| Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
| 2006 | Association of E-Cadherin Gene 3 '-Utr C/T Polymorphism with Primary Open Angle Glaucoma | LIN, HUI-JU; TSAI, FUU-JEN; HUNG, POR- TYING; CHEN, HUEY-YI; FAN, SENG-SHEEN; TSAI, SHIH-WEI | OPHTHALMIC RESEARCH | | | |
| 2006 | Association of E-Cadherin Gene 3'-UTR C/T Polymorphism with Primary Open Angle Glaucoma | Lin, Hui-Ju; Tsai, Fuu-Jen; Hung, Porting; Chen, Wen-Chi; Chen, Huey-Yi; Fan, Seng-Sheen; Tsai, Shih-Wei | Ophthalmic Research | | | |
| 2016 | Cardiac structure and function and effects of enzyme replacement therapy in patients with mucopolysaccharidoses I, II, IVA and VI | Lin, Hsiang-Yu; Chuang, Chih-Kuang; Chen, Ming-Ren; Lin, Shan-Miao; Hung, Chung-Lieh; Chang, Chia-Ying; Chiu, Pao Chin; Tsai, Wen-Hui; Niu, Dau-Ming; Tsai, Fuu-Jen; Lin, Shio Jean; WUH-LIANG HWU ; Lin, Ju-Li; SHAU-PING LIN | Molecular Genetics and Metabolism | 28 | 28 | |
| 2016 | Causes of death and clinical characteristics of 34 patients with Mucopolysaccharidosis II in Taiwan from 1995-2012 Dr. Segolene Ayme | Lin, Hsiang-Yu; Chuang, Chih-Kuang; Huang, Yu-Hsiu; Tu, Ru-Yi; Lin, Fang-Ju; Lin, Shio Jean; Chiu, Pao Chin; Niu, Dau-Ming; Tsai, Fuu-Jen; WUH-LIANG HWU ; YIN-HSIU CHIEN ; Lin, Ju-Li; Chou, Yen-Yin; Tsai, Wen-Hui; Chang, Tung-Ming; SHAU-PING LIN | Orphanet Journal of Rare Diseases | 19 | 21 | |
| 2018 | Clinical characteristics and surgical history of Taiwanese patients with mucopolysaccharidosis type II: Data from the hunter outcome survey (HOS) | Lin, Hsiang-Yu; Chuang, Chih-Kuang; Chen, Ming-Ren; Lin, Shio Jean; Chiu, Pao Chin; Niu, Dau-Ming; Tsai, Fuu-Jen; WUH-LIANG HWU ; YIN-HSIU CHIEN ; Lin, Ju-Li; SHAU-PING LIN | Orphanet Journal of Rare Diseases | 9 | 9 | |
| 2004 | Detection of a Homozygous D645e Mutation of the Acid Alpha-Glucosidase Gene and Glycogen Deposition in Tissues in a Second-Trimester Fetus with Infantile Glycogen Storage Disease Type Ii | CHEN, CHIH-PING; LIN, SHUAN-PEI; TZEN, CHIN-YUAN; TSAI, FUU-JEN; HWU, WUH-LIANG | PRENATAL DIAGNOSIS | | | |
| 2005 | Dopamine Receptor D2 Gene Polymorphisms Are Associated in Taiwanese Children with Tourette Syndrome | TSAI, FUU-JEN; LI, TSAI-CHUNG; WANG, TSO- REN; TSAI, CHANG-HAI; CHOU, I.-CHING; LEE, CHENG-CHUN | PEDIATRIC NEUROLOGY | | | |
| 2013 | Dung-shen (Codonopsis pilosula) attenuated the cardiac-impaired insulin-like growth factor II receptor pathway on myocardial cells | Tsai, Kun-Hsi; Lee, Nien-Hung; Chen, Guei-Ying; Hu, Wei-Syun; Tsai, Chen-Yen; Chang, Mu-Hsin; Jong, Gwo-Ping; Kuo, Chia-Hua; Tzang, Bor-Show; Tsai, Fuu-Jen; Tsai, Chang-Hai; Huang, Chih-Yang | Food Chemistry | 27 | 24 |  |
