Ulisses Gazos Lopes

3.2k total citations
81 papers, 2.6k citations indexed

About

Ulisses Gazos Lopes is a scholar working on Public Health, Environmental and Occupational Health, Epidemiology and Molecular Biology. According to data from OpenAlex, Ulisses Gazos Lopes has authored 81 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Public Health, Environmental and Occupational Health, 40 papers in Epidemiology and 28 papers in Molecular Biology. Recurrent topics in Ulisses Gazos Lopes's work include Research on Leishmaniasis Studies (50 papers), Trypanosoma species research and implications (34 papers) and Leprosy Research and Treatment (8 papers). Ulisses Gazos Lopes is often cited by papers focused on Research on Leishmaniasis Studies (50 papers), Trypanosoma species research and implications (34 papers) and Leprosy Research and Treatment (8 papers). Ulisses Gazos Lopes collaborates with scholars based in Brazil, United States and United Kingdom. Ulisses Gazos Lopes's co-authors include Geoffrey M. Cooper, Ryoji Yao, Péter Erhardt, Marcelo T. Bozza, Teresa Calegari-Silva, Octávio Fernandes, Renata M. Pereira, Alessandra Mattos Saliba, Dyann F. Wirth and Bartira Rossi‐Bergmann and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Immunology and PLoS ONE.

In The Last Decade

Ulisses Gazos Lopes

81 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ulisses Gazos Lopes Brazil	28	1.3k	982	932	353	332	81	2.6k
Núria Gironès Spain	32	833 0.7×	1.0k 1.0×	748 0.8×	323 0.9×	382 1.2×	70	2.3k
Marcos A. Vannier‐Santos Brazil	35	1.1k 0.9×	939 1.0×	709 0.8×	229 0.6×	494 1.5×	102	2.8k
Farhat Afrin India	33	1.1k 0.9×	593 0.6×	573 0.6×	462 1.3×	176 0.5×	66	2.5k
Janis Lazdins Switzerland	24	750 0.6×	978 1.0×	491 0.5×	611 1.7×	415 1.3×	41	2.6k
Takeshi Nara Japan	29	406 0.3×	666 0.7×	1.0k 1.1×	150 0.4×	478 1.4×	106	2.3k
Souvenir D. Tachado United States	28	703 0.6×	660 0.7×	705 0.8×	904 2.6×	183 0.6×	43	2.4k
Célio Geraldo Freire-de-Lima Brazil	32	978 0.8×	1.6k 1.6×	1.1k 1.2×	1.3k 3.8×	373 1.1×	100	3.7k
Ulrike Schleicher Germany	29	844 0.7×	786 0.8×	666 0.7×	1.4k 4.1×	318 1.0×	60	3.1k
Hira L. Nakhasi United States	42	3.0k 2.3×	2.3k 2.4×	1.5k 1.7×	875 2.5×	847 2.6×	164	5.4k
Ali Ouaissi France	34	1.8k 1.4×	1.7k 1.7×	668 0.7×	425 1.2×	634 1.9×	92	2.9k

Countries citing papers authored by Ulisses Gazos Lopes

Since Specialization

Citations

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

Fields of papers citing papers by Ulisses Gazos Lopes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ulisses Gazos Lopes. 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 Ulisses Gazos Lopes. The network helps show where Ulisses Gazos Lopes may publish in the future.

Co-authorship network of co-authors of Ulisses Gazos Lopes

This figure shows the co-authorship network connecting the top 25 collaborators of Ulisses Gazos Lopes. A scholar is included among the top collaborators of Ulisses Gazos Lopes 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 Ulisses Gazos Lopes. Ulisses Gazos Lopes 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

Attias, Ma�rcia, Gilberto B. Domont, Fábio César Sousa Nogueira, et al.. (2024). Leishmania amazonensis-derived extracellular vesicles (EVs) induce neutrophil extracellular traps (NETs). Journal of Leukocyte Biology. 117(1). 2 indexed citations

Chorev, Michael, et al.. (2024). Activity of the Di-Substituted Urea-Derived Compound I-17 in Leishmania In Vitro Infections. Pathogens. 13(2). 104–104. 1 indexed citations

Caldas, Lúcio Ayres, et al.. (2022). Endoplasmic Stress Affects the Coinfection of Leishmania Amazonensis and the Phlebovirus (Bunyaviridae) Icoaraci. Viruses. 14(9). 1948–1948. 2 indexed citations

Costa, Leandro Silva da, Deivid Costa Soares, Amanda Brito Wardini, et al.. (2020). DH82 Canine and RAW264.7 Murine Macrophage Cell Lines Display Distinct Activation Profiles Upon Interaction With Leishmania infantum and Leishmania amazonensis. Frontiers in Cellular and Infection Microbiology. 10. 247–247. 10 indexed citations

