Risultati della ricerca - Jer‐Yuarn Wu
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A marker for Stevens–Johnson syndrome di Wen‐Hung Chung, Wen‐Hung Chung, Hong‐Shang Hong, Mo‐Song Hsih, Li‐Cheng Yang, Hsin‐Chun Ho, Jer‐Yuarn Wu, Yuan-Tsong Chen
Pubblicazione 2004Artigo -
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Genome-wide transcriptome analysis to further understand neutrophil activation and lncRNA transcript profiles in Kawasaki disease di Tai‐Ming Ko, Jeng-Sheng Chang, Shih‐Ping Chen, Yi-Min Liu, Chia-Jung Chang, Fuu‐Jen Tsai, Yi‐Ching Lee, Chien‐Hsiun Chen, Yuan-Tsong Chen, Jer-Yuarn Wu
Pubblicazione 2019Artigo -
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A genome-wide association study identifies a novel susceptibility locus for the immunogenicity of polyethylene glycol di Chia-Jung Chang, Chien‐Hsiun Chen, Bing-Mae Chen, Yu-Cheng Su, Ying‐Ting Chen, Michael S. Hershfield, Ming Ta Michael Lee, Tian−Lu Cheng, Yuan-Tsong Chen, Steve R. Roffler, Jer‐Yuarn Wu
Pubblicazione 2017Artigo -
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Genome-wide expression profiles of subchondral bone in osteoarthritis di Ching‐Heng Chou, Chia‐Chun Wu, I-Wen Song, Hui-Ping Chuang, Liang-Suei Lu, Jen-Huei Chang, San‐Yuan Kuo, Chian‐Her Lee, Jer‐Yuarn Wu, Yuan-Tsong Chen, Virginia B. Kraus, Ming Ta Michael Lee
Pubblicazione 2013Artigo -
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Dysregulation of C/EBPα by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease di Ming‐Chang Chiang, Huimei Chen, Yi-Hsin Lee, Hao‐Hung Chang, Yi‐Chih Wu, Bing‐Wen Soong, Chiung‐Mei Chen, Yih‐Ru Wu, Chin‐San Liu, Dau‐Ming Niu, Jer‐Yuarn Wu, Yuan-Tsong Chen, Yijuang Chern
Pubblicazione 2007Artigo -
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Overlapping High-Resolution Copy Number Alterations in Cancer Genomes Identified Putative Cancer Genes in Hepatocellular Carcinoma di Chian‐Feng Chen, En‐Chi Hsu, Kuen‐Tyng Lin, Pang‐Hsien Tu, Hung-Wei Chang, Chin-Hui Lin, Yann-Jang Chen, De-Leung Gu, Chi-Hung Lin, Jer-Yuarn Wu, Yuan-Tsong Chen, Ming‐Ta Hsu, Yuh‐Shan Jou
Pubblicazione 2010Artigo -
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Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations di Yukinori Okada, Michiaki Kubo, Hiroko Ohmiya, Atsushi Takahashi, Natsuhiko Kumasaka, Naoya Hosono, Shiro Maeda, Wanqing Wen, Rajkumar Dorajoo, Min Jin Go, Wei Zheng, Norihiro Kato, Jer‐Yuarn Wu, Lu Qi, Tatsuhiko Tsunoda, Kazuhiko Yamamoto, Yusuke Nakamura, Naoyuki Kamatani, Toshihiro Tanaka
Pubblicazione 2012Artigo -
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Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population di Po‐Hsiu Kuo, Li-Chung Chuang, Mei‐Hsin Su, Chia‐Hsiang Chen, Chien-Hsiun Chen, Jer‐Yuarn Wu, Chung‐Jen Yen, Yu‐Yu Wu, Shih-Kai Liu, Miao‐Chun Chou, Wen‐Jiun Chou, Yen‐Nan Chiu, Wen‐Che Tsai, Susan Shur‐Fen Gau
Pubblicazione 2015Artigo -
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Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder di Chia‐Lin Yin, Hsin-I Chen, Ling‐Hui Li, Yi‐Ling Chien, Hsiao‐Mei Liao, Miao Chun Chou, Wen‐Jiun Chou, Wen‐Che Tsai, Yen‐Nan Chiu, Yu‐Yu Wu, Chen-Zen Lo, Jer‐Yuarn Wu, Yuan-Tsong Chen, Susan Shur‐Fen Gau
Pubblicazione 2016Artigo -
