Ryoichiro Kageyama

36.1k total citations · 10 hit papers
277 papers, 28.3k citations indexed

About

Ryoichiro Kageyama is a scholar working on Molecular Biology, Developmental Neuroscience and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ryoichiro Kageyama has authored 277 papers receiving a total of 28.3k indexed citations (citations by other indexed papers that have themselves been cited), including 232 papers in Molecular Biology, 81 papers in Developmental Neuroscience and 49 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ryoichiro Kageyama's work include Developmental Biology and Gene Regulation (117 papers), Neurogenesis and neuroplasticity mechanisms (81 papers) and Epigenetics and DNA Methylation (45 papers). Ryoichiro Kageyama is often cited by papers focused on Developmental Biology and Gene Regulation (117 papers), Neurogenesis and neuroplasticity mechanisms (81 papers) and Epigenetics and DNA Methylation (45 papers). Ryoichiro Kageyama collaborates with scholars based in Japan, United States and France. Ryoichiro Kageyama's co-authors include Toshiyuki Ohtsuka, Shigetada Nakanishi, Itaru Imayoshi, François Guillemot, Yasumasa Bessho, Hiromi Shimojo, Jun Hatakeyama, Taeko Kobayashi, Yoshiki Sasai and Masayuki Sakamoto and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Ryoichiro Kageyama

272 papers receiving 28.1k citations

Hit Papers

Control of endodermal endocrine development by Hes-1 1991 2026 2002 2014 2000 2008 1995 2002 1991 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
Ryoichiro Kageyama Japan 95 20.8k 6.0k 4.2k 4.0k 2.9k 277 28.3k
François Guillemot France 93 20.1k 1.0× 9.3k 1.6× 6.6k 1.6× 5.5k 1.4× 3.0k 1.0× 243 29.0k
David H. Rowitch United States 93 18.9k 0.9× 9.9k 1.6× 4.9k 1.1× 4.0k 1.0× 2.3k 0.8× 200 31.5k
Michael Wegner Germany 78 12.5k 0.6× 4.4k 0.7× 3.1k 0.7× 4.5k 1.1× 1.8k 0.6× 265 19.9k
Alexandra L. Joyner United States 87 21.0k 1.0× 4.1k 0.7× 5.4k 1.3× 6.5k 1.6× 2.4k 0.8× 194 27.2k
Jonas Frisén Sweden 81 13.7k 0.7× 10.2k 1.7× 9.5k 2.3× 2.0k 0.5× 2.2k 0.8× 162 30.1k
Urban Lendahl Sweden 79 15.4k 0.7× 4.9k 0.8× 4.0k 0.9× 2.2k 0.6× 2.4k 0.8× 215 24.8k
Carmen Birchmeier Germany 87 17.9k 0.9× 2.7k 0.5× 5.3k 1.3× 2.4k 0.6× 3.3k 1.1× 182 28.6k
Luis F. Parada United States 94 17.4k 0.8× 5.3k 0.9× 9.4k 2.2× 4.6k 1.1× 2.5k 0.9× 231 33.7k
Constance L. Cepko United States 92 23.6k 1.1× 4.4k 0.7× 8.5k 2.0× 4.2k 1.0× 4.0k 1.4× 232 28.8k
Jeffrey Milbrandt United States 106 18.1k 0.9× 3.7k 0.6× 12.5k 3.0× 4.5k 1.1× 3.3k 1.1× 297 34.7k

