Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
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2010 | The association between lumican gene polymorphisms and high myopia | Lin H.-J.; Wan L.; Tsai Y.; Chen W.-C.; SHIH-WEI TSAI ; Tsai F.-J. | Eye | 32 | 32 | |
2004 | Characterization of trans- and cis-cleavage activity of the SARS coronavirus 3CLpro protease: Basis for the in vitro screening of anti-SARS drugs | Lin C.-W.; Tsai C.-H.; Tsai F.-J.; PEI-JER CHEN ; Lai C.-C.; Wan L.; Chiu H.-H.; Lin K.-H. | FEBS Letters | 37 | 36 | |
2008 | Identification of eight novel mutations of the acid α-glucosidase gene causing the infantile or juvenile form of glycogen storage disease type II | Wan L.; Lee C.-C.; Hsu C.-M.; WUH-LIANG HWU ; Yang C.-C.; Tsai C.-H.; Tsai F.-J. | Journal of Neurology | 50 | 46 | |
2006 | Increased prevalence of interleukin-1 receptor antagonist gene polymorphism in patients with chronic rhinosinusitis | Cheng Y.-K.; Lin C.-D.; Chang W.-C.; Hwang G.-Y.; SHIH-WEI TSAI ; Wan L.; Tsai M.-H.; Tsai J.J.P.; Tsai F.-J. | Archives of Otolaryngology - Head and Neck Surgery | 32 | 30 | |
2009 | Muscarinic acetylcholine receptor 1 gene polymorphisms associated with high myopia | Lin H.-J.; Wan L.; Tsai Y.; Chen W.-C.; SHIH-WEI TSAI ; Tsai F.-J. | Molecular Vision | 20 | 15 | |
2006 | Mutation analysis of Gaucher disease patients in Taiwan: High prevalence of the RecNciI and L444P mutations | Wan L.; Hsu C.-M.; Tsai C.-H.; Lee C.-C.; WUH-LIANG HWU ; Tsai F.-J. | Blood Cells, Molecules, and Diseases | 46 | 41 | |
2010 | Reply to Guggenheim et al | Lin H.-J.; Wan L.; Tsai Y.; Chen W.-C.; SHIH-WEI TSAI ; Tsai F.-J. | Eye | 0 | 0 | |
2009 | Sclera-related gene polymorphisms in high myopia | Lin H.-J.; Wan L.; Tsai Y.; Liu S.-C.; Chen W.-C.; SHIH-WEI TSAI ; Tsai F.-J. | Molecular Vision | 40 | 35 |