Yaowaluck Maprang Roshorm

905 total citations
20 papers, 735 citations indexed

About

Yaowaluck Maprang Roshorm is a scholar working on Immunology, Molecular Biology and Genetics. According to data from OpenAlex, Yaowaluck Maprang Roshorm has authored 20 papers receiving a total of 735 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Immunology, 7 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Yaowaluck Maprang Roshorm's work include Virus-based gene therapy research (5 papers), Viral gastroenteritis research and epidemiology (4 papers) and Invertebrate Immune Response Mechanisms (4 papers). Yaowaluck Maprang Roshorm is often cited by papers focused on Virus-based gene therapy research (5 papers), Viral gastroenteritis research and epidemiology (4 papers) and Invertebrate Immune Response Mechanisms (4 papers). Yaowaluck Maprang Roshorm collaborates with scholars based in Thailand, United Kingdom and United States. Yaowaluck Maprang Roshorm's co-authors include Sakol Panyim, Witoon Tirasophon, Supansa Yodmuang, Tomáš Hanke, Chalermporn Ongvarrasopone, Nicholas W. Gale, Kayla A. Holder, David G. Jackson, Louise A. Johnson and Vincenzo Cerundolo and has published in prestigious journals such as Nature Immunology, Scientific Reports and Biochemical and Biophysical Research Communications.

In The Last Decade

Yaowaluck Maprang Roshorm

18 papers receiving 728 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yaowaluck Maprang Roshorm Thailand 13 407 314 104 87 75 20 735
Adel M. Nour United States 9 279 0.7× 512 1.6× 41 0.4× 78 0.9× 98 1.3× 13 779
Ana Marisa Chudzinski‐Tavassi Brazil 21 142 0.3× 375 1.2× 239 2.3× 82 0.9× 93 1.2× 82 1.2k
Chang-Jun Guo China 16 529 1.3× 209 0.7× 39 0.4× 77 0.9× 80 1.1× 40 787
Mizuho Kajikawa Japan 17 444 1.1× 412 1.3× 28 0.3× 114 1.3× 82 1.1× 40 986
Stéphanie Eyquem France 7 276 0.7× 575 1.8× 25 0.2× 56 0.6× 59 0.8× 8 939
Tsuyoshi Tokusumi United States 16 408 1.0× 368 1.2× 190 1.8× 65 0.7× 59 0.8× 23 808
Stuart Sims United Kingdom 14 458 1.1× 213 0.7× 22 0.2× 63 0.7× 80 1.1× 25 864
Eve Diefenbach Australia 12 273 0.7× 285 0.9× 18 0.2× 93 1.1× 31 0.4× 19 775
Alexey A. Matskevich Switzerland 16 789 1.9× 429 1.4× 559 5.4× 73 0.8× 88 1.2× 24 1.3k
John C. Tan United States 17 166 0.4× 287 0.9× 42 0.4× 31 0.4× 63 0.8× 27 668

Countries citing papers authored by Yaowaluck Maprang Roshorm

Since Specialization
Citations

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

Fields of papers citing papers by Yaowaluck Maprang Roshorm

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yaowaluck Maprang Roshorm. 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 Yaowaluck Maprang Roshorm. The network helps show where Yaowaluck Maprang Roshorm may publish in the future.

