| 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 | | | |
| 2010 | Ectopic and High CXCL13 Chemokine Expression in Myasthenia Gravis with Thymic Lymphoid Hyperplasia | Shiao, Y. M.; Lee, C. C.; Hsu, Y. H.; Huang, S. F.; Lin, C. Y.; Li, L. H.; Fann, C. S. J.; Tsai, C. Y.; Tsai, S. F.; Chiu, H. C. | Journal of Neuroimmunology 221(1-2), 101-106 | | | |
| 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 | | | |
| 2004 | Genomic Shotgun Array: A Procedure Linking Large-Scale DNA Sequencing with Regional Transcript Mapping. | Li, L. H.; Li, J. C.; Lin, Y. F.; Lin, C. Y.; Chen, C. Y.; Tsai, S. F. | Nucleic Acids Research 32, 27-35 | | | |
| 2010 | Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2-13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high-density oligonucleotide array-a recognizable syndrome | Chang, C. F.; Li, L. H.; Wang, C. H.; Tsai, F. J.; Chen, T. C.; Wu, J. Y.; Chen, Y. T.; Tsai, A. C. H. | American J of Medical Genetics Part A 152A(9), 2365-2371 | | | |
| 2006 | Long contiguous stretches of homozygosity in the human genome | Li, L. H.; Ho, S. F.; Chen, C. H.; Wei, C. Y.; Wong, W. C.; Li, L. Y.; Hung, S. I.; Chung, W. H.; Pan, W. H.; Lee, M. T.; Tsai, F. J.; Chang, C. F.; Wu, J. Y.; Chen, Y. T. | Hum Mutat 27(11), 1115-1121 | | | |
| 2011 | Molecular profile and copy number analysis of sporadic colorectal cancer in Taiwan | Lin, C. H.; Lin, J. K.; Chang, S. C.; Chang, Y. H.; Chang, H. M.; Liu, J. H.; Li, L. H.; Chen, Y. T.; Tsai, S. F.; Chen, W. S | Journal of Biomedical Science 18, 36 | | | |
| 2005 | Type II collagen gene variants and inherited osteonecrosis of the femoral head | Liu, Y. F.; Chen, W. M.; Lin, Y. F.; Yang, R. C.; Lin, M. W.; Li, L. H.; Chang, Y. H.; Jou, Y. S.; Lin, P. Y.; Su, J. S.; Huang, S. F.; Hsiao, K. J.; Fann, C. S. J.; Hwang, H. W.; Chen, Y. T.; Tsai, S. F. | NEW ENGLAND JOURNAL OF MEDICINE 352, 2294-2301 | | | |
| 2005 | Type II collagen gene variants and inherited osteonecrosis of the frmoral head | Liu, Y. F.; Chen, W. M.; Lin, Y. F.; Yang, R. C.; Lin, M. W.; Li, L. H.; Chang, Y. H.; Jou, J. S.; Lin, P. Y.; Su, J. S.; Huang, S. F.; Hsiao, K. J.; Fann, C. S.; Hwang, H. W.; Chen, Y. T.; Tsai, S. F. | New England Journal of Medicine 352, 2294-2301 | | | |
