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Jer-Yuarn Wu

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Taiwan
China

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Asian Continental Ancestry Group

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Hui-Ju Lin; Jane-Ming Lin; Jer-Yuarn Wu; Chien-Hsiun Chen; Liuh-An Chen; Yi-Chun Chou; Yu-Chuen Huang; Wen-Ling Liao; Chao-Jen Lin; Fuu-Jen Tsai
Novel susceptibility genes associated with diabetic cataract in a Taiwanese population.
Hui-Ju Lin; Jane-Ming Lin; Liuh-An Chen; Yu-Chuen Huang; Jer-Yuarn Wu; Fuu-Jen Tsai
Association of genes on chromosome 6, GRIK2 , TMEM217 and TMEM63B (linked to MRPL14 ) with diabetic retinopathy.
Catherine T Jordan; Cailin E Joyce; Yin Liu; Michelle A Lowes; Alison A McBride; Alan Menter; Katherine C Pierson; Elisha D O Roberson; Caitriona Ryan; Jer-Yuarn Wu; Chi-Fan Yang; Li Cao; Yongqing Chen; Yuan-Tsong Chen; Shenghui Duan; Raphaela Goldbach-Mansky; Cynthia A Helms; Wuh-Liang Hwu; Anne M Bowcock
PSORS2 is due to mutations in CARD14.

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All Publications

2013: Hui-Ju Lin; Jane-Ming Lin; Jer-Yuarn Wu; Chien-Hsiun Chen; Liuh-An Chen; Yi-Chun Chou; Yu-Chuen Huang; Wen-Ling Liao; Chao-Jen Lin; Fuu-Jen Tsai
Novel susceptibility genes associated with diabetic cataract in a Taiwanese population.
Ophthalmic genetics 2013;34(1-2):35-42.
2013: Hui-Ju Lin; Jane-Ming Lin; Liuh-An Chen; Yu-Chuen Huang; Jer-Yuarn Wu; Fuu-Jen Tsai
Association of genes on chromosome 6, GRIK2 , TMEM217 and TMEM63B (linked to MRPL14 ) with diabetic retinopathy.
Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift für Augenheilkunde 2013;229(1):54-60.
2012: Catherine T Jordan; Cailin E Joyce; Yin Liu; Michelle A Lowes; Alison A McBride; Alan Menter; Katherine C Pierson; Elisha D O Roberson; Caitriona Ryan; Jer-Yuarn Wu; Chi-Fan Yang; Li Cao; Yongqing Chen; Yuan-Tsong Chen; Shenghui Duan; Raphaela Goldbach-Mansky; Cynthia A Helms; Wuh-Liang Hwu; Anne M Bowcock
PSORS2 is due to mutations in CARD14.
American journal of human genetics 2012;90(5):784-95.
2012: Yi-Ching Lee; Chi-Di Liang; Yi-Min Liu; Fuu-Jen Tsai; Jeng-Sheng Chang; Li-Ching Chang; Luan-Yin Chang; Chien-Hsiun Chen; Ming-Ren Chen; Ying-Ju Chen; Yuan-Tsong Chen; Hsin Chi; Nan-Chang Chiu; Fu-Yuan Huang; Li-Min Huang; Yhu-Chering Huang; Betau Hwang; Kao-Pin Hwang; Kuo Ho-Chang; Meng-Luen Lee; Pi-Chang Lee; Jer-Yuarn Wu
Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis.
Nature genetics 2012;44(5):522-5.
2012: Yung-Hsiu Lu; Jer-Yuarn Wu; Tina Jui-Ting Wu; Hsiao-Chi Yu; Li-Mei Cheng; Ju-Hui Hsu; Yu-Hsiu Huang; Andrew Lin; Ching-Yuang Lin; Ming-Yu Lo; Dau-Ming Niu
Homocystinuria in Taiwan: an inordinately high prevalence in an Austronesian aboriginal tribe, Tao.
Molecular genetics and metabolism 2012;105(4):590-5.
2012: Yukinori Okada; Atsushi Takahashi; Tatsuhiko Tsunoda; Wanqing Wen; Jer-Yuarn Wu; Kazuhiko Yamamoto; Wei Zheng; Rajkumar Dorajoo; Min Jin Go; Naoya Hosono; Naoyuki Kamatani; Norihiro Kato; Michiaki Kubo; Natsuhiko Kumasaka; Qi Lu; Shiro Maeda; Yusuke Nakamura; Hiroko Ohmiya; Toshihiro Tanaka
Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations.
Nature genetics 2012;44(3):302-6.
2012: Ying-Jay Liou; Chih-Min Liu; Hui-Fen Liu; Yu-Li Liu; Shih-Jen Tsai; Hui-Hung Wang; Sheng-Chang Wang; Ching-Kuan Wu; Cheng-Chung Chen; Chien-Hsiun Chen; Chia-Hsiang Chen; Yuan-Tsong Chen; Hung-Lun Chiang; Yi-Chun Chou; Ming-Shun Chung; Chen-Jee Hong; Hai-Gwo Hwu; Chien-Cheng Kuo; I-Ching Lai; Ming-Ta Michael Lee; Ding-Lieh Liao; Ching-Hua Lin; Jer-Yuarn Wu
Genome-wide association study of treatment refractory schizophrenia in Han Chinese.
PloS one 2012;7(3):e33598.
