Da‐Qiao Ding

2.3k total citations
35 papers, 1.9k citations indexed

About

Da‐Qiao Ding is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Da‐Qiao Ding has authored 35 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 10 papers in Cell Biology and 6 papers in Plant Science. Recurrent topics in Da‐Qiao Ding's work include DNA Repair Mechanisms (21 papers), Fungal and yeast genetics research (17 papers) and Genomics and Chromatin Dynamics (17 papers). Da‐Qiao Ding is often cited by papers focused on DNA Repair Mechanisms (21 papers), Fungal and yeast genetics research (17 papers) and Genomics and Chromatin Dynamics (17 papers). Da‐Qiao Ding collaborates with scholars based in Japan, United States and Switzerland. Da‐Qiao Ding's co-authors include Yasushi Hiraoka, Tokuko Haraguchi, Yuji Chikashige, Ayumu Yamamoto, Hironori Funabiki, Mitsuhiro Yanagida, Shinro Mashiko, Kasumi Okamasa, Masayuki Yamamoto and Mizuki Shimanuki and has published in prestigious journals such as Science, Nucleic Acids Research and Nature Communications.

In The Last Decade

Da‐Qiao Ding

33 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Da‐Qiao Ding Japan 18 1.7k 623 456 95 86 35 1.9k
Anton Khmelinskii Germany 20 1.4k 0.8× 759 1.2× 198 0.4× 35 0.4× 87 1.0× 34 1.7k
Ivan Rupeš Canada 9 1.4k 0.8× 418 0.7× 213 0.5× 32 0.3× 69 0.8× 12 1.5k
Itaru Samejima United Kingdom 21 1.9k 1.1× 884 1.4× 467 1.0× 19 0.2× 121 1.4× 30 2.0k
Sue L. Jaspersen United States 32 3.5k 2.0× 1.9k 3.1× 703 1.5× 102 1.1× 215 2.5× 69 3.8k
Satoru Uzawa United States 18 2.2k 1.3× 860 1.4× 671 1.5× 61 0.6× 170 2.0× 22 2.5k
Neil Adames United States 14 1.2k 0.7× 924 1.5× 245 0.5× 23 0.2× 49 0.6× 22 1.4k
Aliona Bogdanova Germany 17 1.1k 0.6× 602 1.0× 198 0.4× 65 0.7× 94 1.1× 24 1.3k
Stefan Heidmann Germany 23 1.7k 1.0× 659 1.1× 663 1.5× 25 0.3× 129 1.5× 28 2.0k
Per O. Widlund Sweden 19 1.4k 0.8× 1.2k 1.9× 185 0.4× 21 0.2× 141 1.6× 27 1.8k
Masamitsu Sato Japan 21 1.2k 0.7× 829 1.3× 231 0.5× 27 0.3× 61 0.7× 57 1.4k

Countries citing papers authored by Da‐Qiao Ding

Since Specialization
Citations

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

Fields of papers citing papers by Da‐Qiao Ding

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Da‐Qiao Ding. 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 Da‐Qiao Ding. The network helps show where Da‐Qiao Ding may publish in the future.

