Manuel Mendoza

1.4k total citations
27 papers, 935 citations indexed

About

Manuel Mendoza is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Manuel Mendoza has authored 27 papers receiving a total of 935 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 12 papers in Cell Biology and 7 papers in Plant Science. Recurrent topics in Manuel Mendoza's work include Microtubule and mitosis dynamics (11 papers), Genomics and Chromatin Dynamics (10 papers) and Fungal and yeast genetics research (8 papers). Manuel Mendoza is often cited by papers focused on Microtubule and mitosis dynamics (11 papers), Genomics and Chromatin Dynamics (10 papers) and Fungal and yeast genetics research (8 papers). Manuel Mendoza collaborates with scholars based in Spain, France and United States. Manuel Mendoza's co-authors include Michael Glotzer, Verena Jantsch, Susanne Kaitna, Yves Barral, Jeroen Dobbelaere, Caren Norden, Chitra V. Kotwaliwale, Sue Biggins, Anthony A. Hyman and Gabriel E. Neurohr and has published in prestigious journals such as Science, Cell and Nature Communications.

In The Last Decade

Manuel Mendoza

23 papers receiving 928 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manuel Mendoza Spain 12 792 593 220 84 58 27 935
Pedro A. San-Segundo Spain 22 1.3k 1.6× 306 0.5× 205 0.9× 56 0.7× 41 0.7× 39 1.4k
Neus Colomina Spain 14 718 0.9× 225 0.4× 103 0.5× 87 1.0× 33 0.6× 23 808
Marie‐Noëlle Simon France 16 786 1.0× 417 0.7× 100 0.5× 50 0.6× 89 1.5× 25 998
Caroline E. Alfa United Kingdom 9 1.1k 1.4× 632 1.1× 175 0.8× 140 1.7× 23 0.4× 13 1.2k
Kanji Furuya Japan 19 1.8k 2.3× 743 1.3× 345 1.6× 236 2.8× 17 0.3× 40 1.9k
Susanne Prinz United States 12 1.9k 2.4× 1.3k 2.2× 416 1.9× 212 2.5× 37 0.6× 12 2.1k
Frank van Drogen Switzerland 15 839 1.1× 294 0.5× 146 0.7× 149 1.8× 15 0.3× 20 922
Gislene Pereira Germany 14 1.1k 1.4× 814 1.4× 296 1.3× 48 0.6× 17 0.3× 19 1.3k
Françoise M. Roelants United States 14 1.0k 1.3× 532 0.9× 222 1.0× 15 0.2× 35 0.6× 19 1.2k
Klaus Leonhard Germany 9 966 1.2× 286 0.5× 70 0.3× 74 0.9× 19 0.3× 9 1.1k

