Vito Türk

46.4k total citations · 8 hit papers
424 papers, 25.3k citations indexed

About

Vito Türk is a scholar working on Molecular Biology, Cancer Research and Oncology. According to data from OpenAlex, Vito Türk has authored 424 papers receiving a total of 25.3k indexed citations (citations by other indexed papers that have themselves been cited), including 246 papers in Molecular Biology, 148 papers in Cancer Research and 84 papers in Oncology. Recurrent topics in Vito Türk's work include Protease and Inhibitor Mechanisms (144 papers), Peptidase Inhibition and Analysis (70 papers) and Enzyme Production and Characterization (45 papers). Vito Türk is often cited by papers focused on Protease and Inhibitor Mechanisms (144 papers), Peptidase Inhibition and Analysis (70 papers) and Enzyme Production and Characterization (45 papers). Vito Türk collaborates with scholars based in Slovenia, Germany and United States. Vito Türk's co-authors include Boris Turk, Wolfram Bode, Veronika Stoka, Janko Kos, Olga Vasiljeva, Brigita Lenar≷cic̆, Anka Ritonja, Gregor Gunčar, M. Renko and Iztok Dolenc and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Vito Türk

419 papers receiving 24.8k citations

Hit Papers

Cysteine cathepsins: From... 1988 2026 2000 2013 2011 1991 2000 2001 1992 250 500 750 1000

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Vito Türk 12.8k 7.1k 4.3k 3.0k 2.8k 424 25.3k
Richard J. Simpson 27.6k 2.2× 9.4k 1.3× 5.2k 1.2× 2.2k 0.7× 1.8k 0.6× 558 42.5k
Boris Turk 7.7k 0.6× 4.6k 0.7× 3.0k 0.7× 2.2k 0.7× 1.3k 0.5× 231 16.1k
William S. Lane 28.0k 2.2× 6.8k 1.0× 5.5k 1.3× 3.9k 1.3× 2.3k 0.8× 201 36.8k
Christopher M. Overall 11.8k 0.9× 10.8k 1.5× 9.5k 2.2× 2.2k 0.7× 1.1k 0.4× 297 28.1k
Geoffrey M. Wahl 21.7k 1.7× 4.8k 0.7× 11.1k 2.6× 2.6k 0.9× 1.4k 0.5× 178 30.1k
James Travis 7.4k 0.6× 5.1k 0.7× 3.0k 0.7× 1.4k 0.5× 1.2k 0.4× 286 19.6k
Philip S. Low 15.7k 1.2× 1.7k 0.2× 4.7k 1.1× 2.8k 0.9× 5.8k 2.1× 521 36.9k
Wolfram Bode 15.0k 1.2× 6.6k 0.9× 5.5k 1.3× 2.2k 0.7× 998 0.4× 282 28.0k
Yue Xiong 24.3k 1.9× 5.4k 0.8× 11.3k 2.6× 5.0k 1.7× 2.2k 0.8× 254 34.2k
William M. Bonner 25.4k 2.0× 5.5k 0.8× 6.2k 1.4× 2.6k 0.8× 1.8k 0.6× 143 33.4k

Countries citing papers authored by Vito Türk

Since Specialization
Citations

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

Fields of papers citing papers by Vito Türk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vito Türk