2011: Shu-Chi Mu; Jer-Yuarn Wu; Liang-Kuang Chen; Ching-Heng Chou; Sing-Chung Li; Yi-Jung Lin; Hwa-Chang Liu; Ming-Ta Michael Lee; Yuan-Tsong Chen
A mutation in cartilage oligomeric matrix protein (COMP) causes early-onset osteoarthritis in a large kindred study.
Annals of human genetics 2011;75(5):575-83.
2011: Nagham George Abd Al-Ahad Sabbagha; Woan-Yuh Tarn; Fuu-Jen Tsai; Jer-Yuarn Wu; Chih-Fu Yang; Tzu-Ho Chen; Cheng-Chih Huang; Hsiao-Jung Kao; Wei-De Lin; Yuan-Tsong Chen
Alternative splicing in Acad8 resulting a mitochondrial defect and progressive hepatic steatosis in mice.
Pediatric research 2011;70(1):31-6.
2011: Jae-Jung Kim; Young Mi Hong; Saejung Sohn; Gi Young Jang; Kee-Soo Ha; Sin Weon Yun; Myung Ki Han; Kyung-Yil Lee; Min Seob Song; Hyoung Doo Lee; Dong Soo Kim; Jong-Eun Lee; Eun-Soon Shin; Ji-Hyun Jang; Yeon-Su Lee; Sook-Young Kim; Jong-Young Lee; Bok Ghee Han; Jer-Yuarn Wu; Kwi-Joo Kim; Young-Mi Park; Eul-Joo Seo; In-Sook Park; Jong-Keuk Lee
A genome-wide association analysis reveals 1p31 and 2p13.3 as susceptibility loci for Kawasaki disease.
Human genetics 2011;129(5):487-95.
2011: Hsin-Chou Yang; Hsin-Chi Lin; Meijyh Kang; Chun-Houh Chen; Chien-Wei Lin; Ling-Hui Li; Jer-Yuarn Wu; Yuan-Tsong Chen; Wen-Harn Pan
SAQC: SNP array quality control.
BMC bioinformatics 2011;12():100.
2011: 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
Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study.
PloS one 2011;6(2):e16853.
2010: 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
Overlapping high-resolution copy number alterations in cancer genomes identified putative cancer genes in hepatocellular carcinoma.
Hepatology (Baltimore, Md.) 2010;52(5):1690-701.
2010: Ching-Fen Chang; Ling-Hui Li; Chung-Hsing Wang; Fuu-Jen Tsai; Tsai-Chuan Chen; Jer-Yuarn Wu; Yuan-Tsong Chen; Anne Chun-Hui Tsai
Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2-13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high-density oligonucleotide array-a recognizable syndrome.
American journal of medical genetics. Part A 2010;152A(9):2365-71.
2010: Shu-Chin Chien; Yueh-Chun Li; Ling-Hui Li; Jer-Yuarn Wu; Pei-Ching Hsu; Sue-Lin Shi; Fuu-Jen Tsai; Chyi-Chyang Lin
A new familial insertion, ins(18;9)(q12.2;q33.1q31.1) with a 9q31.1-9q33.1 deletion in a girl with a cleft lip and palate.
American journal of medical genetics. Part A 2010;152A(7):1862-7.
2010: Amir N Saleem; Yen-Hui Chen; Hwa Jin Baek; Ya-Wen Hsiao; Hong-Wen 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; Jeffrey Jong-Young Yen; Yuan-Tsong Chen
Mice with alopecia, osteoporosis, and systemic amyloidosis due to mutation in Zdhhc13, a gene coding for palmitoyl acyltransferase.
PLoS genetics 2010;6(6):e1000985.
2010: 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 Chen; Chien-Hsiun Chen; Cathy S J Fann; Yuan-Tsong Chen; Jer-Yuarn Wu
A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese.
PLoS genetics 2010;6(2):e1000847.
2010: Chi-Fan Yang; Jer-Yuarn Wu; Fuu-Jen Tsai
Three novel beta-galactosidase gene mutations in Han Chinese patients with GM1 gangliosidosis are correlated with disease severity.
Journal of biomedical science 2010;17():79.
2010: Hui-Ju Lin; Yu-Chuen Huang; Jane-Ming Lin; Jer-Yuarn Wu; Liuh-An Chen; Chao-Jen Lin; Yung-Ping Tsui; Chih-Ping Chen; Fuu-Jen Tsai
Single-nucleotide polymorphisms in chromosome 3p14.1- 3p14.2 are associated with susceptibility of type 2 diabetes with cataract.
Molecular vision 2010;16():1206-14.
2010: Hsin-Chou Yang; Hsin-Chi Lin; Mei-Chu Huang; Ling-Hui Li; Wen-Harn Pan; Jer-Yuarn Wu; Yuan-Tsong Chen
A new analysis tool for individual-level allele frequency for genomic studies.
BMC genomics 2010;11():415.
2009: M T Michael Lee; Chien-Hsiun Chen; Ching-Heng Chou; Liang-Suei Lu; Hui-Ping Chuang; Yuan-Tsong Chen; Amir N Saleem; Ming-Shien Wen; Jin-Jer Chen; Jer-Yuarn Wu; Yuan-Tsong Chen
Genetic determinants of warfarin dosing in the Han-Chinese population.
Pharmacogenomics 2009;10(12):1905-13.
2009: Ching-Chu Chen; Jer-Yuarn Wu; Chwen-Tzuei Chang; Fuu-Jen Tsai; Tzu-Yuan Wang; Yi-Min Liu; Huai-Chih Tsui; Rong-Hsing Chen; Shyh-Ching Chiou
Levels of retinol-binding protein 4 and uric acid in patients with type 2 diabetes mellitus.
