Ricardo Borges

3.5k total citations
125 papers, 2.8k citations indexed

About

Ricardo Borges is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ricardo Borges has authored 125 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Molecular Biology, 50 papers in Cell Biology and 45 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ricardo Borges's work include Cellular transport and secretion (46 papers), Lipid Membrane Structure and Behavior (38 papers) and Ion channel regulation and function (18 papers). Ricardo Borges is often cited by papers focused on Cellular transport and secretion (46 papers), Lipid Membrane Structure and Behavior (38 papers) and Ion channel regulation and function (18 papers). Ricardo Borges collaborates with scholars based in Spain, United States and United Kingdom. Ricardo Borges's co-authors include José David Machado, Antonio G. Garcı́a, Marcial Camacho, R. Mark Wightman, Luis Gandı́a, Natalia Domínguez, Javier García‐Sancho, Mónica S. Montesinos, Jésica Díaz‐Vera and Karin Pihel and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neuroscience.

In The Last Decade

Ricardo Borges

122 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ricardo Borges Spain 30 1.9k 1.1k 1.0k 363 202 125 2.8k
Ling-Gang Wu United States 23 2.6k 1.4× 1.4k 1.2× 1.3k 1.3× 341 0.9× 139 0.7× 26 3.5k
Nael Nadif Kasri Netherlands 37 2.3k 1.2× 959 0.8× 516 0.5× 277 0.8× 186 0.9× 103 3.5k
Xiaoyan Bao China 13 2.6k 1.4× 522 0.5× 312 0.3× 438 1.2× 331 1.6× 21 3.5k
Hiromu Yawo Japan 40 1.7k 0.9× 2.8k 2.4× 373 0.4× 261 0.7× 91 0.5× 115 4.9k
Kevin D. Gillis United States 31 1.6k 0.9× 1.1k 1.0× 611 0.6× 167 0.5× 175 0.9× 55 2.8k
Zhuan Zhou China 38 3.1k 1.6× 2.6k 2.3× 701 0.7× 624 1.7× 197 1.0× 124 5.2k
Ali Salahpour Canada 33 3.7k 2.0× 2.7k 2.3× 470 0.5× 280 0.8× 104 0.5× 63 5.1k
Hidekazu Tanaka Japan 28 3.3k 1.7× 2.4k 2.1× 1.1k 1.0× 496 1.4× 59 0.3× 74 6.4k
Akikazu Fujita Japan 35 2.9k 1.5× 1.0k 0.9× 966 1.0× 677 1.9× 185 0.9× 102 4.4k
Felix E. Schweizer United States 26 1.7k 0.9× 1.4k 1.2× 1.0k 1.0× 404 1.1× 81 0.4× 54 2.7k

