Peter Chi

3.1k total citations
60 papers, 2.3k citations indexed

About

Peter Chi is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Peter Chi has authored 60 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 12 papers in Oncology and 7 papers in Genetics. Recurrent topics in Peter Chi's work include DNA Repair Mechanisms (43 papers), CRISPR and Genetic Engineering (22 papers) and Genomics and Chromatin Dynamics (12 papers). Peter Chi is often cited by papers focused on DNA Repair Mechanisms (43 papers), CRISPR and Genetic Engineering (22 papers) and Genomics and Chromatin Dynamics (12 papers). Peter Chi collaborates with scholars based in Taiwan, United States and South Korea. Peter Chi's co-authors include Patrick Sung, Michael G. Sehorn, Youngho Kwon, Grzegorz Ira, Hengyao Niu, Changhyun Seong, Stephen Van Komen, Joseph San Filippo, Weixing Zhao and Stefán Sigurðsson and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Peter Chi

57 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter Chi Taiwan 25 2.0k 409 371 295 250 60 2.3k
Caixia Guo China 27 2.1k 1.0× 339 0.8× 579 1.6× 263 0.9× 152 0.6× 73 2.4k
Alexias Safi United States 20 2.2k 1.1× 210 0.5× 289 0.8× 590 2.0× 148 0.6× 36 2.6k
Alison L. Clayton United Kingdom 16 2.3k 1.2× 211 0.5× 206 0.6× 283 1.0× 171 0.7× 18 2.7k
Shin‐ichiro Hiraga Japan 24 1.4k 0.7× 223 0.5× 142 0.4× 189 0.6× 118 0.5× 44 1.9k
Hugh P. Cam United States 19 2.9k 1.4× 308 0.8× 227 0.6× 209 0.7× 1.1k 4.3× 31 3.3k
Nicholas S. Tolwinski Singapore 27 2.0k 1.0× 279 0.7× 188 0.5× 206 0.7× 139 0.6× 57 2.6k
Emily M. Hatch United States 14 1.7k 0.8× 151 0.4× 163 0.4× 219 0.7× 135 0.5× 20 2.0k
Elisabetta Mattei Italy 22 1.4k 0.7× 197 0.5× 162 0.4× 263 0.9× 263 1.1× 51 1.8k
Francesco Nicassio Italy 25 1.9k 0.9× 305 0.7× 1.1k 2.9× 133 0.5× 65 0.3× 47 2.4k
Sachiko Kamakura Japan 16 1.2k 0.6× 194 0.5× 164 0.4× 113 0.4× 146 0.6× 33 1.7k

Countries citing papers authored by Peter Chi

Since Specialization
Citations

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

Fields of papers citing papers by Peter Chi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter Chi