Metabolism: clinical and experimental 2009;58(12):1812-6.
2009: Sue-Hwa Lin; Chia-Ming Liu; Yu-Li Liu; C Shen-Jang Fann; P-C Hsiao; Jer-Yuarn Wu; Shuen-Iu Hung; Chien-Hung Chen; Hui-Min Wu; Yuh-Shan Jou; Shih-Kai Liu; Tzung-Jeng Hwang; Ming Hsieh; Chih-Ching Chang; Wen-Chen Ou Yang; Jin-Jia Lin; Frank Huang-Chih Chou; Stephen Faraone; Ming T Tsuang; Hai-Gwo Hwu; Wen-Jone Chen
Clustering by neurocognition for fine mapping of the schizophrenia susceptibility loci on chromosome 6p.
Genes, brain, and behavior 2009;8(8):785-94.
2009: Ming Ta Michael Lee; Chien-Hsiun Chen; Hui-Ping Chuang; Liang-Suei Lu; Ching-Heng Chou; Yuan-Tsong Chen; Chih-Yang Liu; Ming-Shien Wen; Jang-Jih Lu; Chi-Feng Chang; Jer-Yuarn Wu; Yuan-Tsong Chen
VKORC1 haplotypes in five East-Asian populations and Indians.
Pharmacogenomics 2009;10(10):1609-16.
2009: Chien-Hsing Lin; Ying-Chao Lin; Jer-Yuarn Wu; Wen-Harn Pan; Yuan-Tsong Chen; Cathy S J Fann
A genome-wide survey of copy number variations in Han Chinese residing in Taiwan.
Genomics 2009;94(4):241-6.
2009: Shu-Chi Mu; Hwa-Chang Liu; Jer-Yuarn Wu; Ming-Ta Michael Lee; Hui-Ping Chuang; Liang-Kuang Chen; Yuan-Tsong Chen
A large kindred of early-onset osteoarthritis of the knee and hip: excluding the link to COL2A1 gene.
Rheumatology (Oxford, England) 2009;48(4):371-4.
2009: Hui-Hung Wang; Yie-Wen Liao; Hung-Lun Chiang; Jer-Yuarn Wu; Yuan-Tsong Chen
Novel DNA sequence variations of cytochrome P450 genes in the Han Chinese population.
Pharmacogenomics 2009;10(3):359-74.
2009: Wei-De Lin; Chung-Hsing Wang; Chien-Chen Lai; Yuhsin Tsai; Jer-Yuarn Wu; Chih-Ping Chen; Fuu-Jen Tsai
Molecular analysis of Taiwanese patients with 3-hydroxy-3-methylglutaryl CoA lyase deficiency.
Clinica chimica acta; international journal of clinical chemistry 2009;401(1-2):33-6.
2009: Ming-Jen Lee; Ching-Pang Chang; Yi-Hsin Lee; Yi-Chih Wu; Hsu-Wen Tseng; Yu-Ying Tung; Min-Tzu Wu; Yen-Hui Chen; Lu-Ting Kuo; Dennis Stephenson; Shuen-Iu Hung; Jer-Yuarn Wu; Chen Chang; Yuan-Tsong Chen; Yijuang Chern
Longitudinal evaluation of an N-ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus.
PloS one 2009;4(11):e7868.
2009: 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
Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan.
PloS one 2009;4(5):e5459.
2008: Wen-Hung Chung; Shuen-Iu Hung; Jui-yung Yang; Shih-Chi Su; Shien-Ping Huang; Chun-Yu Wei; See-Wen Chin; Chien-Chun Chiou; Sung-Chao Chu; Hsin-Chun Ho; Chih-Hsun Yang; Chi-Fang Lu; Jer-Yuarn Wu; You-Di Liao; Yuan-Tsong Chen
Granulysin is a key mediator for disseminated keratinocyte death in Stevens-Johnson syndrome and toxic epidermal necrolysis.
Nature medicine 2008;14(12):1343-50.
2008: Yu-Li Liu; Cathy S J Fann; Chih-Min Liu; Wei J Chen; Jer-Yuarn Wu; Shuen-Iu Hung; Chun-Houh Chen; Yuh-Shan Jou; Shih-Kai Liu; Tzung-Jeng Hwang; Ming Hsieh; Chien Ching Chang; Wei-Chih Yang; Jin-Jia Lin; Frank Huang-Chih Chou; Stephen Faraone; Ming T Tsuang; Hai-Gwo Hwu
RASD2, MYH9, and CACNG2 genes at chromosome 22q12 associated with the subgroup of schizophrenia with non-deficit in sustained attention and executive function.
Biological psychiatry 2008;64(9):789-96.
2008: Chien-hsing Lin; Mei-chu Huang; Ling-hui Li; Jer-Yuarn Wu; Yuan-Tsong Chen; Cathy S J Fann
Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling.
Human mutation 2008;29(8):1055-62.
2008: CH Lin; Ling-Hui Li; Sheng-Feng Ho; Tzu-Po Chuang; Jer-Yuarn Wu; Yuan-Tsong Chen; Cathy S J Fann
A large-scale survey of genetic copy number variations among Han Chinese residing in Taiwan.
BMC genetics 2008;9():92.
2008: Ming Ta Michael Lee; Anne Chun-Hui Tsai; Ching-Heng Chou; Feng-Mei Sun; Li-Chen Huang; Pauline Yen; Chyi-Chyang Lin; Chih-Yang Liu; Jer-Yuarn Wu; Yuan-Tsong Chen; Fuu-Jen Tsai
Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia.
