Prabuddha S. Pathinayake

1.4k total citations
25 papers, 684 citations indexed

About

Prabuddha S. Pathinayake is a scholar working on Pulmonary and Respiratory Medicine, Physiology and Immunology. According to data from OpenAlex, Prabuddha S. Pathinayake has authored 25 papers receiving a total of 684 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pulmonary and Respiratory Medicine, 9 papers in Physiology and 9 papers in Immunology. Recurrent topics in Prabuddha S. Pathinayake's work include Asthma and respiratory diseases (7 papers), Respiratory viral infections research (6 papers) and Chronic Obstructive Pulmonary Disease (COPD) Research (6 papers). Prabuddha S. Pathinayake is often cited by papers focused on Asthma and respiratory diseases (7 papers), Respiratory viral infections research (6 papers) and Chronic Obstructive Pulmonary Disease (COPD) Research (6 papers). Prabuddha S. Pathinayake collaborates with scholars based in Australia, South Korea and Bangladesh. Prabuddha S. Pathinayake's co-authors include Peter Wark, Alan Hsu, David W. Waters, Christopher Grainge, Philip M. Hansbro, Steven E. Mutsaers, Michael Schuliga, Kaj E. C. Blokland, Janette K. Burgess and Cecilia M. Prêle and has published in prestigious journals such as PLoS ONE, American Journal of Respiratory and Critical Care Medicine and Journal of Virology.

In The Last Decade

Prabuddha S. Pathinayake

25 papers receiving 676 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Prabuddha S. Pathinayake Australia 14 234 199 168 145 141 25 684
Yue Jia China 14 131 0.6× 144 0.7× 144 0.9× 175 1.2× 218 1.5× 19 683
John A. Christian United States 13 114 0.5× 131 0.7× 160 1.0× 324 2.2× 308 2.2× 27 792
Jun-ichi Ashitani Japan 19 257 1.1× 176 0.9× 256 1.5× 171 1.2× 182 1.3× 48 1.1k
Tomoyuki Masaki Japan 11 106 0.5× 168 0.8× 182 1.1× 164 1.1× 76 0.5× 17 649
Ian Toma United States 12 69 0.3× 278 1.4× 106 0.6× 113 0.8× 40 0.3× 24 615
Kunal P. Patel United States 12 89 0.4× 173 0.9× 190 1.1× 185 1.3× 39 0.3× 15 723
Carles Saus Spain 11 197 0.8× 128 0.6× 69 0.4× 124 0.9× 84 0.6× 23 565
Anna Kłopot United States 13 50 0.2× 263 1.3× 81 0.5× 96 0.7× 48 0.3× 20 1.1k
Shinji Toki United States 18 208 0.9× 135 0.7× 632 3.8× 131 0.9× 486 3.4× 44 1.2k

Countries citing papers authored by Prabuddha S. Pathinayake

Since Specialization
Citations

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

Fields of papers citing papers by Prabuddha S. Pathinayake

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Prabuddha S. Pathinayake. 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 Prabuddha S. Pathinayake. The network helps show where Prabuddha S. Pathinayake may publish in the future.

