Prapaporn Pisitkun

3.3k total citations · 1 hit paper
51 papers, 2.4k citations indexed

About

Prapaporn Pisitkun is a scholar working on Immunology, Rheumatology and Molecular Biology. According to data from OpenAlex, Prapaporn Pisitkun has authored 51 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Immunology, 21 papers in Rheumatology and 12 papers in Molecular Biology. Recurrent topics in Prapaporn Pisitkun's work include Systemic Lupus Erythematosus Research (20 papers), T-cell and B-cell Immunology (12 papers) and Immune Cell Function and Interaction (11 papers). Prapaporn Pisitkun is often cited by papers focused on Systemic Lupus Erythematosus Research (20 papers), T-cell and B-cell Immunology (12 papers) and Immune Cell Function and Interaction (11 papers). Prapaporn Pisitkun collaborates with scholars based in Thailand, United States and Denmark. Prapaporn Pisitkun's co-authors include Silvia Bolland, Jonathan A. Deane, Т. Н. Тарасенко, Anne B. Satterthwaite, Michael J. Difilippantonio, Terrence Town, Lionel Feigenbaum, Jerrold M. Ward, Richard A. Flavell and Asada Leelahavanichkul and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Prapaporn Pisitkun

50 papers receiving 2.4k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Autoreactive B Cell Responses to RNA-Related Antigens Due to TLR7 Gene Duplication

2006 694 citations Prapaporn Pisitkun, Jonathan A. Deane et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Prapaporn Pisitkun Thailand	21	1.9k	725	569	301	222	51	2.4k
Iwao Sekigawa Japan	29	1.1k 0.6×	866 1.2×	509 0.9×	323 1.1×	166 0.7×	112	2.2k
Christiane Pfeiffer Germany	22	1.4k 0.7×	521 0.7×	370 0.7×	243 0.8×	130 0.6×	39	2.5k
Jan‐Eric Turner Germany	29	2.1k 1.1×	465 0.6×	413 0.7×	329 1.1×	128 0.6×	44	2.9k
Ajay Nirula United States	24	1.2k 0.7×	509 0.7×	354 0.6×	168 0.6×	199 0.9×	51	2.1k
Yoshinaga Ito Japan	16	1.6k 0.8×	302 0.4×	689 1.2×	556 1.8×	156 0.7×	27	2.4k
Christina Trollmo Sweden	24	1.6k 0.9×	754 1.0×	363 0.6×	240 0.8×	121 0.5×	43	2.6k
Paul A. Blair United Kingdom	11	1.9k 1.0×	432 0.6×	471 0.8×	297 1.0×	190 0.9×	14	2.9k
Joan Ní Gabhann Ireland	19	1.0k 0.5×	316 0.4×	583 1.0×	258 0.9×	94 0.4×	35	1.6k
Diego Catalán Chile	22	941 0.5×	314 0.4×	468 0.8×	220 0.7×	98 0.4×	42	1.7k
Chau‐Ching Liu United States	26	1.1k 0.6×	433 0.6×	405 0.7×	206 0.7×	131 0.6×	52	1.8k

Countries citing papers authored by Prapaporn Pisitkun

Since Specialization

Citations

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

Fields of papers citing papers by Prapaporn Pisitkun

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Prapaporn Pisitkun

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

All Works

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20 of 20 papers shown

Ngamjanyaporn, Pintip, et al.. (2024). The role of trimethoprim/sulfamethoxazole in preventing opportunistic infections in systemic lupus erythematosus patients receiving low-level immunosuppressive treatment: an open-label, randomized, controlled trial. Clinical and Experimental Medicine. 24(1). 241–241.

Leelahavanichkul, Asada, et al.. (2024). Elucidating the function of STING in systemic lupus erythematosus through the STING Goldenticket mouse mutant. Scientific Reports. 14(1). 13968–13968. 3 indexed citations

Suchonwanit, Poonkiat, et al.. (2023). Optimal time for COVID-19 vaccination in rituximab-treated dermatologic patients. Frontiers in Immunology. 14. 1138765–1138765. 7 indexed citations

Ngamjanyaporn, Pintip, Suchin Worawichawong, Prapaporn Pisitkun, et al.. (2022). Predicting treatment response and clinicopathological findings in lupus nephritis with urine epidermal growth factor, monocyte chemoattractant protein-1 or their ratios. PLoS ONE. 17(3). e0263778–e0263778. 8 indexed citations

