Chek Meng Poh

6.2k total citations · 1 hit paper
17 papers, 3.6k citations indexed

About

Chek Meng Poh is a scholar working on Immunology, Public Health, Environmental and Occupational Health and Neurology. According to data from OpenAlex, Chek Meng Poh has authored 17 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Immunology, 10 papers in Public Health, Environmental and Occupational Health and 4 papers in Neurology. Recurrent topics in Chek Meng Poh's work include Malaria Research and Control (9 papers), Complement system in diseases (8 papers) and Mosquito-borne diseases and control (6 papers). Chek Meng Poh is often cited by papers focused on Malaria Research and Control (9 papers), Complement system in diseases (8 papers) and Mosquito-borne diseases and control (6 papers). Chek Meng Poh collaborates with scholars based in Singapore, United States and Australia. Chek Meng Poh's co-authors include Laurent Rénia, Lisa F. P. Ng, Paul A. MacAry, Matthew Zirui Tay, Shanshan Wu Howland, Sin Yee Gun, Carla Claser, Gijsbert M. Grotenbreg, Rebecca J. Faleiro and Deshapriya S. Karunarathne and has published in prestigious journals such as Immunity, Nature reviews. Immunology and Scientific Reports.

In The Last Decade

Chek Meng Poh

17 papers receiving 3.5k citations

Hit Papers

The trinity of COVID-19: ... 2020 2026 2022 2024 2020 500 1000 1.5k 2.0k 2.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chek Meng Poh Singapore 12 2.1k 926 712 573 471 17 3.6k
Xiaoyun Zhang China 16 2.6k 1.2× 1.5k 1.6× 428 0.6× 935 1.6× 247 0.5× 69 4.3k
Carolina Ramı́rez-Santana Colombia 25 1.2k 0.6× 690 0.7× 421 0.6× 415 0.7× 351 0.7× 67 2.8k
Willem van de Veen Switzerland 27 1.3k 0.6× 594 0.6× 1.3k 1.8× 446 0.8× 145 0.3× 47 4.5k
Haizhou Wang China 20 1.3k 0.6× 589 0.6× 246 0.3× 372 0.6× 342 0.7× 62 2.5k
Matthew Zirui Tay Singapore 10 2.1k 1.0× 937 1.0× 588 0.8× 759 1.3× 107 0.2× 17 3.7k
Guangcai Duan China 24 1.4k 0.7× 492 0.5× 304 0.4× 470 0.8× 145 0.3× 122 2.9k
Yong Cao China 22 2.9k 1.4× 1.5k 1.7× 633 0.9× 1.6k 2.7× 217 0.5× 37 5.4k
Yuanhong Xu China 27 1.3k 0.6× 413 0.4× 309 0.4× 756 1.3× 236 0.5× 158 3.6k
Milena Sokołowska Switzerland 35 1.7k 0.8× 718 0.8× 1.1k 1.5× 1.1k 2.0× 142 0.3× 78 5.5k

Countries citing papers authored by Chek Meng Poh

Since Specialization
Citations

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

Fields of papers citing papers by Chek Meng Poh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chek Meng Poh. 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 Chek Meng Poh. The network helps show where Chek Meng Poh may publish in the future.

