Reiko Kuno

1.9k total citations · 1 hit paper
16 papers, 1.5k citations indexed

About

Reiko Kuno is a scholar working on Neurology, Oncology and Molecular Biology. According to data from OpenAlex, Reiko Kuno has authored 16 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Neurology, 7 papers in Oncology and 6 papers in Molecular Biology. Recurrent topics in Reiko Kuno's work include Neuroinflammation and Neurodegeneration Mechanisms (8 papers), Cancer Cells and Metastasis (7 papers) and Digestive system and related health (3 papers). Reiko Kuno is often cited by papers focused on Neuroinflammation and Neurodegeneration Mechanisms (8 papers), Cancer Cells and Metastasis (7 papers) and Digestive system and related health (3 papers). Reiko Kuno collaborates with scholars based in Japan, Germany and United States. Reiko Kuno's co-authors include Tetsuya Mizuno, Akio Suzumura, Hideyuki Takeuchi, Jun Kawanokuchi, Jinyan Wang, Guiqin Zhang, Shijie Jin, Yoshifumi Sonobe, Toshitaka Nabeshima and Atsumi Nitta and has published in prestigious journals such as Journal of Biological Chemistry, Brain Research and Biochemical and Biophysical Research Communications.

In The Last Decade

Reiko Kuno

16 papers receiving 1.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Tumor Necrosis Factor-α Induces Neurotoxicity via Glutamate Release from Hemichannels of Activated Microglia in an Autocrine Manner

2006 619 citations Hideyuki Takeuchi, Shijie Jin et al. Journal of Biological Chemistry profile →

Peers

Reiko Kuno

NEURO

CMN

PHYSI

IMMUN

Sergey Kalinin United States

Yu-Ping Peng China

Emanuela Colombo Italy

Erik Nutma Netherlands

Agnieszka M. Jurga Poland

Isaías Glezer Brazil

Tony Heurtaux Luxembourg

Pascal F. Durrenberger United Kingdom

Bijay Parajuli Japan

G. Aleph Prieto United States

Sergey Kalinin United States

Reiko Kuno

587 ×0.8

NEURO

642 ×1.4

354 ×0.9

CMN

490 ×1.8

PHYSI

305 ×1.2

IMMUN

Citations per year, relative to Reiko Kuno Reiko Kuno (= 1×) peers Sergey Kalinin

Countries citing papers authored by Reiko Kuno

Since Specialization

Citations

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

Fields of papers citing papers by Reiko Kuno

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Reiko Kuno

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

All Works

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16 of 16 papers shown

Takahashi, Junichi, Tomohiro Mizutani, Sayaka Nagata, et al.. (2022). Suspension culture in a rotating bioreactor for efficient generation of human intestinal organoids. Cell Reports Methods. 2(11). 100337–100337. 18 indexed citations

Kuno, Reiko, Go Ito, Ami Kawamoto, et al.. (2021). Notch and TNF-α signaling promote cytoplasmic accumulation of OLFM4 in intestinal epithelium cells and exhibit a cell protective role in the inflamed mucosa of IBD patients. Biochemistry and Biophysics Reports. 25. 100906–100906. 12 indexed citations

Ito, Go, Sayaka Nagata, Ami Kawamoto, et al.. (2021). Functional analysis of isoflavones using patient-derived human colonic organoids. Biochemical and Biophysical Research Communications. 542. 40–47. 5 indexed citations

Kawamoto, Ami, Sayaka Nagata, Junichi Takahashi, et al.. (2020). TGF-β promotes fetal gene expression and cell migration velocity in a wound repair model of untransformed intestinal epithelial cells. Biochemical and Biophysical Research Communications. 524(3). 533–541. 9 indexed citations

Kawamoto, Ami, Sayaka Nagata, Junichi Takahashi, et al.. (2018). Ubiquitin D is Upregulated by Synergy of Notch Signalling and TNF-α in the Inflamed Intestinal Epithelia of IBD Patients. Journal of Crohn s and Colitis. 13(4). 495–509. 29 indexed citations

Ishibashi, Fumiaki, Hiromichi Shimizu, Toru Nakata, et al.. (2017). Contribution of ATOH1+ Cells to the Homeostasis, Repair, and Tumorigenesis of the Colonic Epithelium. Stem Cell Reports. 10(1). 27–42. 55 indexed citations

Nakata, Toru, Hiromichi Shimizu, Sayaka Nagata, et al.. (2016). Indispensable role of Notch ligand-dependent signaling in the proliferation and stem cell niche maintenance of APC-deficient intestinal tumors. Biochemical and Biophysical Research Communications. 482(4). 1296–1303. 11 indexed citations

Nakata, Toru, Hiromichi Shimizu, Sayaka Nagata, et al.. (2016). Data showing proliferation and differentiation of intestinal epithelial cells under targeted depletion of Notch ligands in mouse intestine. Data in Brief. 10. 551–556. 3 indexed citations

Kuno, Reiko, Yusuke Yoshida, Atsumi Nitta, et al.. (2006). The role of TNF-alpha and its receptors in the production of NGF and GDNF by astrocytes. Brain Research. 1116(1). 12–18. 105 indexed citations

10.

Takeuchi, Hideyuki, Shijie Jin, Jinyan Wang, et al.. (2006). Tumor Necrosis Factor-α Induces Neurotoxicity via Glutamate Release from Hemichannels of Activated Microglia in an Autocrine Manner. Journal of Biological Chemistry. 281(30). 21362–21368. 619 indexed citations breakdown →

11.

Doi, Yukiko, Jianfeng Liang, Reiko Kuno, et al.. (2006). The Direct and Indirect Effects of Serofendic Acid on Neuroprotection. Annals of the New York Academy of Sciences. 1086(1). 91–103. 5 indexed citations

12.

Suzumura, Akio, Hideyuki Takeuchi, Guiqin Zhang, Reiko Kuno, & Tetsuya Mizuno. (2006). Roles of Glia‐Derived Cytokines on Neuronal Degeneration and Regeneration. Annals of the New York Academy of Sciences. 1088(1). 219–229. 97 indexed citations

13.

Mizuno, Tetsuya, Reiko Kuno, Atsumi Nitta, et al.. (2005). Protective effects of nicergoline against neuronal cell death induced by activated microglia and astrocytes. Brain Research. 1066(1-2). 78–85. 44 indexed citations

14.

Takeuchi, Hideyuki, Tetsuya Mizuno, Guiqin Zhang, et al.. (2005). Neuritic Beading Induced by Activated Microglia Is an Early Feature of Neuronal Dysfunction Toward Neuronal Death by Inhibition of Mitochondrial Respiration and Axonal Transport. Journal of Biological Chemistry. 280(11). 10444–10454. 239 indexed citations

15.

Kuno, Reiko, Jinyan Wang, Jun Kawanokuchi, et al.. (2005). Autocrine activation of microglia by tumor necrosis factor-α. Journal of Neuroimmunology. 162(1-2). 89–96. 187 indexed citations

16.

Banno, Masahiro, Tetsuya Mizuno, Hideki Kato, et al.. (2004). The radical scavenger edaravone prevents oxidative neurotoxicity induced by peroxynitrite and activated microglia. Neuropharmacology. 48(2). 283–290. 82 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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