Genomic medicine 2008;2(1-2):45-9.
2008: Hsin-Chou Yang; Mei-Chu Huang; Ling-Hui Li; Chien-Hsing Lin; Alice L Yu; Mitchell B Diccianni; Jer-Yuarn Wu; Yuan-Tsong Chen; Cathy S J Fann
MPDA: microarray pooled DNA analyzer.
BMC bioinformatics 2008;9():196.
2007: Yu-Li Liu; Cathy S J Fann; Chih-Min Liu; Chien Ching Chang; Wei-Chih Yang; Jer-Yuarn Wu; Shuen-Iu Hung; Hung-Yu Chan; Jiahn-Jyh Chen; Ming Hsieh; Tzung-Jeng Hwang; Stephen Faraone; Ming T Tsuang; Weijun Chen; Hai-Gwo Hwu
HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention.
Psychiatric genetics 2007;17(6):333-8.
2007: Chih-Min Liu; Yu-Li Liu; Cathy S J Fann; Wei-Chih Yang; Jer-Yuarn Wu; Shuen-Iu Hung; Weijun Chen; Ching-Mo Chueh; Wei-Ming Liu; Chen-Chung Liu; Ming Hsieh; Tzung-Jeng Hwang; Stephen Faraone; Ming T Tsuang; Hai-Gwo Hwu
No association evidence between schizophrenia and dystrobrevin-binding protein 1 (DTNBP1) in Taiwanese families.
Schizophrenia research 2007;93(1-3):391-8.
2007: Ming-Chang Chiang; Hui-Mei 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
Dysregulation of C/EBPalpha by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease.
Human molecular genetics 2007;16(5):483-98.
2006: Hsiao-Jung Kao; Ching-Feng Cheng; Yen-Hui Chen; Shuen-Iu Hung; Cheng-Chih Huang; David S Millington; Tateki Kikuchi; Jer-Yuarn Wu; Yuan-Tsong Chen
ENU mutagenesis identifies mice with cardiac fibrosis and hepatic steatosis caused by a mutation in the mitochondrial trifunctional protein beta-subunit.
Human molecular genetics 2006;15(24):3569-77.
2006: Ling-Hui Li; Sheng-Feng Ho; Chien-Hsiun Chen; Chun-Yu Wei; Wan-Ching Wong; Li-Ying Li; Shuen-Iu Hung; Wen-Hung Chung; Wen-Han Pan; M T Michael Lee; Fuu-Jen Tsai; Ching-Fen Chang; Jer-Yuarn Wu; Yuan-Tsong Chen
Long contiguous stretches of homozygosity in the human genome.
Human mutation 2006;27(11):1115-21.
2006: Yu-Li Liu; Cathy S J Fann; Chih-Min Liu; Chien Ching Chang; Jer-Yuarn Wu; Shuen-Iu Hung; Shih-Kai Liu; Ming Hsieh; Tzung-Jeng Hwang; Hung-Yu Chan; Jiahn-Jyh Chen; Stephen Faraone; Ming T Tsuang; Weijun Chen; Hai-Gwo Hwu
No association of G72 and D-amino acid oxidase genes with schizophrenia.
Schizophrenia research 2006;87(1-3):15-20.
2006: Dau-Ming Niu; Betau Hwang; Han-Wei Hwang; Nana H Wang; Jer-Yuarn Wu; Pi-Chang Lee; Jen-Chung Chien; Ru-Chi Shieh; Yuan-Tsong Chen
A common SCN5A polymorphism attenuates a severe cardiac phenotype caused by a nonsense SCN5A mutation in a Chinese family with an inherited cardiac conduction defect.
Journal of medical genetics 2006;43(10):817-21.
2006: Yu-Li Liu; Cathy S J Fann; Chih-Min Liu; Weijun Chen; Jer-Yuarn Wu; Shuen-Iu Hung; Chun-Houh Chen; Yuh-Shan Jou; Shih-Kai Liu; Tzung-Jeng Hwang; Ming Hsieh; Wen-Chen OuYang; Hung-Yu Chan; Jiann-Jyh Chen; Wei-Chih Yang; Chin-Yu Lin; Sandy F C Lee; Hai-Gwo Hwu
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.
Biological psychiatry 2006;60(6):554-62.
2006: Yu-Li Liu; Cathy Shen-Jang Fann; Chih-Min Liu; Jer-Yuarn Wu; Shuen-Iu Hung; Hung-Yu Chan; Jiahn-Jyh Chen; Chin-Yu Lin; Shih-Kai Liu; Ming Hsieh; Tzung-Jeng Hwang; Wen-Chen OuYang; Chun-Ying Chen; Jin-Jia Lin; Frank Huang-Chih Chou; Ching-Mo Chueh; Wei-Ming Liu; Ming-Min Tsuang; Stephen Faraone; Ming T Tsuang; Weijun Chen; Hai-Gwo Hwu
Evaluation of RGS4 as a candidate gene for schizophrenia.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006;141B(4):418-20.
2006: Yu-Li Liu; Cathy S J Fann; Chih-Min Liu; Jer-Yuarn Wu; Shuen-Iu Hung; Hung-Yu Chan; Jiahn-Jyh Chen; Chia-Ching Pan; Shih-Kai Liu; Ming Hsieh; Tzung-Jeng Hwang; Wen-Chen OuYang; Chun-Ying Chen; Jin-Jia Lin; Frank Huang-Chih Chou; Ching-Mo Chueh; Wei-Ming Liu; Ming-Ming Tsuang; Stephen Faraone; Ming T Tsuang; Weijun Chen; Hai-Gwo Hwu
Absence of significant associations between four AKT1 SNP markers and schizophrenia in the Taiwanese population.
