Naoki Mochizuki

23.2k total citations · 2 hit papers
250 papers, 17.0k citations indexed

About

Naoki Mochizuki is a scholar working on Molecular Biology, Cell Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Naoki Mochizuki has authored 250 papers receiving a total of 17.0k indexed citations (citations by other indexed papers that have themselves been cited), including 154 papers in Molecular Biology, 76 papers in Cell Biology and 35 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Naoki Mochizuki's work include Angiogenesis and VEGF in Cancer (33 papers), Protein Kinase Regulation and GTPase Signaling (29 papers) and Zebrafish Biomedical Research Applications (27 papers). Naoki Mochizuki is often cited by papers focused on Angiogenesis and VEGF in Cancer (33 papers), Protein Kinase Regulation and GTPase Signaling (29 papers) and Zebrafish Biomedical Research Applications (27 papers). Naoki Mochizuki collaborates with scholars based in Japan, United States and Germany. Naoki Mochizuki's co-authors include Michiyuki Matsuda, Shigetomo Fukuhara, Yusuke Ohba, Kazuo Kurokawa, Koji Ando, Ann M. Graybiel, Michitaka Masuda, Shinichiro Toki, Hiroaki Kawasaki and Gregory M. Springett and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Naoki Mochizuki

249 papers receiving 16.8k citations

Hit Papers

A molecular atlas of cell... 1998 2026 2007 2016 2018 1998 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Naoki Mochizuki Japan 64 10.4k 4.5k 1.9k 1.9k 1.5k 250 17.0k
Mutsuki Amano Japan 52 11.4k 1.1× 6.7k 1.5× 1.5k 0.8× 2.6k 1.4× 971 0.6× 100 17.1k
Toshiaki Katada Japan 69 13.1k 1.3× 3.7k 0.8× 941 0.5× 3.5k 1.9× 1.7k 1.1× 300 18.1k
Yoh Takuwa Japan 57 7.6k 0.7× 2.2k 0.5× 1.3k 0.7× 1.1k 0.6× 1.3k 0.8× 182 11.7k
Wouter H. Moolenaar Netherlands 84 18.7k 1.8× 5.6k 1.2× 669 0.3× 2.7k 1.4× 2.0k 1.3× 198 23.4k
David L. Brautigan United States 70 12.4k 1.2× 3.6k 0.8× 835 0.4× 1.6k 0.8× 1.2k 0.8× 249 16.5k
Yuko Fukata Japan 54 9.5k 0.9× 6.0k 1.3× 982 0.5× 3.9k 2.0× 761 0.5× 99 15.3k
Tetsuo Noda Japan 80 15.6k 1.5× 2.7k 0.6× 955 0.5× 2.1k 1.1× 2.7k 1.8× 260 24.3k
Thomas Franke United States 36 11.8k 1.1× 1.6k 0.4× 1.4k 0.7× 1.9k 1.0× 2.1k 1.4× 49 17.6k
Ushio Kikkawa Japan 74 18.9k 1.8× 3.9k 0.9× 915 0.5× 3.7k 1.9× 2.4k 1.6× 203 24.5k
Masaki Inagaki Japan 73 13.1k 1.3× 7.7k 1.7× 750 0.4× 2.3k 1.2× 1.1k 0.7× 223 18.7k

Countries citing papers authored by Naoki Mochizuki

Since Specialization
Citations

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

Fields of papers citing papers by Naoki Mochizuki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Naoki Mochizuki

