Dima Kozakov

15.7k total citations · 6 hit papers
129 papers, 10.1k citations indexed

About

Dima Kozakov is a scholar working on Molecular Biology, Computational Theory and Mathematics and Materials Chemistry. According to data from OpenAlex, Dima Kozakov has authored 129 papers receiving a total of 10.1k indexed citations (citations by other indexed papers that have themselves been cited), including 118 papers in Molecular Biology, 55 papers in Computational Theory and Mathematics and 44 papers in Materials Chemistry. Recurrent topics in Dima Kozakov's work include Protein Structure and Dynamics (76 papers), Computational Drug Discovery Methods (55 papers) and Enzyme Structure and Function (42 papers). Dima Kozakov is often cited by papers focused on Protein Structure and Dynamics (76 papers), Computational Drug Discovery Methods (55 papers) and Enzyme Structure and Function (42 papers). Dima Kozakov collaborates with scholars based in United States, Russia and Israel. Dima Kozakov's co-authors include Sándor Vajda, Dmitri Beglov, David R. Hall, Kathryn A. Porter, Christine Yueh, Ryan Brenke, Dzmitry Padhorny, Bing Xia, Tanggis Bohnuud and Stephen R. Comeau and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Chemical Society Reviews.

In The Last Decade

Dima Kozakov

127 papers receiving 10.0k citations

Hit Papers

The ClusPro web server for protein–pro... 2006 2026 2012 2019 2017 2006 2013 2015 2020 500 1000 1.5k 2.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dima Kozakov United States 44 7.7k 2.1k 1.3k 1.2k 1.0k 129 10.1k
Dina Schneidman‐Duhovny United States 41 7.2k 0.9× 1.3k 0.6× 1.8k 1.5× 862 0.7× 701 0.7× 84 10.0k
Maxim Totrov United States 44 6.2k 0.8× 2.8k 1.3× 1.5k 1.2× 724 0.6× 621 0.6× 117 9.0k
Dmitri Beglov United States 30 5.1k 0.7× 1.2k 0.6× 626 0.5× 877 0.7× 752 0.7× 51 6.9k
Marc A. Martı́-Renom Spain 45 11.5k 1.5× 980 0.5× 1.6k 1.3× 583 0.5× 897 0.9× 123 15.4k
David B. Ascher Australia 46 6.9k 0.9× 2.6k 1.2× 853 0.7× 564 0.5× 537 0.5× 187 11.8k
Gabriel Studer Switzerland 17 9.5k 1.2× 977 0.5× 953 0.8× 505 0.4× 1.1k 1.1× 22 15.2k
Koushik Kasavajhala United States 7 6.7k 0.9× 1.4k 0.7× 1.3k 1.1× 422 0.3× 500 0.5× 9 9.4k
Martino Bertoni Switzerland 11 8.4k 1.1× 904 0.4× 841 0.7× 462 0.4× 1.0k 1.0× 17 13.5k
Min‐Yi Shen United States 14 7.6k 1.0× 900 0.4× 1.3k 1.1× 546 0.4× 782 0.8× 20 10.4k
András Fiser United States 43 8.0k 1.0× 951 0.4× 1.9k 1.5× 571 0.5× 1.2k 1.1× 144 11.3k

Countries citing papers authored by Dima Kozakov

Since Specialization
Citations

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

Fields of papers citing papers by Dima Kozakov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dima Kozakov

