Hideya Sakaguchi

3.6k total citations · 1 hit paper
33 papers, 2.6k citations indexed

About

Hideya Sakaguchi is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Hideya Sakaguchi has authored 33 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Cellular and Molecular Neuroscience and 10 papers in Neurology. Recurrent topics in Hideya Sakaguchi's work include Neurogenesis and neuroplasticity mechanisms (8 papers), Pluripotent Stem Cells Research (7 papers) and Neuroscience and Neural Engineering (4 papers). Hideya Sakaguchi is often cited by papers focused on Neurogenesis and neuroplasticity mechanisms (8 papers), Pluripotent Stem Cells Research (7 papers) and Neuroscience and Neural Engineering (4 papers). Hideya Sakaguchi collaborates with scholars based in Japan, United States and United Kingdom. Hideya Sakaguchi's co-authors include Yoshio Kuramoto, Mototsugu Eiraku, Taisuke Kadoshima, Yoshiki Sasai, Mika Soen, Jun Takahashi, Satoshi Ando, Tokushige Nakano, Shigeru Shinomoto and Susumu Miyamoto and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and PLoS ONE.

In The Last Decade

Hideya Sakaguchi

32 papers receiving 2.6k citations

Hit Papers

Self-organization of axial polarity, inside-out layer pat... 2013 2026 2017 2021 2013 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hideya Sakaguchi Japan 19 1.3k 606 585 471 454 33 2.6k
Hiroshi Kori Japan 23 731 0.5× 216 0.4× 846 1.4× 170 0.4× 474 1.0× 71 2.3k
Jordi Soriano Spain 26 552 0.4× 295 0.5× 133 0.2× 111 0.2× 919 2.0× 80 2.2k
Ronald W. Joyner United States 34 1.5k 1.1× 183 0.3× 109 0.2× 114 0.2× 1.5k 3.2× 97 3.1k
Christoph Kirst United States 14 589 0.4× 225 0.4× 155 0.3× 58 0.1× 315 0.7× 23 1.5k
Akihiro Isomura Japan 17 1.0k 0.8× 118 0.2× 176 0.3× 171 0.4× 230 0.5× 33 1.6k
Leonardo Sacconi Italy 32 936 0.7× 758 1.3× 108 0.2× 41 0.1× 780 1.7× 124 3.1k
Mario Delmar United States 58 6.2k 4.6× 159 0.3× 94 0.2× 35 0.1× 996 2.2× 176 8.8k
Netta Cohen United Kingdom 19 405 0.3× 131 0.2× 71 0.1× 169 0.4× 550 1.2× 48 1.6k
Gwendal Le Masson France 25 489 0.4× 94 0.2× 64 0.1× 22 0.0× 1.2k 2.7× 86 2.4k
J.‐C. Floyd Sarria Switzerland 7 632 0.5× 121 0.2× 18 0.0× 179 0.4× 987 2.2× 7 2.1k

Countries citing papers authored by Hideya Sakaguchi

Since Specialization
Citations

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

Fields of papers citing papers by Hideya Sakaguchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hideya Sakaguchi

