| Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
| 2016 | 3-O-methyldopa levels in newborns: Result of newborn screening for aromatic L-amino-acid decarboxylase deficiency | Chien Y.-H.; Chen P.-W.; NI-CHUNG LEE ; Hsieh W.-S.; Chiu P.-C.; Hwu W.-L.; Tsai F.-J.; Lin S.-P.; Chu S.-Y.; Jong Y.-J.; Chao M.-C. | Molecular Genetics and Metabolism | 30 | 28 | |
| 2016 | 3-O-methyldopa levels in newborns: Result of newborn screening for aromatic L-amino-acid decarboxylase deficiency | Chien Y.-H.; Chen P.-W.; Lee N.-C.; Hsieh W.-S.; Chiu P.-C.; WUH-LIANG HWU ; Tsai F.-J.; Lin S.-P.; Chu S.-Y.; Jong Y.-J.; Chao M.-C. | Molecular Genetics and Metabolism | 30 | 28 | |
| 2016 | 3-O-methyldopa levels in newborns: Result of newborn screening for aromatic L-amino-acid decarboxylase deficiency | YIN-HSIU CHIEN ; Chen P.-W.; Lee N.-C.; Hsieh W.-S.; Chiu P.-C.; Hwu W.-L.; Tsai F.-J.; Lin S.-P.; Chu S.-Y.; Jong Y.-J.; Chao M.-C. | Molecular Genetics and Metabolism | 30 | 28 | |
| 2009 | Altered homeostasis of CD4 + FoxP3 + regulatory T-cell subpopulations in systemic lupus erythematosus | Suen J.-L.; Li H.-T.; Jong Y.-J.; BOR-LUEN CHIANG ; Yen J.-H. | Immunology | | 72 | |
| 2011 | Computational analysis of a novel mutation in ETFDH gene highlights its long-range effects on the FAD-binding motif | Er T.-K.; Chen C.-C.; Liu Y.-Y.; Chang H.-C.; YIN-HSIU CHIEN ; Chang J.-G.; Hwang J.-K.; Jong Y.-J. | BMC Structural Biology | | 26 | |
| 2014 | Development of a feasible assay for the detection of GAA mutations in patients with Pompe disease | Er T.-K.; Chen C.-C.; YIN-HSIU CHIEN ; Liang W.-C.; Kan T.-M.; Jong Y.-J. | Clinica Chimica Acta | 5 | 4 | |
| 2006 | The F-box protein Fbxo7 interacts with human inhibitor of apoptosis protein cIAP1 and promotes cIAP1 ubiquitination | Chang Y.-F.; Cheng C.-M.; Chang L.-K.; Jong Y.-J.; Yuo C.-Y.; LI-KWAN CHANG | Biochemical and Biophysical Research Communications | 43 | 51 | |
| 2008 | Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis | Hung C.-C.; Lee C.-N.; Chang C.-H.; Jong Y.-J.; Chen C.-P.; Hsieh W.-S.; Su Y.-N.; Win-Li Lin | Clinical Biochemistry | 24 | 25 | |
| 2008 | Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis | Hung C.-C.; CHIEN-NAN LEE ; Chang C.-H.; Jong Y.-J.; Chen C.-P.; Hsieh W.-S.; Su Y.-N.; Lin W.-L. | Clinical Biochemistry | | 25 | |
| 2008 | Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: A comparison | Hung C.-C.; Lee C.-N.; Lin C.-Y.; Cheng W.-F.; CHI-AN CHEN ; Hsieh S.-T.; Yang C.-C.; Jong Y.-J.; Su Y.-N.; Lin W.-L. | Electrophoresis | 11 | 10 | |
| 2008 | Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: A comparison | Hung C.-C.; Lee C.-N.; Lin C.-Y.; WEN-FANG CHENG ; Chen C.-A.; Hsieh S.-T.; Yang C.-C.; Jong Y.-J.; Su Y.-N.; Lin W.-L. | Electrophoresis | 11 | 10 | |
| 2008 | Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: A comparison | Hung C.-C.; CHIEN-NAN LEE ; Lin C.-Y.; Cheng W.-F.; Chen C.-A.; Hsieh S.-T.; Yang C.-C.; Jong Y.-J.; Su Y.-N.; Lin W.-L. | Electrophoresis | | 10 | |
| 2008 | Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: A comparison | Hung C.-C.; Lee C.-N.; Lin C.-Y.; Cheng W.-F.; Chen C.-A.; Hsieh S.-T.; Yang C.-C.; Jong Y.-J.; Su Y.-N.; Win-Li Lin | Electrophoresis | 11 | 10 | |
| 2008 | Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: A comparison | Hung C.-C.; Lee C.-N.; Lin C.-Y.; Cheng W.-F.; Chen C.-A.; SUNG-TSANG HSIEH ; Yang C.-C.; Jong Y.-J.; Su Y.-N.; Lin W.-L. | Electrophoresis | 11 | 10 | |
| 2016 | Increased risk of epilepsy in children with Tourette syndrome: A population-based case-control study | Wong L.C.; Huang H.-L.; WEN-CHIN WENG ; Jong Y.-J.; Yin Y.-J.; Chen H.-A.; Lee W.-T.; Ho S.-Y. | Research in Developmental Disabilities | 9 | 9 | |
| 2016 | Increased risk of epilepsy in children with Tourette syndrome: A population-based case-control study | Wong L.C.; Huang H.-L.; Weng W.-C.; Jong Y.-J.; Yin Y.-J.; Chen H.-A.; WANG-TSO LEE ; Ho S.-Y. | Research in Developmental Disabilities | 7 | 9 | |
| 2016 | Increased risk of epilepsy in children with Tourette syndrome: A population-based case-control study | LEE-CHIN WONG ; Huang H.-L.; Weng W.-C.; Jong Y.-J.; Yin Y.-J.; Chen H.-A.; Lee W.-T.; Ho S.-Y. | Research in Developmental Disabilities | | 9 | |
| 2016 | Increased risks of tic disorders in children with epilepsy: A nation-wide population-based case-control study in Taiwan | Weng W.-C.; Huang H.-L.; Wong L.C.; Jong Y.-J.; Yin Y.-J.; Chen H.-A.; WANG-TSO LEE ; Ho S.-Y. | Research in Developmental Disabilities | 8 | 8 | |
| 2016 | Increased risks of tic disorders in children with epilepsy: A nation-wide population-based case-control study in Taiwan | Weng W.-C.; Huang H.-L.; LEE-CHIN WONG ; Jong Y.-J.; Yin Y.-J.; Chen H.-A.; Lee W.-T.; Ho S.-Y. | Research in Developmental Disabilities | | 8 | |
| 2016 | Increased risks of tic disorders in children with epilepsy: A nation-wide population-based case-control study in Taiwan | WEN-CHIN WENG ; Huang H.-L.; Wong L.C.; Jong Y.-J.; Yin Y.-J.; Chen H.-A.; Lee W.-T.; Ho S.-Y. | Research in Developmental Disabilities | 6 | 7 | |
