Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
2010 | Garlic accelerates red blood cell turnover and splenic erythropoietic gene expression in mice: evidence for erythropoietin-independent erythropoiesis | Akgül, Bünyamin; Lin, K. W.; Ou Yang, H. M.; Chen, Y. H.; Lu, T. H.; Chen, C. H.; Kikuchi, T.; Chen, Y. T.; Tu, C. P. D. | PLoS ONE 5(12), e15385 | | | |
2000 | Genetic analysis of enterovirus 71 isolated from fatal and non-fatal cases of hand, foot and mouth disease during an epidemic in Taiwan, 1998 | Shih, S. R.; Ho, M. S.; Lin, K. H.; Wu, S. L.; Chen, Y. T.; Wu, C. N.; Lin, T. Y.; Chang, L. Y.; Tsao, K. C.; Ning, H. C.; Chang, P. Y.; Jung, S. M.; Hsueh, C.; Chang, K. S. | Virus Res 68, 127-136 | | | |
2009 | Genetic determinants of warfarin dosing in the Han-Chinese population | Lee, M. T.; Chen, C. H.; Chou, C. H.; Lu, L. S.; Chuang, H. P.; Chen, Y. T.; Saleem, A. N.; Wen, M. S.; Chen, J. J.; Wu, J. Y.; Chen, Y. T. | PHARMACOGENOMICS 10(12), 1905-1913 | | | |
2010 | Genetic Predisposition of life treatening antiepileptic-induced skin reactions | Chung, W. H.; Hung, S. I.; Chen, Y. T. | Expert Opinion on Drug Safety 9(1), 15-21 | | | |
2010 | Genetic susceptibility and pharmacogenomics of severe cutaneous adverse drug reactions | Chen, Y. T. | Epilepsy & Seizure 3(1), 51-58 | | | |
2006 | Genetic susceptibility to carbamazepine-induced cutaneous adverse drug reactions | Hung, S. I.; Chung, W. H.; Jee, S. H.; Chen, W. C.; Chang, Y. T.; Lee, W. R.; Hu, S. L.; Wu, M. T.; Chen, G. S.; Wong, T. W.; Hsiao, P. F.; Chen, W. H.; Shih, H. Y.; Fang, W. H.; Wei, C. Y.; Lou, Y. H.; Huang, Y. L.; Lin, J. J.; Chen, Y. T. | Pharmacogenet Genomics 16, 297-306 | | | |
2007 | Genetics of severe drug hypersensitivity reactions in Han Chinese | Hung, S. I.; Chung, W. H.; Chen, Y. T. | Drug Hypersensitity (Switzerland : S. Karger AG) | | | |
2010 | Genome-wide Association study of bipolar I disorder in the Han Chinese population | Lee, M. T. M.; Chen, C. H.; Lee, C. S.; Chen, C. C.; Chong, M. Y.; Ou-Yang, W. C.; Chiu, N. Y.; Chuo, L. J.; Chen, C. Y.; Tan, H. K. L.; Lane, H. Y.; Chang, T. J.; Lin, C. H.; Jou, S. H.; Hou, Y. M.; Feng, J.; Lai, T. J.; Tung, C. L.; Chen, T. J.; Chang, C. J.; Lung, F. W.; Chen, C. K.; Shiah, I. S.; Liu, C. Y.; Teng, P. R.; Chen, K. H.; Shen, L. J.; Chen, C. S.; Chang, T. P.; Li, C. F.; Chou, C. H.; Chen, C. Y.; Wang, K. H. T.; Fann, C. S. J.; Wu, J. Y.; Chen, Y. T.; Cheng, A. T. A. | Molecular Psychiatry 16, 548-556 | | | |
2008 | Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling | Lin, C. H.; Huang, M. C.; Li, L. H.; Wu, J. Y.; Chen, Y. T.; Fann, C. S. J. | Hum Mutat 29(8), 1055-1062 | | | |
2000 | Genotype-phenotype correlation in two frequent mutations and mutation update in type III glycogen storage disease | Shaiu, W. L.; Kishnani, P. S.; Shen, J.; Liu, H. M.; Chen, Y. T. | Mol Genet Metab 69, 16-23 | | | |
2005 | Glucose tetrasaccharide as a biomarker for monitoring the therapeutic response to enzyme replacement therapy for Pompe disease | An, Y.; Young, S. P.; Kishnani, P. S.; Millington, D. S.; Amalfitano, A.; Corz, D.; Chen, Y. T. | Mol Genet Metab 85, 247-254 | | | |
2000 | Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotype | Weston, B. W.; Lin, J. L.; Muenzer, J.; Cameron, H. S.; Arnold, R. R.; Seydewitz, H. H.; Mayatepek, E.; Van Schaftingen, E.; Veiga-da-Cunha, M.; Matern, D.; Chen, Y. T. | Pediatr Res 48, 329-334 | | | |
1992 | Glycogen debranching enzyme deficiency: long-term study of serum enzyme activities and clinical features | Coleman, R. A.; Winter, H. S.; Wolf, B.; Chen, Y. T. | J Inherit Metab Dis 15, 869-881 | | | |
1987 | Glycogen debranching enzyme: purification, antibody characterization, and immunoblot analyses of type III glycogen storage disease | Chen, Y. T.; He, J. K.; Ding, J. H.; Brown, B. I. | Am J Hum Genet 41, 1002-1015 | | | |
2001 | Glycogen storage disease and other inherited disorders of carbohydrate | Chen, Y. T. | Harrison’s Principles of Internal Medicine, 15th Edition (New York : McGraw Hill) | | | |
2007 | Glycogen storage disease and other inherited disorders of carbohydrate | Chen, Y. T. | Harrison’s Principles of Internal Medicine, 17th Edition (New York : McGraw-Hill) | | | |
1999 | Glycogen storage disease III subtypes and muscle weakness during childhood | Chen, Y. T. | Hum Genet 104, 112 | | | |
2002 | Glycogen storage disease type I: diagnosis and phenotype/genotype correlation | Matern, D.; Seydewitz, H. H.; Bali, D.; Lang, C.; Chen, Y. T. | Eur J Pediatr 161, S10-S19 | | | |
1995 | Glycogen storage disease type Ia in two littermate Maltese puppies | Brix, A. E.; Howerth, E. W.; McConkie-Rosell, A.; Peterson, D.; Egnor, D.; Wells, M. R.; Chen, Y. T. | Vet Pathol 32, 460-465 | | | |
1992 | Glycogen storage disease type III (glycogen debranching enzyme deficiency): correlation of biochemical defects with myopathy and cardiomyopathy | Coleman, R. A.; Winter, H. S.; Wolf, B.; Gilchrist, J. M.; Chen, Y. T. | Ann Intern Med 116, 896-900 | | | |