| Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
| 2006 | A common SCN5A polymorphsim attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a chinese family with an inherited cardiac conduction defect | Niu, D. M.; Hwang, B.; Hwang, H. W.; Wang, N. H.; Wu, J. Y.; Lee, P. C.; Chien, J. C.; Shieh, R. C.; Chen, Y. T. | J Med Genet 43(10), 817-821 | | | |
| 2005 | R1193Q of SCN5A, a Brugada and long QT mutation, is a common polymorphism in Han Chinese | Hwang, H. W.; Chen, J. J.; Lin, Y. J.; Shieh, R. C.; Lee, M. T.; Hung, S. I.; Wu, J. Y.; Chen, Y. T.; Niu, D. M.; Hwang, B. T. | J Med Genet 42, e7 | | | |
| 2005 | Type II collagen gene variants and inherited osteonecrosis of the femoral head | Liu, Y. F.; Chen, W. M.; Lin, Y. F.; Yang, R. C.; Lin, M. W.; Li, L. H.; Chang, Y. H.; Jou, Y. S.; Lin, P. Y.; Su, J. S.; Huang, S. F.; Hsiao, K. J.; Fann, C. S. J.; Hwang, H. W.; Chen, Y. T.; Tsai, S. F. | NEW ENGLAND JOURNAL OF MEDICINE 352, 2294-2301 | | | |
| 2005 | Type II collagen gene variants and inherited osteonecrosis of the frmoral head | Liu, Y. F.; Chen, W. M.; Lin, Y. F.; Yang, R. C.; Lin, M. W.; Li, L. H.; Chang, Y. H.; Jou, J. S.; Lin, P. Y.; Su, J. S.; Huang, S. F.; Hsiao, K. J.; Fann, C. S.; Hwang, H. W.; Chen, Y. T.; Tsai, S. F. | New England Journal of Medicine 352, 2294-2301 | | | |
