Lee-Jun Wong

5.4k total citations
59 papers, 2.6k citations indexed

About

Lee-Jun Wong is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Lee-Jun Wong has authored 59 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 30 papers in Clinical Biochemistry and 6 papers in Rheumatology. Recurrent topics in Lee-Jun Wong's work include Mitochondrial Function and Pathology (31 papers), Metabolism and Genetic Disorders (30 papers) and ATP Synthase and ATPases Research (11 papers). Lee-Jun Wong is often cited by papers focused on Mitochondrial Function and Pathology (31 papers), Metabolism and Genetic Disorders (30 papers) and ATP Synthase and ATPases Research (11 papers). Lee-Jun Wong collaborates with scholars based in United States, Taiwan and Canada. Lee-Jun Wong's co-authors include Margherita Milone, Robert K. Naviaux, Russell P. Saneto, Dinithi Senadheera, Richard Haas, Shulin Zhang, Marni J. Falk, Sumit Parikh, Nicole I. Wolf and Victor Wei Zhang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Annals of Internal Medicine.

In The Last Decade

Lee-Jun Wong

59 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lee-Jun Wong United States 28 1.8k 1.1k 377 203 199 59 2.6k
Yolanda Campos Spain 31 1.9k 1.0× 1.1k 1.0× 274 0.7× 105 0.5× 292 1.5× 118 2.7k
Khaled K. Abu‐Amero Saudi Arabia 33 1.7k 0.9× 379 0.4× 791 2.1× 250 1.2× 137 0.7× 184 4.0k
Majid Alfadhel Saudi Arabia 28 1.4k 0.7× 625 0.6× 920 2.4× 301 1.5× 232 1.2× 157 2.5k
Garry K. Brown United Kingdom 39 2.8k 1.5× 2.2k 2.0× 333 0.9× 210 1.0× 363 1.8× 91 3.8k
Maria Alice Donati Italy 31 2.5k 1.3× 1.4k 1.3× 334 0.9× 319 1.6× 915 4.6× 136 3.9k
Ulrika von Döbeln Sweden 31 1.3k 0.7× 919 0.9× 456 1.2× 235 1.2× 270 1.4× 79 2.4k
Sebastian Gidlöf Sweden 20 2.0k 1.1× 631 0.6× 176 0.5× 207 1.0× 539 2.7× 41 3.1k
Irini Manoli United States 26 1.0k 0.6× 541 0.5× 281 0.7× 149 0.7× 346 1.7× 58 2.0k
Katrina M. Dipple United States 24 1.1k 0.6× 265 0.2× 466 1.2× 123 0.6× 272 1.4× 66 1.9k
Donald R. Dunbar United Kingdom 23 1.0k 0.6× 272 0.3× 215 0.6× 87 0.4× 197 1.0× 37 2.6k

Countries citing papers authored by Lee-Jun Wong

Since Specialization
Citations

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

Fields of papers citing papers by Lee-Jun Wong

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lee-Jun Wong. 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 Lee-Jun Wong. The network helps show where Lee-Jun Wong may publish in the future.

