Masayuki Itoh

4.9k total citations
151 papers, 3.4k citations indexed

About

Masayuki Itoh is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Masayuki Itoh has authored 151 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Molecular Biology, 51 papers in Genetics and 35 papers in Cellular and Molecular Neuroscience. Recurrent topics in Masayuki Itoh's work include Genetics and Neurodevelopmental Disorders (36 papers), Neuroscience and Neuropharmacology Research (27 papers) and Neonatal and fetal brain pathology (17 papers). Masayuki Itoh is often cited by papers focused on Genetics and Neurodevelopmental Disorders (36 papers), Neuroscience and Neuropharmacology Research (27 papers) and Neonatal and fetal brain pathology (17 papers). Masayuki Itoh collaborates with scholars based in Japan, United States and Canada. Masayuki Itoh's co-authors include Sachio Takashima, Yu‐ichi Goto, Masashi Mizuguchi, Tetsuya Fukuda, Kazuo Washiyama, Tomio Ichikawa, Yasushi Kuraishi, Yuri Ozawa, Tsugunobu Andoh and Osamu Saitoh and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Masayuki Itoh

148 papers receiving 3.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Masayuki Itoh Japan 32 1.6k 890 801 745 396 151 3.4k
Jennifer M. Kwon United States 29 1.2k 0.8× 634 0.7× 861 1.1× 718 1.0× 331 0.8× 77 3.4k
Christopher J. Phiel United States 20 2.5k 1.6× 749 0.8× 656 0.8× 741 1.0× 193 0.5× 30 3.9k
Guoyin Feng China 40 2.6k 1.6× 1.3k 1.5× 933 1.2× 404 0.5× 430 1.1× 172 5.0k
Jyoti J. Watters United States 38 1.1k 0.7× 955 1.1× 637 0.8× 600 0.8× 284 0.7× 100 5.1k
Guojun Chen China 33 1.8k 1.1× 408 0.5× 1.2k 1.5× 778 1.0× 266 0.7× 130 3.5k
Jan Mulder Sweden 35 1.6k 1.0× 285 0.3× 1.4k 1.7× 739 1.0× 406 1.0× 114 4.6k
Leo Paljärvi Finland 34 1.0k 0.6× 386 0.4× 1.2k 1.5× 840 1.1× 411 1.0× 84 4.0k
Angela M. Kaindl Germany 34 2.0k 1.3× 568 0.6× 960 1.2× 386 0.5× 188 0.5× 166 4.6k
Mehrdad Shamloo United States 41 2.7k 1.7× 543 0.6× 1.8k 2.2× 1.1k 1.4× 466 1.2× 74 5.5k
Diego J. Walther Germany 21 1.5k 1.0× 435 0.5× 1.2k 1.5× 625 0.8× 162 0.4× 30 4.9k

Countries citing papers authored by Masayuki Itoh

Since Specialization
Citations

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

Fields of papers citing papers by Masayuki Itoh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masayuki Itoh

