Fong‐Fong Chu

4.9k total citations · 1 hit paper
63 papers, 3.9k citations indexed

About

Fong‐Fong Chu is a scholar working on Molecular Biology, Nutrition and Dietetics and Immunology. According to data from OpenAlex, Fong‐Fong Chu has authored 63 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 22 papers in Nutrition and Dietetics and 11 papers in Immunology. Recurrent topics in Fong‐Fong Chu's work include Selenium in Biological Systems (20 papers), Redox biology and oxidative stress (11 papers) and Trace Elements in Health (9 papers). Fong‐Fong Chu is often cited by papers focused on Selenium in Biological Systems (20 papers), Redox biology and oxidative stress (11 papers) and Trace Elements in Health (9 papers). Fong‐Fong Chu collaborates with scholars based in United States, China and United Kingdom. Fong‐Fong Chu's co-authors include R. Steven Esworthy, James H. Doroshow, Oliver Hankinson, Emily C. Hoffman, Fred Sander, Herminio Reyes, Barbara A. Brooks, Ye‐Shih Ho, Steven A. Akman and Richard Aranda and has published in prestigious journals such as Science, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Fong‐Fong Chu

63 papers receiving 3.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Cloning of a Factor Required for Activity of the Ah (Dioxin) Receptor

1991 809 citations Fong‐Fong Chu, Oliver Hankinson et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fong‐Fong Chu United States	33	1.9k	1.4k	613	541	396	63	3.9k
R. Steven Esworthy United States	35	1.7k 0.9×	1.5k 1.0×	283 0.5×	179 0.3×	292 0.7×	59	3.3k
Antonella Roveri Italy	37	2.8k 1.5×	2.6k 1.8×	410 0.7×	683 1.3×	138 0.3×	77	6.3k
Cheng Jiang United States	38	1.8k 0.9×	1.5k 1.0×	386 0.6×	540 1.0×	314 0.8×	106	4.1k
Saul R. Powell United States	33	1.7k 0.9×	1.0k 0.7×	469 0.8×	169 0.3×	255 0.6×	58	4.1k
Yasuhito Nakagawa Japan	33	2.6k 1.4×	1.2k 0.8×	223 0.4×	398 0.7×	121 0.3×	79	4.7k
Marla J. Berry United States	33	1.8k 1.0×	2.3k 1.6×	574 0.9×	186 0.3×	289 0.7×	44	4.7k
Kunitoshi Mitsumori Japan	35	2.0k 1.0×	367 0.3×	883 1.4×	1.1k 2.1×	415 1.0×	356	5.0k
Shigeru Sassa United States	49	5.7k 3.0×	568 0.4×	620 1.0×	298 0.6×	281 0.7×	215	8.2k
Paul Amstad Switzerland	33	2.5k 1.3×	426 0.3×	213 0.3×	852 1.6×	322 0.8×	55	4.6k
Kimihiko Satoh Japan	31	5.5k 2.9×	444 0.3×	351 0.6×	737 1.4×	389 1.0×	105	7.3k

Countries citing papers authored by Fong‐Fong Chu

Since Specialization

Citations

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

Fields of papers citing papers by Fong‐Fong Chu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fong‐Fong Chu. 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 Fong‐Fong Chu. The network helps show where Fong‐Fong Chu may publish in the future.

Co-authorship network of co-authors of Fong‐Fong Chu

This figure shows the co-authorship network connecting the top 25 collaborators of Fong‐Fong Chu. A scholar is included among the top collaborators of Fong‐Fong Chu 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 Fong‐Fong Chu. Fong‐Fong Chu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Esworthy, R. Steven & Fong‐Fong Chu. (2023). Using Information from Public Databases to Critically Evaluate Studies Linking the Antioxidant Enzyme Selenium-Dependent Glutathione Peroxidase 2 (GPX2) to Cancer. SHILAP Revista de lepidopterología. 3(4). 985–1014. 2 indexed citations

Esworthy, R. Steven, James H. Doroshow, & Fong‐Fong Chu. (2022). The beginning of GPX2 and 30 years later. Free Radical Biology and Medicine. 188. 419–433. 40 indexed citations

Chu, Fong‐Fong, R. Steven Esworthy, Binghui Shen, & James H. Doroshow. (2020). Role of the microbiota in ileitis of a mouse model of inflammatory bowel disease—Glutathione peroxide isoenzymes 1 and 2‐double knockout mice on a C57BL background. MicrobiologyOpen. 9(10). e1107–e1107. 6 indexed citations

Doroshow, James H., R. Steven Esworthy, & Fong‐Fong Chu. (2019). Control of doxorubicin-induced, reactive oxygen-related apoptosis by glutathione peroxidase 1 in cardiac fibroblasts. Biochemistry and Biophysics Reports. 21. 100709–100709. 18 indexed citations

Chen, Menglu, Pan Chen, Dandan Feng, et al.. (2018). 5‐Hydroxytryptamine (5‐HT)‐exacerbated DSS‐induced colitis is associated with elevated NADPH oxidase expression in the colon. Journal of Cellular Biochemistry. 120(6). 9230–9242. 21 indexed citations