Leepiyasakulchai, Chaniya, et al.. (2022). CD4⁺T-cell cooperation promoted pathogenic function of activated naïve B cells of patients with SLE. Lupus Science & Medicine. 9(1). e000739–e000739. 14 indexed citations

Thim-uam, Arthid, et al.. (2022). cGAS deficiency enhances inflammasome activation in macrophages and inflammatory pathology in pristane-induced lupus. Frontiers in Immunology. 13. 1010764–1010764. 14 indexed citations

Leepiyasakulchai, Chaniya, Pintip Ngamjanyaporn, Ladawan Khowawisetsut, et al.. (2021). The expansion of activated naive DNA autoreactive B cells and its association with disease activity in systemic lupus erythematosus patients. Arthritis Research & Therapy. 23(1). 179–179. 20 indexed citations

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

Saisorn, Wilasinee, Pornpimol Phuengmaung, Peerapat Visitchanakun, et al.. (2021). Acute Kidney Injury Induced Lupus Exacerbation Through the Enhanced Neutrophil Extracellular Traps (and Apoptosis) in Fcgr2b Deficient Lupus Mice With Renal Ischemia Reperfusion Injury. Frontiers in Immunology. 12. 669162–669162. 49 indexed citations

10.

Pisitkun, Prapaporn, et al.. (2020). Efficacy and safety of rituximab biosimilar in refractory lupus. Lupus Science & Medicine. 7(1). e000442–e000442. 4 indexed citations

11.

Tangtanatakul, Pattarin, Yongfei Wang, Wei Wei, et al.. (2020). Meta-analysis of genome-wide association study identifies FBN2 as a novel locus associated with systemic lupus erythematosus in Thai population. Arthritis Research & Therapy. 22(1). 185–185. 15 indexed citations

12.

Thim-uam, Arthid, Jiraphorn Issara-Amphorn, Thiranut Jaroonwitchawan, et al.. (2020). Leaky-gut enhanced lupus progression in the Fc gamma receptor-IIb deficient and pristane-induced mouse models of lupus. Scientific Reports. 10(1). 777–777. 79 indexed citations

13.

Visitchanakun, Peerapat, et al.. (2019). Lupus-like Disease in FcγRIIB−/− Mice Induces Osteopenia. Scientific Reports. 9(1). 17342–17342. 7 indexed citations

14.

Issara-Amphorn, Jiraphorn, Navaporn Worasilchai, Arthid Thim-uam, et al.. (2018). The Synergy of Endotoxin and (1→3)-β-D-Glucan, from Gut Translocation, Worsens Sepsis Severity in a Lupus Model of Fc Gamma Receptor IIb-Deficient Mice. Journal of Innate Immunity. 10(3). 189–201. 62 indexed citations

15.

Thim-uam, Arthid, Peerapat Visitchanakun, Prapaporn Pisitkun, et al.. (2018). Cortical Bone Loss in a Spontaneous Murine Model of Systemic Lupus Erythematosus. Calcified Tissue International. 103(6). 686–697. 7 indexed citations

16.

Ondee, Thunnicha, et al.. (2017). The role of macrophages in the susceptibility of Fc gamma receptor IIb deficient mice to Cryptococcus neoformans. Scientific Reports. 7(1). 40006–40006. 24 indexed citations

17.

Sun, Chenglong, Stefan Schattgen, Prapaporn Pisitkun, et al.. (2015). Evasion of Innate Cytosolic DNA Sensing by a Gammaherpesvirus Facilitates Establishment of Latent Infection. The Journal of Immunology. 194(4). 1819–1831. 80 indexed citations

18.

Walsh, Elizabeth R., Prapaporn Pisitkun, Elisaveta Voynova, et al.. (2012). Dual signaling by innate and adaptive immune receptors is required for TLR7-induced B-cell–mediated autoimmunity. Proceedings of the National Academy of Sciences. 109(40). 16276–16281. 82 indexed citations

19.

Richter, Kathleen, Sukhdev S. Brar, Madhumita Ray, et al.. (2009). Speckled-like Pattern in the Germinal Center (SLIP-GC), a Nuclear GTPase Expressed in Activation-induced Deaminase-expressing Lymphomas and Germinal Center B Cells. Journal of Biological Chemistry. 284(44). 30652–30661. 13 indexed citations

20.

Pisitkun, Prapaporn, Jonathan A. Deane, Michael J. Difilippantonio, et al.. (2006). Autoreactive B Cell Responses to RNA-Related Antigens Due to TLR7 Gene Duplication. Science. 312(5780). 1669–1672. 694 indexed citations breakdown →

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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