Jaime Gosálvez

10.3k total citations
328 papers, 6.6k citations indexed

About

Jaime Gosálvez is a scholar working on Reproductive Medicine, Public Health, Environmental and Occupational Health and Molecular Biology. According to data from OpenAlex, Jaime Gosálvez has authored 328 papers receiving a total of 6.6k indexed citations (citations by other indexed papers that have themselves been cited), including 170 papers in Reproductive Medicine, 127 papers in Public Health, Environmental and Occupational Health and 101 papers in Molecular Biology. Recurrent topics in Jaime Gosálvez's work include Sperm and Testicular Function (169 papers), Reproductive Biology and Fertility (124 papers) and Chromosomal and Genetic Variations (57 papers). Jaime Gosálvez is often cited by papers focused on Sperm and Testicular Function (169 papers), Reproductive Biology and Fertility (124 papers) and Chromosomal and Genetic Variations (57 papers). Jaime Gosálvez collaborates with scholars based in Spain, Australia and United Kingdom. Jaime Gosálvez's co-authors include José Luís Fernández, Carmen López‐Fernández, V. Goyanes, R. Roy, Ashok Agarwal, Stephen D. Johnston, María Enciso, C. González-Marín, Sandro C. Esteves and Rebeca Santiso and has published in prestigious journals such as The Science of The Total Environment, Applied and Environmental Microbiology and Hepatology.

In The Last Decade

Jaime Gosálvez

320 papers receiving 6.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jaime Gosálvez Spain 40 4.3k 3.4k 1.6k 1.3k 874 328 6.6k
B. Colenbrander Netherlands 52 4.9k 1.2× 4.9k 1.5× 1.7k 1.1× 1.8k 1.4× 689 0.8× 232 8.4k
John C. Herr United States 51 4.2k 1.0× 2.9k 0.9× 1.7k 1.0× 3.0k 2.3× 294 0.3× 207 7.7k
Donald P. Evenson United States 44 6.0k 1.4× 4.9k 1.5× 1.6k 1.0× 840 0.7× 406 0.5× 81 7.3k
Marc Yeste Spain 44 4.9k 1.2× 4.2k 1.2× 816 0.5× 1.2k 1.0× 400 0.5× 279 6.7k
Anders Johannisson Sweden 45 4.1k 1.0× 3.7k 1.1× 1.1k 0.7× 630 0.5× 407 0.5× 199 6.5k
Dickson D. Varner United States 42 3.3k 0.8× 2.7k 0.8× 838 0.5× 711 0.6× 284 0.3× 222 4.7k
Fernando J. Peña Spain 50 4.9k 1.2× 4.0k 1.2× 753 0.5× 764 0.6× 440 0.5× 179 6.1k
J.M. Vázquez Spain 48 4.7k 1.1× 4.7k 1.4× 1.7k 1.0× 993 0.8× 260 0.3× 233 7.0k
Jordi Roca Spain 50 5.4k 1.3× 5.0k 1.5× 1.6k 1.0× 1.3k 1.0× 258 0.3× 224 7.2k
Barry A. Ball United States 43 3.8k 0.9× 3.4k 1.0× 735 0.5× 691 0.5× 301 0.3× 219 6.1k

Countries citing papers authored by Jaime Gosálvez

Since Specialization
Citations

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

Fields of papers citing papers by Jaime Gosálvez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jaime Gosálvez