Countries citing papers authored by Ryoichiro Kageyama

Since Specialization
Citations

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

Fields of papers citing papers by Ryoichiro Kageyama

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ryoichiro Kageyama

This figure shows the co-authorship network connecting the top 25 collaborators of Ryoichiro Kageyama. A scholar is included among the top collaborators of Ryoichiro Kageyama 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 Ryoichiro Kageyama. Ryoichiro Kageyama 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.
Kageyama, Ryoichiro, et al.. (2021). Oscillatory expression of Ascl1 in oligodendrogenesis. Gene Expression Patterns. 41. 119198–119198. 6 indexed citations
2.
Isomura, Akihiro, et al.. (2019). Dynamic Delta-like1 expression in presomitic mesoderm cells during somite segmentation. Gene Expression Patterns. 35. 119094–119094. 3 indexed citations
3.
Sanaki-Matsumiya, Marina, et al.. (2018). ES cell-derived presomitic mesoderm-like tissues for analysis of synchronized oscillations in the segmentation clock. Development. 145(4). 43 indexed citations
4.
Ando, Mitsushige, Masanori Goto, Masato Hojo, et al.. (2018). The proneural bHLH genes Mash1, Math3 and NeuroD are required for pituitary development. Journal of Molecular Endocrinology. 61(3). 127–138. 14 indexed citations
5.
Kobayashi, Taeko, Yumiko Iwamoto, Akihiro Isomura, et al.. (2015). Deubiquitinating enzymes regulate Hes1 stability and neuronal differentiation. FEBS Journal. 282(13). 2411–2423. 46 indexed citations
6.
Kitagawa, Masashi, Masato Hojo, Itaru Imayoshi, et al.. (2013). Hes1 and Hes5 regulate vascular remodeling and arterial specification of endothelial cells in brain vascular development. Mechanisms of Development. 130(9-10). 458–466. 39 indexed citations
7.
Harima, Yukiko & Ryoichiro Kageyama. (2013). Oscillatory links of Fgf signaling and Hes7 in the segmentation clock. Current Opinion in Genetics & Development. 23(4). 484–490. 14 indexed citations
8.
Karlsson, Camilla, Camilla Brantsing, Ryoichiro Kageyama, & Anders Lindahl. (2010). HES1 and HES5 Are Dispensable for Cartilage and Endochondral Bone Formation. Cells Tissues Organs. 192(1). 17–27. 11 indexed citations
9.
Ishii, Akiko, Taeko Kobayashi, & Ryoichiro Kageyama. (2008). Requirement of multiple lysine residues for the transcriptional activity and the instability of Hes7. Biochemical and Biophysical Research Communications. 372(1). 142–146. 5 indexed citations
10.
Kageyama, Ryoichiro, Toshiyuki Ohtsuka, & Taeko Kobayashi. (2007). The Hes gene family: repressors and oscillators that orchestrate embryogenesis. Development. 134(7). 1243–1251. 510 indexed citations breakdown →
11.
Kokubu, Hiroshi, Toshiyuki Ohtsuka, & Ryoichiro Kageyama. (2007). Mash1 is required for neuroendocrine cell development in the glandular stomach. Genes to Cells. 13(1). 41–51. 26 indexed citations
12.
Bai, Ge, Nengyin Sheng, Zhihui Xie, et al.. (2007). Id Sustains Hes1 Expression to Inhibit Precocious Neurogenesis by Releasing Negative Autoregulation of Hes1. Developmental Cell. 13(2). 283–297. 161 indexed citations
13.
Moriyama, Mariko, Masatake Osawa, Siu‐Shan Mak, et al.. (2006). Notch signaling via Hes1 transcription factor maintains survival of melanoblasts and melanocyte stem cells. The Journal of Cell Biology. 173(3). 333–339. 197 indexed citations
14.
Masamizu, Yoshito, Toshiyuki Ohtsuka, Yoshiki Takashima, et al.. (2006). Real-time imaging of the somite segmentation clock: Revelation of unstable oscillators in the individual presomitic mesoderm cells. Proceedings of the National Academy of Sciences. 103(5). 1313–1318. 269 indexed citations
15.
Hatakeyama, Jun, Susumu Sakamoto, & Ryoichiro Kageyama. (2006). <i>Hes1 </i>and <i>Hes5</i> Regulate the Development of the Cranial and Spinal Nerve Systems. Developmental Neuroscience. 28(1-2). 92–101. 44 indexed citations
16.
Ong, Chin‐Tong, Hui‐Teng Cheng, Li‐Wei Chang, et al.. (2005). Target Selectivity of Vertebrate Notch Proteins. Journal of Biological Chemistry. 281(8). 5106–5119. 183 indexed citations
17.
Tsunematsu, Ryosuke, Keiko Nakayama, Keiko Nakayama, et al.. (2004). Mouse Fbw7/Sel-10/Cdc4 Is Required for Notch Degradation during Vascular Development. Journal of Biological Chemistry. 279(10). 9417–9423. 212 indexed citations
18.
Kageyama, Ryoichiro, Toshiyuki Ohtsuka, & Koichi Tomita. (2000). The bHLH Gene Hes1 Regulates Differentiation of Multiple Cell Types. Molecules and Cells. 10(1). 1–7. 128 indexed citations
19.
Nishimura, Masataka, Mākoto Ishibashi, Koichi Tomita, et al.. (1998). Structure, Chromosomal Locus, and Promoter of MouseHes2Gene, a Homologue ofDrosophila hairyandEnhancer of split. Genomics. 49(1). 69–75. 107 indexed citations
20.
Ishibashi, Masami, S L Ang, Kohei Shiota, et al.. (1995). Targeted disruption of mammalian hairy and Enhancer of split homolog-1 (HES-1) leads to up-regulation of neural helix-loop-helix factors, premature neurogenesis, and severe neural tube defects.. Genes & Development. 9(24). 3136–3148. 594 indexed citations breakdown →

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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