Yong‐Hwan Moon

3.1k total citations
62 papers, 2.4k citations indexed

About

Yong‐Hwan Moon is a scholar working on Plant Science, Molecular Biology and Mechanics of Materials. According to data from OpenAlex, Yong‐Hwan Moon has authored 62 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Plant Science, 44 papers in Molecular Biology and 3 papers in Mechanics of Materials. Recurrent topics in Yong‐Hwan Moon's work include Plant Molecular Biology Research (39 papers), Plant Stress Responses and Tolerance (25 papers) and Photosynthetic Processes and Mechanisms (22 papers). Yong‐Hwan Moon is often cited by papers focused on Plant Molecular Biology Research (39 papers), Plant Stress Responses and Tolerance (25 papers) and Photosynthetic Processes and Mechanisms (22 papers). Yong‐Hwan Moon collaborates with scholars based in South Korea, United States and Mongolia. Yong‐Hwan Moon's co-authors include Z. Renee Sung, Hye‐Yeon Seok, Sun-Young Lee, Gynheung An, Dong-Hyuk Woo, Justin Goodrich, Anthony Bishopp, Daniel Schubert, Clara Stock and Hee-Yeon Park and has published in prestigious journals such as The Plant Cell, Development and PLANT PHYSIOLOGY.

In The Last Decade

Yong‐Hwan Moon

62 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yong‐Hwan Moon South Korea	28	2.1k	1.7k	113	88	46	62	2.4k
Ying‐Hsuan Sun United States	23	2.4k 1.1×	2.2k 1.2×	57 0.5×	88 1.0×	46 1.0×	35	3.2k
Sunchung Park United States	18	1.7k 0.8×	1.2k 0.7×	45 0.4×	83 0.9×	27 0.6×	46	1.9k
Kyung-Hwan Han United States	21	1.2k 0.6×	1.2k 0.7×	66 0.6×	45 0.5×	35 0.8×	33	1.6k
Mitra Mazarei United States	26	1.3k 0.6×	1.0k 0.6×	58 0.5×	49 0.6×	11 0.2×	68	1.9k
Dongsu Choi South Korea	15	1.5k 0.7×	899 0.5×	47 0.4×	112 1.3×	22 0.5×	28	1.7k
Brian G. Ayre United States	26	2.0k 0.9×	1.1k 0.6×	38 0.3×	78 0.9×	21 0.5×	51	2.3k
Nobuyuki Nishikubo Japan	17	2.2k 1.1×	1.6k 0.9×	40 0.4×	62 0.7×	86 1.9×	32	2.6k
Ramiro E. Rodríguez Argentina	21	2.4k 1.1×	1.7k 1.0×	44 0.4×	93 1.1×	14 0.3×	30	2.7k
Arun Sampathkumar Germany	26	2.1k 1.0×	1.5k 0.9×	61 0.5×	38 0.4×	122 2.7×	50	2.5k
Haodong Chen China	29	2.4k 1.1×	1.8k 1.0×	74 0.7×	291 3.3×	11 0.2×	54	2.8k

Countries citing papers authored by Yong‐Hwan Moon

Since Specialization

Citations

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

Fields of papers citing papers by Yong‐Hwan Moon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yong‐Hwan Moon. 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 Yong‐Hwan Moon. The network helps show where Yong‐Hwan Moon may publish in the future.

Co-authorship network of co-authors of Yong‐Hwan Moon

This figure shows the co-authorship network connecting the top 25 collaborators of Yong‐Hwan Moon. A scholar is included among the top collaborators of Yong‐Hwan Moon 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 Yong‐Hwan Moon. Yong‐Hwan Moon 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

Seok, Hye‐Yeon, et al.. (2025). A Novel Mechanism of the p53 Isoform Δ40p53α in Regulating Collagen III Expression in TGFβ1 ‐Induced LX ‐2 Human Hepatic Stellate Cells. The FASEB Journal. 39(8). e70541–e70541. 2 indexed citations

Seok, Hye‐Yeon, et al.. (2024). AtC3H3, an Arabidopsis Non-TZF Gene, Enhances Salt Tolerance by Increasing the Expression of Both ABA-Dependent and -Independent Stress-Responsive Genes. International Journal of Molecular Sciences. 25(20). 10943–10943. 2 indexed citations

Tran, Huyen Thi Thanh, et al.. (2022). An Efficient Hairy Root System for Validation of Plant Transformation Vector and CRISPR/Cas Construct Activities in Cucumber (Cucumis sativus L.). Frontiers in Plant Science. 12. 770062–770062. 21 indexed citations

Linh, Nguyen Vu, Sugunya Mahatheeranont, Phumon Sookwong, et al.. (2022). Influence of black rice (Oryza sativa L.) bran derived anthocyanin-extract on growth rate, immunological response, and immune-antioxidant gene expression in Nile tilapia (Oreochromis niloticus) cultivated in a biofloc system. Fish & Shellfish Immunology. 128. 604–611. 6 indexed citations

