Shih‐Che Weng

573 total citations
21 papers, 394 citations indexed

About

Shih‐Che Weng is a scholar working on Public Health, Environmental and Occupational Health, Insect Science and Molecular Biology. According to data from OpenAlex, Shih‐Che Weng has authored 21 papers receiving a total of 394 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Public Health, Environmental and Occupational Health, 10 papers in Insect Science and 8 papers in Molecular Biology. Recurrent topics in Shih‐Che Weng's work include Mosquito-borne diseases and control (12 papers), Insect symbiosis and bacterial influences (10 papers) and Viral Infections and Vectors (5 papers). Shih‐Che Weng is often cited by papers focused on Mosquito-borne diseases and control (12 papers), Insect symbiosis and bacterial influences (10 papers) and Viral Infections and Vectors (5 papers). Shih‐Che Weng collaborates with scholars based in Taiwan, United States and France. Shih‐Che Weng's co-authors include Shin-Hong Shiao, Michael M. C. Lai, Wen‐Chi Su, Ti‐Chun Chao, King-Song Jeng, Yih‐Leh Huang, Po‐Nien Tsao, Wu‐Chun Tu, Omar S. Akbari and Chun‐Hong Chen and has published in prestigious journals such as PLoS ONE, Journal of Virology and Frontiers in Immunology.

In The Last Decade

Shih‐Che Weng

20 papers receiving 392 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shih‐Che Weng Taiwan 12 176 117 116 95 81 21 394
Claudia Umaña-Diaz France 7 189 1.1× 35 0.3× 65 0.6× 134 1.4× 87 1.1× 7 395
Luiza de Oliveira Ramos Pereira Brazil 13 337 1.9× 174 1.5× 109 0.9× 78 0.8× 66 0.8× 27 492
Étienne Frumence France 11 232 1.3× 67 0.6× 98 0.8× 71 0.7× 212 2.6× 24 439
Jeffrey M. Grabowski United States 12 255 1.4× 61 0.5× 99 0.9× 137 1.4× 203 2.5× 17 488
Jerônimo Conceição Ruiz Brazil 13 202 1.1× 229 2.0× 50 0.4× 118 1.2× 27 0.3× 23 374
Kelly N. DuBois United Kingdom 9 71 0.4× 151 1.3× 32 0.3× 279 2.9× 65 0.8× 12 485
Patrícia H. Alvarenga United States 12 329 1.9× 98 0.8× 260 2.2× 128 1.3× 74 0.9× 20 623
Erwan Atcheson United Kingdom 11 109 0.6× 45 0.4× 12 0.1× 120 1.3× 27 0.3× 19 327
Caroline Clucas United Kingdom 15 302 1.7× 419 3.6× 87 0.8× 190 2.0× 47 0.6× 20 683
Mathew G. Lyman United States 11 101 0.6× 360 3.1× 22 0.2× 126 1.3× 24 0.3× 13 515

Countries citing papers authored by Shih‐Che Weng

Since Specialization
Citations

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

Fields of papers citing papers by Shih‐Che Weng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shih‐Che Weng. 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 Shih‐Che Weng. The network helps show where Shih‐Che Weng may publish in the future.

