Patcharee Ritprajak

1.8k total citations
46 papers, 1.4k citations indexed

About

Patcharee Ritprajak is a scholar working on Immunology, Molecular Biology and Infectious Diseases. According to data from OpenAlex, Patcharee Ritprajak has authored 46 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Immunology, 15 papers in Molecular Biology and 10 papers in Infectious Diseases. Recurrent topics in Patcharee Ritprajak's work include Immunotherapy and Immune Responses (13 papers), Immune Cell Function and Interaction (11 papers) and Immune cells in cancer (8 papers). Patcharee Ritprajak is often cited by papers focused on Immunotherapy and Immune Responses (13 papers), Immune Cell Function and Interaction (11 papers) and Immune cells in cancer (8 papers). Patcharee Ritprajak collaborates with scholars based in Thailand, Japan and United States. Patcharee Ritprajak's co-authors include Miyuki Azuma, Masaaki Hashiguchi, Yosuke Kamimura, Asada Leelahavanichkul, Haruo Kozono, Nattiya Hirankarn, Tanapat Palaga, Numpon Insin, Thanaphum Osathanon and Prasit Pavasant and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The Journal of Immunology.

In The Last Decade

Patcharee Ritprajak

44 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Patcharee Ritprajak Thailand 19 702 513 378 107 98 46 1.4k
Flávia Castro Portugal 16 753 1.1× 554 1.1× 499 1.3× 109 1.0× 121 1.2× 31 1.6k
Ritobrata Goswami India 19 1.3k 1.8× 315 0.6× 306 0.8× 101 0.9× 73 0.7× 52 2.2k
Anne Richter Germany 21 875 1.2× 314 0.6× 470 1.2× 98 0.9× 121 1.2× 59 1.8k
Feiran Cheng China 10 493 0.7× 321 0.6× 729 1.9× 144 1.3× 78 0.8× 17 1.4k
Luciana Cavalheiro Marti Brazil 20 487 0.7× 344 0.7× 440 1.2× 154 1.4× 105 1.1× 74 1.6k
Zhijun Jiao China 22 934 1.3× 364 0.7× 399 1.1× 82 0.8× 73 0.7× 32 1.7k
Xuejiao Han China 12 504 0.7× 289 0.6× 540 1.4× 62 0.6× 85 0.9× 21 1.1k
Jiali Sun China 19 328 0.5× 373 0.7× 278 0.7× 82 0.8× 96 1.0× 74 1.2k
Sachiko Hirosue Switzerland 16 933 1.3× 560 1.1× 787 2.1× 100 0.9× 61 0.6× 21 1.7k
Jae Yoon Jung South Korea 22 425 0.6× 230 0.4× 561 1.5× 102 1.0× 96 1.0× 47 1.7k