This figure shows the co-authorship network connecting the top 25 collaborators of Jaime Gosálvez. A scholar is included among the top collaborators of Jaime Gosálvez 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 Jaime Gosálvez. Jaime Gosálvez 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.
Johnston, Stephen D., et al.. (2025). The Nexus Between Sperm Membrane Integrity, Sperm Motility, and DNA Fragmentation. Membranes. 15(4). 109–109. 1 indexed citations
2.
Gosálvez, Jaime, et al.. (2024). Role of DNase Activity in Human Sperm DNA Fragmentation. Biomolecules. 14(3). 304–304. 2 indexed citations
3.
4.
Gosálvez, Jaime, et al.. (2021). Antibiotic toxicity on human spermatozoa assessed using the sperm DNA fragmentation dynamic assay. Andrologia. 54(2). e14328–e14328. 7 indexed citations
5.
Gallego, Raquel Del, Ernesto A. Gómez, J.L. Yániz, et al.. (2020). Effect of Sperm Concentration and Storage Temperature on Goat Spermatozoa during Liquid Storage. Biology. 9(9). 300–300. 21 indexed citations
6.
Ortíz, I., et al.. (2019). Effect of permeable cryoprotectant‐free vitrification on DNA fragmentation of equine oocyte–cumulus cells. Reproduction in Domestic Animals. 54(S3). 53–56. 5 indexed citations
7.
Dorado, J., et al.. (2019). Relationship between DNA fragmentation of equine granulosa cells and oocyte meiotic competence after in vitro maturation. Reproduction in Domestic Animals. 54(S4). 78–81. 3 indexed citations
8.
Santiso, Rebeca, et al.. (2018). Rapid Determination of Resistance to Antibiotic Inhibitors of Protein Synthesis in Staphylococcus aureus Through In Situ Evaluation of DNase Activity. Microbial Drug Resistance. 24(6). 739–746. 1 indexed citations
9.
Gosálvez, Jaime, et al.. (2018). DNA fragmentation in epididymal freeze-dried ram spermatozoa impairs embryo development. Zenodo (CERN European Organization for Nuclear Research). 24 indexed citations
10.
Ortíz, I., J. Dorado, Jane M. Morrell, et al.. (2017). New approach to assess sperm DNA fragmentation dynamics: Fine-tuning mathematical models. Journal of Animal Science and Biotechnology. 8(1). 23–23. 5 indexed citations
11.
Gosálvez, Jaime, Carmen López‐Fernández, & Stephen D. Johnston. (2016). Whole extra-charged DNA spermatozoa in the saltwater crocodile (Crocodylus porosus) ejaculate. Herpetological Journal. 26(4). 313–316. 3 indexed citations
12.
Barrachina, Laura, Ana Rosa Remacha, Antonio Romero, et al.. (2016). Priming Equine Bone Marrow-Derived Mesenchymal Stem Cells with Proinflammatory Cytokines: Implications in Immunomodulation–Immunogenicity Balance, Cell Viability, and Differentiation Potential. Stem Cells and Development. 26(1). 15–24. 79 indexed citations
13.
14.
Ortíz, I., J. Dorado, Jane M. Morrell, et al.. (2015). Effect of single-layer centrifugation or washing on frozen–thawed donkey semen quality: Do they have the same effect regardless of the quality of the sample?. Theriogenology. 84(2). 294–300. 30 indexed citations
15.
López, Carlos Monge, et al.. (2010). Mejora de la calidad seminal en inseminación artificial. 21(225). 28–33. 1 indexed citations
16.
Johnston, Stephen D., Robert Hermes, F. Arroyo, et al.. (2009). Frozen-thawed rhinoceros sperm exhibit DNA damage shortly after thawing when assessed by the sperm chromatin dispersion assay. Theriogenology. 72(5). 711–720. 23 indexed citations
17.
Pita, Miguel, Mario Zabal‐Aguirre, F. Arroyo, et al.. (2007). Arcyptera fusca and Arcyptera tornosi repetitive DNA families: whole‐comparative genomic hybridization (W‐CGH) as a novel approach to the study of satellite DNA libraries. Journal of Evolutionary Biology. 21(1). 352–361. 7 indexed citations
18.
Gosálvez, Jaime, et al.. (2000). DNA breakage detection-fish (DBD-FISH): effect of unwinding time. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 453(1). 83–88. 12 indexed citations
19.
Fernández, José Luís, Jaime Gosálvez, & V. Goyanes. (1993). Detection of DNA strand breaks induced by hydroxyl radicals in nuclear and chromosomal chromatin by electron microscopy.. PubMed. 73(294-295). 189–95. 3 indexed citations
20.
Gosálvez, Jaime & V. Goyanes. (1988). Selective digestion of mouse chromosomes with restriction endonucleases. Cytogenetic and Genome Research. 48(4). 198–200. 12 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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