Sage Chaiyapechara

1.3k total citations
23 papers, 1.0k citations indexed

About

Sage Chaiyapechara is a scholar working on Immunology, Aquatic Science and Ecology. According to data from OpenAlex, Sage Chaiyapechara has authored 23 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Immunology, 12 papers in Aquatic Science and 7 papers in Ecology. Recurrent topics in Sage Chaiyapechara's work include Aquaculture disease management and microbiota (20 papers), Aquaculture Nutrition and Growth (12 papers) and Invertebrate Immune Response Mechanisms (9 papers). Sage Chaiyapechara is often cited by papers focused on Aquaculture disease management and microbiota (20 papers), Aquaculture Nutrition and Growth (12 papers) and Invertebrate Immune Response Mechanisms (9 papers). Sage Chaiyapechara collaborates with scholars based in Thailand, United States and United Kingdom. Sage Chaiyapechara's co-authors include Pikul Jiravanichpaisal, Wanilada Rungrassamee, Nitsara Karoonuthaisiri, Amornpan Klanchui, Sawarot Maibunkaew, Faye M. Dong, Ronald W. Hardy, Sithichoke Tangphatsornruang, Wipasiri Soonthornchai and Padermsak Jarayabhand and has published in prestigious journals such as PLoS ONE, Scientific Reports and Aquaculture.

In The Last Decade

Sage Chaiyapechara

21 papers receiving 990 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sage Chaiyapechara Thailand 15 717 569 232 226 109 23 1.0k
Vikash Kumar India 20 908 1.3× 682 1.2× 319 1.4× 267 1.2× 43 0.4× 73 1.4k
Suvra Roy India 16 727 1.0× 508 0.9× 214 0.9× 220 1.0× 44 0.4× 47 1.1k
Jose L. González Vecino United Kingdom 13 1.1k 1.5× 806 1.4× 139 0.6× 261 1.2× 66 0.6× 13 1.3k
Ya‐Li Shiu Taiwan 15 988 1.4× 1.0k 1.8× 89 0.4× 202 0.9× 80 0.7× 26 1.3k
Quanxin Gao China 17 490 0.7× 291 0.5× 206 0.9× 187 0.8× 28 0.3× 57 835
Che Roos Saad Malaysia 21 946 1.3× 1.3k 2.3× 224 1.0× 159 0.7× 50 0.5× 76 1.7k
Eleonor A. Tendencia Philippines 18 529 0.7× 395 0.7× 170 0.7× 122 0.5× 51 0.5× 32 900
Adolfo Jatobá Brazil 19 914 1.3× 922 1.6× 136 0.6× 83 0.4× 20 0.2× 64 1.1k
Ioannis N. Vatsos Norway 14 340 0.5× 323 0.6× 109 0.5× 112 0.5× 27 0.2× 36 624

Countries citing papers authored by Sage Chaiyapechara

Since Specialization
Citations

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

Fields of papers citing papers by Sage Chaiyapechara

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sage Chaiyapechara

This figure shows the co-authorship network connecting the top 25 collaborators of Sage Chaiyapechara. A scholar is included among the top collaborators of Sage Chaiyapechara 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 Sage Chaiyapechara. Sage Chaiyapechara 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
2.
Uengwetwanit, Tanaporn, et al.. (2025). Investigating a novel β-glucan source to enhance disease resistance in Pacific white shrimp (Penaeus vannamei). Scientific Reports. 15(1). 15377–15377.
3.
Powtongsook, Sorawit, Worarat Kruasuwan, Piroon Jenjaroenpun, et al.. (2024). Integrating short- and full-length 16S rRNA gene sequencing to elucidate microbiome profiles in Pacific white shrimp ( Litopenaeus vannamei ) ponds. Microbiology Spectrum. 12(11). e0096524–e0096524. 1 indexed citations
5.
6.
Uengwetwanit, Tanaporn, Umaporn Uawisetwathana, Jasper J. Koehorst, et al.. (2023). Investigating host-gut microbial relationship in Penaeus monodon upon exposure to Vibrio harveyi. Aquaculture. 567. 739252–739252. 19 indexed citations
7.
Chaiyapechara, Sage, et al.. (2023). Shrimp microbiome and immune development in the early life stages. Developmental & Comparative Immunology. 147. 104765–104765. 20 indexed citations
8.
Yongkiettrakul, Suganya, et al.. (2021). Biochemical characterization of the cyclooxygenase enzyme in penaeid shrimp. PLoS ONE. 16(4). e0250276–e0250276. 6 indexed citations
10.
Uengwetwanit, Tanaporn, Umaporn Uawisetwathana, Sopacha Arayamethakorn, et al.. (2020). Multi-omics analysis to examine microbiota, host gene expression and metabolites in the intestine of black tiger shrimp (Penaeus monodon) with different growth performance. PeerJ. 8. e9646–e9646. 33 indexed citations
11.
Taengchaiyaphum, Suparat, Jiraporn Srisala, Premruethai Supungul, et al.. (2019). Mendelian inheritance of endogenous viral elements (EVE) of white spot syndrome virus (WSSV) in shrimp. Developmental & Comparative Immunology. 96. 144–149. 12 indexed citations
12.
Tepaamorndech, Surapun, Yutthana Kingcha, Sage Chaiyapechara, et al.. (2018). Effects of Bacillus aryabhattai TBRC8450 on vibriosis resistance and immune enhancement in Pacific white shrimp, Litopenaeus vannamei. Fish & Shellfish Immunology. 86. 4–13. 53 indexed citations
13.
Rungrassamee, Wanilada, et al.. (2017). Bacterial community composition and distribution in different segments of the gastrointestinal tract of wild-caught adultPenaeus monodon. Aquaculture Research. 49(1). 378–392. 22 indexed citations
14.
Soonthornchai, Wipasiri, Sage Chaiyapechara, Sirawut Klinbunga, et al.. (2016). Differentially expressed transcripts in stomach of Penaeus monodon in response to AHPND infection. Developmental & Comparative Immunology. 65. 53–63. 51 indexed citations
15.
Soonthornchai, Wipasiri, Sage Chaiyapechara, Padermsak Jarayabhand, Kenneth Söderhäll, & Pikul Jiravanichpaisal. (2015). Interaction of Vibrio spp. with the Inner Surface of the Digestive Tract of Penaeus monodon. PLoS ONE. 10(8). e0135783–e0135783. 77 indexed citations
16.
Rungrassamee, Wanilada, Amornpan Klanchui, Sawarot Maibunkaew, et al.. (2014). Characterization of Intestinal Bacteria in Wild and Domesticated Adult Black Tiger Shrimp (Penaeus monodon). PLoS ONE. 9(3). e91853–e91853. 233 indexed citations
17.
Rungrassamee, Wanilada, Amornpan Klanchui, Sage Chaiyapechara, et al.. (2013). Bacterial Population in Intestines of the Black Tiger Shrimp (Penaeus monodon) under Different Growth Stages. PLoS ONE. 8(4). e60802–e60802. 140 indexed citations
18.
Chaiyapechara, Sage, et al.. (2011). Bacterial Community Associated with the Intestinal Tract of P. monodon in Commercial Farms. Microbial Ecology. 63(4). 938–953. 106 indexed citations
20.
Chaiyapechara, Sage, et al.. (2003). Proximate Composition, Lipid Oxidation, and Sensory Characteristics of Fillets from Rainbow Trout Oncorhynchus mykiss Fed Diets Containing 10% to 30% Lipid. Journal of the World Aquaculture Society. 34(3). 266–277. 24 indexed citations

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