Co-authorship network of co-authors of Lee-Jun Wong

This figure shows the co-authorship network connecting the top 25 collaborators of Lee-Jun Wong. A scholar is included among the top collaborators of Lee-Jun Wong 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 Lee-Jun Wong. Lee-Jun Wong 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.
Wang, Julia, Emily Kim, Hannes Vogel, et al.. (2018). Clinical and molecular spectrum of thymidine kinase 2-related mtDNA maintenance defect. Molecular Genetics and Metabolism. 124(2). 124–130. 26 indexed citations
2.
Wang, Jing, Victor Wei Zhang, Tian Xia, et al.. (2015). Capture-based high-coverage NGS: a powerful tool to uncover a wide spectrum of mutation types. Genetics in Medicine. 18(5). 513–521. 21 indexed citations
3.
Granadillo, Jorge L., et al.. (2014). Early onset and severe clinical course associated with the m.5540G>A mutation in MT-TW. Molecular Genetics and Metabolism Reports. 1. 61–65. 3 indexed citations
4.
Burrage, Lindsay C., Sha Tang, Jing Wang, et al.. (2014). Mitochondrial myopathy, lactic acidosis, and sideroblastic anemia (MLASA) plus associated with a novel de novo mutation (m.8969G>A) in the mitochondrial encoded ATP6 gene. Molecular Genetics and Metabolism. 113(3). 207–212. 52 indexed citations
5.
Chanprasert, Sirisak, Jing Wang, Gregory M. Enns, et al.. (2013). Molecular and clinical characterization of the myopathic form of mitochondrial DNA depletion syndrome caused by mutations in the thymidine kinase (TK2) gene. Molecular Genetics and Metabolism. 110(1-2). 153–161. 27 indexed citations
6.
Milone, Margherita & Lee-Jun Wong. (2013). Diagnosis of mitochondrial myopathies. Molecular Genetics and Metabolism. 110(1-2). 35–41. 55 indexed citations
7.
Massie, Rami, Jing Wang, Victor Wei Zhang, et al.. (2012). Mitochondrial myopathy due to novel missense mutation in the cytochrome c oxidase 1 gene. Journal of the Neurological Sciences. 319(1-2). 158–163. 6 indexed citations
8.
Tu, Yi‐Fang, Benny Abraham Kaipparettu, Yewei Ma, & Lee-Jun Wong. (2011). Mitochondria of highly metastatic breast cancer cell line MDA-MB-231 exhibits increased autophagic properties. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1807(9). 1125–1132. 38 indexed citations
9.
Tang, Sha, Elliot L. Dimberg, Margherita Milone, & Lee-Jun Wong. (2011). Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)-like phenotype: an expanded clinical spectrum of POLG1 mutations. Journal of Neurology. 259(5). 862–868. 49 indexed citations
10.
Thorburn, David R., Lee-Jun Wong, Georgirene D. Vladutiu, et al.. (2011). Quality improvement of mitochondrial respiratory chain complex enzyme assays using Caenorhabditis elegans. Genetics in Medicine. 13(9). 794–799. 17 indexed citations
11.
Wiszniewska, Joanna, Mark Lipson, David R. Witt, et al.. (2011). Detection of uniparental isodisomy in autosomal recessive mitochondrial DNA depletion syndrome by high-density SNP array analysis. Journal of Human Genetics. 56(12). 834–839. 16 indexed citations
12.
Wang, Guo-Li, Jing Wang, Ganka Douglas, et al.. (2011). Expanded molecular features of carnitine acyl-carnitine translocase (CACT) deficiency by comprehensive molecular analysis. Molecular Genetics and Metabolism. 103(4). 349–357. 23 indexed citations
13.
El‐Hattab, Ayman W., et al.. (2009). MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome: New patients and novel mutations. Molecular Genetics and Metabolism. 99(3). 300–308. 59 indexed citations
14.
Zhang, Shulin, Harold N. Bass, Amber N. Pursley, et al.. (2009). Application of oligonucleotide array CGH to the simultaneous detection of a deletion in the nuclear TK2 gene and mtDNA depletion. Molecular Genetics and Metabolism. 99(1). 53–57. 14 indexed citations
15.
Shaibani, Aziz, Oleg A. Shchelochkov, Shulin Zhang, et al.. (2009). Mitochondrial Neurogastrointestinal Encephalopathy Due to Mutations in RRM2B. Archives of Neurology. 66(8). 1028–32. 89 indexed citations
16.
Brunetti‐Pierri, Nicola, Aziz Shaibani, Shulin Zhang, Lee-Jun Wong, & Marwan Shinawi. (2009). Progressive Myopathy With Multiple Symmetric Lipomatosis. Archives of Neurology. 66(12). 1576–7. 2 indexed citations
17.
Dimmock, David, Bruno Maranda, Carlo Dionisi‐Vici, et al.. (2008). Citrin deficiency, a perplexing global disorder. Molecular Genetics and Metabolism. 96(1). 44–49. 77 indexed citations
18.
Wong, Lee-Jun, et al.. (2006). AIB1 gene amplification and the instability of polyQ encoding sequence in breast cancer cell lines. BMC Cancer. 6(1). 111–111. 11 indexed citations
19.
Vladutiu, Georgirene D., Michael J. Bennett, David Smail, et al.. (2000). A Variable Myopathy Associated with Heterozygosity for the R503C Mutation in the Carnitine Palmitoyltransferase II Gene. Molecular Genetics and Metabolism. 70(2). 134–141. 44 indexed citations
20.
Wertz, Karin, et al.. (1998). 3849 + 10 kb C → T Splicing Mutation in Hispanic CF Patients. Molecular Genetics and Metabolism. 64(3). 213–216. 9 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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