This figure shows the co-authorship network connecting the top 25 collaborators of Hideya Sakaguchi. A scholar is included among the top collaborators of Hideya Sakaguchi 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 Hideya Sakaguchi. Hideya Sakaguchi 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.
Sakaguchi, Hideya. (2025). Self-organization and applications of neural organoids. European Journal of Cell Biology. 104(2). 151496–151496.
2.
Arioka, Yuko, Hiroki Okumura, Hideya Sakaguchi, & Norio Ozaki. (2023). Shedding light on latent pathogenesis and pathophysiology of mental disorders: The potential ofiPScell technology. Psychiatry and Clinical Neurosciences. 77(6). 308–314. 2 indexed citations
3.
Sawai, Tsutomu, Joshua Shepherd, E. S. Thomas, et al.. (2021). Mapping the Ethical Issues of Brain Organoid Research and Application. AJOB Neuroscience. 13(2). 81–94. 57 indexed citations
4.
Sawai, Tsutomu, Hideya Sakaguchi, E. S. Thomas, Jun Takahashi, & Misao Fujita. (2019). The Ethics of Cerebral Organoid Research: Being Conscious of Consciousness. Stem Cell Reports. 13(3). 440–447. 59 indexed citations
5.
Shimogawa, Takafumi, Hideya Sakaguchi, Tetsuhiro Kikuchi, et al.. (2019). Therapeutic effects of combined cell transplantation and locomotor training in rats with brain injury. npj Regenerative Medicine. 4(1). 13–13. 5 indexed citations
6.
Sakaguchi, Hideya, et al.. (2019). Self-Organized Synchronous Calcium Transients in a Cultured Human Neural Network Derived from Cerebral Organoids. Stem Cell Reports. 13(3). 458–473. 98 indexed citations
7.
Shimogawa, Takafumi, et al.. (2017). Enhanced Axonal Extension of Subcortical Projection Neurons Isolated from Murine Embryonic Cortex using Neuropilin-1. Frontiers in Cellular Neuroscience. 11. 123–123. 7 indexed citations
8.
Kadoshima, Taisuke, Hideya Sakaguchi, & Mototsugu Eiraku. (2017). Generation of Various Telencephalic Regions from Human Embryonic Stem Cells in Three-Dimensional Culture. Methods in molecular biology. 1597. 1–16. 3 indexed citations
9.
Sakaguchi, Hideya, Taisuke Kadoshima, Mika Soen, et al.. (2015). Generation of functional hippocampal neurons from self-organizing human embryonic stem cell-derived dorsomedial telencephalic tissue. Nature Communications. 6(1). 8896–8896. 375 indexed citations
10.
Piazza, Fabrizio, S Greenberg, M. Savoiardo, et al.. (2013). Anti-Aß autoantibodies in cerebral amyloid angiopathy-related inflammation: a human spontaneous model of amyloid-related imaging abnormalities (ARIA) in Alzheimer’s disease. BOA (University of Milano-Bicocca). 28. 1–2. 2 indexed citations
11.
Piazza, Fabrizio, Steven M. Greenberg, M. Savoiardo, et al.. (2012). Immune-mediated mechanisms in the pathogenesis of cerebral amyloid angiopathy-related inflammation and Alzheimer's disease: Role of anti-A beta auto-antibodies. PubMed Central. 253. 64–65. 1 indexed citations
12.
Sakaguchi, Hideya, Satoshi Yamashita, Teruyuki Hirano, et al.. (2012). Myasthenic crisis patients who require intensive care unit management. Muscle & Nerve. 46(3). 440–442. 16 indexed citations
13.
Yamashita, Satoshi, En Kimura, Nozomu Tawara, et al.. (2012). Optineurin is potentially associated with TDP‐43 and involved in the pathogenesis of inclusion body myositis. Neuropathology and Applied Neurobiology. 39(4). 406–416. 27 indexed citations
14.
Nasu, Makoto, Nozomu Takata, Teruko Danjo, et al.. (2012). Robust Formation and Maintenance of Continuous Stratified Cortical Neuroepithelium by Laminin-Containing Matrix in Mouse ES Cell Culture. PLoS ONE. 7(12). e53024–e53024. 71 indexed citations
15.
Yamashita, Satoshi, Sachi Kojima, Hideya Sakaguchi, et al.. (2011). Heatstroke in patients with Parkinson’s disease. Neurological Sciences. 33(3). 685–687. 9 indexed citations
16.
Yamashita, Satoshi, Akira Mori, Hideya Sakaguchi, et al.. (2011). Sporadic juvenile amyotrophic lateral sclerosis caused by mutant FUS/TLS: possible association of mental retardation with this mutation. Journal of Neurology. 259(6). 1039–1044. 36 indexed citations
17.
Sakaguchi, Hideya, Akihiko Ueda, Takayuki Kosaka, et al.. (2011). Cerebral amyloid angiopathy-related inflammation presenting with steroid-responsive higher brain dysfunction: case report and review of the literature. Journal of Neuroinflammation. 8(1). 116–116. 33 indexed citations
18.
Yamashita, Satoshi, Hideya Sakaguchi, Akira Mori, et al.. (2011). Significant CMAP decrement by repetitive nerve stimulation is more frequent in median than ulnar nerves of patients with amyotrophic lateral sclerosis. Muscle & Nerve. 45(3). 426–428. 18 indexed citations
19.
Sakaguchi, Hideya. (1988). Oscillatory and Excitable Behaviors in a Population of Model Neurons. Progress of Theoretical Physics. 79(5). 1061–1068. 5 indexed citations
20.
Sakaguchi, Hideya, Shigeru Shinomoto, & Yoshio Kuramoto. (1987). Local and Grobal Self-Entrainments in Oscillator Lattices. Progress of Theoretical Physics. 77(5). 1005–1010. 171 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026