Atsushi Mizoguchi

10.6k total citations · 4 hit papers
87 papers, 8.3k citations indexed

About

Atsushi Mizoguchi is a scholar working on Immunology, Genetics and Molecular Biology. According to data from OpenAlex, Atsushi Mizoguchi has authored 87 papers receiving a total of 8.3k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Immunology, 32 papers in Genetics and 22 papers in Molecular Biology. Recurrent topics in Atsushi Mizoguchi's work include Immune Cell Function and Interaction (33 papers), Inflammatory Bowel Disease (31 papers) and Microscopic Colitis (21 papers). Atsushi Mizoguchi is often cited by papers focused on Immune Cell Function and Interaction (33 papers), Inflammatory Bowel Disease (31 papers) and Microscopic Colitis (21 papers). Atsushi Mizoguchi collaborates with scholars based in United States, Japan and Canada. Atsushi Mizoguchi's co-authors include Emiko Mizoguchi, Atul K. Bhan, Richard S. Blumberg, Daren Low, Hidetoshi Takedatsu, Ken Sugimoto, Yasuyo Shimomura, Ramnik J. Xavier, Atsuhiro Ogaẃa and Akira Andoh 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

Atsushi Mizoguchi

87 papers receiving 8.1k citations

Hit Papers

IL-22 ameliorates intesti... 2002 2026 2010 2018 2008 2002 2016 2002 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
Atsushi Mizoguchi United States 43 4.6k 2.4k 1.9k 1.1k 1.1k 87 8.3k
Atsushi Kitani Japan 41 6.5k 1.4× 2.3k 0.9× 1.8k 0.9× 1.1k 1.0× 1.1k 1.0× 95 9.7k
Michael W. Leach United States 33 6.4k 1.4× 1.4k 0.6× 2.0k 1.1× 1.1k 1.0× 1.2k 1.1× 72 9.4k
Christoph Mueller Switzerland 49 3.6k 0.8× 1.8k 0.7× 1.2k 0.6× 1.0k 0.9× 882 0.8× 145 6.9k
Edward E. S. Nieuwenhuis Netherlands 43 3.3k 0.7× 3.5k 1.4× 1.9k 1.0× 1.2k 1.0× 1.1k 1.0× 122 9.5k
Stella C. Knight United Kingdom 53 6.9k 1.5× 2.5k 1.1× 1.3k 0.7× 762 0.7× 1.3k 1.2× 231 11.4k
Hilde Cheroutre United States 54 7.8k 1.7× 2.9k 1.2× 1.2k 0.6× 929 0.8× 1.1k 1.0× 110 11.8k
Rodney D. Newberry United States 44 4.8k 1.0× 2.2k 0.9× 1.1k 0.6× 1.5k 1.4× 697 0.6× 117 8.2k
Kevin J. Maloy United Kingdom 43 6.5k 1.4× 3.0k 1.2× 2.1k 1.1× 1.5k 1.3× 1.2k 1.1× 63 10.1k
Holm H. Uhlig United Kingdom 41 4.8k 1.0× 2.3k 1.0× 2.3k 1.2× 1.9k 1.7× 1.5k 1.4× 127 8.9k
Theresa T. Pizarro United States 51 4.4k 1.0× 3.5k 1.5× 2.7k 1.4× 2.0k 1.8× 1.3k 1.2× 142 9.4k

Countries citing papers authored by Atsushi Mizoguchi

Since Specialization
Citations

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

Fields of papers citing papers by Atsushi Mizoguchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Atsushi Mizoguchi

