Atsushi Kittaka

3.2k total citations
186 papers, 2.6k citations indexed

About

Atsushi Kittaka is a scholar working on Pathology and Forensic Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Atsushi Kittaka has authored 186 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 109 papers in Pathology and Forensic Medicine, 75 papers in Genetics and 57 papers in Molecular Biology. Recurrent topics in Atsushi Kittaka's work include Vitamin D Research Studies (107 papers), Estrogen and related hormone effects (73 papers) and Biotin and Related Studies (34 papers). Atsushi Kittaka is often cited by papers focused on Vitamin D Research Studies (107 papers), Estrogen and related hormone effects (73 papers) and Biotin and Related Studies (34 papers). Atsushi Kittaka collaborates with scholars based in Japan, United States and Taiwan. Atsushi Kittaka's co-authors include Hiroaki Takayama, Tai C. Chen, Nozomi Saito, Toshie Fujishima, Yoshitomo Suhara, Toshiyuki Sakaki, Masashi Takano, Masaaki Kurihara, Toru Sugiyama and Shinobu Honzawa and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Atsushi Kittaka

181 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Atsushi Kittaka Japan 28 1.4k 878 854 709 434 186 2.6k
Daniela Gallo Italy 30 474 0.3× 533 0.6× 1.4k 1.6× 134 0.2× 460 1.1× 72 2.9k
Surinder K. Chander United Kingdom 23 278 0.2× 933 1.1× 853 1.0× 325 0.5× 89 0.2× 38 1.7k
Lawrence M. Ballas United States 24 137 0.1× 389 0.4× 2.2k 2.6× 548 0.8× 327 0.8× 37 3.5k
Hiroyuki Masuno Japan 19 407 0.3× 246 0.3× 309 0.4× 219 0.3× 118 0.3× 37 1.1k
Pierre De Clercq Belgium 15 449 0.3× 196 0.2× 208 0.2× 252 0.4× 130 0.3× 40 860
Emmanuelle J. Meuillet United States 30 128 0.1× 152 0.2× 1.7k 1.9× 331 0.5× 261 0.6× 65 2.4k
Lisa M. Shewchuk United States 27 95 0.1× 243 0.3× 1.6k 1.9× 690 1.0× 266 0.6× 45 3.0k
Atul Purohit United Kingdom 41 105 0.1× 2.6k 2.9× 2.4k 2.8× 1.4k 2.0× 141 0.3× 102 4.7k
Daniel H. Albert United States 29 120 0.1× 105 0.1× 1.3k 1.6× 582 0.8× 105 0.2× 88 2.7k
Karen R. Grotzinger United States 13 318 0.2× 179 0.2× 1.6k 1.8× 306 0.4× 114 0.3× 18 3.3k

Countries citing papers authored by Atsushi Kittaka

Since Specialization
Citations

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

Fields of papers citing papers by Atsushi Kittaka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Atsushi Kittaka