Psychiatric genetics 2006;16(1):39-41.
2006: Wen-Harn Pan; Cathy S J Fann; Jer-Yuarn Wu; Yung-Tai Hung; Mei-Shang Ho; Terence Hua Tai; Ying-Ju Chen; Chung-Ju Liao; Meng-Li Yang; Andrew T A Cheng; Yuan-Tsong Chen
Han Chinese cell and genome bank in Taiwan: purpose, design and ethical considerations.
Human heredity 2006;61(1):27-30.
2005: Hsiang-Yu Yuan; Jin-Jer Chen; M T Michael Lee; Ju-Chieh Wung; Ying-Fu Chen; Min-Ji Charng; Ming-Jen Lu; Chen-Road Hung; Chun-Yu Wei; Chien-Hsiun Chen; Jer-Yuarn Wu; Yuan-Tsong Chen
A novel functional VKORC1 promoter polymorphism is associated with inter-individual and inter-ethnic differences in warfarin sensitivity.
Human molecular genetics 2005;14(13):1745-51.
2005: Shuen-Iu Hung; Wen-Hung Chung; Lieh-Bang Liou; Chen-Chung 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
HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(11):4134-9.
2005: H W Hwang; J J Chen; Y J Lin; Ru-Chi Shieh; M T Lee; Shuen-Iu Hung; Jer-Yuarn Wu; Yuan-Tsong Chen; Dau-Ming Niu; Be-Tau Hwang
R1193Q of SCN5A, a Brugada and long QT mutation, is a common polymorphism in Han Chinese.
Journal of medical genetics 2005;42(2):e7; author reply e8.
2005: Long-Kuang Lin; Yin-Hsiu Chien; Jer-Yuarn Wu; Ai-Hou Wang; Shu-Chuan Chiang; Wuh-Liang Hwu
KIF21A gene c.2860C>T mutation in congenital fibrosis of extraocular muscles type 1 and 3.
Molecular vision 2005;11():245-8.
2004: Hsiang-Tai Chou; Yng-Tay Chen; Jer-Yuarn Wu; Fuu-Jen Tsai
Association between urokinase-plasminogen activator gene T4065C polymorphism and risk of mitral valve prolapse.
International journal of cardiology 2004;96(2):165-70.
2004: Wei-Ming Chen; Yu-Fen Liu; Ming-Wei Lin; I-Chun Chen; Pei-Yu Lin; Guan-Lu Lin; Yuh-Shan Jou; Yang-Te Lin; Cathy S J Fann; Jer-Yuarn Wu; Kwang-Jen Hsiao; Shih-Feng Tsai
Autosomal dominant avascular necrosis of femoral head in two Taiwanese pedigrees and linkage to chromosome 12q13.
American journal of human genetics 2004;75(2):310-7.
2004: Chang-Ching Wei; Wei-De Lin; Fuu-Jen Tsai; Jer-Yuarn Wu; Ching-Tien Peng; Chang-Hai Tsai
Isovaleric acidemia diagnosed promptly by tandem mass spectrometry: report of one case.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2004;45(4):236-8.
2004: Hsiang-Tai Chou; Jui-Sung Hung; Yng-Tay Chen; Jer-Yuarn Wu; Fuu-Jen Tsai
Association between COL3A1 collagen gene exon 31 polymorphism and risk of floppy mitral valve/mitral valve prolapse.
International journal of cardiology 2004;95(2-3):299-305.
2004: Chung-Ming Huang; Liang-Wen Hang; Chi-Lan Chen; Jer-Yuarn Wu; Fuu-Jen Tsai
Polymorphisms of TAP1 transporter genes in Chinese patients with systemic lupus erythematosus in Taiwan.
Rheumatology international 2004;24(3):130-2.
2004: Wen-Hung Chung; Shuen-Iu Hung; Hong-Shang Hong; Mo-Song Hsih; Li-Cheng Yang; Hsin-Chun Ho; Jer-Yuarn Wu; Yuan-Tsong Chen
Medical genetics: a marker for Stevens-Johnson syndrome.
Nature 2004;428(6982):486.
2004: Jer-Yuarn Wu; Hsiao-Jung Kao; Sing-Chung Li; Robert Stevens; Steven Hillman; David S Millington; Yuan-Tsong Chen
ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease.
The Journal of clinical investigation 2004;113(3):434-40.
2004: Min-Chien Yu; Chung-Ming Huang; Mei-Chen Wu; Jer-Yuarn Wu; Fuu-Jen Tsai
Association of TAP2 gene polymorphisms in Chinese patients with rheumatoid arthritis.
Clinical rheumatology 2004;23(1):35-9.
2004: Hsiang-Tai Chou; Yng-Tay Chen; Jer-Yuarn Wu; Fuu-Jen Tsai
Lack of association between perlecan gene intron 6 BamHI polymorphism and risk of mitral valve prolapse in Taiwan Chinese.
Japanese heart journal 2004;45(1):109-18.
2003: I-Ching Chou; Cheng-Chun Lee; Chao-Ching Huang; Jer-Yuarn Wu; Jeffrey J P Tsai; Chang-Hai Tsai; Fuu-Jen Tsai
Association of the neuronal nicotinic acetylcholine receptor subunit alpha4 polymorphisms with febrile convulsions.
