Hirotake Yamaguchi

1.1k total citations
16 papers, 921 citations indexed

About

Hirotake Yamaguchi is a scholar working on Molecular Biology, Genetics and Ecology. According to data from OpenAlex, Hirotake Yamaguchi has authored 16 papers receiving a total of 921 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Ecology. Recurrent topics in Hirotake Yamaguchi's work include Bacterial Genetics and Biotechnology (8 papers), Bacteriophages and microbial interactions (7 papers) and RNA and protein synthesis mechanisms (3 papers). Hirotake Yamaguchi is often cited by papers focused on Bacterial Genetics and Biotechnology (8 papers), Bacteriophages and microbial interactions (7 papers) and RNA and protein synthesis mechanisms (3 papers). Hirotake Yamaguchi collaborates with scholars based in Japan, South Korea and France. Hirotake Yamaguchi's co-authors include Yasutaro Fujita, Yoshiko Nakaura, Naotake Ogasawara, Ken‐ichi Yoshida, Kazuo Kobayashi, Teruo Tanaka, Mitsuo Ogura, Virginie Molle, Robert P. Shivers and Abraham L. Sonenshein and has published in prestigious journals such as Journal of Biological Chemistry, Biochemical and Biophysical Research Communications and Journal of Bacteriology.

In The Last Decade

Hirotake Yamaguchi

16 papers receiving 911 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hirotake Yamaguchi Japan 12 658 538 310 102 65 16 921
V. James Hernandez United States 16 955 1.5× 648 1.2× 249 0.8× 111 1.1× 97 1.5× 18 1.2k
Elisabeth Vaganay France 15 617 0.9× 285 0.5× 196 0.6× 70 0.7× 57 0.9× 25 922
Martin Haardt Canada 10 801 1.2× 504 0.9× 93 0.3× 47 0.5× 66 1.0× 10 1.2k
K L Strauch United States 12 712 1.1× 471 0.9× 136 0.4× 143 1.4× 37 0.6× 13 1.1k
S Kimura Japan 9 439 0.7× 312 0.6× 191 0.6× 40 0.4× 81 1.2× 19 800
Miki Jishage Japan 13 1.2k 1.8× 893 1.7× 391 1.3× 93 0.9× 73 1.1× 19 1.5k
Stéphanie Marsin France 18 1.1k 1.6× 399 0.7× 165 0.5× 84 0.8× 88 1.4× 33 1.3k
Jill Gough Australia 4 631 1.0× 346 0.6× 112 0.4× 34 0.3× 86 1.3× 6 1.1k
Arnim Weber Germany 19 769 1.2× 164 0.3× 66 0.2× 48 0.5× 48 0.7× 27 1.1k
Michelle A. Alting-Mees Canada 11 1.1k 1.7× 167 0.3× 220 0.7× 27 0.3× 175 2.7× 15 1.5k

Countries citing papers authored by Hirotake Yamaguchi

Since Specialization
Citations

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

Fields of papers citing papers by Hirotake Yamaguchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hirotake Yamaguchi

