Gustavo Sánchez‐Chávez

434 total citations
21 papers, 345 citations indexed

About

Gustavo Sánchez‐Chávez is a scholar working on Molecular Biology, Pharmacology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Gustavo Sánchez‐Chávez has authored 21 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 7 papers in Pharmacology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Gustavo Sánchez‐Chávez's work include Retinal Development and Disorders (8 papers), Cholinesterase and Neurodegenerative Diseases (6 papers) and Retinal Diseases and Treatments (4 papers). Gustavo Sánchez‐Chávez is often cited by papers focused on Retinal Development and Disorders (8 papers), Cholinesterase and Neurodegenerative Diseases (6 papers) and Retinal Diseases and Treatments (4 papers). Gustavo Sánchez‐Chávez collaborates with scholars based in Mexico, Spain and Italy. Gustavo Sánchez‐Chávez's co-authors include Rocı́o Salceda, Rocío Salceda, Juan R. Riesgo‐Escovar, Luis M. Salgado, Alejandro Martı́nez-Martı́nez, Cecilio J. Vidal, María Luisa Fanjul‐Moles, Piero Giulio Giulianini, Leticia Ramı́rez-Lugo and Federico Bermúdez‐Rattoni and has published in prestigious journals such as PLoS ONE, Diabetes and Journal of Cerebral Blood Flow & Metabolism.

In The Last Decade

Gustavo Sánchez‐Chávez

21 papers receiving 339 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gustavo Sánchez‐Chávez Mexico 11 159 85 61 59 43 21 345
Giacoma Galizzi Italy 14 230 1.4× 47 0.6× 53 0.9× 199 3.4× 29 0.7× 19 522
Pallavi Sharma India 12 197 1.2× 89 1.0× 101 1.7× 47 0.8× 49 1.1× 25 480
Yasutaka Takagi Japan 10 221 1.4× 61 0.7× 187 3.1× 73 1.2× 42 1.0× 20 475
Juliet A. Moncaster United States 10 220 1.4× 37 0.4× 89 1.5× 114 1.9× 49 1.1× 21 460
Mónica G. Ilincheta de Boschero Argentina 12 324 2.0× 99 1.2× 40 0.7× 133 2.3× 13 0.3× 22 540
Elena E. Korbolina Russia 11 242 1.5× 67 0.8× 86 1.4× 181 3.1× 30 0.7× 20 407
Luísa de Lemos Spain 10 211 1.3× 77 0.9× 12 0.2× 75 1.3× 25 0.6× 19 374
Jack P. Smith United States 14 320 2.0× 149 1.8× 47 0.8× 91 1.5× 35 0.8× 23 478
Rocı́o Salceda Mexico 16 331 2.1× 217 2.6× 96 1.6× 172 2.9× 60 1.4× 43 701
Feng Qian China 11 167 1.1× 71 0.8× 60 1.0× 55 0.9× 16 0.4× 17 386

Countries citing papers authored by Gustavo Sánchez‐Chávez

Since Specialization
Citations

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

Fields of papers citing papers by Gustavo Sánchez‐Chávez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gustavo Sánchez‐Chávez. 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 Gustavo Sánchez‐Chávez. The network helps show where Gustavo Sánchez‐Chávez may publish in the future.

