Reo Maeda

1.1k total citations
19 papers, 737 citations indexed

About

Reo Maeda is a scholar working on Molecular Biology, Cognitive Neuroscience and Genetics. According to data from OpenAlex, Reo Maeda has authored 19 papers receiving a total of 737 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 6 papers in Cognitive Neuroscience and 6 papers in Genetics. Recurrent topics in Reo Maeda's work include Developmental Biology and Gene Regulation (12 papers), Hemispheric Asymmetry in Neuroscience (6 papers) and Hearing, Cochlea, Tinnitus, Genetics (4 papers). Reo Maeda is often cited by papers focused on Developmental Biology and Gene Regulation (12 papers), Hemispheric Asymmetry in Neuroscience (6 papers) and Hearing, Cochlea, Tinnitus, Genetics (4 papers). Reo Maeda collaborates with scholars based in Japan, United States and France. Reo Maeda's co-authors include Kenji Matsuno, Kiichiro Taniguchi, Shunya Hozumi, Teresa Nicolson, Naotaka Nakazawa, Ryo Hatori, Takashi Okumura, Mitsutoshi Nakamura, Timothy Erickson and Takeshi Sasamura and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Reo Maeda

19 papers receiving 733 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Reo Maeda Japan 13 423 197 180 102 98 19 737
Mark Eddison United States 15 696 1.6× 186 0.9× 301 1.7× 107 1.0× 365 3.7× 24 1.3k
Olga Alexandrova Germany 18 374 0.9× 107 0.5× 198 1.1× 249 2.4× 210 2.1× 25 958
Joseph L. Dynes United States 14 601 1.4× 296 1.5× 156 0.9× 39 0.4× 287 2.9× 17 1.1k
Edmund J. Koundakjian United States 8 739 1.7× 254 1.3× 313 1.7× 96 0.9× 191 1.9× 8 1.1k
Ikuko Fujiwara Japan 16 460 1.1× 669 3.4× 123 0.7× 41 0.4× 143 1.5× 29 1.3k
Shan Meltzer United States 11 388 0.9× 153 0.8× 156 0.9× 32 0.3× 398 4.1× 14 888
Agnieszka Rzadzinska United Kingdom 12 716 1.7× 261 1.3× 550 3.1× 128 1.3× 64 0.7× 20 1.2k
Jonathan E. Bird United States 14 402 1.0× 166 0.8× 449 2.5× 111 1.1× 32 0.3× 24 802
Anna M. Steyer Germany 15 561 1.3× 201 1.0× 65 0.4× 45 0.4× 82 0.8× 32 914
Margaret S. Saha United States 23 965 2.3× 222 1.1× 60 0.3× 78 0.8× 268 2.7× 79 1.6k

Countries citing papers authored by Reo Maeda

Since Specialization
Citations

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

Fields of papers citing papers by Reo Maeda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Reo Maeda

