Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
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2006 | Molecular and clinical analyses of 84 patients with tuberous sclerosis complex | Hung C.-C.; Su Y.N.; Chien S.-C.; HORNG-HUEI LIOU ; Chen C.-C.; PAU-CHUNG CHEN ; Hsieh C.-J.; Chen C.-P.; WANG-TSO LEE ; Lin, Win-Li ; CHIEN-NAN LEE | BMC Medical Genetics | 57 | 54 | |
2007 | Molecular assay of -α3.7 and -α4.2 deletions causing α-thalassemia by denaturing high-performance liquid chromatography | Hung C.-C.; CHIEN-NAN LEE ; Chen C.-P.; Jong Y.-J.; WU-SHIUN HSIEH ; Win-Li Lin ; Su Y.-N.; Hsu S.-M. | Clinical Biochemistry | 20 | 18 | |
2005 | Molecular genetic analysis of the TSC genes in two families with prenatally diagnosed rhabdomyomas [1] | Chen C.-P.; Su Y.-N.; Hung C.-C.; CHIEN-NAN LEE ; FON-JOU HSIEH ; Chang T.-Y.; Chen M.-R.; Wang W. | Prenatal Diagnosis | 16 | 11 | |
2008 | Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM | SHIN-YU LIN ; Su Y.-N.; Hung C.-C.; WOEI TSAY ; Chiou S.-S.; Chang C.-T.; HONG-NERNG HO ; CHIEN-NAN LEE | BMC Medical Genetics | 39 | 36 | |
2009 | Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome | Hung C.-C.; SHIN-YU LIN ; CHIEN-NAN LEE ; Cheng H.-Y.; Lin S.-P.; Chen M.-R.; Chen C.-P.; Chang C.-H.; Lin C.-Y.; CHIH-CHIEH YU ; Chiu H.-H.; WEN-FANG CHENG ; HONG-NERNG HO ; Niu D.-M.; Su Y. | Annals of Human Genetics | 27 | 27 | |
2017 | Newborn genetic screening for hearing impairment: a population-based longitudinal study | Chen-Chi Wu ; Tsai C.-H.; Hung C.-C.; Lin Y.-H.; Lin Y.-H.; Huang F.-L.; PO-NIEN TSAO ; Su Y.-N.; Lee Y.L.; Hsieh W.-S.; Hsu C.-J. | Genetics in Medicine | 53 | 50 | |
2011 | Newborn genetic screening for hearing impairment: A preliminary study at a tertiary center | Chen-Chi Wu ; Hung C.-C.; SHIN-YU LIN ; Hsieh W.-S.; PO-NIEN TSAO ; CHIEN-NAN LEE ; Su Y.-N.; Hsu C.-J. | PLoS ONE | 42 | 26 | |
2018 | Noninvasive glucose monitoring with a contact lens and smartphone | Lin Y.-R.; Hung C.-C.; HSIEN-YI CHIU ; Chang B.-H.; Li B.-R.; Cheng S.-J.; Yang J.-W.; Lin S.-F.; Chen G.-Y. | Sensors (Switzerland) | 57 | 52 | |
2006 | Novel mutation in the TSC2 gene associated with prenatally diagnosed cardiac rhabdomyomas and cerebral tuberous sclerosis | Chen C.-P.; Su Y.-N.; Hung C.-C.; JIN-CHUNG SHIH ; Wang W. | Journal of the Formosan Medical Association | 18 | 15 | |
2010 | Preimplantation genetic diagnosis of β-thalassemia using real-time polymerase chain reaction with fluorescence resonance energy transfer hybridization probes | Hung C.-C.; SHEE-UAN CHEN ; SHIN-YU LIN ; Fang M.-Y.; Chang L.-J.; Tsai Y.-Y.; Lin L.-T.; YU-SHIH YANG ; CHIEN-NAN LEE ; Su Y.-N. | Analytical Biochemistry | 12 | 12 | |
2012 | Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH) | Hung C.-C.; Lin C.-H.; SHIN-YU LIN ; JIN-CHUNG SHIH ; CHIEN-NAN LEE ; Su Y.-N. | Gene | 10 | 9 | |
2005 | Quantification of relative gene dosage by single-base extension and high-performance liquid chromatography: Application to the SMN1/SMN2 gene | Hung C.-C.; CHIEN-NAN LEE ; Chen C.-P.; Jong Y.-J.; CHI-AN CHEN ; WEN-FANG CHENG ; Lin, Win-Li ; Su Y.-N. | Analytical Chemistry | 22 | 21 | |
2005 | Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: A highly efficient and reliable carrier-screening test | Su Y.-N.; Hung C.-C.; Li H.; CHIEN-NAN LEE ; WEN-FANG CHENG ; PO-NIEN TSAO ; Chang M.-C.; CHIA-LI YU ; Hsieh W.-S.; Lin, Win-Li ; Hsu S.-M. | Human Mutation | 64 | 57 | |
2011 | Quantitative and qualitative analyses of the SNRPN gene using real-time PCR with melting curve analysis | Hung C.-C.; SHIN-YU LIN ; Lin S.-P.; Chen C.-P.; Chen L.-Y.; CHIEN-NAN LEE ; Su Y.-N. | Journal of Molecular Diagnostics | 5 | 3 | |
2006 | Quantitative assay of deletion or duplication genotype by capillary electrophoresis system: Application in prader-willi syndrome and duchenne muscular dystrophy | Hung C.-C.; Chen C.-P.; Lin S.-P.; Chien S.-C.; CHIEN-NAN LEE ; WEN-FANG CHENG ; WU-SHIUN HSIEH ; Liu M.S.; Su Y.-N.; Lin, Win-Li | Clinical Chemistry | 18 | 15 | |
2006 | A rapid and reliable detection system for the analysis of PMP22 gene dosage by MP/DHPLC assay | Lin C.-Y.; Su Y.-N.; CHIEN-NAN LEE ; Hung C.-C.; WEN-FANG CHENG ; Win-Li Lin ; CHI-AN CHEN ; SUNG-TSANG HSIEH | Journal of Human Genetics | 12 | 10 | |
2004 | Rapid detection of FGFR3 gene mutation in achondroplasia by DHPLC system-coupling heteroduplex and fluorescence-enhanced primer-extension analysis | Su Y.-N.; CHIEN-NAN LEE ; Chien S.-C.; Hung C.-C.; YIN-HSIU CHIEN ; CHI-AN CHEN | Journal of Human Genetics | 9 | 9 | |
2003 | Rapid detection of β-globin gene (HBB) mutations coupling heteroduplex and primer-extension analysis by DHPLC | Su Y.-N.; CHIEN-NAN LEE ; Hung C.-C.; CHI-AN CHEN ; WEN-FANG CHENG ; PO-NIEN TSAO ; CHIA-LI YU ; FON-JOU HSIEH | Human Mutation | 36 | 34 | |
2007 | Rapid prenatal diagnosis of Duchenne muscular dystrophy with gene duplications by ion-pair reversed-phase high-performance liquid chromatography coupled with competitive multiplex polymerase chain reaction strategy | Huang W.-Y.; Hung C.-C.; CHIEN-NAN LEE ; Su Y.-N.; Chen C.-P. | Prenatal Diagnosis | 3 | 3 | |
2003 | Rapid prenatal diagnosis of X-linked chronic granulomatous disease using a denaturing high-performance liquid chromatography (DHPLC) system | Chien S.-C.; CHIEN-NAN LEE ; Hung C.-C.; PO-NIEN TSAO ; Su Y.-N.; FON-JOU HSIEH | Prenatal Diagnosis | 7 | 7 |