Tomoo Ogi

8.3k total citations · 1 hit paper
123 papers, 5.3k citations indexed

About

Tomoo Ogi is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Tomoo Ogi has authored 123 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 91 papers in Molecular Biology, 24 papers in Genetics and 18 papers in Cancer Research. Recurrent topics in Tomoo Ogi's work include DNA Repair Mechanisms (43 papers), Carcinogens and Genotoxicity Assessment (15 papers) and CRISPR and Genetic Engineering (12 papers). Tomoo Ogi is often cited by papers focused on DNA Repair Mechanisms (43 papers), Carcinogens and Genotoxicity Assessment (15 papers) and CRISPR and Genetic Engineering (12 papers). Tomoo Ogi collaborates with scholars based in Japan, United Kingdom and United States. Tomoo Ogi's co-authors include E. Peter Greenberg, Phoebe Lostroh, Martín Schuster, Alan R. Lehmann, Haruo Ohmori, Yuka Nakazawa, Shunichi Yamashita, Sayura Aoyagi, Jeffrey J. Hayes and David Chafin 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

Tomoo Ogi

113 papers receiving 5.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Identification, Timing, and Signal Specificity ofPseudomonas aeruginosaQuorum-Controlled Genes: a Transcriptome Analysis

2003 885 citations Tomoo Ogi et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tomoo Ogi Japan	32	4.2k	1.2k	904	553	358	123	5.3k
Tatsuya Nakamura Japan	44	5.2k 1.2×	647 0.5×	1.0k 1.1×	453 0.8×	230 0.6×	118	7.2k
Shih-Feng Tsai Taiwan	28	2.5k 0.6×	676 0.6×	414 0.5×	735 1.3×	325 0.9×	49	4.3k
Jason Wright United States	12	7.9k 1.9×	1.5k 1.3×	936 1.0×	843 1.5×	992 2.8×	16	9.8k
Maria Sandkvist United States	39	2.3k 0.6×	1.5k 1.3×	719 0.8×	136 0.2×	404 1.1×	65	5.1k
Jun Fu China	38	4.4k 1.0×	1.5k 1.2×	378 0.4×	409 0.7×	409 1.1×	115	5.9k
Albrecht Bindereif Germany	43	4.7k 1.1×	552 0.5×	1.7k 1.8×	166 0.3×	120 0.3×	103	5.9k
Simon J. McGowan United Kingdom	36	2.8k 0.7×	835 0.7×	350 0.4×	184 0.3×	210 0.6×	67	4.0k
Christopher K. Raymond United States	19	2.8k 0.7×	583 0.5×	609 0.7×	188 0.3×	957 2.7×	27	3.9k
Guoliang Qing China	31	3.0k 0.7×	534 0.4×	1.5k 1.7×	644 1.2×	285 0.8×	54	4.2k
Wei Yu China	36	3.2k 0.8×	713 0.6×	305 0.3×	352 0.6×	440 1.2×	104	4.0k

Countries citing papers authored by Tomoo Ogi

Since Specialization

Citations

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

Fields of papers citing papers by Tomoo Ogi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tomoo Ogi

This figure shows the co-authorship network connecting the top 25 collaborators of Tomoo Ogi. A scholar is included among the top collaborators of Tomoo Ogi 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 Tomoo Ogi. Tomoo Ogi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Nakazawa, Yuka, Yasuyoshi Oka, Hironobu Morinaga, et al.. (2025). TFIIH-p52ΔC defines a ninth xeroderma pigmentosum complementation–group XP-J and restores TFIIH stability to p8-defective trichothiodystrophy. Journal of Clinical Investigation. 135(22). 1 indexed citations

Kurahashi, Hirokazu, Yoshiteru Azuma, Mayuko Shimada, et al.. (2025). Paroxysmal Kinesigenic Dyskinesia in Two Siblings With Novel Heterozygous TMEM151A Frameshift Variant: The First Case Report in Japan. American Journal of Medical Genetics Part A. 197(8). e64079–e64079.

Nishikawa, Masashi, Shin Hayashi, Hidenori Ito, et al.. (2024). Pathophysiological significance of the p.E31G variant in RAC1 responsible for a neurodevelopmental disorder with microcephaly. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1871(1). 167520–167520. 1 indexed citations

Takeichi, Takuya, Yasushi Ogawa, Sumihisa Imakado, et al.. (2024). Updated mutational spectrum and genotype–phenotype correlations in ichthyosis patients with ABCA12 pathogenic variants. Experimental Dermatology. 33(4). e15072–e15072. 1 indexed citations

Nyuzuki, Hiromi, et al.. (2024). A severe case of cardiospondylocarpofacial syndrome with a novel MAP3K7 variant. Human Genome Variation. 11(1). 8–8.

