Bilge Argunhan

509 total citations
21 papers, 344 citations indexed

About

Bilge Argunhan is a scholar working on Molecular Biology, Oncology and Cell Biology. According to data from OpenAlex, Bilge Argunhan has authored 21 papers receiving a total of 344 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 4 papers in Oncology and 4 papers in Cell Biology. Recurrent topics in Bilge Argunhan's work include DNA Repair Mechanisms (17 papers), CRISPR and Genetic Engineering (7 papers) and Fungal and yeast genetics research (7 papers). Bilge Argunhan is often cited by papers focused on DNA Repair Mechanisms (17 papers), CRISPR and Genetic Engineering (7 papers) and Fungal and yeast genetics research (7 papers). Bilge Argunhan collaborates with scholars based in Japan, United States and United Kingdom. Bilge Argunhan's co-authors include Hideo Tsubouchi, Hiroshi Iwasaki, Wing‐Kit Leung, Tomomi Tsubouchi, Yasuto Murayama, Martina Dvořáčková, Kentaro Ito, Sarah Farmer, Masayuki Takahashi and Shuji Kanamaru and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Bilge Argunhan

21 papers receiving 344 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bilge Argunhan Japan 11 326 95 44 39 29 21 344
Nathaniel H. Thayer United States 6 296 0.9× 64 0.7× 21 0.5× 49 1.3× 32 1.1× 10 332
Anna Travesa United States 8 275 0.8× 87 0.9× 41 0.9× 31 0.8× 13 0.4× 9 290
Sarah Farmer United Kingdom 9 413 1.3× 171 1.8× 79 1.8× 65 1.7× 57 2.0× 11 479
Emanuele Roscioli United Kingdom 11 384 1.2× 297 3.1× 52 1.2× 72 1.8× 20 0.7× 15 451
Lætitia Delabaere United States 8 575 1.8× 118 1.2× 48 1.1× 107 2.7× 45 1.6× 8 638
Firaz Mohideen United States 6 279 0.9× 39 0.4× 59 1.3× 20 0.5× 33 1.1× 9 296
Maikel Castellano‐Pozo Spain 7 345 1.1× 62 0.7× 31 0.7× 61 1.6× 34 1.2× 9 378
Taehyun Ryu United States 6 575 1.8× 113 1.2× 55 1.3× 94 2.4× 39 1.3× 8 624
Scott Rata United Kingdom 6 201 0.6× 129 1.4× 39 0.9× 28 0.7× 12 0.4× 8 242
Sally Fujiyama‐Nakamura Japan 7 274 0.8× 63 0.7× 34 0.8× 52 1.3× 37 1.3× 8 327

Countries citing papers authored by Bilge Argunhan

Since Specialization
Citations

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

Fields of papers citing papers by Bilge Argunhan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bilge Argunhan