This figure shows the co-authorship network connecting the top 25 collaborators of Peter Chi. A scholar is included among the top collaborators of Peter Chi 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 Peter Chi. Peter Chi 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.
Tsai, Y.-T., et al.. (2025). SWI5–SFR1 reduces RAD51 recombinase extending units during filament assembly. Nucleic Acids Research. 53(14). 1 indexed citations
2.
Li, Mengyun, Ching‐Hui Tsai, Michael Binder, et al.. (2025). Mug20–Rec25–Rec27 binds DNA and enhances meiotic DNA break formation via phase-separated condensates. Nucleic Acids Research. 53(5). 1 indexed citations
3.
Sun, Yuting, et al.. (2024). Hop2-Mnd1 functions as a DNA sequence fidelity switch in Dmc1-mediated DNA recombination. Nature Communications. 15(1). 9266–9266.
4.
Chen, Yi‐An, et al.. (2023). RAD51 paralogs synergize with RAD51 to protect reversed forks from cellular nucleases. Nucleic Acids Research. 51(21). 11717–11731. 9 indexed citations
5.
Yeh, Hsin‐Yi, et al.. (2023). A RAD51–ADP double filament structure unveils the mechanism of filament dynamics in homologous recombination. Nature Communications. 14(1). 4993–4993. 5 indexed citations
6.
Zhang, Hanwen, Wen‐Tai Chiu, Song‐Bin Chang, et al.. (2022). PARP1 recruits DNA translocases to restrain DNA replication and facilitate DNA repair. PLoS Genetics. 18(12). e1010545–e1010545. 17 indexed citations
7.
Yeh, Hsin‐Yi, Baptiste Roelens, Kei Yamaya, et al.. (2021). Caenorhabditis elegans DSB-3 reveals conservation and divergence among protein complexes promoting meiotic double-strand breaks. Proceedings of the National Academy of Sciences. 118(33). 17 indexed citations
8.
Li, Wan-Chen, Wei-Hsuan Lan, Hsin‐Yi Yeh, et al.. (2021). Trichoderma reesei Rad51 tolerates mismatches in hybrid meiosis with diverse genome sequences. Proceedings of the National Academy of Sciences. 118(8). 13 indexed citations
9.
Yeh, Hsin‐Yi, Wei-Hsuan Lan, Yimin Wu, et al.. (2021). Identification of fidelity-governing factors in human recombinases DMC1 and RAD51 from cryo-EM structures. Nature Communications. 12(1). 115–115. 25 indexed citations
10.
Chen, Wei‐Ting, Huan‐Yi Tseng, Chih‐Ying Lee, et al.. (2021). Elp1 facilitates RAD51-mediated homologous recombination repair via translational regulation. Journal of Biomedical Science. 28(1). 81–81. 7 indexed citations
11.
Huang, Wen‐Yen, Hsien‐Yi Chiu, Michael Chang, et al.. (2017). Mobilizing Transit-Amplifying Cell-Derived Ectopic Progenitors Prevents Hair Loss from Chemotherapy or Radiation Therapy. Cancer Research. 77(22). 6083–6096. 34 indexed citations
12.
Yeh, Hsin‐Yi, Sheng‐Wei Lin, Chan-I Chung, et al.. (2016). Role of the RAD51–SWI5–SFR1 Ensemble in homologous recombination. Nucleic Acids Research. 44(13). 6242–6251. 12 indexed citations
13.
Lin, Sheng‐Wei, et al.. (2015). Functional Relationship of ATP Hydrolysis, Presynaptic Filament Stability, and Homologous DNA Pairing Activity of the Human Meiotic Recombinase DMC1. Journal of Biological Chemistry. 290(32). 19863–19873. 13 indexed citations
14.
Wilson, Marenda A., Youngho Kwon, Yuanyuan Xu, et al.. (2013). Pif1 helicase and Polδ promote recombination-coupled DNA synthesis via bubble migration. Nature. 502(7471). 393–396. 254 indexed citations
15.
Chi, Peter, Youngho Kwon, Mari‐Liis Visnapuu, et al.. (2011). Analyses of the yeast Rad51 recombinase A265V mutant reveal different in vivo roles of Swi2-like factors. Nucleic Acids Research. 39(15). 6511–6522. 13 indexed citations
16.
Moses, Dana N., Youngho Kwon, Pamela Chan, et al.. (2009). Structural transitions within human Rad51 nucleoprotein filaments. Proceedings of the National Academy of Sciences. 106(31). 12688–12693. 44 indexed citations
17.
Moses, Dana N., Youngho Kwon, Pamela Chan, et al.. (2009). Visualizing the Disassembly of S. cerevisiae Rad51 Nucleoprotein Filaments. Journal of Molecular Biology. 388(4). 703–720. 20 indexed citations
18.
Filippo, Joseph San, Peter Chi, Michael G. Sehorn, et al.. (2006). Recombination Mediator and Rad51 Targeting Activities of a Human BRCA2 Polypeptide. Journal of Biological Chemistry. 281(17). 11649–11657. 105 indexed citations
19.
Chi, Peter, Stephen Van Komen, Michael G. Sehorn, Stefán Sigurðsson, & Patrick Sung. (2006). Roles of ATP binding and ATP hydrolysis in human Rad51 recombinase function. DNA repair. 5(3). 381–391. 147 indexed citations
20.
Chi, Peter, Youngho Kwon, Changhyun Seong, et al.. (2006). Yeast Recombination Factor Rdh54 Functionally Interacts with the Rad51 Recombinase and Catalyzes Rad51 Removal from DNA. Journal of Biological Chemistry. 281(36). 26268–26279. 63 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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