José Ayté

3.0k total citations
81 papers, 2.4k citations indexed

About

José Ayté is a scholar working on Molecular Biology, Cell Biology and Clinical Biochemistry. According to data from OpenAlex, José Ayté has authored 81 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 78 papers in Molecular Biology, 19 papers in Cell Biology and 8 papers in Clinical Biochemistry. Recurrent topics in José Ayté's work include Fungal and yeast genetics research (42 papers), Genomics and Chromatin Dynamics (18 papers) and RNA Research and Splicing (17 papers). José Ayté is often cited by papers focused on Fungal and yeast genetics research (42 papers), Genomics and Chromatin Dynamics (18 papers) and RNA Research and Splicing (17 papers). José Ayté collaborates with scholars based in Spain, United States and United Kingdom. José Ayté's co-authors include Elena Hidalgo, Ana Vivancos, Sarela García‐Santamarina, Fausto G. Hegardt, Susanna Boronat, Miriam Sansó, Natalia Gabrielli, Isabel A. Calvo, Mercè Carmona and Alice Zuin and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

José Ayté

80 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
José Ayté Spain 31 2.1k 362 272 168 161 81 2.4k
Aleš Vančura United States 26 1.8k 0.9× 319 0.9× 197 0.7× 132 0.8× 248 1.5× 74 2.3k
Mário H. Barros Brazil 23 1.6k 0.7× 142 0.4× 90 0.3× 181 1.1× 192 1.2× 56 2.0k
Nadine Camougrand France 30 2.0k 1.0× 422 1.2× 248 0.9× 143 0.9× 163 1.0× 64 2.6k
Joanna Rytka Poland 24 1.8k 0.8× 318 0.9× 236 0.9× 60 0.4× 77 0.5× 77 2.0k
Byungchan Ahn South Korea 19 1.2k 0.6× 184 0.5× 148 0.5× 335 2.0× 42 0.3× 41 2.0k
Alaattin Kaya United States 20 882 0.4× 208 0.6× 198 0.7× 213 1.3× 142 0.9× 37 1.4k
Andréa Hamann Germany 21 1.2k 0.6× 181 0.5× 267 1.0× 203 1.2× 24 0.1× 50 1.6k
Gino Heeren Austria 14 885 0.4× 120 0.3× 145 0.5× 203 1.2× 66 0.4× 17 1.2k
Masaki Mizunuma Japan 18 1.1k 0.5× 158 0.4× 193 0.7× 183 1.1× 58 0.4× 52 1.6k
Takemitsu Furuchi Japan 22 1.2k 0.6× 294 0.8× 104 0.4× 113 0.7× 552 3.4× 62 1.8k

