Naoki Harada

7.8k total citations
203 papers, 3.8k citations indexed

About

Naoki Harada is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Naoki Harada has authored 203 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 85 papers in Molecular Biology, 65 papers in Genetics and 44 papers in Oncology. Recurrent topics in Naoki Harada's work include Genomic variations and chromosomal abnormalities (45 papers), Prenatal Screening and Diagnostics (26 papers) and Genetic Syndromes and Imprinting (18 papers). Naoki Harada is often cited by papers focused on Genomic variations and chromosomal abnormalities (45 papers), Prenatal Screening and Diagnostics (26 papers) and Genetic Syndromes and Imprinting (18 papers). Naoki Harada collaborates with scholars based in Japan, United States and Netherlands. Naoki Harada's co-authors include Norio Niikawa, Naomichi Matsumoto, Osamu Shimokawa, Tohru Ohta, Toshihiro Miyamoto, Tatsuya Kishino, Katsuto Takenaka, Naomichi Matsumoto, Koh-ichiro Yoshiura and Takanori Teshima and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nucleic Acids Research.

In The Last Decade

Naoki Harada

197 papers receiving 3.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Naoki Harada Japan 33 1.5k 1.3k 567 555 418 203 3.8k
Ferdinand von Eggeling Germany 36 1.9k 1.3× 562 0.4× 571 1.0× 338 0.6× 226 0.5× 155 3.7k
Charles D. Scher United States 36 3.1k 2.1× 1.1k 0.8× 907 1.6× 206 0.4× 152 0.4× 81 5.9k
Rolf Marschalek Germany 40 3.3k 2.2× 397 0.3× 569 1.0× 319 0.6× 272 0.7× 225 5.4k
Uwe Claussen Germany 30 1.5k 1.0× 1.4k 1.0× 190 0.3× 527 0.9× 808 1.9× 105 2.9k
Michael Kiefer United States 42 4.1k 2.7× 756 0.6× 1.1k 2.0× 101 0.2× 278 0.7× 68 6.9k
W. Edward Highsmith United States 32 1.8k 1.2× 434 0.3× 687 1.2× 136 0.2× 92 0.2× 99 4.2k
Kathryn Graham Canada 32 988 0.7× 567 0.4× 729 1.3× 133 0.2× 92 0.2× 45 2.8k
Paul A. Edwards United Kingdom 38 3.0k 2.0× 921 0.7× 1.2k 2.1× 70 0.1× 329 0.8× 128 5.2k
Kenzaburo Tani Japan 38 2.4k 1.6× 1.1k 0.8× 1.2k 2.0× 199 0.4× 65 0.2× 225 5.4k
Hidenori Kato Japan 33 1.8k 1.2× 366 0.3× 612 1.1× 245 0.4× 587 1.4× 167 4.4k

