公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
---|---|---|---|---|---|---|
2012 | Maternal ascites after thoracoamniotic shunting | Lin T.-H.; JIN-CHUNG SHIH ; Su Y.-N.; CHIEN-NAN LEE | Prenatal Diagnosis | 0 | 0 | |
2011 | Maternal psychosocial factors around delivery on development of 2-year-old children: A prospective cohort study | Chuang C.-H.; Liao H.-F.; Hsieh W.-S.; SUH-FANG JENG ; Su Y.-N.; PAU-CHUNG CHEN | Journal of Paediatrics and Child Health | 15 | 13 | |
2011 | Maternal psychosocial factors around delivery, and the behavior of 2-year-old children | Chuang C.-H.; SUH-FANG JENG ; Hsieh W.-S.; Liao H.-F.; Su Y.-N.; PAU-CHUNG CHEN | Pediatrics International | 9 | 8 | |
2012 | Maternal-reported behavioral and emotional problems in Taiwanese preschool children | YEN-TZU WU ; WEI J. CHEN ; Hsieh W.-S.; PAU-CHUNG CHEN ; Liao H.-F.; Su Y.-N.; SUH-FANG JENG | Research in Developmental Disabilities | 37 | 32 | |
2009 | Mesothelin inhibits paclitaxel-induced apoptosis through the PI3K pathway | Chang M.-C.; CHI-AN CHEN ; CHANG-YAO HSIEH ; CHIEN-NAN LEE ; Su Y.-N.; Hu Y.-H.; WEN-FANG CHENG | Biochemical Journal | 57 | 55 | |
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 | |
2019 | Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith–Wiedemann spectrum | CHENG-TING LEE ; YI-CHING TUNG ; WUH-LIANG HWU ; JIN-CHUNG SHIH ; WEN-HSI LIN ; MU-ZON WU ; KUAN-TING KUO ; YUNG-LI YANG ; HUEY-LING CHEN ; Chen M.; Su Y.-N.; Jong Y.-J.; SHIH-YAO LIU ; Tsai W.-Y.; NI-CHUNG LEE | American Journal of Medical Genetics, Part A | 5 | 5 | |
2012 | Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndrome | Wang S.-H.; Chen-Chi Wu ; Lu Y.-C.; Lin Y.-H.; Su Y.-N.; WUH-LIANG HWU ; Yu I.-S.; Hsu C.-J. | Laryngoscope | 27 | 19 | |
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 | Mutational spectrum of multiple endocrine neoplasia type 2 and sporadic medullary thyroid carcinoma in Taiwan | Chang C.-F.; WEI-SHIUNG YANG ; Su Y.-N.; Wu I.-L.; TIEN-CHUN CHANG | Journal of the Formosan Medical Association | 20 | 11 | |
2004 | Naked RNA vaccine controls tumors with down-regulated MHC class I expression through NK cells and perforin-dependent pathways | WEN-FANG CHENG ; Hung C.-F.; CHIEN-NAN LEE ; Su Y.-N.; Chang M.-C.; He L.; Wu T.-C.; CHI-AN CHEN ; CHANG-YAO HSIEH | European Journal of Immunology | 15 | 14 | |
2006 | Nationwide singleton birth weight percentiles by gestational age in Taiwan, 1998-2002 | WU-SHIUN HSIEH ; Wu H.-C.; SUH-FANG JENG ; Liao H.-F.; Su Y.-N.; Lin S.-J.; Hsieh C.-J.; PAU-CHUNG CHEN | Acta Paediatrica Taiwanica | 96 | 0 | |
2012 | A nationwide survey of risk factors for stillbirth in Taiwan, 2001-2004 | Hu I.-J.; PAU-CHUNG CHEN ; SUH-FANG JENG ; Hsieh C.-J.; Liao H.-F.; Su Y.-N.; Lin S.-J.; Hsieh W.-S. | Pediatrics and Neonatology | 11 | 10 | |
2009 | Neonatal and Pregnancy Outcome in Primary Antiphospholipid Syndrome: A 10-year Experience in One Medical Center | Chou A.-K.; SONG-CHOU HSIEH ; Su Y.-N.; SUH-FANG JENG ; CHIEN-YI CHEN ; HUNG-CHIEH CHOU ; PO-NIEN TSAO ; Hsieh W.-S. | Pediatrics and Neonatology | 14 | 11 | |
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 | |
2012 | Novel heterozygous tissue-nonspecific alkaline phosphatase (TNAP) gene mutations causing lethal perinatal hypophosphatasia | KAI-CHI CHANG ; PO-HAN LIN ; Su Y.-N.; STEVEN SHINN-FORNG PENG ; NI-CHUNG LEE ; HUNG-CHIEH CHOU ; CHIEN-YI CHEN ; Hsieh W.-S.; PO-NIEN TSAO | Journal of Bone and Mineral Metabolism | 14 | 12 | |
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 | Novel neurotrophic tyrosine kinase receptor type 1 gene mutation associated with congenital insensitivity to pain with anhidrosis | Lin Y.-P.; Su Y.-N.; WEN-CHIN WENG ; WANG-TSO LEE | Journal of Child Neurology | 16 | 15 |