Yoichi Matsuo

4.1k total citations
153 papers, 3.0k citations indexed

About

Yoichi Matsuo is a scholar working on Oncology, Surgery and Molecular Biology. According to data from OpenAlex, Yoichi Matsuo has authored 153 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Oncology, 54 papers in Surgery and 45 papers in Molecular Biology. Recurrent topics in Yoichi Matsuo's work include Pancreatic and Hepatic Oncology Research (27 papers), Colorectal Cancer Surgical Treatments (15 papers) and Gastric Cancer Management and Outcomes (13 papers). Yoichi Matsuo is often cited by papers focused on Pancreatic and Hepatic Oncology Research (27 papers), Colorectal Cancer Surgical Treatments (15 papers) and Gastric Cancer Management and Outcomes (13 papers). Yoichi Matsuo collaborates with scholars based in Japan, United States and Greece. Yoichi Matsuo's co-authors include Hiroki Takahashi, Hiromitsu Takeyama, Hirozumi Sawai, Hitoshi Funahashi, Nobuo Ochi, Akira Yasuda, Yuji Okada, Sushovan Guha, Tadao Manabe and Zhimin Tong and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gastroenterology and Cancer Research.

In The Last Decade

Yoichi Matsuo

137 papers receiving 3.0k citations

Peers

Yoichi Matsuo
Hiromitsu Takeyama Japan
Zhihong Chi China
Maciej Szmitkowski Poland
Arimichi Takabayashi Japan
Maria Napolitano Italy
Hitoshi Funahashi Japan
Yanhong Gu China
Mona F. Melhem United States
Kazuhiro Yoshida Japan
Markus W. Büchler Germany
Hiromitsu Takeyama Japan
Yoichi Matsuo
Citations per year, relative to Yoichi Matsuo Yoichi Matsuo (= 1×) peers Hiromitsu Takeyama

Countries citing papers authored by Yoichi Matsuo

Since Specialization
Citations

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

Fields of papers citing papers by Yoichi Matsuo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoichi Matsuo

This figure shows the co-authorship network connecting the top 25 collaborators of Yoichi Matsuo. A scholar is included among the top collaborators of Yoichi Matsuo 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 Yoichi Matsuo. Yoichi Matsuo 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.
Fujii, Yoshiaki, Sho Kimura, Shogo Suzuki, et al.. (2025). Optimal Intracorporeal Anastomosis for Colectomy: A Comparative Experimental Evaluation Using 3D Anastomosis Models. Asian Journal of Endoscopic Surgery. 18(1). e70048–e70048.
2.
Watanabe, K., Hiroki Takahashi, Takeshi Yanagita, et al.. (2024). Visualization of cecal tumor by near-infrared laparoscopy and intraoperative colonoscopy. Surgical Case Reports. 10(1).
3.
Kato, Hiroyuki, Aya Naiki‐Ito, Shingo Inaguma, et al.. (2024). The role of DPYD and the effects of DPYD suppressor luteolin combined with 5‐FU in pancreatic cancer. Cancer Medicine. 13(16). e70124–e70124. 4 indexed citations
4.
Takahashi, Hiroki, K. Watanabe, Takeshi Yanagita, et al.. (2024). Bcl‑xL‑specific BH3 mimetic A‑1331852 suppresses proliferation of fluorouracil‑resistant colorectal cancer cells by inducing apoptosis. Oncology Reports. 53(2). 1 indexed citations
5.
6.
Matsuo, Yoichi, Kenta Saito, Hiroyuki Kato, et al.. (2023). Simultaneous presentation and resection of esophageal cancer and metastasis to the pancreas: Α case report and literature review. Molecular and Clinical Oncology. 20(1). 2–2. 1 indexed citations
7.
Suzuki, Takuya, Hiroki Takahashi, Takahisa Hirokawa, et al.. (2023). AZD6738 promotes the tumor suppressive effects of trifluridine in colorectal cancer cells. Oncology Reports. 49(3). 2 indexed citations
8.
Nakai, Nozomu, Takeshi Yanagita, Takuya Suzuki, et al.. (2023). Elevated Preoperative Serum Vascular Endothelial Growth Factor Does Not Predict Poor Outcomes in Curatively Resected Non-metastatic Colorectal Cancer Treated Without Neoadjuvant Therapy. Anticancer Research. 43(5). 2333–2341. 1 indexed citations
9.
Saito, Kenta, et al.. (2023). Neuroendocrine carcinoma of the minor papilla with pancreas divisum: a case report and review of the literature. Journal of Medical Case Reports. 17(1). 127–127.
10.
11.
Shimasaki, Takeo, Satoko Yamamoto, Kagenori Ito, et al.. (2021). Novel Platform for Regulation of Extracellular Vesicles and Metabolites Secretion from Cells Using a Multi-Linkable Horizontal Co-Culture Plate. Micromachines. 12(11). 1431–1431. 9 indexed citations
12.
Matsuo, Yoichi, et al.. (2021). A Case of Inguinal Endometriosis Treated with Exploratory Laparoscopy. The Japanese Journal of Gastroenterological Surgery. 54(4). 285–292. 2 indexed citations
13.
Matsuo, Yoichi, Kenta Saito, Ken Tsuboi, et al.. (2020). [A Case of Gallbladder Cancer with Para-Aortic Lymph Node Metastasis Successfully Treated by Gemcitabine plus Cisplatin Combination Chemotherapy and Conversion Surgery].. Gan to kagaku ryōhō. 47(13). 2204–2206. 2 indexed citations
14.
Yasuda, Akira, Hirozumi Sawai, Nobuo Ochi, et al.. (2011). Solid variant of serous cystadenoma of the pancreas. Archives of Medical Science. 2(2). 353–355. 21 indexed citations
15.
Matsuo, Yoichi, Paul M. Campbell, Rolf A. Brekken, et al.. (2009). K-Ras Promotes Angiogenesis Mediated by Immortalized Human Pancreatic Epithelial Cells through Mitogen-Activated Protein Kinase Signaling Pathways. Molecular Cancer Research. 7(6). 799–808. 68 indexed citations
16.
Ma, Jiachi, Hirozumi Sawai, Yoichi Matsuo, et al.. (2009). IGF-1 and PTEN regulate the proliferation and invasiveness of colon cancer cells through opposite effects on PI3K/Akt signalling. Archives of Medical Science. 5(2). 195–206. 4 indexed citations
17.
Tong, Zhimin, Ajaikumar B. Kunnumakkara, Huamin Wang, et al.. (2008). Neutrophil Gelatinase–Associated Lipocalin: A Novel Suppressor of Invasion and Angiogenesis in Pancreatic Cancer. Cancer Research. 68(15). 6100–6108. 144 indexed citations
18.
Funahashi, Hitoshi, Hirozumi Sawai, Akira Yasuda, et al.. (2008). Glial cell line-derived neurotrophic factor enhances the invasive ability of pancreatic cancer cells by regulating urokinase-type plasminogen activator and matrix metalloproteinase. Archives of Medical Science. 3(4). 323–329. 2 indexed citations
19.
Sawai, Hirozumi, Akira Yasuda, Nobuo Ochi, et al.. (2007). Basic research TGF-β regulates invasive behavior of human pancreatic cancer cells by controlling Smad expression. Archives of Medical Science. 3(3). 185–191. 3 indexed citations
20.
Takahashi, Hiroki, Yoichi Matsuo, Minoru Yamamoto, et al.. (2007). Reactive Lymphoid Hyperplasia of the Liver in a Patient with Ascending Colon Cancer: Report of a Case. The Japanese Journal of Gastroenterological Surgery. 40(3). 331–336. 4 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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