Valéria M. Borges
About
Valéria M. Borges is a scholar working on Public Health, Environmental and Occupational Health, Epidemiology and Molecular Biology.
According to data from OpenAlex, Valéria M. Borges has authored 92 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 69 papers in Public Health, Environmental and Occupational Health, 38 papers in Epidemiology and 21 papers in Molecular Biology. Recurrent topics in Valéria M. Borges's work include Research on Leishmaniasis Studies (66 papers), Trypanosoma species research and implications (34 papers) and Phagocytosis and Immune Regulation (11 papers). Valéria M. Borges is often cited by papers focused on Research on Leishmaniasis Studies (66 papers), Trypanosoma species research and implications (34 papers) and Phagocytosis and Immune Regulation (11 papers). Valéria M. Borges collaborates with scholars based in Brazil, United States and Belgium. Valéria M. Borges's co-authors include Aldina Barral, Manoel Barral‐Netto, Cláudia Brodskyn, Camila I. de Oliveira, George A. DosReis, Nívea F. Luz, Théo Araújo-Santos, Bruno B. Andrade, Patrı́cia T. Bozza and Walter A. Zin and has published in prestigious journals such as The Journal of Experimental Medicine, The Journal of Immunology and PLoS ONE.
In The Last Decade
Valéria M. Borges
92 papers receiving 3.1k citations
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late) cites · hero ref
| Name | h | Career | Trend | Papers | Cites | |||||
|---|---|---|---|---|---|---|---|---|---|---|
| Valéria M. Borges Brazil | 33 | 1.5k | 933 | 801 | 722 | 288 | 92 | 3.1k | ||
| Farhat Afrin India | 33 | 1.1k 0.7× | 593 0.6× | 462 0.6× | 573 0.8× | 176 0.6× | 66 | 2.5k | ||
| Steve Oghumu United States | 27 | 775 0.5× | 535 0.6× | 672 0.8× | 448 0.6× | 276 1.0× | 88 | 2.2k | ||
| Ulrike Schleicher Germany | 29 | 844 0.6× | 786 0.8× | 1.4k 1.8× | 666 0.9× | 318 1.1× | 60 | 3.1k | ||
| Dhafer Laouini Tunisia | 23 | 354 0.2× | 344 0.4× | 1.3k 1.7× | 790 1.1× | 116 0.4× | 68 | 3.2k | ||
| Eishin Morita Japan | 38 | 288 0.2× | 288 0.3× | 879 1.1× | 686 1.0× | 134 0.5× | 187 | 5.0k | ||
| Barbara Bohle Austria | 49 | 193 0.1× | 230 0.2× | 1.4k 1.8× | 946 1.3× | 72 0.3× | 183 | 8.0k | ||
| Ana Paula Campanelli Brazil | 35 | 439 0.3× | 744 0.8× | 1.2k 1.5× | 630 0.9× | 121 0.4× | 95 | 3.4k | ||
| Huiying Yang China | 27 | 395 0.3× | 1.3k 1.4× | 1.2k 1.5× | 825 1.1× | 94 0.3× | 100 | 4.1k | ||
| Stephanie L. Constant United States | 34 | 400 0.3× | 522 0.6× | 3.8k 4.7× | 1.6k 2.2× | 367 1.3× | 55 | 6.1k | ||
| Zhibin Zhang China | 26 | 538 0.4× | 592 0.6× | 2.4k 3.0× | 6.2k 8.6× | 265 0.9× | 46 | 8.2k |
Countries citing papers authored by Valéria M. Borges
Since
Specialization
Citations
This map shows the geographic impact of Valéria M. Borges'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 Valéria M. Borges with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Valéria M. Borges more than expected).
Fields of papers citing papers by Valéria M. Borges
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Valéria M. Borges. 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 Valéria M. Borges. The network helps show where Valéria M. Borges may publish in the future.
Co-authorship network of co-authors of Valéria M. Borges
This figure shows the co-authorship network connecting the top 25 collaborators of Valéria M. Borges. A scholar is included among the top collaborators of Valéria M. Borges 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 Valéria M. Borges. Valéria M. Borges is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Covre, Luciana Polaco, Débora Decotè-Ricardo, Célio Geraldo Freire-de-Lima, et al.. (2024). Senescence-related genes are associated with the immunopathology signature of American tegumentary leishmaniasis lesions and may predict progression to mucosal leishmaniasis. Clinical & Experimental Immunology. 219(1).
2.
Rebouças-Silva, Jéssica, et al.. (2023). Leishmanicidal and immunomodulatory properties of Brazilian green propolis extract (EPP-AF®) and a gel formulation in a pre-clinical model. Frontiers in Pharmacology. 14. 1013376–1013376.
3.
Faccioli, Lúcia Helena, et al.. (2023). Polyunsaturated fatty acids alter the formation of lipid droplets and eicosanoid production in Leishmania promastigotes. Memórias do Instituto Oswaldo Cruz. 118. e220160–e220160.
4.
Rebouças-Silva, Jéssica, et al.. (2023). In vitro leishmanicidal effect of Yangambin and Epi-yangambin lignans isolated from Ocotea fasciculata (Nees) Mez. Frontiers in Cellular and Infection Microbiology. 12. 1045732–1045732.
