Celia Quevedo

2.5k total citations · 1 hit paper
27 papers, 1.7k citations indexed

About

Celia Quevedo is a scholar working on Molecular Biology, Health, Toxicology and Mutagenesis and Cell Biology. According to data from OpenAlex, Celia Quevedo has authored 27 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 7 papers in Health, Toxicology and Mutagenesis and 7 papers in Cell Biology. Recurrent topics in Celia Quevedo's work include Zebrafish Biomedical Research Applications (6 papers), Environmental Toxicology and Ecotoxicology (6 papers) and Animal testing and alternatives (4 papers). Celia Quevedo is often cited by papers focused on Zebrafish Biomedical Research Applications (6 papers), Environmental Toxicology and Ecotoxicology (6 papers) and Animal testing and alternatives (4 papers). Celia Quevedo collaborates with scholars based in Spain, United States and Canada. Celia Quevedo's co-authors include Victoria Cepeda, Carlos Alonso‐Moreno, Miguel A. Fuertes, Jose M. Pérez, Alberto Alcázar, Matilde Salinas, Arantza Muriana, David R. Kaplan, Freda D. Miller and Ainhoa Alzualde and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Cell Biology and PLoS ONE.

In The Last Decade

Celia Quevedo

27 papers receiving 1.6k citations

Hit Papers

Biochemical Mechanisms of Cisplatin Cytotoxicity 2007 2026 2013 2019 2007 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Celia Quevedo Spain 18 879 410 332 163 162 27 1.7k
Michael Huang Australia 26 1.5k 1.7× 418 1.0× 253 0.8× 139 0.9× 81 0.5× 49 2.7k
Susumu Takekoshi Japan 30 941 1.1× 263 0.6× 396 1.2× 97 0.6× 44 0.3× 166 2.6k
Régis Delage-Mourroux France 23 1.6k 1.8× 374 0.9× 175 0.5× 84 0.5× 66 0.4× 49 2.7k
Yasukazu Takanezawa Japan 19 1.2k 1.4× 275 0.7× 289 0.9× 68 0.4× 134 0.8× 51 2.3k
Július Brtko Slovakia 23 691 0.8× 208 0.5× 99 0.3× 184 1.1× 123 0.8× 144 1.6k
Masaya Ueno Japan 28 1.6k 1.8× 364 0.9× 237 0.7× 82 0.5× 67 0.4× 61 2.7k
Tino Kurz Sweden 25 1.4k 1.6× 156 0.4× 359 1.1× 83 0.5× 193 1.2× 36 3.4k
Richard R. Vaillancourt United States 24 1.6k 1.8× 393 1.0× 271 0.8× 35 0.2× 108 0.7× 37 2.3k
Alfonso León‐Del‐Río Mexico 16 882 1.0× 178 0.4× 486 1.5× 220 1.3× 30 0.2× 39 1.5k
Nobuyuki Yamagishi Japan 25 834 0.9× 212 0.5× 232 0.7× 70 0.4× 47 0.3× 68 1.3k

Countries citing papers authored by Celia Quevedo

Since Specialization
Citations

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

Fields of papers citing papers by Celia Quevedo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Celia Quevedo

