Lee‐Jun Wong

1.0k total citations
28 papers, 762 citations indexed

About

Lee‐Jun Wong is a scholar working on Molecular Biology, Clinical Biochemistry and Epidemiology. According to data from OpenAlex, Lee‐Jun Wong has authored 28 papers receiving a total of 762 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 17 papers in Clinical Biochemistry and 4 papers in Epidemiology. Recurrent topics in Lee‐Jun Wong's work include Metabolism and Genetic Disorders (17 papers), Mitochondrial Function and Pathology (16 papers) and Biochemical and Molecular Research (5 papers). Lee‐Jun Wong is often cited by papers focused on Metabolism and Genetic Disorders (17 papers), Mitochondrial Function and Pathology (16 papers) and Biochemical and Molecular Research (5 papers). Lee‐Jun Wong collaborates with scholars based in United States, United Arab Emirates and Switzerland. Lee‐Jun Wong's co-authors include David Dimmock, Victor Venegas, Jing Wang, Fernando Scaglia, Perry A. Frey, I A Rose, Richard A. Lewis, Marwan Shinawi, Aziz Shaibani and Ayman W. El‐Hattab and has published in prestigious journals such as Journal of Biological Chemistry, Hepatology and Biochemistry.

In The Last Decade

Lee‐Jun Wong

28 papers receiving 735 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lee‐Jun Wong United States	17	525	344	80	76	73	28	762
Yanling Yang China	17	576 1.1×	373 1.1×	46 0.6×	97 1.3×	125 1.7×	56	856
Shlomo Almashanu Israel	16	390 0.7×	271 0.8×	128 1.6×	134 1.8×	67 0.9×	45	838
Catherine Brunel‐Guitton Canada	14	454 0.9×	203 0.6×	66 0.8×	41 0.5×	57 0.8×	28	621
Marinus Duran Netherlands	9	584 1.1×	232 0.7×	86 1.1×	44 0.6×	43 0.6×	9	732
Sunita Bijarnia‐Mahay India	13	257 0.5×	241 0.7×	75 0.9×	133 1.8×	65 0.9×	63	522
Cristina Amat Di San Filippo United States	13	554 1.1×	594 1.7×	178 2.2×	134 1.8×	115 1.6×	13	858
Jun Ye China	15	312 0.6×	305 0.9×	127 1.6×	105 1.4×	156 2.1×	50	590
J. M. Saudubray France	18	717 1.4×	615 1.8×	164 2.0×	100 1.3×	93 1.3×	49	1.0k
Zuhair Rahbeeni Saudi Arabia	18	537 1.0×	453 1.3×	152 1.9×	150 2.0×	110 1.5×	63	989
Hélène Ogier France	13	443 0.8×	415 1.2×	292 3.6×	76 1.0×	113 1.5×	16	877

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

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20 of 20 papers shown

Wang, Yongxing, Miguel M. Leiva‐Juárez, Lisandra Vila Ellis, et al.. (2023). Antimicrobial mitochondrial reactive oxygen species induction by lung epithelial immunometabolic modulation. PLoS Pathogens. 19(9). e1011138–e1011138. 3 indexed citations

Demirbas, Didem, David J. Harris, Pamela Arn, et al.. (2019). Phenotypic variability in deficiency of the α subunit of succinate‐CoA ligase. JIMD Reports. 46(1). 63–69. 7 indexed citations

Wong, Lee‐Jun, et al.. (2014). PTU-115 Identifying Nafld In Patients Attending A Lipid Clinic – Do Non-invasive Scoring Systems For Fibrosis Have A Role?. Gut. 63(Suppl 1). A89.2–A90. 1 indexed citations

Shaibani, Aziz, Lee‐Jun Wong, Victor Wei Zhang, Richard A. Lewis, & Marwan Shinawi. (2014). Autosomal recessive posterior column ataxia with retinitis pigmentosa caused by novel mutations in theFLVCR1gene. International Journal of Neuroscience. 125(1). 43–49. 22 indexed citations

Bhoj, Elizabeth, M. Li, Rebecca C. Ahrens‐Nicklas, et al.. (2014). Pathologic Variants of the Mitochondrial Phosphate Carrier SLC25A3: Two New Patients and Expansion of the Cardiomyopathy/Skeletal Myopathy Phenotype With and Without Lactic Acidosis. JIMD Reports. 19. 59–66. 34 indexed citations

