Robert Kypta

6.3k total citations · 2 hit papers
59 papers, 5.3k citations indexed

About

Robert Kypta is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Robert Kypta has authored 59 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 11 papers in Pulmonary and Respiratory Medicine and 10 papers in Cellular and Molecular Neuroscience. Recurrent topics in Robert Kypta's work include Wnt/β-catenin signaling in development and cancer (33 papers), Cancer-related gene regulation (23 papers) and Prostate Cancer Treatment and Research (11 papers). Robert Kypta is often cited by papers focused on Wnt/β-catenin signaling in development and cancer (33 papers), Cancer-related gene regulation (23 papers) and Prostate Cancer Treatment and Research (11 papers). Robert Kypta collaborates with scholars based in United Kingdom, Spain and Germany. Robert Kypta's co-authors include Yoshiaki Kawano, Jonathan Waxman, Sara A. Courtneidge, Emin T. Ulug, Yves Goldberg, María dM Vivanco, Nora Bengoa‐Vergniory, Hua Su, Louis F. Reichardt and Pinar Uysal‐Onganer and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Robert Kypta

58 papers receiving 5.2k citations

Hit Papers

Secreted antagonists of the Wnt signalling pathway 1990 2026 2002 2014 2003 1990 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert Kypta United Kingdom 32 4.0k 991 656 629 611 59 5.3k
Yoshiki Murakumo Japan 38 3.3k 0.8× 1.1k 1.1× 849 1.3× 338 0.5× 432 0.7× 129 4.7k
M. Graziella Persico Italy 41 4.4k 1.1× 1.2k 1.2× 722 1.1× 478 0.8× 949 1.6× 69 6.4k
Valérie Ferreira Netherlands 22 3.4k 0.8× 904 0.9× 1.0k 1.6× 364 0.6× 749 1.2× 30 5.0k
Gretchen Frantz United States 34 3.7k 0.9× 1.6k 1.7× 831 1.3× 451 0.7× 493 0.8× 45 6.1k
Drazen B. Zimonjic United States 40 4.2k 1.0× 1.6k 1.6× 1.2k 1.8× 500 0.8× 855 1.4× 91 6.5k
Anthony M.C. Brown United States 41 4.7k 1.2× 1.1k 1.1× 698 1.1× 329 0.5× 1.3k 2.1× 66 6.3k
Lisa Garrett United States 25 3.1k 0.8× 1.3k 1.3× 503 0.8× 252 0.4× 874 1.4× 50 5.0k
Noriko Gotoh Japan 39 5.0k 1.2× 1.3k 1.3× 1.9k 3.0× 439 0.7× 351 0.6× 116 6.4k
Craig A. Dionne United States 37 3.9k 1.0× 804 0.8× 469 0.7× 304 0.5× 484 0.8× 56 5.5k
Michael R. Bösl Germany 28 3.4k 0.9× 429 0.4× 269 0.4× 394 0.6× 498 0.8× 40 5.0k

Countries citing papers authored by Robert Kypta

Since Specialization
Citations

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

Fields of papers citing papers by Robert Kypta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert Kypta

