Shinichiro Nakada

4.5k total citations · 2 hit papers
51 papers, 3.3k citations indexed

About

Shinichiro Nakada is a scholar working on Molecular Biology, Oncology and Surgery. According to data from OpenAlex, Shinichiro Nakada has authored 51 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 16 papers in Oncology and 9 papers in Surgery. Recurrent topics in Shinichiro Nakada's work include DNA Repair Mechanisms (24 papers), CRISPR and Genetic Engineering (9 papers) and Ubiquitin and proteasome pathways (9 papers). Shinichiro Nakada is often cited by papers focused on DNA Repair Mechanisms (24 papers), CRISPR and Genetic Engineering (9 papers) and Ubiquitin and proteasome pathways (9 papers). Shinichiro Nakada collaborates with scholars based in Japan, United States and Canada. Shinichiro Nakada's co-authors include Daniel Durocher, Stephanie Panier, Laurence Pelletier, Jarkko Ylanko, Nadine K. Kolas, Jan Wildenhain, Megan Mendez, Anne‐Claude Gingras, Timothy M. Thomson and J. Ross Chapman and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Shinichiro Nakada

47 papers receiving 3.2k citations

Hit Papers

Orchestration of the DNA-... 2007 2026 2013 2019 2007 2009 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
Shinichiro Nakada Japan 24 3.0k 1.1k 348 326 326 51 3.3k
Yaron Galanty United Kingdom 20 2.9k 1.0× 1.0k 0.9× 353 1.0× 263 0.8× 367 1.1× 27 3.1k
Andrew N. Blackford United Kingdom 24 3.1k 1.0× 1.3k 1.2× 457 1.3× 403 1.2× 424 1.3× 30 3.6k
Regina Groisman France 15 3.0k 1.0× 776 0.7× 373 1.1× 260 0.8× 376 1.2× 27 3.2k
Andrea C. Carrano United States 15 2.5k 0.8× 1.5k 1.3× 297 0.9× 576 1.8× 269 0.8× 17 3.1k
Zhongsheng You United States 25 2.6k 0.9× 976 0.9× 501 1.4× 449 1.4× 180 0.6× 49 2.8k
Evi Soutoglou France 32 3.5k 1.2× 739 0.7× 362 1.0× 265 0.8× 446 1.4× 48 3.9k
Rémi Buisson United States 22 2.2k 0.7× 923 0.8× 397 1.1× 173 0.5× 361 1.1× 44 2.5k
Grzegorz Nalepa United States 21 2.0k 0.7× 724 0.6× 285 0.8× 597 1.8× 258 0.8× 42 2.5k
Mark A. Subler United States 32 2.0k 0.7× 1.5k 1.3× 412 1.2× 226 0.7× 268 0.8× 65 3.0k
Richard A. DiTullio United States 9 2.8k 0.9× 1.4k 1.2× 604 1.7× 408 1.3× 260 0.8× 9 3.1k