Co-authorship network of co-authors of Prabuddha S. Pathinayake

This figure shows the co-authorship network connecting the top 25 collaborators of Prabuddha S. Pathinayake. A scholar is included among the top collaborators of Prabuddha S. Pathinayake 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 Prabuddha S. Pathinayake. Prabuddha S. Pathinayake 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.
Dey, Surajit, Wenying Lu, Heinrich C. Weber, et al.. (2024). Large airway wall vascularity in patients with asthma–COPD overlap: a bronchoscopy study. ERJ Open Research. 10(4). 2–2024. 3 indexed citations
3.
Pathinayake, Prabuddha S., Alan Hsu, Kristy Nichol, et al.. (2024). Endoplasmic reticulum stress enhances the expression of TLR3-induced TSLP by airway epithelium. American Journal of Physiology-Lung Cellular and Molecular Physiology. 326(5). L618–L626. 3 indexed citations
4.
Chen, Ling, Prabuddha S. Pathinayake, Andrew T. Reid, et al.. (2024). Inflammation‐induced loss of CFTR ‐expressing airway ionocytes in non‐eosinophilic asthma. Respirology. 30(1). 25–40. 2 indexed citations
5.
Pathinayake, Prabuddha S., Nikhil T Awatade, & Peter Wark. (2023). Type 2 Immunity and Its Impact on COVID-19 Infection in the Airways. Viruses. 15(2). 402–402. 6 indexed citations
6.
Dey, Surajit, Wenying Lu, Greg Haug, et al.. (2023). Airway inflammatory changes in the lungs of patients with asthma-COPD overlap (ACO): a bronchoscopy endobronchial biopsy study. Respiratory Research. 24(1). 221–221. 11 indexed citations
7.
Awatade, Nikhil T, Andrew T. Reid, Kristy Nichol, et al.. (2023). Comparison of commercially available differentiation media on cell morphology, function, and anti-viral responses in conditionally reprogrammed human bronchial epithelial cells. Scientific Reports. 13(1). 11200–11200. 8 indexed citations
8.
Johansen, Matt D., Duc Hai Nguyen, Prabuddha S. Pathinayake, et al.. (2022). Increased SARS-CoV-2 Infection, Protease, and Inflammatory Responses in Chronic Obstructive Pulmonary Disease Primary Bronchial Epithelial Cells Defined with Single-Cell RNA Sequencing. American Journal of Respiratory and Critical Care Medicine. 206(6). 712–729. 31 indexed citations
9.
Dey, Surajit, Wenying Lu, Heinrich C. Weber, et al.. (2022). Differential airway remodeling changes were observed in patients with asthma COPD overlap compared to patients with asthma and COPD alone. American Journal of Physiology-Lung Cellular and Molecular Physiology. 323(4). L473–L483. 12 indexed citations
10.
Uddin, Md Bashir, et al.. (2022). Foot-and-mouth disease virus non-structural protein 2B downregulates the RLR signaling pathway via degradation of RIG-I and MDA5. Frontiers in Immunology. 13. 1020262–1020262. 13 indexed citations
11.
Pathinayake, Prabuddha S., David W. Waters, Kristy Nichol, et al.. (2021). Endoplasmic reticulum-unfolded protein response signalling is altered in severe eosinophilic and neutrophilic asthma. Thorax. 77(5). 443–451. 27 indexed citations
12.
Chong, Wai Chin, Madhur D. Shastri, Gregory M. Peterson, et al.. (2021). The complex interplay between endoplasmic reticulum stress and the NLRP3 inflammasome: a potential therapeutic target for inflammatory disorders. Clinical & Translational Immunology. 10(2). e1247–e1247. 42 indexed citations
13.
Waters, David W., Kaj E. C. Blokland, Prabuddha S. Pathinayake, et al.. (2019). STAT3 Regulates the Onset of Oxidant-induced Senescence in Lung Fibroblasts. American Journal of Respiratory Cell and Molecular Biology. 61(1). 61–73. 56 indexed citations
14.
Pathinayake, Prabuddha S., W. A. Gayan Chathuranga, Hyun‐Cheol Lee, et al.. (2018). Inactivated enterovirus 71 with poly-γ-glutamic acid/Chitosan nano particles (PC NPs) induces high cellular and humoral immune responses in BALB/c mice. Archives of Virology. 163(8). 2073–2083. 8 indexed citations
15.
Pathinayake, Prabuddha S., Alan Hsu, David W. Waters, et al.. (2018). Understanding the Unfolded Protein Response in the Pathogenesis of Asthma. Frontiers in Immunology. 9. 175–175. 42 indexed citations
16.
Pathinayake, Prabuddha S., et al.. (2018). Respiratory Viruses and Asthma. Seminars in Respiratory and Critical Care Medicine. 39(1). 45–55. 22 indexed citations
17.
Kim, Jaehoon, Tae‐Hwan Kim, Hyun‐Cheol Lee, et al.. (2017). Rubicon Modulates Antiviral Type I Interferon (IFN) Signaling by Targeting IFN Regulatory Factor 3 Dimerization. Journal of Virology. 91(14). 29 indexed citations
18.
Li, Rui, Mohammed Yousuf Elahi Chowdhury, Tae-Hwan Kim, et al.. (2015). Mucosally administered Lactobacillus surface-displayed influenza antigens (sM2 and HA2) with cholera toxin subunit A1 (CTA1) Induce broadly protective immune responses against divergent influenza subtypes. Veterinary Microbiology. 179(3-4). 250–263. 29 indexed citations
19.
Chowdhury, Mohammed Yousuf Elahi, Rui Li, Jae Hoon Kim, et al.. (2014). Mucosal Vaccination with Recombinant Lactobacillus casei-Displayed CTA1-Conjugated Consensus Matrix Protein-2 (sM2) Induces Broad Protection against Divergent Influenza Subtypes in BALB/c Mice. PLoS ONE. 9(4). e94051–e94051. 37 indexed citations
20.
Kim, Ki-Sun, Jin‐Moo Lee, Won‐Kyu Lee, et al.. (2013). Single-stranded DNA aptamer that specifically binds to the influenza virus NS1 protein suppresses interferon antagonism. Antiviral Research. 100(2). 337–345. 41 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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