This figure shows the co-authorship network connecting the top 25 collaborators of Bilge Argunhan. A scholar is included among the top collaborators of Bilge Argunhan 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 Bilge Argunhan. Bilge Argunhan 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.
Yates, Luke A., et al.. (2023). Phosphoregulation of DNA repair via the Rad51 auxiliary factor Swi5–Sfr1. Journal of Biological Chemistry. 299(8). 104929–104929. 2 indexed citations
2.
Argunhan, Bilge, Kentaro Ito, Yumiko Kurokawa, et al.. (2021). Rrp1 translocase and ubiquitin ligase activities restrict the genome destabilising effects of Rad51 in fission yeast. Nucleic Acids Research. 49(12). 6832–6848. 7 indexed citations
3.
Daley, James M., Arijit Dutta, Tatsuya Niwa, et al.. (2021). A conserved Ctp1/CtIP C-terminal peptide stimulates Mre11 endonuclease activity. Proceedings of the National Academy of Sciences. 118(11). 16 indexed citations
4.
Argunhan, Bilge, Hiroshi Iwasaki, & Hideo Tsubouchi. (2021). Post-translational modification of factors involved in homologous recombination. DNA repair. 104. 103114–103114. 9 indexed citations
5.
Tsubouchi, Hideo, Bilge Argunhan, & Hiroshi Iwasaki. (2021). Biochemical properties of fission yeast homologous recombination enzymes. Current Opinion in Genetics & Development. 71. 19–26. 9 indexed citations
6.
Tsubouchi, Hideo, Bilge Argunhan, Rei Kajitani, et al.. (2021). Homology length dictates the requirement for Rad51 and Rad52 in gene targeting in the Basidiomycota yeast Naganishia liquefaciens. Current Genetics. 67(6). 919–936. 1 indexed citations
7.
Argunhan, Bilge, et al.. (2021). A novel motif of Rad51 serves as an interaction hub for recombination auxiliary factors. eLife. 10. 13 indexed citations
8.
Han, Yong-Woon, Rei Kajitani, Yumiko Kurokawa, et al.. (2020). Draft Genome Sequence of Naganishia liquefaciens Strain N6, Isolated from the Japan Trench. Microbiology Resource Announcements. 9(47). 6 indexed citations
9.
Ito, Kentaro, Yasuto Murayama, Yumiko Kurokawa, et al.. (2020). Real-time tracking reveals catalytic roles for the two DNA binding sites of Rad51. Nature Communications. 11(1). 2950–2950. 18 indexed citations
10.
Argunhan, Bilge, Masayoshi Sakakura, Kentaro Ito, et al.. (2020). Cooperative interactions facilitate stimulation of Rad51 by the Swi5-Sfr1 auxiliary factor complex. eLife. 9. 10 indexed citations
11.
Tsubouchi, Hideo, Bilge Argunhan, Kentaro Ito, Masayuki Takahashi, & Hiroshi Iwasaki. (2020). Two auxiliary factors promote Dmc1-driven DNA strand exchange via stepwise mechanisms. Proceedings of the National Academy of Sciences. 117(22). 12062–12070. 12 indexed citations
12.
Ito, Kentaro, Bilge Argunhan, Hideo Tsubouchi, & Hiroshi Iwasaki. (2019). Real-time Observation of the DNA Strand Exchange Reaction Mediated by Rad51. Journal of Visualized Experiments. 5 indexed citations
13.
Argunhan, Bilge, Wing‐Kit Leung, Vijayalakshmi V. Subramanian, et al.. (2017). Fundamental cell cycle kinases collaborate to ensure timely destruction of the synaptonemal complex during meiosis. The EMBO Journal. 36(17). 2488–2509. 41 indexed citations
14.
Argunhan, Bilge, Yasuto Murayama, & Hiroshi Iwasaki. (2017). The differentiated and conserved roles of Swi5‐Sfr1 in homologous recombination. FEBS Letters. 591(14). 2035–2047. 21 indexed citations
15.
Tsubouchi, Hideo, Bilge Argunhan, & Tomomi Tsubouchi. (2017). Exiting prophase I: no clear boundary. Current Genetics. 64(2). 423–427. 10 indexed citations
16.
17.
Argunhan, Bilge, et al.. (2013). Direct and Indirect Control of the Initiation of Meiotic Recombination by DNA Damage Checkpoint Mechanisms in Budding Yeast. PLoS ONE. 8(6). e65875–e65875. 22 indexed citations
18.
Leung, Wing‐Kit, et al.. (2013). The Ecm11-Gmc2 Complex Promotes Synaptonemal Complex Formation through Assembly of Transverse Filaments in Budding Yeast. PLoS Genetics. 9(1). e1003194–e1003194. 73 indexed citations
19.
20.
Farmer, Sarah, et al.. (2012). Budding Yeast Pch2, a Widely Conserved Meiotic Protein, Is Involved in the Initiation of Meiotic Recombination. PLoS ONE. 7(6). e39724–e39724. 29 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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