Shingo Yasuhara

2.5k total citations
56 papers, 2.0k citations indexed

About

Shingo Yasuhara is a scholar working on Molecular Biology, Epidemiology and Physiology. According to data from OpenAlex, Shingo Yasuhara has authored 56 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 19 papers in Epidemiology and 13 papers in Physiology. Recurrent topics in Shingo Yasuhara's work include Burn Injury Management and Outcomes (11 papers), Autophagy in Disease and Therapy (9 papers) and Adipose Tissue and Metabolism (8 papers). Shingo Yasuhara is often cited by papers focused on Burn Injury Management and Outcomes (11 papers), Autophagy in Disease and Therapy (9 papers) and Adipose Tissue and Metabolism (8 papers). Shingo Yasuhara collaborates with scholars based in United States, Japan and China. Shingo Yasuhara's co-authors include J. A. Jeevendra Martyn, Masao Kaneki, Hiroki Sugita, Takashi Okamoto, Charles C. Wykoff, Jeffrey A. Engelman, Michael P. Lisanti, Kenneth Song, Michiko Sugita and Ronald G. Tompkins and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Circulation.

In The Last Decade

Shingo Yasuhara

52 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shingo Yasuhara United States 21 1.0k 508 405 402 261 56 2.0k
Chien‐Te Lin United States 21 1.4k 1.4× 1.3k 2.7× 350 0.9× 342 0.9× 256 1.0× 35 2.5k
Dominique Fortin France 30 1.4k 1.4× 902 1.8× 402 1.0× 291 0.7× 748 2.9× 51 2.7k
Maurizio Ragni Italy 21 795 0.8× 841 1.7× 347 0.9× 240 0.6× 296 1.1× 44 2.0k
Nicolas J. Pillon Sweden 27 1.0k 1.0× 1.0k 2.1× 383 0.9× 247 0.6× 114 0.4× 46 2.3k
Giovanni Corsetti Italy 22 762 0.7× 667 1.3× 227 0.6× 308 0.8× 130 0.5× 69 1.7k
Christopher G. R. Perry Canada 25 1.1k 1.1× 1.2k 2.3× 236 0.6× 473 1.2× 220 0.8× 65 2.1k
Tianzheng Yu United States 20 2.0k 2.0× 800 1.6× 438 1.1× 218 0.5× 178 0.7× 39 2.8k
Miriam Hoene Germany 29 1.3k 1.2× 899 1.8× 362 0.9× 269 0.7× 108 0.4× 51 2.2k
Katsuhiko Funai United States 26 1.3k 1.2× 1.2k 2.4× 354 0.9× 366 0.9× 120 0.5× 64 2.2k
Alessandro Arduini Spain 23 1.2k 1.1× 501 1.0× 318 0.8× 398 1.0× 362 1.4× 35 2.9k

