Toru Furukawa

17.0k total citations · 2 hit papers
318 papers, 10.5k citations indexed

About

Toru Furukawa is a scholar working on Oncology, Surgery and Molecular Biology. According to data from OpenAlex, Toru Furukawa has authored 318 papers receiving a total of 10.5k indexed citations (citations by other indexed papers that have themselves been cited), including 200 papers in Oncology, 110 papers in Surgery and 82 papers in Molecular Biology. Recurrent topics in Toru Furukawa's work include Pancreatic and Hepatic Oncology Research (150 papers), Cholangiocarcinoma and Gallbladder Cancer Studies (54 papers) and Pancreatitis Pathology and Treatment (50 papers). Toru Furukawa is often cited by papers focused on Pancreatic and Hepatic Oncology Research (150 papers), Cholangiocarcinoma and Gallbladder Cancer Studies (54 papers) and Pancreatitis Pathology and Treatment (50 papers). Toru Furukawa collaborates with scholars based in Japan, United States and United Kingdom. Toru Furukawa's co-authors include Akira Horii, Makoto Sunamura, Stanley A. Plotkin, Masakazu Yamamoto, Daitoku Sakamuro, Tsutomu Takegami, Takashi Hatori, Fuyuhiko Motoi, Ming‐Sound Tsao and Ralph H. Hruban and has published in prestigious journals such as Nature, JAMA and Journal of Biological Chemistry.

In The Last Decade

Toru Furukawa

307 papers receiving 10.2k citations

Hit Papers

An Illustrated Consensus ... 2004 2026 2011 2018 2004 2023 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
Toru Furukawa Japan 53 6.1k 3.7k 3.6k 2.2k 1.8k 318 10.5k
Hiroaki Nagano Japan 60 4.2k 0.7× 5.0k 1.3× 3.5k 1.0× 2.2k 1.0× 3.2k 1.8× 451 13.1k
Boudewijn J.M. Braakhuis Netherlands 53 3.9k 0.6× 4.4k 1.2× 2.3k 0.6× 1.3k 0.6× 2.4k 1.3× 142 10.7k
Mengchao Wu China 59 3.7k 0.6× 4.8k 1.3× 3.5k 1.0× 3.3k 1.5× 3.8k 2.1× 312 13.7k
Charles Balabaud France 55 2.4k 0.4× 4.7k 1.3× 3.4k 0.9× 3.5k 1.6× 2.5k 1.4× 238 12.5k
Masamichi Kojiro Japan 66 3.3k 0.5× 3.6k 1.0× 4.2k 1.2× 5.0k 2.3× 2.6k 1.4× 281 15.6k
Young Nyun Park South Korea 64 2.7k 0.4× 3.7k 1.0× 3.6k 1.0× 5.4k 2.5× 2.1k 1.2× 391 14.5k
Antonio Tito Fojo United States 48 8.4k 1.4× 6.9k 1.8× 2.1k 0.6× 800 0.4× 1.5k 0.8× 137 13.6k
Daniel C. Chung United States 46 5.2k 0.8× 4.0k 1.1× 1.4k 0.4× 2.4k 1.1× 1.9k 1.1× 155 10.3k
Hiromitsu Saisho Japan 53 3.1k 0.5× 2.1k 0.6× 2.5k 0.7× 2.9k 1.3× 1.1k 0.6× 260 9.3k
Mary P. Bronner United States 53 3.4k 0.6× 2.5k 0.7× 3.7k 1.0× 1.5k 0.7× 1.9k 1.0× 173 10.1k

Countries citing papers authored by Toru Furukawa

Since Specialization
Citations

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

Fields of papers citing papers by Toru Furukawa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Toru Furukawa

