| Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
| 2008 | A case of congenital glycogen storage disease type IV with a novel GBE1 mutation | Raju, G. P.; Li, H. C.; Bali, D. S.; Chen, Y. T.; Urion, D. K.; Lidov, H. G. W.; Kang, P. B. | J Child Neurol 23(3), 349-352 | | | |
| 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 | | | |
| 1998 | A gene on chromosome 11q23 coding for a putative glucose- 6-phosphate translocase is mutated in glycogen-storage disease types Ib and Ic | Veiga-da-Cunha, M.; Gerin, I.; Chen, Y. T.; de Barsy, T.; de Lonlay, P.; Dionisi-Vici, C.; Fenske, C. D.; Lee, P. J.; Leonard, J. V.; Maire, I.; McConkie-Rosell, A.; Schweitzer, S.; Vikkula, M.; Van Schaftingen, E. | Am J Hum Genet 63, 976-983 | | | |
| 2010 | A genome-wide association study identifies susceptibility variants for Type 2 Diabetes in Han Chinese | Tsai, F. J.; Yang, C. F.; Chen, C. C.; Chuang, L. M.; Lu, C. H.; Chang, C. T.; Wang, T. Y.; Chen, R. H.; Shiu, C. F.; Liu, Y. M.; Chang, C. C.; Chen, P.; Chen, C. H.; Fann, C. S. J.; Chen, Y. T.; Wu, J. Y. | PLoS Genetics 6(2), e1000847 | | | |
| 2006 | A genome-wide study of preferential amplification/hybridization in microarray-based pooled DNA experiments | Yang, H. C. ; Liang, Y. J.; Huang, M. C.; Li, L. H.; Lin, C. H.; Wu, J. Y.; Chen, Y. T.; Fann, C. S. J. | Nucleic Acids Research 34(15), e106 | | | |
| 1993 | A man with type III glycogenosis associated with cirrhosis and portal hypertension | Markowitz, A. J.; Chen, Y. T.; Muenzer, J.; Delbuono, E. A.; Lucey, M. R. | Gastroenterology 105, 1882-1885 | | | |
| 2011 | A Mutation in Cartilage Oligomeric Matrix Protein (COMP) Causes Early- Onset Osteoarthritis in a Large Kindred Study | Mu, S. C.; Lin, Y. J.; Liu, W. C.; Wu, J. Y.; Li, S. C.; Lee, M. T. M.; Chen, L. K.; Chen, Y. T. | Annals of Human Genetics 75(5), 575-583 | | | |
| 1997 | A nonsense mutation due to a single base insertion in the 3'-coding region of glycogen debranching enzyme gene associated with a severe phenotype in a patient with glycogen storage disease type IIIa | Shen, J.; Bao, Y.; Chen, Y. T. | Hum Mutat 9, 37-40 | | | |
| 2005 | A novel functional VKORC1 promoter polymorphism is associated with inter-individual and inter-ethnic differences in warfarin sensitivity | Yuan, H. Y.; Chen, J. J.; Lee, M. T.; Wung, J. C.; Chen, Y. F.; Charng, M. J.; Lu, M. J.; Hung, C. R.; Wei, C. Y.; Chen, C. H.; Wu, J. Y.; Chen, Y. T. | Hum Mol Genet 14, 1745-1751 | | | |
| 2008 | A promoter sequence variant of ZNF750 is linked with familial psoriasis | Yang, C. F.; Hwu, W. L.; Yang, L. C.; Chung, W. H.; Chien, Y. H.; Hung, C. F.; Chen, H. C.; Tsai, P. J.; Fann, C. S. J.; Liao, F.; Chen, Y. T. | J Invest Dermatol 128(7), 1662-1668 | | | |
| 2008 | A rpomoter sequence variant of ZNF750 is linked with familial psoriasis | Yang, C. F.; Hwu, W. L.; Yang, L. C.; Chung, W. H.; Chien, Y. H.; Hung, C. F.; Chen, H. C.; Tsai, P. J.; Fann, C. S. J.; Liao, F.; Chen, Y. T. | J Invest Dermatol 128(7), 1662-8 | | | |
| 2015 | A search for subkilometer-sized ordinary chondrite like asteroids in the main-belt | Lin, H. W.; Yoshida, Fumi; Chen, Y. T.; Ip, W. H.; Chang, C. K. | ICARUS 254, 202-212 | | | |
| 1997 | A single-base deletion in the 3'-coding region of glycogen-debranching enzyme is prevalent in glycogen storage disease type IIIA in a population of North African Jewish patients | Parvari, R.; Moses, S.; Shen, J.; Hershkovitz, E.; Lerner, A.; Chen, Y. T. | Eur J Hum Genet 5, 266-270 | | | |
| 1994 | A splice junction mutation in a new myopathic variant of phosphoglycerate kinase deficiency (PGK North Carolina) | Tsujino, S.; Tonin, P.; Shanske, S.; Nohria, V.; Boustany, R. M.; Lewis, D.; Chen, Y. T.; DiMauro, S. | Ann Neurol 35, 349-353 | | | |
| 2013 | A stable silicon/graphene composite using solvent exchange method as anode material for lithium ion battery | Wong, D. P.; Tseng, H. P.; Chen, Y. T.; Hwang, B. J.; Chen, L. C.; Chen, K. H. | CARBON | | | |
| 2008 | AAV vector-mediated reversal of hypoglycemia in canine and murine glycogen storage disease type Ia | Koeberl, D. D.; Pinto, C.; Sun, B.; Kozink, D. M.; Benjamin, D. K.; Demaster, A. K.; Kruse, M. A.; Vaughn, V.; Hillman, S.; Bird, A.; Jackson, M.; Brown, T.; Kishnani, P. S.; Chen, Y. T. | Mol Ther 16, 665-672 | | | |
| 2000 | Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders | Shen, J. J.; Matern, D.; Millington, D. S.; Hillman, S.; Feezor, M. D.; Bennett, M. J.; Qumsiyeh, M.; Kahler, S. G.; Chen, Y. T.; Van Hove, J. L. | J Inherit Metab Dis 23, 27-44 | | | |
| 1999 | Age-associated rapid and Stat6-independent IL-4 production by NK1-CD4+8- thymus T lymphocytes | Chen, Y. T.; Chen, F. L.; Kung, J. T. | J Immunol 163, 4747-4753 | | | |
| 2011 | Allopurinol | Chen, P.; Hung, S. -I.; Chen, S. -Y.; Chen, Y. T. | Molecular and Translational Medicine, Pharmacogenomic Testing in Current Clinical Practice (USA : Humana Press) | | | |
| 2006 | Ambulatory electrocardiogram analysis in infants treated with recombinant human acid alpha-glucosidase enzyme replacement therapy for Pompe disease | Cook, A. L.; Kishnani, P. S.; Carboni, M. P.; Kanter, R. J.; Chen, Y. T.; Ansong, A. K.; Kravitz, R. M.; Rice, H.; Li, J. S. | Genet Med 8, 313-317 | | | |
