Mamoru Ito
About
Mamoru Ito is a scholar working on Immunology, Molecular Biology and Hematology.
According to data from OpenAlex, Mamoru Ito has authored 220 papers receiving a total of 10.0k indexed citations (citations by other indexed papers that have themselves been cited), including 103 papers in Immunology, 52 papers in Molecular Biology and 46 papers in Hematology. Recurrent topics in Mamoru Ito's work include Immune Cell Function and Interaction (53 papers), T-cell and B-cell Immunology (37 papers) and Hematopoietic Stem Cell Transplantation (29 papers). Mamoru Ito is often cited by papers focused on Immune Cell Function and Interaction (53 papers), T-cell and B-cell Immunology (37 papers) and Hematopoietic Stem Cell Transplantation (29 papers). Mamoru Ito collaborates with scholars based in Japan, United States and China. Mamoru Ito's co-authors include Tatsutoshi Nakahata, Kimio Kobayashi, Yoshio Koyanagi, Ryoji Ito, Ikumi Katano, Kohichiro Tsuji, Takeshi Takahashi, Kazutomo Suzue, Toshio Heike and Hidefumi Hiramatsu and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.
In The Last Decade
Mamoru Ito
216 papers receiving 9.8k citations
Hit Papers
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late) cites · hero ref
| Name | h | Career | Trend | Papers | Cites | |||||
|---|---|---|---|---|---|---|---|---|---|---|
| Mamoru Ito Japan | 53 | 4.1k | 3.0k | 1.9k | 1.6k | 1.3k | 220 | 10.0k | ||
| Kenneth I. Weinberg United States | 51 | 4.1k 1.0× | 3.9k 1.3× | 2.2k 1.2× | 2.1k 1.4× | 1.7k 1.3× | 180 | 10.8k | ||
| Michael Eckhaus United States | 47 | 2.0k 0.5× | 4.8k 1.6× | 1.5k 0.8× | 1.6k 1.0× | 1.4k 1.1× | 114 | 10.2k | ||
| Angel F. López Australia | 63 | 6.9k 1.7× | 3.6k 1.2× | 2.9k 1.5× | 2.3k 1.4× | 922 0.7× | 275 | 13.7k | ||
| Phillip I. Bird Australia | 50 | 3.1k 0.8× | 4.2k 1.4× | 1.1k 0.6× | 1.6k 1.0× | 916 0.7× | 189 | 9.2k | ||
| Masaki Yasukawa Japan | 47 | 4.0k 1.0× | 2.0k 0.7× | 2.6k 1.3× | 1.5k 1.0× | 821 0.6× | 249 | 8.1k | ||
| Mikael Jondal Sweden | 55 | 6.4k 1.6× | 3.2k 1.1× | 2.8k 1.4× | 755 0.5× | 831 0.6× | 199 | 12.2k | ||
| Pamela L. Schwartzberg United States | 72 | 11.2k 2.8× | 4.9k 1.6× | 3.7k 1.9× | 1.3k 0.9× | 1.1k 0.9× | 153 | 17.7k | ||
| John Atkinson United States | 59 | 5.2k 1.3× | 2.1k 0.7× | 682 0.4× | 1.3k 0.8× | 1.0k 0.8× | 160 | 9.6k | ||
| Kathryn Calame United States | 66 | 8.7k 2.1× | 7.0k 2.4× | 2.3k 1.2× | 1.0k 0.6× | 1.5k 1.1× | 144 | 15.8k | ||
| Leonard Chess United States | 60 | 8.4k 2.1× | 2.3k 0.8× | 1.5k 0.8× | 1.1k 0.7× | 649 0.5× | 148 | 12.5k |
Countries citing papers authored by Mamoru Ito
Since
Specialization
Citations
This map shows the geographic impact of Mamoru Ito'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 Mamoru Ito with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mamoru Ito more than expected).
Fields of papers citing papers by Mamoru Ito
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Mamoru Ito. 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 Mamoru Ito. The network helps show where Mamoru Ito may publish in the future.
Co-authorship network of co-authors of Mamoru Ito
This figure shows the co-authorship network connecting the top 25 collaborators of Mamoru Ito. A scholar is included among the top collaborators of Mamoru Ito 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 Mamoru Ito. Mamoru Ito is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Takeda, Kazuyoshi, Masaki Harada, Yuko Kojima, et al.. (2024). CD8+ T cell-mediated rejection of allogenic human-induced pluripotent stem cell-derived cardiomyocyte sheets in human PBMC-transferred NOG MHC double knockout mice. The Journal of Heart and Lung Transplantation. 43(8). 1348–1357.
2.
Kametani, Fuyuki, Ryoji Ito, Banri Tsuda, et al.. (2021). HER2-antigen-specific humoral immune response in breast cancer lymphocytes transplanted in hu-PBL hIL-4 NOG mice. Scientific Reports. 11(1). 12798–12798.
3.