This figure shows the co-authorship network connecting the top 25 collaborators of Vito Türk. A scholar is included among the top collaborators of Vito Türk 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 Vito Türk. Vito Türk 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.
Loboda, Jure, Emmanuelle Merquiol, Boris Turk, et al.. (2025). Development and Application of Small Molecule–Peptide Conjugates as Cathepsin K-Specific Covalent Irreversible Inhibitors in Human Osteoclast and Lung Cancer. JACS Au. 5(3). 1104–1120. 4 indexed citations
2.
Ladányi, Márta, Meta Sterniša, Milica Perišić Nanut, et al.. (2024). Exposure to specific fungal lectins during adhesion impairs biofilm formation of Listeria on polystyrene. Microbial Biotechnology. 17(12). e70040–e70040. 1 indexed citations
3.
Loboda, Jure, Francis Impens, Robert Vidmar, et al.. (2023). Proteomic data and structure analysis combined reveal interplay of structural rigidity and flexibility on selectivity of cysteine cathepsins. Communications Biology. 6(1). 450–450. 4 indexed citations
4.
Kordiš, Dušan & Vito Türk. (2023). Origin and Early Diversification of the Papain Family of Cysteine Peptidases. International Journal of Molecular Sciences. 24(14). 11761–11761. 5 indexed citations
5.
Stoka, Veronika, Olga Vasiljeva, Hiroshi Nakanishi, & Vito Türk. (2023). The Role of Cysteine Protease Cathepsins B, H, C, and X/Z in Neurodegenerative Diseases and Cancer. International Journal of Molecular Sciences. 24(21). 15613–15613. 16 indexed citations
6.
Petek, Marko, Tjaša Lukan, Katja Stare, et al.. (2022). A mini-TGA protein modulates gene expression through heterogeneous association with transcription factors. PLANT PHYSIOLOGY. 191(3). 1934–1952. 7 indexed citations
7.
Mikhaylov, Georgy, Miha Butinar, Vito Türk, et al.. (2022). Theranostic Applications of an Ultra-Sensitive T1 and T2 Magnetic Resonance Contrast Agent Based on Cobalt Ferrite Spinel Nanoparticles. Cancers. 14(16). 4026–4026. 5 indexed citations
8.
Mons, Elma, Ineke D.C. Jansen, Jure Loboda, et al.. (2019). The Alkyne Moiety as a Latent Electrophile in Irreversible Covalent Small Molecule Inhibitors of Cathepsin K. Journal of the American Chemical Society. 141(8). 3507–3514. 79 indexed citations
9.
Tomašič, Tihomir, et al.. (2018). Application of fragment based virtual screening towards inhibition of bacterial N- acetyglucosaminidase $. SAR and QSAR in environmental research. 29(9). 647–660. 2 indexed citations
10.
Vidmar, Robert, Matej Vizovišek, Vito Türk, Boris Turk, & Marko Fonovič. (2017). Protease cleavage site fingerprinting by label‐free in‐gel degradomics reveals pH ‐dependent specificity switch of legumain. The EMBO Journal. 36(16). 2455–2465. 63 indexed citations
11.
Renko, M., Jerica Sabotič, Jože Brzin, & Vito Türk. (2009). Structural studies of mycocypins, a new family of cysteine protease inhibitors. Acta Crystallographica Section A Foundations of Crystallography. 65(a1). s136–s136. 1 indexed citations
12.
Ivanova, Saška, et al.. (2008). Chapter Nine Lysosomes in Apoptosis. Methods in enzymology on CD-ROM/Methods in enzymology. 442. 183–199. 71 indexed citations
13.
Štefanić, Zoran, et al.. (2007). Preliminary crystallographic study of Streptomyces coelicolor single-stranded DNA-binding protein. Croatica Chemica Acta. 80(1). 35–39. 4 indexed citations
14.
Golouh, Rastko, et al.. (2001). Immunochemical Localisation of Cathepsin S, Cathepsin L and MHC Class II-Associated p41 Isoform of Invariant Chain in Human Lymph Node Tissue. Biological Chemistry. 382(5). 799–804. 15 indexed citations
15.
Štrukelj, Borut, et al.. (2000). Cloning and Expression of Functional Equistatin. Biological Chemistry. 381(1). 85–8. 8 indexed citations
16.
Cimerman, Nina, et al.. (1999). Interaction of Cystatin C Variants with Papain and Human Cathepsins B, H and L. Journal of enzyme inhibition. 14(2). 167–174. 41 indexed citations
18.
Štrukelj, Borut, et al.. (1995). Molecular cloning and sequence analysis of human preprocathepsin C. FEBS Letters. 369(2-3). 326–330. 71 indexed citations
19.
Lenar≷cic̆, Brigita, Anka Ritonja, Boris Turk, Iztok Dolenc, & Vito Türk. (1992). Characterization and Structure of Pineapple Stem Inhibitor of Cysteine Proteinases. Biological Chemistry Hoppe-Seyler. 373(2). 459–464. 16 indexed citations
20.
Keil-Dlouhá, V. & Vito Türk. (1988). Structural analogies between adhesive proteins and cysteine proteinase inhibitors.. Biological Chemistry Hoppe-Seyler. 199–204. 1 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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