László Buday

7.1k total citations · 2 hit papers
93 papers, 6.0k citations indexed

About

László Buday is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, László Buday has authored 93 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 73 papers in Molecular Biology, 29 papers in Cell Biology and 17 papers in Oncology. Recurrent topics in László Buday's work include Protein Kinase Regulation and GTPase Signaling (29 papers), PI3K/AKT/mTOR signaling in cancer (13 papers) and Cellular Mechanics and Interactions (10 papers). László Buday is often cited by papers focused on Protein Kinase Regulation and GTPase Signaling (29 papers), PI3K/AKT/mTOR signaling in cancer (13 papers) and Cellular Mechanics and Interactions (10 papers). László Buday collaborates with scholars based in Hungary, United Kingdom and United States. László Buday's co-authors include Julian Downward, Sean E. Egan, Péter Tompa, Mary W. Brooks, Andrew Sizeland, Robert A. Weinberg, Anna F. Farago, Péter Tamás, Lívius Wunderlich and Szabolcs Sipeki and has published in prestigious journals such as Nature, Cell and Journal of Biological Chemistry.

In The Last Decade

László Buday

92 papers receiving 5.9k citations

Hit Papers

Association of Sos Ras exchange protein with Grb2 is impl... 1993 2026 2004 2015 1993 1993 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
László Buday Hungary 36 4.3k 1.4k 1.1k 936 519 93 6.0k
Michael F. Moran Canada 44 5.5k 1.3× 1.5k 1.1× 1.2k 1.1× 816 0.9× 521 1.0× 120 7.3k
Henrik Daub Germany 35 5.4k 1.3× 1.7k 1.2× 1.1k 1.0× 705 0.8× 453 0.9× 56 7.6k
Stephan M. Feller United Kingdom 39 2.9k 0.7× 837 0.6× 822 0.8× 836 0.9× 371 0.7× 104 4.5k
Nick Totty United Kingdom 29 4.3k 1.0× 851 0.6× 914 0.9× 1.1k 1.2× 523 1.0× 39 6.1k
Francis Burrows United States 39 4.9k 1.1× 1.1k 0.8× 828 0.8× 1.1k 1.1× 162 0.3× 109 6.5k
Sara Sigismund Italy 27 3.9k 0.9× 1.3k 1.0× 2.0k 1.9× 693 0.7× 423 0.8× 38 5.9k
Raymond B. Birge United States 47 3.6k 0.8× 1.1k 0.8× 1.0k 1.0× 3.2k 3.4× 836 1.6× 112 7.6k
Luisa Lanfrancone Italy 38 4.9k 1.1× 1.6k 1.2× 839 0.8× 1.2k 1.3× 503 1.0× 95 7.8k
Tohru Kataoka Japan 48 6.7k 1.6× 651 0.5× 1.7k 1.6× 763 0.8× 308 0.6× 122 8.2k
Deborah H. Anderson Canada 24 2.8k 0.7× 732 0.5× 780 0.7× 641 0.7× 302 0.6× 59 3.9k