This figure shows the co-authorship network connecting the top 25 collaborators of Masayuki Itoh. A scholar is included among the top collaborators of Masayuki Itoh 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 Masayuki Itoh. Masayuki Itoh 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.
Ninomiya, Hiromasa, Issei S. Shimada, Shinji Kawai, et al.. (2025). Aberrant activation of IL-6/JAK/STAT3/FOSL1 signaling induces renal abnormalities in a Xenopus model of Joubert syndrome-related disorders. Journal of Biological Chemistry. 301(8). 110413–110413.
2.
Suzuki, Nami, Masayuki Itoh, Maya Yamazaki, et al.. (2024). Limb-Clasping Response in NMDA Receptor Palmitoylation-Deficient Mice. Molecular Neurobiology. 61(11). 9125–9135. 2 indexed citations
3.
Wada, Takashi, et al.. (2023). Alteration of monoaminergic systems in the caudal medulla and its possible link to diurnal increase of apnea in a mouse model of Rett syndrome. Journal of Oral Science. 65(2). 96–101. 1 indexed citations
4.
Takahashi, Satoru, Ryosuke Tanaka, Shin Nabatame, et al.. (2021). Early diagnosis of MECP2 duplication syndrome: Insights from a nationwide survey in Japan. Journal of the Neurological Sciences. 422. 117321–117321. 9 indexed citations
5.
Sugiyama, Takehiro, Yoshinori Aoki, Keiji Goishi, et al.. (2021). Lectin-Like Oxidized Low-Density Lipoprotein Receptor-1–Related Microglial Activation in Neonatal Hypoxic-Ischemic Encephalopathy. American Journal Of Pathology. 191(7). 1303–1313. 6 indexed citations
6.
Itoh, Masayuki, Mariko Yamashita, Hiroyuki Okuno, et al.. (2018). Deficiency of AMPAR–Palmitoylation Aggravates Seizure Susceptibility. Journal of Neuroscience. 38(47). 10220–10235. 29 indexed citations
7.
Gage, Blair K., Ali Asadi, Robert K. Baker, et al.. (2015). The Role of ARX in Human Pancreatic Endocrine Specification. PLoS ONE. 10(12). e0144100–e0144100. 30 indexed citations
8.
Itoh, Masayuki & Makoto Takano. (2014). Identification of palmitoylation enzymes for the HCN2 channel.. The Journal of Physiological Sciences. 64. 123. 1 indexed citations
9.
Maegaki, Yoshihiro, Kei Murayama, Taro Yamazaki, et al.. (2014). Myocerebrohepatopathy spectrum disorder due to POLG mutations: A clinicopathological report. Brain and Development. 37(7). 719–724. 11 indexed citations
10.
Wang, Wenze, Sachio Takashima, Masayuki Itoh, et al.. (2011). The developmental changes of Nav1.1 and Nav1.2 expression in the human hippocampus and temporal lobe. Brain Research. 1389. 61–70. 38 indexed citations
11.
Itoh, Masayuki, Shin Okazaki, Rie Miyata, et al.. (2010). Partial loss of pancreas endocrine and exocrine cells of human ARX-null mutation: Consideration of pancreas differentiation. Differentiation. 80(2-3). 118–122. 19 indexed citations
12.
13.
Kitamura, Kunio, Masako Yanazawa, Maki Ohsawa, et al.. (2009). Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice. Human Molecular Genetics. 18(19). 3708–3724. 69 indexed citations
14.
Yamada, Takahisa, Masayuki Itoh, S. Nishimura, et al.. (2008). Association of single nucleotide polymorphisms in the endothelial differentiation sphingolipid G‐protein‐coupled receptor 1 gene with marbling in Japanese Black beef cattle. Animal Genetics. 40(2). 209–216. 31 indexed citations
15.
Munakata, Mitsutoshi, Mika Watanabe, Taisuke Otsuki, et al.. (2007). Altered Distribution of KCC2 in Cortical Dysplasia in Patients with Intractable Epilepsy. Epilepsia. 48(4). 837–844. 48 indexed citations
16.
Mizuguchi, Masashi, Hideo Yamanouchi, Laurence E. Becker, Masayuki Itoh, & Sachio Takashima. (2002). Doublecortin immunoreactivity in giant cells of tuberous sclerosis and focal cortical dysplasia. Acta Neuropathologica. 104(4). 418–424. 37 indexed citations
17.
Itoh, Masayuki, et al.. (2002). [A case of FK 506-induced leukoencephalopathy].. PubMed. 54(1). 51–5. 1 indexed citations
18.
Koyama, Hirofumi, Masayuki Itoh, Kohji Miyahara, & Eiko Tsuchiya. (2002). Abundance of the RSC nucleosome‐remodeling complex is important for the cells to tolerate DNA damage in Saccharomyces cerevisiae. FEBS Letters. 531(2). 215–221. 31 indexed citations
19.
Itoh, Masayuki. (1999). [Perinatal ischemic brain damages and apoptosis].. PubMed. 31(2). 140–5. 1 indexed citations
20.
Itoh, Masayuki, Kinji Ohno, Yutaka Tomita, & Kyosuke Takeshita. (1993). Abnormal short‐latency somatosensory evoked potentials in two patients with carbohydrate‐deficient glycoprotein syndrome. Acta Paediatrica. 82(6-7). 607–608. 5 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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