| 2017 | Genetically Determined Plasma Lipid Levels and Risk of Diabetic Retinopathy: A Mendelian Randomization Study | Sobrin, Lucia; Chong, Yong He; Fan, Qiao; Gan, Alfred; Stanwyck, Lynn K; Kaidonis, Georgia; Craig, Jamie E; Kim, Jihye; Liao, Wen-Ling; Huang, Yu-Chuen; Lee, Wen-Jane; Hung, Yi-Jen; Guo, Xiuqing; Hai, Yang; Ipp, Eli; Pollack, Samuela; Hancock, Heather; Price, Alkes; Penman, Alan; Mitchell, Paul; Liew, Gerald; Smith, Albert V; Gudnason, Vilmundur; Tan, Gavin; Klein, Barbara E K; Kuo, Jane; Li, Xiaohui; Christiansen, Mark W; Psaty, Bruce M; Sandow, Kevin; Jensen, Richard A; Klein, Ronald; Cotch, Mary Frances; Wang, Jie Jin; Jia, Yucheng; Chen, Ching J; Chen, Yii-Der Ida; Rotter, Jerome I; Tsai, Fuu-Jen; Hanis, Craig L; Burdon, Kathryn P; Wong, Tien Yin; Cheng, Ching-Yu; JYH-MING JIMMY JUANG | Diabetes | 12 | 11 | |
| 2010 | A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese | Tsai, Fuu-Jen; Yang, Chi-Fan; Chen, Ching-Chu; LEE-MING CHUANG ; Lu, Chieh-Hsiang; Chang, Chwen-Tzuei; Wang, Tzu-Yuan; Chen, Rong-Hsing; Shiu, Chiung-Fang; Liu, Yi-Min; Chang, Chih-Chun; Chen, Pei; Chen, Chien-Hsiun; Fann, Cathy S J; Chen, Yuan-Tsong; Wu, Jer-Yuarn | PLoS genetics | 276 | 268 | |
| 2008 | Identification of Eight Novel Mutations of the Acid Alpha-Glucosidase Gene Causing the Infantile or Juvenile Form of Glycogen Storage Disease Type Ii | WAN, LEI; LEE, CHENG-CHUN; HSU, CHIN-MOO; HWU, WUH-LIANG; YANG, CHIH-CHAO; TSAI, CHANG-HAI; TSAI, FUU-JEN | JOURNAL OF NEUROLOGY | | | |
| 2019 | Long-term effects of enzyme replacement therapy for Taiwanese patients with mucopolysaccharidosis IVA | Lin, Hsiang-Yu; Chuang, Chih-Kuang; Ke, Yu-Yuan; Hsu, Chia-Chi; Chiu, Pao Chin; Niu, Dau-Ming; Tsai, Fuu-Jen; WUH-LIANG HWU ; Lin, Ju-Li; SHAU-PING LIN | Pediatrics and Neonatology | 8 | 6 | |
| 2013 | Long-term follow-up results in patients with classic infantile Pompe disease receiving enzyme therapy since newborn | Chien, Yin-Hsiu; Hwu, Wuh-Liang; Lee, Ni-Chung; Chen, Chun-An; Tsai, Fuu-Jen; Tsai, Wen-Hui; Huang, Hsiang-Ju; Hsu, Wei-Chung; Tsai, Tzu-Hsun; Shieh, Jeng-Yi; WEI-CHUNG HSU | Molecular Genetics and Metabolism | 0 | 0 | |
| 2016 | Long-term galsulfase enzyme replacement therapy in Taiwanese mucopolysaccharidosis VI patients: A case series | Lin, Hsiang-Yu; Chuang, Chih-Kuang; Wang, Chung-Hsing; YIN-HSIU CHIEN ; Wang, Yu-Mei; Tsai, Fuu-Jen; Chou, Yen-Yin; Lin, Shio Jean; Pan, Hui-Ping; Niu, Dau-Ming; WUH-LIANG HWU ; Ke, Yu-Yuan; SHAU-PING LIN | Molecular Genetics and Metabolism Reports | 19 | 17 | |
