公開日期 | 題名 | 作者 | 關聯 | scopus | WOS | 全文 |
2006 | A comparison of individual genotyping and pooled DNA analysis for polymorphism validation prior to large-scale genetic studies | Yang, H. C. ; Lin, C. H.; Hung, S. I.; Fann, C. S. J. | ANNALS OF HUMAN GENETICS 70(3), 350-359 | | | |
2022 | A Deep Learning-enabled Electrocardiogram Model for the Identification of a Rare Inherited Arrhythmia: Brugada Syndrome | Liu, CM; Liu, CL; Hu, KW; Tseng, VS; Chang, SL; Lin, YJ; Lo, LW; Chung, FP; Chao, TF; Tuan, TC; Liao, JN; Lin, CY; Chang, TY; Fann, CS ; Higa, S; Yagi, N; Hu, YF; Chen, SA | Canadian Journal of Cardiology 38(2), 152-159 | | | |
2005 | A genome-wide scanning and fine mapping study of COGA data | Yang, H. C. ; Chang, C. C.; Lin, C. Y.; Chen, C. L.; Lin, C. Y.; Fann, C. S. J | BMC Genetics 6, S30 | | | |
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 | | | |
2017 | A non-threshold region-specific method for detecting rare variants in complex diseases | Hsieh, AR; Chen, DP; Chattopadhyay, AS; Li, YJ; Chang, CC; Fann, CSJ | PLOS ONE 12(11), e0188566 | | | |
2006 | A Single Nucleotide Polymorphism Fine Mapping Study of Chromosome 1q42.1 Reveals the Vulnerability Genes for Schizophrenia, GNPAT and DISC1: Association with Impairment of Sustained Attention | Liu, Y. L.; Fann, C. S. J. ; Liu, C. M.; Wu, J. W.; Hung, S. I.; Chen, C. H. ; Jou, Y. S.; Liu, S. K.; Hwang, T. J.; Hsieh, M. H.; Ouyang, W. C.; Chan, H. Y.; Chen, J. J.; Yang, W. C.; Lin, C. Y.; Lee, S. F. C.; Hwu, H. W. | Biological Psychiatry 60(6), 554-562 | | | |
2006 | A sliding-window weighted linkage disequilibrium test | Yang, H. C. ; Lin, C. Y.; Fann, C. S. J. | GENETIC EPIDEMIOLOGY 30(6), 531-545 | | | |
2006 | A sliding-window weighted linkage disequilibrium test | Yang, H. C. ; Lin, C. Y.; Fann, C. S. J. | | | | |
2021 | Accelerated cardiovascular risk after viral clearance in hepatitis C patients with the NAMPT-rs61330082 TT genotype: An 8-year prospective cohort study | Chang, ML; Lin, YS; Chang, MY; Hsu, CL; Chien, RN; Fann, CS | Virulence 12(1), 270-280 | | | |
2021 | Analysis of site-specific glycan profiles of serum proteins in patients with multiple sclerosis or neuromyelitis optica spectrum disorder - a pilot study | Ip, PP; Li, Q; Lin, WH; Chang, CC; Fann, CS ; Chen, HY; Liu, FT; Lebrilla, CB; Yang, CC; Liao, F | Glycobiology, cwab053 | | | |
2015 | Association of circadian genes with diurnal blood pressure changes and non-dipper essential hypertension: a genetic association with young-onset hypertension | Leu, HB; Chung, CM; Lin, SJ; Chiang, KM; Yang, HC ; Ho, HY; Ting, CT; Lin, TH; Sheu, SH; Tsai, WC; Chen, JH; Yin, WH; Chiu, TY; Chen, CI; Fann, CS ; Chen, YT ; Pan, WH ; Chen, JW | Hypertension research 38(2), 155-162 | | | |
2005 | Breast cancer risk associated with genotypic polymorphism of the mitosis-regulating gene Aurora-A/STK15/BTAK | Lo, Y. L.; Yu, J. C.; Chen, S. T.; Yang, H. C. ; Fann, C. S. J. ; Mau, Y. C.; Shen, C. Y. | International Journal of Cancer 115(2), 276~283 | | | |
2019 | Determining population stratification and subgroup effects in association studies of rare genetic variants for nicotine dependence. | Hsieh, AR; Chen, LS; Li, YJ; Fann, CSJ | Psychiatric Genetics 29(4), 111-119 | | | |
2023 | Effects of insomnia and non-vasomotor menopausal symptoms on coronary heart disease risk: a mendelian randomization study | Lian, IB; Sie, JJ; Chang, CC; Fann, CSJ ; Huang, CH | Heliyon 9(2), e13569 | | | |
2023 | Extracellular Nicotinamide Phosphoribosyltransferase as a Surrogate Marker of Prominent Malignant Potential in Colonic Polyps: A 2-Year Prospective Study | Chen, TH; Hsu, HC; You, JF; Lai, CC; Tsou, YK; Hsu, CL; Fann, CSJ ; Chien, RN; Chang, ML | Cancers 15(6), 1702 | | | |
2013 | Fine-mapping angiotensin-converting enzyme gene: separate QTLs identified for hypertension and for ACE activity. | Chung, CM; Wang, RY; Fann, CS ; Chen, JW; Jong, YS; Jou, YS ; Yang, HC ; Kang, CS; Chen, CC; Chang, HC; Pan, WH | PloS one 8(3), e56119 | | | |
2021 | Genetic Association of Hepatitis C-Related Mixed Cryoglobulinemia: A 10-Year Prospective Study of Asians Treated with Antivirals | Chang, ML; Chang, SW; Chen, SC; Chien, RN; Hsu, CL; Chang, MY; Fann, CSJ | Viruses 13(3), 464 | | | |
2022 | Genome-wide analyses identify novel risk loci for cluster headache in Han Chinese residing in Taiwan | Chen, SP; Hsu, CL; Wang, YF; Yang, FC; Chen, TH; Huang, JH; Pan, LH; Fuh, JL; Chang, HC; Lee, YL; Chang, HC; Lee, KH; Chang, YC; Fann, CS ; Wang, SJ | The Journal of Headache and Pain 23(1), 147 | | | |
2022 | Genome-wide analysis identified novel susceptible genes of restless legs syndrome in migraineurs | Jiang, YJ; Fann, CS ; Fuh, JL; Chung, MY; Huang, HY; Chu, KC; Wang, YF; Hsu, CL; Kao, LS; Chen, SP; Wang, SJ | J Headache Pain 23, 39 | | | |
2021 | Genome-wide association analysis in host genetic characteristics of progression to high-grade cervical intraepithelial neoplasia or more severe for women with human papillomavirus infection and normal cytology. | Chyong-Huey Lai; Su-Wei Chang; Lan Yan Yang; Shuen-Iu Hung; Chiao-Yun Lin; Angel Chao; Yun-Shien Lee; Swei Hsueh; Chu-Chun Huang; Hsuan-Yu Chen; Hung-Hsueh Chou; Cheng-Tao Lin; Chin-Jung Wang; Huei-Jean Huang; Kung-Gen Huang; Min-Yu Chen; Yun-Hsin Tang; Ren-Chin Wu; Ting-Chang Chang; Chee-Jen Chang; Chien-Ching Chang; Chia-Lin Hsu; Yuan-Tsong Chen; Jer-Yuarn Wu; Cathy S-J Fann | | | | |