Lee‐Jun Wong - Concepedia

Author

Lee‐Jun Wong

Baylor College of Medicine

Also Known As

L J Wong, L Wong, L ‐J. C. Wong, L. J. Wong, L. Wong, L.-J. Wong, L.J.C. Wong, Lee-Jun Wong, Lee‐Jun Wong

Publications

Citations

H-Index

Concepts

All Affiliations

Baylor College of Medicine Baylor Genetics Fox Chase Cancer Center Medical College of Wisconsin

About

Lee‐Jun Wong is an author at Baylor College of Medicine specializing in medicine, genetics, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	544
2	Natural Sciences	4	4	143
3	Engineering	2	2	161
4	Public Health	2	2	124
5	Health Sciences	1	1	19

Lee‐Jun Wong

Publications

845

Citations

H-Index

Page 1

	Year	Citations
Real‐Time Quantitative PCR Analysis of Mitochondrial DNA Content Victor Venegas, Jing Wang, David Dimmock, Current Protocols in Human Genetics DnaEngineeringGeneticsDna AnalysisMolecular Biology	2011	132
Maternal systemic primary carnitine deficiency uncovered by newborn screening: Clinical, biochemical, and molecular aspects Ayman W. El‐Hattab, Fangyuan Li, Joseph Shen, Genetics in Medicine NutritionNewborn ScreeningPediatricsMaternal HealthMolecular Aspects	2010	107
Early-onset severe neuromuscular phenotype associated with compound heterozygosity for OPA1 mutations Christian P. Schaaf, Maria Blazo, Richard A. Lewis, Molecular Genetics and Metabolism Systems BiologyMendelian DisorderGenetic DisorderMedicineGenetics	2011	83
Galactose-1-phosphate uridylyltransferase. Rate studies confirming a uridylyl-enzyme intermediate on the catalytic pathway Lee‐Jun Wong, Perry A. Frey Biochemistry GlycobiologyAltmetric Attention ScoreMolecular BiologySecondary MetaboliteChemical Biology	1974	51
Extensive investigations of mitochondrial DNA genome in treated HIV-infected subjects: beyond mitochondrial DNA depletion. Grace A. McComsey, Renkui Bai, Jen‐Fue Maa, PubMed	2005	51
Pathologic Variants of the Mitochondrial Phosphate Carrier SLC25A3: Two New Patients and Expansion of the Cardiomyopathy/Skeletal Myopathy Phenotype With and Without Lactic Acidosis Elizabeth Bhoj, M. Li, Rebecca C. Ahrens‐Nicklas, JIMD Reports	2014	48
Small heterodimer partner deletion prevents hepatic steatosis and when combined with farnesoid X receptor loss protects against type 2 diabetes in mice Oludemilade Akinrotimi, Ryan Riessen, Philip VanDuyne, Hepatology	2017	45
Biochemical, molecular, and clinical diagnoses of patients with cerebral creatine deficiency syndromes Matthew S. Comeaux, Jing Wang, Guoli Wang, Molecular Genetics and Metabolism Neurological DisorderPhysiologyNutritional NeuroscienceBrain InjuryNeurology	2013	43
Analysis of Mitochondrial DNA Point Mutation Heteroplasmy by ARMS Quantitative PCR Jing Wang, Victor Venegas, Fangyuan Li, Current Protocols in Human Genetics DnaGeneticsDna AnalysisMolecular BiologyPathology	2011	37
Autosomal recessive posterior column ataxia with retinitis pigmentosa caused by novel mutations in the<i>FLVCR1</i>gene Aziz Shaibani, Lee‐Jun Wong, Victor Wei Zhang, International Journal of Neuroscience	2014	33

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