Masumi Ichikawa

3.7k total citations
120 papers, 3.1k citations indexed

About

Masumi Ichikawa is a scholar working on Cellular and Molecular Neuroscience, Sensory Systems and Nutrition and Dietetics. According to data from OpenAlex, Masumi Ichikawa has authored 120 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Cellular and Molecular Neuroscience, 65 papers in Sensory Systems and 36 papers in Nutrition and Dietetics. Recurrent topics in Masumi Ichikawa's work include Olfactory and Sensory Function Studies (65 papers), Biochemical Analysis and Sensing Techniques (36 papers) and Neurobiology and Insect Physiology Research (35 papers). Masumi Ichikawa is often cited by papers focused on Olfactory and Sensory Function Studies (65 papers), Biochemical Analysis and Sensing Techniques (36 papers) and Neurobiology and Insect Physiology Research (35 papers). Masumi Ichikawa collaborates with scholars based in Japan, United States and France. Masumi Ichikawa's co-authors include Masato Matsuoka, Yoichiro Kuroda, Yuji Mori, Kazuyo Muramoto, Yoshitaka Oka, Toshiya Osada, Kazuo Ueda, Masaki Nakane, Takeo Deguchi and Kazuo Kobayashi 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

Masumi Ichikawa

117 papers receiving 3.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Masumi Ichikawa Japan 31 1.5k 959 797 622 389 120 3.1k
Jean‐Didier Vincent France 42 2.3k 1.6× 869 0.9× 1.8k 2.3× 429 0.7× 342 0.9× 111 5.2k
Brian Key Australia 42 2.7k 1.8× 1.6k 1.7× 1.4k 1.8× 1.1k 1.7× 70 0.2× 172 5.1k
Lisa Stowers United States 25 1.6k 1.1× 1.7k 1.7× 1.5k 1.8× 1.0k 1.6× 126 0.3× 33 4.5k
Peter C. Brunjes United States 33 1.7k 1.2× 2.2k 2.2× 554 0.7× 1.0k 1.7× 64 0.2× 92 3.8k
Christopher S. von Bartheld United States 42 2.4k 1.6× 1.2k 1.2× 1.8k 2.2× 362 0.6× 108 0.3× 126 6.0k
Yojiro Yanagawa Japan 27 943 0.6× 214 0.2× 930 1.2× 146 0.2× 351 0.9× 122 2.7k
Pablo Chamero Germany 22 956 0.6× 976 1.0× 704 0.9× 532 0.9× 60 0.2× 36 2.0k
Marc Spehr Germany 31 1.8k 1.2× 2.1k 2.2× 635 0.8× 1.4k 2.3× 322 0.8× 83 3.6k
K. H. Andres Germany 33 1.7k 1.2× 625 0.7× 946 1.2× 350 0.6× 42 0.1× 71 4.0k
Trese Leinders‐Zufall Germany 41 3.7k 2.5× 4.1k 4.2× 1.1k 1.4× 2.7k 4.3× 176 0.5× 88 6.0k

Countries citing papers authored by Masumi Ichikawa

Since Specialization
Citations

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

Fields of papers citing papers by Masumi Ichikawa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masumi Ichikawa

