Ramón Cueto

1.7k total citations
23 papers, 1.1k citations indexed

About

Ramón Cueto is a scholar working on Molecular Biology, Immunology and Rheumatology. According to data from OpenAlex, Ramón Cueto has authored 23 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Immunology and 6 papers in Rheumatology. Recurrent topics in Ramón Cueto's work include Folate and B Vitamins Research (6 papers), Immune cells in cancer (4 papers) and Immune responses and vaccinations (3 papers). Ramón Cueto is often cited by papers focused on Folate and B Vitamins Research (6 papers), Immune cells in cancer (4 papers) and Immune responses and vaccinations (3 papers). Ramón Cueto collaborates with scholars based in United States, China and Spain. Ramón Cueto's co-authors include Xiaofeng Yang, Hong Wang, Ying Shao, William Y. Yang, Gayani Nanayakkara, Xuebin Qin, Lixiao Zhang, Eric T. Choi, Jiali Cheng and Xianwei Wang and has published in prestigious journals such as Journal of Biological Chemistry, Arteriosclerosis Thrombosis and Vascular Biology and Frontiers in Immunology.

In The Last Decade

Ramón Cueto

23 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ramón Cueto United States 17 570 332 140 124 92 23 1.1k
Mingyo Kim South Korea 11 334 0.6× 269 0.8× 134 1.0× 90 0.7× 77 0.8× 30 892
Rahul Shinde United States 15 543 1.0× 647 1.9× 97 0.7× 115 0.9× 50 0.5× 25 1.5k
Peiliang Shi China 19 912 1.6× 338 1.0× 149 1.1× 129 1.0× 145 1.6× 28 1.5k
Sarah E. Headland United Kingdom 8 659 1.2× 498 1.5× 109 0.8× 114 0.9× 150 1.6× 13 1.3k
Gayani Nanayakkara United States 22 675 1.2× 440 1.3× 155 1.1× 211 1.7× 30 0.3× 33 1.4k
Gianluca Grassia Italy 25 557 1.0× 550 1.7× 177 1.3× 71 0.6× 59 0.6× 38 1.4k
Xiaoliang Wang China 20 482 0.8× 372 1.1× 155 1.1× 181 1.5× 53 0.6× 48 1.2k
Michelle T. Barati United States 20 741 1.3× 213 0.6× 89 0.6× 122 1.0× 65 0.7× 52 1.5k
Jing Luo China 22 642 1.1× 351 1.1× 159 1.1× 179 1.4× 191 2.1× 110 1.7k

Countries citing papers authored by Ramón Cueto

Since Specialization
Citations

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

Fields of papers citing papers by Ramón Cueto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ramón Cueto

