Nathália Rocco-Machado

497 total citations
15 papers, 403 citations indexed

About

Nathália Rocco-Machado is a scholar working on Molecular Biology, Epidemiology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Nathália Rocco-Machado has authored 15 papers receiving a total of 403 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Epidemiology and 4 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Nathália Rocco-Machado's work include Trypanosoma species research and implications (5 papers), Research on Leishmaniasis Studies (4 papers) and Redox biology and oxidative stress (4 papers). Nathália Rocco-Machado is often cited by papers focused on Trypanosoma species research and implications (5 papers), Research on Leishmaniasis Studies (4 papers) and Redox biology and oxidative stress (4 papers). Nathália Rocco-Machado collaborates with scholars based in Brazil and United States. Nathália Rocco-Machado's co-authors include José Roberto Meyer‐Fernandes, Daniela Cosentino‐Gomes, J.R. Meyer-Fernandes, Lisvane Paes‐Vieira, Cláudia F. Dick, Michelle T. C. Nascimento, Kátia C. Gondim, Lucélia Santi, Walter O. Beys‐da‐Silva and Marilene Henning Vainstein and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Free Radical Biology and Medicine.

In The Last Decade

Nathália Rocco-Machado

14 papers receiving 399 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nathália Rocco-Machado Brazil 9 198 77 69 57 31 15 403
Rebecca Caffrey United States 9 223 1.1× 69 0.9× 39 0.6× 136 2.4× 27 0.9× 14 504
Anna K. McNeil United States 8 326 1.6× 88 1.1× 43 0.6× 32 0.6× 11 0.4× 8 539
Zhongchi Li United States 14 290 1.5× 114 1.5× 59 0.9× 97 1.7× 44 1.4× 22 617
Seon Hwa Park South Korea 12 309 1.6× 62 0.8× 170 2.5× 84 1.5× 97 3.1× 22 721
Yuan Chi Japan 17 384 1.9× 54 0.7× 52 0.8× 31 0.5× 23 0.7× 20 736
Hiromasa Ono Japan 14 199 1.0× 103 1.3× 42 0.6× 29 0.5× 35 1.1× 20 457
Mario Ruiz Sweden 17 347 1.8× 147 1.9× 71 1.0× 98 1.7× 10 0.3× 27 726
Perinur Bozaykut Türkiye 11 251 1.3× 126 1.6× 35 0.5× 113 2.0× 9 0.3× 19 542
Ping Jiang China 15 281 1.4× 34 0.4× 92 1.3× 52 0.9× 55 1.8× 50 552

Countries citing papers authored by Nathália Rocco-Machado

Since Specialization
Citations

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

Fields of papers citing papers by Nathália Rocco-Machado

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nathália Rocco-Machado. 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 Nathália Rocco-Machado. The network helps show where Nathália Rocco-Machado may publish in the future.

Co-authorship network of co-authors of Nathália Rocco-Machado

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

All Works

15 of 15 papers shown
1.
Rocco-Machado, Nathália, et al.. (2024). Oxidation of CaMKIIα cysteines inhibits autonomous activation induced by phosphorylation. Archives of Biochemistry and Biophysics. 764. 110268–110268.
2.
Rocco-Machado, Nathália, Lo Lai, Geumsoo Kim, et al.. (2022). Oxidative stress–induced autonomous activation of the calcium/calmodulin-dependent kinase II involves disulfide formation in the regulatory domain. Journal of Biological Chemistry. 298(11). 102579–102579. 12 indexed citations
3.
Dick, Cláudia F., Nathália Rocco-Machado, André L.A. Dos-Santos, et al.. (2022). An Iron Transporter Is Involved in Iron Homeostasis, Energy Metabolism, Oxidative Stress, and Metacyclogenesis in Trypanosoma cruzi. Frontiers in Cellular and Infection Microbiology. 11. 789401–789401. 6 indexed citations
4.
Dick, Cláudia F., et al.. (2022). Anaerobic ATP synthesis pathways and inorganic phosphate transport and their possible roles in encystment in Acanthamoeba castellanii. Cell Biology International. 46(8). 1288–1298. 8 indexed citations
5.
Paes‐Vieira, Lisvane, et al.. (2021). Differential regulation of E-NTPdases during Leishmania amazonensis lifecycle and effect of their overexpression on parasite infectivity and virulence. Parasitology International. 85. 102423–102423. 4 indexed citations
6.
Rocco-Machado, Nathália, et al.. (2021). Hydrogen Peroxide Generation as an Underlying Response to High Extracellular Inorganic Phosphate (Pi) in Breast Cancer Cells. International Journal of Molecular Sciences. 22(18). 10096–10096. 10 indexed citations
7.
Rocco-Machado, Nathália, et al.. (2020). Acanthamoeba castellanii phosphate transporter (AcPHS) is important to maintain inorganic phosphate influx and is related to trophozoite metabolic processes. Journal of Bioenergetics and Biomembranes. 52(2). 93–102. 10 indexed citations
8.
Rocco-Machado, Nathália, Daniela Cosentino‐Gomes, Michelle T. C. Nascimento, et al.. (2019). Leishmania amazonensis ferric iron reductase (LFR1) is a bifunctional enzyme: Unveiling a NADPH oxidase activity. Free Radical Biology and Medicine. 143. 341–353. 10 indexed citations
9.
Dos-Santos, André L.A., Cláudia F. Dick, Nathália Rocco-Machado, et al.. (2019). Tartrate-resistant phosphatase type 5 in Trypanosoma cruzi is important for resistance to oxidative stress promoted by hydrogen peroxide. Experimental Parasitology. 205. 107748–107748. 7 indexed citations
10.
Rocco-Machado, Nathália, Daniela Cosentino‐Gomes, & José Roberto Meyer‐Fernandes. (2015). Modulation of Na+/K+ ATPase Activity by Hydrogen Peroxide Generated through Heme in L. amazonensis. PLoS ONE. 10(6). e0129604–e0129604. 10 indexed citations
11.
Alves‐Bezerra, Michele, Daniela Cosentino‐Gomes, Lisvane Paes‐Vieira, et al.. (2014). Identification of uncoupling protein 4 from the blood-sucking insect Rhodnius prolixus and its possible role on protection against oxidative stress. Insect Biochemistry and Molecular Biology. 50. 24–33. 19 indexed citations
12.
Cosentino‐Gomes, Daniela, Nathália Rocco-Machado, & José Roberto Meyer‐Fernandes. (2014). Rhodnius prolixus: Modulation of antioxidant defenses by Trypanosoma rangeli. Experimental Parasitology. 145. 118–124. 7 indexed citations
13.
Cosentino‐Gomes, Daniela, Nathália Rocco-Machado, Lucélia Santi, et al.. (2013). Inhibition of Ecto-Phosphatase Activity in Conidia Reduces Adhesion and Virulence of Metarhizium anisopliae on the Host Insect Dysdercus peruvianus. Current Microbiology. 66(5). 467–474. 25 indexed citations
14.
Rocco-Machado, Nathália, et al.. (2013). NADPH Oxidase Biology and the Regulation of Tyrosine Kinase Receptor Signaling and Cancer Drug Cytotoxicity. International Journal of Molecular Sciences. 14(2). 3683–3704. 59 indexed citations
15.
Cosentino‐Gomes, Daniela, Nathália Rocco-Machado, & José Roberto Meyer‐Fernandes. (2012). Cell Signaling through Protein Kinase C Oxidation and Activation. International Journal of Molecular Sciences. 13(9). 10697–10721. 216 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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