Countries citing papers authored by Shinichiro Nakada

Since Specialization
Citations

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

Fields of papers citing papers by Shinichiro Nakada

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shinichiro Nakada

This figure shows the co-authorship network connecting the top 25 collaborators of Shinichiro Nakada. A scholar is included among the top collaborators of Shinichiro Nakada 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 Shinichiro Nakada. Shinichiro Nakada 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.
Tadagaki, Kenjiro, et al.. (2024). The combination of venetoclax and quercetin exerts a cytotoxic effect on acute myeloid leukemia. Scientific Reports. 14(1). 26418–26418. 4 indexed citations
2.
Nakada, Shinichiro, Nicolas Golse, Matthieu Faron, et al.. (2024). Initial laparoscopic liver resection is associated with reduced adhesions and transfusions at the time of salvage liver transplantation. HPB. 26(9). 1190–1199.
3.
Mishima, Takashi, Shigetsugu Takano, Tsukasa Takayashiki, et al.. (2023). Serum elastase-1 predicts malignancy in intraductal papillary mucinous neoplasm of the pancreas. Pancreatology. 24(1). 93–99. 3 indexed citations
4.
Nakada, Shinichiro, Yuichiro Otsuka, Jun Ishii, et al.. (2022). Predictors of a difficult Pringle maneuver in laparoscopic liver resection and evaluation of alternative procedures to assist bleeding control. Surgery Today. 52(12). 1688–1697. 3 indexed citations
5.
Kitano, Yuki, Marc‐Antoine Allard, Shinichiro Nakada, et al.. (2020). Early‐ and long‐term outcomes of liver transplantation with rescue allocation grafts. Clinical Transplantation. 35(1). e14046–e14046. 1 indexed citations
6.
Saha, Liton Kumar, Masataka Tsuda, Kouji Hirota, et al.. (2020). UBC13-Mediated Ubiquitin Signaling Promotes Removal of Blocking Adducts from DNA Double-Strand Breaks. iScience. 23(4). 101027–101027. 18 indexed citations
7.
Yoshimi, Kazuto, Yuya Okuzaki, Peter Gee, et al.. (2019). CRISPR-Cas3 induces broad and unidirectional genome editing in human cells. Nature Communications. 10(1). 5302–5302. 130 indexed citations
8.
Nakada, Shinichiro, Marc‐Antoine Allard, M. Lewin, et al.. (2019). Ischemic Cholangiopathy Following Transcatheter Arterial Chemoembolization for Recurrent Hepatocellular Carcinoma After Hepatectomy: an Underestimated and Devastating Complication. Journal of Gastrointestinal Surgery. 24(11). 2517–2525. 7 indexed citations
9.
Sasanuma, Hiroyuki, Masataka Tsuda, Liton Kumar Saha, et al.. (2018). BRCA1 ensures genome integrity by eliminating estrogen-induced pathological topoisomerase II–DNA complexes. Proceedings of the National Academy of Sciences. 115(45). E10642–E10651. 77 indexed citations
10.
Yasuhara, Takaaki, Reona Kato, Yoshihiko Hagiwara, et al.. (2018). Human Rad52 Promotes XPG-Mediated R-loop Processing to Initiate Transcription-Associated Homologous Recombination Repair. Cell. 175(2). 558–570.e11. 241 indexed citations
11.
Nibe, Yoichi, Shigeru Oshima, Masanori Kobayashi, et al.. (2017). Novel polyubiquitin imaging system, PolyUb-FC, reveals that K33-linked polyubiquitin is recruited by SQSTM1/p62. Autophagy. 14(2). 347–358. 29 indexed citations
12.
Sato, Koichi, Y Katsuki, Wataru Kobayashi, et al.. (2017). RFWD3-Mediated Ubiquitination Promotes Timely Removal of Both RPA and RAD51 from DNA Damage Sites to Facilitate Homologous Recombination. Molecular Cell. 66(5). 622–634.e8. 131 indexed citations
14.
Sato, Yusuke, Atsushi Yamagata, Sakurako Goto‐Ito, et al.. (2015). Structural Basis for Ubiquitin Recognition by Ubiquitin-Binding Zinc Finger of FAAP20. PLoS ONE. 10(3). e0120887–e0120887. 10 indexed citations
15.
Kato, Kiyoko, et al.. (2014). Fine-Tuning of DNA Damage-Dependent Ubiquitination by OTUB2 Supports the DNA Repair Pathway Choice. Molecular Cell. 53(4). 617–630. 80 indexed citations
16.
Nakada, Shinichiro, et al.. (2012). RNF8 Regulates Assembly of RAD51 at DNA Double-Strand Breaks in the Absence of BRCA1 and 53BP1. Cancer Research. 72(19). 4974–4983. 50 indexed citations
17.
Kolas, Nadine K., J. Ross Chapman, Shinichiro Nakada, et al.. (2007). Orchestration of the DNA-Damage Response by the RNF8 Ubiquitin Ligase. Science. 318(5856). 1637–1640. 719 indexed citations breakdown →
18.
Nakada, Shinichiro. (2005). Early G2/M checkpoint failure as a molecular mechanism underlying etoposide-induced chromosomal aberrations. Journal of Clinical Investigation. 116(1). 80–89. 32 indexed citations
19.
Omata, Taku, et al.. (2002). Clinical Study of Convulsions with Mild Gastroenteritis. 106(3). 368–371. 3 indexed citations
20.
Huang, Yinyin, Takatoshi Ishiko, Shinichiro Nakada, et al.. (1997). Role for E2F in DNA damage-induced entry of cells into S phase.. PubMed. 57(17). 3640–3. 44 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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