5.
Silveira, Marcelo Augusto Duarte, Jéssica Rebouças-Silva, Flávio Teles, et al.. (2022). Effects of Standardized Brazilian Green Propolis Extract (EPP-AF®) on Inflammation in Haemodialysis Patients: A Clinical Trial. International Journal of Nephrology. 2022. 1–9.
6.
Solcà, Manuela da Silva, Leila Denise Alves Ferreira Amorim, Valéria M. Borges, et al.. (2021). Immune response dynamics and Lutzomyia longipalpis exposure characterize a biosignature of visceral leishmaniasis susceptibility in a canine cohort. PLoS neglected tropical diseases. 15(2). e0009137–e0009137.
7.
Santiago, Rayra Pereira, Sètondji Cocou Modeste Alexandre Yahouédéhou, Valma Maria Lopes Nascimento, et al.. (2021). Associations between TGF‐β1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients. Mediators of Inflammation. 2021(1). 4651891–4651891.
8.
Coutinho-Abreu, Iliano V., Timothy R. Wilson, Claudio Meneses, et al.. (2020). Binding of Leishmania infantum Lipophosphoglycan to the Midgut Is Not Sufficient To Define Vector Competence in Lutzomyia longipalpis Sand Flies. mSphere. 5(5).
9.
Cardoso, Thiago M., Jonilson Berlink Lima, Daniel F. Feijó, et al.. (2020). Inflammasome Activation by CD8+ T Cells from Patients with Cutaneous Leishmaniasis Caused by Leishmania braziliensis in the Immunopathogenesis of the Disease. Journal of Investigative Dermatology. 141(1). 209–213.e2.
10.
DeSouza‐Vieira, Thiago, Eva Iniguez, Tiago D. Serafim, et al.. (2020). Heme Oxygenase-1 Induction by Blood-Feeding Arthropods Controls Skin Inflammation and Promotes Disease Tolerance. Cell Reports. 33(4). 108317–108317.
11.
Rebouças-Silva, Jéssica, Paulo S. Silveira-Mattos, Camila I. de Oliveira, et al.. (2020). <p>Evaluation of in vitro and in vivo Efficacy of a Novel Amphotericin B-Loaded Nanostructured Lipid Carrier in the Treatment of <em>Leishmania braziliensis</em> Infection</p>. International Journal of Nanomedicine. Volume 15. 8659–8672.
12.
Luz, Nívea F., Jonilson Berlink Lima, Roque Pacheco de Almeida, et al.. (2018). RIPK1–RIPK3–MLKL-Associated Necroptosis Drives Leishmania infantum Killing in Neutrophils. Frontiers in Immunology. 9. 1818–1818.
13.
Lima, Jonilson Berlink, Théo Araújo-Santos, Alan Brito Carneiro, et al.. (2017). Leishmania infantum lipophosphoglycan induced-Prostaglandin E2 production in association with PPAR-γ expression via activation of Toll like receptors-1 and 2. Scientific Reports. 7(1). 14321–14321.
14.
Bezerra‐Santos, Márcio, Lucas Sousa Magalhães, Rodrigo Anselmo Cazzaniga, et al.. (2017). sCD163 levels as a biomarker of disease severity in leprosy and visceral leishmaniasis. PLoS neglected tropical diseases. 11(3). e0005486–e0005486.
15.
Andrade, Bruno B., Nívea F. Luz, Fabiana S. Celes, et al.. (2017). Heme Drives Oxidative Stress-Associated Cell Death in Human Neutrophils Infected with Leishmania infantumNeutrophils Infected with Leishmania infantum.
16.
Andrade, Bruno B., Ricardo Khouri, Johan Van Weyenbergh, et al.. (2015). Differential Expression of the Eicosanoid Pathway in Patients With Localized or Mucosal Cutaneous Leishmaniasis. The Journal of Infectious Diseases. 213(7). 1143–1147.
17.
Araújo-Santos, Théo, Nilda E. Rodríguez, Daniel R. Abánades, et al.. (2014). Role of Prostaglandin F2α Production in Lipid Bodies From Leishmania infantum chagasi: Insights on Virulence. The Journal of Infectious Diseases. 210(12). 1951–1961.
18.
Correia, Luís Cláudio Lemos, Bruno B. Andrade, Valéria M. Borges, et al.. (2010). Prognostic value of cytokines and chemokines in addition to the GRACE Score in non-ST-elevation acute coronary syndromes. Clinica Chimica Acta. 411(7-8). 540–545.
19.
Novais, Fernanda O., André Báfica, Ricardo Khouri, et al.. (2009). Neutrophils and Macrophages Cooperate in Host Resistance against Leishmania braziliensis Infection. The Journal of Immunology. 183(12). 8088–8098.
20.
Morimoto, Konosuke, William J. Janssen, Michael B. Fessler, et al.. (2006). Lovastatin Enhances Clearance of Apoptotic Cells (Efferocytosis) with Implications for Chronic Obstructive Pulmonary Disease. The Journal of Immunology. 176(12). 7657–7665.
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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