Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
2020 | MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemia | Yu, Chih-Hsiang; Lin, Tze-Kang; SHIANN-TANG JOU ; Lin, Chien-Yu; Lin, Kai-Hsin; MENG-YAO LU ; Chen, Shu-Huey; Cheng, Chao-Neng; Wu, Kang-Hsi; Wang, Shih-Chung; HSIU-HAO CHANG ; MENG-JU LI ; Ni, Yu-Ling; Su, Yi-Ning; Lin, Dong-Tsamn; Chen, Hsuan-Yu; Harrison, Christine J; Hung, Chia-Cheng; SHU-WHA LIN ; YUNG-LI YANG | Scientific Reports | 12 | 10 | |
2007 | Molecular Assay of -Alpha(3.7) and -Alpha(4.2) Deletions Causing Alpha- Thalassemia by Denaturing High-Performance Liquid Chromatography | HUNG, CHIA-CHENG; LEE, CHIEN-NAN; CHEN, CHIH-PING; JONG, YUH-JYH; HSIEH, WU-SHIUN; LIN, WIN-LI; SU, YI-NING; HSU, SU-MING; 洪加政; 李建南; 陳持平; 鐘育志; 謝武勳; 林文澧; 蘇怡寧; 許世明 | CLINICAL BIOCHEMISTRY | | | |
2012 | MOLECULAR IMAGING PATTERN AT DIAGNOSIS DISTINGUISHES THE GENOMIC TYPE AND TREATMENT OUTCOME OF NEUROBLASTOMA | Liu, Yen-Lin; Tzen, Kai-Yuan; Lu, Meng-Yao; Chang, Hsiu-Hao; Jou, Shiann-Tarng; Yang, Yung-Li; Lin, Dong-Tsamn; Lin, Kai-Hsin; Su, Yi-Ning; Hsu, Wen-Ming | Pediatr. Blood Cancer | | | |
2024 | Neonatal Filaggrin Genetic Screening and Counseling to Prevent Atopic Dermatitis in High-Risk Infants | HAN-YING CHEN ; CHIH-LING CHEN ; Wu, Yu-Hui; Lin, Tze-Kang; Su, Yi-Ning; YUE-LIANG GUO ; SHIN-YU LIN ; CHIEN-NAN LEE | Dermatitis : contact, atopic, occupational, drug | | | |
2005 | Parallel minisequencing followed by multiplex matrix-assisted laser desorption/ionization mass spectrometry assay for β-thalassemia mutations | Liao, Hsin-Kai; Su, Yi-Ning; Kao, Hung-Yi; Hung, Chia-Cheng; Wang, Hsueh-Ting; Chen, Yu-Ju | Journal of Human Genetics | 21 | 19 | |
2021 | The Prenatal Diagnosis and Clinical Outcomes of Fetuses With 15q11.2 Copy Number Variants: A Case Series of 36 Patients | Jessica KANG ; CHIEN-NAN LEE ; Su, Yi-Ning; MING-WEI LIN ; YI-YUN TAI ; Hsu, Wen-Wei; Huang, Kuan-Ying; CHI-LING CHEN ; Hung, Chien-Hui; SHIN-YU LIN | Frontiers in medicine | 2 | 3 | |
2013 | Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2→q11.21) | Chen, Chih-Ping; TSANG-MING KO ; Su, Yi-Ning; Su, Jun-Wei; Chen, Yu-Ting; Lee, Chen-Chi; Chen, Li-Feng; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 3 | 2 | |
2010 | Prenatal Diagnosis and Molecular Cytogenetic Characterization of De Novo Partial Trisomy 7p (7p15.3 -> Pter) and Partial Monosomy 13q (13q33.3 -> Qter) Associated with Dandy-Walker Malformation) Abnormal Skull Development and Microcephaly | CHEN, CHIH-PING; CHEN, MING; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; HSU, CHIN-YUAN; WU, PEI-CHEN; LEE, DONG-JAY; MA, GWO-CHIN; WANG, WAYSEEN | TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY | | | |
2016 | Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion | Chen, Chih-Ping; TSANG-MING KO ; Su, Yi-Ning; Wang, Liang-Kai; Chern, Schu-Rern; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Shin-Wen; Ko, Kevin; Lee, Chen-Chi; Chen, Li-Feng; Yang, Chien-Wen; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 7 | 6 | |
2012 | Prenatal diagnosis of mosaic tetrasomy 18p | Chen, Chih-Ping; TSANG-MING KO ; Su, Yi-Ning; Chern, Schu-Rern; Su, Jun-Wei; Chen, Yu-Ting; Town, Dai-Dyi; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 16 | 15 | |
2011 | Prenatal diagnosis of mosaic trisomy 2: discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction | Chen, Chih-Ping; Su, Yi-Ning; SHIN-YU LIN ; Chern, Schu-Rern; Chen, Yu-Ting; Lee, Meng-Shan; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 24 | 23 | |
2012 | Prenatal diagnosis of partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31→qter) associated with increased nuchal translucency and abnormal maternal serum biochemistry in the first trimester | Chen, Chih-Ping; TSANG-MING KO ; Su, Yi-Ning; Hsu, Chin-Yuan; Chen, Yi-Yung; Su, Jun-Wei; Chen, Wen-Lin; Pan, Chen-Wen; Wang, Wayseen | Taiwanese journal of obstetrics & gynecology | 9 | 9 | |
1997 | Puerperal Lactation Suppression by Metergoline Versus Bromocriptione | LIN, HO-HSIUNG; SU, YI-NING; WEI, LIN- HUNG; HUANG, SU-CHENG; 林鶴雄; 蘇怡寧; 魏凌鴻; 黃思誠 | TAIWANESE JOURNAL OF OBSTETRICS AND GYNECOLOGY | | | |
2005 | Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: a highly efficient and reliable carrier-screening test | Su, Yi-Ning; Hung, Chia-Cheng; Li, Hung | Human Mutation | | | |
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, WAN-YI; HUNG, CHIA-CHENG; LEE, CHIEN-NAN; SU, YI-NING; CHEN, CHIH-PING | PRENATAL DIAGNOSIS | | | |
2001 | Risk Factor and Early Identification of Treatment Failure in Patients of Gestational Trophoblastic Tumor Treated with Single Agent Chemotherapy | LEE, CHIEN-NAN; SU, YI-NING; WEI, LIN- HUNG; CHENG, WEN-FANG; CHEN, CHI-AN | TJOG | | | |
2009 | 台灣眼睛皮膚型白化症患者之基因分析基因型-表現型之研究:基因檢測之重要性 | 盧曉穎; Lu, Hsiao-Yin | | | | |
2009 | 體染色體隱性遺傳之先天性眼球震顫個案家庭之遺傳分析 | 曾黎雲; Tseng, Li-Yun | | | | |