Chilman Bae

2.4k total citations · 1 hit paper
27 papers, 1.8k citations indexed

About

Chilman Bae is a scholar working on Physiology, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Chilman Bae has authored 27 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Physiology, 15 papers in Molecular Biology and 8 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Chilman Bae's work include Erythrocyte Function and Pathophysiology (15 papers), Ion channel regulation and function (14 papers) and Blood properties and coagulation (7 papers). Chilman Bae is often cited by papers focused on Erythrocyte Function and Pathophysiology (15 papers), Ion channel regulation and function (14 papers) and Blood properties and coagulation (7 papers). Chilman Bae collaborates with scholars based in United States, China and Australia. Chilman Bae's co-authors include Frederick Sachs, Philip A. Gottlieb, Radhakrishnan Gnanasambandam, Lynn Ziegler, Paul R. Rohde, Vesna Nikolova-Krstevski, Boris Martinac, Charles D. Cox, Chai‐Ann Ng and Jin Mo Chung 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

Chilman Bae

26 papers receiving 1.8k citations

Hit Papers

Removal of the mechanoprotective influence of the cytoske... 2016 2026 2019 2022 2016 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chilman Bae United States 15 1.4k 1.0k 596 359 158 27 1.8k
Shaopeng Chi China 16 1.1k 0.8× 926 0.9× 488 0.8× 340 0.9× 107 0.7× 23 1.5k
Jason Wu United States 14 648 0.5× 762 0.7× 275 0.5× 270 0.8× 256 1.6× 15 1.5k
Martine Jodar France 11 621 0.4× 820 0.8× 257 0.4× 186 0.5× 279 1.8× 12 1.3k
Keiko Nonomura Japan 7 374 0.3× 434 0.4× 171 0.3× 152 0.4× 54 0.3× 11 794
Radhakrishnan Gnanasambandam United States 11 611 0.4× 493 0.5× 271 0.5× 133 0.4× 100 0.6× 15 846
Ning Huang China 21 206 0.1× 913 0.9× 97 0.2× 371 1.0× 44 0.3× 54 1.8k
Benjamin D. McNeil United States 15 801 0.6× 853 0.8× 66 0.1× 431 1.2× 280 1.8× 16 2.6k
Radek Dobrowolski United States 25 355 0.2× 1.8k 1.7× 63 0.1× 400 1.1× 38 0.2× 41 2.4k
Darren Fernandes Australia 19 432 0.3× 434 0.4× 265 0.4× 85 0.2× 19 0.1× 34 1.1k
Karl Bellvé United States 24 204 0.1× 1.1k 1.1× 36 0.1× 444 1.2× 104 0.7× 36 1.6k

