Yuta Koui

441 total citations
13 papers, 332 citations indexed

About

Yuta Koui is a scholar working on Hepatology, Molecular Biology and Surgery. According to data from OpenAlex, Yuta Koui has authored 13 papers receiving a total of 332 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Hepatology, 8 papers in Molecular Biology and 5 papers in Surgery. Recurrent topics in Yuta Koui's work include Liver physiology and pathology (8 papers), Pluripotent Stem Cells Research (6 papers) and Organ Transplantation Techniques and Outcomes (3 papers). Yuta Koui is often cited by papers focused on Liver physiology and pathology (8 papers), Pluripotent Stem Cells Research (6 papers) and Organ Transplantation Techniques and Outcomes (3 papers). Yuta Koui collaborates with scholars based in Japan, United States and France. Yuta Koui's co-authors include Taketomo Kido, Atsushi Miyajima, Katsuhiko Shirahige, Yuki Katou, Hiroki Oyama, Minoru Tanaka, Ayaka Kobayashi, Edward Chern, Kaori Suzuki and Yasushi Miura and has published in prestigious journals such as Biomaterials, Scientific Reports and Pharmacology & Therapeutics.

In The Last Decade

Yuta Koui

10 papers receiving 328 citations

Peers

Yuta Koui
Ayla Smout Belgium
Juliana Puppi United Kingdom
Ryotaro Ito United States
Cai-Bin Cui United States
Yuta Koui
Citations per year, relative to Yuta Koui Yuta Koui (= 1×) peers Noushin Dianat

Countries citing papers authored by Yuta Koui

Since Specialization
Citations

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

Fields of papers citing papers by Yuta Koui

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yuta Koui

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

All Works

13 of 13 papers shown
1.
Koui, Yuta, Minoru Tanaka, & Taketomo Kido. (2025). Human PSC-derived liver cells and their applications for disease models and drug discovery. Pharmacology & Therapeutics. 274. 108907–108907.
3.
Koui, Yuta, Taketomo Kido, Miwa Tamura‐Nakano, et al.. (2024). Establishment of human induced pluripotent stem cell-derived hepatobiliary organoid with bile duct for pharmaceutical research use. Biomaterials. 310. 122621–122621. 10 indexed citations
4.
Koui, Yuta & Taketomo Kido. (2023). Using human induced pluripotent stem cell-derived liver cells to investigate the mechanisms of liver fibrosis in vitro. Biochemical Society Transactions. 51(3). 1271–1277. 2 indexed citations
5.
Koui, Yuta, Matthew J. Anderson, Motomi Osato, et al.. (2022). Hepatic leukemia factor-expressing paraxial mesoderm cells contribute to the developing brain vasculature. Biology Open. 11(9).
6.
Tsuchiya, Atsunori, Takahiro Iwasawa, Shunsuke Nojiri, et al.. (2021). Small extracellular vesicles derived from interferon-γ pre-conditioned mesenchymal stromal cells effectively treat liver fibrosis. npj Regenerative Medicine. 6(1). 19–19. 70 indexed citations
7.
Koui, Yuta, Yusuke Mori, Yasuhiro Nakano, et al.. (2021). Development of human iPSC-derived quiescent hepatic stellate cell-like cells for drug discovery and in vitro disease modeling. Stem Cell Reports. 16(12). 3050–3063. 23 indexed citations
8.
Danoy, Mathieu, Yannick Tauran, Stéphane Poulain, et al.. (2021). Investigation of the hepatic development in the coculture of hiPSCs-derived LSECs and HLCs in a fluidic microenvironment. APL Bioengineering. 5(2). 26104–26104. 9 indexed citations
9.
Danoy, Mathieu, Stéphane Poulain, Yuta Koui, et al.. (2020). Transcriptome profiling of hiPSC-derived LSECs with nanoCAGE. Molecular Omics. 16(2). 138–146. 11 indexed citations
10.
Koui, Yuta, Masaya Sugiyama, Hironori Nishitsuji, et al.. (2020). Modulation of hepatitis B virus infection by epidermal growth factor secreted from liver sinusoidal endothelial cells. Scientific Reports. 10(1). 14349–14349. 18 indexed citations
11.
Kido, Taketomo & Yuta Koui. (2018). Induction of Functional Hepatocytes from Human iPSCs. Methods in molecular biology. 1905. 131–142. 8 indexed citations
12.
Koui, Yuta, Taketomo Kido, Hiroki Oyama, et al.. (2017). An In Vitro Human Liver Model by iPSC-Derived Parenchymal and Non-parenchymal Cells. Stem Cell Reports. 9(2). 490–498. 126 indexed citations
13.
Kido, Taketomo, Yuta Koui, Kaori Suzuki, et al.. (2015). CPM Is a Useful Cell Surface Marker to Isolate Expandable Bi-Potential Liver Progenitor Cells Derived from Human iPS Cells. Stem Cell Reports. 5(4). 508–515. 55 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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