Rommel Chacón‐Salinas

1.7k total citations
63 papers, 1.3k citations indexed

About

Rommel Chacón‐Salinas is a scholar working on Immunology, Infectious Diseases and Epidemiology. According to data from OpenAlex, Rommel Chacón‐Salinas has authored 63 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Immunology, 16 papers in Infectious Diseases and 13 papers in Epidemiology. Recurrent topics in Rommel Chacón‐Salinas's work include Mast cells and histamine (15 papers), Tuberculosis Research and Epidemiology (10 papers) and Immune Cell Function and Interaction (10 papers). Rommel Chacón‐Salinas is often cited by papers focused on Mast cells and histamine (15 papers), Tuberculosis Research and Epidemiology (10 papers) and Immune Cell Function and Interaction (10 papers). Rommel Chacón‐Salinas collaborates with scholars based in Mexico, United States and United Kingdom. Rommel Chacón‐Salinas's co-authors include Iris Estrada‐García, Sergio Estrada‐Parra, Alma Chávez‐Blanco, Jeanet Serafín‐López, Stephen E. Ullrich, Marcia Campillo-Navarro, Sirenia González‐Pozos, Alberto Yairh Limón-Flores, Sonia Mayra Pérez‐Tapia and Saé Muñiz‐Hernández and has published in prestigious journals such as The Journal of Immunology, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Rommel Chacón‐Salinas

59 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rommel Chacón‐Salinas Mexico	21	732	414	326	325	113	63	1.3k
Mary Fafutis‐Morris Mexico	19	613 0.8×	387 0.9×	243 0.7×	247 0.8×	139 1.2×	49	1.3k
Aleh Bobr United States	10	598 0.8×	628 1.5×	274 0.8×	548 1.7×	117 1.0×	25	1.5k
Denise Morais da Fonseca Brazil	19	808 1.1×	330 0.8×	263 0.8×	245 0.8×	211 1.9×	49	1.5k
Emmanuel Stephen‐Victor France	21	647 0.9×	386 0.9×	154 0.5×	221 0.7×	245 2.2×	42	1.4k
Óscar Medina‐Contreras Mexico	19	712 1.0×	565 1.4×	142 0.4×	138 0.4×	127 1.1×	55	1.5k
Fotini Paliogianni Greece	22	599 0.8×	430 1.0×	332 1.0×	252 0.8×	122 1.1×	46	1.7k
Takuma Misawa Japan	15	1.0k 1.4×	1.0k 2.5×	231 0.7×	165 0.5×	112 1.0×	20	1.9k
Mingjian Fei United States	9	1.2k 1.6×	285 0.7×	288 0.9×	187 0.6×	333 2.9×	19	1.8k
Michihiro Takahama Japan	12	913 1.2×	1000 2.4×	288 0.9×	155 0.5×	107 0.9×	21	1.8k
Shresh Pathak United States	19	587 0.8×	513 1.2×	396 1.2×	500 1.5×	140 1.2×	28	1.6k

Countries citing papers authored by Rommel Chacón‐Salinas

Since Specialization

Citations

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

Fields of papers citing papers by Rommel Chacón‐Salinas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rommel Chacón‐Salinas. 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 Rommel Chacón‐Salinas. The network helps show where Rommel Chacón‐Salinas may publish in the future.

Co-authorship network of co-authors of Rommel Chacón‐Salinas

This figure shows the co-authorship network connecting the top 25 collaborators of Rommel Chacón‐Salinas. A scholar is included among the top collaborators of Rommel Chacón‐Salinas 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 Rommel Chacón‐Salinas. Rommel Chacón‐Salinas 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

Chacón‐Salinas, Rommel, et al.. (2025). N-Glycosylation of Antibodies: Biological Effects During Infections and Therapeutic Applications. Antibodies. 14(4). 93–93.

Gómez‐Martín, Diana, Jiram Torres‐Ruiz, José Francisco Muñóz-Valle, et al.. (2025). Mast cell activation signature as a potential biomarker in COVID-19. Immunology Letters. 275. 107026–107026.

Schcolnik‐Cabrera, Alejandro, Rommel Chacón‐Salinas, Rocío Morales‐Bárcenas, et al.. (2025). Epigenetic reprogramming of mast and cancer cells modifies tumor-promoting cytokine networks. Medical Oncology. 42(9). 371–371.

