| Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
| 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 | | | |
| 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 | | | |
| 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 | | | |
| 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 | | | |
| 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 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 | | | | |
| 2021 | Genome-wide association study of early-onset bipolar I disorder in the Han Taiwanese population | Wu, LS; Huang, MC; Fann, CS ; Lane, HY; Kuo, CJ; Chiu, WC; Kwok, PY ; Cheng, AT | Translational psychiatry 11, 301 | | | |
| 2021 | Genome-Wide Association Study of Lithium-Induced Dry Mouth in Bipolar I Disorder | Wu, LS; Huang, MC; Chen, CK; Shen, CY ; Fann, CS ; Lin, CY; Lin, CC; Cheng, AT | Journal of personalized medicine 11(12), 1265 | | | |
| 2022 | Genome-wide association study reveals susceptibility loci for self-reported headache in a large community-based Asian population | Tsao, YC; Wang, SJ; Hsu, CL; Wang, YF; Fuh, JL; Chen, SP; Fann, CS | Cephalalgia 42(3), 229-238 | | | |
| 2021 | Hepatitis B virus persistent infection-related single nucleotide polymorphisms in HLA regions are associated with viral load in hepatoma families | Hsieh, AR; Fann, CSJ ; Lin, HC; Tai, J; Hsieh, SY; Tai, DI | WORLD JOURNAL OF GASTROENTEROLOGY 27(37), 6262-6276 | | | |
| 2019 | Heterozygosity mapping for human dominant trait variants. | Imai-Okazaki, A; Li, Y; Horpaopan, S; Riazalhosseini, Y; Garshasbi, M; Mosse, YP; Zhang, D; Schrauwen, I; Sharma, A; Fann, CSJ ; Leal, SM; Lathrop, M; Ott, J | Human Mutation 40(7), 996-1004 | | | |
| 2020 | Maximal Segmental Score method for localizing recessive disease variants based on sequence data | Ai-Ru Hsieh; Jia Jyun Sie; Chien Ching Chang; Jurg Ott; Ie-Bin Lian; Cathy SJ Fann | Frontiers in Genetics 11, 555 | | | |
| 2022 | Patient-Derived Organoid Serves as a Platform for Personalized Chemotherapy in Advanced Colorectal Cancer Patients | K Geevimaan; J.Y. Guo; C.N. Shen ; J.K. Jiang; C.S.J. Fann ; M.J. Hwang ; J.W. Shui ; H.T. Lin; M.J. Wang; H.C. Shih; A. F.Y. Li; S.C. Chang; S.H. Yang; J.Y. Chen | Frontiers in Oncology 12, 883437 | | | |
| 2020 | Shared genomic segment analysis with equivalence testing | Horpaopan, Sukanya; Fann, Cathy S. J. ; Lathrop, Mark; Ott, Jurg | Genetic Epidemiology 44(7), 741-747 | | | |
| 2020 | Source identification of HIV-1 transmission in three lawsuits Using Ultra-Deep pyrosequencing and phylogenetic analysis | Li, WY; Huang, SW; Wang, SF; Liu, HF; Chou, CH; Wu, SJ; Huang, HD; Lu, PL; Fann, CSJ ; Chen, M; Chen, YH; Chen, YA | Journal of Microbiology, Immunology and Infection | | | |
| 2019 | TRPM8 genetic variant is associated with chronic migraine and allodynia. | Ling, YH; Chen, SP; Fann, CS ; Wang, SJ; Wang, YF | The Journal of Headache and Pain 20(1), 115 | | | |
| 2019 | Weight loss and metabolic improvements in obese patients undergoing gastric banding and gastric banded plication: A comparison | Weu Wang; Fann, Cathy SJ ; Shwu-Huey Yang; Hsin-Hung Chen; Chih-Yen Chen | Nutrition 57, 290-299 | | | |
