Makoto Michikawa

7.8k total citations
155 papers, 6.2k citations indexed

About

Makoto Michikawa is a scholar working on Physiology, Molecular Biology and Cell Biology. According to data from OpenAlex, Makoto Michikawa has authored 155 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 91 papers in Physiology, 79 papers in Molecular Biology and 27 papers in Cell Biology. Recurrent topics in Makoto Michikawa's work include Alzheimer's disease research and treatments (81 papers), Cholesterol and Lipid Metabolism (20 papers) and Neuroinflammation and Neurodegeneration Mechanisms (16 papers). Makoto Michikawa is often cited by papers focused on Alzheimer's disease research and treatments (81 papers), Cholesterol and Lipid Metabolism (20 papers) and Neuroinflammation and Neurodegeneration Mechanisms (16 papers). Makoto Michikawa collaborates with scholars based in Japan, United States and Canada. Makoto Michikawa's co-authors include Katsuhiko Yanagisawa, Kun Zou, Jian-Sheng Gong, Naoya Sawamura, Qiwen Fan, Takashi Hosono, Ichiro Isobe, Mi-Hee Ko, Wenxin Yu and Kazuchika Nishitsuji and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neuroscience.

In The Last Decade

Makoto Michikawa

155 papers receiving 6.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Makoto Michikawa Japan 42 3.1k 2.9k 1.0k 865 825 155 6.2k
Ruth B. Caldwell United States 60 2.4k 0.8× 4.6k 1.6× 753 0.7× 788 0.9× 626 0.8× 218 11.5k
Hong Jiang China 43 2.0k 0.6× 2.9k 1.0× 410 0.4× 756 0.9× 506 0.6× 204 7.5k
Sylvain Chemtob Canada 59 1.6k 0.5× 4.5k 1.6× 636 0.6× 1.1k 1.3× 417 0.5× 328 11.8k
Bertrand Joseph Sweden 49 2.4k 0.7× 5.3k 1.9× 346 0.3× 649 0.8× 895 1.1× 130 8.8k
Zhao Zhong Chong United States 65 1.6k 0.5× 5.1k 1.8× 752 0.7× 886 1.0× 413 0.5× 125 9.3k
Roberto Chiesa Italy 43 1.7k 0.5× 4.3k 1.5× 762 0.7× 586 0.7× 429 0.5× 186 7.5k
Gary A. Weisman United States 57 1.8k 0.6× 3.7k 1.3× 618 0.6× 1.4k 1.6× 299 0.4× 159 9.6k
Ying Jiang United States 33 3.1k 1.0× 1.7k 0.6× 264 0.3× 777 0.9× 1.1k 1.3× 74 5.7k
Robert E. Pitas United States 51 4.2k 1.3× 4.7k 1.6× 3.2k 3.1× 1.5k 1.8× 821 1.0× 88 11.0k
Maria Ankarcrona Sweden 36 2.8k 0.9× 4.9k 1.7× 284 0.3× 2.2k 2.5× 868 1.1× 70 8.0k

Countries citing papers authored by Makoto Michikawa

Since Specialization
Citations

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

Fields of papers citing papers by Makoto Michikawa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Makoto Michikawa

