Takashi Ueda

20.8k total citations · 1 hit paper
358 papers, 14.7k citations indexed

About

Takashi Ueda is a scholar working on Molecular Biology, Plant Science and Surgery. According to data from OpenAlex, Takashi Ueda has authored 358 papers receiving a total of 14.7k indexed citations (citations by other indexed papers that have themselves been cited), including 153 papers in Molecular Biology, 100 papers in Plant Science and 86 papers in Surgery. Recurrent topics in Takashi Ueda's work include Plant Reproductive Biology (80 papers), Cellular transport and secretion (69 papers) and Pancreatitis Pathology and Treatment (53 papers). Takashi Ueda is often cited by papers focused on Plant Reproductive Biology (80 papers), Cellular transport and secretion (69 papers) and Pancreatitis Pathology and Treatment (53 papers). Takashi Ueda collaborates with scholars based in Japan, United States and Germany. Takashi Ueda's co-authors include Akihiko Nakano, Tomohiro Uemura, Kazuo Ebine, Yoshifumi Takeyama, Masa H. Sato, Masaru Fujimoto, Yoshikazu Kuroda, Yoshimi Takai, Alan H. Jobe and Emi Ito and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Takashi Ueda

336 papers receiving 14.5k citations

Hit Papers

The Arabidopsis GNOM ARF-GEF Mediates Endosomal Recycling... 2003 2026 2010 2018 2003 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Takashi Ueda Japan 65 8.5k 6.7k 3.9k 1.6k 1.4k 358 14.7k
Tatsuya Hirano Japan 78 13.0k 1.5× 3.9k 0.6× 4.2k 1.1× 1.0k 0.6× 542 0.4× 339 19.5k
Joël Vandekerckhove Belgium 68 8.4k 1.0× 1.9k 0.3× 3.4k 0.9× 995 0.6× 456 0.3× 181 13.8k
Yasushi Ishihama Japan 61 13.7k 1.6× 2.4k 0.4× 1.9k 0.5× 397 0.3× 397 0.3× 253 21.5k
Hiroshi Kimurâ Japan 71 15.9k 1.9× 2.5k 0.4× 1.7k 0.4× 601 0.4× 427 0.3× 461 19.8k
Ming Zhou China 62 9.7k 1.1× 955 0.1× 1.0k 0.3× 729 0.5× 2.0k 1.4× 346 14.1k
Anthony Bretscher United States 70 11.9k 1.4× 834 0.1× 9.1k 2.3× 730 0.5× 815 0.6× 148 19.0k
Matthias W. Hentze Germany 107 25.4k 3.0× 1.7k 0.3× 1.8k 0.5× 536 0.3× 1.3k 0.9× 306 40.1k
Nagarjuna Nagaraj Germany 30 11.9k 1.4× 1.0k 0.2× 2.0k 0.5× 551 0.4× 511 0.4× 39 17.2k
Hiroshi Nojima Japan 62 10.6k 1.2× 1.1k 0.2× 3.5k 0.9× 759 0.5× 422 0.3× 300 15.8k
Alfred Nordheim Germany 74 13.2k 1.6× 1.2k 0.2× 1.7k 0.4× 501 0.3× 442 0.3× 204 17.7k

Countries citing papers authored by Takashi Ueda

Since Specialization
Citations

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

Fields of papers citing papers by Takashi Ueda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Takashi Ueda

