Judit Villén

27.6k total citations · 14 hit papers
105 papers, 19.6k citations indexed

About

Judit Villén is a scholar working on Molecular Biology, Spectroscopy and Cell Biology. According to data from OpenAlex, Judit Villén has authored 105 papers receiving a total of 19.6k indexed citations (citations by other indexed papers that have themselves been cited), including 91 papers in Molecular Biology, 34 papers in Spectroscopy and 8 papers in Cell Biology. Recurrent topics in Judit Villén's work include Advanced Proteomics Techniques and Applications (34 papers), Mass Spectrometry Techniques and Applications (22 papers) and RNA and protein synthesis mechanisms (15 papers). Judit Villén is often cited by papers focused on Advanced Proteomics Techniques and Applications (34 papers), Mass Spectrometry Techniques and Applications (22 papers) and RNA and protein synthesis mechanisms (15 papers). Judit Villén collaborates with scholars based in United States, Spain and Canada. Judit Villén's co-authors include Steven P. Gygi, Sean A. Beausoleil, David P. Bartel, Chanseok Shin, Daehyun Baek, Fernando D. Camargo, Scott A. Gerber, A. John Rush, Joshua E. Elias and Mark P. Jedrychowski and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Judit Villén

104 papers receiving 19.4k citations

Hit Papers

The impact of microRNAs o... 2004 2026 2011 2018 2008 2010 2008 2006 2004 500 1000 1.5k 2.0k 2.5k
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. The impact of microRNAs on protein output
    2008 2.9k citations Judit Villén, Steven P. Gygi et al. profile →
  2. A Tissue-Specific Atlas of Mouse Protein Phosphorylation and Expression
    2010 1.3k citations Mark P. Jedrychowski, Joshua E. Elias et al. profile →
  3. A quantitative atlas of mitotic phosphorylation
    2008 1.3k citations Noah Dephoure, Chunshui Zhou et al. Proceedings of the National Academy of Sciences profile →
  4. A probability-based approach for high-throughput protein phosphorylation analysis and site localization
    2006 1.3k citations Sean A. Beausoleil, Judit Villén et al. profile →
  5. Large-scale characterization of HeLa cell nuclear phosphoproteins
    2004 1.2k citations Sean A. Beausoleil, Mark P. Jedrychowski et al. Proceedings of the National Academy of Sciences profile →
  6. Angiogenin-Induced tRNA Fragments Inhibit Translation Initiation
    2011 758 citations Judit Villén, Steven P. Gygi et al. profile →