This figure shows the co-authorship network connecting the top 25 collaborators of Masumi Ichikawa. A scholar is included among the top collaborators of Masumi Ichikawa 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 Masumi Ichikawa. Masumi Ichikawa 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.
Sugiura, Hiroko, Shin Yasuda, Shutaro Katsurabayashi, et al.. (2015). Rheb activation disrupts spine synapse formation through accumulation of syntenin in tuberous sclerosis complex. Nature Communications. 6(1). 6842–6842. 28 indexed citations
2.
Ichikawa, Masumi, et al.. (2012). Illusory motion and motion capture in terms of oblique components. Perception. 41. 92–92. 1 indexed citations
3.
Murata, Koshi, Yoshihiro Wakabayashi, Hiromi Ohara, et al.. (2009). Modulation of Gonadotrophin‐Releasing Hormone Pulse Generator Activity by the Pheromone in Small Ruminants. Journal of Neuroendocrinology. 21(4). 346–350. 15 indexed citations
4.
Yokosuka, Makoto, Akiko Hagiwara, Tôru Saitô, et al.. (2009). Morphological and Histochemical Study of the Nasal Cavity and Fused Olfactory Bulb of the Brown-Eared Bulbul,Hysipetes amaurotis. ZOOLOGICAL SCIENCE. 26(10). 713–721. 10 indexed citations
5.
Wakabayashi, Yoshihiro & Masumi Ichikawa. (2008). Localization of G Protein Alpha Subunits and Morphology of Receptor Neurons in Olfactory and Vomeronasal Epithelia in Reeve's Turtle, Geoclemys reevesii. ZOOLOGICAL SCIENCE. 25(2). 178–187. 24 indexed citations
6.
Yokosuka, Makoto, et al.. (2008). p‐Chloroamphetamine‐induced rat ejaculation is not associated with the preoptic nucleus or medial nucleus amygdala. Reproductive Medicine and Biology. 7(1). 37–43. 3 indexed citations
7.
Makino, Nobuko, Shigeo Ookawara, Kazuo Katoh, et al.. (2008). The Morphological Change of Supporting Cells in the Olfactory Epithelium after Bulbectomy. Chemical Senses. 34(2). 171–179. 9 indexed citations
8.
Muramoto, Kazuyo, et al.. (2006). Modification of Synapse Formation of Accessory Olfactory Bulb Neurons by Coculture with Vomeronasal Neurons. Chemical Senses. 31(4). 371–378. 3 indexed citations
9.
Hayashi, Hiroshi, Naoki Kunugita, Keiichi Arashidani, Hidekazu Fujimaki, & Masumi Ichikawa. (2004). Long-term exposure to low levels of formaldehyde increases the number of tyrosine hydroxylase-immunopositive periglomerular cells in mouse main olfactory bulb. Brain Research. 1007(1-2). 192–197. 13 indexed citations
10.
Hagino‐Yamagishi, Kimiko, Hideo Kubo, Yoshihiro Wakabayashi, et al.. (2004). Expression of vomeronasal receptor genes in Xenopus laevis. The Journal of Comparative Neurology. 472(2). 246–256. 58 indexed citations
11.
Yasui, Kohichiroh, Takaji Wakita, Kyoko Tsukiyama–Kohara, et al.. (1998). The Native Form and Maturation Process of Hepatitis C Virus Core Protein. Journal of Virology. 72(7). 6048–6055. 203 indexed citations
12.
Yokoyama, Kiyoko, et al.. (1998). Evaluation Method of the Autonomic Function of Elderies in Response to the Postural Change. IEEJ Transactions on Fundamentals and Materials. 118(3). 227–232. 1 indexed citations
13.
Ichikawa, Masumi & Toshiya Osada. (1995). Morphology of vomeronasal organ cultures from fetal rat. Anatomy and Embryology. 191(1). 25–32. 8 indexed citations
14.
Ichikawa, Masumi, et al.. (1993). Formation and maturation of synapses in primary cultures of rat cerebral cortical cells: an electron microscopic study. Neuroscience Research. 16(2). 95–103. 123 indexed citations
15.
Ichikawa, Masumi, Toshiya Osada, & Atsushi Ikai. (1992). Bandeiraea simplicifolia lectin I and Vicia villosa agglutinin bind specifically to the vomeronasal axons in the accessory olfactory bulb of the rat. Neuroscience Research. 13(1). 73–79. 37 indexed citations
18.
Nakane, Masaki, Masumi Ichikawa, & Takeo Deguchi. (1983). Light and electron microscopic demonstration of guanylate cyclase in rat brain. Brain Research. 273(1). 9–15. 139 indexed citations
19.
Matsuo, Akifumi, et al.. (1981). Mechanical energy output and joint movements in sprint running. Ergonomics. 24(10). 765–772. 15 indexed citations
20.
Ichikawa, Masumi & Kazuo Ueda. (1977). Fine structure of the olfactory epithelium in the goldfish, Carassius auratus. Cell and Tissue Research. 183(4). 445–55. 86 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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