未登录Functional sequence variants of intergenic long noncoding RNA on chromosome 17q21 are associated with asthma刘KY, Sie JJ, 高Y, Lo YL, Wu CC, 王CC, 等. 染色体17q21上基因间长链非编码RNA的功能性序列变异与哮喘相关。欧洲呼吸杂志。(2025)。doi: 10.1183/13993003.00847-2025
Liu, Kwei-Yan; Sie, Jia-Jyun; Gao, Yajing; Lo, Yen-Li; Wu, Chao-Chien; Wang, Chin-Chou; Sheu, Chau-Chyun; Lai, Ruay-Sheng; Leung, Sum-Yee; Lin, Chi-Cheng; Wei, Yu-Feng; Lin, Ching-Hsiung; Lin, Sheng-Hao; Hsu, Jeng-Yuan; Wei-Chang Huang; Tseng, Chia-Cheng; Lai, Yung-Fa; Cheng, Meng-Hsuan; Chen, Huang-Chi; Yang, Chih-Jen; Hsu, Yuan-Ting; Su, Chian-Heng; Hsu, Shih-Chang; Chung, Wen-Yu; Hsieh, Ming-Tsuen; Chen, Li-Chen; Hung, Chih-Hsing; Lee, Chon-Lin; Huang, Ming-Shyan; Zhou, Yufeng; Fann, Cathy S. J.; Huang, Shau-Ku .png)
分享.png)
收藏分享 收藏 分享 收藏 A genome-wide association study identifies novel loci of vertigo in an Asian population-based cohort全基因组关联研究在亚洲人群队列中确定眩晕的新基因座Chen, Shih-Pin; Hsu, Chia-Lin; Chen, Ting-Huei; Pan, Li-Ling Hope; Wang, Yen-Feng; Ling, Yu-Hsiang; Chang, Hsueh-Chen; Chen, Yi-Ming; Fann, Cathy Shen-Jang; Wang, Shuu-Jiun 分享 收藏 分享 收藏 Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor丛集性头痛全基因组关联研究和荟萃分析确定了八个基因座，并暗示吸烟是因果危险因素Winsvold, Bendik; Harder, Aster V. E. A.; Ran, Caroline; Chalmer, Mona; Dalmasso, Maria Carolina; Ferkingstad, Egil; Tripathi, Kumar Parijat; Bacchelli, Elena; Borte, Sigrid; Fourier, Carmen S.; Petersen, Anja H.; Vijfhuizen, Lisanne; Magnusson, Sigurdur; O'Connor, Emer; Bjornsdottir, Gyda; Happola, Paavo; Wang, Yen-Feng; Callesen, Ida; Kelderman, Tim; Gallardo, Victor J.; de Boer, Irene; Olofsgard, Felicia Jennysdotter; Heinze, Katja; Lund, Nunu; Thomas, Laurent F.; Hsu, Chia-Lin; Pirinen, Matti; Hautakangas, Heidi; Ribases, Marta; Guerzoni, Simona; Sivakumar, Prasanth; Yip, Janice; Heinze, Axel; Kucukali, Fahri B.; Ostrowski, Sisse S.; Pedersen, Ole E.; Kristoffersen, Espen S.; Martinsen, Amy E.; Artigas, Maria S.; Lagrata, Susie; Cainazzo, Maria Michela; Adebimpe, Joycee; Quinn, Olivia; Goebel, Carl E.; Cirkel, Anna; Volk, Alexander; Heilmann-Heimbach, Stefanie E.; Skogholt, Anne Heidi; Gabrielsen, Maiken E.; Wilbrink, Leopoldine A.; Danno, Daisuke; Mehta, Dwij R.; Guobjartsson, Daniel F.; Rosendaal, Frits R.; van Dijk, Ko Willems; Fronczek, Rolf A.; Wagner, Michael; Scherer, Martin; Goebel, Hartmut A.; Sleegers, Kristel; Sveinsson, Olafur; Pani, Luca; Zoli, Michele; Ramos-Quiroga, Josep A.; Dardiotis, Efthimios; Steinberg, Anna; Riedel-Heller, Steffi; Sjostrand, Christina; Thorgeirsson, Thorgeir E.; Stefansson, Hreinn; Southgate, Laura; Trembath, Richard C.; Vandrovcova, Jana; Noordam, Raymond; Paemeleire, Koen H.; Stefansson, Kari; Fann, Cathy Shen-Jang; Waldenlind, Elisabet; Tronvik, Erling; Jensen, Rigmor