Epilepsia 2003;44(8):1089-93.
2003: Sui-Foon Lo; Chung-Ming Huang; Mei-Chen Wu; Jer-Yuarn Wu; Fuu-Jen Tsai
Lack of association of tumor necrosis factor alpha gene polymorphism in patients with rheumatoid arthritis in central Taiwan.
Rheumatology international 2003;23(4):151-3.
2003: Yi-Ru Shi; Kai-Sheng Hsieh; Jer-Yuarn Wu; Cheng-Chun Lee; Chang-Hai Tsai; Ming-Tsung Yu; Jeng-Sheng Chang; Fuu-Jen Tsai
Genetic analysis of chromosome 22q11.2 markers in congenital heart disease.
Journal of clinical laboratory analysis 2003;17(1):28-35.
2002: Wei-De Lin; Jer-Yuarn Wu; Fuu-Jen Tsai; Ming-Tsong Gau; Cheng-Chung Lee
Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers.
Journal of the Formosan Medical Association = Taiwan yi zhi 2002;101(8):567-71.
2002: Chung-Ming Huang; Mei-Chen Wu; Jer-Yuarn Wu; Fuu-Jen Tsai
Interleukin-1 receptor antagonist gene polymorphism in chinese patients with systemic lupus erythematosus.
Clinical rheumatology 2002;21(3):255-7.
2002: Chung-Ming Huang; Mei-Chen Wu; Jer-Yuarn Wu; Fuu-Jen Tsai
No association of vitamin D receptor gene start codon fok 1 polymorphisms in Chinese patients with systemic lupus erythematosus.
The Journal of rheumatology 2002;29(6):1211-3.
2002: Yi-Ru Shi; Kai-Sheng Hsieh; Jer-Yuarn Wu; Cheng-Chun Lee; Chang-Hai Tsai; Fuu-Jen Tsai
Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method.
Pediatrics international : official journal of the Japan Pediatric Society 2002;44(3):264-8.
2002: Chung-Ming Huang; Mei-Chen Wu; Jer-Yuarn Wu; Fuu-Jen Tsai
Lack of association of interleukin-1beta gene polymorphisms in Chinese patients with systemic lupus erythematosus.
Rheumatology international 2002;21(5):173-5.
2002: Hsiang-Tai Chou; Yi-Ru Shi; Jer-Yuarn Wu; Fuu-Jen Tsai
Angiotensin II type 1 receptor gene adenine/cytosine1166 polymorphism is not associated with mitral valve prolapse syndrome in Taiwan Chinese.
Circulation journal : official journal of the Japanese Circulation Society 2002;66(2):163-6.
2002: Chien-Chen Lai; Chang-Hai Tsai; Fuu-Jen Tsai; Jer-Yuarn Wu; Wei-De Lin; Cheng-Chun Lee
Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots.
Clinical chemistry 2002;48(2):354-6.
2002: Yi-Ru Shi; Jer-Yuarn Wu; Yu-An Hsu; Cheng-Chun Lee; Chang-Hai Tsai; Fuu-Jen Tsai
Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan.
Genetic testing 2002;6(3):237-43.
2002: Chung-Ming Huang; Mei-Chen Wu; Jer-Yuarn Wu; Fuu-Jen Tsai
Association of vitamin D receptor gene BsmI polymorphisms in Chinese patients with systemic lupus erythematosus.
Lupus 2002;11(1):31-4.
2002: Chien-Chen Lai; Chang-Hai Tsai; Fuu-Jen Tsai; Jer-Yuarn Wu; Wei-De Lin; Cheng-Chun Lee
Rapid screening assay of congenital adrenal hyperplasia by measuring 17 alpha-hydroxyprogesterone with high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots.
Journal of clinical laboratory analysis 2002;16(1):20-5.
2001: CF Yang; Jer-Yuarn Wu; S P Lin; Fuu-Jen Tsai
Mucopolysaccharidosis type VI: Report of two Taiwanese patients and identification of one novel mutation.
Journal of the Formosan Medical Association = Taiwan yi zhi 2001;100(12):820-3.
2001: Wei-De Lin; Jer-Yuarn Wu; Hsiu-Bao Hsu; Fuu-Jen Tsai; Cheng-Chun Lee; Chang-Hai Tsai
Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation.
Journal of the Formosan Medical Association = Taiwan yi zhi 2001;100(12):817-9.
2001: Yao-Yuan Hsieh; Chi Chen Chang; Fuu-Jen Tsai; Jer-Yuarn Wu; Yi-Ru Shi; Horng-Der Tsai; Chang-Hai Tsai
Polymorphisms for interleukin-1 beta (IL-1 beta)-511 promoter, IL-1 beta exon 5, and IL-1 receptor antagonist: nonassociation with endometriosis.
Journal of assisted reproduction and genetics 2001;18(9):506-11.
2001: CF Yang; Fuu-Jen Tsai; SP Lin; Cheng-Chun Lee; Jer-Yuarn Wu
A novel in-frame deletion mutation (c106-111del) identified in a Taiwan Chinese patient with type IVA mucopolysaccharidosis.
Human mutation 2001;18(3):254.
2001: Fuu-Jen Tsai; Cheng-Chun Lee; Mei-Chen Wu; SP Lin; C Y Lin; Chang-Hai Tsai; H Kodama; Jer-Yuarn Wu
Mutation analysis of type II Gaucher disease in five Taiwanese children: identification of two novel mutations.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2001;42(4):231-5.
