Jue D. Wang

5.1k total citations
58 papers, 3.6k citations indexed

About

Jue D. Wang is a scholar working on Molecular Biology, Genetics and Materials Chemistry. According to data from OpenAlex, Jue D. Wang has authored 58 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 40 papers in Genetics and 18 papers in Materials Chemistry. Recurrent topics in Jue D. Wang's work include Bacterial Genetics and Biotechnology (39 papers), Enzyme Structure and Function (18 papers) and Bacteriophages and microbial interactions (15 papers). Jue D. Wang is often cited by papers focused on Bacterial Genetics and Biotechnology (39 papers), Enzyme Structure and Function (18 papers) and Bacteriophages and microbial interactions (15 papers). Jue D. Wang collaborates with scholars based in United States, China and Germany. Jue D. Wang's co-authors include Anjana Srivatsan, Alan D. Grossman, Ashley K. Tehranchi, Petra Anne Levin, Kuanqing Liu, Alycia N. Bittner, Glenn M. Sanders, Rui Chen, Yan Zhang and Christophe Herman and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Jue D. Wang

54 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jue D. Wang United States 32 2.8k 2.0k 771 417 348 58 3.6k
Philippe Bouloc France 31 2.4k 0.9× 1.7k 0.8× 839 1.1× 278 0.7× 299 0.9× 73 3.3k
Jan‐Willem De Gier Sweden 38 3.3k 1.2× 2.0k 1.0× 883 1.1× 272 0.7× 263 0.8× 68 4.2k
Douglas F. Browning United Kingdom 30 2.4k 0.9× 1.7k 0.9× 757 1.0× 267 0.6× 309 0.9× 71 3.6k
Ulrike Mäder Germany 38 2.7k 0.9× 1.5k 0.8× 954 1.2× 462 1.1× 198 0.6× 75 3.9k
Chris van der Does Germany 35 2.5k 0.9× 1.8k 0.9× 752 1.0× 272 0.7× 256 0.7× 78 3.4k
Charles L. Turnbough United States 39 3.2k 1.1× 1.7k 0.9× 1.2k 1.6× 353 0.8× 247 0.7× 80 4.1k
Pierre Genevaux France 31 2.5k 0.9× 1.1k 0.5× 548 0.7× 433 1.0× 304 0.9× 64 3.2k
Kürşad Turgay Germany 30 2.5k 0.9× 1.4k 0.7× 554 0.7× 607 1.5× 176 0.5× 45 3.1k
Alberto Marina Spain 32 2.4k 0.9× 980 0.5× 791 1.0× 389 0.9× 178 0.5× 82 3.3k
Gemma C. Atkinson Sweden 30 2.3k 0.8× 1.0k 0.5× 631 0.8× 180 0.4× 490 1.4× 62 3.1k

Countries citing papers authored by Jue D. Wang

Since Specialization
Citations

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

Fields of papers citing papers by Jue D. Wang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jue D. Wang. 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 Jue D. Wang. The network helps show where Jue D. Wang may publish in the future.

