Yung‐Hsiao Chiang

4.5k total citations
158 papers, 3.5k citations indexed

About

Yung‐Hsiao Chiang is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Yung‐Hsiao Chiang has authored 158 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Neurology, 35 papers in Cellular and Molecular Neuroscience and 34 papers in Molecular Biology. Recurrent topics in Yung‐Hsiao Chiang's work include Traumatic Brain Injury and Neurovascular Disturbances (32 papers), Traumatic Brain Injury Research (25 papers) and Spine and Intervertebral Disc Pathology (17 papers). Yung‐Hsiao Chiang is often cited by papers focused on Traumatic Brain Injury and Neurovascular Disturbances (32 papers), Traumatic Brain Injury Research (25 papers) and Spine and Intervertebral Disc Pathology (17 papers). Yung‐Hsiao Chiang collaborates with scholars based in Taiwan, United States and Sweden. Yung‐Hsiao Chiang's co-authors include Barry J. Hoffer, Marisela Morales, Kai‐Yun Chen, Nigel H. Greig, Jia‐Yi Wang, Shinn‐Zong Lin, Yuan-Hao Chen, Hsin-I Ma, Shin‐Han Tsai and Wen‐Ta Chiu and has published in prestigious journals such as JAMA, Journal of Neuroscience and SHILAP Revista de lepidopterología.

In The Last Decade

Yung‐Hsiao Chiang

150 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
Yung‐Hsiao Chiang Taiwan 34 1.0k 841 767 584 557 158 3.5k
Jianhua Qiu United States 33 1.5k 1.5× 878 1.0× 540 0.7× 778 1.3× 875 1.6× 70 4.0k
Paco S. Herson United States 40 1.5k 1.5× 457 0.5× 939 1.2× 1.0k 1.7× 604 1.1× 132 4.6k
Ronen R. Leker Israel 35 1.4k 1.3× 1.4k 1.7× 643 0.8× 561 1.0× 1.3k 2.2× 181 4.7k
Kristin Engelhard Germany 34 982 1.0× 1.9k 2.3× 522 0.7× 515 0.9× 841 1.5× 113 4.5k
Ruxiang Xu China 32 970 1.0× 319 0.4× 706 0.9× 353 0.6× 373 0.7× 125 2.8k
Yuji Kaneko United States 36 1.3k 1.2× 892 1.1× 533 0.7× 952 1.6× 596 1.1× 90 3.6k
Naoki Tajiri United States 37 1.5k 1.5× 1.2k 1.5× 869 1.1× 1.1k 1.9× 648 1.2× 102 4.3k
Toshiho Ohtsuki Japan 35 1.2k 1.2× 472 0.6× 943 1.2× 1.2k 2.1× 630 1.1× 91 4.1k
Kenji Dohi Japan 29 940 0.9× 439 0.5× 937 1.2× 483 0.8× 260 0.5× 151 3.0k
Stuart W. Hoffman United States 30 1.2k 1.2× 1.6k 1.9× 660 0.9× 579 1.0× 883 1.6× 44 3.9k

Countries citing papers authored by Yung‐Hsiao Chiang

Since Specialization
Citations

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

Fields of papers citing papers by Yung‐Hsiao Chiang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yung‐Hsiao Chiang. 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 Yung‐Hsiao Chiang. The network helps show where Yung‐Hsiao Chiang may publish in the future.

