Thanh T. Luong

2.2k total citations
28 papers, 1.8k citations indexed

About

Thanh T. Luong is a scholar working on Infectious Diseases, Molecular Biology and Genetics. According to data from OpenAlex, Thanh T. Luong has authored 28 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Infectious Diseases, 22 papers in Molecular Biology and 13 papers in Genetics. Recurrent topics in Thanh T. Luong's work include Antimicrobial Resistance in Staphylococcus (22 papers), Bacterial biofilms and quorum sensing (19 papers) and Bacterial Genetics and Biotechnology (13 papers). Thanh T. Luong is often cited by papers focused on Antimicrobial Resistance in Staphylococcus (22 papers), Bacterial biofilms and quorum sensing (19 papers) and Bacterial Genetics and Biotechnology (13 papers). Thanh T. Luong collaborates with scholars based in United States, Sweden and India. Thanh T. Luong's co-authors include Chia Y. Lee, Paul M. Dunman, Marat R. Sadykov, Greg A. Somerville, Charlotte D. Majerczyk, Abraham L. Sonenshein, Steven W. Newell, Yong Lim, Malabendu Jana and Steven J. Projan and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Bacteriology and Infection and Immunity.

In The Last Decade

Thanh T. Luong

26 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thanh T. Luong United States 21 1.4k 1.3k 491 198 157 28 1.8k
Yinduo Ji United States 23 1.3k 0.9× 1.0k 0.8× 425 0.9× 241 1.2× 278 1.8× 72 2.2k
Tobias Geiger Germany 18 1.1k 0.7× 914 0.7× 528 1.1× 186 0.9× 148 0.9× 32 1.5k
Soraya L. Moghazeh United States 20 1.5k 1.0× 1.8k 1.3× 544 1.1× 213 1.1× 223 1.4× 22 2.6k
Anne‐Kathrin Ziebandt Germany 11 1.0k 0.7× 822 0.6× 335 0.7× 204 1.0× 155 1.0× 12 1.4k
Chia Y. Lee United States 32 2.4k 1.6× 2.1k 1.6× 782 1.6× 338 1.7× 259 1.6× 55 3.0k
Ralph Bertram Germany 25 1.2k 0.8× 575 0.4× 697 1.4× 143 0.7× 345 2.2× 56 1.8k
Clarissa Pozzi United States 13 1.2k 0.8× 1.0k 0.8× 151 0.3× 318 1.6× 78 0.5× 15 1.6k
Devin L. Stauff United States 16 1.0k 0.7× 490 0.4× 387 0.8× 110 0.6× 135 0.9× 24 1.6k
Kati Seidl Switzerland 19 832 0.6× 934 0.7× 209 0.4× 127 0.6× 82 0.5× 34 1.3k
Rajan P. Adhikari United States 18 816 0.6× 942 0.7× 226 0.5× 162 0.8× 123 0.8× 29 1.2k

Countries citing papers authored by Thanh T. Luong

Since Specialization
Citations

This map shows the geographic impact of Thanh T. Luong'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 Thanh T. Luong with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thanh T. Luong more than expected).

Fields of papers citing papers by Thanh T. Luong

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thanh T. Luong. 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 Thanh T. Luong. The network helps show where Thanh T. Luong may publish in the future.