Countries citing papers authored by Naoki Harada

Since Specialization
Citations

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

Fields of papers citing papers by Naoki Harada

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Naoki Harada

This figure shows the co-authorship network connecting the top 25 collaborators of Naoki Harada. A scholar is included among the top collaborators of Naoki Harada 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 Naoki Harada. Naoki Harada 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.
Harada, Naoki, et al.. (2025). Use of the LEONIS Mova Steerable Catheter in the Treatment of Cavernous Sinus Dural Arteriovenous Fistula with Occluded Inferior Petrosal Sinus. Journal of Neuroendovascular Therapy. 19(1). n/a–n/a. 1 indexed citations
2.
Morihiro, Kunihiko, Naoki Harada, Mitsuru Naito, et al.. (2024). RNA Oncological Therapeutics: Intracellular Hairpin RNA Assembly Enables MicroRNA-Triggered Anticancer Functionality. Journal of the American Chemical Society. 146(2). 1346–1355. 17 indexed citations
3.
Yamashita‐Kashima, Yoriko, Natsumi Kawasaki, Mitsue Kurasawa, et al.. (2022). Coadministration with bendamustine restores the antitumor activity of obinutuzumab in obinutuzumab-resistant tumors. International Journal of Hematology. 115(6). 860–872. 1 indexed citations
4.
Kawasaki, Natsumi, et al.. (2022). Resistance to obinutuzumab-induced antibody-dependent cellular cytotoxicity caused by abnormal Fas signaling is overcome by combination therapies. Molecular Biology Reports. 49(6). 4421–4433. 9 indexed citations
5.
Yamashita‐Kashima, Yoriko, et al.. (2021). Obinutuzumab in Combination with Chemotherapy Enhances Direct Cell Death in CD20-Positive Obinutuzumab-resistant Non-Hodgkin Lymphoma Cells. Molecular Cancer Therapeutics. 20(6). 1133–1141. 8 indexed citations
6.
Yamashita‐Kashima, Yoriko, Mieko Yanagisawa, Hayao Nakanishi, et al.. (2019). Trastuzumab in combination with paclitaxel enhances antitumor activity by promoting apoptosis in human epidermal growth factor receptor 2-positive trastuzumab-resistant gastric cancer xenograft models. Anti-Cancer Drugs. 31(3). 241–250. 3 indexed citations
7.
Takamura, Hiroyoshi, Takahiro Kikuchi, Naoki Harada, et al.. (2018). Unified Total Synthesis, Stereostructural Elucidation, and Biological Evaluation of Sarcophytonolides. The Journal of Organic Chemistry. 83(18). 11028–11056. 19 indexed citations
8.
Ishii, Nobuya, Naoki Harada, Eric W. Joseph, et al.. (2013). Enhanced Inhibition of ERK Signaling by a Novel Allosteric MEK Inhibitor, CH5126766, That Suppresses Feedback Reactivation of RAF Activity. Cancer Research. 73(13). 4050–4060. 128 indexed citations
9.
Saitsu, Hirotomo, Kenji Kurosawa, Takeshi Mizuguchi, et al.. (2009). Characterization of the complex 7q21.3 rearrangement in a patient with bilateral split‐foot malformation and hearing loss. American Journal of Medical Genetics Part A. 149A(6). 1224–1230. 14 indexed citations
10.
Mori, Yasuo, Takatoshi Aoki, Katsuto Takenaka, et al.. (2009). Successful treatment of refractory advanced nasal NK/T cell lymphoma with unrelated cord blood stem cell transplantation incorporating focal irradiation. International Journal of Hematology. 91(1). 107–111. 8 indexed citations
11.
Harada, Naoki, et al.. (2008). One Case of Stercoral Colonic Perforation During Treatment of Hemodialysis and Polycythemia Vera. The Japanese Journal of Gastroenterological Surgery. 41(2). 247–252. 1 indexed citations
12.
Harada, Naoki, et al.. (2007). A CASE OF DEDIFFERENTIATED LIPOSARCOMA OF THE SPERMATIC CORD WHICH RECURRED REPEATEDLY. Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association). 68(10). 2610–2616.
13.
Miura, Kiyonori, Koh‐ichiro Yoshiura, Shoko Miura, et al.. (2006). Clinical outcome of infants with confined placental mosaicism and intrauterine growth restriction of unknown cause. American Journal of Medical Genetics Part A. 140A(17). 1827–1833. 23 indexed citations
14.
Kurotaki, Naohiro, Joseph Shen, Tatsuro Kondoh, et al.. (2005). Phenotypic consequences of genetic variation at hemizygous alleles: Sotos syndrome is a contiguous gene syndrome incorporating coagulation factor twelve (FXII) deficiency. Genetics in Medicine. 7(7). 479–483. 33 indexed citations
15.
Yamamoto, Toshiyuki, Motoyoshi Kawataki, Michiko Yamanaka, et al.. (2005). A large interstitial deletion of 17p13.1p11.2 involving the Smith–Magenis chromosome region in a girl with multiple congenital anomalies. American Journal of Medical Genetics Part A. 140A(1). 88–91. 13 indexed citations
16.
Shimokawa, Osamu, Kenji Kurosawa, Naoki Harada, et al.. (2004). Molecular characterization of inv dup del(8p): Analysis of five cases. American Journal of Medical Genetics Part A. 128A(2). 133–137. 61 indexed citations
17.
Kondoh, Tatsuro, et al.. (2004). Genotype-phenotype correlation of 5p- syndrome: pitfall of diagnosis. Journal of Human Genetics. 50(1). 26–29. 17 indexed citations
19.
Yamamoto, Tohru, Nobuaki Matsuo, Hiroyasu Ishikura, et al.. (1991). An Adult Case of Idiopathic Intussusception and Review of the Literature. 43(4). 444–449. 1 indexed citations
20.
Fukushima, Yoshimitsu, Naoki Harada, Kyohko Abe, et al.. (1991). Molecular study of the Prader‐Willi syndrome: Deletion, RFLP, and phenotype analyses of 50 patients. American Journal of Medical Genetics. 41(1). 54–63. 58 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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