Guan-Chung Wu

1.3k total citations
42 papers, 1.0k citations indexed

About

Guan-Chung Wu is a scholar working on Genetics, Physiology and Reproductive Medicine. According to data from OpenAlex, Guan-Chung Wu has authored 42 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 27 papers in Physiology and 16 papers in Reproductive Medicine. Recurrent topics in Guan-Chung Wu's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (30 papers), Reproductive biology and impacts on aquatic species (27 papers) and Sperm and Testicular Function (16 papers). Guan-Chung Wu is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (30 papers), Reproductive biology and impacts on aquatic species (27 papers) and Sperm and Testicular Function (16 papers). Guan-Chung Wu collaborates with scholars based in Taiwan, France and Japan. Guan-Chung Wu's co-authors include Ching‐Fong Chang, Chien‐Ju Lin, Sherly Tomy, Sylvie Dufour, Yan‐Horn Lee, Wen‐Shiun Yueh, Mong‐Fong Lee, Shan-Ru Jeng, Jin‐Lien Du and Xiaofeng Zhang and has published in prestigious journals such as PLoS ONE, The Science of The Total Environment and Journal of Hazardous Materials.

In The Last Decade

Guan-Chung Wu

38 papers receiving 986 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Guan-Chung Wu Taiwan 19 770 643 270 230 96 42 1.0k
Ayaka Yano France 13 997 1.3× 621 1.0× 192 0.7× 204 0.9× 62 0.6× 19 1.2k
Sullip Kumar Majhi India 9 517 0.7× 411 0.6× 157 0.6× 106 0.5× 28 0.3× 29 681
Wen‐Shiun Yueh Taiwan 15 609 0.8× 631 1.0× 238 0.9× 64 0.3× 59 0.6× 24 799
Kagayaki Morishima Japan 21 889 1.2× 566 0.9× 117 0.4× 186 0.8× 53 0.6× 38 1.1k
Noëlle Richard‐Mercier France 12 630 0.8× 235 0.4× 241 0.9× 267 1.2× 119 1.2× 18 769
Vojtěch Kašpar Czechia 16 349 0.5× 500 0.8× 208 0.8× 79 0.3× 24 0.3× 50 735
Tomoyuki Okutsu Japan 15 780 1.0× 743 1.2× 204 0.8× 128 0.6× 11 0.1× 28 1.1k
Iranı́ Quagio-Grassiotto Brazil 19 366 0.5× 606 0.9× 235 0.9× 76 0.3× 26 0.3× 76 983
Jacky Cosson Czechia 16 272 0.4× 790 1.2× 524 1.9× 130 0.6× 49 0.5× 24 1.1k
Marina Govoroun France 17 1.1k 1.4× 863 1.3× 347 1.3× 338 1.5× 27 0.3× 24 1.4k

Countries citing papers authored by Guan-Chung Wu

Since Specialization
Citations

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

Fields of papers citing papers by Guan-Chung Wu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Guan-Chung Wu. 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 Guan-Chung Wu. The network helps show where Guan-Chung Wu may publish in the future.

