Toshiko Yamochi

498 total citations
38 papers, 294 citations indexed

About

Toshiko Yamochi is a scholar working on Oncology, Pathology and Forensic Medicine and Surgery. According to data from OpenAlex, Toshiko Yamochi has authored 38 papers receiving a total of 294 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Oncology, 10 papers in Pathology and Forensic Medicine and 8 papers in Surgery. Recurrent topics in Toshiko Yamochi's work include Genetic factors in colorectal cancer (6 papers), Colorectal Cancer Screening and Detection (5 papers) and Neuroendocrine Tumor Research Advances (4 papers). Toshiko Yamochi is often cited by papers focused on Genetic factors in colorectal cancer (6 papers), Colorectal Cancer Screening and Detection (5 papers) and Neuroendocrine Tumor Research Advances (4 papers). Toshiko Yamochi collaborates with scholars based in Japan and Ireland. Toshiko Yamochi's co-authors include Kazuo Konishi, Kazuhiro Kaneko, Hidekazu Ota, Reiko Makino, Keiji Mitamura, Atsushi Katagiri, Michio Imawari, Shin‐ei Kudo, Noriyuki Ogata and Yasuharu Maeda and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Toshiko Yamochi

33 papers receiving 292 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Toshiko Yamochi Japan 10 182 127 65 60 49 38 294
Hosub Park South Korea 9 129 0.7× 78 0.6× 78 1.2× 42 0.7× 72 1.5× 28 290
J. Morreau Netherlands 5 194 1.1× 53 0.4× 87 1.3× 54 0.9× 47 1.0× 7 296
Kanita Kayasut Thailand 9 147 0.8× 187 1.5× 39 0.6× 33 0.6× 65 1.3× 28 336
Yi-Hong Ling China 10 123 0.7× 59 0.5× 120 1.8× 39 0.7× 87 1.8× 12 333
Gabriele Delconte Italy 11 323 1.8× 210 1.7× 102 1.6× 54 0.9× 43 0.9× 20 450
Liisa Chang United Kingdom 4 183 1.0× 83 0.7× 107 1.6× 23 0.4× 100 2.0× 5 332
M. Svrcek France 8 178 1.0× 176 1.4× 74 1.1× 30 0.5× 98 2.0× 9 373
Hideki Kanazawa Japan 10 289 1.6× 108 0.9× 93 1.4× 28 0.5× 119 2.4× 23 435
Shawn Steen United States 11 148 0.8× 60 0.5× 45 0.7× 30 0.5× 80 1.6× 22 334
Bisong Haupt United States 11 201 1.1× 91 0.7× 85 1.3× 21 0.3× 69 1.4× 11 386

Countries citing papers authored by Toshiko Yamochi

Since Specialization
Citations

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

Fields of papers citing papers by Toshiko Yamochi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Toshiko Yamochi

This figure shows the co-authorship network connecting the top 25 collaborators of Toshiko Yamochi. A scholar is included among the top collaborators of Toshiko Yamochi 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 Toshiko Yamochi. Toshiko Yamochi 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
2.
Yamashita, Takeshi, Koji Otsuka, Akira Saito, et al.. (2025). Efficacy of Esophagectomy Following Neoadjuvant Chemotherapy for Esophageal Neuroendocrine Carcinoma. Anticancer Research. 45(5). 2051–2058. 1 indexed citations
3.
Hayashi, Hidenori, Yohei Sasaki, Nana Arai, et al.. (2024). High Ki-67 Expression Predicting a Risk Factor for the Progression of Disease within 24 Months and Microenvironment in Follicular Lymphoma. International Journal of Molecular Sciences. 25(20). 11057–11057. 1 indexed citations
4.
Ito, Takayoshi, et al.. (2024). Simultaneous gastric, pancreatic, and renal metastasis from poorly differentiated hepatocellular carcinoma. Clinical Journal of Gastroenterology. 17(3). 497–504.
5.
Igarashi, Katsuhide, Toshiko Yamochi, Hirotaka Ota, et al.. (2024). Blood endocan as a biomarker for breast cancer recurrence. Cancer Biomarkers. 41(2). 145–154.
7.
Hamada, Kazuyuki, Ryotaro Ohkuma, Tomoyuki Ishiguro, et al.. (2023). Case Report: Combined pembrolizumab, 5-fluorouracil, and cisplatin therapy were remarkably effective in p16-positive squamous cell carcinoma of unknown primary. Frontiers in Oncology. 13. 1231986–1231986. 1 indexed citations
8.
Hirose, Yusuke, Takashi Mimura, Mamiko Onuki, et al.. (2023). Risk-reducing salpingo-oophorectomy for Japanese women with hereditary breast and ovarian cancer: a single-institution 10-year experience. Japanese Journal of Clinical Oncology. 53(6). 472–479. 3 indexed citations
10.
Yamochi, Tadanori, et al.. (2021). Plasmid analysis of clinically isolated <i>Enterobacter cloacae</i> in Showa University Hospital. The Showa University Journal of Medical Sciences. 33(4). 97–102. 1 indexed citations
11.
Ishikawa, Hiroki, Toshiko Yamochi, Hiraku Sasaki, et al.. (2020). NKT cells are responsible for the clearance of murine norovirus through the virus-specific secretory IgA pathway. Biochemistry and Biophysics Reports. 21. 100722–100722. 1 indexed citations
12.
Urushibara, Fumihiko, Eisuke Shiozawa, Hideyuki Miyachi, et al.. (2018). Expression of matrix metalloproteinase-7 correlates with the invasion of T1 colorectal carcinoma. Oncology Letters. 15(3). 3614–3620. 2 indexed citations
13.
Matsui, Yuki, Jun Morita, Michio Naoe, et al.. (2018). Systematic review and two new cases of primary upper urinary tract neuroendocrine carcinomas. Cancer Treatment and Research Communications. 17. 23–30. 3 indexed citations
14.
Cho, Tomonari, Eisuke Shiozawa, Fumihiko Urushibara, et al.. (2017). The role of microvessel density, lymph node metastasis, and tumor size as prognostic factors of distant metastasis in colorectal cancer. Oncology Letters. 13(6). 4327–4333. 22 indexed citations
16.
Kohda, Chikara, Hiroki Ishikawa, Tomoko Norose, et al.. (2016). Oral tolerance is inducible during active dextran sulfate sodium-induced colitis. World Journal of Gastrointestinal Pharmacology and Therapeutics. 7(2). 242–242. 4 indexed citations
17.
Konishi, Kazuo, Toshiko Yamochi, Yoichi M. Ito, et al.. (2014). Distinct Molecular Features of Different Macroscopic Subtypes of Colorectal Neoplasms. PLoS ONE. 9(8). e103822–e103822. 17 indexed citations
18.
Shinmura, Kensuke, Kazuo Konishi, Toshiko Yamochi, et al.. (2014). Molecular features of colorectal polyps presenting Kudo’s type II mucosal crypt pattern: are they based on the same mechanism of tumorigenesis?. SHILAP Revista de lepidopterología. 2(3). E171–E177. 3 indexed citations
19.
Konishi, Kazuo, Katsumi Sasaki, Toshinori Kurahashi, et al.. (2003). Primary small cell carcinoma of the stomach. Journal of Gastroenterology and Hepatology. 18(6). 743–747. 39 indexed citations
20.
Yamamoto, Tomoaki, Kazuo Konishi, Toshiko Yamochi, et al.. (2003). No major tumorigenic role for β-catenin in serrated as opposed to conventional colorectal adenomas. British Journal of Cancer. 89(1). 152–157. 23 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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