This figure shows the co-authorship network connecting the top 25 collaborators of Celia Quevedo. A scholar is included among the top collaborators of Celia Quevedo 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 Celia Quevedo. Celia Quevedo 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
2.
Gallego, Miguel, et al.. (2023). Validation of a zebrafish developmental defects assay as a qualified alternative test for its regulatory use following the ICH S5(R3) guideline. Reproductive Toxicology. 123. 108513–108513. 16 indexed citations
3.
Quevedo, Celia, et al.. (2020). Computational approach for collection and prediction of molecular initiating events in developmental toxicity. Reproductive Toxicology. 94. 55–64. 5 indexed citations
4.
Alzualde, Ainhoa, Mamta Behl, Nisha S. Sipes, et al.. (2018). Toxicity profiling of flame retardants in zebrafish embryos using a battery of assays for developmental toxicity, neurotoxicity, cardiotoxicity and hepatotoxicity toward human relevance. Neurotoxicology and Teratology. 70. 40–50. 127 indexed citations
5.
Alzualde, Ainhoa, Aintzane Alday, Mamta Behl, et al.. (2015). Toxicity profiling of flame retardants in zebrafish embryos using a battery of assays for teratogenicity, behavior, cardiotoxicity, and hepatotoxicity. Reproductive Toxicology. 56. 13–14. 1 indexed citations
6.
Delcourt, Nicolas, Celia Quevedo, Christelle Nonne, et al.. (2014). Targeted Identification of Sialoglycoproteins in Hypoxic Endothelial Cells and Validation in Zebrafish Reveal Roles for Proteins in Angiogenesis. Journal of Biological Chemistry. 290(6). 3405–3417. 24 indexed citations
7.
Letamendı́a, Ainhoa, et al.. (2012). Development and Validation of an Automated High-Throughput System for Zebrafish In Vivo Screenings. PLoS ONE. 7(5). e36690–e36690. 76 indexed citations
8.
Camus, Suzanne, Celia Quevedo, Sergio Ménendez, et al.. (2011). Identification of phosphorylase kinase as a novel therapeutic target through high-throughput screening for anti-angiogenesis compounds in zebrafish. Oncogene. 31(39). 4333–4342. 40 indexed citations
9.
Quevedo, Celia, Vincent Sauzeau, Mauricio Menacho-Márquez, Antonio Castro-Castro, & Xosé R. Bustelo. (2010). Vav3-deficient Mice Exhibit a Transient Delay in Cerebellar Development. Molecular Biology of the Cell. 21(6). 1125–1139. 35 indexed citations
10.
Quevedo, Celia, David R. Kaplan, & W. Brent Derry. (2007). AKT-1 Regulates DNA-Damage-Induced Germline Apoptosis in C. elegans. Current Biology. 17(3). 286–292. 58 indexed citations
11.
Cepeda, Victoria, et al.. (2007). Biochemical Mechanisms of Cisplatin Cytotoxicity. Anti-Cancer Agents in Medicinal Chemistry. 7(1). 3–18. 549 indexed citations breakdown →
12.
Cepeda, Victoria, et al.. (2006). Poly(ADP-Ribose) Polymerase-1 (PARP-1) Inhibitors in Cancer Chemotherapy. Recent Patents on Anti-Cancer Drug Discovery. 1(1). 39–53. 76 indexed citations
13.
Pérez, José M., Manuel Soto, Celia Quevedo, et al.. (2005). Poly(ADP-ribose) Polymerase-1 Inhibitor 3-Aminobenzamide Enhances Apoptosis Induction by Platinum Complexes in Cisplatin-Resistant Tumor Cells. Medicinal Chemistry. 2(1). 47–53. 47 indexed citations
14.
Quevedo, Celia, Matilde Salinas, & Alberto Alcázar. (2003). Initiation Factor 2B Activity Is Regulated by Protein Phosphatase 1, Which Is Activated by the Mitogen-activated Protein Kinase-dependent Pathway in Insulin-like Growth Factor 1-stimulated Neuronal Cells. Journal of Biological Chemistry. 278(19). 16579–16586. 25 indexed citations
15.
Dubreuil, Catherine, Celia Quevedo, Anna F. Lee, et al.. (2003). SHP-1 negatively regulates neuronal survival by functioning as a TrkA phosphatase. The Journal of Cell Biology. 163(5). 999–1010. 76 indexed citations
16.
Quevedo, Celia, Matilde Salinas, & Alberto Alcázar. (2002). Regulation of Cap-Dependent Translation by Insulin-like Growth Factor-1 in Neuronal Cells. Biochemical and Biophysical Research Communications. 291(3). 560–566. 30 indexed citations
17.
Vega, Cristina Martín de la, Jozef Bürda, Miroslava Némethová, et al.. (2001). Possible mechanisms involved in the down-regulation of translation during transient global ischaemia in the rat brain. Biochemical Journal. 357(3). 819–819. 84 indexed citations
18.
Quevedo, Celia, Alberto Alcázar, & Matilde Salinas. (2000). Two Different Signal Transduction Pathways Are Implicated in the Regulation of Initiation Factor 2B Activity in Insulin-like Growth Factor-1-stimulated Neuronal Cells. Journal of Biological Chemistry. 275(25). 19192–19197. 58 indexed citations
19.
Vega, Cristina Martín de la, Ana Maria Garcı́a, M. Elena Martı́n, et al.. (1999). Resistance of Initiation Factor 2 (eIF-2α) Kinases to Staurosporine. Cellular Signalling. 11(6). 399–404. 6 indexed citations
20.
Quevedo, Celia, et al.. (1998). Increased Activity of Eukaryotic Initiation Factor 2B in PC12 Cells in Response to Differentiation by Nerve Growth Factor. Journal of Neurochemistry. 71(5). 1905–1911. 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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