Ryu Maeda

840 total citations
14 papers, 722 citations indexed

About

Ryu Maeda is a scholar working on Molecular Biology, Developmental Neuroscience and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ryu Maeda has authored 14 papers receiving a total of 722 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 3 papers in Developmental Neuroscience and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ryu Maeda's work include Developmental Biology and Gene Regulation (7 papers), Wnt/β-catenin signaling in development and cancer (3 papers) and Congenital heart defects research (3 papers). Ryu Maeda is often cited by papers focused on Developmental Biology and Gene Regulation (7 papers), Wnt/β-catenin signaling in development and cancer (3 papers) and Congenital heart defects research (3 papers). Ryu Maeda collaborates with scholars based in Japan, United States and Russia. Ryu Maeda's co-authors include Ira Daar, Hitoshi Okamoto, Ichiro Masai, Atsuko Komori, Haichang Li, Masahiro Yamaguchi, Yasuhiro Nojima, Noriko Tonou‐Fujimori, Mitsugu Maéno and Arthur M. Buchberg and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Development and Oncogene.

In The Last Decade

Ryu Maeda

14 papers receiving 714 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ryu Maeda Japan 12 591 151 120 94 58 14 722
Thomas Schmitt‐John Germany 20 564 1.0× 168 1.1× 150 1.3× 139 1.5× 42 0.7× 39 1.1k
C. H. Koster Netherlands 8 520 0.9× 131 0.9× 112 0.9× 80 0.9× 33 0.6× 12 639
Agnès Degrave France 7 409 0.7× 168 1.1× 94 0.8× 39 0.4× 22 0.4× 7 603
Nick R. Love United Kingdom 10 506 0.9× 110 0.7× 49 0.4× 78 0.8× 42 0.7× 11 732
Sinnakaruppan Mathavan Singapore 15 377 0.6× 199 1.3× 125 1.0× 63 0.7× 39 0.7× 30 707
Emily K. Pugach United States 13 531 0.9× 391 2.6× 96 0.8× 39 0.4× 28 0.5× 14 825
Violaine Alunni France 6 594 1.0× 172 1.1× 261 2.2× 99 1.1× 22 0.4× 7 741
Samantha Carruthers United Kingdom 8 462 0.8× 234 1.5× 132 1.1× 38 0.4× 30 0.5× 9 667
Atsushi Shimomura Japan 14 361 0.6× 84 0.6× 70 0.6× 134 1.4× 34 0.6× 25 577
Sheryl M. Sato United States 16 606 1.0× 103 0.7× 129 1.1× 135 1.4× 79 1.4× 27 854

Countries citing papers authored by Ryu Maeda

Since Specialization
Citations

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

Fields of papers citing papers by Ryu Maeda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ryu Maeda

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

All Works

14 of 14 papers shown
1.
Maeda, Ryu, Naoki Takeda, Ryuji Hiramatsu, et al.. (2024). Morc1 reestablishes H3K9me3 heterochromatin on piRNA-targeted transposons in gonocytes. Proceedings of the National Academy of Sciences. 121(13). e2317095121–e2317095121. 2 indexed citations
2.
Jiang, Yiming, Chun‐Yi Chen, Daisuke Yamane, et al.. (2023). Specimen size effect on the strength of nickel-boron alloys. Materials Letters. 349. 134742–134742. 1 indexed citations
3.
Uesato, Shinichi, Hirofumi Yamashita, Ryu Maeda, et al.. (2014). Synergistic Antitumor Effect of a Combination of Paclitaxel and Carboplatin with Nobiletin from Citrus depressa on Non-Small-Cell Lung Cancer Cell Lines. Planta Medica. 80(6). 452–457. 28 indexed citations
4.
Tanaka, Hideomi, Ryu Maeda, Wataru Shoji, et al.. (2007). Novel mutations affecting axon guidance in zebrafish and a role for plexin signalling in the guidance of trigeminal and facial nerve axons. Development. 134(18). 3259–3269. 36 indexed citations
5.
Yamaguchi, Masahiro, Noriko Tonou‐Fujimori, Atsuko Komori, et al.. (2005). Histone deacetylase 1 regulates retinal neurogenesis in zebrafish by suppressing Wnt and Notch signaling pathways. Development. 132(13). 3027–3043. 186 indexed citations
6.
Park, Eui Kyun, Neil Warner, Yong‐Sik Bong, et al.. (2004). Ectopic EphA4 Receptor Induces Posterior Protrusions via FGF Signaling inXenopusEmbryos. Molecular Biology of the Cell. 15(4). 1647–1655. 34 indexed citations
7.
Escalante‐Alcalde, Diana, Lídia Hernandez, Hervé Le Stunff, et al.. (2003). The lipid phosphatase LPP3 regulates extra-embryonic vasculogenesis and axis patterning. Development. 130(19). 4623–4637. 144 indexed citations
8.
Maeda, Ryu, Akihiko Ishimura, Kathleen Mood, et al.. (2002). Xpbx1b and Xmeis1b play a collaborative role in hindbrain and neural crest gene expression in Xenopus embryos. Proceedings of the National Academy of Sciences. 99(8). 5448–5453. 46 indexed citations
9.
Maeda, Ryu, et al.. (2001). Xmeis1, a protooncogene involved in specifying neural crest cell fate in Xenopus embryos. Oncogene. 20(11). 1329–1342. 56 indexed citations
10.
Takeda, Masatoshi, et al.. (2000). Xenopus msx-1 regulates dorso-ventral axis formation by suppressing the expression of organizer genes. Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology. 126(2). 157–168. 14 indexed citations
11.
Ishimura, Akihiko, Ryu Maeda, Masatoshi Takeda, et al.. (2000). Involvement of BMP‐4/msx‐1 and FGF pathways in neural induction in the Xenopus embryo. Development Growth & Differentiation. 42(4). 307–316. 27 indexed citations
12.
Katagiri, Chiaki, et al.. (1997). Molecular cloning of Xenopus hatching enzyme and its specific expression in hatching gland cells. The International Journal of Developmental Biology. 41(1). 19–25. 56 indexed citations
13.
Lin, Jih‐Jing, et al.. (1997). XBMP‐1B (Xtld), a Xenopus homolog of dorso–ventral polarity gene in Drosophila, modifies tissue phenotypes of ventral explants. Development Growth & Differentiation. 39(1). 43–51. 23 indexed citations
14.
Maeda, Ryu, et al.. (1997). Xmsx-1 modifies mesodermal tissue pattern along dorsoventral axis in Xenopus laevis embryo. Development. 124(13). 2553–2560. 69 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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