Krassimir Yankulov

2.9k total citations · 1 hit paper
50 papers, 2.3k citations indexed

About

Krassimir Yankulov is a scholar working on Molecular Biology, Plant Science and Cell Biology. According to data from OpenAlex, Krassimir Yankulov has authored 50 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 10 papers in Plant Science and 4 papers in Cell Biology. Recurrent topics in Krassimir Yankulov's work include Genomics and Chromatin Dynamics (24 papers), DNA Repair Mechanisms (13 papers) and CRISPR and Genetic Engineering (13 papers). Krassimir Yankulov is often cited by papers focused on Genomics and Chromatin Dynamics (24 papers), DNA Repair Mechanisms (13 papers) and CRISPR and Genetic Engineering (13 papers). Krassimir Yankulov collaborates with scholars based in Canada, United States and France. Krassimir Yankulov's co-authors include David L. Bentley, Susan McCracken, Nova Fong, Scott Ballantyne, Jack Greenblatt, Marvin Wickens, Guohua Pan, Scott D. Patterson, Justin Blau and David P. Siderovski and has published in prestigious journals such as Nature, Cell and Nucleic Acids Research.

In The Last Decade

Krassimir Yankulov

49 papers receiving 2.3k citations

Hit Papers

The C-terminal domain of RNA polymerase II couples mRNA p... 1997 2026 2006 2016 1997 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Krassimir Yankulov Canada 17 2.1k 223 176 171 133 50 2.3k
Oliver Pusch Austria 22 1.1k 0.5× 236 1.1× 250 1.4× 84 0.5× 184 1.4× 39 1.5k
Stéphanie Pébernard Switzerland 17 1.7k 0.8× 272 1.2× 362 2.1× 111 0.6× 85 0.6× 25 2.0k
Laura I. Davis United States 12 2.1k 1.0× 90 0.4× 150 0.9× 91 0.5× 142 1.1× 15 2.3k
Isabelle C. Kos‐Braun Germany 18 2.2k 1.0× 99 0.4× 112 0.6× 192 1.1× 45 0.3× 23 2.4k
Emmanuel Käs France 24 2.4k 1.1× 182 0.8× 471 2.7× 450 2.6× 132 1.0× 32 2.7k
Ludwig Englmeier Germany 9 1.4k 0.7× 106 0.5× 145 0.8× 54 0.3× 115 0.9× 10 1.6k
Graeme R. Grimes United Kingdom 18 2.0k 1.0× 127 0.6× 313 1.8× 245 1.4× 64 0.5× 30 2.4k
Grant A. Hartzog United States 18 2.0k 1.0× 64 0.3× 170 1.0× 159 0.9× 78 0.6× 28 2.1k
Erica Pascal United States 8 1.0k 0.5× 165 0.7× 162 0.9× 378 2.2× 86 0.6× 10 1.5k
Allison Lange United States 9 1.1k 0.5× 166 0.7× 151 0.9× 99 0.6× 29 0.2× 11 1.4k

Countries citing papers authored by Krassimir Yankulov

Since Specialization
Citations

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

Fields of papers citing papers by Krassimir Yankulov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Krassimir Yankulov

