Thomas J. Lie

2.1k total citations
27 papers, 1.4k citations indexed

About

Thomas J. Lie is a scholar working on Molecular Biology, Biochemistry and Building and Construction. According to data from OpenAlex, Thomas J. Lie has authored 27 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Biochemistry and 7 papers in Building and Construction. Recurrent topics in Thomas J. Lie's work include Amino Acid Enzymes and Metabolism (7 papers), Anaerobic Digestion and Biogas Production (7 papers) and Metalloenzymes and iron-sulfur proteins (5 papers). Thomas J. Lie is often cited by papers focused on Amino Acid Enzymes and Metabolism (7 papers), Anaerobic Digestion and Biogas Production (7 papers) and Metalloenzymes and iron-sulfur proteins (5 papers). Thomas J. Lie collaborates with scholars based in United States, China and Czechia. Thomas J. Lie's co-authors include John A. Leigh, Edward R. Leadbetter, Kyle C. Costa, Kristina L. Hillesland, Sergey Stolyar, David A. Stahl, Nicolás Pinel, Walter Godchaux, Jared R. Leadbetter and Murray Hackett and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Applied and Environmental Microbiology.

In The Last Decade

Thomas J. Lie

26 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
Thomas J. Lie United States 18 810 338 277 272 262 27 1.4k
Kyle C. Costa United States 17 517 0.6× 334 1.0× 313 1.1× 159 0.6× 223 0.9× 34 1.0k
Nicolai Müller Germany 18 474 0.6× 374 1.1× 194 0.7× 181 0.7× 165 0.6× 31 1.0k
John C. Willison France 25 862 1.1× 233 0.7× 351 1.3× 146 0.5× 99 0.4× 46 1.7k
Housna Mouttaki United States 16 499 0.6× 334 1.0× 361 1.3× 197 0.7× 222 0.8× 19 1.3k
Cheryl Ingram‐Smith United States 16 562 0.7× 279 0.8× 147 0.5× 145 0.5× 158 0.6× 34 1.0k
Sandra Baena Colombia 19 638 0.8× 182 0.5× 590 2.1× 241 0.9× 286 1.1× 38 1.5k
Anita S. Gößner Germany 12 438 0.5× 237 0.7× 221 0.8× 220 0.8× 129 0.5× 14 952
Somkiet Techkarnjanaruk Thailand 19 278 0.3× 220 0.7× 190 0.7× 249 0.9× 140 0.5× 34 1.0k
Kai Schuchmann Germany 14 1.1k 1.4× 457 1.4× 194 0.7× 538 2.0× 155 0.6× 14 2.0k
Ginro Endo Japan 22 339 0.4× 392 1.2× 305 1.1× 328 1.2× 173 0.7× 64 1.6k

Countries citing papers authored by Thomas J. Lie

Since Specialization
Citations

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

Fields of papers citing papers by Thomas J. Lie

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas J. Lie. 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 Thomas J. Lie. The network helps show where Thomas J. Lie may publish in the future.