Co-authorship network of co-authors of Shih‐Che Weng

This figure shows the co-authorship network connecting the top 25 collaborators of Shih‐Che Weng. A scholar is included among the top collaborators of Shih‐Che Weng 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 Shih‐Che Weng. Shih‐Che Weng 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.
2.
Weng, Shih‐Che, et al.. (2024). Establishing a dominant early larval sex-selection strain in the Asian malaria vector Anopheles stephensi. Infectious Diseases of Poverty. 13(1). 83–83. 5 indexed citations
3.
Yeh, Chun‐Ting, Shih‐Che Weng, Po‐Nien Tsao, & Shin-Hong Shiao. (2023). The chaperone BiP promotes dengue virus replication and mosquito vitellogenesis in Aedes aegypti. Insect Biochemistry and Molecular Biology. 155. 103930–103930. 3 indexed citations
4.
Weng, Shih‐Che, et al.. (2023). Advances and challenges in synthetic biology for mosquito control. Trends in Parasitology. 40(1). 75–88. 16 indexed citations
5.
Weng, Shih‐Che, Igor Antoshechkin, Éric Marois, & Omar S. Akbari. (2023). Efficient sex separation by exploiting differential alternative splicing of a dominant marker in Aedes aegypti. PLoS Genetics. 19(11). e1011065–e1011065. 10 indexed citations
6.
Weng, Shih‐Che, et al.. (2023). Co-infection of dengue and Zika viruses mutually enhances viral replication in the mosquito Aedes aegypti. Parasites & Vectors. 16(1). 18 indexed citations
7.
Weng, Shih‐Che & Shin-Hong Shiao. (2022). SUMOylation Is Essential for Dengue Virus Replication and Transmission in the Mosquito Aedes aegypti. Frontiers in Microbiology. 13. 801284–801284. 4 indexed citations
8.
Weng, Shih‐Che, et al.. (2022). A flavivirus-inducible gene expression system that modulates broad-spectrum antiviral activity against dengue and Zika viruses. Insect Biochemistry and Molecular Biology. 142. 103723–103723. 4 indexed citations
9.
Weng, Shih‐Che, Po‐Nien Tsao, & Shin-Hong Shiao. (2021). Blood glucose promotes dengue virus infection in the mosquito Aedes aegypti. Parasites & Vectors. 14(1). 376–376. 19 indexed citations
10.
Weng, Shih‐Che, et al.. (2021). A Thioester-Containing Protein Controls Dengue Virus Infection in Aedes aegypti Through Modulating Immune Response. Frontiers in Immunology. 12. 21 indexed citations
11.
Weng, Shih‐Che, et al.. (2020). A simplified method for blood feeding, oral infection, and saliva collection of the dengue vector mosquitoes. PLoS ONE. 15(5). e0233618–e0233618. 23 indexed citations
12.
Sun, Chin‐Hung, et al.. (2020). DNA topoisomerase IIIβ promotes cyst generation by inducing cyst wall protein gene expression in Giardia lamblia. Open Biology. 10(2). 190228–190228. 14 indexed citations
13.
Weng, Shih‐Che & Shin-Hong Shiao. (2020). The unfolded protein response modulates the autophagy‐mediated egg production in the mosquito Aedes aegypti . Insect Molecular Biology. 29(4). 404–416. 6 indexed citations
14.
Shiao, Shin-Hong, Shih‐Che Weng, Liqiang Luan, et al.. (2019). Novel phthalocyanines activated by dim light for mosquito larva- and cell-inactivation with inference for their potential as broad-spectrum photodynamic insecticides. PLoS ONE. 14(5). e0217355–e0217355. 18 indexed citations
15.
Lin, Shuting, et al.. (2019). Transcription Factor Elf3 Modulates Vasopressin-Induced Aquaporin-2 Gene Expression in Kidney Collecting Duct Cells. Frontiers in Physiology. 10. 1308–1308. 11 indexed citations
16.
Weng, Shih‐Che, et al.. (2019). A salivary protein of Aedes aegypti promotes dengue-2 virus replication and transmission. Insect Biochemistry and Molecular Biology. 111. 103181–103181. 25 indexed citations
17.
Chang, Chia-Hao, et al.. (2018). The non-canonical Notch signaling is essential for the control of fertility in Aedes aegypti. PLoS neglected tropical diseases. 12(3). e0006307–e0006307. 19 indexed citations
18.
Li, Shih-Wei, et al.. (2015). A case of human infection with Anisakis simplex in Taiwan. Gastrointestinal Endoscopy. 82(4). 757–758. 14 indexed citations
19.
Weng, Shih‐Che & Shin-Hong Shiao. (2015). Frizzled 2 is a key component in the regulation of TOR signaling-mediated egg production in the mosquito Aedes aegypti. Insect Biochemistry and Molecular Biology. 61. 17–24. 22 indexed citations
20.
Su, Li‐Hsin, et al.. (2013). DNA Topoisomerase II Is Involved in Regulation of Cyst Wall Protein Genes and Differentiation in Giardia lamblia. PLoS neglected tropical diseases. 7(5). e2218–e2218. 9 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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