Countries citing papers authored by José Ayté

Since Specialization
Citations

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

Fields of papers citing papers by José Ayté

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of José Ayté

This figure shows the co-authorship network connecting the top 25 collaborators of José Ayté. A scholar is included among the top collaborators of José Ayté 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 José Ayté. José Ayté 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.
Boronat, Susanna, et al.. (2025). The glutathione system maintains the thiol redox balance in the mitochondria of fission yeast. Free Radical Biology and Medicine. 234. 100–112. 1 indexed citations
2.
Vega, Montserrat Rojo de la, Susanna Boronat, Sarela García‐Santamarina, et al.. (2025). Distinct roles of histone H2B ubiquitination at promoters and coding regions of Pol II-transcribed stress genes. Genome biology. 26(1). 419–419. 1 indexed citations
3.
Vega, Montserrat Rojo de la, Isabel Alves‐Rodrigues, Roger Anglada, et al.. (2025). Nrm1 is a bistable switch connecting cell cycle progression to transcriptional control. EMBO Reports. 26(20). 5048–5069.
4.
Vega, Montserrat Rojo de la, David Castillo, Roger Anglada, et al.. (2023). Topoisomerase 1 facilitates nucleosome reassembly at stress genes during recovery. Nucleic Acids Research. 51(22). 12161–12173. 5 indexed citations
5.
Albà, M. Mar, et al.. (2023). Comparing Mitochondrial Activity, Oxidative Stress Tolerance, and Longevity of Thirteen Ascomycota Yeast Species. Antioxidants. 12(10). 1810–1810. 6 indexed citations
6.
Pérez, Pilar, et al.. (2022). Stress-induced cell depolarization through the MAP kinase–Cdc42 axis. Trends in Cell Biology. 33(2). 124–137. 4 indexed citations
7.
Corral-Ramos, Cristina, et al.. (2021). TOR and MAP kinase pathways synergistically regulate autophagy in response to nutrient depletion in fission yeast. Autophagy. 18(2). 375–390. 32 indexed citations
8.
Ayté, José, et al.. (2020). Phosphorylation of the Transcription Factor Atf1 at Multiple Sites by the MAP Kinase Sty1 Controls Homologous Recombination and Transcription. Journal of Molecular Biology. 432(19). 5430–5446. 8 indexed citations
9.
Cabrera, Margarita, Susanna Boronat, Montserrat Rojo de la Vega, et al.. (2020). Chaperone-Facilitated Aggregation of Thermo-Sensitive Proteins Shields Them from Degradation during Heat Stress. Cell Reports. 30(7). 2430–2443.e4. 37 indexed citations
10.
Boronat, Susanna, et al.. (2019). Identification of ubiquitin-proteasome system components affecting the degradation of the transcription factor Pap1. Redox Biology. 28. 101305–101305. 9 indexed citations
11.
Carmona, Mercè, Iria Medraño-Fernández, Roberto Sitia, et al.. (2019). Monitoring cytosolic H2O2 fluctuations arising from altered plasma membrane gradients or from mitochondrial activity. Nature Communications. 10(1). 4526–4526. 37 indexed citations
12.
Schmidt, Henning, et al.. (2016). Prp4 Kinase Grants the License to Splice: Control of Weak Splice Sites during Spliceosome Activation. PLoS Genetics. 12(1). e1005768–e1005768. 25 indexed citations
13.
García‐Santamarina, Sarela, et al.. (2014). Monitoring in vivo reversible cysteine oxidation in proteins using ICAT and mass spectrometry. Nature Protocols. 9(5). 1131–1145. 78 indexed citations
14.
Gabrielli, Natalia, José Ayté, & Elena Hidalgo. (2012). Cells Lacking Pfh1, a Fission Yeast Homolog of Mammalian Frataxin Protein, Display Constitutive Activation of the Iron Starvation Response. Journal of Biological Chemistry. 287(51). 43042–43051. 15 indexed citations
15.
Guerra-Moreno, Ángel, Isabel Alves‐Rodrigues, Elena Hidalgo, & José Ayté. (2012). Chemical genetic induction of meiosis inSchizosaccharomyces pombe. Cell Cycle. 11(8). 1621–1625. 26 indexed citations
16.
Zuin, Alice, Ana Vivancos, Miriam Sansó, et al.. (2005). The Glycolytic Metabolite Methylglyoxal Activates Pap1 and Sty1 Stress Responses in Schizosaccharomyces pombe. Journal of Biological Chemistry. 280(44). 36708–36713. 49 indexed citations
17.
Vivancos, Ana, et al.. (2003). Schizosaccharomyces pombe Cells Lacking the Ran-binding Protein Hba1 Show a Multidrug Resistance Phenotype Due to Constitutive Nuclear Accumulation of Pap1. Journal of Biological Chemistry. 278(42). 40565–40572. 33 indexed citations
18.
Borgne, Annie, Hiroshi Murakami, José Ayté, & Paul Nurse. (2002). The G1/S Cyclin Cig2p during Meiosis in Fission Yeast. Molecular Biology of the Cell. 13(6). 2080–2090. 35 indexed citations
19.
20.
Haro, Diego, Pedro F. Marrero, José Ayté, & Fausto G. Hegardt. (1990). Identification of a cholesterol‐regulated 180‐kDA microsomal protein in rat hepatocytes. European Journal of Biochemistry. 188(1). 123–129. 4 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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