Seok, Hye‐Yeon, Dong-Hyuk Woo, Hee-Yeon Park, et al.. (2016). AtC3H17, a Non-Tandem CCCH Zinc Finger Protein, Functions as a Nuclear Transcriptional Activator and Has Pleiotropic Effects on Vegetative Development, Flowering and Seed Development in Arabidopsis. Plant and Cell Physiology. 57(3). 603–615. 37 indexed citations

Seok, Hye‐Yeon, Dong-Hyuk Woo, Nguyen Vu Linh, et al.. (2016). Arabidopsis AtNAP functions as a negative regulator via repression of AREB1 in salt stress response. Planta. 245(2). 329–341. 62 indexed citations

Seok, Hye‐Yeon, Dong-Hyuk Woo, Hương Thanh Trần, et al.. (2015). Arabidopsis Qc-SNARE gene AtSFT12 is involved in salt and osmotic stress responses and Na+ accumulation in vacuoles. Plant Cell Reports. 34(7). 1127–1138. 28 indexed citations

Lee, Sun‐Young, et al.. (2014). The Arabidopsis chloroplast protein S-RBP11 is involved in oxidative and salt stress responses. Plant Cell Reports. 33(6). 837–847. 6 indexed citations

Lee, Sun-Young, Eun Young Hwang, Hye‐Yeon Seok, et al.. (2014). Arabidopsis AtERF71/HRE2 functions as transcriptional activator via cis-acting GCC box or DRE/CRT element and is involved in root development through regulation of root cell expansion. Plant Cell Reports. 34(2). 223–231. 56 indexed citations

10.

Kim, Jae‐Min, Dong-Hyuk Woo, Sunho Kim, et al.. (2011). Arabidopsis MKKK20 is involved in osmotic stress response via regulation of MPK6 activity. Plant Cell Reports. 31(1). 217–224. 61 indexed citations

11.

Nguyen, Xuan Canh, Sun Ho Kim, Kyunghee Lee, et al.. (2011). Identification of a C2H2-type zinc finger transcription factor (ZAT10) from Arabidopsis as a substrate of MAP kinase. Plant Cell Reports. 31(4). 737–745. 62 indexed citations

12.

Park, Hee-Yeon, Hye‐Yeon Seok, Dong-Hyuk Woo, et al.. (2011). AtERF71/HRE2 transcription factor mediates osmotic stress response as well as hypoxia response in Arabidopsis. Biochemical and Biophysical Research Communications. 414(1). 135–141. 85 indexed citations

13.

Lee, Sun-Young, et al.. (2011). EMF1 Interacts with EIP1, EIP6 or EIP9 Involved in the Regulation of Flowering Time in Arabidopsis. Plant and Cell Physiology. 52(8). 1376–1388. 71 indexed citations

14.

Woo, Dong-Hyuk, Hee-Yeon Park, In Soon Kang, et al.. (2010). Arabidopsis lenc1 mutant displays reduced ABA accumulation by low AtNCED3 expression under osmotic stress. Journal of Plant Physiology. 168(2). 140–147. 12 indexed citations

15.

Park, Hee-Yeon, et al.. (2009). OsDEG10 encoding a small RNA-binding protein is involved in abiotic stress signaling. Biochemical and Biophysical Research Communications. 380(3). 597–602. 22 indexed citations

16.

Moon, Yong‐Hwan, et al.. (2003). Increased Stability of LHCII by Aggregate Formation during Dark-Induced Leaf Senescence in the Arabidopsis Mutant, ore10. Plant and Cell Physiology. 44(12). 1368–1377. 31 indexed citations

17.

Moon, Yong‐Hwan, et al.. (1999). Identification of a rice APETALA3 homologue by yeast two-hybrid screening. Plant Molecular Biology. 40(1). 167–177. 121 indexed citations

18.

Han, Oksoo, Hee Jae Lee, Young Won Yun, et al.. (1998). Generation of Resistance to the Diphenyl Ether Herbicide, Oxyfluorfen, via Expression of the Bacillus subtilis Protoporphyrinogen Oxidase Gene in Transgenic Tobacco Plants.. Bioscience Biotechnology and Biochemistry. 62(3). 558–560. 32 indexed citations

19.

Moon, Yong‐Hwan, et al.. (1996). Isolation and characterization of a homeodomain-leucine zipper gene, Gmh1, from soybean somatic embryo. Molecules and Cells. 6(3). 366–373. 8 indexed citations

20.

Moon, Yong‐Hwan, et al.. (1996). ISOLATION AND CHARACTERIZATION OF THREE HOMEO-DOMAIN-LEUCINE ZIPPER GENES,PHZ1, PPHZ2, AND PHZ4 FROM PIMPINELLA BRACHYCARPA SHOOT TIPS. Molecules and Cells. 6(6). 697–703. 2 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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