  7. Global Analysis of Cdk1 Substrate Phosphorylation Sites Provides Insights into Evolution
    2009 716 citations Judit Villén, Steven P. Gygi et al. profile →
  8. A Conserved MST-FOXO Signaling Pathway Mediates Oxidative-Stress Responses and Extends Life Span
    2006 696 citations Judit Villén, Steven P. Gygi et al. profile →
  9. Phosphoproteomic Analysis Identifies Grb10 as an mTORC1 Substrate That Negatively Regulates Insulin Signaling
    2011 672 citations Yonghao Yu, Judit Villén et al. profile →
  10. An AMPK-FOXO Pathway Mediates Longevity Induced by a Novel Method of Dietary Restriction in C. elegans
    2007 624 citations Judit Villén, Steven P. Gygi et al. profile →
  11. Large-scale phosphorylation analysis of mouse liver
    2007 606 citations Judit Villén, Sean A. Beausoleil et al. Proceedings of the National Academy of Sciences profile →
  12. The SCX/IMAC enrichment approach for global phosphorylation analysis by mass spectrometry
    2008 508 citations Judit Villén, Steven P. Gygi profile →
  13. Global analysis of phosphorylation and ubiquitylation cross-talk in protein degradation
    2013 478 citations Danielle L. Swaney, Pedro Beltrão et al. profile →
  14. Chromatogram libraries improve peptide detection and quantification by data independent acquisition mass spectrometry
    2018 345 citations Robert Lawrence, Judit Villén et al. Nature Communications profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Judit Villén United States 53 16.1k 4.1k 3.6k 2.7k 1.5k 105 19.6k
Tamar Geiger Israel 43 8.9k 0.6× 2.7k 0.7× 1.4k 0.4× 1.6k 0.6× 1.4k 0.9× 100 12.8k
Wilhelm Haas United States 53 11.0k 0.7× 2.7k 0.7× 1.5k 0.4× 1.8k 0.6× 2.0k 1.4× 101 15.3k
Blagoy Blagoev Denmark 42 10.6k 0.7× 4.9k 1.2× 1.1k 0.3× 1.8k 0.7× 1.6k 1.1× 108 14.1k
Junmin Peng United States 78 16.9k 1.1× 2.6k 0.6× 1.8k 0.5× 3.4k 1.2× 2.8k 1.9× 257 23.0k
Shao‐En Ong United States 36 11.5k 0.7× 4.9k 1.2× 920 0.3× 1.7k 0.6× 1.5k 1.0× 81 14.3k
Shabaz Mohammed Netherlands 61 11.5k 0.7× 4.8k 1.2× 888 0.2× 1.6k 0.6× 2.4k 1.6× 182 15.4k
Florian Gnad Germany 37 11.3k 0.7× 3.3k 0.8× 808 0.2× 1.7k 0.6× 1.9k 1.3× 54 13.6k
Brian Raught Canada 60 13.9k 0.9× 1.1k 0.3× 1.5k 0.4× 2.7k 1.0× 2.2k 1.4× 172 17.3k
Tobias C. Walther United States 64 16.0k 1.0× 1.4k 0.3× 2.3k 0.7× 4.6k 1.7× 1.2k 0.8× 121 23.1k
Michael J.O. Wakelam United Kingdom 64 10.5k 0.6× 1.4k 0.3× 1.6k 0.4× 2.5k 0.9× 1.1k 0.7× 241 15.0k