This figure shows the co-authorship network connecting the top 25 collaborators of Takashi Ueda. A scholar is included among the top collaborators of Takashi Ueda 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 Takashi Ueda. Takashi Ueda 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.
Segami, Shoji, et al.. (2025). Amyloplasts are necessary for full gravitropism in thallus of Marchantia polymorpha. Journal of Experimental Botany. 76(22). 6741–6757. 1 indexed citations
2.
Sakil, Md. Arif, et al.. (2025). Autophagic cell death in plants. Plant and Cell Physiology. 66(10). 1389–1396. 1 indexed citations
4.
Ohta, Daisaku, Atsushi Okazawa, Takumi Ogawa, et al.. (2024). Characterization of Subcellular Dynamics of Sterol Methyltransferases Clarifies Defective Cell Division in smt2 smt3, a C-24 Ethyl Sterol-Deficient Mutant of Arabidopsis. Biomolecules. 14(7). 868–868. 1 indexed citations
5.
Hirano, Tomoko, Kazuo Ebine, Takashi Ueda, et al.. (2023). The SYP123–VAMP727 SNARE complex delivers secondary cell wall components for root hair shank hardening in Arabidopsis. The Plant Cell. 35(12). 4347–4365. 1 indexed citations
6.
Minamino, Naoki, Tomoaki Nishiyama, Mayuko Sato, et al.. (2022). Phylogenetic distribution and expression pattern analyses identified a divergent basal body assembly protein involved in land plant spermatogenesis. New Phytologist. 236(3). 1182–1196. 4 indexed citations
7.
Takagi, Junpei, Emi Ito, Yoko Ito, et al.. (2021). Cargo sorting zones in the trans-Golgi network visualized by super-resolution confocal live imaging microscopy in plants. Nature Communications. 12(1). 1901–1901. 71 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.
Shimada, Takashi, Takashi Ueda, & Ikuko Hara‐Nishimura. (2021). Excess sterol accumulation affects seed morphology and physiology in Arabidopsis thaliana. Plant Signaling & Behavior. 16(4). 1872217–1872217. 9 indexed citations
10.
Kanazawa, Takehiko, Takeshi Haraguchi, Atsuko Era, et al.. (2020). Characterization of ancestral myosin XI from Marchantia polymorpha by heterologous expression in Arabidopsis thaliana. The Plant Journal. 104(2). 460–473. 4 indexed citations
11.
Minamino, Naoki, Manjinder S. Cheema, Dina L. Bai, et al.. (2019). Protamines from liverwort are produced by post-translational cleavage and C-terminal di-aminopropanelation of several male germ-specific H1 histones. Journal of Biological Chemistry. 294(44). 16364–16373. 17 indexed citations
12.
Shimada, Takashi, Shigeyuki Betsuyaku, Noriko Inada, et al.. (2019). Enrichment of Phosphatidylinositol 4,5-Bisphosphate in the Extra-Invasive Hyphal Membrane Promotes Colletotrichum Infection of Arabidopsis thaliana. Plant and Cell Physiology. 60(7). 1514–1524. 36 indexed citations
13.
Ebine, Kazuo, Falco Krüger, Zaida Andrés, et al.. (2018). Distinct sets of tethering complexes, SNARE complexes, and Rab GTPases mediate membrane fusion at the vacuole in Arabidopsis. Proceedings of the National Academy of Sciences. 115(10). E2457–E2466. 107 indexed citations
14.
Minamino, Naoki, Takehiko Kanazawa, Atsuko Era, et al.. (2018). RAB GTPases in the Basal Land Plant Marchantia polymorpha. Plant and Cell Physiology. 59(4). 850–861. 13 indexed citations
15.
Ito, Emi, Kazuo Ebine, Seungwon Choi, et al.. (2018). Integration of two RAB5 groups during endosomal transport in plants. eLife. 7. 24 indexed citations
16.
Kurusu, Takamitsu, Nobutaka Kitahata, Tomokazu Tsutsui, et al.. (2018). Involvement of S-type anion channels in disease resistance against an oomycete pathogen in Arabidopsis seedlings. Communicative & Integrative Biology. 11(3). 1–6. 3 indexed citations
17.
Cui, Yong, Wenhan Cao, Yilin He, et al.. (2018). A whole-cell electron tomography model of vacuole biogenesis in Arabidopsis root cells. Nature Plants. 5(1). 95–105. 112 indexed citations
18.
Kawai‐Toyooka, Hiroko, Toshiyuki Mori, Takashi Hamaji, et al.. (2014). Sex-Specific Posttranslational Regulation of the Gamete Fusogen GCS1 in the Isogamous Volvocine Alga Gonium pectorale. Eukaryotic Cell. 13(5). 648–656. 16 indexed citations
19.
Fujimoto, Masaru, Shin‐ichi Arimura, Takashi Ueda, et al.. (2010). Arabidopsis dynamin-related proteins DRP2B and DRP1A participate together in clathrin-coated vesicle formation during endocytosis. Proceedings of the National Academy of Sciences. 107(13). 6094–6099. 111 indexed citations
20.
Dhonukshe, Pankaj, Ilya Grigoriev, Rainer Fischer, et al.. (2008). Auxin transport inhibitors impair vesicle motility and actin cytoskeleton dynamics in diverse eukaryotes. Proceedings of the National Academy of Sciences. 105(11). 4489–4494. 187 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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