Toru Hirota

8.4k total citations · 2 hit papers
85 papers, 6.0k citations indexed

About

Toru Hirota is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, Toru Hirota has authored 85 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 51 papers in Cell Biology and 21 papers in Oncology. Recurrent topics in Toru Hirota's work include Microtubule and mitosis dynamics (49 papers), Genomics and Chromatin Dynamics (33 papers) and DNA Repair Mechanisms (16 papers). Toru Hirota is often cited by papers focused on Microtubule and mitosis dynamics (49 papers), Genomics and Chromatin Dynamics (33 papers) and DNA Repair Mechanisms (16 papers). Toru Hirota collaborates with scholars based in Japan, United States and Austria. Toru Hirota's co-authors include Jan‐Michael Peters, Hideyuki Saya, Tomotoshi Marumoto, Jan Ellenberg, Daniel W. Gerlich, Jesse Lipp, Ban‐Hock Toh, Jan‐Michael Peters, Masayuki Nitta and Takashi Sasayama and has published in prestigious journals such as Nature, Cell and Nucleic Acids Research.

In The Last Decade

Toru Hirota

84 papers receiving 6.0k citations

Hit Papers

Histone H3 serine 10 phosphorylation by Aurora B causes H... 2003 2026 2010 2018 2005 2003 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Toru Hirota Japan 38 4.8k 3.4k 1.3k 1.1k 347 85 6.0k
Gary J. Gorbsky United States 46 5.8k 1.2× 4.8k 1.4× 1.1k 0.8× 1.2k 1.1× 388 1.1× 96 7.0k
Andrew J. Holland United States 38 4.4k 0.9× 3.7k 1.1× 978 0.8× 950 0.9× 1.1k 3.2× 67 5.6k
Elena V. Ivanova United States 26 3.1k 0.6× 1.3k 0.4× 984 0.8× 318 0.3× 569 1.6× 80 4.7k
Reiko Honda Japan 23 4.1k 0.8× 1.7k 0.5× 2.7k 2.1× 344 0.3× 230 0.7× 29 5.0k
Xiaomu Wei United States 20 3.4k 0.7× 2.9k 0.9× 819 0.6× 511 0.5× 269 0.8× 26 5.1k
Hidemasa Goto Japan 41 3.4k 0.7× 2.2k 0.7× 727 0.6× 295 0.3× 650 1.9× 62 4.3k
Paul R. Andreassen United States 45 5.8k 1.2× 1.9k 0.6× 1.6k 1.2× 692 0.6× 1.2k 3.4× 101 6.8k
William P. Tansey United States 39 5.4k 1.1× 699 0.2× 1.4k 1.1× 381 0.3× 677 2.0× 98 6.4k
Gordon K. Chan Canada 33 3.9k 0.8× 3.1k 0.9× 831 0.6× 745 0.7× 250 0.7× 53 4.4k
Pengbo Zhou United States 37 3.4k 0.7× 787 0.2× 1.1k 0.8× 219 0.2× 431 1.2× 68 4.4k