Countries citing papers authored by Patcharee Ritprajak

Since Specialization
Citations

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

Fields of papers citing papers by Patcharee Ritprajak

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patcharee Ritprajak

This figure shows the co-authorship network connecting the top 25 collaborators of Patcharee Ritprajak. A scholar is included among the top collaborators of Patcharee Ritprajak 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 Patcharee Ritprajak. Patcharee Ritprajak 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
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Leelahavanichkul, Asada, et al.. (2024). Complement receptor 3-dependent engagement by Candida glabrata β-glucan modulates dendritic cells to induce regulatory T-cell expansion. Open Biology. 14(5). 230315–230315. 7 indexed citations
3.
Saisorn, Wilasinee, et al.. (2024). Lupus exacerbation in ovalbumin-induced asthma in Fc gamma receptor IIb deficient mice, partly due to hyperfunction of dendritic cells. Asian Pacific Journal of Allergy and Immunology. 43(2). 300–311. 6 indexed citations
4.
Phuengmaung, Pornpimol, Jiraphorn Issara-Amphorn, Patcharee Ritprajak, et al.. (2023). Less Severe Sepsis in Cecal Ligation and Puncture Models with and without Lipopolysaccharide in Mice with Conditional Ezh2-Deleted Macrophages (LysM-Cre System). International Journal of Molecular Sciences. 24(10). 8517–8517. 4 indexed citations
5.
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Palaga, Tanapat, et al.. (2023). Impaired functions of human monocyte-derived dendritic cells and induction of regulatory T cells by pathogenic Leptospira. PLoS neglected tropical diseases. 17(11). e0011781–e0011781. 3 indexed citations
7.
Ritprajak, Patcharee, et al.. (2022). Cell Wall Mannan of Candida Attenuates Osteogenic Differentiation by Human Dental Pulp Cells. Journal of Endodontics. 49(2). 190–197. 1 indexed citations
8.
Visitchanakun, Peerapat, Paweena Susantitaphong, Prapaporn Pisitkun, et al.. (2021). Interference on Cytosolic DNA Activation Attenuates Sepsis Severity: Experiments on Cyclic GMP–AMP Synthase (cGAS) Deficient Mice. International Journal of Molecular Sciences. 22(21). 11450–11450. 29 indexed citations
9.
Saisorn, Wilasinee, et al.. (2021). Interaction Between Dendritic Cells and Candida krusei β-Glucan Partially Depends on Dectin-1 and It Promotes High IL-10 Production by T Cells. Frontiers in Cellular and Infection Microbiology. 10. 566661–566661. 10 indexed citations
10.
Ritprajak, Patcharee, et al.. (2021). Effect of metal ions released from orthodontic mini-implants on osteoclastogenesis. Dental and Medical Problems. 58(3). 327–333.
11.
Ritprajak, Patcharee, et al.. (2020). Dendritic cells as key players in systemic lupus erythematosus. Asian Pacific Journal of Allergy and Immunology. 38(4). 225–232. 32 indexed citations
12.
Thammahong, Arsa, et al.. (2019). Alteration of macrophage immune phenotype in a murine sepsis model is associated with susceptibility to secondary fungal infection. Asian Pacific Journal of Allergy and Immunology. 40(2). 162–171. 18 indexed citations
13.
Palaga, Tanapat, et al.. (2018). Oxidized Carbon Black: Preparation, Characterization and Application in Antibody Delivery across Cell Membrane. Scientific Reports. 8(1). 2489–2489. 26 indexed citations
14.
Sa‐Ard‐Iam, Noppadol, et al.. (2018). Cell wall mannan of Candida krusei mediates dendritic cell apoptosis and orchestrates Th17 polarization via TLR-2/MyD88-dependent pathway. Scientific Reports. 8(1). 17123–17123. 20 indexed citations
15.
Ritprajak, Patcharee, et al.. (2016). Generation of potent porcine monocyte-derived dendritic cells (MoDCs) by modified culture protocol. Veterinary Immunology and Immunopathology. 182. 63–68. 12 indexed citations
16.
Manokawinchoke, Jeeranan, Patcharee Ritprajak, Thanaphum Osathanon, & Prasit Pavasant. (2014). Estradiol induces osteoprotegerin expression by human dental pulp cells. Odontology. 104(1). 10–18. 10 indexed citations
17.
Ritprajak, Patcharee & Miyuki Azuma. (2014). Intrinsic and extrinsic control of expression of the immunoregulatory molecule PD-L1 in epithelial cells and squamous cell carcinoma. Oral Oncology. 51(3). 221–228. 268 indexed citations
18.
Zhang, Lu, Yosuke Kamimura, Patcharee Ritprajak, et al.. (2010). B7-H1 Overexpression Regulates Epithelial–Mesenchymal Transition and Accelerates Carcinogenesis in Skin. Cancer Research. 71(4). 1235–1243. 83 indexed citations
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Azuma, Miyuki, Patcharee Ritprajak, & Masaaki Hashiguchi. (2010). Topical Application of siRNA Targeting Cutaneous Dendritic Cells in Allergic Skin Disease. Methods in molecular biology. 623. 373–381. 12 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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