Stoyno Stoynov

4.3k total citations · 2 hit papers
28 papers, 2.6k citations indexed

About

Stoyno Stoynov is a scholar working on Molecular Biology, Oncology and Cell Biology. According to data from OpenAlex, Stoyno Stoynov has authored 28 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 8 papers in Oncology and 4 papers in Cell Biology. Recurrent topics in Stoyno Stoynov's work include DNA Repair Mechanisms (17 papers), PARP inhibition in cancer therapy (8 papers) and Genomics and Chromatin Dynamics (8 papers). Stoyno Stoynov is often cited by papers focused on DNA Repair Mechanisms (17 papers), PARP inhibition in cancer therapy (8 papers) and Genomics and Chromatin Dynamics (8 papers). Stoyno Stoynov collaborates with scholars based in Bulgaria, Germany and United States. Stoyno Stoynov's co-authors include Stephan W. Grill, Ina Poser, Marcus Jahnel, Titus M. Franzmann, Simon Alberti, Anthony A. Hyman, Shambaditya Saha, Julia Mahamid, Nicola Maghelli and Shovamayee Maharana and has published in prestigious journals such as Cell, Nucleic Acids Research and Nature Communications.

In The Last Decade

Stoyno Stoynov

25 papers receiving 2.6k citations

Hit Papers

A Liquid-to-Solid Phase Transition of the ALS Protein FUS... 2015 2026 2018 2022 2015 2024 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
Stoyno Stoynov Bulgaria 11 2.3k 340 281 221 166 28 2.6k
Saskia Hutten Germany 21 2.5k 1.1× 421 1.2× 194 0.7× 208 0.9× 278 1.7× 31 2.9k
Jamie Longgood United States 10 2.0k 0.9× 239 0.7× 158 0.6× 82 0.4× 140 0.8× 10 2.5k
Nicola Maghelli Germany 14 2.2k 0.9× 350 1.0× 585 2.1× 58 0.3× 167 1.0× 21 2.8k
Avinash Patel Germany 9 2.9k 1.2× 455 1.3× 465 1.7× 61 0.3× 219 1.3× 10 3.3k
Frédéric Frottin France 11 1.2k 0.5× 320 0.9× 288 1.0× 171 0.8× 146 0.9× 13 1.6k
Saumya Jain United States 11 3.4k 1.5× 220 0.6× 435 1.5× 50 0.2× 115 0.7× 19 3.7k
Dierk Niessing Germany 30 2.3k 1.0× 126 0.4× 247 0.9× 132 0.6× 92 0.6× 70 2.6k
Sudeep Banjade United States 10 3.1k 1.3× 82 0.2× 596 2.1× 164 0.7× 52 0.3× 14 3.6k
Gregory L. Dignon United States 17 3.4k 1.5× 263 0.8× 194 0.7× 39 0.2× 119 0.7× 26 3.7k

Countries citing papers authored by Stoyno Stoynov

Since Specialization
Citations

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

Fields of papers citing papers by Stoyno Stoynov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stoyno Stoynov

This figure shows the co-authorship network connecting the top 25 collaborators of Stoyno Stoynov. A scholar is included among the top collaborators of Stoyno Stoynov 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 Stoyno Stoynov. Stoyno Stoynov 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.
Aleksandrov, Radoslav, et al.. (2025). In and out of Replication Stress: PCNA/RPA1-Based Dynamics of Fork Stalling and Restart in the Same Cell. International Journal of Molecular Sciences. 26(2). 667–667.
2.
Panova, Greta, B. D. Keister, G. Georgiev, et al.. (2024). Diffusion of activated ATM explains γH2AX and MDC1 spread beyond the DNA damage site. iScience. 27(9). 110826–110826. 2 indexed citations
4.
Chappidi, Nagaraja, Thomas Quail, Radoslav Aleksandrov, et al.. (2024). PARP1-DNA co-condensation drives DNA repair site assembly to prevent disjunction of broken DNA ends. Cell. 187(4). 945–961.e18. 74 indexed citations breakdown →
5.
Lukarska, Maria, et al.. (2024). A unified mechanism for PARP inhibitor-induced PARP1 chromatin retention at DNA damage sites in living cells. Cell Reports. 43(5). 114234–114234. 17 indexed citations
6.
Aleksandrov, Radoslav, et al.. (2023). CellTool: An Open-Source Software Combining Bio-Image Analysis and Mathematical Modeling for the Study of DNA Repair Dynamics. International Journal of Molecular Sciences. 24(23). 16784–16784. 6 indexed citations
7.
Stoynov, Stoyno, et al.. (2023). PARP1 roles in DNA repair and DNA replication: The basi(c)s of PARP inhibitor efficacy and resistance. Seminars in Oncology. 51(1-2). 2–18. 32 indexed citations
8.
Aleksandrov, Radoslav, et al.. (2021). DNArepairK: An Interactive Database for Exploring the Impact of Anticancer Drugs onto the Dynamics of DNA Repair Proteins. Biomedicines. 9(9). 1238–1238. 7 indexed citations
9.
Stoynov, Stoyno, et al.. (2021). Approach To Ship’s It And Ot Systems Cybersecurity Improvement. 93(7s). 185–196. 2 indexed citations
10.
Stoynov, Stoyno, et al.. (2020). Deregulated levels of RUVBL1 induce transcription-dependent replication stress. The International Journal of Biochemistry & Cell Biology. 128. 105839–105839. 6 indexed citations
11.
Aleksandrov, Radoslav, Ina Poser, Dragomir B. Krastev, et al.. (2018). Protein Dynamics in Complex DNA Lesions. Molecular Cell. 69(6). 1046–1061.e5. 116 indexed citations
12.
Krastev, Dragomir B., Stephen J. Pettitt, James Campbell, et al.. (2018). Coupling bimolecular PARylation biosensors with genetic screens to identify PARylation targets. Nature Communications. 9(1). 2016–2016. 23 indexed citations
14.
Patel, Avinash, Hyun O. Lee, Louise Jawerth, et al.. (2015). A Liquid-to-Solid Phase Transition of the ALS Protein FUS Accelerated by Disease Mutation. Cell. 162(5). 1066–1077. 2097 indexed citations breakdown →
15.
Sarov, Mihail, et al.. (2013). The thermodynamic patterns of eukaryotic genes suggest a mechanism for intron–exon recognition. Nature Communications. 4(1). 2101–2101. 7 indexed citations
16.
Vasilev, Aleksey, et al.. (2013). Novel Fluorescent Dyes for Single DNA Molecule Techniques. Molecular Imaging. 12(2). 90–9. 8 indexed citations
17.
Krastev, Dragomir B., et al.. (2006). Coordination of DNA synthesis and replicative unwinding by the S-phase checkpoint pathways. Nucleic Acids Research. 34(15). 4138–4146. 15 indexed citations
18.
Roguev, Assen, Andrej Shevchenko, Hristo Taskov, et al.. (2005). Uncoupling of Unwinding from DNA Synthesis Implies Regulation of MCM Helicase by Tof1/Mrc1/Csm3 Checkpoint Complex. Journal of Molecular Biology. 347(3). 509–521. 111 indexed citations
19.
Stoynov, Stoyno, et al.. (2001). Supercoiling unwinds two-micrometer plasmid yeast DNA at the origin of replication. The International Journal of Biochemistry & Cell Biology. 33(2). 175–180. 1 indexed citations
20.
Stoynov, Stoyno, et al.. (1997). Single‐strand‐specific DNase activity is an inherent property of the 140‐kDa protein of the snake venom exonuclease1. FEBS Letters. 409(2). 151–154. 13 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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