This figure shows the co-authorship network connecting the top 25 collaborators of Atsushi Mizoguchi. A scholar is included among the top collaborators of Atsushi Mizoguchi 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 Atsushi Mizoguchi. Atsushi Mizoguchi 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.
Mizoguchi, Emiko, et al.. (2024). Recently Updated Role of Chitinase 3-like 1 on Various Cell Types as a Major Influencer of Chronic Inflammation. Cells. 13(8). 678–678. 5 indexed citations
2.
Nishida, Atsushi, et al.. (2014). Regulatory B Cells in Mouse Models of Intestinal Inflammation. Methods in molecular biology. 1190. 227–241. 4 indexed citations
3.
Mizoguchi, Atsushi. (2012). Healing of intestinal inflammation by IL-22. Inflammatory Bowel Diseases. 18(9). 1777–1784. 102 indexed citations
4.
Nagatani, Katsuya, Sen Wang, Victoria Lladó, et al.. (2012). Chitin microparticles for the control of intestinal inflammation. Inflammatory Bowel Diseases. 18(9). 1698–1710. 42 indexed citations
5.
Chen, Chun‐Chuan, Joel Pekow, Victoria Lladó, et al.. (2011). Chitinase 3-Like-1 Expression in Colonic Epithelial Cells as a Potentially Novel Marker for Colitis-Associated Neoplasia. American Journal Of Pathology. 179(3). 1494–1503. 73 indexed citations
6.
Nishida, Atsushi, Mei Zhang, Akira Andoh, et al.. (2011). The Membrane-Bound Mucin Muc1 Regulates T Helper 17-Cell Responses and Colitis in Mice. Gastroenterology. 142(4). 865–874.e2. 69 indexed citations
7.
Biswas, Amlan, Yuen-Joyce Liu, Liming Hao, et al.. (2010). Induction and rescue of Nod2-dependent Th1-driven granulomatous inflammation of the ileum. Proceedings of the National Academy of Sciences. 107(33). 14739–14744. 128 indexed citations
8.
Sugimoto, Ken, Atsuhiro Ogaẃa, Emiko Mizoguchi, et al.. (2008). IL-22 ameliorates intestinal inflammation in a mouse model of ulcerative colitis. Journal of Clinical Investigation. 118(2). 534–44. 855 indexed citations breakdown →
9.
Hokama, Akira, Emiko Mizoguchi, & Atsushi Mizoguchi. (2008). Roles of galectins in inflammatory bowel disease. World Journal of Gastroenterology. 14(33). 5133–5133. 35 indexed citations
10.
Mizoguchi, Atsushi, Hidetoshi Takedatsu, Ken Sugimoto, et al.. (2007). Dependence of intestinal granuloma formation on unique myeloid DC-like cells. Journal of Clinical Investigation. 117(3). 605–615. 37 indexed citations
11.
Nanno, Masanobu, Yasuyoshi Kanari, Tomoaki Naito, et al.. (2007). Exacerbating Role of γδ T Cells in Chronic Colitis of T-Cell Receptor α Mutant Mice. Gastroenterology. 134(2). 481–490. 45 indexed citations
12.
Nagahama, Kiyotaka, et al.. (2007). Protein Kinase C θ Plays a Fundamental Role in Different Types of Chronic Colitis. Gastroenterology. 134(2). 459–469. 32 indexed citations
13.
Mizoguchi, Emiko, Yuriko Hachiya, Mayumi Kawada, et al.. (2007). TNF Receptor Type I-Dependent Activation of Innate Responses to Reduce Intestinal Damage-Associated Mortality. Gastroenterology. 134(2). 470–480. 44 indexed citations
14.
Mizoguchi, Atsushi & Atul K. Bhan. (2006). A Case for Regulatory B Cells. The Journal of Immunology. 176(2). 705–710. 462 indexed citations
15.
Hokama, Akira, Emiko Mizoguchi, Ken Sugimoto, et al.. (2004). Induced Reactivity of Intestinal CD4+ T Cells with an Epithelial Cell Lectin, Galectin-4, Contributes to Exacerbation of Intestinal Inflammation. Immunity. 20(6). 681–693. 134 indexed citations
16.
Beck, Paul L., Ricardo Machado Xavier, Jennifer Wong, et al.. (2004). Paradoxical roles of different nitric oxide synthase isoforms in colonic injury. American Journal of Physiology-Gastrointestinal and Liver Physiology. 286(1). G137–G147. 85 indexed citations
17.
Colgan, Sean P., Richard S. Pitman, Takashi Nagaishi, et al.. (2003). Intestinal heat shock protein 110 regulates expression of CD1d on intestinal epithelial cells. Journal of Clinical Investigation. 112(5). 745–754. 25 indexed citations
19.
Bhan, Atul K., Emiko Mizoguchi, R. Neal Smith, & Atsushi Mizoguchi. (1999). Lessons for human inflammatory bowel disease from experimental models. Current Opinion in Gastroenterology. 15(4). 285–285. 13 indexed citations
20.
Yano, Hirohisa, Akihiro Iemura, Kazunori Fukuda, et al.. (1993). Establishment of two distinct human hepatocellular carcinoma cell lines from a single nodule showing clonal dedifferentiation of cancer cells. Hepatology. 18(2). 320–327. 65 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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