Co-authorship network of co-authors of Yung‐Hsiao Chiang

This figure shows the co-authorship network connecting the top 25 collaborators of Yung‐Hsiao Chiang. A scholar is included among the top collaborators of Yung‐Hsiao Chiang 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 Yung‐Hsiao Chiang. Yung‐Hsiao Chiang 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, Kai‐Yun, Shih‐Chang Hsueh, David Tweedie, et al.. (2025). 3-Monothiopomalidomide, a new immunomodulatory imide drug (IMiD), blunts inflammation and mitigates ischemic stroke in the rat. GeroScience. 47(4). 5763–5783. 1 indexed citations
2.
Liu, Ziyu, Qian Xiao, Hitoshi Shirakawa, et al.. (2024). Effects of fish oil on insulin resistance in the brains of rats with alcoholic liver damage. Journal of Functional Foods. 120. 106369–106369. 1 indexed citations
3.
Tsai, Yih‐Jeng, Thierry Burnouf, Yun Wang, et al.. (2024). CCL5 is essential for axonogenesis and neuronal restoration after brain injury. Journal of Biomedical Science. 31(1). 91–91. 10 indexed citations
4.
Yang, Yishan, Huy Tran, Phạm Anh Tuấn, et al.. (2024). Age- and gender-dependent impact of titanium vertebral augmentation implants combined with cementing on subsequent vertebral fracture incidence: A comparative study with cementing alone. European Spine Journal. 33(12). 4513–4520. 2 indexed citations
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Hsieh, Yi‐Chen, et al.. (2022). Timing of symptomatic subsequent vertebral compression fracture associated with different demographic factors. European Spine Journal. 31(9). 2439–2447. 2 indexed citations
8.
Lo, Yu‐Chun, You‐Yin Chen, Yun Wang, et al.. (2021). CCL5 promotion of bioenergy metabolism is crucial for hippocampal synapse complex and memory formation. Molecular Psychiatry. 26(11). 6451–6468. 27 indexed citations
9.
Yen, Chia‐Hung, Tsung-Hsun Hsieh, Tzu‐Jen Kao, et al.. (2021). CCL5 via GPX1 activation protects hippocampal memory function after mild traumatic brain injury. Redox Biology. 46. 102067–102067. 36 indexed citations
10.
Chang, Wei‐Chiao, Wei‐Chiao Chang, Yung‐Hsiao Chiang, et al.. (2019). Increased short- and long-term risk of sleep disorders in people with traumatic brain injury. Neuropsychological Rehabilitation. 31(2). 211–230. 5 indexed citations
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Lai, Jing-Huei, Tobias E. Karlsson, John Wu, et al.. (2018). Role of Nogo Receptor-1 for Recovery of Balance, Cognition, and Emotion after Mild Traumatic Brain Injury in Mice. Journal of Neurotrauma. 36(7). 1054–1059. 10 indexed citations
14.
Lin, Ching‐Yu, Shun‐Tai Yang, Shing‐Chuan Shen, et al.. (2018). Serum amyloid A1 in combination with integrin αVβ3 increases glioblastoma cells mobility and progression. Molecular Oncology. 12(5). 756–771. 27 indexed citations
15.
Hoffer, Barry J., Chaim G. Pick, Michael E. Hoffer, et al.. (2017). Repositioning drugs for traumatic brain injury - N-acetyl cysteine and Phenserine. Journal of Biomedical Science. 24(1). 71–71. 25 indexed citations
16.
Ma, Hon‐Ping, et al.. (2015). Sleep Duration and Sleep Quality following Acute Mild Traumatic Brain Injury: A Propensity Score Analysis. Behavioural Neurology. 2015. 1–7. 10 indexed citations
17.
Greig, Nigel H., David Tweedie, Lital Rachmany, et al.. (2014). Incretin mimetics as pharmacological tools to elucidate and as a new drug strategy to treat traumatic brain injury. PMC. 25 indexed citations
18.
Chen, Yuan-Hao, et al.. (2013). Postnatal Systemic Inflammation Exacerbates Impairment of Hippocampal Synaptic Plasticity in an Animal Seizure Model. NeuroImmunoModulation. 20(4). 223–232. 24 indexed citations
19.
Wu, John, et al.. (2012). Location and Level of Etk Expression in Neurons Are Associated with Varied Severity of Traumatic Brain Injury. PLoS ONE. 7(6). e39226–e39226. 6 indexed citations
20.
Chiang, Yung‐Hsiao, Hui‐Wen Lin, Shih‐Yi Huang, et al.. (2011). Early Enteral Nutrition and Clinical Outcomes of Severe Traumatic Brain Injury Patients in Acute Stage: A Multi-Center Cohort Study. Journal of Neurotrauma. 29(1). 75–80. 47 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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