2001: Wei-De Lin; Jer-Yuarn Wu; Chien-Chen Lai; Fuu-Jen Tsai; Chang-Hai Tsai; SP Lin; D M Niu
A pilot study of neonatal screening by electrospray ionization tandem mass spectrometry in Taiwan.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2001;42(4):224-30.
2001: Fuu-Jen Tsai; C F Yang; Jer-Yuarn Wu; Chang-Hai Tsai; Cheng-Chun Lee
Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients.
Pediatrics international : official journal of the Japan Pediatric Society 2001;43(3):263-6.
2001: Chang-Hai Tsai; Wei-De Lin; Fuu-Jen Tsai; Ching-Tien Peng; Jer-Yuarn Wu
Pitfalls of PCR-based genotyping in patients with 21-hydroxylase deficiency.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2001;42(3):145-50.
2001: Wen-Chi Chen; Huey-Yi Chen; Jer-Yuarn Wu; Y T Chen; Fuu-Jen Tsai
Osteocalcin gene Hind III polymorphism is not correlated with calcium oxalate stone disease.
Urological research 2001;29(2):98-101.
2001: Yi-Ru Shi; Jer-Yuarn Wu; Fuu-Jen Tsai; Cheng-Chun Lee; Chang-Hai Tsai
A new polymorphism (c28C>A) of EXT2 gene identified in a Taiwan Chinese family.
Human mutation 2001;17(4):356.
2001: Wei-De Lin; Yi-Ru Shi; Fuu-Jen Tsai; Cheng-Chun Lee; H J Lin; Jer-Yuarn Wu
Identification of a polymorphism (D168N) in the XRP2 gene in Chinese.
Human mutation 2001;17(4):354.
2001: Yao-Yuan Hsieh; Jer-Yuarn Wu; CC Chang; Fuu-Jen Tsai; Cheng-Chun Lee; HD Tsai; Chang-Hai Tsai
Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele.
Prenatal diagnosis 2001;21(3):200-1.
2001: Jer-Yuarn Wu; Mei-Chen Wu; Cheng-Chun Lee; Fuu-Jen Tsai
Identification of a novel three-nucleotide insertion mutation (c.841-842insTGA) in the acid beta-glucosidase gene of a Taiwan Chinese patient with type II Gaucher disease.
Human mutation 2001;17(3):238.
2001: Mei-Chen Wu; Jer-Yuarn Wu; Cheng-Chun Lee; Chang-Hai Tsai; Fuu-Jen Tsai
Two novel polymorphisms (c954T>C and c1038A>G) in exon8 of NPHS2 gene identified in Taiwan Chinese.
Human mutation 2001;17(3):237.
2001: Yi-Ru Shi; Jer-Yuarn Wu; Fuu-Jen Tsai; Cheng-Chun Lee; Chang-Hai Tsai
A 651-665delinsTT mutation in EXT1 causes hereditary multiple exostoses.
Human mutation 2001;17(2):158.
2001: Wen-Chi Chen; Huey-Yi Chen; Cheng-Der Hsu; Jer-Yuarn Wu; Fuu-Jen Tsai
No association of vitamin D receptor gene BsmI polymorphisms with calcium oxalate stone formation.
Molecular urology 2001;5(1):7-10.
2001: Chung-Ming Huang; Fuu-Jen Tsai; Jer-Yuarn Wu; Mei-Chen Wu
Interleukin-1beta and interleukin-1 receptor antagonist gene polymorphisms in rheumatoid arthritis.
Scandinavian journal of rheumatology 2001;30(4):225-8.
2001: Huey-Yi Chen; Horng-Der Tsai; Wen-Chi Chen; Jer-Yuarn Wu; Fuu-Jen Tsai; Chang-Hai Tsai
Relation of polymorphism in the promotor region for the human osteocalcin gene to bone mineral density and occurrence of osteoporosis in postmenopausal Chinese women in Taiwan.
Journal of clinical laboratory analysis 2001;15(5):251-5.
2001: Mei-Chen Wu; Jer-Yuarn Wu; Cheng-Chun Lee; Chang-Hai Tsai; Fuu-Jen Tsai
A novel polymorphism (c288C>T) of the NPHS2 gene identified in a Taiwan Chinese family.
Human mutation 2001;17(1):81-2.
2000: Fuu-Jen Tsai; C Yang; Jer-Yuarn Wu; H J Lin; Cheng-Chun Lee; Chang-Hai Tsai
A novel mutation K167X of the XLRS1 gene (RS1) in a Taiwanese family with X-linked juvenile retinoschisis.
Human mutation 2000;16(5):449.
2000: CF Yang; Jer-Yuarn Wu; Fuu-Jen Tsai; Cheng-Chun Lee; Wei-De Lin
Identification of a polymorphism (G83S) in the TWIST gene in Taiwanese.
Human mutation 2000;16(5):448.
2000: Mei-Chen Wu; Fuu-Jen Tsai; Cheng-Chun Lee; Chang-Hai Tsai; Jer-Yuarn Wu
A novel missense mutation (H119L) identified in a Taiwan Chinese family with glycogen storage disease Ia (Von Gierke disease).
Human mutation 2000;16(5):447.
2000: Wen-Chi Chen; Fuu-Jen Tsai; Jer-Yuarn Wu; Hsi-Chin Wu; Hsu-Feng Lu; C W Li
Distributions of p53 codon 72 polymorphism in bladder cancer--proline form is prominent in invasive tumor.
Urological research 2000;28(5):293-6.
