al.. (2009). Cigarette smoking, oxidative stress, the anti-oxidant response through Nrf2 signaling, and Age-related Macular Degeneration. Vision Research. 50(7). 652–664. 154 indexed citations
18.
Soliman, Mohamed S., et al.. (2008). In vitro Evaluation of Predicted Antiangiogenic Peptides in Human Retinal Endothelial Cells. Investigative Ophthalmology & Visual Science. 49(13). 4594–4594. 1 indexed citations
19.
Sikder, Shameema, Samantha Herretes, Elia J. Duh, et al.. (2006). Topical Human Amniotic Fluid vs. Potent Antiangiogenesis Protein in the Inhibition of Induced Corneal Neovascularization. Investigative Ophthalmology & Visual Science. 47(13). 1650–1650. 1 indexed citations
20.
Gehlbach, Peter, Stacey Hose, Bo Lei, et al.. (2005). Developmental abnormalities in the Nuc1 rat retina: A spontaneous mutation that affects neuronal and vascular remodeling and retinal function. Neuroscience. 137(2). 447–461. 18 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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