Countries citing papers authored by Chilman Bae

Since Specialization
Citations

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

Fields of papers citing papers by Chilman Bae

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chilman Bae

This figure shows the co-authorship network connecting the top 25 collaborators of Chilman Bae. A scholar is included among the top collaborators of Chilman Bae 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 Chilman Bae. Chilman Bae 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.
Hascup, Erin R., et al.. (2024). Microglial Piezo1 mechanosensitive channel as a therapeutic target in Alzheimer’s disease. Frontiers in Cellular Neuroscience. 18. 1423410–1423410. 7 indexed citations
2.
Bae, Chilman, et al.. (2023). Inflammation condition sensitizes Piezo1 mechanosensitive channel in mouse cerebellum astrocyte. Frontiers in Cellular Neuroscience. 17. 1200946–1200946. 17 indexed citations
3.
Bae, Chilman, et al.. (2022). Effects of substrate stiffness on astrocyte migration: Piezo1 regulation in neuroinflammatory condition. Biophysical Journal. 121(3). 492a–492a. 1 indexed citations
4.
Liu, Xin, Chilman Bae, Bolong Liu, et al.. (2022). Development of opioid-induced hyperalgesia depends on reactive astrocytes controlled by Wnt5a signaling. Molecular Psychiatry. 28(2). 767–779. 13 indexed citations
5.
Liu, Xin, Jigong Wang, Yuqiang Shi, et al.. (2021). Neuron Type-Dependent Synaptic Activity in the Spinal Dorsal Horn of Opioid-Induced Hyperalgesia Mouse Model. Frontiers in Synaptic Neuroscience. 13. 748929–748929. 2 indexed citations
6.
Liu, Xin, Chilman Bae, Yuqiang Shi, et al.. (2019). Microglia Mediate HIV-1 gp120-Induced Synaptic Degeneration in Spinal Pain Neural Circuits. Journal of Neuroscience. 39(42). 8408–8421. 50 indexed citations
8.
Gnanasambandam, Radhakrishnan, Chilman Bae, Lynn Ziegler, Frederick Sachs, & Philip A. Gottlieb. (2018). Functional analyses of heteromeric human PIEZO1 Channels. PLoS ONE. 13(11). e0207309–e0207309. 5 indexed citations
9.
Bae, Chilman, Thomas M. Suchyna, Lynn Ziegler, Frederick Sachs, & Philip A. Gottlieb. (2016). Human PIEZO1 Ion Channel Functions as a Split Protein. PLoS ONE. 11(3). e0151289–e0151289. 10 indexed citations
10.
Cox, Charles D., Chilman Bae, Lynn Ziegler, et al.. (2016). Removal of the mechanoprotective influence of the cytoskeleton reveals PIEZO1 is gated by bilayer tension. Nature Communications. 7(1). 10366–10366. 380 indexed citations breakdown →
11.
Gnanasambandam, Radhakrishnan, Chilman Bae, Philip A. Gottlieb, & Frederick Sachs. (2015). Ionic Selectivity and Permeation Properties of Human PIEZO1 Channels. PLoS ONE. 10(5). e0125503–e0125503. 136 indexed citations
12.
Bae, Chilman, Frederick Sachs, & Philip A. Gottlieb. (2015). Protonation of the Human PIEZO1 Ion Channel Stabilizes Inactivation. Journal of Biological Chemistry. 290(8). 5167–5173. 52 indexed citations
13.
Huang, Haixia, Chilman Bae, Frederick Sachs, & Thomas M. Suchyna. (2013). Caveolae Regulation of Mechanosensitive Channel Function in Myotubes. PLoS ONE. 8(8). e72894–e72894. 33 indexed citations
14.
Gottlieb, Philip A., et al.. (2013). Piezo1 Mutations Identified in Xerocytosis alter the Inactivation Rate. Biophysical Journal. 104(2). 467a–467a. 2 indexed citations
15.
Bae, Chilman, Philip A. Gottlieb, & Frederick Sachs. (2013). Human PIEZO1: Removing Inactivation. Biophysical Journal. 105(4). 880–886. 61 indexed citations
16.
Gottlieb, Philip A., Chilman Bae, & Frederick Sachs. (2012). Gating the mechanical channel Piezo1. Channels. 6(4). 282–289. 159 indexed citations
17.
Bae, Chilman, Vladislav S. Markin, Thomas M. Suchyna, & Frederick Sachs. (2011). Modeling Ion Channels in the Gigaseal. Biophysical Journal. 101(11). 2645–2651. 11 indexed citations
18.
Bae, Chilman, et al.. (2011). Focal Adhesion Induction at the Tip of a Functionalized Nanoelectrode. Cellular and Molecular Bioengineering. 4(4). 616–626. 7 indexed citations
19.
Bae, Chilman, Frederick Sachs, & Philip A. Gottlieb. (2011). The Mechanosensitive Ion Channel Piezo1 Is Inhibited by the Peptide GsMTx4. Biochemistry. 50(29). 6295–6300. 387 indexed citations
20.
Bae, Chilman & Peter C. Butler. (2007). Finite element analysis of microelectrotension of cell membranes. Biomechanics and Modeling in Mechanobiology. 7(5). 379–386. 15 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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