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

All Works

16 of 16 papers shown
1.
Yamaguchi, Hirotake, et al.. (2025). Integrating LC–MS/MS and In Silico Methods to Uncover Bioactive Compounds with Lipase Inhibitory Potential in the Antarctic Moss Warnstorfia fontinaliopsis. Applied Biochemistry and Biotechnology. 197(4). 2734–2756. 1 indexed citations
2.
Ozaki, Takenori, Shoichi Maruyama, Masato Kobori, et al.. (2008). Novel Culture System of Mesenchymal Stromal Cells from Human Subcutaneous Adipose Tissue. Stem Cells and Development. 18(4). 533–544. 51 indexed citations
3.
Koparal, Ayşe Tansu, Hirotake Yamaguchi, Kaoru Omae, Shuhei Torii, & Yasuo Kitagawa. (2004). Differential effect of green tea catechins on three endothelial cell clones isolated from rat adipose tissue and on human umbilical vein endothelial cells. Cytotechnology. 46(1). 25–36. 3 indexed citations
4.
Serizawa, Masakuni, Hiroki Yamamoto, Hirotake Yamaguchi, et al.. (2004). Systematic analysis of SigD-regulated genes in Bacillus subtilis by DNA microarray and Northern blotting analyses. Gene. 329. 125–136. 62 indexed citations
5.
Kakeshita, Hiroshi, Keigo Bunai, Shigeo Tojo, et al.. (2003). Mannitol-1-Phosphate Dehydrogenase (MtlD) Is Required for Mannitol and Glucitol Assimilation in Bacillus subtilis : Possible Cooperation of mtl and gut Operons. Journal of Bacteriology. 185(16). 4816–4824. 32 indexed citations
6.
Doan, Thierry, Pascale Servant, Shigeo Tojo, et al.. (2003). The Bacillus subtilis ywkA gene encodes a malic enzyme and its transcription is activated by the YufL/YufM two-component system in response to malate. Microbiology. 149(9). 2331–2343. 48 indexed citations
7.
Molle, Virginie, Yoshiko Nakaura, Robert P. Shivers, et al.. (2003). Additional Targets of theBacillus subtilisGlobal Regulator CodY Identified by Chromatin Immunoprecipitation and Genome-Wide Transcript Analysis. Journal of Bacteriology. 185(6). 1911–1922. 244 indexed citations
8.
Yoshida, Ken‐ichi, et al.. (2003). Identification of additional TnrA‐regulated genes of Bacillus subtilis associated with a TnrA box. Molecular Microbiology. 49(1). 157–165. 87 indexed citations
9.
Asai, Kei, Hirotake Yamaguchi, Choong‐Min Kang, et al.. (2003). DNA microarray analysis ofBacillus subtilissigma factors of extracytoplasmic function family. FEMS Microbiology Letters. 220(1). 155–160. 56 indexed citations
10.
Yatagai, Fumio, Takehiko Nohmi, Kenichi Masumura, et al.. (2002). Heavy‐ion‐induced mutations in the gpt delta transgenic mouse: Effect of p53 gene knockout. Environmental and Molecular Mutagenesis. 40(3). 216–225. 37 indexed citations
11.
Ogura, Mitsuo, Hirotake Yamaguchi, Kazuo Kobayashi, et al.. (2002). Whole-Genome Analysis of Genes Regulated by theBacillus subtilisCompetence Transcription Factor ComK. Journal of Bacteriology. 184(9). 2344–2351. 125 indexed citations
12.
Kobayashi, Kazuo, Mitsuo Ogura, Hirotake Yamaguchi, et al.. (2001). Comprehensive DNA Microarray Analysis of Bacillus subtilis Two-Component Regulatory Systems. Journal of Bacteriology. 183(24). 7365–7370. 121 indexed citations
13.
Yamaguchi, Hirotake, Hironobu Yamashita, Hitoshi Mori, et al.. (2000). High and Low Affinity Heparin-binding Sites in the G Domain of the Mouse Laminin α4 Chain. Journal of Biological Chemistry. 275(38). 29458–29465. 27 indexed citations
14.
Yamaguchi, Hirotake, Yasuo Kitagawa, & Kiyoshi Miki. (1999). BrachyuryRegulatory Region Active in Embryonal Carcinoma P19 Cells. Bioscience Biotechnology and Biochemistry. 63(3). 608–609. 2 indexed citations
15.
Yamaguchi, Hirotake, Tomoaki Niimi, Yasuo Kitagawa, & Kiyoshi Miki. (1999). Brachyury (T) expression in embryonal carcinoma P19 cells resembles its expression in primitive streak and tail‐bud but not that in notochord. Development Growth & Differentiation. 41(3). 253–264. 14 indexed citations
16.
Yamaguchi, Hirotake, Kimiko Tanaka, Yasuo Kitagawa, & Kiyoshi Miki. (1999). A PEA3 Site Flanked by SP1, SP4, and GATA Sites Positively Regulates the Differentiation-Dependent Expression ofBrachyuryin Embryonal Carcinoma P19 Cells. Biochemical and Biophysical Research Communications. 254(3). 542–547. 11 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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