This figure shows the co-authorship network connecting the top 25 collaborators of Robert Kypta. A scholar is included among the top collaborators of Robert Kypta 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 Robert Kypta. Robert Kypta 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.
Aurrekoetxea-Rodríguez, Iskander, So Young Lee, Miriam Rábano, et al.. (2024). Polyoxometalate inhibition of SOX2-mediated tamoxifen resistance in breast cancer. Cell Communication and Signaling. 22(1). 425–425. 2 indexed citations
2.
Soliman, Sameh S. M., et al.. (2022). Dickkopf-3: An Update on a Potential Regulator of the Tumor Microenvironment. Cancers. 14(23). 5822–5822. 3 indexed citations
3.
Gorroño‐Etxebarria, Irantzu, Urko Aguirre, Nerea González, et al.. (2019). Wnt-11 as a Potential Prognostic Biomarker and Therapeutic Target in Colorectal Cancer. Cancers. 11(7). 908–908. 17 indexed citations
4.
Gorroño‐Etxebarria, Irantzu, Malin Åkerfelt, Mikael C. Puustinen, et al.. (2018). Frizzled-8 integrates Wnt-11 and transforming growth factor-β signaling in prostate cancer. Nature Communications. 9(1). 1747–1747. 84 indexed citations
5.
González‐Gualda, Estela, et al.. (2018). CRISPR-Mediated Reactivation of DKK3 Expression Attenuates TGF-β Signaling in Prostate Cancer. Cancers. 10(6). 165–165. 37 indexed citations
6.
Mazo, Claudia, et al.. (2018). In Silico Approach for Immunohistochemical Evaluation of a Cytoplasmic Marker in Breast Cancer. Cancers. 10(12). 517–517. 5 indexed citations
7.
Ramos, Adriana, Isaac Rosa, Irantzu Gorroño‐Etxebarria, et al.. (2018). Proteomic Studies Reveal Disrupted in Schizophrenia 1 as a Player in Both Neurodevelopment and Synaptic Function. International Journal of Molecular Sciences. 20(1). 119–119. 4 indexed citations
8.
Domenici, Giacomo, Jennifer H. Steel, Miriam Rábano, et al.. (2018). Protective effect of stromal Dickkopf-3 in prostate cancer: opposing roles for TGFBI and ECM-1. Oncogene. 37(39). 5305–5324. 48 indexed citations
9.
Kypta, Robert, et al.. (2017). WNT signalling in prostate cancer. Nature Reviews Urology. 14(11). 683–696. 266 indexed citations
10.
Bengoa‐Vergniory, Nora, et al.. (2016). Identification of Noncanonical Wnt Receptors Required for Wnt-3a-Induced Early Differentiation of Human Neural Stem Cells. Molecular Neurobiology. 54(8). 6213–6224. 18 indexed citations
11.
Porlan, Eva, José Manuel Morante‐Redolat, Antonella Consiglio, et al.. (2014). MT5-MMP regulates adult neural stem cell functional quiescence through the cleavage of N-cadherin. Nature Cell Biology. 16(7). 629–638. 87 indexed citations
12.
Romero, Diana, Yoshiaki Kawano, Nora Bengoa‐Vergniory, et al.. (2013). Downregulation of Dickkopf-3 disrupts prostate acinar morphogenesis through TGF-β/Smad signaling. Journal of Cell Science. 126(Pt 8). 1858–67. 29 indexed citations
13.
Uysal‐Onganer, Pinar & Robert Kypta. (2011). Wnt11 in 2011 – the regulation and function of a non‐canonical Wnt. Acta Physiologica. 204(1). 52–64. 63 indexed citations
14.
Uysal‐Onganer, Pinar, Yoshiaki Kawano, Marjorie M. Walker, et al.. (2010). Wnt-11 promotes neuroendocrine-like differentiation, survival and migration of prostate cancer cells. Molecular Cancer. 9(1). 55–55. 137 indexed citations
16.
Kawano, Yohei, et al.. (2009). Secreted Frizzled-related protein-1 is a negative regulator of androgen receptor activity in prostate cancer. British Journal of Cancer. 100(7). 1165–1174. 39 indexed citations
17.
Giannini, Ana L.M., María dM Vivanco, & Robert Kypta. (2000). α-Catenin Inhibits β-Catenin Signaling by Preventing Formation of a β-Catenin·T-cell Factor·DNA Complex. Journal of Biological Chemistry. 275(29). 21883–21888. 76 indexed citations
18.
Giannini, Ana L.M., María dM Vivanco, & Robert Kypta. (2000). Analysis of β-Catenin Aggregation and Localization Using GFP Fusion Proteins: Nuclear Import of α-Catenin by the β-Catenin/Tcf Complex. Experimental Cell Research. 255(2). 207–220. 39 indexed citations
19.
Yoshida, Cathleen K., et al.. (1995). Identification of integrin α3β1 as a neuronal thrombospondin receptor mediating neurite outgrowth. Neuron. 15(2). 333–343. 148 indexed citations
20.
Kypta, Robert, Yves Goldberg, Emin T. Ulug, & Sara A. Courtneidge. (1990). Association between the PDGF receptor and members of the src family of tyrosine kinases. Cell. 62(3). 481–492. 581 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026