Masahiro Maruoka

703 total citations
22 papers, 530 citations indexed

About

Masahiro Maruoka is a scholar working on Molecular Biology, Immunology and Hematology. According to data from OpenAlex, Masahiro Maruoka has authored 22 papers receiving a total of 530 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 7 papers in Immunology and 5 papers in Hematology. Recurrent topics in Masahiro Maruoka's work include Chronic Myeloid Leukemia Treatments (5 papers), Protein Kinase Regulation and GTPase Signaling (4 papers) and Galectins and Cancer Biology (3 papers). Masahiro Maruoka is often cited by papers focused on Chronic Myeloid Leukemia Treatments (5 papers), Protein Kinase Regulation and GTPase Signaling (4 papers) and Galectins and Cancer Biology (3 papers). Masahiro Maruoka collaborates with scholars based in Japan, Taiwan and Germany. Masahiro Maruoka's co-authors include Naoki Watanabe, Tai Kiuchi, S. Norimatsu, Tatsuo Takeya, Jun Suzuki, Norihiro Ishida‐Kitagawa, Takuya Ogawa, Kensaku Mizuno, Chiharu Higashida and Hiroaki Mizuno and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Molecular Cell.

In The Last Decade

Masahiro Maruoka

21 papers receiving 525 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Masahiro Maruoka Japan 12 252 140 111 103 63 22 530
Sébastien Mailfert France 14 257 1.0× 72 0.5× 293 2.6× 61 0.6× 88 1.4× 22 622
Bálint Balázs Germany 10 252 1.0× 40 0.3× 61 0.5× 201 2.0× 69 1.1× 12 565
Jason Yi United States 8 209 0.8× 222 1.6× 313 2.8× 117 1.1× 125 2.0× 19 642
Stephan Daetwyler United States 12 223 0.9× 135 1.0× 19 0.2× 179 1.7× 36 0.6× 24 479
Leila Nahidiazar Netherlands 11 534 2.1× 292 2.1× 37 0.3× 125 1.2× 26 0.4× 11 882
Daniela Leyton-Puig Netherlands 9 228 0.9× 194 1.4× 34 0.3× 75 0.7× 24 0.4× 9 422
Kazuaki Sawada Japan 7 116 0.5× 29 0.2× 38 0.3× 117 1.1× 85 1.3× 12 392
Volker Andresen Germany 12 276 1.1× 72 0.5× 60 0.5× 374 3.6× 258 4.1× 20 861
Omer Shafraz United States 7 226 0.9× 258 1.8× 19 0.2× 53 0.5× 19 0.3× 12 496
Asier Jayo United Kingdom 14 235 0.9× 327 2.3× 55 0.5× 54 0.5× 71 1.1× 25 656

Countries citing papers authored by Masahiro Maruoka

Since Specialization
Citations

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

Fields of papers citing papers by Masahiro Maruoka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masahiro Maruoka