Countries citing papers authored by Ricardo Borges

Since Specialization
Citations

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

Fields of papers citing papers by Ricardo Borges

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ricardo Borges

This figure shows the co-authorship network connecting the top 25 collaborators of Ricardo Borges. A scholar is included among the top collaborators of Ricardo Borges 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 Ricardo Borges. Ricardo Borges 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.
Carabelli, Valentina, et al.. (2023). Multielectrode Arrays as a Means to Study Exocytosis in Human Platelets. Biosensors. 13(1). 86–86. 5 indexed citations
2.
Castañeyra-Ruiz, Leandro, Ibrahim González-Marrero, Emilia M. Carmona-Calero, et al.. (2022). AQP4 labels a subpopulation of white matter-dependent glial radial cells affected by pediatric hydrocephalus, and its expression increased in glial microvesicles released to the cerebrospinal fluid in obstructive hydrocephalus. Acta Neuropathologica Communications. 10(1). 41–41. 16 indexed citations
3.
Estévez‐Herrera, Judith, et al.. (2021). Glucagon-like peptide-1 receptor controls exocytosis in chromaffin cells by increasing full-fusion events. Cell Reports. 36(8). 109609–109609. 8 indexed citations
4.
5.
Estévez‐Herrera, Judith, et al.. (2016). ATP: The crucial component of secretory vesicles. Proceedings of the National Academy of Sciences. 113(28). E4098–106. 63 indexed citations
6.
Domínguez, Natalia, et al.. (2012). Preparation and Culture of Adrenal Chromaffin Cells. Methods in molecular biology. 846. 223–234. 11 indexed citations
7.
Borges, Ricardo, et al.. (2012). Vesicular Ca2+ mediates granule motion and exocytosis. Cell Calcium. 51(3-4). 338–341. 15 indexed citations
8.
Montesinos, Mónica S., José David Machado, Ricardo Borges, et al.. (2011). Ouabain enhances exocytosis through the regulation of calcium handling by the endoplasmic reticulum of chromaffin cells. Cell Calcium. 50(4). 332–342. 11 indexed citations
9.
Díaz‐Vera, Jésica, Juan R. Hernández‐Fernaud, Marcial Camacho, et al.. (2010). Chromogranin B Gene Ablation Reduces the Catecholamine Cargo and Decelerates Exocytosis in Chromaffin Secretory Vesicles. Journal of Neuroscience. 30(3). 950–957. 45 indexed citations
10.
Machado, José David, et al.. (2010). Chromogranins A and B as Regulators of Vesicle Cargo and Exocytosis. Cellular and Molecular Neurobiology. 30(8). 1181–1187. 32 indexed citations
11.
Montesinos, Mónica S., et al.. (2010). The quantal secretion of catecholamines is impaired by the accumulation of β‐adrenoceptor antagonists into chromaffin cell vesicles. British Journal of Pharmacology. 159(7). 1548–1556. 18 indexed citations
12.
Machado, José David, Marcial Camacho, Javier Álvarez, & Ricardo Borges. (2009). On the role of intravesicular calcium in the motion and exocytosis of secretory organelles. Communicative & Integrative Biology. 2(2). 71–73. 20 indexed citations
13.
Carabelli, Valentina, Andrea Marcantoni, Valentina Comunanza, et al.. (2007). Chronic hypoxia up‐regulates α1HT‐type channels and low‐threshold catecholamine secretion in rat chromaffin cells. The Journal of Physiology. 584(1). 149–165. 85 indexed citations
14.
Garcı́a, Antonio G., et al.. (2006). Calcium Signaling and Exocytosis in Adrenal Chromaffin Cells. Physiological Reviews. 86(4). 1093–1131. 272 indexed citations
15.
Machado, José David, et al.. (2001). cAMP Modulates Exocytotic Kinetics and Increases Quantal Size in Chromaffin Cells. Molecular Pharmacology. 60(3). 514–520. 72 indexed citations
16.
Machado, José David, et al.. (2000). Nitric Oxide Modulates a Late Step of Exocytosis. Journal of Biological Chemistry. 275(27). 20274–20279. 69 indexed citations
17.
Álvarez, Consuelo Vélez, et al.. (1997). Interaction between G protein-operated receptors eliciting secretion in rat adrenals. Biochemical Pharmacology. 53(3). 317–325. 7 indexed citations
18.
Gandı́a, Luis, Mércedes Villarroya, Baldomero Lara, et al.. (1996). Otilonium: a potent blocker of neuronal nicotinic ACh receptors in bovine chromaffin cells. British Journal of Pharmacology. 117(3). 463–470. 9 indexed citations
19.
Borges, Ricardo. (1994). Histamine H1 receptor activation mediates the preferential release of adrenaline in the rat adrenal gland. Life Sciences. 54(9). 631–640. 26 indexed citations
20.
López, Manuela G., Consuelo Sancho, Ricardo de Pascual, et al.. (1991). Membrane-mediated effects of the steroid 17-alpha-estradiol on adrenal catecholamine release.. Journal of Pharmacology and Experimental Therapeutics. 259(1). 279–285. 29 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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