Damaso, Clarissa R., Luciana Barros de Arruda, Pedro Fernando da Costa Vasconcelos, et al.. (2019). Amazonian Phlebovirus (Bunyaviridae) potentiates the infection of Leishmania (Leishmania) amazonensis: Role of the PKR/IFN1/IL-10 axis. PLoS neglected tropical diseases. 13(6). e0007500–e0007500. 21 indexed citations

Lima, Jonilson Berlink, Guillermo Arango Duque, Cláudio Pereira Figueira, et al.. (2018). Leishmania infantum Lipophosphoglycan-Deficient Mutants: A Tool to Study Host Cell-Parasite Interplay. Frontiers in Microbiology. 9. 626–626. 17 indexed citations

Pereira, Renata M., et al.. (2016). Unveiling the Role of the Integrated Endoplasmic Reticulum Stress Response in Leishmania Infection – Future Perspectives. Frontiers in Immunology. 7. 283–283. 6 indexed citations

Calegari-Silva, Teresa, et al.. (2012). ExoU Activates NF-κB and Increases IL-8/KC Secretion during Pseudomonas aeruginosa Infection. PLoS ONE. 7(7). e41772–e41772. 31 indexed citations

Pinheiro, Roberta Olmo, et al.. (2011). Thalidomide modulates Mycobacterium leprae-induced NF-κB pathway and lower cytokine response. European Journal of Pharmacology. 670(1). 272–279. 18 indexed citations

10.

Pereira, Renata M., Teresa Calegari-Silva, Maria Bellio, et al.. (2011). Human cutaneous leishmaniasis: interferon‐dependent expression of double‐stranded RNA‐dependent protein kinase (PKR) via TLR2. The FASEB Journal. 25(12). 4162–4173. 50 indexed citations

11.

Vale, André M., Jeremy B. Foote, Alessandra Granato, et al.. (2011). A rapid and quantitative method for the evaluation of V gene usage, specificities and the clonal size of B cell repertoires. Journal of Immunological Methods. 376(1-2). 143–149. 5 indexed citations

12.

Rocha, Juliana Dutra Barbosa da, Débora Decotè-Ricardo, Ulisses Gazos Lopes, et al.. (2009). Inhibitory Effect of the Alkaloid Warifteine Purified fromCissampelos sympodialison B Lymphocyte FunctionIn VitroandIn Vivo. Planta Medica. 76(4). 325–330. 14 indexed citations

13.

Sant’Anna, Celso, et al.. (2008). Evolutionary conservation of actin-binding proteins inTrypanosoma cruziand unusual subcellular localization of the actin homologue. Parasitology. 135(8). 955–965. 16 indexed citations

14.

Ribeiro-Gomes, Flávia Lima, Juliana de Meis, Renata M. Pereira, et al.. (2005). Caspase-8 Activity Prevents Type 2 Cytokine Responses and Is Required for Protective T Cell-Mediated Immunity against Trypanosoma cruzi Infection. The Journal of Immunology. 174(10). 6314–6321. 31 indexed citations

15.

Lopes, Ulisses Gazos, et al.. (2004). RJLs: a new family of Ras-related GTP-binding proteins. Gene. 327(2). 221–232. 22 indexed citations

16.

Pinheiro, Roberta Olmo, et al.. (2004). The T-cell anergy induced by Leishmania amazonensis antigens is related with defective antigen presentation and apoptosis. Anais da Academia Brasileira de Ciências. 76(3). 519–527. 42 indexed citations

17.

Freitas, Marta Sampaio de, et al.. (2002). Neurite outgrowth is impaired on HSP70-positive astrocytes through a mechanism that requires NF-κB activation. Brain Research. 958(2). 359–370. 21 indexed citations

18.

Yokoyama, Kohei, Rudi Baron, Jean‐Charles Faye, et al.. (2001). TcRho1, a Farnesylated Rho Family Homologue fromTrypanosoma cruzi. Journal of Biological Chemistry. 276(32). 29711–29718. 29 indexed citations

19.

Cunha‐e‐Silva, Narcisa L., et al.. (2000). Characterization of a Rab11 homologue in Trypanosoma cruzi. Gene. 243(1-2). 179–185. 33 indexed citations

20.

Bozza, Marcelo T., Octávio Fernandes, Wim Degrave, & Ulisses Gazos Lopes. (1995). Characterization of ‘Old World’ Leishmania species using amplified minicircle variable regions as molecular probes. Transactions of the Royal Society of Tropical Medicine and Hygiene. 89(3). 333–334. 10 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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