This figure shows the co-authorship network connecting the top 25 collaborators of Ramón Cueto. A scholar is included among the top collaborators of Ramón Cueto 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 Ramón Cueto. Ramón Cueto 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.
Sun, Yu, Yifan Lu, Fatma Saaoud, et al.. (2024). Caspase-4/11 promotes hyperlipidemia and chronic kidney disease-accelerated vascular inflammation by enhancing trained immunity. JCI Insight. 9(16). 7 indexed citations
2.
Cueto, Ramón, Wen Shen, Xianwei Wang, et al.. (2024). SAH is a major metabolic sensor mediating worsening metabolic crosstalk in metabolic syndrome. Redox Biology. 73. 103139–103139. 12 indexed citations
3.
Yang, William Y., Fatma Saaoud, Keman Xu, et al.. (2024). Perspective: Pathological transdifferentiation—a novel therapeutic target for cardiovascular diseases and chronic inflammation. Frontiers in Cardiovascular Medicine. 11. 1500775–1500775. 1 indexed citations
4.
Wang, Xianwei, Lu Liu, Xiaohua Jiang, et al.. (2023). Identification of methylation-regulated genes modulating microglial phagocytosis in hyperhomocysteinemia-exacerbated Alzheimer’s disease. Alzheimer s Research & Therapy. 15(1). 164–164. 4 indexed citations
5.
Drummer, Charles, Fatma Saaoud, Nirag Jhala, et al.. (2023). Caspase-11 promotes high-fat diet-induced NAFLD by increasing glycolysis, OXPHOS, and pyroptosis in macrophages. Frontiers in Immunology. 14. 1113883–1113883. 41 indexed citations
6.
Saaoud, Fatma, Lu Liu, Keman Xu, et al.. (2022). Aorta- and liver-generated TMAO enhances trained immunity for increased inflammation via ER stress/mitochondrial ROS/glycolysis pathways. JCI Insight. 8(1). 80 indexed citations
7.
Jan, Michael, Ramón Cueto, Xiaohua Jiang, et al.. (2021). Molecular processes mediating hyperhomocysteinemia-induced metabolic reprogramming, redox regulation and growth inhibition in endothelial cells. Redox Biology. 45. 102018–102018. 31 indexed citations
8.
Zhang, Lixiao, Xianwei Wang, Ramón Cueto, et al.. (2019). Biochemical basis and metabolic interplay of redox regulation. Redox Biology. 26. 101284–101284. 234 indexed citations
9.
10.
Shen, Wen, Chao Gao, Ramón Cueto, et al.. (2019). Homocysteine-methionine cycle is a metabolic sensor system controlling methylation-regulated pathological signaling. Redox Biology. 28. 101322–101322. 78 indexed citations
11.
Cueto, Ramón, Lixiao Zhang, Xiao Huang, et al.. (2018). Identification of homocysteine-suppressive mitochondrial ETC complex genes and tissue expression profile – Novel hypothesis establishment. Redox Biology. 17. 70–88. 28 indexed citations
12.
Shao, Ying, Gayani Nanayakkara, Jiali Cheng, et al.. (2017). Lysophospholipids and Their Receptors Serve as Conditional DAMPs and DAMP Receptors in Tissue Oxidative and Inflammatory Injury. Antioxidants and Redox Signaling. 28(10). 973–986. 55 indexed citations
13.
Cheng, Jiali, Gayani Nanayakkara, Ying Shao, et al.. (2017). Mitochondrial Proton Leak Plays a Critical Role in Pathogenesis of Cardiovascular Diseases. Advances in experimental medicine and biology. 982. 359–370. 130 indexed citations
14.
Dai, Jin, Pu Fang, Jason Saredy, et al.. (2017). Metabolism-associated danger signal-induced immune response and reverse immune checkpoint-activated CD40+ monocyte differentiation. Journal of Hematology & Oncology. 10(1). 141–141. 28 indexed citations
15.
Li, Yafeng, Gayani Nanayakkara, Yu Sun, et al.. (2017). Analyses of caspase-1-regulated transcriptomes in various tissues lead to identification of novel IL-1β-, IL-18- and sirtuin-1-independent pathways. Journal of Hematology & Oncology. 10(1). 40–40. 45 indexed citations
16.
17.
Ferrer, Lucas, Jahaira Lopez‐Pastrana, Gayani Nanayakkara, et al.. (2016). Caspase-1 Plays a Critical Role in Accelerating Chronic Kidney Disease-Promoted Neointimal Hyperplasia in the Carotid Artery. Journal of Cardiovascular Translational Research. 9(2). 135–144. 41 indexed citations
18.
Shao, Ying, Candice Johnson, William Y. Yang, et al.. (2016). Metabolic Diseases Downregulate the Majority of Histone Modification Enzymes, Making a Few Upregulated Enzymes Novel Therapeutic Targets—“Sand Out and Gold Stays”. Journal of Cardiovascular Translational Research. 9(1). 49–66. 33 indexed citations
19.
Lopez‐Pastrana, Jahaira, Lucas Ferrer, Yafeng Li, et al.. (2015). Inhibition of Caspase-1 Activation in Endothelial Cells Improves Angiogenesis. Journal of Biological Chemistry. 290(28). 17485–17494. 79 indexed citations
20.
Lucena, M. Isabel, et al.. (2010). Genética y hepatotoxicidad. Gastroenterología y Hepatología. 33. 10–21. 1 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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