Ikuo Masuho

3.4k total citations · 1 hit paper
50 papers, 2.3k citations indexed

About

Ikuo Masuho is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Ikuo Masuho has authored 50 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 17 papers in Cellular and Molecular Neuroscience and 8 papers in Genetics. Recurrent topics in Ikuo Masuho's work include Receptor Mechanisms and Signaling (31 papers), Protein Kinase Regulation and GTPase Signaling (20 papers) and Ion channel regulation and function (7 papers). Ikuo Masuho is often cited by papers focused on Receptor Mechanisms and Signaling (31 papers), Protein Kinase Regulation and GTPase Signaling (20 papers) and Ion channel regulation and function (7 papers). Ikuo Masuho collaborates with scholars based in United States, Japan and United Kingdom. Ikuo Masuho's co-authors include Kirill A. Martemyanov, Keqiang Xie, Sreenivas Chavali, David E. Gloriam, Alexander S. Hauser, Leonie Johanna Jahn, M. Madan Babu, Olga Ostrovskaya, Nickolas K. Skamangas and Christopher D. Jones and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Ikuo Masuho

48 papers receiving 2.3k citations

Hit Papers

Pharmacogenomics of GPCR Drug Targets 2017 2026 2020 2023 2017 100 200 300 400

Peers

Ikuo Masuho
Alexey Pronin United States
Geoffrey C. Owens United States
Monique Howard Australia
Amantha Thathiah United States
Ursula Boschert United States
Seung Kwak United States
Alexey Pronin United States
Ikuo Masuho
Citations per year, relative to Ikuo Masuho Ikuo Masuho (= 1×) peers Alexey Pronin

Countries citing papers authored by Ikuo Masuho

Since Specialization
Citations

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

Fields of papers citing papers by Ikuo Masuho

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ikuo Masuho

This figure shows the co-authorship network connecting the top 25 collaborators of Ikuo Masuho. A scholar is included among the top collaborators of Ikuo Masuho 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 Ikuo Masuho. Ikuo Masuho 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.
Shiimura, Yuki, Dohyun Im, Hidetsugu Asada, et al.. (2025). The structure and function of the ghrelin receptor coding for drug actions. Nature Structural & Molecular Biology. 32(3). 531–542. 3 indexed citations
2.
Masuho, Ikuo, et al.. (2024). Receptor-dependent influence of R7 RGS proteins on neuronal GIRK channel signaling dynamics. Progress in Neurobiology. 243. 102686–102686.
3.
Masuho, Ikuo, Ryoji Kise, Pablo Gaínza, et al.. (2023). Rules and mechanisms governing G protein coupling selectivity of GPCRs. Cell Reports. 42(10). 113173–113173. 32 indexed citations
4.
Masuho, Ikuo, Dongjun Ren, Wei Lv, et al.. (2022). Effects of Small Molecule Ligands on ACKR3 Receptors. Molecular Pharmacology. 102(3). 128–138. 4 indexed citations
5.
Moo, Ee Von, Kasper Harpsøe, Alexander S. Hauser, et al.. (2021). Ligand-directed bias of G protein signaling at the dopamine D2 receptor. Cell chemical biology. 29(2). 226–238.e4. 22 indexed citations
6.
Masuho, Ikuo, Balaji Santhanam, Brian S. Muntean, et al.. (2020). A Global Map of G Protein Signaling Regulation by RGS Proteins. Cell. 183(2). 503–521.e19. 100 indexed citations
7.
Masuho, Ikuo, Ezequiel Marrón Fernández de Velasco, Atsushi Nakano, et al.. (2020). GPCR-dependent biasing of GIRK channel signaling dynamics by RGS6 in mouse sinoatrial nodal cells. Proceedings of the National Academy of Sciences. 117(25). 14522–14531. 16 indexed citations
8.
Wang, Dandan, Hannah M. Stoveken, Stefano Zucca, et al.. (2019). Genetic behavioral screen identifies an orphan anti-opioid system. Science. 365(6459). 1267–1273. 43 indexed citations
9.
Gulati, Sahil, Hui Jin, Ikuo Masuho, et al.. (2018). Targeting G protein-coupled receptor signaling at the G protein level with a selective nanobody inhibitor. Nature Communications. 9(1). 1996–1996. 68 indexed citations
10.
Desbois, Muriel, et al.. (2018). PAM forms an atypical SCF ubiquitin ligase complex that ubiquitinates and degrades NMNAT2. Journal of Biological Chemistry. 293(36). 13897–13909. 36 indexed citations
11.
Masuho, Ikuo, Francisco Pereira da Silva‐Júnior, Egberto Reis Barbosa, et al.. (2016). Screening of GNAL variants in Brazilian patients with isolated dystonia reveals a novel mutation with partial loss of function. Journal of Neurology. 263(4). 665–668. 12 indexed citations
12.
Shamseldin, Hanan E., Ikuo Masuho, Ahmed Alenizi, et al.. (2016). GNB5 mutation causes a novel neuropsychiatric disorder featuring attention deficit hyperactivity disorder, severely impaired language development and normal cognition. Genome biology. 17(1). 195–195. 28 indexed citations
13.
Masuho, Ikuo, Kirill A. Martemyanov, & Nevin A. Lambert. (2015). Monitoring G Protein Activation in Cells with BRET. Methods in molecular biology. 1335. 107–113. 81 indexed citations
14.
Masuho, Ikuo, et al.. (2011). Establishment of clonal cell lines of taste buds from a p53 −/− mouse tongue. In Vitro Cellular & Developmental Biology - Animal. 47(4). 333–340. 6 indexed citations
15.
Cao, Yan, Alexander V. Kolesnikov, Ikuo Masuho, Vladimir J. Kefalov, & Kirill A. Martemyanov. (2010). Membrane Anchoring Subunits Specify Selective Regulation of RGS9·Gβ5 GAP Complex in Photoreceptor Neurons. Journal of Neuroscience. 30(41). 13784–13793. 9 indexed citations
16.
Cao, Yan, Ikuo Masuho, Haruhisa Okawa, et al.. (2009). Retina-Specific GTPase Accelerator RGS11/Gβ5S/R9AP Is a Constitutive Heterotrimer Selectively Targeted to mGluR6 in ON-Bipolar Neurons. Journal of Neuroscience. 29(29). 9301–9313. 71 indexed citations
17.
Masuho, Ikuo, Michihiro Tateyama, & Osamu Saitoh. (2005). Characterization of Bitter Taste Responses of Intestinal STC-1 Cells. Chemical Senses. 30(4). 281–290. 32 indexed citations
18.
Saitoh, Osamu, et al.. (2003). Distribution of regulator of G protein signaling 8 (RGS8) protein in the cerebellum. The Cerebellum. 2(2). 154–160. 15 indexed citations
19.
Masuho, Ikuo, Masayuki Itoh, Hiroshi Itoh, & Osamu Saitoh. (2003). The mechanism of membrane‐translocation of regulator of G‐protein signaling (RGS) 8 induced by Gα expression. Journal of Neurochemistry. 88(1). 161–168. 13 indexed citations
20.
Saitoh, Osamu, et al.. (2000). Molecular Cloning and Characterization of Xenopus RGS5. Biochemical and Biophysical Research Communications. 270(1). 34–39. 4 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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