| 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 | | | |
| 2007 | Dysregulation of C/EBPalpha by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease | Chiang, M. C.; Chen, H. M.; Lee, Y. H.; Chang, H. H.; Wu, Y. C.; Soong, B. W.; Chen, C. M.; Wu, Y. R.; Liu, C. S.; Niu, D. M.; Wu, J. Y.; Chen, Y. T.; Chern, Y. | Hum Mol Genet 16(5), 483-498 | | | |
| 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 | | | |
