Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
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 | | | |
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 | | | |
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 | | | |
2006 | Absence of significant associations between four AKT1 SNP markers and schizophrenia in the Taiwanese population | Liu, Y. L.; Fann, C. S. J.; Liu, C. M.; Wu, J. Y.; Hung, S. I.; Chan, H. Y.; Chen, J. J.; Pan, C. C.; Liu, S. K.; Hsieh, M. H.; Hwang, T. J.; Ouyang, W. C.; Chen, C. Y.; Lin, J. J.; Chou, F. H.; Chueh, C. M.; Liu, W. M.; Tsuang, M. M.; Faraone, S. V.; Tsuang, M. T.; Chen, W. J.; Hwu, H. G. | Psychiatric Genetics 16, 39-41 | | | |
2019 | Asian Culturally Specific Predictors in a Large-Scale Land Use Regression Model to Predict Spatial-Temporal Variability of Ozone Concentration | Hsu, C.Y.; Wu, J. Y.; Chen, Y.C.; Chen, N. T; Chen, M. J.; Pan, W. C.; Lung, S.C.C. ; Guo, Y. L.; Wu, C.D. | International Journal of Environmental Research and Public Health 16(7), 1300 | | | |
2004 | Autosomal dominant avascular necrosis of femoral head in two Taiwanese pedigrees and linkage to chromosome 12q13 | Chen, W. M.; Liu, Y. F.; Lin, M. W.; Chen, I. C.; Lin, P. Y.; Lin, G. L.; Jou, Y. S.; Lin, Y. T.; Fann, C. S. J.; Wu, J. Y.; Hsiao, K. J.; Tsai, S. F. | Am J Hum Genet 75, 310-317 | | | |
1997 | Chemoenzymatic preparation of novel cyclic imine sugars and rapid biological activity evaluation using electrospray mass spectrometry and kinetic analysis | Takayama, S.; Martin, R.; Wu, J. Y.; Laslo, K.; Siuzdak, G.; Wong, C. H. | J Am Chem Soc 119, 8146-8151 | | | |
2009 | Clustering by neurocognition for fine mapping of the schizophrenia susceptibility loci on chromosome 6p | Lin, S. H.; Liu, C. M.; Liu, Y. L.; Fann, C. S. J.; Hsiao, P. C.; Wu, J. Y.; Hung, S. I.; Chen, C. H. ; Wu, H. M.; 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.; Chen, W. J. | Genes, Brain and Behavior 8(8), 785-794 | | | |
2002 | Co-dominant RAPD markers closely linked with two morphological genes in rice (Oryza sativa L.) | Wu, J. Y.; Wu, H. K.; Chung, M. C. | Bot Bull Acad Sin 43, 171-180 | | | |
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 | | | |
2006 | ENU mutagenesis identifies mice with cardiac fibrosis and hepatic steatosis caused by a mutation in mitochondrial trifunctional protein beta-subunit | Kao, H. J.; Cheng, C. F.; Chen, Y. H.; Hung, S. I.; Huang, C. C.; Millington, D.; Kikuchi, T.; Wu, J. Y.; Chen, Y. T. | Hum Mol Genet 15(24), 3569-3577 | | | |
2004 | ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease | Wu, J. Y.; Kao, H. J.; Li, S. C.; Stevens, R.; Hillman, S.; Millington, D.; Chen, Y. T. | J Clin Invest 113, 434-440 | | | |
1995 | Epitaxial Growth of Diamond Films for Electronic Applications | Chen, K. H.; Wu, J. Y.; Chen, L. C.; Juan, C. C.; Hsu, T. | Wide Bandgap Semiconductors and Devices: State-of-the-Art Program on Compound Semiconductors XXIII 95-21, 55-69 | | | |
1996 | Expression of catalytically active human multifunctional glycogen-debranching enzyme and lysosomal acid alpha-glucosidase in insect cells | Wu, J. Y.; Van Hove, J. L.; Huang, Y. S.; Chen, Y. T. | Biochem Mol Biol Int 39, 755-764 | | | |
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 | 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 | | | |
2010 | Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder | Li, S. C.; Chen, C. M.; Goldstein, J. L.; Wu, J. Y.; Lemyre, E.; Burrow, T. A.; Kang, P. B.; Chen, Y. T.; Bali, D. S. | JOURNAL OF INHERITED METABOLIC DISEASE online:08 January | | | |
2008 | Granulysin is a key mediator for disseminated keratinocyte death in Stevens-Johnson syndrome and toxic epidermal necrolysis | Chung, W. H.; Hung, S. I.; Yang, J. Y.; Su, S. C.; Huang, S. P.; Wei, C. Y.; Chin, S. W.; Chiou, C. C.; Chu, S. C.; Ho, H. C.; Yang, C. H.; Lu, C. F.; Wu, J. Y.; Liao, Y. D.; Chen, Y. T. | NATURE MEDICINE 14(12), 1345-1350 | | | |
1996 | Hepatic and neuromuscular forms of glycogen storage disease type IV caused by mutations in the same glycogen-branching enzyme gene | Bao, Y.; Kishnani, P.; Wu, J. Y.; Chen, Y. T. | J Clin Invest 97, 941-948 | | | |