Hieu Vu

3.1k total citations · 1 hit paper
30 papers, 1.6k citations indexed

About

Hieu Vu is a scholar working on Molecular Biology, Biochemistry and Cancer Research. According to data from OpenAlex, Hieu Vu has authored 30 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 13 papers in Biochemistry and 6 papers in Cancer Research. Recurrent topics in Hieu Vu's work include Lipid metabolism and biosynthesis (12 papers), Metabolomics and Mass Spectrometry Studies (7 papers) and Cancer, Hypoxia, and Metabolism (6 papers). Hieu Vu is often cited by papers focused on Lipid metabolism and biosynthesis (12 papers), Metabolomics and Mass Spectrometry Studies (7 papers) and Cancer, Hypoxia, and Metabolism (6 papers). Hieu Vu collaborates with scholars based in United States, China and Canada. Hieu Vu's co-authors include John Blenis, David Shahbazian, Michael S. Cohen, Philippe P. Roux, Jack Taunton, Marina K. Holz, Nahum Sonenberg, Ruth Welti, Mary R. Roth and Lewis C. Cantley and has published in prestigious journals such as Cell, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Hieu Vu

28 papers receiving 1.6k citations

Hit Papers

RAS/ERK Signaling Promote... 2007 2026 2013 2019 2007 100 200 300 400 500

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Hieu Vu 1.1k 272 264 224 148 30 1.6k
Xiaoming Gong 743 0.7× 212 0.8× 96 0.4× 156 0.7× 118 0.8× 47 1.4k
Werner J. Kovacs 1.4k 1.3× 155 0.6× 185 0.7× 378 1.7× 276 1.9× 42 2.1k
Philipp Ternes 1.4k 1.2× 364 1.3× 320 1.2× 78 0.3× 271 1.8× 31 1.9k
Isabelle Riezman 1.2k 1.0× 207 0.8× 153 0.6× 161 0.7× 158 1.1× 22 1.6k
Yasuyuki Fujimoto 752 0.7× 561 2.1× 183 0.7× 90 0.4× 228 1.5× 40 1.4k
Pasquale Scarcia 1.5k 1.4× 182 0.7× 85 0.3× 148 0.7× 290 2.0× 30 1.8k
Amy K. Walker 1.1k 1.0× 171 0.6× 83 0.3× 134 0.6× 202 1.4× 29 1.6k
Xin Gu 1.5k 1.4× 83 0.3× 205 0.8× 208 0.9× 228 1.5× 34 2.1k
André S. Bachmann 1.9k 1.7× 278 1.0× 250 0.9× 191 0.9× 48 0.3× 82 2.4k
Xiaojie Li 2.1k 1.9× 85 0.3× 564 2.1× 244 1.1× 152 1.0× 88 2.8k

Countries citing papers authored by Hieu Vu

Since Specialization
Citations

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

Fields of papers citing papers by Hieu Vu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hieu Vu. 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 Hieu Vu. The network helps show where Hieu Vu may publish in the future.