Co-authorship network of co-authors of Chek Meng Poh

This figure shows the co-authorship network connecting the top 25 collaborators of Chek Meng Poh. A scholar is included among the top collaborators of Chek Meng Poh 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 Chek Meng Poh. Chek Meng Poh is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Yeo, Siok Ping, Lindsay Kua, Chek Meng Poh, et al.. (2024). B7-H3–Targeting Chimeric Antigen Receptors Epstein-Barr Virus–specific T Cells Provides a Tumor Agnostic Off-The-Shelf Therapy Against B7-H3–positive Solid Tumors. Cancer Research Communications. 4(6). 1410–1429. 3 indexed citations
2.
Cross, Gail Brenda, Claire M. Naftalin, Jinghao Nicholas Ngiam, et al.. (2022). Discrepant serological findings in SARS‐CoV‐2 PCR‐negative hospitalized patients with fever and acute respiratory symptoms during the pandemic. Journal of Medical Virology. 94(6). 2460–2470. 2 indexed citations
3.
Poh, Chek Meng, Jian Zheng, Rudragouda Channappanavar, et al.. (2020). Multiplex Screening Assay for Identifying Cytotoxic CD8+ T Cell Epitopes. Frontiers in Immunology. 11. 400–400. 10 indexed citations
4.
Poh, Chek Meng, Yi‐Hao Chan, & Lisa F. P. Ng. (2020). Role of T Cells in Chikungunya Virus Infection and Utilizing Their Potential in Anti-Viral Immunity. Frontiers in Immunology. 11. 287–287. 21 indexed citations
5.
Tay, Matthew Zirui, Chek Meng Poh, Laurent Rénia, Paul A. MacAry, & Lisa F. P. Ng. (2020). The trinity of COVID-19: immunity, inflammation and intervention. Nature reviews. Immunology. 20(6). 363–374. 2926 indexed citations breakdown →
7.
Li, Olive T. W., Chek Meng Poh, Ranawaka A. P. M. Perera, et al.. (2018). Combined use of live-attenuated and inactivated influenza vaccines to enhance heterosubtypic protection. Virology. 525. 73–82. 3 indexed citations
8.
Teo, Teck‐Hui, Shanshan Wu Howland, Carla Claser, et al.. (2017). Co‐infection with Chikungunya virus alters trafficking of pathogenic CD 8 + T cells into the brain and prevents Plasmodium ‐induced neuropathology. EMBO Molecular Medicine. 10(1). 121–138. 25 indexed citations
9.
Gun, Sin Yee, Carla Claser, Teck‐Hui Teo, et al.. (2017). Interferon regulatory factor 1 is essential for pathogenic CD8+ T cell migration and retention in the brain during experimental cerebral malaria. Cellular Microbiology. 20(5). e12819–e12819. 14 indexed citations
10.
Karunarathne, Deshapriya S., Joshua M. Horne‐Debets, Johnny X. Huang, et al.. (2016). Programmed Death-1 Ligand 2-Mediated Regulation of the PD-L1 to PD-1 Axis Is Essential for Establishing CD4 + T Cell Immunity. Immunity. 45(2). 333–345. 84 indexed citations
11.
Horne‐Debets, Joshua M., Deshapriya S. Karunarathne, Rebecca J. Faleiro, et al.. (2016). Mice lacking Programmed cell death-1 show a role for CD8+ T cells in long-term immunity against blood-stage malaria. Scientific Reports. 6(1). 26210–26210. 19 indexed citations
12.
Howland, Shanshan Wu, Chek Meng Poh, & Laurent Rénia. (2015). Activated Brain Endothelial Cells Cross-Present Malaria Antigen. PLoS Pathogens. 11(6). e1004963–e1004963. 80 indexed citations
13.
Howland, Shanshan Wu, Carla Claser, Chek Meng Poh, Sin Yee Gun, & Laurent Rénia. (2015). Pathogenic CD8+ T cells in experimental cerebral malaria. Seminars in Immunopathology. 37(3). 221–231. 74 indexed citations
14.
Howland, Shanshan Wu, Sin Yee Gun, Carla Claser, Chek Meng Poh, & Laurent Rénia. (2015). Measuring antigen presentation in mouse brain endothelial cells ex vivo and in vitro. Nature Protocols. 10(12). 2016–2026. 21 indexed citations
15.
Poh, Chek Meng, Shanshan Wu Howland, Gijsbert M. Grotenbreg, & Laurent Rénia. (2014). Damage to the Blood-Brain Barrier during Experimental Cerebral Malaria Results from Synergistic Effects of CD8+T Cells with Different Specificities. Infection and Immunity. 82(11). 4854–4864. 33 indexed citations
16.
Howland, Shanshan Wu, Chek Meng Poh, Sin Yee Gun, et al.. (2013). Brain microvessel cross‐presentation is a hallmark of experimental cerebral malaria. EMBO Molecular Medicine. 5(7). 984–999. 114 indexed citations
17.
Horne‐Debets, Joshua M., Rebecca J. Faleiro, Deshapriya S. Karunarathne, et al.. (2013). PD-1 Dependent Exhaustion of CD8+ T Cells Drives Chronic Malaria. Cell Reports. 5(5). 1204–1213. 119 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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