Satoh, K., Kazumasa Kanemaru, Masafumi Muratani, et al.. (2021). DNAM-1 regulates Foxp3 expression in regulatory T cells by interfering with TIGIT under inflammatory conditions. Proceedings of the National Academy of Sciences. 118(21).
4.
Satō, Masaki, Mitsuyo Matsumoto, Yuriko Saiki, et al.. (2020). BACH1 Promotes Pancreatic Cancer Metastasis by Repressing Epithelial Genes and Enhancing Epithelial–Mesenchymal Transition. Cancer Research. 80(6). 1279–1292.
5.
Ashizawa, Tadashi, Akira Iizuka, Ryota Kondou, et al.. (2016). Antitumor Effect of Programmed Death-1 (PD-1) Blockade in Humanized the NOG-MHC Double Knockout Mouse. Clinical Cancer Research. 23(1). 149–158.
6.
Wong, Won Fen, Toshio Watanabe, Kazuyoshi Kohu, et al.. (2010). Over‐expression of Runx1 transcription factor impairs the development of thymocytes from the double‐negative to double‐positive stages. Immunology. 130(2). 243–253.
7.
Muguruma, Yukari, Hiromichi Matsushita, Takashi Yahata, et al.. (2010). Establishment of a xenograft model of human myelodysplastic syndromes. Haematologica. 96(4). 543–551.
8.
Ogawa, Daisuke, Yohei Okada, Masaya Nakamura, et al.. (2008). Evaluation of human fetal neural stem/progenitor cells as a source for cell replacement therapy for neurological disorders: Properties and tumorigenicity after long‐term in vitro maintenance. Journal of Neuroscience Research. 87(2). 307–317.
9.
Yahata, Takashi, Yukari Muguruma, Sheng Yin, et al.. (2008). Quiescent Human Hematopoietic Stem Cells in the Bone Marrow Niches Organize the Hierarchical Structure of Hematopoiesis. Stem Cells. 26(12). 3228–3236.
10.
Masuda, Hirotaka, Tetsuo Maruyama, Junichi Yamane, et al.. (2007). Noninvasive and real-time assessment of reconstructed functional human endometrium in NOD/SCID/γ c null immunodeficient mice. Proceedings of the National Academy of Sciences. 104(6). 1925–1930.
11.
Kametani, Yoshie, Masashi Shiina, Ikumi Katano, et al.. (2006). Development of human–human hybridoma from anti-Her-2 peptide–producing B cells in immunized NOG mouse. Experimental Hematology. 34(9). 1239–1247.
12.
Terabe, Masaki, Shigeharu Wakana, Ken Katakura, et al.. (2004). Influence of H2 complex and non-H2 genes on progression of cutaneous lesions in mice infected with Leishmania amazonensis. Parasitology International. 53(3). 217–221.
13.
Matsumura, Takuya, Yoshie Kametani, Kiyoshi Ando, et al.. (2003). Functional CD5+ B cells develop predominantly in the spleen of NOD/SCID/γcnull (NOG) mice transplanted either with human umbilical cord blood, bone marrow, or mobilized peripheral blood CD34+ cells. Experimental Hematology. 31(9). 789–797.
14.
Hagiwara, Katsuro, et al.. (2001). Seroprevalence of Borna disease virus in domestic animals in Xinjiang, China. Veterinary Microbiology. 80(4). 383–389.
15.
Ono, Yoshikuni, Nobuyuki Shimozawa, K Hioki, et al.. (2001). Production of cloned mice from embryonic stem cells arrested at metaphase. Reproduction. 122(5). 731–736.
16.
Fukuchi, Yumi, Masahiro Kizaki, Kentaro Kinjo, et al.. (1998). Establishment of a retinoic acid-resistant human acute promyelocytic leukaemia (APL) model in human granulocyte-macrophage colony-stimulating factor (hGM-CSF) transgenic severe combined immunodeficiency (SCID) mice. British Journal of Cancer. 78(7). 878–884.
17.
Lichtenfels, J. Ralph, V. Kharchenko, Christina Sommer, & Mamoru Ito. (1997). Key characters for the microscopical identification of Cylicocyclus nassatus and Cylicocyclus ashworthi (Nematoda: Cyathostominae) of the horse, Equus caballus. Comparative Parasitology. 64(1). 120–127.
18.
Igarashi, Ikuo, Seiji Waki, Mamoru Ito, et al.. (1994). Role of CD4⁺ T Cells in the Control of Primary Infection with Babesia microti in Mice. Obihiro University of Agriculture and Veterinary Medicine Institutional Repository. 4(4). 164–171.
19.
Okudaira, Hirokazu, Akio Mori, Kazuhiko Yamamoto, et al.. (1991). Interleukin-4 Gene Expression and IgE Responsiveness. International Archives of Allergy and Immunology. 94(1-4). 184–186.
20.
Harada, Yasuo, et al.. (1985). Three Dimensional Ultrastructure of the Vestibular Ganglion of the Bull Frog. Practica Oto-Rhino-Laryngologica. 78(11special). 2469–2478.
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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