This figure shows the co-authorship network connecting the top 25 collaborators of Atsushi Kittaka. A scholar is included among the top collaborators of Atsushi Kittaka 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 Atsushi Kittaka. Atsushi Kittaka 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.
Kimura, Shinzo, S. Tagami, Hiroki Mano, et al.. (2025). Divergent roles of 25-hydroxyvitamin D3 and 1α,25-dihydroxyvitamin D3 in neural fate determination: A CYP27B1-dependent neuron formation and VDR-dependent astrocyte development. Biochemical and Biophysical Research Communications. 755. 151547–151547. 1 indexed citations
3.
Ishizawa, Michiyasu, Masashi Takano, Atsushi Kittaka, Tarô Matsumoto, & Makoto Makishima. (2024). 2α-Substituted Vitamin D Derivatives Effectively Enhance the Osteoblast Differentiation of Dedifferentiated Fat Cells. Biomolecules. 14(6). 706–706. 1 indexed citations
4.
Peluso‐Iltis, Carole, Daniela Rovito, Judit Ősz, et al.. (2024). 4-Hydroxy-1α,25-Dihydroxyvitamin D3: Synthesis and Structure–Function Study. Biomolecules. 14(5). 551–551. 1 indexed citations
5.
Takemoto, Yasushi, et al.. (2023). Structure–activity relationship studies on vitamin D-based selective SREBP/SCAP inhibitor KK-052. RSC Medicinal Chemistry. 14(10). 2030–2034. 6 indexed citations
6.
Kittaka, Atsushi, et al.. (2023). An Improved and Scalable Synthesis of the Potent SREBP Inhibitor KK-052 via [3+2] Cycloaddition. Synthesis. 56(9). 1460–1464. 1 indexed citations
7.
Yasuda, Kaori, Hiroki Mano, Akiko Takeuchi, et al.. (2023). Synthesis of New 26,27-Difluoro- and 26,26,27,27-Tetrafluoro-25-hydroxyvitamin D<sub>3</sub>: Effects of Terminal Fluorine Atoms on Biological Activity and Half-life. Chemical and Pharmaceutical Bulletin. 71(9). 717–723. 7 indexed citations
9.
Sakamoto, Ryota, et al.. (2022). Synthesis of C2-Alkoxy-Substituted 19-Nor Vitamin D3 Derivatives: Stereoselectivity and Biological Activity. Biomolecules. 12(1). 69–69. 3 indexed citations
10.
Hayata, Yuki, Satoshi Kawamura, Yasushi Takemoto, et al.. (2021). Discovery of a Vitamin D Receptor-Silent Vitamin D Derivative That Impairs Sterol Regulatory Element-Binding Protein In Vivo. Journal of Medicinal Chemistry. 64(9). 5689–5709. 23 indexed citations
11.
Yasui, Koji, et al.. (2019). Synthetic Chemical Probes That Dissect Vitamin D Activities. ACS Chemical Biology. 14(12). 2851–2858. 15 indexed citations
12.
Yamanaka, Masahiro, et al.. (2019). Stereoselective Synthesis of Four Calcitriol Lactone Diastereomers at C23 and C25. The Journal of Organic Chemistry. 84(12). 7630–7641. 12 indexed citations
13.
Yasuda, Kaori, et al.. (2019). Synthesis and CYP24A1-Dependent Metabolism of 23-Fluorinated Vitamin D3 Analogues. ACS Omega. 4(6). 11332–11337. 12 indexed citations
14.
Chiang, Kun‐Chun, Chun‐Nan Yeh, Ta‐Sen Yeh, et al.. (2018). MART-10, a 1α,25(OH)2D3 Analog, Potently Represses Metastasis of ER+ Breast Cancer Cells with VEGF-A Overexpression. Anticancer Research. 38(7). 3879–3887. 8 indexed citations
15.
Chiang, Kun‐Chun, Ming‐Huang Chen, Chi‐Ying F. Huang, et al.. (2015). MART-10, the new brand of 1α,25(OH)2D3 analog, is a potent anti-angiogenic agent in vivo and in vitro. The Journal of Steroid Biochemistry and Molecular Biology. 155(Pt A). 26–34. 9 indexed citations
16.
Chiang, Kun‐Chun, Chun‐Nan Yeh, Kun‐Ju Lin, et al.. (2014). Chemopreventive and chemotherapeutic effects of dietary supplementation of vitamin D on cholangiocarcinoma in a Chemical-Induced animal model. Oncotarget. 5(11). 3849–3861. 14 indexed citations
17.
Takano, Masashi, Daisuke Sawada, Nozomi Saito, et al.. (2012). C15-functionalized 16-ene-1α,25-dihydroxyvitamin D3 is a new vitamin D analog with unique biological properties.. PubMed. 32(1). 311–7. 3 indexed citations
18.
Chen, Tai C., Kelly S. Persons, Shasha Zheng, et al.. (2007). Evaluation of C-2-substituted 19-nor-1α,25-dihydroxyvitamin D3 analogs as therapeutic agents for prostate cancer. The Journal of Steroid Biochemistry and Molecular Biology. 103(3-5). 717–720. 29 indexed citations
19.
Kittaka, Atsushi, Nozomi Saito, & Masashi Takano. (2006). [Recent progress of study on vitamin D analogs].. PubMed. 16(7). 1154–65. 2 indexed citations
20.
Arizono, Ikuo, Atsushi Kittaka, & Hiroshi Ota. (1989). A Test for Normality Based on Generalized Entropy. Osaka Prefecture University Repository (Osaka Prefecture University). 37(2). 153–160. 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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