Israela Balderas

1.3k total citations
18 papers, 1.0k citations indexed

About

Israela Balderas is a scholar working on Cellular and Molecular Neuroscience, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Israela Balderas has authored 18 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cellular and Molecular Neuroscience, 15 papers in Cognitive Neuroscience and 5 papers in Molecular Biology. Recurrent topics in Israela Balderas's work include Memory and Neural Mechanisms (14 papers), Neuroscience and Neuropharmacology Research (12 papers) and Receptor Mechanisms and Signaling (4 papers). Israela Balderas is often cited by papers focused on Memory and Neural Mechanisms (14 papers), Neuroscience and Neuropharmacology Research (12 papers) and Receptor Mechanisms and Signaling (4 papers). Israela Balderas collaborates with scholars based in Mexico, United States and France. Israela Balderas's co-authors include Federico Bermúdez‐Rattoni, Carlos J. Rodríguez‐Ortiz, Victor Ramı́rez-Amaya, Martha L. Escobar, James L. McGaugh, Perla Moreno‐Castilla, Paola Torre, Antonello Bonci, Ross A. McDevitt and Rosa Anna Maria Marino and has published in prestigious journals such as Journal of Neuroscience, Neuroscience and Journal of Cerebral Blood Flow & Metabolism.

In The Last Decade

Israela Balderas

18 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Israela Balderas Mexico 16 665 549 239 160 129 18 1.0k
Jeff L. Weiner United States 22 883 1.3× 363 0.7× 370 1.5× 246 1.5× 123 1.0× 38 1.3k
Chris Barkus United Kingdom 15 523 0.8× 321 0.6× 278 1.2× 92 0.6× 161 1.2× 19 943
Olusegun J. Ariwodola United States 18 628 0.9× 276 0.5× 242 1.0× 179 1.1× 110 0.9× 22 923
Tali Kobilo United States 9 520 0.8× 501 0.9× 221 0.9× 137 0.9× 187 1.4× 10 1.1k
Marvin R. Diaz United States 21 689 1.0× 286 0.5× 250 1.0× 168 1.1× 88 0.7× 39 1.2k
Amy Taylor United Kingdom 15 699 1.1× 560 1.0× 304 1.3× 115 0.7× 240 1.9× 35 1.4k
Volker Korz Germany 18 598 0.9× 502 0.9× 238 1.0× 358 2.2× 136 1.1× 53 1.1k
Torfi Sigurdsson Germany 14 898 1.4× 1.1k 1.9× 356 1.5× 224 1.4× 124 1.0× 18 1.6k
Loren M. DeVito United States 12 575 0.9× 486 0.9× 349 1.5× 89 0.6× 175 1.4× 14 1.3k
Sophie Dix United Kingdom 16 717 1.1× 829 1.5× 265 1.1× 119 0.7× 118 0.9× 24 1.4k

Countries citing papers authored by Israela Balderas

Since Specialization
Citations

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

Fields of papers citing papers by Israela Balderas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Israela Balderas

This figure shows the co-authorship network connecting the top 25 collaborators of Israela Balderas. A scholar is included among the top collaborators of Israela Balderas 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 Israela Balderas. Israela Balderas is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Balderas, Israela, et al.. (2023). The anterior insula and its projection to amygdala nuclei modulate the abstinence-exacerbated expression of conditioned place preference. Psychopharmacology. 241(3). 445–459. 4 indexed citations
2.
Balderas, Israela, Perla Moreno‐Castilla, Ross A. McDevitt, et al.. (2020). Glutamatergic basolateral amygdala to anterior insular cortex circuitry maintains rewarding contextual memory. Communications Biology. 3(1). 139–139. 28 indexed citations
3.
Moreno‐Castilla, Perla, et al.. (2017). Hippocampal release of dopamine and norepinephrine encodes novel contextual information. Hippocampus. 27(5). 547–557. 41 indexed citations
4.
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
5.
McDevitt, Ross A., Hui Shen, Israela Balderas, et al.. (2014). Serotonergic versus Nonserotonergic Dorsal Raphe Projection Neurons: Differential Participation in Reward Circuitry. Cell Reports. 8(6). 1857–1869. 153 indexed citations
6.
Balderas, Israela, Carlos J. Rodríguez‐Ortiz, & Federico Bermúdez‐Rattoni. (2014). Consolidation and reconsolidation of object recognition memory. Behavioural Brain Research. 285. 213–222. 42 indexed citations
7.
Rodríguez‐Ortiz, Carlos J., et al.. (2014). Retrieval is not necessary to trigger reconsolidation of object recognition memory in the perirhinal cortex. Learning & Memory. 21(9). 452–456. 27 indexed citations
8.
Balderas, Israela, Carlos J. Rodríguez‐Ortiz, & Federico Bermúdez‐Rattoni. (2013). Retrieval and reconsolidation of object recognition memory are independent processes in the perirhinal cortex. Neuroscience. 253. 398–405. 48 indexed citations
9.
Balderas, Israela, Perla Moreno‐Castilla, & Federico Bermúdez‐Rattoni. (2013). Dopamine D1 receptor activity modulates object recognition memory consolidation in the perirhinal cortex but not in the hippocampus. Hippocampus. 23(10). 873–878. 39 indexed citations
10.
Rodríguez‐Ortiz, Carlos J., Israela Balderas, Paola Torre, & Federico Bermúdez‐Rattoni. (2012). Taste aversion memory reconsolidation is independent of its retrieval. Neurobiology of Learning and Memory. 98(3). 215–219. 51 indexed citations
11.
Balderas, Israela, et al.. (2012). Muscarinic receptors activity in the perirhinal cortex and hippocampus has differential involvement in the formation of recognition memory. Neurobiology of Learning and Memory. 97(4). 418–424. 22 indexed citations
12.
Torre, Paola, Carlos J. Rodríguez‐Ortiz, Israela Balderas, & Federico Bermúdez‐Rattoni. (2010). Differential participation of temporal structures in the consolidation and reconsolidation of taste aversion extinction. European Journal of Neuroscience. 32(6). 1018–1023. 31 indexed citations
13.
Rodríguez‐Ortiz, Carlos J., et al.. (2010). Long-term aversive taste memory requires insular and amygdala protein degradation. Neurobiology of Learning and Memory. 95(3). 311–315. 40 indexed citations
14.
Balderas, Israela, et al.. (2008). The consolidation of object and context recognition memory involve different regions of the temporal lobe. Learning & Memory. 15(9). 618–624. 179 indexed citations
15.
Cruz, Vanesa De la, Carlos J. Rodríguez‐Ortiz, Israela Balderas, & Federico Bermúdez‐Rattoni. (2008). Medial temporal lobe structures participate differentially in consolidation of safe and aversive taste memories. European Journal of Neuroscience. 28(7). 1377–1381. 35 indexed citations
16.
17.
Balderas, Israela, et al.. (2004). Cambios morfológicos asociados a la memoria. Revista de Neurología. 38(10). 944–944. 3 indexed citations
18.
Ramı́rez-Amaya, Victor, et al.. (2001). Spatial Long-Term Memory Is Related to Mossy Fiber Synaptogenesis. Journal of Neuroscience. 21(18). 7340–7348. 149 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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