Co-authorship network of co-authors of Da‐Qiao Ding

This figure shows the co-authorship network connecting the top 25 collaborators of Da‐Qiao Ding. A scholar is included among the top collaborators of Da‐Qiao Ding 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 Da‐Qiao Ding. Da‐Qiao Ding 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.
Ding, Da‐Qiao, Kasumi Okamasa, Atsushi Matsuda, et al.. (2024). Proteins and noncoding RNAs that promote homologous chromosome recognition and pairing in fission yeast meiosis undergo condensate formation in vitro. The FASEB Journal. 38(21). e70163–e70163.
2.
Sakuno, Takeshi, Hideki Tanizawa, Osamu Iwasaki, et al.. (2022). Rec8 Cohesin-mediated Axis-loop chromatin architecture is required for meiotic recombination. Nucleic Acids Research. 50(7). 3799–3816. 11 indexed citations
3.
Ding, Da‐Qiao, Atsushi Matsuda, Kasumi Okamasa, & Yasushi Hiraoka. (2021). Linear elements are stable structures along the chromosome axis in fission yeast meiosis. Chromosoma. 130(2-3). 149–162. 7 indexed citations
4.
Yamada, Takatomi, Shintaro Yamada, Da‐Qiao Ding, et al.. (2020). Maintenance of meiotic crossover against reduced double-strand break formation in fission yeast lacking histone H2A.Z. Gene. 743. 144615–144615. 2 indexed citations
5.
Ding, Da‐Qiao, et al.. (2019). Torsional Turning Motion of Chromosomes as an Accelerating Force to Align Homologous Chromosomes during Meiosis. Journal of the Physical Society of Japan. 88(2). 23801–23801. 6 indexed citations
6.
Yamada, Shintaro, Kazuto Kugou, Da‐Qiao Ding, et al.. (2018). The conserved histone variant H2A.Z illuminates meiotic recombination initiation. Current Genetics. 64(5). 1015–1019. 9 indexed citations
7.
Ding, Da‐Qiao & Yasushi Hiraoka. (2017). Visualization of a Specific Genome Locus by the lacO/LacI-GFP System. Cold Spring Harbor Protocols. 2017(10). pdb.prot091934–pdb.prot091934. 8 indexed citations
8.
Ding, Da‐Qiao, Tokuko Haraguchi, & Yasushi Hiraoka. (2016). A cohesin-based structural platform supporting homologous chromosome pairing in meiosis. Current Genetics. 62(3). 499–502. 17 indexed citations
9.
Ding, Da‐Qiao, et al.. (2015). Meiotic cohesin-based chromosome structure is essential for homologous chromosome pairing in Schizosaccharomyces pombe. Chromosoma. 125(2). 205–214. 43 indexed citations
10.
Matsuda, Atsushi, Yuji Chikashige, Da‐Qiao Ding, et al.. (2015). Highly condensed chromatins are formed adjacent to subtelomeric and decondensed silent chromatin in fission yeast. Nature Communications. 6(1). 7753–7753. 53 indexed citations
11.
Ding, Da‐Qiao, Tokuko Haraguchi, & Yasushi Hiraoka. (2013). The role of chromosomal retention of noncoding RNA in meiosis. Chromosome Research. 21(6-7). 665–672. 14 indexed citations
12.
Ding, Da‐Qiao, Kasumi Okamasa, Miho Yamane, et al.. (2012). Meiosis-Specific Noncoding RNA Mediates Robust Pairing of Homologous Chromosomes in Meiosis. Science. 336(6082). 732–736. 101 indexed citations
13.
Ding, Da‐Qiao, Tokuko Haraguchi, & Yasushi Hiraoka. (2012). Chromosomally-retained RNA mediates homologous pairing. Nucleus. 3(6). 516–519. 6 indexed citations
14.
Asakawa, Haruhiko, Tomoko Kojidani, Chie Mori, et al.. (2010). Virtual Breakdown of the Nuclear Envelope in Fission Yeast Meiosis. Current Biology. 20(21). 1919–1925. 56 indexed citations
15.
Ding, Da‐Qiao, Yuki Tomita, Ayumu Yamamoto, et al.. (2000). Large‐scale screening of intracellular protein localization in living fission yeast cells by the use of a GFP‐fusion genomic DNA library. Genes to Cells. 5(3). 169–190. 115 indexed citations
16.
Hiraoka, Yasushi, Da‐Qiao Ding, Ayumu Yamamoto, Chihiro Tsutsumi, & Yuji Chikashige. (2000). Characterization of fission yeast meiotic mutants based on live observation of meiotic prophase nuclear movement. Chromosoma. 109(1-2). 103–109. 29 indexed citations
17.
Tange, Yoshie, Tetsuya Horio, Mizuki Shimanuki, et al.. (1998). A Novel Fission Yeast Gene, tht1+, Is Required for the Fusion of Nuclear Envelopes during Karyogamy. The Journal of Cell Biology. 140(2). 247–258. 31 indexed citations
18.
Shimanuki, Mizuki, Da‐Qiao Ding, Yuji Chikashige, et al.. (1997). A novel fission yeast gene, kms1 +, is required for the formation of meiotic prophase-specific nuclear architecture. Molecular and General Genetics MGG. 254(3). 238–249. 113 indexed citations
19.
Ding, Da‐Qiao, et al.. (1991). Intercellular Transport and Photosynthetic Differentiation inChara corallina. Journal of Experimental Botany. 42(1). 33–38. 11 indexed citations
20.

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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