Co-authorship network of co-authors of Yaowaluck Maprang Roshorm

This figure shows the co-authorship network connecting the top 25 collaborators of Yaowaluck Maprang Roshorm. A scholar is included among the top collaborators of Yaowaluck Maprang Roshorm 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 Yaowaluck Maprang Roshorm. Yaowaluck Maprang Roshorm 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.
Roshorm, Yaowaluck Maprang, et al.. (2025). Influenza Neuraminidase Virus-Like Particle-Based Nanocarriers as a New Platform for the Delivery of Small-Peptide Antigens. Molecular Biotechnology. 68(2). 723–734.
5.
Ruengjitchatchawalya, Marasri, et al.. (2022). Immunodominant and Neutralizing Linear B-Cell Epitopes Spanning the Spike and Membrane Proteins of Porcine Epidemic Diarrhea Virus. Frontiers in Immunology. 12. 785293–785293. 13 indexed citations
6.
Chonkaew, Wunpen, et al.. (2022). Amphiphilic Chitosan Bearing Double Palmitoyl Chains and Quaternary Ammonium Moieties as a Nanocarrier for Plasmid DNA. ACS Omega. 7(12). 10056–10068. 11 indexed citations
7.
Phoolcharoen, Waranyoo, et al.. (2021). Immunodominant linear B cell epitopes in the spike and membrane proteins of SARS-CoV-2 identified by immunoinformatics prediction and immunoassay. Scientific Reports. 11(1). 20383–20383. 26 indexed citations
8.
Roshorm, Yaowaluck Maprang, et al.. (2020). Co-expression of self-cleaved multiple proteins derived from Porcine Reproductive and Respiratory Syndrome Virus by bi-cistronic and tri-cistronic DNA vaccines. Protein Expression and Purification. 177. 105763–105763. 5 indexed citations
9.
Roshorm, Yaowaluck Maprang, et al.. (2020). Direct suppression of human islet dedifferentiation, progenitor genes, but not epithelial to mesenchymal transition by liraglutide. Heliyon. 6(9). e04951–e04951. 5 indexed citations
10.
Johnson, Louise A., Suneale Banerji, Uzi Gileadi, et al.. (2017). Dendritic cells enter lymph vessels by hyaluronan-mediated docking to the endothelial receptor LYVE-1. Nature Immunology. 18(7). 762–770. 146 indexed citations
11.
Roshorm, Yaowaluck Maprang, et al.. (2017). Functional Pancreatic Isolated Islets from Cryopreserved Porcine and Human Pancreatic Tissues Based on GLUT2 Receptor Sensitivity. 100(11). 250.
12.
Roshorm, Yaowaluck Maprang, et al.. (2016). Antiviral Compounds Against Nucleocapsid Protein of Porcine Epidemic Diarrhea Virus. Animal Biotechnology. 28(2). 120–130. 12 indexed citations
13.
Roshorm, Yaowaluck Maprang, et al.. (2012). T cells induced by recombinant chimpanzee adenovirus alone and in prime‐boost regimens decrease chimeric EcoHIV/NDK challenge virus load. European Journal of Immunology. 42(12). 3243–3255. 17 indexed citations
14.
Im, Eung‐Jun, Yaowaluck Maprang Roshorm, Anne Bridgeman, et al.. (2011). Protective Efficacy of Serially Up-Ranked Subdominant CD8+ T Cell Epitopes against Virus Challenges. PLoS Pathogens. 7(5). e1002041–e1002041. 59 indexed citations
15.
Roshorm, Yaowaluck Maprang, Naoki Kobayashi, Andrew J. McMichael, et al.. (2009). Novel HIV‐1 clade B candidate vaccines designed for HLA‐B*5101+ patients protected mice against chimaeric ecotropic HIV‐1 challenge. European Journal of Immunology. 39(7). 1831–1840. 19 indexed citations
16.
Bridgeman, Anne, Yaowaluck Maprang Roshorm, Linda J. Lockett, et al.. (2009). Ovine atadenovirus, a novel and highly immunogenic vector in prime-boost studies of a candidate HIV-1 vaccine. Vaccine. 28(2). 474–483. 21 indexed citations
17.
Ongvarrasopone, Chalermporn, Yaowaluck Maprang Roshorm, & Sakol Panyim. (2007). . ScienceAsia. 33(1). 35–35. 48 indexed citations
18.
Yodmuang, Supansa, et al.. (2006). YHV-protease dsRNA inhibits YHV replication in Penaeus monodon and prevents mortality. Biochemical and Biophysical Research Communications. 341(2). 351–356. 165 indexed citations
19.
Ongvarrasopone, Chalermporn, et al.. (2006). Molecular cloning and functional expression of the Penaeus monodon 5-HT receptor. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1759(7). 328–339. 38 indexed citations
20.
Tirasophon, Witoon, Yaowaluck Maprang Roshorm, & Sakol Panyim. (2005). Silencing of yellow head virus replication in penaeid shrimp cells by dsRNA. Biochemical and Biophysical Research Communications. 334(1). 102–107. 131 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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