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Identification of Novel Susceptibility Loci for Kawasaki Disease in a Han Chinese Population by a Genome-Wide Association Study di Fuu‐Jen Tsai, Yi‐Ching Lee, Jeng-Sheng Chang, Li‐Min Huang, Fu-Yuan Huang, Nan-Chang Chiu, Ming-Ren Chen, Hsin Chi, Yann-Jinn Lee, Li-Ching Chang, Yi-Min Liu, Hsiang-Hua Wang, Chien‐Hsiun Chen, Yuan-Tsong Chen, Jer‐Yuarn Wu
Pubblicazione 2011Artigo -
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Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase di Amir n. Saleem, Yen‐Hui Chen, Hwa Jin Baek, Ya‐Wen Hsiao, Hongwen Huang, Hsiao‐Jung Kao, Kai-Ming Liu, Li-Fen Shen, I-Wen Song, Chen‐Pei D. Tu, Jer‐Yuarn Wu, Tateki Kikuchi, Monica J. Justice, J. J. Yen, Yuan-Tsong Chen
Pubblicazione 2010Artigo -
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A Genome-Wide Association Study Identifies Susceptibility Variants for Type 2 Diabetes in Han Chinese di Fuu‐Jen Tsai, Chi-Fan Yang, Ching-Chu Chen, Lee‐Ming Chuang, Chieh-Hsiang Lu, Chwen-Tzuei Chang, Tzu-Yuan Wang, Rong-Hsing Chen, Chiung-Fang Shiu, Yi-Min Liu, Chih-Chun Chang, Pei‐Jer Chen, Chien‐Hsiun Chen, Cathy S.J. Fann, Yuan-Tsong Chen, Jer-Yuarn Wu
Pubblicazione 2010Artigo -
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PSORS2 Is Due to Mutations in CARD14 di Catherine T. Jordan, Li Cao, Elisha Roberson, Katherine C. Pierson, Chi-Fan Yang, Cailin E. Joyce, Caitriona Ryan, Shenghui Duan, Cynthia Helms, Yin Liu, Yongqing Chen, Alison A. McBride, Wuh‐Liang Hwu, Jer-Yuarn Wu, Yuan-Tsong Chen, Alan Menter, Raphaela Goldbach‐Mansky, Michelle A. Lowes, A. Bowcock
Pubblicazione 2012Artigo -
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HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol di Wen‐Hung Chung, Wen‐Hung Chung, Lieh-Bang Liou, C.C. Chu, Marie Lin, Hsien-Ping Huang, Yen-Ling Lin, Joung-Liang Lan, Li-Cheng Yang, Hong-shang Hong, Ming-Jing Chen, Ping-Chin Lai, Mai-Szu Wu, Chia‐Yu Chu, Kuo-Hsien Wang, Chien‐Hsiun Chen, Cathy S.J. Fann, Jer-Yuarn Wu, Yuan-Tsong Chen
Pubblicazione 2005Artigo -
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Genetic profiles of 103,106 individuals in the Taiwan Biobank provide insights into the health and history of Han Chinese di Chun-Yu Wei, Jenn-Hwai Yang, Erh‐Chan Yeh, Ming-Fang Tsai, Hsiao‐Jung Kao, Chen-Zen Lo, Lung-Pao Chang, Wan-Jia Lin, Feng‐Jen Hsieh, Saurabh Belsare, Anand Bhaskar, Ming‐Wei Su, Te‐Chang Lee, Yi‐Ling Lin, Fu‐Tong Liu, Chen‐Yang Shen, Ling‐Hui Li, Chien-Hsiun Chen, Jeffrey D. Wall, Jer‐Yuarn Wu, Pui‐Yan Kwok
Pubblicazione 2021Artigo -
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Genome-Wide Association Study of Young-Onset Hypertension in the Han Chinese Population of Taiwan di Hsin‐Chou Yang, Yu-Jen Liang, Yi-Lin Wu, Chia-Min Chung, Kuang-Mao Chiang, Hung‐Yun Ho, Chih-Tai Ting, Tsung‐Hsien Lin, Sheng-Hsiung Sheu, Wei-Chuan Tsai, Jyh-Hong Chen, Hsin-Bang Leu, Wei‐Hsian Yin, Ting‐Yu Chiu, Chin-Iuan Chen, Cathy S.J. Fann, Jer‐Yuarn Wu, Teng‐Nan Lin, Shing‐Jong Lin, Yuan-Tsong Chen, Jaw‐Wen Chen, Wen-Harn Pan
Pubblicazione 2009Artigo
Strumenti per la ricerca:
Soggetti correlati
Biology
Gene
Genetics
Medicine
Genotype
Single-nucleotide polymorphism
Genome-wide association study
Genetic association
Internal medicine
Endocrinology
Population
Allele
Environmental health
Genome
Immunology
SNP
Biochemistry
Locus (genetics)
Pathology
Computational biology
Dermatology
Disease
Haplotype
Diabetes mellitus
Gene expression
Linkage disequilibrium
Psychiatry
Toxic epidermal necrolysis
Type 2 diabetes
Antibody