Co-authorship network of co-authors of Hieu Vu

This figure shows the co-authorship network connecting the top 25 collaborators of Hieu Vu. A scholar is included among the top collaborators of Hieu Vu 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 Hieu Vu. Hieu Vu 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.
Chamseddin, Bahir, Hieu Vu, Divya Srivastava, et al.. (2025). Metabolic profiles of cutaneous lupus have abnormalities in the nicotinamide adenine dinucleotide pathway. Lupus Science & Medicine. 12(1). e001401–e001401.
2.
Mukherjee, Abir, Divya Bezwada, Francesco Greco, et al.. (2023). Adipocytes reprogram cancer cell metabolism by diverting glucose towards glycerol-3-phosphate thereby promoting metastasis. Nature Metabolism. 5(9). 1563–1577. 30 indexed citations
3.
Webb, Bryn D., Sara M. Nowinski, Ashley Solmonson, et al.. (2023). Recessive pathogenic variants in MCAT cause combined oxidative phosphorylation deficiency. eLife. 12. 4 indexed citations
4.
Yang, Chendong, Carlos Caro, Hieu Vu, et al.. (2023). New insights in the targets of action of dimethyl fumarate in endothelial cells: effects on energetic metabolism and serine synthesis in vitro and in vivo. Communications Biology. 6(1). 1084–1084. 6 indexed citations
5.
Chen, Rui, Jipeng Wang, Hieu Vu, et al.. (2022). A male-derived nonribosomal peptide pheromone controls female schistosome development. Cell. 185(9). 1506–1520.e17. 30 indexed citations
6.
Parida, Pravat Kumar, Akash Kaushik, Vidhya R. Nair, et al.. (2022). Optimized protocol for stable isotope tracing and steady-state metabolomics in mouse HER2+ breast cancer brain metastasis. STAR Protocols. 3(2). 101345–101345.
7.
Kasuga, Ikuro, Aki Hirabayashi, Hieu Vu, et al.. (2022). Emergence of mobile tigecycline resistance gene tet(X4)-harbouring Shewanella xiamenensis in a water environment. Journal of Global Antimicrobial Resistance. 28. 140–142. 15 indexed citations
8.
Gu, Zhimin, Gen Zhang, Richard Wynn, et al.. (2022). Metabolon formation regulates branched-chain amino acid oxidation and homeostasis. Nature Metabolism. 4(12). 1775–1791. 22 indexed citations
9.
Liao, Chengheng, Cherise Ryan Glodowski, Cheng Fan, et al.. (2021). Integrated Metabolic Profiling and Transcriptional Analysis Reveals Therapeutic Modalities for Targeting Rapidly Proliferating Breast Cancers. Cancer Research. 82(4). 665–680. 19 indexed citations
10.
Pachnis, Panayotis, Alpaslan Tasdogan, Brandon Faubert, et al.. (2021). Isotope tracing reveals glycolysis and oxidative metabolism in childhood tumors of multiple histologies. Med. 2(4). 395–410.e4. 29 indexed citations
11.
Tran, Diem Hong, R. Kesavan, Mona Hoseini Soflaee, et al.. (2021). Mitochondrial NADP+ is essential for proline biosynthesis during cell growth. Nature Metabolism. 3(4). 571–585. 75 indexed citations
12.
Conn, Crystal S., Haojun Yang, Kenji Ikeda, et al.. (2021). The major cap-binding protein eIF4E regulates lipid homeostasis and diet-induced obesity. Nature Metabolism. 3(2). 244–257. 36 indexed citations
13.
Song, Yu, Hieu Vu, Sunitha Shiva, et al.. (2020). A Lipidomic Approach to Identify Cold-Induced Changes in Arabidopsis Membrane Lipid Composition. Methods in molecular biology. 187–202. 3 indexed citations
14.
Xiong, Nanxiang, Xiaofei Gao, Hongyang Zhao, et al.. (2020). Using arterial–venous analysis to characterize cancer metabolic consumption in patients. Nature Communications. 11(1). 3169–3169. 30 indexed citations
16.
Massaro, C. Flavia, Mohammad Katouli, Tanja Grkovic, et al.. (2014). Anti-staphylococcal activity of C-methyl flavanones from propolis of Australian stingless bees (Tetragonula carbonaria) and fruit resins of Corymbia torelliana (Myrtaceae). Fitoterapia. 95. 247–257. 76 indexed citations
17.
Shiva, Sunitha, et al.. (2013). Lipidomic Analysis of Plant Membrane Lipids by Direct Infusion Tandem Mass Spectrometry. Methods in molecular biology. 1009. 79–91. 37 indexed citations
18.
Yang, Wenyu, Yong Zheng, Sung Chul Bahn, et al.. (2012). The Patatin-Containing Phospholipase A pPLAIIα Modulates Oxylipin Formation and Water Loss in Arabidopsis thaliana. Molecular Plant. 5(2). 452–460. 64 indexed citations
19.
Choo, Andrew Y., Sang Gyun Kim, Matthew G. Vander Heiden, et al.. (2010). Glucose Addiction of TSC Null Cells Is Caused by Failed mTORC1-Dependent Balancing of Metabolic Demand with Supply. Molecular Cell. 38(4). 487–499. 204 indexed citations
20.
Roux, Philippe P., David Shahbazian, Hieu Vu, et al.. (2007). RAS/ERK Signaling Promotes Site-specific Ribosomal Protein S6 Phosphorylation via RSK and Stimulates Cap-dependent Translation. Journal of Biological Chemistry. 282(19). 14056–14064. 575 indexed citations breakdown →

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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