Countries citing papers authored by Toru Hirota

Since Specialization
Citations

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

Fields of papers citing papers by Toru Hirota

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Toru Hirota

This figure shows the co-authorship network connecting the top 25 collaborators of Toru Hirota. A scholar is included among the top collaborators of Toru Hirota 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 Toru Hirota. Toru Hirota 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.
Kakui, Yasutaka, Tereza Clarence, Todd Fallesen, et al.. (2025). Progressive chromosome shape changes during cell divisions. EMBO Reports. 26(21). 5199–5215.
2.
Furukawa, Ayako, et al.. (2024). Bipartite binding interface recruiting HP1 to chromosomal passenger complex at inner centromeres. The Journal of Cell Biology. 223(9). 3 indexed citations
3.
Jo, Minji, Izuma Nakayama, Motohiro Morioka, et al.. (2022). Profiling chromosomal‐level variations in gastric malignancies. Cancer Science. 113(11). 3864–3876. 4 indexed citations
4.
Uchida, Kazuhiko, Minji Jo, Kota Nagasaka, et al.. (2021). Kinetochore stretching-mediated rapid silencing of the spindle-assembly checkpoint required for failsafe chromosome segregation. Current Biology. 31(8). 1581–1591.e3. 17 indexed citations
5.
Sakamoto, Shinichi, Masahiro Sugiura, Yasutaka Yamada, et al.. (2021). Functional analysis of LAT3 in prostate cancer: Its downstream target and relationship with androgen receptor. Cancer Science. 112(9). 3871–3883. 19 indexed citations
6.
Jo, Minji, et al.. (2021). Unraveling pathologies underlying chromosomal instability in cancers. Cancer Science. 112(8). 2975–2983. 14 indexed citations
7.
Shindo, Norihisa, Makoto Otsuki, Kazuhiko Uchida, & Toru Hirota. (2021). Prolonged mitosis causes separase deregulation and chromosome nondisjunction. Cell Reports. 34(3). 108652–108652. 11 indexed citations
8.
Cartwright, Tyrell N., et al.. (2020). Kinase inhibition profiles as a tool to identify kinases for specific phosphorylation sites. Nature Communications. 11(1). 1684–1684. 18 indexed citations
9.
Nishimura, Koutarou, Yoshikazu Johmura, Katashi Deguchi, et al.. (2019). Cdk1-mediated DIAPH1 phosphorylation maintains metaphase cortical tension and inactivates the spindle assembly checkpoint at anaphase. Nature Communications. 10(1). 981–981. 15 indexed citations
10.
Hirota, Toru, et al.. (2018). Dynamics of sister chromatids through the cell cycle: Together and apart. The Journal of Cell Biology. 217(6). 1887–1889. 2 indexed citations
11.
Itoh, Go, Masanori Ikeda, Shin‐ichiro Kanno, et al.. (2013). Nucleoporin Nup188 is required for chromosome alignment in mitosis. Cancer Science. 104(7). 871–879. 36 indexed citations
12.
Shindo, Norihisa, Kazuki Kumada, & Toru Hirota. (2012). Separase Sensor Reveals Dual Roles for Separase Coordinating Cohesin Cleavage and Cdk1 Inhibition. Developmental Cell. 23(1). 112–123. 58 indexed citations
13.
Abe, Satoshi, Kota Nagasaka, Youko Hirayama, et al.. (2011). The initial phase of chromosome condensation requires Cdk1-mediated phosphorylation of the CAP-D3 subunit of condensin II. Genes & Development. 25(8). 863–874. 114 indexed citations
14.
Ohishi, Tomokazu, Toru Hirota, Takashi Tsuruo, & Hiroyuki Seimiya. (2010). TRF1 Mediates Mitotic Abnormalities Induced by Aurora-A Overexpression. Cancer Research. 70(5). 2041–2052. 26 indexed citations
15.
Itoh, Go, Shin‐ichiro Kanno, Kazuhiko Uchida, et al.. (2010). CAMP (C13orf8, ZNF828) is a novel regulator of kinetochore–microtubule attachment. The EMBO Journal. 30(1). 130–144. 47 indexed citations
16.
Uchida, Kazuhiko, Kentaro Takagaki, Kazuki Kumada, et al.. (2009). Kinetochore stretching inactivates the spindle assembly checkpoint. The Journal of Cell Biology. 184(3). 383–390. 182 indexed citations
17.
Tanaka, Kozo & Toru Hirota. (2009). Chromosome segregation machinery and cancer. Cancer Science. 100(7). 1158–1165. 31 indexed citations
18.
Honda, Shinobu, Tomotoshi Marumoto, Toru Hirota, et al.. (2004). Activation of m-Calpain Is Required for Chromosome Alignment on the Metaphase Plate during Mitosis. Journal of Biological Chemistry. 279(11). 10615–10623. 34 indexed citations
19.
Nishiyama, Yasuyuki, Toru Hirota, Tetsuro Morisaki, et al.. (1999). A human homolog of Drosophila warts tumor suppressor, h‐warts, localized to mitotic apparatus and specifically phosphorylated during mitosis. FEBS Letters. 459(2). 159–165. 91 indexed citations
20.
Muto, Masahiko, et al.. (1996). Allergic Contact Dermatitis due to Propolis.. The Nishinihon Journal of Dermatology. 58(1). 6–9. 1 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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