Luis Chávez-Sanchéz

969 total citations
37 papers, 755 citations indexed

About

Luis Chávez-Sanchéz is a scholar working on Immunology, Rheumatology and Oncology. According to data from OpenAlex, Luis Chávez-Sanchéz has authored 37 papers receiving a total of 755 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Immunology, 12 papers in Rheumatology and 7 papers in Oncology. Recurrent topics in Luis Chávez-Sanchéz's work include Systemic Lupus Erythematosus Research (11 papers), Immune Cell Function and Interaction (10 papers) and T-cell and B-cell Immunology (10 papers). Luis Chávez-Sanchéz is often cited by papers focused on Systemic Lupus Erythematosus Research (11 papers), Immune Cell Function and Interaction (10 papers) and T-cell and B-cell Immunology (10 papers). Luis Chávez-Sanchéz collaborates with scholars based in Mexico, United States and United Kingdom. Luis Chávez-Sanchéz's co-authors include Adriana Karina Chávez-Rueda, Francisco Blanco-Favéla, María Victoria Legorreta-Haquet, Eduardo Montoya-Díaz, Emiliano Tesoro-Cruz, Ezequiel M. Fuentes‐Pananá, Edgar Zenteno, Lourdes Arriaga‐Pizano, Mariela Bernabe-Garcı́a and Yadira Ledesma‐Soto and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Annals of the New York Academy of Sciences.

In The Last Decade

Luis Chávez-Sanchéz

34 papers receiving 739 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luis Chávez-Sanchéz Mexico 15 413 196 113 108 108 37 755
María Victoria Legorreta-Haquet Mexico 14 361 0.9× 167 0.9× 100 0.9× 108 1.0× 106 1.0× 26 704
Heather L. Caslin United States 14 402 1.0× 216 1.1× 202 1.8× 69 0.6× 51 0.5× 34 853
Daniel Crean Ireland 16 319 0.8× 323 1.6× 110 1.0× 84 0.8× 46 0.4× 33 889
Fernando Alvarez Canada 17 332 0.8× 352 1.8× 201 1.8× 210 1.9× 46 0.4× 31 1.1k
Erna Sziksz Hungary 14 167 0.4× 207 1.1× 93 0.8× 118 1.1× 34 0.3× 29 665
Anne Lise Ferrara Italy 15 344 0.8× 302 1.5× 38 0.3× 67 0.6× 41 0.4× 39 795
Adriaan Duijvestijn Netherlands 11 257 0.6× 187 1.0× 159 1.4× 93 0.9× 26 0.2× 14 596
Claus Haase Denmark 20 485 1.2× 201 1.0× 46 0.4× 95 0.9× 107 1.0× 32 897
Jennifer Kench United States 10 424 1.0× 214 1.1× 55 0.5× 99 0.9× 47 0.4× 12 792
M. Zaeem Cader United Kingdom 9 365 0.9× 296 1.5× 71 0.6× 115 1.1× 218 2.0× 13 883

Countries citing papers authored by Luis Chávez-Sanchéz

Since Specialization
Citations

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

Fields of papers citing papers by Luis Chávez-Sanchéz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Luis Chávez-Sanchéz. 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 Luis Chávez-Sanchéz. The network helps show where Luis Chávez-Sanchéz may publish in the future.