| 2015 | Long-term prognosis of patients with infantile-onset pompe disease diagnosed by newborn screening and treated since birth | YIN-HSIU CHIEN ; NI-CHUNG LEE ; CHUN-AN CHEN ; Tsai, Fuu-Jen; Tsai, Wen-Hui; JENG-YI SHIEH ; Huang, Hsiang-Ju; Hsu, Wei-Chung; Tsai, Tzu-Hsun ; WEI-CHUNG HSU | Journal of Pediatrics | 88 | 81 | |
| 2012 | Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians | Cho, Yoon Shin; Chen, Chien-Hsiun; Hu, Cheng; Long, Jirong; Ong, Rick Twee Hee; Sim, Xueling; Takeuchi, Fumihiko; Wu, Ying; Go, Min Jin; Yamauchi, Toshimasa; YI-CHENG CHANG ; Kwak, Soo Heon; Ma, Ronald C W; Yamamoto, Ken; Adair, Linda S; Aung, Tin; Cai, Qiuyin; Chang, Li-Ching; Chen, Yuan-Tsong; Gao, Yutang; Hu, Frank B; Kim, Hyung-Lae; Kim, Sangsoo; Kim, Young Jin; Lee, Jeannette Jen-Mai; Lee, Nanette R; Li, Yun; Liu, Jian Jun; Lu, Wei; Nakamura, Jiro; Nakashima, Eitaro; Ng, Daniel Peng-Keat; Tay, Wan Ting; Tsai, Fuu-Jen; Wong, Tien Yin; Yokota, Mitsuhiro; Zheng, Wei; Zhang, Rong; Wang, Congrong; So, Wing Yee; Ohnaka, Keizo; Ikegami, Hiroshi; Hara, Kazuo; Cho, Young Min; Cho, Nam H; TIEN-JYUN CHANG ; Bao, Yuqian; Hedman, Åsa K; Morris, Andrew P; McCarthy, Mark I; Takayanagi, Ryoichi; Park, Kyong Soo; Jia, Weiping; LEE-MING CHUANG ; Chan, Juliana C N; Maeda, Shiro; Kadowaki, Takashi; Lee, Jong-Young; Wu, Jer-Yuarn; Teo, Yik Ying; Tai, E Shyong; Shu, Xiao Ou; Mohlke, Karen L; Kato, Norihiro; Han, Bok-Ghee; Seielstad, Mark | Nature genetics | 482 | 472 | |
| 2006 | Mutation Analysis of Gaucher Disease Patients in Taiwan: High Prevalence of the Recncii and L444p Mutations | HSU, CHIN-MOO; TSAI, C-H; LEE, CHENG-CHUN; HWU, WUH-LIANG; TSAI, FUU-JEN | BLOOD CELLS MOLECULES AND DISEASES | | | |
| 2003 | No association between the dopamine transproter gene polymorphism and sporadic Parkinson’s disease among Chinese in Taiwan | Tsai, Tzung-Chang; Wu, Jer-Yuam; Lee, Cheng-Chung; Tsai, Chon-Haw; Tsai, Fuu-Jen; Chang, Fang-Chia ; Kuo, Chi-Chung | Mid Taiwan Journal of Medicine | | | |
| 2008 | Osteoblast-derive TGF-β1 Stimulates IL-8 Release via AP-1 and NF-κB in Human Cancer Cells | Fong, Yi-Chin; Maa, Ming-Chei; Tsai, Fuu-Jen; Chen, Wen-Chi; Lin, Jaung-Geng; Jeng, Long-Bin; 楊榮森; Fu, Wen-Mei; Tang, Chih-Hsin | J Bone Miner Res | | | |
| 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 | | | |
