第 1 到 46 筆結果，共 46 筆。
| 公開日期 | 題名 | 作者 | 關聯 | scopus | WOS | 全文 | |
|---|---|---|---|---|---|---|---|
| 1 | 2024 | Unsupervised clustering identified clinically relevant metabolic syndrome endotypes in UK and Taiwan Biobanks | AM Lim; EU Lim; PL Chen; CS Fann | iScience 27(7), 109815 | |||
| 2 | 2023 | Genotype-phenotype correlation in Taiwanese children with diazoxide-unresponsive congenital hyperinsulinism | Cheng-Ting Lee; Wen-Hao Tsai; Chien-Ching Chang; Pei-Chun Chen; Cathy Shen-Jang Fann ; Hsueh-Kai Chang; Shih-Yao Liu; Mu-Zon Wu; Pao-Chin Chiu; Wen-Ming Hsu; Wei-Shiung Yang; Ling-Ping Lai; Wen-Yu Tsai; Shi-Bing Yang ; Pei-Lung Chen | FRONTIERS IN ENDOCRINOLOGY 14, 1283907 | |||
| 3 | 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 | |||
| 4 | 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 | |||
| 5 | 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 | |||
| 6 | 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 | |||
| 7 | 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 | |||
| 8 | 2022 | Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes | Lee, CJ; Chen, TH; Lim, AMW; Chang, CC; Sie, JJ; Chen, PL; Chang, SW; Wu, SJ; Hsu, CL; Hsieh, AR; Yang, WS; Fann, CSJ | Communications Biology 5(1), 1175 | |||
| 9 | 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 | |||
| 10 | 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 | |||
| 11 | 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 | |||
| 12 | 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 | |||
| 13 | 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 | |||
| 14 | 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 | ||||
| 15 | 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 | |||
| 16 | 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 | |||
| 17 | 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 | |||
| 18 | 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 | |||
| 19 | 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 | |||
| 20 | 2020 | Shared genomic segment analysis with equivalence testing | Horpaopan, Sukanya; Fann, Cathy S. J. ; Lathrop, Mark; Ott, Jurg | Genetic Epidemiology 44(7), 741-747 | |||
| 21 | 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 | |||
| 22 | 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 | |||
| 23 | 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 | |||
| 24 | 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 | |||
| 25 | 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 | |||
| 26 | 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 | |||
| 27 | 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 | |||
| 28 | 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 | |||
| 29 | 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 | |||
| 30 | 2009 | Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan | Yang, H. -C. ; Liang, Y. -J.; Wu, Y. -L.; Chung, C. -M.; Chiang, K. -M.; Ho, H. -Y.; Ting, C. -T.; Lin, T. -H.; Sheu, S. -H.; Tsai, W. -C.; Chen, J. -H.; Leu, H. -B.; Yin, W. -H.; Chiu, T. -Y.; Chen, C. -I.; Fann, C. S. J. ; Wu, J. -Y.; Lin, T. -N.; Lin, S. -J; Chen, Y. -T. ; Chen, J. -W.; Pan, W. -H. | PLoS One 4(5), e5459 | |||
| 31 | 2008 | RASD2, MYH9, and CACNG2 Genes at Chromosome 22q12 Associated with the Subgroup of Schizophrenia with Non-Deficit in Sustained Attention and Executive Function | Liu, Y. L.; Fann, C. S. J. ; Liu, C. M.; Chen, W. J.; Wu, J. Y.; Hung, S. I.; Chen, C. H. ; Jou, Y. S. ; Liu, S. K.; Hwang, T. J.; Hsieh, M. H.; Chang, C. C.; Yang, W. C.; Lin, J. J.; Chou, F. H.; Faraone, S. V.; Tsuang, M. T.; Hwu, H. G. | Biological Psychiatry 64(9), 789-796 | |||
| 32 | 2008 | KBAT: Kernel-based association test | Yang, H. -C. ; Hsieh, H. -Y.; Fann, C. S. J. | GENETICS 179, 1057-1068 | |||
| 33 | 2008 | Using the Longest Significance Run to Estimate Region-Specific P-values in Genetic Association Mapping Studies | Lian, IB; Lin, YH; Lin, YC; Yang, HC ; Chang, CJ; Fann, CS | BMC Bioinformatics 9(1), 246 | |||
| 34 | 2008 | MPDA: Microarray pooled DNA analyzer | Yang, H. -C. ; Huang, M. -C.; Li, L. -H.; Lin, C. -H.; Yu, L. T.; Diccianni, M. B.; Wu, J. -Y.; Chen, Y. -T. ; Fann, C. S. J. | BMC BIOINFORMATICS 9, 196 | |||
| 35 | 2007 | Genome-Wide Scan for Quantitative ACE Activity in Taiwan Young-Onset Hypertension Study | Wang, R. Y.; Chung, C. M.; Fann, C. S. J. ; Yang, H. C. ; Chen, J. W.; Jong, Y. S.; Jou, Y. S. ; Lo, H. M.; Ho, F. M.; Kang, C. S.; Chen, C. C.; Chang, H. C.; Shyue, S. K. ; Pan, W. P. | HUMAN HEREDITY 65(2), 85-90 | |||
| 36 | 2007 | Association mapping using pooled DNA | Yang, H. -C. ; Fann, C. S. J. | Linkage Disequilibrium and Association Mapping (USA : Humana Press Inc.) | |||
| 37 | 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 | |||
| 38 | 2006 | A sliding-window weighted linkage disequilibrium test | Yang, H. C. ; Lin, C. Y.; Fann, C. S. J. | Genet Epidemiol 30(6), 531-545 | |||
| 39 | 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 | |||
| 40 | 2006 | PDA: pooled DNA analyzer | Yang, H. C. ; Pan, C. C.; Lin, C. Y.; Fann, C. S. J. | BMC Bioinformatics 7, 233 | |||
| 41 | 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 | |||
| 42 | 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 | |||
| 43 | 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 | |||
| 44 | 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 | |||
| 45 | 2005 | New adjustment factors and sample size calculation in a DNA-pooling experiment with preferential amplification | Yang, H. C. ; Pan, C. C.; Luand, R. C. Y.; Fann, C. S. J. | Genetics 169(1), 399-410 | |||
| 46 | 2003 | Receptor mediated effect of serotonergic transmission in patients with bipolar affective disorder | Lin, Y. M. J.; Yang, H. -C. ; Lai, T. J.; Fann, C. S. J. ; Sun, H. S. | JOURNAL OF MEDICAL GENETICS 40, 781-78 |
