Deshou Wang

7.6k total citations · 1 hit paper
177 papers, 5.7k citations indexed

About

Deshou Wang is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Deshou Wang has authored 177 papers receiving a total of 5.7k indexed citations (citations by other indexed papers that have themselves been cited), including 132 papers in Genetics, 65 papers in Molecular Biology and 63 papers in Physiology. Recurrent topics in Deshou Wang's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (110 papers), Reproductive biology and impacts on aquatic species (63 papers) and Animal Genetics and Reproduction (60 papers). Deshou Wang is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (110 papers), Reproductive biology and impacts on aquatic species (63 papers) and Animal Genetics and Reproduction (60 papers). Deshou Wang collaborates with scholars based in China, Japan and United States. Deshou Wang's co-authors include Minghui Li, Linyan Zhou, Lina Sun, Yoshitaka Nagahama, Wenjing Tao, Hongjuan Shi, Dongneng Jiang, Tohru Kobayashi, Fumie Sakai and Thomas D. Kocher and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Development.

In The Last Decade

Deshou Wang

168 papers receiving 5.6k citations

Hit Papers

A Tandem Duplicate of Anti-Müllerian Hormone with a Misse... 2015 2026 2018 2022 2015 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
Deshou Wang China 40 4.3k 2.7k 1.7k 988 983 177 5.7k
Yann Guiguen France 46 5.0k 1.2× 3.7k 1.4× 1.6k 1.0× 1.3k 1.3× 958 1.0× 116 6.8k
Julien Bobe France 35 1.9k 0.5× 3.0k 1.1× 1.0k 0.6× 2.2k 2.3× 675 0.7× 116 5.2k
Jean‐François Baroiller France 38 2.8k 0.7× 2.4k 0.9× 610 0.4× 1.7k 1.7× 466 0.5× 87 4.5k
Ching‐Fong Chang Taiwan 38 2.4k 0.6× 2.5k 0.9× 477 0.3× 1.3k 1.3× 841 0.9× 153 4.3k
Yasutoshi Yoshiura Japan 38 1.5k 0.3× 1.4k 0.5× 724 0.4× 833 0.8× 747 0.8× 98 3.8k
David J. Penman United Kingdom 40 3.3k 0.8× 1.7k 0.6× 853 0.5× 1.7k 1.7× 206 0.2× 117 4.6k
Linyan Zhou China 25 1.9k 0.4× 1.2k 0.5× 747 0.4× 313 0.3× 503 0.5× 59 2.4k
Jean‐Jacques Lareyre France 25 2.0k 0.5× 2.2k 0.8× 515 0.3× 792 0.8× 1.3k 1.3× 51 3.4k
Igor Babiak Norway 33 930 0.2× 1.6k 0.6× 461 0.3× 1.1k 1.1× 582 0.6× 99 2.7k
Andrzej Ciereszko Poland 40 1.9k 0.4× 3.9k 1.4× 383 0.2× 2.1k 2.1× 3.0k 3.1× 266 5.9k

Countries citing papers authored by Deshou Wang

Since Specialization
Citations

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

Fields of papers citing papers by Deshou Wang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Deshou Wang

This figure shows the co-authorship network connecting the top 25 collaborators of Deshou Wang. A scholar is included among the top collaborators of Deshou Wang 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 Deshou Wang. Deshou Wang 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.
Zhang, Liang, et al.. (2025). Highly efficient disruption of tyrb gene using CRISPR/Cas9 in grass carp (Ctenopharyngodon idella). SHILAP Revista de lepidopterología. 5(1). 38–44. 1 indexed citations
2.
Bayır, Abdulkadir, et al.. (2025). CRISPR-Based Genetic Improvement of Aquaculture Species. Fishes. 10(2). 84–84. 4 indexed citations
3.
Zhang, Bo, Deshou Wang, Dongneng Jiang, et al.. (2025). Metabolism, Function, Molecular Mechanism, and Application of Carotenoids in Coloration of Aquatic Animals. Reviews in Aquaculture. 17(2). 4 indexed citations
4.
Zhang, Tingting, Liping Zhang, Zhixiong He, et al.. (2025). A novel modified peptide derived from tilapia piscidin 4 with improved cytotoxicity, stability and antibacterial activity against fish pathogens and its underlying antibacterial mechanism. Fish & Shellfish Immunology. 162. 110309–110309. 2 indexed citations
5.
Wen, Zilong, et al.. (2025). Carotenoids, instead of pteridines, determine color of xanthophores and erythrophores in tilapia. Journal of Heredity. 116(4). 466–478.
6.
Liu, Xingyong, Zhou Li, Wenbo Li, et al.. (2024). Production of fertile YY pseudofemales in Nile tilapia with LG23 as the sex chromosome. Aquaculture. 587. 740870–740870. 1 indexed citations
8.
Su, Yun, Maolin Ye, Lu Li, et al.. (2024). Star1 gene mutation reveals the essentiality of 11-ketotestosterone and glucocorticoids for male fertility in Nile Tilapia (Oreochromis niloticus). Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology. 273. 110985–110985. 4 indexed citations
9.
10.
Xiao, Hesheng, et al.. (2024). Maternal dnd1 is essential for migration and maintenance of PGCs in Nile tilapia at larval stage. Aquaculture Reports. 38. 102319–102319. 2 indexed citations
11.
Sun, Lina, Tian Gao, Zhiqiang Li, et al.. (2024). Creation of body color mutants by CRISPR/Cas9 gene editing in largemouth bass, Micropterus salmoides. Aquaculture Reports. 40. 102593–102593.
12.
13.
Kocher, Thomas D., et al.. (2023). Knockout of Hermansky-Pudlak syndrome 5 (hps5) leads to red tilapia with reduced melanophores and iridophores. Aquaculture. 582. 740496–740496. 4 indexed citations
14.
Tao, Wenjing, Haowen Yang, Limin Wu, et al.. (2023). Characterization of the male-specific region containing the candidate sex-determining gene in Amur catfish (Silurus asotus) using third-generation- and pool-sequencing data. International Journal of Biological Macromolecules. 248. 125908–125908. 9 indexed citations
15.
Xu, Chunmei, Qingqing Zhang, Kang Du, et al.. (2022). Genome-Wide Identification and Characterization of the BRD Family in Nile Tilapia (Oreochromis niloticus). Animals. 12(17). 2266–2266. 3 indexed citations
16.
Liu, Xingyong, Xueyan Wei, Xin Zhou, et al.. (2021). Roles of anti-Müllerian hormone and its duplicates in sex determination and germ cell proliferation of Nile tilapia. Genetics. 220(3). 35 indexed citations
17.
Yang, Lanying, et al.. (2021). Cyp17a1 is Required for Female Sex Determination and Male Fertility by Regulating Sex Steroid Biosynthesis in Fish. Endocrinology. 162(12). 39 indexed citations
18.
Wei, Xueyan, Xingyong Liu, Yibing Li, et al.. (2021). Germline sexual fate is determined by the antagonistic action of dmrt1 and foxl3/foxl2 in tilapia. Development. 148(8). 65 indexed citations
19.
Tao, Wenjing, Luohao Xu, Lin Zhao, et al.. (2020). High‐quality chromosome‐level genomes of two tilapia species reveal their evolution of repeat sequences and sex chromosomes. Molecular Ecology Resources. 21(2). 543–560. 55 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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