Co-authorship network of co-authors of Luis Chávez-Sanchéz

This figure shows the co-authorship network connecting the top 25 collaborators of Luis Chávez-Sanchéz. A scholar is included among the top collaborators of Luis Chávez-Sanchéz 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 Luis Chávez-Sanchéz. Luis Chávez-Sanchéz 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.
Ferreira‐Hermosillo, Aldo, et al.. (2025). Circulating T Cell Subsets in Type 1 Diabetes. Cells. 14(1). 48–48.
2.
Bonifaz, Laura C., et al.. (2025). Cytotoxic Molecules as Potential Biomarkers for Active and Inactive Systemic Lupus Erythematosus. Biomedicines. 13(7). 1559–1559.
3.
Chávez-Rueda, Adriana Karina, et al.. (2024). Exosomes as Regulators of Macrophages in Cardiovascular Diseases. Biomedicines. 12(12). 2683–2683. 5 indexed citations
4.
Legorreta-Haquet, María Victoria, et al.. (2024). Hormones and B-cell development in health and autoimmunity. Frontiers in Immunology. 15. 1385501–1385501. 18 indexed citations
5.
Montesinos, Juan José, et al.. (2023). Human Bone Marrow Mesenchymal Stem Cells Promote the M2 Phenotype in Macrophages Derived from STEMI Patients. International Journal of Molecular Sciences. 24(22). 16257–16257. 3 indexed citations
6.
Legorreta-Haquet, María Victoria, et al.. (2022). The effect of prolactin on immune cell subsets involved in SLE pathogenesis. Frontiers in Immunology. 13. 1016427–1016427. 20 indexed citations
7.
Fuentes‐Pananá, Ezequiel M., et al.. (2021). Prolactin Increases the Frequency of Follicular T Helper Cells with Enhanced IL21 Secretion and OX40 Expression in Lupus-Prone MRL/lpr Mice. Journal of Immunology Research. 2021. 1–15. 8 indexed citations
8.
Bernabe-Garcı́a, Mariela, et al.. (2021). Efficacy of Docosahexaenoic Acid for the Prevention of Necrotizing Enterocolitis in Preterm Infants: A Randomized Clinical Trial. Nutrients. 13(2). 648–648. 13 indexed citations
9.
Chávez-Sanchéz, Luis, et al.. (2020). Effect of Interleukin‐17 in the Activation of Monocyte Subsets in Patients with ST‐Segment Elevation Myocardial Infarction. Journal of Immunology Research. 2020(1). 13 indexed citations
10.
Blanco-Favéla, Francisco, et al.. (2019). Role of interleukin-17 in acute myocardial infarction. Molecular Immunology. 107. 71–78. 36 indexed citations
11.
Blanco-Favéla, Francisco, et al.. (2017). Effect of Native and Minimally Modified Low-density Lipoprotein on the Activation of Monocyte Subsets. Archives of Medical Research. 48(5). 432–440. 1 indexed citations
12.
Blanco-Favéla, Francisco, et al.. (2017). IL-17-differentiated macrophages secrete pro-inflammatory cytokines in response to oxidized low-density lipoprotein. Lipids in Health and Disease. 16(1). 196–196. 44 indexed citations
13.
Legorreta-Haquet, María Victoria, Adriana Karina Chávez-Rueda, Luis Chávez-Sanchéz, et al.. (2016). Function of Treg Cells Decreased in Patients With Systemic Lupus Erythematosus Due To the Effect of Prolactin. Medicine. 95(5). e2384–e2384. 32 indexed citations
14.
Bernabe-Garcı́a, Mariela, Mardia López‐Alarcón, Francisco Blanco-Favéla, et al.. (2014). Oral administration of n-3 long-chain fatty acids reduce inflammatory response and improve clinical outcomes in patients with cardiovascular surgery. 20(6). 145–160. 8 indexed citations
15.
Chávez-Sanchéz, Luis, et al.. (2014). Clinical outcome in patients with acute coronary syndrome and outward remodeling is associated with a predominant inflammatory response. BMC Research Notes. 7(1). 669–669. 4 indexed citations
16.
Blanco-Favéla, Francisco, María Victoria Legorreta-Haquet, Adriana Karina Chávez-Rueda, et al.. (2012). Participación de la prolactina en la respuesta inmune. Boletín Médico del Hospital Infantil de México. 69(5). 329–336. 4 indexed citations
17.
Ledesma‐Soto, Yadira, Francisco Blanco-Favéla, Ezequiel M. Fuentes‐Pananá, et al.. (2012). Increased levels of prolactin receptor expression correlate with the early onset of lupus symptoms and increased numbers of transitional-1 B cells after prolactin treatment. BMC Immunology. 13(1). 11–11. 30 indexed citations
18.
Montoya-Díaz, Eduardo, et al.. (2011). Prolactin Promoter Polymorphism (−1149 G/T) is Associated with ANTI–DNA Antibodies in Mexican Patients with Systemic Lupus Erythematosus. Immunological Investigations. 40(6). 614–626. 9 indexed citations
19.
Chávez-Sanchéz, Luis, et al.. (2010). Activation of TLR2 and TLR4 by minimally modified low-density lipoprotein in human macrophages and monocytes triggers the inflammatory response. Human Immunology. 71(8). 737–744. 75 indexed citations
20.
Chávez-Rueda, Adriana Karina, et al.. (2007). Effect of Prolactin on Lymphocyte Activation from Systemic Lupus Erythematosus Patients. Annals of the New York Academy of Sciences. 1108(1). 157–165. 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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