Hernández‐Chiñas, Ulises, Armando Gamboa‐Domínguez, Juan Carlos León‐Contreras, et al.. (2024). Mast Cell Carboxypeptidase A3 Is Associated with Pulmonary Fibrosis Secondary to COVID-19. International Journal of Molecular Sciences. 25(22). 12258–12258. 2 indexed citations

Campillo-Navarro, Marcia, Jorge Barrios‐Payán, Dulce Mata‐Espinosa, et al.. (2024). Impaired control of Mycobacterium tuberculosis infection in mast cell-deficient KitW-sh/W−sh mice. Tuberculosis. 150. 102587–102587. 1 indexed citations

Díaz, L., et al.. (2023). Dengue Virus Increases the Expression of TREM-1 and CD10 on Human Neutrophils. Viral Immunology. 36(3). 176–185. 3 indexed citations

García‐Rocha, Rosario, Alberto Monroy, Jorge Hernández‐Montes, et al.. (2022). Evidence that cervical cancer cells cultured as tumorspheres maintain high CD73 expression and increase their protumor characteristics through TGF‐β production. Cell Biochemistry and Function. 40(7). 760–772. 10 indexed citations

Campillo-Navarro, Marcia, Juan Carlos Yam‐Puc, Sergio Estrada‐Parra, et al.. (2021). TLR2 Regulates Mast Cell IL-6 and IL-13 Production During Listeria monocytogenes Infection. Frontiers in Immunology. 12. 650779–650779. 12 indexed citations

Pedraza‐Escalona, Martha, et al.. (2021). Isolation and characterization of high affinity and highly stable anti-Chikungunya virus antibodies using ALTHEA Gold Libraries™. BMC Infectious Diseases. 21(1). 1121–1121. 4 indexed citations

10.

Mora‐García, María de Lourdes, Benny Weiss‐Steider, Juan José Montesinos, et al.. (2020). Detection of CD39 and a Highly Glycosylated Isoform of Soluble CD73 in the Plasma of Patients with Cervical Cancer: Correlation with Disease Progression. Mediators of Inflammation. 2020. 1–14. 10 indexed citations

11.

Mora‐García, María de Lourdes, Rosario García‐Rocha, Jorge Hernández‐Montes, et al.. (2019). Mesenchymal Stromal Cells Derived from Normal Cervix and Cervical Cancer Tumors Increase CD73 Expression in Cervical Cancer Cells Through TGF-β1 Production. Stem Cells and Development. 28(7). 477–488. 21 indexed citations

12.

Castrejón-Jiménez, Nayeli Shantal, Marcia Campillo-Navarro, Rommel Chacón‐Salinas, et al.. (2019). Ursolic and Oleanolic Acids Induce Mitophagy in A549 Human Lung Cancer Cells. Molecules. 24(19). 3444–3444. 66 indexed citations

13.

Ibáñez-Hernández, Miguel Ángel, Luvia Enid Sánchez‐Torres, Jorge Barrios‐Payán, et al.. (2019). <p>Extracellular vesicles released by J774A.1 macrophages reduce the bacterial load in macrophages and in an experimental mouse model of tuberculosis</p>. International Journal of Nanomedicine. Volume 14. 6707–6719. 22 indexed citations

14.

Mora‐García, María de Lourdes, Rosario García‐Rocha, Benny Weiss‐Steider, et al.. (2019). HPV-16 Infection Is Associated with a High Content of CD39 and CD73 Ectonucleotidases in Cervical Samples from Patients with CIN-1. Mediators of Inflammation. 2019. 1–13. 18 indexed citations

15.

Serafín‐López, Jeanet, Isabel Wong‐Baeza, Sonia Mayra Pérez‐Tapia, et al.. (2019). Valproic acid promotes a decrease in mycobacterial survival by enhancing nitric oxide production in macrophages stimulated with IFN-γ. Tuberculosis. 114. 123–126. 17 indexed citations

16.

Medina‐Rivero, Emilio, Lenin Pavón, Gabriela Mellado‐Sánchez, et al.. (2017). Transferon™, a peptide mixture with immunomodulatory properties is not immunogenic when administered with various adjuvants. Journal of Immunotoxicology. 14(1). 169–177. 3 indexed citations

17.

Campillo-Navarro, Marcia, Luis Donis‐Maturano, Jeanet Serafín‐López, et al.. (2016). Listeria monocytogenes induces mast cell extracellular traps. Immunobiology. 222(2). 432–439. 46 indexed citations

18.

Nieto-Patlán, Alejandro, Teresa Santos-Mendoza, Jeanet Serafín‐López, et al.. (2014). Differential activation of dendritic cells by Mycobacterium tuberculosis Beijing genotype. Immunological Investigations. 43(5). 436–446. 8 indexed citations

19.

Helguera‐Repetto, Addy Cecilia, Rommel Chacón‐Salinas, Jorge Francisco Cerna-Cortés, et al.. (2014). Differential Macrophage Response to Slow- and Fast-Growing Pathogenic Mycobacteria. BioMed Research International. 2014. 1–10. 29 indexed citations

20.

Limón-Flores, Alberto Yairh, et al.. (2009). Mast Cells Mediate the Immune Suppression Induced by Dermal Exposure to JP-8 Jet Fuel. Toxicological Sciences. 112(1). 144–152. 15 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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