Countries citing papers authored by Judit Villén

Since Specialization
Citations

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

Fields of papers citing papers by Judit Villén

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Judit Villén

This figure shows the co-authorship network connecting the top 25 collaborators of Judit Villén. A scholar is included among the top collaborators of Judit Villén 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 Judit Villén. Judit Villén 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.
Maes, Michal, Julián Ávila-Pacheco, Jan Sklenář, et al.. (2025). Preventing inappropriate signals pre- and post-ligand perception by a toggle switch mechanism of ERECTA. Proceedings of the National Academy of Sciences. 122(4). e2420196122–e2420196122. 2 indexed citations
2.
Leydon, Alexander R., Raphaël Loll‐Krippleber, Nathan M. Belliveau, et al.. (2024). A function of TPL/TBL1-type corepressors is to nucleate the assembly of the preinitiation complex. The Journal of Cell Biology. 224(2). 2 indexed citations
3.
Bradley, David, Alexander Hogrebe, Alexandre K. Dubé, et al.. (2024). The fitness cost of spurious phosphorylation. The EMBO Journal. 43(20). 4720–4751. 2 indexed citations
4.
Genereaux, Julie, et al.. (2023). Anticodon sequence determines the impact of mistranslating tRNA Ala variants. RNA Biology. 20(1). 791–804. 6 indexed citations
5.
Leutert, Mario, et al.. (2023). The regulatory landscape of the yeast phosphoproteome. Nature Structural & Molecular Biology. 30(11). 1761–1773. 19 indexed citations
6.
Berg, Matthew D., et al.. (2022). A novel mistranslating tRNA model in Drosophila melanogaster has diverse, sexually dimorphic effects. G3 Genes Genomes Genetics. 12(5). 4 indexed citations
7.
Berg, Matthew D., Raphaël Loll‐Krippleber, Bryan-Joseph San Luis, et al.. (2022). Genetic background and mistranslation frequency determine the impact of mistranslating tRNASerUGG. G3 Genes Genomes Genetics. 12(7). 1 indexed citations
8.
Lu, Yang Young, Jeff Bilmes, Ricard A. Rodríguez‐Mias, Judit Villén, & William Stafford Noble. (2021). DIAmeter: matching peptides to data-independent acquisition mass spectrometry data. Bioinformatics. 37(Supplement_1). i434–i442. 17 indexed citations
9.
Berg, Matthew D., Raphaël Loll‐Krippleber, Bryan-Joseph San Luis, et al.. (2021). The amino acid substitution affects cellular response to mistranslation. G3 Genes Genomes Genetics. 11(10). 9 indexed citations
10.
Calejman, Camila Martínez, Sophie Trefely, Amelia K. Luciano, et al.. (2020). mTORC2-AKT signaling to ATP-citrate lyase drives brown adipogenesis and de novo lipogenesis. Nature Communications. 11(1). 575–575. 106 indexed citations
11.
Entwisle, Samuel, Camila Martínez Calejman, Robert Lawrence, et al.. (2020). Proteome and Phosphoproteome Analysis of Brown Adipocytes Reveals That RICTOR Loss Dampens Global Insulin/AKT Signaling. Molecular & Cellular Proteomics. 19(7). 1104–1119. 6 indexed citations
12.
Ochoa, David, Robert Lawrence, Bachir El Debs, et al.. (2016). An atlas of human kinase regulation. Molecular Systems Biology. 12(12). 888–888. 69 indexed citations
13.
Pruneda, Jonathan N., F. Donelson Smith, Danielle L. Swaney, et al.. (2014). E2~Ub conjugates regulate the kinase activity of Shigella effector OspG during pathogenesis. The EMBO Journal. 33(5). n/a–n/a. 58 indexed citations
14.
Xiao, Kunhong, Jin‐Peng Sun, Ji‐Hee Kim, et al.. (2010). Global phosphorylation analysis of β-arrestin–mediated signaling downstream of a seven transmembrane receptor (7TMR). Proceedings of the National Academy of Sciences. 107(34). 15299–15304. 164 indexed citations
15.
Villén, Judit, Cristina Lacasa, M. Teresa Bertran, et al.. (2010). The γTuRC Revisited: A Comparative Analysis of Interphase and Mitotic Human γTuRC Redefines the Set of Core Components and Identifies the Novel Subunit GCP8. Molecular Biology of the Cell. 21(22). 3963–3972. 85 indexed citations
16.
Yu, Yonghao, Rana Anjum, Kazuishi Kubota, et al.. (2009). A site-specific, multiplexed kinase activity assay using stable-isotope dilution and high-resolution mass spectrometry. Proceedings of the National Academy of Sciences. 106(28). 11606–11611. 62 indexed citations
17.
Dephoure, Noah, Chunshui Zhou, Judit Villén, et al.. (2008). A quantitative atlas of mitotic phosphorylation. Proceedings of the National Academy of Sciences. 105(31). 10762–10767. 1303 indexed citations breakdown →
18.
Villén, Judit, Sean A. Beausoleil, Scott A. Gerber, & Steven P. Gygi. (2007). Large-scale phosphorylation analysis of mouse liver. Proceedings of the National Academy of Sciences. 104(5). 1488–1493. 606 indexed citations breakdown →
19.
Haas, Wilhelm, Brendan K. Faherty, Scott A. Gerber, et al.. (2006). Optimization and Use of Peptide Mass Measurement Accuracy in Shotgun Proteomics. Molecular & Cellular Proteomics. 5(7). 1326–1337. 233 indexed citations
20.
Beausoleil, Sean A., Mark P. Jedrychowski, Daniel Schwartz, et al.. (2004). Large-scale characterization of HeLa cell nuclear phosphoproteins. Proceedings of the National Academy of Sciences. 101(33). 12130–12135. 1190 indexed citations breakdown →

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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