Gladis Sánchez

1.1k total citations
27 papers, 936 citations indexed

About

Gladis Sánchez is a scholar working on Molecular Biology, Reproductive Medicine and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Gladis Sánchez has authored 27 papers receiving a total of 936 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 14 papers in Reproductive Medicine and 9 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Gladis Sánchez's work include Ion Transport and Channel Regulation (17 papers), Sperm and Testicular Function (14 papers) and Reproductive Biology and Fertility (9 papers). Gladis Sánchez is often cited by papers focused on Ion Transport and Channel Regulation (17 papers), Sperm and Testicular Function (14 papers) and Reproductive Biology and Fertility (9 papers). Gladis Sánchez collaborates with scholars based in United States, Brazil and France. Gladis Sánchez's co-authors include Gustavo Blanco, Robert W. Mercer, Tamara Jiménez, Jeffrey McDermott, Roger J. Melton, Joseph S. Tash, Joseph C. Koster, Eva Wertheimer, Warren G. Tourtellotte and William H. Kinsey and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Biochemistry and International Journal of Molecular Sciences.

In The Last Decade

Gladis Sánchez

25 papers receiving 929 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gladis Sánchez United States 16 521 371 275 133 89 27 936
Winnie Shum United States 19 421 0.8× 318 0.9× 226 0.8× 77 0.6× 47 0.5× 30 866
Emilia Middea Italy 15 458 0.9× 637 1.7× 367 1.3× 299 2.2× 64 0.7× 15 1.3k
Sheng Cui China 19 546 1.0× 278 0.7× 185 0.7× 236 1.8× 73 0.8× 103 1.3k
Anna Hejmej Poland 23 362 0.7× 566 1.5× 200 0.7× 323 2.4× 100 1.1× 60 1.1k
María Agustina Battistone United States 16 426 0.8× 475 1.3× 326 1.2× 113 0.8× 58 0.7× 31 1.0k
Patricia Grasso United States 21 394 0.8× 479 1.3× 201 0.7× 205 1.5× 64 0.7× 78 1.4k
Josep M. Fernández‐Novell Spain 22 465 0.9× 516 1.4× 455 1.7× 157 1.2× 298 3.3× 40 1.3k
Xiaoping Ning United States 9 261 0.5× 640 1.7× 539 2.0× 92 0.7× 41 0.5× 10 958
Xiuxia Wang China 21 521 1.0× 504 1.4× 420 1.5× 280 2.1× 52 0.6× 36 1.1k
Nadine Martinat France 17 346 0.7× 442 1.2× 215 0.8× 261 2.0× 53 0.6× 37 923

Countries citing papers authored by Gladis Sánchez

Since Specialization
Citations

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

Fields of papers citing papers by Gladis Sánchez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gladis Sánchez

