Ji Ho Suh

729 total citations
27 papers, 542 citations indexed

About

Ji Ho Suh is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Ji Ho Suh has authored 27 papers receiving a total of 542 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Genetics and 6 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Ji Ho Suh's work include Estrogen and related hormone effects (8 papers), Hormonal and reproductive studies (4 papers) and Prostate Cancer Treatment and Research (4 papers). Ji Ho Suh is often cited by papers focused on Estrogen and related hormone effects (8 papers), Hormonal and reproductive studies (4 papers) and Prostate Cancer Treatment and Research (4 papers). Ji Ho Suh collaborates with scholars based in United States, South Korea and Sweden. Ji Ho Suh's co-authors include Paul Webb, Keesook Lee, Douglas H. Sieglaff, Eun‐Yeung Gong, Aleksandra Čvoro, Gudrun Toresson, X. Lou, Cindy Benod, Jan-Åke Gustafsson and Aijun Zhang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Ji Ho Suh

26 papers receiving 535 citations

Peers

Ji Ho Suh
Ji Ho Suh
Citations per year, relative to Ji Ho Suh Ji Ho Suh (= 1×) peers Daniela Fliegner

Countries citing papers authored by Ji Ho Suh

Since Specialization
Citations

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

Fields of papers citing papers by Ji Ho Suh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ji Ho Suh

This figure shows the co-authorship network connecting the top 25 collaborators of Ji Ho Suh. A scholar is included among the top collaborators of Ji Ho 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 Ji Ho Suh. Ji Ho 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
1.
Suh, Ji Ho, Xiangjun Tian, Meng Luo, et al.. (2024). Probiotic Limosilactobacillus reuteri DSM 17938 Changes Foxp3 Deficiency-Induced Dyslipidemia and Chronic Hepatitis in Mice. Nutrients. 16(4). 511–511. 2 indexed citations
2.
Lee, Sung Ho, Ji Ho Suh, Mi Jeong Heo, et al.. (2024). The Hepatokine Orosomucoid 2 Mediates Beneficial Metabolic Effects of Bile Acids. Diabetes. 73(5). 701–712. 5 indexed citations
3.
Gustafsson, Jan-Ακε, Li X, Ji Ho Suh, & X. Lou. (2023). A structural perspective of liver X receptors. Vitamins and hormones. 123. 231–247. 1 indexed citations
4.
Heo, Mi Jeong, Ji Ho Suh, Kyle L. Poulsen, Cynthia Ju, & Kang Ho Kim. (2023). Updates on the Immune Cell Basis of Hepatic Ischemia-Reperfusion Injury. Molecules and Cells. 46(9). 527–534. 9 indexed citations
5.
Heo, Mi Jeong, Ji Ho Suh, Sung Ho Lee, et al.. (2023). Aryl hydrocarbon receptor maintains hepatic mitochondrial homeostasis in mice. Molecular Metabolism. 72. 101717–101717. 15 indexed citations
6.
Patterson, Grace, E. Yaneth Osorio, Alex G. Peniche, et al.. (2022). Pathologic Inflammation in Malnutrition Is Driven by Proinflammatory Intestinal Microbiota, Large Intestine Barrier Dysfunction, and Translocation of Bacterial Lipopolysaccharide. Frontiers in Immunology. 13. 846155–846155. 34 indexed citations
7.
Suh, Ji Ho, Kang Ho Kim, Margaret E. Conner, David D. Moore, & Geoffrey A. Preidis. (2022). Hepatic PPARα Is Destabilized by SIRT1 Deacetylase in Undernourished Male Mice. Frontiers in Nutrition. 9. 831879–831879. 11 indexed citations
8.
Preidis, Geoffrey A., Krishnakant G. Soni, Ji Ho Suh, et al.. (2020). Coagulopathy in Malnourished Mice Is Sexually Dimorphic and Regulated by Nutrient‐Sensing Nuclear Receptors. Hepatology Communications. 4(12). 1835–1850. 3 indexed citations
9.
Nam, Deok Hwa, EunAh Kim, Ashley Benham, et al.. (2018). Transient activation of AMPK preceding left ventricular pressure overload reduces adverse remodeling and preserves left ventricular function. The FASEB Journal. 33(1). 711–721. 9 indexed citations
10.
Suh, Ji Ho, Li Lai, Jong Kim, et al.. (2017). Steroid receptor coactivator-2 (SRC-2) coordinates cardiomyocyte paracrine signaling to promote pressure overload–induced angiogenesis. Journal of Biological Chemistry. 292(52). 21643–21652. 7 indexed citations
11.
Kinarivala, Nihar, et al.. (2016). Pharmacophore elucidation of phosphoiodyn A – Potent and selective peroxisome proliferator-activated receptor β/δ agonists with neuroprotective activity. Bioorganic & Medicinal Chemistry Letters. 26(8). 1889–1893. 14 indexed citations
12.
Suh, Ji Ho, et al.. (2015). Similarities and Distinctions in Actions of Surface-Directed and Classic Androgen Receptor Antagonists. PLoS ONE. 10(9). e0137103–e0137103. 7 indexed citations
13.
Suh, Ji Ho, Jeffrey C. Sivils, Prasenjit Dey, et al.. (2015). The FKBP52 Cochaperone Acts in Synergy with β-Catenin to Potentiate Androgen Receptor Signaling. PLoS ONE. 10(7). e0134015–e0134015. 12 indexed citations
14.
Suh, Ji Ho, et al.. (2014). Phosphorylation of glucocorticoid receptor tau1c transactivation domain enhances binding to CREB binding protein (CBP) TAZ2. Biochemical and Biophysical Research Communications. 457(1). 119–123. 8 indexed citations
15.
Zhang, Aijun, Douglas H. Sieglaff, J. Philippe York, et al.. (2014). Thyroid hormone receptor regulates most genes independently of fibroblast growth factor 21 in liver. Journal of Endocrinology. 224(3). 289–301. 24 indexed citations
16.
Lou, X., Gudrun Toresson, Cindy Benod, et al.. (2014). Structure of the retinoid X receptor α–liver X receptor β (RXRα–LXRβ) heterodimer on DNA. Nature Structural & Molecular Biology. 21(3). 277–281. 83 indexed citations
17.
Suh, Ji Ho, Douglas H. Sieglaff, Aijun Zhang, et al.. (2013). SIRT1 is a Direct Coactivator of Thyroid Hormone Receptor β1 with Gene-Specific Actions. PLoS ONE. 8(7). e70097–e70097. 62 indexed citations
18.
Suh, Ji Ho, Eun‐Yeung Gong, Cheol Yi Hong, et al.. (2008). Reduced testicular steroidogenesis in tumor necrosis factor-α knockout mice. The Journal of Steroid Biochemistry and Molecular Biology. 112(1-3). 117–121. 23 indexed citations
19.
Suh, Ji Ho, Jiansheng Huang, Yun‐Yong Park, et al.. (2006). Orphan Nuclear Receptor Small Heterodimer Partner Inhibits Transforming Growth Factor-β Signaling by Repressing SMAD3 Transactivation. Journal of Biological Chemistry. 281(51). 39169–39178. 29 indexed citations
20.
Hong, Cheol Yi, Eun‐Yeung Gong, Kabsun Kim, et al.. (2005). Modulation of the Expression and Transactivation of Androgen Receptor by the Basic Helix-Loop-Helix Transcription Factor Pod-1 through Recruitment of Histone Deacetylase 1. Molecular Endocrinology. 19(9). 2245–2257. 37 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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