This figure shows the co-authorship network connecting the top 25 collaborators of Toru Furukawa. A scholar is included among the top collaborators of Toru Furukawa 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 Toru Furukawa. Toru Furukawa 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.
Wood, Laura D., Volkan Adsay, Olca Baştürk, et al.. (2023). Systematic review of challenging issues in pathology of intraductal papillary mucinous neoplasms. Pancreatology. 23(7). 878–891. 24 indexed citations
2.
Ogawa, Takenori, Ayako Nakanome, Akira Ohkoshi, et al.. (2022). Investigation of the diversity of human papillomavirus 16 variants and L1 antigenic regions relevant for the prevention of human papillomavirus-related oropharyngeal cancer in Japan. Auris Nasus Larynx. 49(6). 1033–1041. 4 indexed citations
3.
Hata, Tatsuo, Masamichi Mizuma, Fuyuhiko Motoi, et al.. (2021). Germline DNA damage repair gene mutations in pancreatic cancer patients with personal/family histories of pancreas/breast/ovarian/prostate cancer in a Japanese population. Annals of Gastroenterological Surgery. 5(6). 853–864. 9 indexed citations
4.
Izumo, Wataru, Ryota Higuchi, Toru Furukawa, et al.. (2020). Evaluation of preoperative prognostic factors in patients with resectable invasive intraductal papillary mucinous carcinoma. Surgery. 168(6). 994–1002. 2 indexed citations
5.
Shibayama, Yuki, Kazuo Takahashi, Hisateru Yamaguchi, et al.. (2020). Aberrant (pro)renin receptor expression induces genomic instability in pancreatic ductal adenocarcinoma through upregulation of SMARCA5/SNF2H. Communications Biology. 3(1). 724–724. 6 indexed citations
6.
Higuchi, Ryota, Takehisa Yazawa, Shuichiro Uemura, et al.. (2018). Surgical Outcomes for Perihilar Cholangiocarcinoma with Vascular Invasion. Journal of Gastrointestinal Surgery. 23(7). 1443–1453. 25 indexed citations
7.
Higuchi, Ryota, et al.. (2018). ENBD is associated with decreased tumor dissemination compared to ptbd in perihilar cholangiocarcinoma. HPB. 20. S184–S185. 1 indexed citations
8.
Matsuda, Yoko, M. Tanaka, Motoji Sawabe, et al.. (2017). Relationship between pancreatic intraepithelial neoplasias, pancreatic ductal adenocarcinomas, and single nucleotide polymorphisms in autopsied elderly patients. Genes Chromosomes and Cancer. 57(1). 12–18. 6 indexed citations
9.
Higuchi, Ryota, Takehisa Yazawa, Shuichiro Uemura, et al.. (2017). ENBD is Associated with Decreased Tumor Dissemination Compared to PTBD in Perihilar Cholangiocarcinoma. Journal of Gastrointestinal Surgery. 21(9). 1506–1514. 24 indexed citations
10.
Maeda, Jun, Matthew Genet, Kelly Mann, et al.. (2015). Validation of 64Cu-ATSM damaging DNA via high-LET Auger electron emission. 1 indexed citations
11.
Furukawa, Toru, Etsuko Tanji, Yuko Kuboki, et al.. (2012). Targeting of MAPK-associated molecules identifies SON as a prime target to attenuate the proliferation and tumorigenicity of pancreatic cancer cells. Molecular Cancer. 11(1). 88–88. 18 indexed citations
12.
Tanji, Etsuko, et al.. (2011). MicroRNAs Associated with Mitogen-Activated Protein Kinase in Human Pancreatic Cancer. Molecular Cancer Research. 10(2). 259–269. 64 indexed citations
13.
Higuchi, Ryota, Takehiro Ota, Tatsuo Araida, et al.. (2010). Prognostic relevance of ductal margins in operative resection of bile duct cancer. Surgery. 148(1). 7–14. 34 indexed citations
14.
Ushikubo, Fernanda Yumi, et al.. (2008). A study of water containing micro and nano-bubbles and its possible effect on physiological activity.. 6 indexed citations
15.
Suzuki, Yutaka, Yutaka Atomi, Masanori Sugiyama, et al.. (2004). Cystic Neoplasm of the Pancreas. Pancreas. 28(3). 241–246. 196 indexed citations
16.
Hruban, Ralph H., Kyoichi Takaori, David S. Klimstra, et al.. (2004). An Illustrated Consensus on the Classification of Pancreatic Intraepithelial Neoplasia and Intraductal Papillary Mucinous Neoplasms. The American Journal of Surgical Pathology. 28(8). 977–987. 761 indexed citations breakdown →
17.
Nakashima, Misako, Naoko Tanese, Masataka Ito, et al.. (2002). A novel gene, GliH1, with homology to the Gli zinc finger domain not required for mouse development. Mechanisms of Development. 119(1). 21–34. 29 indexed citations
18.
Furukawa, Toru, Hirokazu Tanino, Shoji Oura, et al.. (1997). Clinical application of histoculture drug response assay (HDRA) - Distribution pattern of inhibition index and predictability of clinical chemo-therapy effects -. 32(4). 400–409. 2 indexed citations
19.
Kubota, Tetsuro, Toru Furukawa, & Masaki Kitajima. (1993). [High clinical predictability of histoculture drug response assay (HDRA) for drug-sensitivity of cancer of the digestive organs].. PubMed. 20(4). 461–6. 3 indexed citations
20.
Endo, K, Harumi Sakahara, Tetsuo Nakashima, et al.. (1984). Tumor Imaging by Monoclonal Antibodies Labeled with Radioactive Metal Ions. The Korean Journal of Nuclear Medicine. 18(2). 77–85. 1 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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