Chen, Menglu, Lei Gao, Pan Chen, et al.. (2016). Serotonin-Exacerbated DSS-Induced Colitis Is Associated with Increase in MMP-3 and MMP-9 Expression in the Mouse Colon. Mediators of Inflammation. 2016. 1–10. 21 indexed citations

Zhou, Yunfeng, Hong Guo, Lei Gao, et al.. (2016). The Gastric Mucosa from Patients Infected with CagA+ or VacA+ Helicobacter pylori Has a Lower Level of Dual Oxidase-2 Expression than Uninfected or Infected with CagA−/VacA− H. pylori. Digestive Diseases and Sciences. 61(8). 2328–2337. 10 indexed citations

Chu, Fong‐Fong, R. Steven Esworthy, James H. Doroshow, et al.. (2016). Deficiency in Duox2 activity alleviates ileitis in GPx1- and GPx2-knockout mice without affecting apoptosis incidence in the crypt epithelium. Redox Biology. 11. 144–156. 34 indexed citations

Chu, Fong‐Fong, R. Steven Esworthy, James H. Doroshow, & Binghui Shen. (2016). NADPH oxidase-1 deficiency offers little protection in Salmonella typhimurium-induced typhlitis in mice. World Journal of Gastroenterology. 22(46). 10158–10158. 7 indexed citations

10.

Dittrich, Anna‐Maria, Hellmuth‐Alexander Meyer, David Quarcoo, et al.. (2009). Glutathione peroxidase-2 protects from allergen-induced airway inflammation in mice. European Respiratory Journal. 35(5). 1148–1154. 41 indexed citations

11.

Hahn, Maria A., Dong-Hyun Lee, R. Steven Esworthy, et al.. (2008). Methylation of Polycomb Target Genes in Intestinal Cancer Is Mediated by Inflammation. Cancer Research. 68(24). 10280–10289. 154 indexed citations

12.

Kriska, Tamás, Vladislav Levchenko, Fong‐Fong Chu, R. Steven Esworthy, & Albert W. Girotti. (2008). Novel enrichment of tumor cell transfectants expressing high levels of type 4 glutathione peroxidase using 7α-hydroperoxycholesterol as a selection agent. Free Radical Biology and Medicine. 45(5). 700–707. 6 indexed citations

13.

Lee, Dong-Hyun, et al.. (2006). Mutation Accumulation in the Intestine and Colon of Mice Deficient in Two Intracellular Glutathione Peroxidases. Cancer Research. 66(20). 9845–9851. 35 indexed citations

14.

Chu, Fong‐Fong, R. Steven Esworthy, Leslie Lee, & Sharon P. Wilczynski. (1999). Retinoic Acid Induces Gpx2 Gene Expression in MCF-7 Human Breast Cancer Cells. Journal of Nutrition. 129(10). 1846–1854. 45 indexed citations

15.

Esworthy, R. Steven, Kristine M. Swiderek, Ye‐Shih Ho, & Fong‐Fong Chu. (1998). Selenium-dependent glutathione peroxidase-GI is a major glutathione peroxidase activity in the mucosal epithelium of rodent intestine1Portions of this work were presented in the Selenium II minisymposia at Experimental Biology '96. Preliminary accounts of this work appear in the proceedings volumes of the Sixth International Symposium on Selenium in Biology and Medicine (ISSBM, 1996) and The Japanese Society of Chromatography (1996).1. Biochimica et Biophysica Acta (BBA) - General Subjects. 1381(2). 213–226. 91 indexed citations

16.

Chu, Fong‐Fong, R. Steven Esworthy, Kalina Boteva, et al.. (1996). Polymorphism and Chromosomal Localization of the GI-Form of Human Glutathione Peroxidase (GPX2) on 14q24.1 byin SituHybridization. Genomics. 32(2). 272–276. 27 indexed citations

17.

Esworthy, R. Steven, et al.. (1994). Cloning and sequencing of the cDNA encoding a human testis phospholipid hydroperoxide glutathione peroxidase*. Gene. 144(2). 317–318. 77 indexed citations

18.

Chu, Fong‐Fong. (1994). The human glutathione peroxidase genes GPX2, GPX3, and GPX4 map to chromosomes 14, 5, and 19, respectively. Cytogenetic and Genome Research. 66(2). 96–98. 68 indexed citations

19.

Watson, Andrea, Roy Bannister, Fong‐Fong Chu, et al.. (1992). Mechanism of Action of a Repressor of Dioxin-Dependent Induction of Cyplal Gene Transcription. Molecular and Cellular Biology. 12(5). 2115–2123. 48 indexed citations

20.

Doroshow, James H., Steven A. Akman, R. Steven Esworthy, Fong‐Fong Chu, & T. Burke. (1991). Doxorubicin Resistance Conferred by Selective Enhancement of Intracellular Glutathione Peroxidase or Superoxide Dismutase Content in Human MCF-7 Breast Cancer Cells. Free Radical Research Communications. 13(1). 779–781. 38 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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