Wong, Lee‐Jun, et al.. (2014). A novel EBP c.224T>A mutation supports the existence of a male‐specific disorder independent of CDPX2. American Journal of Medical Genetics Part A. 164(7). 1642–1647. 9 indexed citations

Wang, Jing, Guoli Wang, Soledad Kleppe, et al.. (2013). Biochemical, molecular, and clinical diagnoses of patients with cerebral creatine deficiency syndromes. Molecular Genetics and Metabolism. 109(3). 260–268. 29 indexed citations

Wong, Lee‐Jun. (2012). Mitochondrial Syndromes with Leukoencephalopathies. Seminars in Neurology. 32(1). 55–61. 45 indexed citations

Brunetti‐Pierri, Nicola, Ricardo H. Pignatelli, Jeffrey A. Towbin, et al.. (2011). Dilation of the aortic root in mitochondrial disease patients. Molecular Genetics and Metabolism. 103(2). 167–170. 19 indexed citations

10.

Schaaf, Christian P., Maria Blazo, Richard A. Lewis, et al.. (2011). Early-onset severe neuromuscular phenotype associated with compound heterozygosity for OPA1 mutations. Molecular Genetics and Metabolism. 103(4). 383–387. 56 indexed citations

11.

Huang, Jee‐Fu, Yi‐Chu Liao, Renkui Bai, et al.. (2011). Mitochondrial polymorphism 12361A>G is associated with nonalcoholic fatty liver disease. Translational research. 159(1). 58–59. 11 indexed citations

12.

Wang, Jing, Victor Venegas, Fangyuan Li, & Lee‐Jun Wong. (2011). Analysis of Mitochondrial DNA Point Mutation Heteroplasmy by ARMS Quantitative PCR. Current Protocols in Human Genetics. 68(1). Unit 19.6.–Unit 19.6.. 28 indexed citations

13.

Venegas, Victor, Jing Wang, David Dimmock, & Lee‐Jun Wong. (2011). Real‐Time Quantitative PCR Analysis of Mitochondrial DNA Content. Current Protocols in Human Genetics. 68(1). Unit 19.7.–Unit 19.7.. 109 indexed citations

14.

El‐Hattab, Ayman W., Fangyuan Li, Joseph Shen, et al.. (2010). Maternal systemic primary carnitine deficiency uncovered by newborn screening: Clinical, biochemical, and molecular aspects. Genetics in Medicine. 12(1). 19–24. 81 indexed citations

15.

Shchelochkov, Oleg A., Lee‐Jun Wong, Aziz Shaibani, & Marwan Shinawi. (2009). Atypical presentation of VLCAD deficiency associated with a novel ACADVL splicing mutation. Muscle & Nerve. 39(3). 374–382. 17 indexed citations

16.

Edwards, Rebecca L., et al.. (2009). Long‐term neurodevelopmental effects of early detection and treatment in a 6‐year‐old patient with argininaemia diagnosed by newborn screening. Journal of Inherited Metabolic Disease. 32(S1). 197–200. 14 indexed citations

17.

Dimmock, David, Annette Feigenbaum, Rita Horváth, et al.. (2008). Abnormal Neurological Features Predict Poor Survival and Should Preclude Liver Transplantation in Patients with Deoxyguanosine Kinase Deficiency. Liver Transplantation. 14(10). 1480–1485. 56 indexed citations

18.

Johnston, Jennifer J., Uta Lichter‐Konecki, Elizabeth Wilson, et al.. (2004). Discordant PKU phenotype in one family due to disparate genotypes and a novel mutation. Journal of Inherited Metabolic Disease. 27(2). 157–163. 4 indexed citations

19.

Baidas, Said, et al.. (2003). Constitutional trisomy 8 mosaicism due to meiosis II non‐disjunction in a phenotypically normal woman with hematologic abnormalities. American Journal of Medical Genetics Part A. 124A(4). 383–387. 13 indexed citations

20.

Rose, I A, J V Warms, & Lee‐Jun Wong. (1977). Inhibitors of glucose-1,6-bisphosphate synthase.. Journal of Biological Chemistry. 252(12). 4262–4268. 21 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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