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

All Works

19 of 19 papers shown
1.
Lai, Yi‐Ting, Takeshi Sasamura, Junpei Kuroda, et al.. (2023). The Drosophila AWP1 ortholog Doctor No regulates JAK/STAT signaling for left–right asymmetry in the gut by promoting receptor endocytosis. Development. 150(6). 4 indexed citations
2.
Takabatake, Reona, Satoshi IZUMI, Satoshi Nakazawa, et al.. (2019). Novel Bioprinting Application for the Production of Reference Material Containing a Defined Copy Number of Target DNA. Analytical Chemistry. 91(20). 12733–12740. 8 indexed citations
3.
Ishibashi, T., Ryo Hatori, Reo Maeda, et al.. (2019). E and ID proteins regulate cell chirality and left–right asymmetric development in Drosophila. Genes to Cells. 24(3). 214–230. 9 indexed citations
4.
Erickson, Timothy, Clive P. Morgan, Jennifer Olt, et al.. (2017). Integration of Tmc1/2 into the mechanotransduction complex in zebrafish hair cells is regulated by Transmembrane O-methyltransferase (Tomt). eLife. 6. 45 indexed citations
5.
Maeda, Reo, et al.. (2017). Functional Analysis of the Transmembrane and Cytoplasmic Domains of Pcdh15a in Zebrafish Hair Cells. Journal of Neuroscience. 37(12). 3231–3245. 24 indexed citations
6.
Trapani, Josef G., et al.. (2015). Dopamine Modulates the Activity of Sensory Hair Cells. Journal of Neuroscience. 35(50). 16494–16503. 45 indexed citations
7.
Okumura, Takashi, Takeshi Sasamura, Shunya Hozumi, et al.. (2015). Class I Myosins Have Overlapping and Specialized Functions in Left-Right Asymmetric Development inDrosophila. Genetics. 199(4). 1183–1199. 16 indexed citations
8.
Maeda, Reo, Katie S. Kindt, Weike Mo, et al.. (2014). Tip-link protein protocadherin 15 interacts with transmembrane channel-like proteins TMC1 and TMC2. Proceedings of the National Academy of Sciences. 111(35). 12907–12912. 128 indexed citations
9.
Nakamura, Mitsutoshi, Takeshi Muguruma, Naotaka Nakazawa, et al.. (2012). Reduced cell number in the hindgut epithelium disrupts hindgut left–right asymmetry in a mutant of pebble, encoding a RhoGEF, in Drosophila embryos. Mechanisms of Development. 130(2-3). 169–180. 13 indexed citations
10.
Nakazawa, Naotaka, Kiichiro Taniguchi, Takashi Okumura, Reo Maeda, & Kenji Matsuno. (2012). A novel Cre/loxP system for mosaic gene expression in the Drosophila embryo. Developmental Dynamics. 241(5). 965–974. 10 indexed citations
11.
Kuroda, Junpei, Mitsutoshi Nakamura, Masashi Yoshida, et al.. (2011). Canonical Wnt signaling in the visceral muscle is required for left–right asymmetric development of the Drosophila midgut. Mechanisms of Development. 128(11-12). 625–639. 20 indexed citations
12.
Taniguchi, Kiichiro, Reo Maeda, Tadashi Ando, et al.. (2011). Chirality in Planar Cell Shape Contributes to Left-Right Asymmetric Epithelial Morphogenesis. Science. 333(6040). 339–341. 173 indexed citations
13.
Okumura, Takashi, Kiichiro Taniguchi, Junpei Kuroda, et al.. (2010). Left–right asymmetric morphogenesis of the anterior midgut depends on the activation of a non-muscle myosin II in Drosophila. Developmental Biology. 344(2). 693–706. 16 indexed citations
14.
Kuroda, Junpei, Takashi Okumura, Reo Maeda, et al.. (2010). P103. Wnt signal plays essential roles in the left-right asymmetric development of the embryonic gut in Drosophila. Differentiation. 80. S51–S52. 1 indexed citations
15.
Hozumi, Shunya, Reo Maeda, Takashi Okumura, et al.. (2008). Head region of unconventional myosin I family members is responsible for the organ‐specificity of their roles in left–right polarity in Drosophila. Developmental Dynamics. 237(12). 3528–3537. 19 indexed citations
16.
Taniguchi, Kiichiro, Shunya Hozumi, Reo Maeda, et al.. (2007). D-JNK signaling in visceral muscle cells controls the laterality of the Drosophila gut. Developmental Biology. 311(1). 251–263. 20 indexed citations
17.
Taniguchi, Kiichiro, Shunya Hozumi, Reo Maeda, Takashi Okumura, & Kenji Matsuno. (2007). Roles of Type I Myosins in Drosophila Handedness. Fly. 1(5). 287–290. 6 indexed citations
18.
Maeda, Reo, Shunya Hozumi, Kiichiro Taniguchi, et al.. (2006). Roles of single-minded in the left–right asymmetric development of the Drosophila embryonic gut. Mechanisms of Development. 124(3). 204–217. 20 indexed citations
19.
Hozumi, Shunya, Reo Maeda, Kiichiro Taniguchi, et al.. (2006). An unconventional myosin in Drosophila reverses the default handedness in visceral organs. Nature. 440(7085). 798–802. 160 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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