Co-authorship network of co-authors of Guan-Chung Wu

This figure shows the co-authorship network connecting the top 25 collaborators of Guan-Chung Wu. A scholar is included among the top collaborators of Guan-Chung Wu 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 Guan-Chung Wu. Guan-Chung Wu 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.
Yan, Jia-Jiun, Li‐Yih Lin, Pung-Pung Hwang, et al.. (2025). Epigenetic insights into physiological resilience: Multigenerational readouts of CO2-induced seawater acidification effects on fish embryos. iScience. 28(9). 113187–113187.
2.
Wu, Guan-Chung, et al.. (2024). Environmental acidification drives inter-organ energy mobilization to enhance reproductive performance in medaka (Oryzias latipes). Journal of Hazardous Materials. 480. 136197–136197.
3.
Hu, Marian Y., Ying-Jey Guh, Guan-Chung Wu, et al.. (2023). Cellular mechanisms underlying extraordinary sulfide tolerance in a crustacean holobiont from hydrothermal vents. Proceedings of the Royal Society B Biological Sciences. 290(1990). 20221973–20221973. 10 indexed citations
4.
Chen, Chih, et al.. (2023). Transcriptomic profile of symbiotic accessory nidamental gland during female maturation in bigfin reef squid. Frontiers in Marine Science. 9. 2 indexed citations
5.
Chang, Ching‐Fong, et al.. (2023). Accelerated of Sex Reversal use 17α-methyltestosterone Induced Female, Orange-Spotted Grouper <I>Epinephelus coioides</I>. Jurnal Ilmiah Perikanan dan Kelautan. 15(2). 264–277. 1 indexed citations
6.
Wu, Guan-Chung, et al.. (2022). Temperature increases induce metabolic adjustments in the early developmental stages of bigfin reef squid (Sepioteuthis lessoniana). The Science of The Total Environment. 844. 156962–156962. 18 indexed citations
8.
Lin, Chien‐Ju, Gersende Maugars, Shan-Ru Jeng, et al.. (2020). Basal teleosts provide new insights into the evolutionary history of teleost-duplicated aromatase. General and Comparative Endocrinology. 291. 113395–113395. 18 indexed citations
9.
Lin, Chien‐Ju, Guan-Chung Wu, Sylvie Dufour, & Ching‐Fong Chang. (2019). Activation of the brain-pituitary-gonadotropic axis in the black porgy Acanthopagrus schlegelii during gonadal differentiation and testis development and effect of estradiol treatment. General and Comparative Endocrinology. 281. 17–29. 9 indexed citations
10.
Wu, Guan-Chung & Ching‐Fong Chang. (2017). Primary males guide the femaleness through the regulation of testicular Dmrt1 and ovarian Cyp19a1a in protandrous black porgy. General and Comparative Endocrinology. 261. 198–202. 21 indexed citations
11.
Jeng, Shan-Ru, et al.. (2017). Gonadal development and expression of sex-specific genes during sex differentiation in the Japanese eel. General and Comparative Endocrinology. 257. 74–85. 41 indexed citations
12.
13.
Chen, Chien‐Ming, et al.. (2014). Gene Ontology based housekeeping gene selection for RNA-seq normalization. Methods. 67(3). 354–363. 19 indexed citations
14.
Wu, Guan-Chung & Ching‐Fong Chang. (2012). Oocytes Survive in the Testis by Altering the Soma Fate from Male to Female in the Protandrous Black Porgy, Acanthopagrus schlegeli1. Biology of Reproduction. 88(1). 19–19. 17 indexed citations
15.
Wu, Guan-Chung, et al.. (2011). Testicular dmrt1 Is Involved in the Sexual Fate of the Ovotestis in the Protandrous Black Porgy1. Biology of Reproduction. 86(2). 41–41. 79 indexed citations
16.
Rao, Yousheng, et al.. (2011). Mutation Bias is the Driving Force of Codon Usage in the Gallus gallus genome. DNA Research. 18(6). 499–512. 85 indexed citations
17.
Lin, Chien‐Ju, Guan-Chung Wu, Mong‐Fong Lee, et al.. (2010). Regulation of two forms of gonadotropin-releasing hormone receptor gene expression in the protandrous black porgy fish, Acanthopagrus schlegeli. Molecular and Cellular Endocrinology. 323(2). 137–146. 29 indexed citations
18.
Wu, Guan-Chung & Ching‐Fong Chang. (2009). wnt4 Is Associated with the Development of Ovarian Tissue in the Protandrous Black Porgy, Acanthopagrus schlegeli1. Biology of Reproduction. 81(6). 1073–1082. 65 indexed citations
19.
Wu, Guan-Chung, et al.. (2005). Current Status of Genetic and Endocrine Factors in the Sex Change of Protandrous Black Porgy, Acanthopagrus schlegeli (Teleostean). Annals of the New York Academy of Sciences. 1040(1). 206–214. 26 indexed citations
20.
Wu, Guan-Chung, et al.. (2003). Differential Dmrt1 transcripts in gonads of the protandrous black porgy, <i>Acanthopagrus schlegeli</i>. Cytogenetic and Genome Research. 101(3-4). 309–313. 50 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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