Co-authorship network of co-authors of Thomas J. Lie

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas J. Lie. A scholar is included among the top collaborators of Thomas J. Lie 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 Thomas J. Lie. Thomas J. Lie 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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2.
3.
Lie, Thomas J., et al.. (2022). A Genetic Study of Nif -Associated Genes in a Hyperthermophilic Methanogen. Microbiology Spectrum. 10(1). e0209321–e0209321. 9 indexed citations
4.
Ma, Hongyu, et al.. (2020). Promoting photo-fermentative hydrogen production performance by substituting the rnf promoter in Rhodobacter capsulatus. International Journal of Hydrogen Energy. 46(5). 3742–3752. 17 indexed citations
5.
Yoon, Sung Ho, Serdar Turkarslan, David J. Reiss, et al.. (2013). A systems level predictive model for global gene regulation of methanogenesis in a hydrogenotrophic methanogen. Genome Research. 23(11). 1839–1851. 30 indexed citations
6.
Costa, Kyle C., Thomas J. Lie, Xia Qin, & John A. Leigh. (2013). VhuD Facilitates Electron Flow from H 2 or Formate to Heterodisulfide Reductase in Methanococcus maripaludis. Journal of Bacteriology. 195(22). 5160–5165. 40 indexed citations
7.
Costa, Kyle C., Thomas J. Lie, Michael A. Jacobs, & John A. Leigh. (2013). H 2 -Independent Growth of the Hydrogenotrophic Methanogen Methanococcus maripaludis. mBio. 4(2). 33 indexed citations
8.
Lie, Thomas J., Kyle C. Costa, Boguslaw Lupa, et al.. (2012). Essential anaplerotic role for the energy-converting hydrogenase Eha in hydrogenotrophic methanogenesis. Proceedings of the National Academy of Sciences. 109(38). 15473–15478. 95 indexed citations
9.
Costa, Kyle C., Tiansong Wang, Thomas J. Lie, et al.. (2010). Protein complexing in a methanogen suggests electron bifurcation and electron delivery from formate to heterodisulfide reductase. Proceedings of the National Academy of Sciences. 107(24). 11050–11055. 157 indexed citations
10.
Wisedchaisri, Goragot, David M. Dranow, Thomas J. Lie, et al.. (2010). Structural Underpinnings of Nitrogen Regulation by the Prototypical Nitrogen-Responsive Transcriptional Factor NrpR. Structure. 18(11). 1512–1521. 10 indexed citations
11.
Xia, Qiangwei, Tiansong Wang, Erik L. Hendrickson, et al.. (2009). Quantitative proteomics of nutrient limitation in the hydrogenotrophic methanogen Methanococcus maripaludis. BMC Microbiology. 9(1). 149–149. 51 indexed citations
12.
Lie, Thomas J., et al.. (2009). Overlapping repressor binding sites regulate expression of the Methanococcus maripaludis glnK1 operon. Molecular Microbiology. 75(3). 755–762. 15 indexed citations
13.
Lie, Thomas J., Jeremy A. Dodsworth, David C. Nickle, & John A. Leigh. (2007). Diverse homologues of the archaeal repressor NrpR function similarly in nitrogen regulation. FEMS Microbiology Letters. 271(2). 281–288. 19 indexed citations
14.
Lie, Thomas J., Gwendolyn E. Wood, & John A. Leigh. (2004). Regulation of nif Expression in Methanococcus maripaludis. Journal of Biological Chemistry. 280(7). 5236–5241. 80 indexed citations
15.
Backe, Bjørn, Torhild Heggestad, & Thomas J. Lie. (2003). Har keisersnittsepidemien nådd Norge. Tidsskrift for Den Norske Laegeforening. 2 indexed citations
16.
Backe, Bjørn, Torhild Heggestad, & Thomas J. Lie. (2003). [The epidemic of Caesarean section: has it reached Norway?].. PubMed. 123(11). 1522–4. 9 indexed citations
17.
Lie, Thomas J. & John A. Leigh. (2002). Regulatory Response of Methanococcus maripaludis to Alanine, an Intermediate Nitrogen Source. Journal of Bacteriology. 184(19). 5301–5306. 38 indexed citations
18.
Lie, Thomas J., Walter Godchaux, & Edward R. Leadbetter. (2000). Sulfonates as Terminal Electron Acceptors for Growth of Sulfite-Reducing Bacteria ( Desulfitobacterium spp.) and Sulfate-Reducing Bacteria: Effects of Inhibitors of Sulfidogenesis. Applied and Environmental Microbiology. 66(6). 2693–2693. 3 indexed citations
19.
Lie, Thomas J., Jared R. Leadbetter, & Edward R. Leadbetter. (1998). Metabolism of sulfonic acids and other organosulfur compounds by sulfate‐reducing bacteria. Geomicrobiology Journal. 15(2). 135–149. 47 indexed citations
20.
Lie, Thomas J., Thomas P. Pitta, Edward R. Leadbetter, Walter Godchaux, & Jared R. Leadbetter. (1996). Sulfonates: novel electron acceptors in anaerobic respiration. Archives of Microbiology. 166(3). 204–210. 80 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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