This figure shows the co-authorship network connecting the top 25 collaborators of Masahiro Maruoka. A scholar is included among the top collaborators of Masahiro Maruoka 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 Masahiro Maruoka. Masahiro Maruoka 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.
Maruoka, Masahiro, et al.. (2024). Phospholipid scrambling induced by an ion channel/metabolite transporter complex. Nature Communications. 15(1). 7566–7566. 5 indexed citations
2.
Onodera, Yasuhito, et al.. (2024). In vivo CRISPR screening directly targeting testicular cells. Cell Genomics. 4(3). 100510–100510. 4 indexed citations
3.
Maruoka, Masahiro, Ryo Suzuki, Daniel M. Packwood, et al.. (2023). Extracellular calcium functions as a molecular glue for transmembrane helices to activate the scramblase Xkr4. Nature Communications. 14(1). 5592–5592. 2 indexed citations
4.
Ishiyama, Kenichi, et al.. (2021). Paradoxical activation of c-Src as a drug-resistant mechanism. Cell Reports. 34(12). 108876–108876. 25 indexed citations
5.
Maruoka, Masahiro, Panpan Zhang, Hiromi Mori, et al.. (2021). Caspase cleavage releases a nuclear protein fragment that stimulates phospholipid scrambling at the plasma membrane. Molecular Cell. 81(7). 1397–1410.e9. 24 indexed citations
6.
Maruoka, Masahiro & Jun Suzuki. (2021). Regulation of phospholipid dynamics in brain. Neuroscience Research. 167. 30–37. 13 indexed citations
7.
Ishiyama, Kenichi, et al.. (2020). Paradoxical Activation of c-Src as a Drug-Resistant Mechanism. SSRN Electronic Journal.
8.
Ueda, Yuki, et al.. (2018). Roles of the third Ig‐like domain of Necl‐5/PVR and the fifth Ig‐like domain of the PDGF receptor in its signaling. Genes to Cells. 23(3). 214–224. 5 indexed citations
9.
Mizutani, Kiyohito, et al.. (2017). Nectin-like molecule-4/cell adhesion molecule 4 inhibits the ligand-induced dimerization of ErbB3 with ErbB2. Scientific Reports. 7(1). 11375–11375. 7 indexed citations
10.
Maruoka, Masahiro, et al.. (2017). Nectin-4 co-stimulates the prolactin receptor by interacting with SOCS1 and inhibiting its activity on the JAK2-STAT5a signaling pathway. Journal of Biological Chemistry. 292(17). 6895–6909. 23 indexed citations
11.
Mizutani, Kiyohito, Masahiro Maruoka, Kenji Mandai, et al.. (2016). A Novel Nectin-mediated Cell Adhesion Apparatus That Is Implicated in Prolactin Receptor Signaling for Mammary Gland Development. Journal of Biological Chemistry. 291(11). 5817–5831. 17 indexed citations
12.
Kiuchi, Tai, et al.. (2015). Multitarget super-resolution microscopy with high-density labeling by exchangeable probes. Nature Methods. 12(8). 743–746. 101 indexed citations
13.
Higashida, Chiharu, Tai Kiuchi, Hiroaki Mizuno, et al.. (2013). F- and G-actin homeostasis regulates mechanosensitive actin nucleation by formins. Nature Cell Biology. 15(4). 395–405. 80 indexed citations
14.
Ishida‐Kitagawa, Norihiro, et al.. (2012). Siglec-15 Protein Regulates Formation of Functional Osteoclasts in Concert with DNAX-activating Protein of 12 kDa (DAP12). Journal of Biological Chemistry. 287(21). 17493–17502. 81 indexed citations
15.
Maruoka, Masahiro, Masayoshi Kuwano, Akira Matsui, et al.. (2011). Identification and functional analysis of a new phosphorylation site (Y398) in the SH3 domain of Abi-1. FEBS Letters. 585(6). 834–840. 10 indexed citations
16.
Sato, Seiichi, Tetsuya Gotoh, Masahiro Maruoka, et al.. (2006). NESH (Abi‐3) is present in the Abi/WAVE complex but does not promote c‐Abl‐mediated phosphorylation. FEBS Letters. 580(27). 6464–6470. 18 indexed citations
17.
Suzuki, Jun, et al.. (2006). A rapid protein expression and purification system using Chinese hamster ovary cells expressing retrovirus receptor. Journal of Biotechnology. 126(4). 463–474. 8 indexed citations
18.
Suzuki, Jun, Masahiro Maruoka, Norihiro Ishida‐Kitagawa, et al.. (2006). Retrovirus-mediated conditional immortalization and analysis of established cell lines of osteoclast precursor cells. Biochemical and Biophysical Research Communications. 350(1). 97–104. 6 indexed citations
19.
Maruoka, Masahiro, Jun Suzuki, Kayo Yoshida, et al.. (2005). Identification of B cell adaptor for PI3‐kinase (BCAP) as an Abl interactor 1‐regulated substrate of Abl kinases. FEBS Letters. 579(14). 2986–2990. 26 indexed citations
20.
Norimatsu, S. & Masahiro Maruoka. (2002). Accurate Q-factor estimation of optically amplified systems in the presence of waveform distortions. Journal of Lightwave Technology. 20(1). 19–27. 37 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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