Co-authorship network of co-authors of Thanh T. Luong

This figure shows the co-authorship network connecting the top 25 collaborators of Thanh T. Luong. A scholar is included among the top collaborators of Thanh T. Luong 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 Thanh T. Luong. Thanh T. Luong 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.
Reghunathan, Meera, et al.. (2023). Deconstructing the Excellent Plastic Surgeon: A Survey of Key Attributes. Plastic & Reconstructive Surgery Global Open. 11(12). e5460–e5460. 2 indexed citations
2.
Reghunathan, Meera, et al.. (2023). A SWOT Analysis of Hot Topics in Plastic Surgery Resident Education: Consensus From the ACAPS 10th Annual Winter Meeting. Plastic & Reconstructive Surgery Global Open. 11(12). e5461–e5461. 4 indexed citations
3.
4.
Luong, Thanh T. & Carol H. Yan. (2023). Benign Paranasal Sinus Tumors. Current Otorhinolaryngology Reports. 11(3). 332–343.
5.
Lei, Mei G., et al.. (2019). MgrA Negatively Impacts Staphylococcus aureus Invasion by Regulating Capsule and FnbA. Infection and Immunity. 87(12). 9 indexed citations
6.
Gupta, Ravi, Thanh T. Luong, & Chia Y. Lee. (2015). RNAIII of the Staphylococcus aureus agr system activates global regulator MgrA by stabilizing mRNA. Proceedings of the National Academy of Sciences. 112(45). 14036–14041. 82 indexed citations
7.
Zielińska, A., Karen E. Beenken, Hwang‐Soo Joo, et al.. (2011). Defining the Strain-Dependent Impact of the Staphylococcal Accessory Regulator ( sarA ) on the Alpha-Toxin Phenotype of Staphylococcus aureus. Journal of Bacteriology. 193(12). 2948–2958. 68 indexed citations
8.
Zhu, Yefei, Renu Nandakumar, Marat R. Sadykov, et al.. (2011). RpiR Homologues May Link Staphylococcus aureus RNAIII Synthesis and Pentose Phosphate Pathway Regulation. Journal of Bacteriology. 193(22). 6187–6196. 43 indexed citations
9.
Majerczyk, Charlotte D., Paul M. Dunman, Thanh T. Luong, et al.. (2010). Direct Targets of CodY in Staphylococcus aureus. Journal of Bacteriology. 192(11). 2861–2877. 177 indexed citations
10.
Anderson, Kelsi L., Christelle M. Roux, Matthew W. Olson, et al.. (2010). Characterizing the effects of inorganic acid and alkaline shock on theStaphylococcus aureustranscriptome and messenger RNA turnover. FEMS Immunology & Medical Microbiology. 60(3). 208–250. 53 indexed citations
11.
Sadykov, Marat R., Thanh T. Luong, Yefei Zhu, et al.. (2010). Tricarboxylic Acid Cycle-Dependent Synthesis of Staphylococcus aureus Type 5 and 8 Capsular Polysaccharides. Journal of Bacteriology. 192(5). 1459–1462. 44 indexed citations
12.
Cue, David, Mei G. Lei, Thanh T. Luong, et al.. (2009). Rbf Promotes Biofilm Formation by Staphylococcus aureus via Repression of icaR , a Negative Regulator of icaADBC. Journal of Bacteriology. 191(20). 6363–6373. 81 indexed citations
13.
Jonsson, Ing‐Marie, Catharina Lindholm, Thanh T. Luong, Chia Y. Lee, & Andrej Tarkowski. (2008). mgrA regulates staphylococcal virulence important for induction and progression of septic arthritis and sepsis. Microbes and Infection. 10(12-13). 1229–1235. 28 indexed citations
14.
Luong, Thanh T. & Chia Y. Lee. (2007). Improved single-copy integration vectors for Staphylococcus aureus. Journal of Microbiological Methods. 70(1). 186–190. 66 indexed citations
16.
Luong, Thanh T. & Chia Y. Lee. (2006). The arl locus positively regulates Staphylococcus aureus type 5 capsule via an mgrA-dependent pathway. Microbiology. 152(10). 3123–3131. 77 indexed citations
17.
Ingavale, Susham S., Willem J. B. van Wamel, Thanh T. Luong, Chia Y. Lee, & Ambrose L. Cheung. (2005). Rat/MgrA, a Regulator of Autolysis, Is a Regulator of Virulence Genes in Staphylococcus aureus. Infection and Immunity. 73(3). 1423–1431. 129 indexed citations
18.
Lim, Yong, Malabendu Jana, Thanh T. Luong, & Chia Y. Lee. (2004). Control of Glucose- and NaCl-Induced Biofilm Formation by rbf in Staphylococcus aureus. Journal of Bacteriology. 186(3). 722–729. 161 indexed citations
19.
Luong, Thanh T., Shu Ouyang, Kelly Bush, & Chia Y. Lee. (2002). Type 1 Capsule Genes of Staphylococcus aureus Are Carried in a Staphylococcal Cassette Chromosome Genetic Element. Journal of Bacteriology. 184(13). 3623–3629. 73 indexed citations
20.
Luong, Thanh T., Subrata Sau, Marisa Anahí Gómez, Jean C. Lee, & Chia Y. Lee. (2002). Regulation of Staphylococcus aureus Capsular Polysaccharide Expression by agr and sarA. Infection and Immunity. 70(2). 444–450. 74 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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