Countries citing papers authored by Manuel Mendoza

Since Specialization
Citations

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

Fields of papers citing papers by Manuel Mendoza

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuel Mendoza

This figure shows the co-authorship network connecting the top 25 collaborators of Manuel Mendoza. A scholar is included among the top collaborators of Manuel Mendoza 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 Manuel Mendoza. Manuel Mendoza 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.
Moreno, David F., Damien Plassard, Audrey Furst, et al.. (2025). Gene-specific transcript buffering revealed by perturbation of coactivator complexes. Science Advances. 11(12). eadr1492–eadr1492.
2.
Moreno, David F., et al.. (2025). Roles of Srs2/PARI-family DNA helicases in NoCut checkpoint signaling and abscission regulation. The Journal of Cell Biology. 224(12).
3.
Cichocki, B., et al.. (2022). Nuclear pore complex acetylation regulates mRNA export and cell cycle commitment in budding yeast. The EMBO Journal. 41(15). e110271–e110271. 10 indexed citations
4.
Shah, Bhavya, Bingbing Cheng, Manuel Mendoza, et al.. (2021). Probing Cerebral Metabolism with Hyperpolarized 13C Imaging after Opening the Blood–Brain Barrier with Focused Ultrasound. ACS Chemical Neuroscience. 12(15). 2820–2828. 5 indexed citations
5.
Chen, Jun, Junjie Li, Chendong Yang, et al.. (2021). Profiling Carbohydrate Metabolism in Liver and Hepatocellular Carcinoma with [ 13 C]‐Glycerate Probes. Analysis & Sensing. 1(4). 196–202.
6.
Stefano, Marco Di, et al.. (2020). Impact of Chromosome Fusions on 3D Genome Organization and Gene Expression in Budding Yeast. Genetics. 214(3). 651–667. 7 indexed citations
7.
Mendoza, Manuel, et al.. (2020). Modulation of Cell Identity by Modification of Nuclear Pore Complexes. Frontiers in Genetics. 10. 1301–1301. 8 indexed citations
8.
Maier, Michael, et al.. (2020). Budding yeast complete DNA synthesis after chromosome segregation begins. Nature Communications. 11(1). 2267–2267. 33 indexed citations
9.
Mendoza, Manuel, et al.. (2019). The Synthesis and Biological Evaluation of Indolactam Alkaloids. Synthesis. 51(23). 4443–4451. 7 indexed citations
10.
Maya‐Miles, Douglas, Xenia Peñate, Mari Cruz Muñoz-Centeno, et al.. (2018). High levels of histones promote whole-genome-duplications and trigger a Swe1WEE1-dependent phosphorylation of Cdc28CDK1. eLife. 7. 13 indexed citations
11.
Kumar, Arun, et al.. (2018). Daughter-cell-specific modulation of nuclear pore complexes controls cell cycle entry during asymmetric division. Nature Cell Biology. 20(4). 432–442. 30 indexed citations
12.
Pryszcz, Leszek P., et al.. (2017). Distinct roles of the polarity factors Boi1 and Boi2 in the control of exocytosis and abscission in budding yeast. Molecular Biology of the Cell. 28(22). 3082–3094. 18 indexed citations
13.
Amaral, Nuno, Charlotta Funaya, Fátima-Zahra Idrissi, et al.. (2016). The Aurora-B-dependent NoCut checkpoint prevents damage of anaphase bridges after DNA replication stress. Nature Cell Biology. 18(5). 516–526. 46 indexed citations
14.
Neurohr, Gabriel E. & Manuel Mendoza. (2016). Cdc14 Localization as a Marker for Mitotic Exit: In Vivo Quantitative Analysis of Cdc14 Release. Methods in molecular biology. 1505. 59–67. 1 indexed citations
15.
Kumar, Arun & Manuel Mendoza. (2015). Time-Lapse Fluorescence Microscopy of Budding Yeast Cells. Methods in molecular biology. 1369. 1–8. 5 indexed citations
16.
Mendoza, Manuel, et al.. (2014). Chromosome length and perinuclear attachment constrain resolution of DNA intertwines. The Journal of Cell Biology. 206(6). 719–733. 20 indexed citations
17.
Neurohr, Gabriel E., Andreas Naegeli, Dominik Theler, et al.. (2011). A Midzone-Based Ruler Adjusts Chromosome Compaction to Anaphase Spindle Length. Science. 332(6028). 465–468. 75 indexed citations
18.
Mendoza, Manuel, Caren Norden, & Yves Barral. (2005). Division-Plane Positioning: Microtubules Strike Back. Current Biology. 15(15). R595–R597.
19.
Mendoza, Manuel, Stefanie Redemann, & Damian Brunner. (2005). The fission yeast MO25 protein functions in polar growth and cell separation. European Journal of Cell Biology. 84(12). 915–926. 35 indexed citations
20.
Mendoza, Manuel, Anthony A. Hyman, & Michael Glotzer. (2002). GTP Binding Induces Filament Assembly of a Recombinant Septin. Current Biology. 12(21). 1858–1863. 81 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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