H.; Chen, Shih-Pin; Houlden, Henry; Terwindt, Gisela C.; Kubisch, Christian; Maestrini, Elena; Vikelis, Michail; Pozo-Rosich, Patricia; Belin, Andrea C.; Matharu, Manjit; van den Maagdenberg, Arn M. J. M.; Hansen, Thomas F.; Ramirez, Alfredo; Zwart, John-Anker 分享 收藏 Genome-wide analyses identify novel risk loci for cluster headache in Han Chinese residing in Taiwan全基因组分析确定了居住在台湾的汉族人丛集性头痛的新风险位点Chen, Shih-Pin; Hsu, Chia-Lin; Wang, Yen-Feng; Yang, Fu-Chi; Chen, Ting-Huei; Huang, Jia-Hsin; Pan, Li-Ling Hope; Fuh, Jong-Ling; Chang, Hsueh-Chen; Lee, Yi-Lun; Chang, Hung-Ching; Lee, Ko-Han; Chang, Yu-Chuan; Fann, Cathy Shen-Jang; Wang, Shuu-Jiun 分享 收藏 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetesLee, Chia-Jung; Chen, Ting-Huei; Lim, Aylwin Ming Wee; Chang, Chien-Ching; Sie, Jia-Jyun; Chen, Pei-Lung; Chang, Su-Wei; Wu, Shang-Jung; Hsu, Chia-Lin; Hsieh, Ai-Ru; Yang, Wei-Shiung; Fann, Cathy S. J. 分享 收藏 Patient-Derived Organoid Serves as a Platform for Personalized Chemotherapy in Advanced Colorectal Cancer Patients患者来源的类器官可作为晚期结直肠癌患者个性化化疗的平台Geevimaan, Khamushavalli; Guo, Jing-You; Shen, Chia-Ning; Jiang, Jeng-Kai; Fann, Cathy S. J.; Hwang, Ming-Jing; Shui, Jr-Wen; Lin, Hsiu-Ting; Wang, Mei-Jung; Shih, Hsuan-Cheng; Li, Anna Fen-Yau; Chang, Shih-Ching; Yang, Shung-Haur; Chen, Jeou-Yuan 分享 收藏 Genome-wide analysis identified novel susceptible genes of restless legs syndrome in migraineursJiang, Yun-Jin; Fann, Cathy Shen-Jang; Fuh, Jong-Ling; Chung, Ming-Yi; Huang, Hui-Ying; Chu, Kuo-Chang; Wang, Yen-Feng; Hsu, Chia-Lin; Kao, Lung-Sen; Chen, Shih-Pin; Wang, Shuu-Jiun 分享 收藏 A Deep Learning-Enabled Electrocardiogram Model for the Identification of a Rare Inherited Arrhythmia: Brugada SyndromeLiu, Chih-Min; Liu, Chien-Liang; Hu, Kai-Wen; Tseng, Vincent S.; Chang, Shih-Lin; Lin, Yenn-Jiang; Lo, Li-Wei; Chung, Fa-Po; Chao, Tze-Fan; Tuan, Ta-Chuan; Liao, Jo-Nan; Lin, Chin-Yu; Chang, Ting-Yung; Fann, Cathy Shen-Jang; Higa, Satoshi; Yagi, Nobumori; Hu, Yu-Feng; Chen, Shih-Ann 分享 收藏 分享 收藏 分享 收藏 分享 收藏 Analysis of site-specific glycan profiles of serum proteins in patients with multiple sclerosis or neuromyelitis optica spectrum disorder-a pilot studyIp, Peng Peng; Li, Qiongyu; Lin, Wei-Han; Chang, Chien-Ching; Fann, Cathy Shen-Jang; Chen, Huan-Yuan; Liu, Fu-Tong; Lebrilla, Carlito B.; Yang, Chih-Chao; Liao, Fang 分享 收藏 分享 收藏 分享 收藏 Heterozygosity mapping for human dominant trait variants人类显性性状变异的杂合性定位Imai-Okazaki, Atsuko; Li, Yi; Horpaopan, Sukanya; Riazalhosseini, Yasser; Garshasbi, Masoud; Mosse, Yael P.; Zhang, Di; Schrauwen, Isabelle; Sharma, Aarushi; Fann, Cathy S. J.; Leal, Suzanne M.; Lathrop, Mark; Ott, Jurg 分享 收藏 
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
