| 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 | | | |
| 2006 | A comparison of major histocompatibility complex SNPs in Han Chinese residing in Taiwan and Caucasians | Yang, H. C. ; Lin, C. H.; Hsu, C. L.; Hung, S. I.; Wu, J. Y.; Pan, W. H. ; Chen, Y. T. ; Fann, C. S. J. | Journal of biomedical science 13, 489-498 | | | |
| 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. | Genet Epidemiol 30(6), 531-545 | | | |
| 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 | | | |
| 2007 | Association mapping using pooled DNA | Yang, H. -C. ; Fann, C. S. J. | Linkage Disequilibrium and Association Mapping (USA : Humana Press Inc.) | | | |
| 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 | | | |
| 2023 | Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor | Bendik S. Winsvold; Aster V. E. Harder; Caroline Ran; Mona A. Chalmer; Maria Carolina Dalmasso; Egil Ferkingstad; Kumar Parijat Tripathi; Elena Bacchelli; Sigrid Børte; Carmen Fourier; Anja S. Petersen; Lisanne S. Vijfhuizen; Sigurdur H. Magnusson; Emer O'Connor; Gyda Bjornsdottir; Paavo Häppölä; Yen-Feng Wang; Ida Callesen; Tim Kelderman; Victor J Gallardo; Irene de Boer; Felicia Jennysdotter Olofsgård; Katja Heinze; Nunu Lund; Laurent F. Thomas; Chia-Lin Hsu; Matti Pirinen; Heidi Hautakangas; Marta Ribasés; Simona Guerzoni; Prasanth Sivakumar; Janice Yip; Axel Heinze; Fahri Küçükali; Sisse R. Ostrowski D; Ole B. Pedersen; Espen S. Kristoffersen; Amy E. Martinsen; María S. Artigas; Susie Lagrata; Maria Michela Cainazzo; Joycee Adebimpe; Olivia Quinn; Carl Göbel; Anna Cirkel; Alexander E. Volk; Stefanie Heilmann-Heimbach; Anne Heidi Skogholt; Maiken E. Gabrielsen; Leopoldine A. Wilbrink; Daisuke Danno; Dwij Mehta; Daníel F. Guðbjartsson; HUNT All-In Headache; The International Headache Genetics Consortium; DBDS Genomic Consortium; Frits R. Rosendaal; Ko Willems van Dijk; Rolf Fronczek; Michael Wagner; Martin Scherer; Hartmut Göbel; Kristel Sleegers; Olafur A. Sveinsson; Luca Pani; Michele Zoli; Josep A. Ramos-Quiroga; Efthimios Dardiotis; Anna Steinberg; Steffi Riedel-Heller; Christina Sjöstrand; Thorgeir E. Thorgeirsson; Hreinn Stefansson; Laura Southgate; Richard C. Trembath; Jana Vandrovcova; Raymond Noordam; Koen Paemeleire; Kari Stefansson; Cathy Shen-Jang Fann ; Elisabet Waldenlind; Erling Tronvik; Rigmor H. Jensen; Shih-Pin Chen; Henry Houlden; Gisela M. Terwindt; Christian Kubisch; Elena Maestrini; Michail Vikelis; Patricia Pozo-Rosich; Andrea C. Belin; Manjit Matharu; Arn M.J.M. van den Maagdenberg; Thomas F. Hansen; Alfredo Ramirez; John-Anker Zwart; International Consortium for Cluster Headache Genetics | Annals of Neurology 94(4), 713-726 | | | |
| 2023 | Contribution of the APOE Genotype to Cognitive Impairment in Individuals With NOTCH3 Cysteine‐Altering Variants | Cheng, YW; Liao, YC; Chen, CH; Chung, CP; Fann, CSJ ; Chang, CC; Lee, YC; Tang, SC | Journal of the American Heart Association 12(22), e032689 | | | |
| 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 | | | |