This figure shows the co-authorship network connecting the top 25 collaborators of Krassimir Yankulov. A scholar is included among the top collaborators of Krassimir Yankulov 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 Krassimir Yankulov. Krassimir Yankulov 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
2.
Yankulov, Krassimir, et al.. (2023). TOF1 and RRM3 reveal a link between gene silencing and the pausing of replication forks. Current Genetics. 69(4-6). 235–249. 1 indexed citations
3.
Yankulov, Krassimir, et al.. (2021). Variation, Variegation and Heritable Gene Repression in S. cerevisiae. Frontiers in Genetics. 12. 630506–630506. 4 indexed citations
4.
Yankulov, Krassimir, et al.. (2020). Gene repression in S. cerevisiae—looking beyond Sir-dependent gene silencing. Current Genetics. 67(1). 3–17. 9 indexed citations
5.
Jeffery, Daniel, Naoko Kakusho, Zhiying You, et al.. (2015). CDC28 phosphorylates Cac1p and regulates the association of chromatin assembly factor i with chromatin. Cell Cycle. 14(1). 74–85. 16 indexed citations
6.
Yankulov, Krassimir & Richard A. Couto. (2012). Peer review in class: Metrics and variations in a senior course. Biochemistry and Molecular Biology Education. 40(3). 161–168. 8 indexed citations
7.
Yankulov, Krassimir, et al.. (2012). Directional telomeric silencing and lack of canonical B1 elements in two silencer Autonomously Replicating Sequences in S. cerevisiae. BMC Molecular Biology. 13(1). 34–34. 2 indexed citations
8.
Yankulov, Krassimir. (2011). Dare to challenge the silence? Telomeric gene silencing revisited. Nucleus. 2(6). 513–516. 8 indexed citations
9.
Jeffery, Daniel, et al.. (2011). Sub-Telomeric core X and Y' Elements in S.cerevisiae Suppress Extreme Variations in Gene Silencing. PLoS ONE. 6(3). e17523–e17523. 8 indexed citations
10.
Rehman, Muhammad Attiq, Dongliang Wang, Geneviève Fourel, Éric Gilson, & Krassimir Yankulov. (2008). SubtelomericACS-containing Proto-silencers Act as Antisilencers in Replication Factors Mutants inSaccharomyces cerevisiae. Molecular Biology of the Cell. 20(2). 631–641. 7 indexed citations
11.
Yankulov, Krassimir, Emmanuelle Revardel, Pierre Luciano, et al.. (2006). Subtelomeric proteins negatively regulate telomere elongation in budding yeast. The EMBO Journal. 25(4). 846–856. 54 indexed citations
12.
Yankulov, Krassimir, et al.. (2006). Subtelomeric proteins negatively regulate telomere elongation in budding yeast. HAL (Le Centre pour la Communication Scientifique Directe). 1 indexed citations
13.
Pinhero, Reena Grittle, et al.. (2004). Three cyclin‐dependent kinases preferentially phosphorylate different parts of the C‐terminal domain of the large subunit of RNA polymerase II. European Journal of Biochemistry. 271(5). 1004–1014. 40 indexed citations
14.
Tye, Bik K., et al.. (2003). Evidence for a Role of MCM (Mini-chromosome Maintenance)5 in Transcriptional Repression of Sub-telomeric and Ty-proximal Genes in Saccharomyces cerevisiae. Journal of Biological Chemistry. 278(30). 27372–27381. 35 indexed citations
15.
Gauthier, Laura D., et al.. (2002). Higher-accuracy method for measuring minichromosome stability in Saccharomyces cerevisiae.. PubMed. 32(5). 1036, 1038, 1040 passim–1036, 1038, 1040 passim. 6 indexed citations
16.
Yankulov, Krassimir, Иван Тодоров, Piotr Romanowski, et al.. (1999). MCM Proteins Are Associated with RNA Polymerase II Holoenzyme. Molecular and Cellular Biology. 19(9). 6154–6163. 78 indexed citations
17.
Yankulov, Krassimir & David L. Bentley. (1998). Transcriptional control: Tat cofactors and transcriptional elongation. Current Biology. 8(13). R447–R449. 40 indexed citations
18.
Yankulov, Krassimir, et al.. (1996). TFIIH Functions in Regulating Transcriptional Elongation by RNA Polymerase II in Xenopus Oocytes. Molecular and Cellular Biology. 16(7). 3291–3299. 56 indexed citations
19.
Yankulov, Krassimir, Katsumi Yamashita, Richard Roy, Jean‐Marc Egly, & David L. Bentley. (1995). The Transcriptional Elongation Inhibitor 5,6-Dichloro-1-β-D-ribofuranosylbenzimidazole Inhibits Transcription Factor IIH-associated Protein Kinase. Journal of Biological Chemistry. 270(41). 23922–23925. 161 indexed citations
20.
Yankulov, Krassimir, et al.. (1994). Transcriptional elongation by RNA polymerase II is stimulated by transactivators. Cell. 77(5). 749–759. 219 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026