2000: Fuu-Jen Tsai; Jer-Yuarn Wu; Wei-De Lin; Chang-Hai Tsai
A stop codon mutation in the CBFA 1 gene causes cleidocranial dysplasia.
Acta paediatrica (Oslo, Norway : 1992) 2000;89(10):1262-5.
2000: Fuu-Jen Tsai; Jer-Yuarn Wu; Cheng-Chun Lee; C H Tsa
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) causes non-syndromic craniosynostosis.
Acta paediatrica (Oslo, Norway : 1992) 2000;89(6):672-4.
2000: Wei-De Lin; Fuu-Jen Tsai; Cheng-Chun Lee; Jer-Yuarn Wu
Identification of a polymorphism (D366H) in the endoglin gene in Chinese.
Human mutation 2000;15(6):583.
2000: Yi-Ru Shi; Jer-Yuarn Wu; Fuu-Jen Tsai; Cheng-Chun Lee; Chang-Hai Tsai
An R223P mutation in EXT2 gene causes hereditary multiple exostoses.
Human mutation 2000;15(4):390-1.
2000: Mei-Chen Wu; Fuu-Jen Tsai; C C Le; SP Lin; Jer-Yuarn Wu
Identification of a novel missense mutation (T16A) in the glucose-6-phosphatase gene in a Taiwan Chinese patient with glycogen storage disease Ia (Von Gierke disease).
Human mutation 2000;15(4):390.
2000: Jer-Yuarn Wu; CF Yang; Cheng-Chun Lee; Tai-Heng Chen; Fuu-Jen Tsai
A novel mutation (Q239R) identified in a Taiwan Chinese patient with type VI mucopolysaccharidosis (Maroteaux-Lamy syndrome).
Human mutation 2000;15(4):389-90.
2000: Cheng-Chun Lee; Mei-Chen Wu; Jer-Yuarn Wu; Tsai-Chung Li; Fuu-Jen Tsai; Chang-Hai Tsai
Carrier detection of Duchenne/Becker muscular dystrophy by using fluorescent linkage analysis in Taiwan.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2000;41(2):69-74.
2000: Cheng-Chun Lee; Jer-Yuarn Wu; Fuu-Jen Tsai; H Kodama; T Abe; CF Yang; Chang-Hai Tsai
Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation association.
Journal of human genetics 2000;45(5):275-9.
2000: C K Tan; Fuu-Jen Tsai; Cheng-Chieh Lin; Jer-Yuarn Wu; Ming-Tsung Yu; Shih-Lan Hsu; Yi-Ru Shi; J C Chang; SW Lai
Wolf-Hirschhorn (4p deletion) syndrome: report of one case.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 2000;41(1):39-42.
1999: Chang-Hai Tsai; Fuu-Jen Tsai; Jer-Yuarn Wu; SP Lin; Tai-Heng Chen; CF Yang; Cheng-Chun Lee
Insertion/deletion mutations of type I oculocutaneous albinism in chinese patients from Taiwan.
Human mutation 1999;14(6):542.
1999: C Lee; Fuu-Jen Tsai; Jer-Yuarn Wu; Ching-Tien Peng; Chang-Hai Tsai; Wuh-Liang Hwu; Tso-Ren Wang; D S Millington
3-hydroxy-3-methylglutaric aciduria presenting with Reye like syndrome: report of one case.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 1999;40(6):445-7.
1999: C F Yang; Fuu-Jen Tsai; Jer-Yuarn Wu; Yi-Ru Shi; Cheng-Chun Lee; Chang-Hai Tsai
Rapid diagnosis of common aneuploidies by quantitative fluorescent polymerase chain reaction.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 1999;40(5):330-4.
1999: Fuu-Jen Tsai; L P Tsai; SP Lin; Chang-Hai Tsai; Ching-Tien Peng; Tso-Ren Wang; Cheng-Chun Lee; Jer-Yuarn Wu
An R248C mutation of FGFR3 leading to thanatophoric dysplasia type I.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 1999;40(4):262-4.
1999: Fuu-Jen Tsai; Chang-Hai Tsai; Ching-Tien Peng; Jer-Yuarn Wu; C H Lien; T R Wang
Different race, different face: minor anomalies in Chinese newborn infants.
Acta paediatrica (Oslo, Norway : 1992) 1999;88(3):323-6.
1999: Fuu-Jen Tsai; Chang-Hai Tsai; Ching-Tien Peng; SP Lin; Wuh-Liang Hwu; Tso-Ren Wang; Cheng-Chun Lee; Jer-Yuarn Wu
Molecular diagnosis of Apert syndrome in Chinese patients.
Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi 1999;40(1):31-3.
1998: CC Chang; Fuu-Jen Tsai; HD Tsai; Chang-Hai Tsai; Y Y Hseih; Cheng-Chun Lee; T C Yang; Jer-Yuarn Wu
Prenatal diagnosis of Apert syndrome.
Prenatal diagnosis 1998;18(6):621-5.
1998: Ching-Tien Peng; Jer-Yuarn Wu; Chang-Hai Tsai; Fuu-Jen Tsai; Tai-Heng Chen
Molecular diagnosis of patients with beta-thalassemia major in central Taiwan by amplified created restriction site analysis.
Journal of human genetics 1998;43(4):237-41.
1998: Chang-Hai Tsai; Fuu-Jen Tsai; Jer-Yuarn Wu; Tai-Heng Chen; Cheng-Chun Lee; SP Lin; CF Yang; Y J Jong; M C Lo
Mutation analysis of Wilson disease in Taiwan and description of six new mutations.
Human mutation 1998;12(6):370-6.