Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
2010 | Pharmacogenetics of toxic epidermal necrolysis | Lee, M. T. M.; Hung, S. I.; Wei, C. Y.; Chen, Y. T. | EXPERT OPINION ON PHARMACOTHERAPY 13, 2153-2162 | | | |
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 | | | |
2008 | RASD2, MYH9, and CACNG2 Genes at Chromosome 22q12 Associated with the Subgroup of Schizophrenia with Non-deficit in Sustained Attention and Executive Function | Liu, Y. L.; Fann, C. S. J.; Liu, C. M.; Chen, W. J.; Wu, J. Y.; Hung, S. I.; Chen, C. H.; Jou, Y. S.; Liu, S. K.; Hwang, T. J.; Hsieh, M. H.; Chang, C. C.; Yang, W. C.; Lin, J. J.; Chou, F. H. C.; Faraone, S. V.; Tsuang, M. T.; Hwu, H. G. | Biological Psychiatry 64 (9), 789–796 | | | |
2008 | RASD2, MYH9m and CACNG2 genes at chromosome 22q12 associated with the subgroup of schizophrenia with non-deficit in sustained attention and executive function | Liu, Y. L.; Fann, C. S. J.; Liu, C. M.; Chen, W. J.; Wu, J. Y.; Hung, S. I.; Chen, C. H.; Jou, Y. S.; Liu, S. K.; Hwang, T. J.; Hsieh, M. H.; Chang, C. C.; Yang, W. C.; Lin, J. J.; Chou, F. H.; Faraone, S. V.; Tsuang, M. T.; Hwu, H. G. | Biol Psychiatry 64(9), 789-796 | | | |
2011 | Shared and restricted T-cell receptor use is crucial for carbamazepine-induced Stevens-Johnson syndrome | Ko, T. M. ; Chung, W. H.; Wei, C. Y.; Shih, H. Y.; Chen, J. K.; Lin, C. H.; Chen, Y. T. ; Hung, S. I. | Journal of Allergy and Clinical Immunology 128(6), 1266-1276.e11 | | | |
2001 | The crystal structure of a novel mammalian lectin, Ym1, suggests a saccharide binding site | Sun, Y. J.; Chang, N. C.; Hung, S. I.; Chang, A. C.; Chou, C. C.; Hsiao, C. D. | J Biol Chem 276, 17507-17514 | | | |