Ko Noguchi

7.1k total citations
128 papers, 5.7k citations indexed

About

Ko Noguchi is a scholar working on Plant Science, Molecular Biology and Global and Planetary Change. According to data from OpenAlex, Ko Noguchi has authored 128 papers receiving a total of 5.7k indexed citations (citations by other indexed papers that have themselves been cited), including 97 papers in Plant Science, 64 papers in Molecular Biology and 22 papers in Global and Planetary Change. Recurrent topics in Ko Noguchi's work include Photosynthetic Processes and Mechanisms (60 papers), Plant Stress Responses and Tolerance (41 papers) and Plant nutrient uptake and metabolism (24 papers). Ko Noguchi is often cited by papers focused on Photosynthetic Processes and Mechanisms (60 papers), Plant Stress Responses and Tolerance (41 papers) and Plant nutrient uptake and metabolism (24 papers). Ko Noguchi collaborates with scholars based in Japan, United States and Australia. Ko Noguchi's co-authors include Ichiro Terashima, Keisuke Yoshida, Wataru Yamori, Chihiro Watanabe, Takushi Hachiya, Yin Wang, Masaru Kono, Youshi Tazoe, Kouki Hikosaka and Takao Araya and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLANT PHYSIOLOGY.

In The Last Decade

Ko Noguchi

121 papers receiving 5.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ko Noguchi Japan 46 4.4k 2.8k 1.2k 485 238 128 5.7k
Werner M. Kaiser Germany 57 8.1k 1.8× 4.1k 1.5× 669 0.5× 498 1.0× 172 0.7× 155 10.4k
Richard C. Leegood United Kingdom 43 3.9k 0.9× 3.6k 1.3× 673 0.5× 324 0.7× 155 0.7× 89 5.8k
Erik H. Murchie United Kingdom 41 6.3k 1.4× 2.3k 0.8× 1.3k 1.1× 526 1.1× 114 0.5× 123 7.8k
John Burke United States 45 4.7k 1.0× 3.0k 1.1× 507 0.4× 305 0.6× 490 2.1× 204 7.3k
Jeremy Harbinson Netherlands 42 5.3k 1.2× 3.4k 1.2× 1.1k 0.9× 393 0.8× 524 2.2× 103 6.6k
Alistair M. Hetherington United Kingdom 54 9.9k 2.2× 4.8k 1.7× 1.5k 1.3× 795 1.6× 241 1.0× 147 11.9k
Shi‐Bao Zhang China 32 2.0k 0.5× 1.7k 0.6× 709 0.6× 1.0k 2.1× 304 1.3× 160 3.6k
Jörg Fromm Germany 40 3.7k 0.8× 1.2k 0.4× 522 0.4× 372 0.8× 568 2.4× 97 4.7k
Julian M. Hibberd United Kingdom 45 4.8k 1.1× 5.3k 1.9× 399 0.3× 1.1k 2.3× 187 0.8× 120 7.9k
Gregory A. Gambetta France 37 3.8k 0.8× 1.3k 0.5× 1.0k 0.8× 142 0.3× 87 0.4× 89 4.3k

Countries citing papers authored by Ko Noguchi

Since Specialization
Citations

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

Fields of papers citing papers by Ko Noguchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ko Noguchi