Countries citing papers authored by Shingo Yasuhara

Since Specialization
Citations

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

Fields of papers citing papers by Shingo Yasuhara

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shingo Yasuhara

This figure shows the co-authorship network connecting the top 25 collaborators of Shingo Yasuhara. A scholar is included among the top collaborators of Shingo Yasuhara 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 Shingo Yasuhara. Shingo Yasuhara 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.
Chen, Jingyuan, Yoshinori Kitagawa, Haobo Li, et al.. (2025). Activated Microglia Mediate the Motor Neuron‐, Synaptic Denervation‐ and Muscle Wasting‐Changes in Burn Injured Mice. Journal of Cachexia Sarcopenia and Muscle. 16(2). e13755–e13755.
2.
Xie, Fei, et al.. (2024). Morphine induces inflammatory responses via both TLR4 and cGAS-STING signaling pathways. Cytokine. 183. 156737–156737. 8 indexed citations
3.
Yasuda, N., A Kashiwagi, Takahiko Tamura, et al.. (2019). 77 Microtubule Network Disturbance is Likely the Target of Oxidative-Stress-Induced Mitophagy Perturbation. Journal of Burn Care & Research. 40(Supplement_1). S52–S53.
4.
Ma, Li, et al.. (2019). Burn-Induced Microglia Activation is Associated With Motor Neuron Degeneration and Muscle Wasting in Mice. Shock. 51(5). 569–579. 18 indexed citations
5.
Khan, Mohammed Abdul Sattar, William R. Kem, Shingo Yasuhara, et al.. (2017). An ALPHA7 Nicotinic Acetylcholine Receptor Agonist (GTS-21) Promotes C2C12 Myonuclear Accretion in Association with Release of Interleukin-6 (IL-6) and Improves Survival in Burned Mice. Shock. 48(2). 227–235. 13 indexed citations
6.
Yasuhara, Shingo, Takahisa Goto, William R. Kem, et al.. (2016). Prevention of Burn-Induced Inflammatory Responses and Muscle Wasting by GTS-21, a Specific Agonist for α7 Nicotinic Acetylcholine Receptors. Shock. 47(1). 61–69. 28 indexed citations
9.
Andronesi, Ovidiu C., Dionyssios Mintzopoulos, Nikolaos Psychogios, et al.. (2010). Combined off‐resonance imaging and T2 relaxation in the rotating frame for positive contrast MR imaging of infection in a murine burn model. Journal of Magnetic Resonance Imaging. 32(5). 1172–1183. 8 indexed citations
10.
Martyn, J. A. Jeevendra, Masao Kaneki, Shingo Yasuhara, David S. Warner, & Mark A. Warner. (2008). Obesity-induced Insulin Resistance and Hyperglycemia. Anesthesiology. 109(1). 137–148. 200 indexed citations
11.
Asai, Akihiro, et al.. (2007). In vivo Micro-circulation Measurement in Skeletal Muscle by Intra-vital Microscopy. Journal of Visualized Experiments. 210–210. 4 indexed citations
12.
Yasuhara, Shingo, et al.. (2007). Mitochondria, endoplasmic reticulum, and alternative pathways of cell death in critical illness. Critical Care Medicine. 35(Suppl). S488–S495. 34 indexed citations
14.
Sugita, Hiroki, Masao Kaneki, Michiko Sugita, et al.. (2004). Burn injury impairs insulin-stimulated Akt/PKB activation in skeletal muscle. American Journal of Physiology-Endocrinology and Metabolism. 288(3). E585–E591. 81 indexed citations
15.
Fink, Heidrun, Shingo Yasuhara, Manfred Blobner, & J. A. Jeevendra Martyn. (2004). Up-regulation of acetylcholine receptors during subchronic infusion of pancuronium is caused by a posttranscriptional mechanism related to disuse. Critical Care Medicine. 32(2). 509–513. 2 indexed citations
16.
Yasuhara, Shingo, Ying Zhu, Takashi Matsui, et al.. (2003). Comparison of Comet Assay, Electron Microscopy, and Flow Cytometry for Detection of Apoptosis. Journal of Histochemistry & Cytochemistry. 51(7). 873–885. 132 indexed citations
17.
Sugita, Michiko, et al.. (2002). A Critical Role for Inducible Nitric Oxide Synthase in Burn Injury-Induced Insulin Resistance. Journal of Burn Care & Rehabilitation. 23(suppl_2). S76–S76. 1 indexed citations
18.
Yasuhara, Shingo, et al.. (1999). THE 1999 MOYER AWARD Burn Injury Induces Skeletal Muscle Apoptosis and the Activation of Caspase Pathways in Rats. Journal of Burn Care & Rehabilitation. 20(6). 462–470. 41 indexed citations
19.
Ikezu, Tsuneya, Shingo Yasuhara, James G. Granneman, et al.. (1999). A unique mechanism of desensitization to lipolysis mediated by β3-adrenoceptor in rats with thermal injury. American Journal of Physiology-Endocrinology and Metabolism. 277(2). E316–E324. 7 indexed citations
20.
Yamaguchi, Hiroki, Miyako Takaki, Hiromi Matsubara, Shingo Yasuhara, & Hiroyuki Suga. (1996). Constancy and variability of contractile efficiency as a function of calcium and cross-bridge kinetics: simulation. American Journal of Physiology-Heart and Circulatory Physiology. 270(4). H1501–H1508. 7 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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