This figure shows the co-authorship network connecting the top 25 collaborators of Makoto Michikawa. A scholar is included among the top collaborators of Makoto Michikawa 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 Makoto Michikawa. Makoto Michikawa 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.
Sun, Yang, et al.. (2025). Multi-functional role of apolipoprotein E in neurodegenerative diseases. Frontiers in Aging Neuroscience. 17. 1535280–1535280. 3 indexed citations
2.
Sun, Yang, Yuan Gao, Tomohisa Nakamura, et al.. (2024). Presenilin deficiency enhances tau phosphorylation and its secretion. Journal of Neurochemistry. 168(9). 2956–2973. 1 indexed citations
3.
Sun, Yang, et al.. (2024). Presenilin: A Multi-Functional Molecule in the Pathogenesis of Alzheimer’s Disease and Other Neurodegenerative Diseases. International Journal of Molecular Sciences. 25(3). 1757–1757. 14 indexed citations
4.
Jung, Cha‐Gyun, et al.. (2024). Potential Therapeutic Effects of Bifidobacterium breve MCC1274 on Alzheimer’s Disease Pathologies in AppNL-G-F Mice. Nutrients. 16(4). 538–538. 5 indexed citations
5.
Jung, Cha‐Gyun, Hitoshi Yamashita, Chunyu Zhou, et al.. (2023). Deletion of UCP1 in Tg2576 Mice Increases Body Temperature and Exacerbates Alzheimer’s Disease-Related Pathologies. International Journal of Molecular Sciences. 24(3). 2741–2741. 2 indexed citations
6.
Sheikh, Abdullah Md., et al.. (2023). Alzheimer’s Amyloid β Peptide Induces Angiogenesis in an Alzheimer’s Disease Model Mouse through Placental Growth Factor and Angiopoietin 2 Expressions. International Journal of Molecular Sciences. 24(5). 4510–4510. 13 indexed citations
7.
Zhou, Chunyu, et al.. (2022). Probiotic Bifidobacterium breve MCC1274 Mitigates Alzheimer’s Disease-Related Pathologies in Wild-Type Mice. Nutrients. 14(12). 2543–2543. 38 indexed citations
8.
Sun, Yang, Yuan Gao, Tomohisa Nakamura, et al.. (2022). Presenilin Is Essential for ApoE Secretion, a Novel Role of Presenilin Involved in Alzheimer's Disease Pathogenesis. Journal of Neuroscience. 42(8). 1574–1586. 17 indexed citations
9.
Sheikh, Abdullah Md., Shozo Yano, Harumi Osago, et al.. (2022). Analysis of the time-dependent changes of phospholipids in the brain regions of a mouse model of Alzheimer’s disease. Brain Research. 1800. 148197–148197. 7 indexed citations
11.
Ano, Yasuhisa, Misato Yoshikawa, Makoto Michikawa, et al.. (2019). Iso-α-Acids, Bitter Components in Beer, Suppress Inflammatory Responses and Attenuate Neural Hyperactivation in the Hippocampus. Frontiers in Pharmacology. 10. 81–81. 11 indexed citations
12.
Takeda, Yosuke, Hiroshi Oue, Shinsuke Okada, et al.. (2016). Molar loss and powder diet leads to memory deficit and modifies the mRNA expression of brain-derived neurotrophic factor in the hippocampus of adult mice. BMC Neuroscience. 17(1). 81–81. 26 indexed citations
13.
Hosono, Takashi, Akihiro Mouri, Kazuchika Nishitsuji, et al.. (2015). Arachidonic or Docosahexaenoic Acid Diet Prevents Memory Impairment in Tg2576 Mice. Journal of Alzheimer s Disease. 48(1). 149–162. 31 indexed citations
14.
Sheikh, Abdullah Md., Makoto Michikawa, S.U. Kim, & Atsushi Nagai. (2015). Lysophosphatidylcholine increases the neurotoxicity of Alzheimer’s amyloid β1-42 peptide: Role of oligomer formation. Neuroscience. 292. 159–169. 41 indexed citations
15.
Ito, Jin‐ichi, Yuko Nagayasu, Yutaka Miura, Shinji Yokoyama, & Makoto Michikawa. (2014). Astrocyte׳s endogenous apoE generates HDL-like lipoproteins using previously synthesized cholesterol through interaction with ABCA1. Brain Research. 1570. 1–12. 24 indexed citations
16.
Zou, Kun, Junjun Liu, Atsushi Watanabe, et al.. (2013). Aβ43 Is the Earliest-Depositing Aβ Species in APP Transgenic Mouse Brain and Is Converted to Aβ41 by Two Active Domains of ACE. American Journal Of Pathology. 182(6). 2322–2331. 40 indexed citations
17.
Ko, Mi-Hee, Kun Zou, Wenxin Yu, et al.. (2005). Cholesterol-mediated Neurite Outgrowth Is Differently Regulated between Cortical and Hippocampal Neurons. Journal of Biological Chemistry. 280(52). 42759–42765. 75 indexed citations
18.
Zou, Kun, Dae Sung Kim, Atsuko Kakio, et al.. (2003). Amyloid β‐protein (Aβ)1–40 protects neurons from damage induced by Aβ1–42 in culture and in rat brain. Journal of Neurochemistry. 87(3). 609–619. 131 indexed citations
19.
Michikawa, Makoto, Qiwen Fan, Ichiro Isobe, & Katsuhiko Yanagisawa. (2000). Apolipoprotein E Exhibits Isoform‐Specific Promotion of Lipid Efflux from Astrocytes and Neurons in Culture. Journal of Neurochemistry. 74(3). 1008–1016. 207 indexed citations
20.
Isobe, Ichiro, Katsuhiko Yanagisawa, & Makoto Michikawa. (2000). A Possible Model of Senile Plaques Using Synthetic Amyloid β-Protein and Rat Glial Culture. Experimental Neurology. 162(1). 51–60. 20 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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