This figure shows the co-authorship network connecting the top 25 collaborators of Ko Noguchi. A scholar is included among the top collaborators of Ko Noguchi 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 Ko Noguchi. Ko Noguchi 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.
Mizokami, Yusuke, et al.. (2025). Characterization of biochemistry and anatomy for underwater carbon uptake in leaves of the amphibious plant Hygrophila difformis. Journal of Experimental Botany. 76(16). 4581–4597.
3.
Mizokami, Yusuke, et al.. (2024). Effects of nutrient conditions to stem photosynthesis and growth in Ephedra intermedia (Ephedraceae). Soil Science & Plant Nutrition. 70(5-6). 345–352. 2 indexed citations
4.
Miyagi, Atsuko, Kentaro Takahara, Masaru Kono, et al.. (2023). Loss of peroxisomal NAD kinase 3 (NADK3) affects photorespiration metabolism in Arabidopsis. Journal of Plant Physiology. 283. 153950–153950. 1 indexed citations
5.
Takahashi, Yuki, Ko Noguchi, Kentaro Ifuku, et al.. (2023). Effects of drought stress on the oxidation of the reaction center chlorophyll of photosystem I and grain yield in paddy-field grown rice plants. Soil Science & Plant Nutrition. 69(4). 215–220. 1 indexed citations
7.
Wada, Naoki, Ryouichi Tanaka, Atsuko Miyagi, et al.. (2022). Dynamic seasonal changes in photosynthesis systems in leaves ofAsarum tamaense, an evergreen understorey herbaceous species. Annals of Botany. 131(3). 423–436. 6 indexed citations
8.
Otsuka, Kurataka, Mineko Konishi, Atsuko Kinoshita, et al.. (2021). Temperature-dependent fasciation mutants provide a link between mitochondrial RNA processing and lateral root morphogenesis. eLife. 10. 14 indexed citations
9.
Funayama‐Noguchi, Sachiko, Masaru Shibata, Ko Noguchi, & Ichiro Terashima. (2020). Effects of root morphology, respiration and carboxylate exudation on carbon economy in two non‐mycorrhizal lupines under phosphorus deficiency. Plant Cell & Environment. 44(2). 598–612. 20 indexed citations
10.
Takeuchi, Yu, Yasuyuki Fukui, Ko Noguchi, et al.. (2020). Rare Neurologic Disease-Associated Mutations of AIMP1 Are Related with Inhibitory Neuronal Differentiation Which Is Reversed by Ibuprofen. SHILAP Revista de lepidopterología. 7(5). 25–25. 5 indexed citations
11.
Sako, Kaori, Yushi Futamura, Takeshi Shimizu, et al.. (2020). Inhibition of mitochondrial complex I by the novel compound FSL0260 enhances high salinity-stress tolerance in Arabidopsis thaliana. Scientific Reports. 10(1). 8691–8691. 14 indexed citations
12.
Noguchi, Ko, Chihiro Watanabe, & Ichiro Terashima. (2015). Effects of Elevated Atmospheric CO2on Primary Metabolite Levels inArabidopsis thalianaCol-0 Leaves: An Examination of Metabolome Data. Plant and Cell Physiology. 56(11). pcv125–pcv125. 23 indexed citations
13.
Wang, Yin, et al.. (2013). Overexpression of plasma membrane H + -ATPase in guard cells promotes light-induced stomatal opening and enhances plant growth. Proceedings of the National Academy of Sciences. 111(1). 533–538. 187 indexed citations
14.
Nakamura, Takatoshi, et al.. (2012). Functional linkage between N acquisition strategies and aeration capacities of hydrophytes for efficient oxygen consumption in roots. Physiologia Plantarum. 147(2). 135–146. 9 indexed citations
16.
Hachiya, Takushi, Chihiro Watanabe, Danny Tholen, et al.. (2010). Ammonium‐dependent respiratory increase is dependent on the cytochrome pathway in Arabidopsis thaliana shoots. Plant Cell & Environment. 33(11). 1888–1897. 42 indexed citations
17.
Watanabe, Chihiro, T Hachiya, Ichiro Terashima, & Ko Noguchi. (2008). The lack of alternative oxidase at low temperature leads to a disruption of the balance in carbon and nitrogen metabolism, and to an up‐regulation of antioxidant defence systems in Arabidopsis thaliana leaves. Plant Cell & Environment. 31(8). 1190–1202. 113 indexed citations
18.
Noguchi, Ko, et al.. (2001). Costs of protein turnover and carbohydrate export in leaves of sun and shade species. Australian Journal of Plant Physiology. 28(1). 37–47. 43 indexed citations
19.
Noguchi, Ko, et al.. (2001). Activities of the cyanide-resistant respiratory pathway in leaves of sun and shade species. Australian Journal of Plant Physiology. 28(1). 27–35. 50 indexed citations
20.
Noguchi, Ko & Ichiro Terashima. (1996). COMPARATIVE STUDY OF THE RESPIRATORY SYSTEMS OF LEAVES IN SUN AND SHADE PLANTS. Plant and Cell Physiology. 37. 64. 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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