Yamada, Kei, Yu Kobayashi, Hitomi Fujii, et al.. (2024). Neonatal myoclonus in Bryant-Li-Bhoj syndrome associated with a novel H3F3A variant. Human Genome Variation. 11(1). 45–45.

Kushima, Itaru, Hiroki Kimura, Branko Aleksić, et al.. (2024). Whole‐genome sequencing analysis of Japanese autism spectrum disorder trios. Psychiatry and Clinical Neurosciences. 79(3). 87–97. 2 indexed citations

Nakazawa, Yuka, Yasuyoshi Oka, Tomoko Matsunaga, & Tomoo Ogi. (2024). Transcription‐coupled repair – mechanisms of action, regulation, and associated human disorders. FEBS Letters. 599(2). 166–167. 5 indexed citations

Takeichi, Takuya, Takahiro Hamada, Mayuko Yamamoto, et al.. (2023). Patients with keratinization disorders due to ABCA12 variants showing pityriasis rubra pilaris phenotypes. The Journal of Dermatology. 51(1). 101–105. 2 indexed citations

10.

Theil, Arjan F., Gert‐Jan Kremers, Jeroen Demmers, et al.. (2023). Live cell transcription-coupled nucleotide excision repair dynamics revisited. DNA repair. 130. 103566–103566. 4 indexed citations

11.

Tamura, Atsushi, Miyako Tanaka, Yohei Kanamori, et al.. (2023). Lysosomal cholesterol overload in macrophages promotes liver fibrosis in a mouse model of NASH. The Journal of Experimental Medicine. 220(11). 24 indexed citations

12.

Horiba, Kazuhiro, Yuka Torii, Yuta Aizawa, et al.. (2022). Performance of Nanopore and Illumina Metagenomic Sequencing for Pathogen Detection and Transcriptome Analysis in Infantile Central Nervous System Infections. Open Forum Infectious Diseases. 9(10). ofac504–ofac504. 11 indexed citations

13.

Kimura, Hiroki, Masahiro Nakatochi, Branko Aleksić, et al.. (2022). Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genes. Translational Psychiatry. 12(1). 265–265. 8 indexed citations

14.

Utani, Atsushi, Yuta Koike, Yutaka Kuwatsuka, et al.. (2022). Clinical practice guidelines for pseudoxanthoma elasticum (2017). The Journal of Dermatology. 49(3). e91–e98. 5 indexed citations

15.

Takasaki, Yuto, Branko Aleksić, Hiroki Kimura, et al.. (2022). Exome sequencing of Japanese schizophrenia multiplex families supports the involvement of calcium ion channels. PLoS ONE. 17(5). e0268321–e0268321. 1 indexed citations

16.

Konishi, Hiroyuki, Takayuki Okamoto, Yuichiro Hara, et al.. (2020). Astrocytic phagocytosis is a compensatory mechanism for microglial dysfunction. The EMBO Journal. 39(22). e104464–e104464. 131 indexed citations

17.

Saha, Liton Kumar, Mitsuo Wakasugi, Salma Akter, et al.. (2020). Topoisomerase I-driven repair of UV-induced damage in NER-deficient cells. Proceedings of the National Academy of Sciences. 117(25). 14412–14420. 22 indexed citations

18.

Ogi, Tomoo, Yuka Nakazawa, Kensaku Sasaki, et al.. (2013). [Molecular cloning and characterisation of UVSSA, the responsible gene for UV-sensitive syndrome].. PubMed. 85(3). 133–44. 2 indexed citations

19.

Leopoldino, Andréia Machado, Valérie Bergoglio, Jiyang O‐Wang, et al.. (2005). Up-regulation of the error-prone DNA polymerase {kappa} promotes pleiotropic genetic alterations and tumorigenesis.. PubMed. 65(1). 325–30. 81 indexed citations

20.

Ogi, Tomoo, Patricia Kannouche, & Alan R. Lehmann. (2004). Localisation of human Y-family DNA polymerase κ: relationship to PCNA foci. Journal of Cell Science. 118(1). 129–136. 67 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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