Co-authorship network of co-authors of Jue D. Wang

This figure shows the co-authorship network connecting the top 25 collaborators of Jue D. Wang. A scholar is included among the top collaborators of Jue D. Wang 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 Jue D. Wang. Jue D. Wang 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.
Anderson, Brent W., Wieland Steinchen, Danny K. Fung, et al.. (2025). Allosteric regulation of pyruvate kinase enables efficient and robust gluconeogenesis by preventing metabolic conflicts and carbon overflow. mSystems. 10(2). e0113124–e0113124. 1 indexed citations
2.
Fung, Danny K., Jin Yang, Jeremy W. Schroeder, et al.. (2025). A shared alarmone–GTP switch controls persister formation in bacteria. Nature Microbiology. 10(7). 1617–1629. 1 indexed citations
3.
Anderson, Brent W., Tippapha Pisithkul, Yanxiu Li, et al.. (2025). Pyruvate kinase directly generates GTP in glycolysis, supporting growth and contributing to guanosine toxicity. mBio. 16(4). e0379824–e0379824. 3 indexed citations
4.
Sandler, Michael, John T. Sauls, Jeremy W. Schroeder, et al.. (2024). Tools and methods for high-throughput single-cell imaging with the mother machine. eLife. 12. 1 indexed citations
5.
Wang, Jue D., et al.. (2024). MKAN-MMI: empowering traditional medicine-microbe interaction prediction with masked graph autoencoders and KANs. Frontiers in Pharmacology. 15. 1484639–1484639.
6.
Wang, Jue D., et al.. (2024). From dusty shelves toward the spotlight: growing evidence for Ap4A as an alarmone in maintaining RNA stability and proteostasis. Current Opinion in Microbiology. 81. 102536–102536.
7.
Sandler, Michael, John T. Sauls, Jeremy W. Schroeder, et al.. (2023). Tools and methods for high-throughput single-cell imaging with the mother machine. eLife. 12. 10 indexed citations
8.
Schroeder, Jeremy W., et al.. (2023). RNase H genes cause distinct impacts on RNA:DNA hybrid formation and mutagenesis genome wide. Science Advances. 9(30). eadi5945–eadi5945. 8 indexed citations
9.
Fung, Danny K., Jin Yang, Xiaoli Xu, et al.. (2022). Metabolic Promiscuity of an Orphan Small Alarmone Hydrolase Facilitates Bacterial Environmental Adaptation. mBio. 13(6). e0242222–e0242222. 6 indexed citations
10.
Steinchen, Wieland, Georg Hochberg, Jin Yang, et al.. (2022). Diadenosine tetraphosphate regulates biosynthesis of GTP in Bacillus subtilis. Nature Microbiology. 7(9). 1442–1452. 26 indexed citations
11.
Yang, Jin, et al.. (2022). Bacillus subtilis produces (p)ppGpp in response to the bacteriostatic antibiotic chloramphenicol to prevent its potential bactericidal effect. SHILAP Revista de lepidopterología. 1(2). 101–113. 13 indexed citations
12.
Anderson, Brent W., Maria A. Schumacher, Jin Yang, et al.. (2021). The nucleotide messenger (p)ppGpp is an anti-inducer of the purine synthesis transcription regulator PurR in Bacillus. Nucleic Acids Research. 50(2). 847–866. 30 indexed citations
13.
Updegrove, Taylor B., Vivek Anantharaman, Jin Yang, et al.. (2021). Reformulation of an extant ATPase active site to mimic ancestral GTPase activity reveals a nucleotide base requirement for function. eLife. 10. 16 indexed citations
14.
Yang, Jin, Brent W. Anderson, Asan Turdiev, et al.. (2020). The nucleotide pGpp acts as a third alarmone in Bacillus, with functions distinct from those of (p)ppGpp. Nature Communications. 11(1). 5388–5388. 45 indexed citations
15.
Schroeder, Jeremy W., et al.. (2020). The roles of replication-transcription conflict in mutagenesis and evolution of genome organization. PLoS Genetics. 16(8). e1008987–e1008987. 19 indexed citations
16.
Anderson, Brent W., et al.. (2019). Evolution of (p)ppGpp-HPRT regulation through diversification of an allosteric oligomeric interaction. eLife. 8. 34 indexed citations
17.
Vadia, Stephen, Rafael Lucena, Zhizhou Yang, et al.. (2017). Fatty Acid Availability Sets Cell Envelope Capacity and Dictates Microbial Cell Size. Current Biology. 27(12). 1757–1767.e5. 98 indexed citations
18.
Liu, Kuanqing, Alycia N. Bittner, & Jue D. Wang. (2015). Diversity in (p)ppGpp metabolism and effectors. Current Opinion in Microbiology. 24. 72–79. 141 indexed citations
19.
Zhang, Yan, Rachel A. Mooney, Jeffrey A. Grass, et al.. (2014). DksA Guards Elongating RNA Polymerase against Ribosome-Stalling-Induced Arrest. Molecular Cell. 53(5). 766–778. 53 indexed citations
20.
Wang, Jue D., et al.. (1996). ADENOVIRUS-MEDIATED GENE TRANSFER INTO RAT CARDIAC ALLOGRAFTS. Transplantation. 61(12). 1726–1729. 37 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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