This figure shows the co-authorship network connecting the top 25 collaborators of Naoki Mochizuki. A scholar is included among the top collaborators of Naoki Mochizuki 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 Mochizuki. Naoki Mochizuki 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.
Chiba, Ayano, et al.. (2024). Zonated Wnt/β-catenin signal-activated cardiomyocytes at the atrioventricular canal promote coronary vessel formation in zebrafish. Developmental Cell. 60(1). 21–29.e8. 1 indexed citations
2.
Ando, Koji, Keisuke Sako, Urara Hasegawa, et al.. (2024). Angpt1 binding to Tie1 regulates the signaling required for lymphatic vessel development in zebrafish. Development. 151(10). 3 indexed citations
3.
Watanabe‐Takano, Haruko, Katsuhiro Kato, Koji Kobayashi, et al.. (2024). Endothelial cells regulate alveolar morphogenesis by constructing basement membranes acting as a scaffold for myofibroblasts. Nature Communications. 15(1). 1622–1622. 7 indexed citations
4.
Schulte, Dörte, Hiroyuki Nakajima, Naoki Mochizuki, et al.. (2023). Svep1 is a binding ligand of Tie1 and affects specific aspects of facial lymphatic development in a Vegfc-independent manner. eLife. 12. 12 indexed citations
5.
Huang, Ying, Feiyang Ma, Fatma O. Kok, et al.. (2022). Heterogeneous pdgfrb+ cells regulate coronary vessel development and revascularization during heart regeneration. Development. 149(4). 7 indexed citations
6.
Nishimura, Yusuke, Koji Ando, Shinya Yuge, et al.. (2022). Blood Flow Regulates Glomerular Capillary Formation in Zebrafish Pronephros. Kidney360. 3(4). 700–713. 8 indexed citations
7.
Ando, Koji, Renae Skoczylas, Naoki Mochizuki, et al.. (2022). Proper migration of lymphatic endothelial cells requires survival and guidance cues from arterial mural cells. eLife. 11. 11 indexed citations
8.
Fukui, Hajime, Renée Chow, Jing Xie, et al.. (2021). Bioelectric signaling and the control of cardiac cell identity in response to mechanical forces. Science. 374(6565). 351–354. 61 indexed citations
9.
Noishiki, Chikage, Shinya Yuge, Koji Ando, et al.. (2019). Live imaging of angiogenesis during cutaneous wound healing in adult zebrafish. Angiogenesis. 22(2). 341–354. 39 indexed citations
10.
Miyazaki, Takahiro, Kentaro Otani, Ayano Chiba, et al.. (2018). A New Secretory Peptide of Natriuretic Peptide Family, Osteocrin, Suppresses the Progression of Congestive Heart Failure After Myocardial Infarction. Circulation Research. 122(5). 742–751. 39 indexed citations
11.
Stainier, Didier Y. R., Erez Raz, Nathan D. Lawson, et al.. (2017). Guidelines for morpholino use in zebrafish. PLoS Genetics. 13(10). e1007000–e1007000. 237 indexed citations
12.
Chiba, Ayano, Haruko Watanabe‐Takano, Kenta Terai, et al.. (2016). Osteocrin, a peptide secreted from the heart and other tissues, contributes to cranial osteogenesis and chondrogenesis in zebrafish. Development. 144(2). 334–344. 26 indexed citations
13.
Ando, Koji, et al.. (2013). Rap1 potentiates endothelial cell junctions by spatially controlling myosin II activity and actin organization. The Journal of Cell Biology. 202(6). 901–916. 113 indexed citations
14.
Fukuhara, Shigetomo, Szandor Simmons, Shunsuke Kawamura, et al.. (2012). The sphingosine-1-phosphate transporter Spns2 expressed on endothelial cells regulates lymphocyte trafficking in mice. Journal of Clinical Investigation. 122(4). 1416–1426. 264 indexed citations
15.
Ueno, Masaya, S. Miyamoto, Eiichi Morii, et al.. (2010). PSF1, a DNA Replication Factor Expressed Widely in Stem and Progenitor Cells, Drives Tumorigenic and Metastatic Properties. Cancer Research. 70(3). 1215–1224. 57 indexed citations
16.
Makita, Naomasa, Elijah R. Behr, Wataru Shimizu, et al.. (2008). The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome. Journal of Clinical Investigation. 118(6). 2219–29. 160 indexed citations
17.
Wakeno, Masakatsu, Tetsuo Minamino, Osamu Seguchi, et al.. (2006). Long-Term Stimulation of Adenosine A2b Receptors Begun After Myocardial Infarction Prevents Cardiac Remodeling in Rats. Circulation. 114(18). 1923–1932. 84 indexed citations
18.
Watanabe, Takuya, Masumi Tsuda, Yoshinori Makino, et al.. (2006). Adaptor Molecule Crk Is Required for Sustained Phosphorylation of Grb2-Associated Binder 1 and Hepatocyte Growth Factor–Induced Cell Motility of Human Synovial Sarcoma Cell Lines. Molecular Cancer Research. 4(7). 499–510. 53 indexed citations
19.
Yoshizaki, Hisayoshi, Yusuke Ohba, Kazuo Kurokawa, et al.. (2003). Activity of Rho-family GTPases during cell division as visualized with FRET-based probes. The Journal of Cell Biology. 162(2). 223–232. 349 indexed citations
20.
Endo, Akira, et al.. (2003). Selective Inhibition of Vascular Endothelial Growth Factor Receptor‐2 (VEGFR‐2) Identifies a Central Role for VEGFR‐2 in Human Aortic Endothelial Cell Responses to VEGF. Journal of Receptors and Signal Transduction. 23(2-3). 239–254. 36 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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