Minah Suh

4.1k total citations
99 papers, 3.1k citations indexed

About

Minah Suh is a scholar working on Cellular and Molecular Neuroscience, Cognitive Neuroscience and Neurology. According to data from OpenAlex, Minah Suh has authored 99 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Cellular and Molecular Neuroscience, 31 papers in Cognitive Neuroscience and 23 papers in Neurology. Recurrent topics in Minah Suh's work include Neural dynamics and brain function (16 papers), EEG and Brain-Computer Interfaces (12 papers) and Vestibular and auditory disorders (12 papers). Minah Suh is often cited by papers focused on Neural dynamics and brain function (16 papers), EEG and Brain-Computer Interfaces (12 papers) and Vestibular and auditory disorders (12 papers). Minah Suh collaborates with scholars based in South Korea, United States and India. Minah Suh's co-authors include Jamshid Ghajar, Theodore H. Schwartz, Rachel Kolster, Bruce D. McCandliss, Mingrui Zhao, Sonya Bahar, Chaejeong Heo, Hongtao Ma, Sumit N. Niogi and Pratik Mukherjee and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Advanced Materials and Nature Communications.

In The Last Decade

Minah Suh

98 papers receiving 3.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Minah Suh South Korea 29 1.0k 654 612 587 504 99 3.1k
David C. Zhu United States 40 1.2k 1.2× 517 0.8× 422 0.7× 885 1.5× 682 1.4× 131 4.6k
Adrian W. Laxton United States 34 897 0.9× 913 1.4× 328 0.5× 310 0.5× 1.2k 2.4× 120 4.0k
Isabelle Loubinoux France 33 1.1k 1.1× 644 1.0× 732 1.2× 584 1.0× 788 1.6× 83 4.1k
In‐Uk Song South Korea 25 491 0.5× 394 0.6× 719 1.2× 538 0.9× 1.0k 2.1× 137 2.7k
Oren Sagher United States 32 585 0.6× 550 0.8× 662 1.1× 276 0.5× 1.4k 2.8× 85 4.0k
Martin Rausch Switzerland 26 634 0.6× 428 0.7× 354 0.6× 532 0.9× 234 0.5× 59 2.8k
Jonathan P. Dyke United States 39 656 0.6× 544 0.8× 329 0.5× 896 1.5× 485 1.0× 141 5.2k
Fatima Nasrallah Australia 25 478 0.5× 360 0.6× 602 1.0× 477 0.8× 312 0.6× 89 2.0k
Yen‐Yu Ian Shih United States 29 799 0.8× 767 1.2× 396 0.6× 715 1.2× 380 0.8× 115 2.6k
Takeharu Kunieda Japan 32 1.6k 1.5× 661 1.0× 267 0.4× 415 0.7× 453 0.9× 172 3.0k

Countries citing papers authored by Minah Suh

Since Specialization
Citations

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

Fields of papers citing papers by Minah Suh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Minah Suh

This figure shows the co-authorship network connecting the top 25 collaborators of Minah Suh. A scholar is included among the top collaborators of Minah Suh 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 Minah Suh. Minah Suh 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
2.
Yoon, Sujung, Woojin Won, Suji Lee, et al.. (2025). Astrocytic gamma-aminobutyric acid dysregulation as a therapeutic target for posttraumatic stress disorder. Signal Transduction and Targeted Therapy. 10(1). 240–240. 1 indexed citations
3.
Lee, Na Kyeong, S. S. Ryu, Ho‐Keun Kwon, et al.. (2025). Glioma-associated microglia potentiate neuronal hyper-excitability in the glioma environment. Neuro-Oncology. 27(12). 3058–3071. 1 indexed citations
4.
Kang, Bok‐Man, et al.. (2023). Seizure-induced neutrophil adhesion in brain capillaries leads to a decrease in postictal cerebral blood flow. iScience. 26(5). 106655–106655. 5 indexed citations
5.
Biswas, Deblina, Prasanta Dey, Jong Hwan Ko, et al.. (2022). Micro-ultrasonic Assessment of Early Stage Clot Formation and Whole Blood Coagulation Using an All-Optical Ultrasound Transducer and Adaptive Signal Processing Algorithm. ACS Sensors. 7(10). 2940–2950. 7 indexed citations
7.
Kim, Jeongmin, Eun Jung Kim, So Yeon Kim, et al.. (2021). Orthopedic surgery-induced cognitive dysfunction is mediated by CX3CL1/R1 signaling. Journal of Neuroinflammation. 18(1). 93–93. 28 indexed citations
8.
Jung, Woojin, Chaejeong Heo, Jong Uk Kim, et al.. (2021). Design and material for a patternable polysiloxane acrylate-based penetrating intracortical neural probe. Journal of Micromechanics and Microengineering. 31(3). 34002–34002. 8 indexed citations
9.
Lee, Myunghee, et al.. (2020). Excitation-Inhibition Imbalance Leads to Alteration of Neuronal Coherence and Neurovascular Coupling under Acute Stress. Journal of Neuroscience. 40(47). 9148–9162. 26 indexed citations
10.
Kang, Bok‐Man, et al.. (2020). Differential contribution of excitatory and inhibitory neurons in shaping neurovascular coupling in different epileptic neural states. Journal of Cerebral Blood Flow & Metabolism. 41(5). 1145–1161. 17 indexed citations
11.
Son, Soyoung, V. G. Deepagan, Sol Shin, et al.. (2018). Ultrasmall gold nanosatellite-bearing transformable hybrid nanoparticles for deep tumor penetration. Acta Biomaterialia. 79. 294–305. 26 indexed citations
13.
Poplawsky, Alexander John, Mitsuhiro Fukuda, Bok‐Man Kang, et al.. (2017). Dominance of layer-specific microvessel dilation in contrast-enhanced high-resolution fMRI: Comparison between hemodynamic spread and vascular architecture with CLARITY. NeuroImage. 197. 657–667. 16 indexed citations
14.
Kim, Minyoung, Hyuk-Chan Kwon, Yong‐Ho Lee, et al.. (2015). Frontoparietal EEG alpha-phase synchrony reflects differential attentional demands during word recall and oculomotor dual-tasks. Neuroreport. 26(18). 1161–1167. 6 indexed citations
15.
Lee, Eunyoung, Kyung-Hwa Jeon, Jeongeun Sim, et al.. (2014). Development of an Albumin Copper Binding (ACuB) Assay to Detect Ischemia Modified Albumin. Analytical Sciences. 30(10). 985–990. 19 indexed citations
16.
Heo, Chaejeong, et al.. (2013). Direct high-resolution label-free imaging of cellular nanostructure dynamics in living cells. Journal of Biomedical Optics. 18(6). 66016–66016. 1 indexed citations
17.
Oh, Eungseok, Chaejeong Heo, Ji Seon Kim, et al.. (2013). Hyperspectral fluorescence imaging for cellular iron mapping in thein vitromodel of Parkinson’s disease. Journal of Biomedical Optics. 19(5). 51207–51207. 14 indexed citations
18.
Kim, Mi‐Sun, et al.. (2012). Measurements of Location-Dependent Nitric Oxide Levels on Skin Surface in relation to Acupuncture Point. Evidence-based Complementary and Alternative Medicine. 2012. 1–7. 12 indexed citations
20.
Zhao, Mingrui, Hongtao Ma, Minah Suh, & Theodore H. Schwartz. (2009). Spatiotemporal Dynamics of Perfusion and Oximetry during Ictal Discharges in the Rat Neocortex. Journal of Neuroscience. 29(9). 2814–2823. 74 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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