Countries citing papers authored by László Buday

Since Specialization
Citations

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

Fields of papers citing papers by László Buday

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of László Buday

This figure shows the co-authorship network connecting the top 25 collaborators of László Buday. A scholar is included among the top collaborators of László Buday 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 László Buday. László Buday 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.
2.
Pancsa, Rita, et al.. (2024). Unveiling epithelial plasticity regulation in lung cancer: Exploring the cross-talk among Tks4 scaffold protein partners. Molecular Biology of the Cell. 35(8). ar111–ar111. 1 indexed citations
3.
Lovrics, Anna, et al.. (2024). Predictive value analysis of the interaction network of Tks4 scaffold protein in colon cancer. Frontiers in Molecular Biosciences. 11. 1414805–1414805.
4.
Takács, Tamás, et al.. (2024). Insulin receptor substrate 1 is a novel member of EGFR signaling in pancreatic cells. European Journal of Cell Biology. 103(4). 151457–151457. 3 indexed citations
5.
Schád, Éva, et al.. (2023). Absence of Scaffold Protein Tks4 Disrupts Several Signaling Pathways in Colon Cancer Cells. International Journal of Molecular Sciences. 24(2). 1310–1310. 3 indexed citations
6.
Takács, Tamás, et al.. (2023). Studying the Association of TKS4 and CD2AP Scaffold Proteins and Their Implications in the Partial Epithelial–Mesenchymal Transition (EMT) Process. International Journal of Molecular Sciences. 24(20). 15136–15136. 5 indexed citations
7.
Kudlik, Gyöngyi, Tamás Takács, László Radnai, et al.. (2020). Advances in Understanding TKS4 and TKS5: Molecular Scaffolds Regulating Cellular Processes from Podosome and Invadopodium Formation to Differentiation and Tissue Homeostasis. International Journal of Molecular Sciences. 21(21). 8117–8117. 22 indexed citations
8.
Buday, László & Virág Vas. (2020). Novel regulation of Ras proteins by direct tyrosine phosphorylation and dephosphorylation. Cancer and Metastasis Reviews. 39(4). 1067–1073. 22 indexed citations
9.
Vas, Virág, Tamás Kovács, Gyöngyi Kudlik, et al.. (2019). Significance of the Tks4 scaffold protein in bone tissue homeostasis. Scientific Reports. 9(1). 5781–5781. 11 indexed citations
10.
Borbély, Sándor, Viktor Kis, Virág Vas, et al.. (2019). Dendritic spine morphology and memory formation depend on postsynaptic Caskin proteins. Scientific Reports. 9(1). 16843–16843. 23 indexed citations
11.
Róna, Gergely, Máté Borsos, Jonathan J. Ellis, et al.. (2014). Dynamics of re-constitution of the human nuclear proteome after cell division is regulated by NLS-adjacent phosphorylation. Cell Cycle. 13(22). 3551–3564. 18 indexed citations
12.
Tantos, Ágnes, Beáta Szabó, András Láng, et al.. (2013). Multiple fuzzy interactions in the moonlighting function of thymosin-β4. PubMed. 1(1). e26204–e26204. 10 indexed citations
13.
Róna, Gergely, Mary Marfori, Máté Borsos, et al.. (2013). Phosphorylation adjacent to the nuclear localization signal of human dUTPase abolishes nuclear import: structural and mechanistic insights. Acta Crystallographica Section D Biological Crystallography. 69(12). 2495–2505. 32 indexed citations
14.
Lányi, Árpád, Zalán Péterfi, Anna Orient, et al.. (2011). The Homolog of the Five SH3-Domain Protein (HOFI/SH3PXD2B) Regulates Lamellipodia Formation and Cell Spreading. PLoS ONE. 6(8). e23653–e23653. 35 indexed citations
15.
Boussac, Hugues de, Marcin Ratajewski, Attila Tordai, et al.. (2010). The ERK1/2-Hepatocyte Nuclear Factor 4α Axis Regulates Human ABCC6 Gene Expression in Hepatocytes. Journal of Biological Chemistry. 285(30). 22800–22808. 37 indexed citations
16.
Turu, Gábor, László Szidonya, Zsuzsanna Gáborik, et al.. (2005). Differential β‐arrestin binding of AT1and AT2angiotensin receptors. FEBS Letters. 580(1). 41–45. 54 indexed citations
18.
Buday, László, Lívius Wunderlich, & Péter Tamás. (2002). The Nck family of adapter proteins. Cellular Signalling. 14(9). 723–731. 198 indexed citations
19.
Buday, László & Julian Downward. (1993). Epidermal Growth Factor Regulates the Exchange Rate of Guanine Nucleotides on p21 ras in Fibroblasts. Molecular and Cellular Biology. 13(3). 1903–1910. 107 indexed citations
20.
Hajnóczky, György, Péter Várnai, László Buday, Anna F. Farago, & András Spät. (1992). The role of protein kinase-C in control of aldosterone production by rat adrenal glomerulosa cells: activation of protein kinase-C by stimulation with potassium.. Endocrinology. 130(4). 2230–2236. 27 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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