Co-authorship network of co-authors of Gustavo Sánchez‐Chávez

This figure shows the co-authorship network connecting the top 25 collaborators of Gustavo Sánchez‐Chávez. A scholar is included among the top collaborators of Gustavo Sánchez‐Chávez 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 Gustavo Sánchez‐Chávez. Gustavo Sánchez‐Chávez 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.
Sánchez‐Chávez, Gustavo, et al.. (2023). Streptozotocin-Induced Diabetic Rats Showed a Differential Glycine Receptor Expression in the Spinal Cord: A GlyR Role in Diabetic Neuropathy. Neurochemical Research. 49(3). 684–691. 4 indexed citations
2.
Riesgo‐Escovar, Juan R., et al.. (2021). Retinal Nrf2 expression in normal and early streptozotocin-diabetic rats. Neurochemistry International. 145. 105007–105007. 9 indexed citations
3.
Sánchez‐Chávez, Gustavo, et al.. (2020). Mitochondrial bound hexokinase type I in normal and streptozotocin diabetic rat retina. Mitochondrion. 52. 212–217. 6 indexed citations
4.
Sánchez‐Chávez, Gustavo, et al.. (2019). Glycine receptor is differentially expressed in the rat retina at early stages of streptozotocin-induced diabetes. Neuroscience Letters. 712. 134506–134506. 6 indexed citations
5.
Sánchez‐Chávez, Gustavo, et al.. (2017). Nitrosative Stress in the Rat Retina at the Onset of Streptozotocin-Induced Diabetes. Cellular Physiology and Biochemistry. 42(6). 2353–2363. 21 indexed citations
6.
Sánchez‐Chávez, Gustavo, et al.. (2017). Glycine receptor subunits expression in the developing rat retina. Neurochemistry International. 108. 177–182. 6 indexed citations
7.
Montiel, Teresa, Leticia Ramı́rez-Lugo, Israela Balderas, et al.. (2017). Recurrent moderate hypoglycemia exacerbates oxidative damage and neuronal death leading to cognitive dysfunction after the hypoglycemic coma. Journal of Cerebral Blood Flow & Metabolism. 39(5). 808–821. 18 indexed citations
8.
Sánchez‐Chávez, Gustavo, et al.. (2015). Potential Role of Endoplasmic Reticulum Stress in Pathogenesis of Diabetic Retinopathy. Neurochemical Research. 41(5). 1098–1106. 23 indexed citations
9.
Sánchez‐Chávez, Gustavo, et al.. (2012). Insulin Stimulated-Glucose Transporter Glut 4 Is Expressed in the Retina. PLoS ONE. 7(12). e52959–e52959. 26 indexed citations
10.
Sánchez‐Chávez, Gustavo, et al.. (2012). Control of Glycogen Content in Retina: Allosteric Regulation of Glycogen Synthase. PLoS ONE. 7(2). e30822–e30822. 9 indexed citations
11.
Fanjul‐Moles, María Luisa, et al.. (2010). CIRCADIAN MODULATION OF CRUSTACEAN HYPERGLYCEMIC HORMONE IN CRAYFISH EYESTALK AND RETINA. Chronobiology International. 27(1). 34–51. 14 indexed citations
12.
Sánchez‐Chávez, Gustavo & Rocı́o Salceda. (2008). Enzimas polifuncionales: El caso de la acetilcolinesterasa. 27(2). 44–51. 5 indexed citations
13.
Salceda, Rocı́o, et al.. (2008). l-Arginine Uptake in Normal and Diabetic Rat Retina and Retinal Pigment Epithelium. Neurochemical Research. 33(8). 1541–1545. 9 indexed citations
14.
Sánchez‐Chávez, Gustavo, et al.. (2008). Effect of Diabetes on Glycogen Metabolism in Rat Retina. Neurochemical Research. 33(7). 1301–1308. 20 indexed citations
15.
Riesgo‐Escovar, Juan R., et al.. (2008). Glycine transporters (glycine transporter 1 and glycine transporter 2) are expressed in retina. Neuroreport. 19(13). 1295–1299. 8 indexed citations
16.
Sánchez‐Chávez, Gustavo & Rocı́o Salceda. (2001). Acetyl- and butyrylcholinesterase molecular forms in normal and streptozotocin-diabetic rat retinal pigment epithelium. Neurochemistry International. 39(3). 209–215. 5 indexed citations
17.
Sánchez‐Chávez, Gustavo & Rocı́o Salceda. (2001). Acetyl- and Butyrylcholinesterase in Normal and Diabetic Rat Retina. Neurochemical Research. 26(2). 153–159. 16 indexed citations
18.
Salceda, Rocı́o & Gustavo Sánchez‐Chávez. (2000). Calcium uptake, release and ryanodine binding in melanosomes from retinal pigment epithelium. Cell Calcium. 27(4). 223–229. 48 indexed citations
19.
Sánchez‐Chávez, Gustavo & Rocı́o Salceda. (2000). Effect of Streptozotocin‐Induced Diabetes on Activities of Cholinesterases in the Rat Retina. IUBMB Life. 49(4). 283–287. 41 indexed citations
20.
Sánchez‐Chávez, Gustavo, Cecilio J. Vidal, & Rocı́o Salceda. (1995). Acetyl‐ and butyrylcholinesterase activities in the rat retina and retinal pigment epithelium. Journal of Neuroscience Research. 41(5). 655–662. 11 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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