This figure shows the co-authorship network connecting the top 25 collaborators of Dima Kozakov. A scholar is included among the top collaborators of Dima Kozakov 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 Dima Kozakov. Dima Kozakov 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.
Jones, George, et al.. (2025). E-FTMap: A Protein Structure Based Pharmacophore Identification Server for Guiding Fragment Expansion. Journal of Molecular Biology. 437(15). 168956–168956.
2.
Xiao, Zhangping, Fangyuan Cao, Xinyue Zhang, et al.. (2025). Identification of Actionable Targeted Protein Degradation Effector Sites through Site-Specific Ligand Incorporation-Induced Proximity (SLIP). Journal of the American Chemical Society. 147(25). 21549–21559. 1 indexed citations
3.
Li, Yong, David Yin-wei Lin, Bharath Srinivasan, et al.. (2025). Modulating the Binding Kinetics of Bruton’s Tyrosine Kinase Inhibitors through Transition-State Effects. Journal of the American Chemical Society. 147(31). 27876–27891. 1 indexed citations
4.
Zhu, Y., George Jones, Carlos Simmerling, et al.. (2024). MHC-Fine: Fine-tuned AlphaFold for precise MHC-peptide complex prediction. Biophysical Journal. 123(17). 2902–2909. 5 indexed citations
5.
Blum, Benjamin C., Weiwei Lin, Jacob Porter, et al.. (2024). Multiomic profiling of chronically activated CD4+ T cells identifies drivers of exhaustion and metabolic reprogramming. PLoS Biology. 22(12). e3002943–e3002943. 4 indexed citations
6.
Desta, Israel, Sergei Kotelnikov, George Jones, et al.. (2023). The ClusPro AbEMap web server for the prediction of antibody epitopes. Nature Protocols. 18(6). 1814–1840. 14 indexed citations
7.
Davila, Ana, Zichang Xu, Songling Li, et al.. (2022). AbAdapt: an adaptive approach to predicting antibody–antigen complex structures from sequence. Bioinformatics Advances. 2(1). vbac015–vbac015. 21 indexed citations
8.
Havugimana, Pierre C., Raghuveera Kumar Goel, Sadhna Phanse, et al.. (2022). Scalable multiplex co-fractionation/mass spectrometry platform for accelerated protein interactome discovery. Nature Communications. 13(1). 4043–4043. 48 indexed citations
9.
Kounde, Cyrille S., Milon Mondal, Jake L. Greenfield, et al.. (2022). Light-mediated multi-target protein degradation using arylazopyrazole photoswitchable PROTACs (AP-PROTACs). Chemical Communications. 58(78). 10933–10936. 35 indexed citations
10.
Wang, Jinan, Andrey Alekseenko, Dima Kozakov, & Yinglong Miao. (2019). Improved Modeling of Peptide-Protein Binding Through Global Docking and Accelerated Molecular Dynamics Simulations. Frontiers in Molecular Biosciences. 6. 112–112. 70 indexed citations
11.
Beglov, Dmitri, David Hall, Amanda Wakefield, et al.. (2018). Exploring the structural origins of cryptic sites on proteins. Proceedings of the National Academy of Sciences. 115(15). E3416–E3425. 93 indexed citations
12.
Padhorny, Dzmitry, et al.. (2018). Glucose regulation in the methylotrophic yeast Hansenula (Ogataea) polymorpha is mediated by a putative transceptor Gcr1. The International Journal of Biochemistry & Cell Biology. 103. 25–34. 2 indexed citations
13.
Padhorny, Dzmitry, David R. Hall, Artem B. Mamonov, et al.. (2017). Protein–ligand docking using FFT based sampling: D3R case study. Journal of Computer-Aided Molecular Design. 32(1). 225–230. 11 indexed citations
14.
Padhorny, Dzmitry, Andrey Kazennov, Brandon S. Zerbe, et al.. (2016). Protein–protein docking by fast generalized Fourier transforms on 5D rotational manifolds. Proceedings of the National Academy of Sciences. 113(30). E4286–93. 44 indexed citations
15.
Kozakov, Dima, David R. Hall, Stefan Jehle, et al.. (2015). Ligand deconstruction: Why some fragment binding positions are conserved and others are not. Proceedings of the National Academy of Sciences. 112(20). E2585–94. 56 indexed citations
16.
Mottarella, Scott E., Dmitri Beglov, Natalia Beglova, et al.. (2014). Docking Server for the Identification of Heparin Binding Sites on Proteins. Journal of Chemical Information and Modeling. 54(7). 2068–2078. 54 indexed citations
17.
Naser‐Moghadasi, Mohammad, Dima Kozakov, Pirooz Vakili, Sándor Vajda, & Ioannis Ch. Paschalidis. (2013). A new distributed algorithm for side-chain positioning in the process of protein docking. PubMed. 78. 739–744. 3 indexed citations
18.
Bohnuud, Tanggis, Scott E. Mottarella, Dmitri Beglov, et al.. (2012). FTMAP: extended protein mapping with user-selected probe molecules. Nucleic Acids Research. 40(W1). W271–W275. 119 indexed citations
19.
Vajda, Sándor & Dima Kozakov. (2009). Convergence and combination of methods in protein–protein docking. Current Opinion in Structural Biology. 19(2). 164–170. 164 indexed citations
20.
Kozakov, Dima, Karl H. Clodfelter, Sándor Vajda, & Carlos J. Camacho. (2005). Optimal Clustering for Detecting Near-Native Conformations in Protein Docking. Biophysical Journal. 89(2). 867–875. 111 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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