This figure shows the co-authorship network connecting the top 25 collaborators of Gladis Sánchez. A scholar is included among the top collaborators of Gladis Sánchez 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 Gladis Sánchez. Gladis Sánchez 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.
2.
Sánchez, Gladis, et al.. (2024). The cystogenic effects of ouabain in autosomal dominant polycystic kidney disease require cell caveolae. Experimental Cell Research. 444(1). 114356–114356. 1 indexed citations
3.
Sánchez, Gladis, et al.. (2022). The sodium-glucose cotransporter isoform 1 (SGLT-1) is important for sperm energetics, motility, and fertility. Biology of Reproduction. 106(6). 1206–1217. 14 indexed citations
4.
5.
Ahn, Soo Hyun, Manjunatha K. Nanjappa, Jianrong Wang, et al.. (2021). Multiple Lesions Contribute to Infertility in Males Lacking Autoimmune Regulator. American Journal Of Pathology. 191(9). 1592–1609. 12 indexed citations
6.
Sánchez, Gladis, et al.. (2020). The Na+ and K+ transport system of sperm (ATP1A4) is essential for male fertility and an attractive target for male contraception†. Biology of Reproduction. 103(2). 343–356. 29 indexed citations
7.
Sánchez, Gladis, Fernando de Pilla Varotti, Cristóforo Scavone, et al.. (2019). 21-Benzylidene digoxin decreases proliferation by inhibiting the EGFR/ERK signaling pathway and induces apoptosis in HeLa cells. Steroids. 155. 108551–108551. 13 indexed citations
8.
McDermott, Jeffrey, Gladis Sánchez, Madhulika Sharma, et al.. (2017). Ouabain promotes partial epithelial to mesenchymal transition (EMT) changes in human autosomal dominant polycystic kidney disease (ADPKD) cells. Experimental Cell Research. 355(2). 142–152. 14 indexed citations
9.
Sánchez, Gladis, Brenda S. Magenheimer, Gail A. Reif, et al.. (2015). Ouabain Regulates CFTR-Mediated Anion Secretion and Na,K-ATPase Transport in ADPKD Cells. The Journal of Membrane Biology. 248(6). 1145–1157. 14 indexed citations
10.
Jiménez, Tamara, Gladis Sánchez, & Gustavo Blanco. (2012). Activity of the Na,K‐ATPase α4 Isoform Is Regulated During Sperm Capacitation to Support Sperm Motility. Journal of Andrology. 33(5). 1047–1057. 39 indexed citations
11.
McDermott, Jeffrey, Gladis Sánchez, Vargheese M. Chennathukuzhi, & Gustavo Blanco. (2012). Green fluorescence protein driven by the Na,K-ATPase α4 isoform promoter is expressed only in male germ cells of mouse testis. Journal of Assisted Reproduction and Genetics. 29(12). 1313–1325. 25 indexed citations
12.
Luo, Jinping, Vijayalaxmi Gupta, Joseph S. Tash, et al.. (2011). Role of FYN Kinase in Spermatogenesis: Defects Characteristic of Fyn-Null Sperm in Mice1. Biology of Reproduction. 86(1). 1–8. 78 indexed citations
13.
Sánchez, Gladis, et al.. (2011). Ouabain activates the Na-K-ATPase signalosome to induce autosomal dominant polycystic kidney disease cell proliferation. American Journal of Physiology-Renal Physiology. 301(4). F897–F906. 37 indexed citations
14.
Jiménez, Tamara, Gladis Sánchez, Eva Wertheimer, & Gustavo Blanco. (2010). Activity of the Na,K-ATPase α4 isoform is important for membrane potential, intracellular Ca2+, and pH to maintain motility in rat spermatozoa. Reproduction. 139(5). 835–845. 59 indexed citations
15.
Jiménez, Tamara, et al.. (2010). Increased Expression of the Na,K-ATPase alpha4 Isoform Enhances Sperm Motility in Transgenic Mice1. Biology of Reproduction. 84(1). 153–161. 34 indexed citations
16.
Pierre, Sandrine V., et al.. (2007). Isoform specificity of Na-K-ATPase-mediated ouabain signaling. American Journal of Physiology-Renal Physiology. 294(4). F859–F866. 32 indexed citations
17.
Sánchez, Gladis, et al.. (2006). The Na,K-ATPase α4 isoform from humans has distinct enzymatic properties and is important for sperm motility. Molecular Human Reproduction. 12(9). 565–576. 77 indexed citations
18.
Sánchez, Gladis & Gustavo Blanco. (2004). Residues within Transmembrane Domains 4 and 6 of the Na,K-ATPase α Subunit Are Important for Na+ Selectivity. Biochemistry. 43(28). 9061–9074. 6 indexed citations
19.
Blanco, Gustavo, Gladis Sánchez, & Robert W. Mercer. (1998). Differential Regulation of Na,K-ATPase Isozymes by Protein Kinases and Arachidonic Acid. Archives of Biochemistry and Biophysics. 359(2). 139–150. 65 indexed citations
20.
Koster, Joseph C., et al.. (1995). Kinetic Properties of the .alpha.2.beta.1 and .alpha.2.beta.2 Isoenzymes of the Na,K-ATPase. Biochemistry. 34(1). 319–325. 72 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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