| Year |
Citation |
Score |
| 2019 |
Ko TM, Chang JS, Chen SP, Liu YM, Chang CJ, Tsai FJ, Lee YC, Chen CH, Chen YT, Wu JY. Genome-wide transcriptome analysis to further understand neutrophil activation and lncRNA transcript profiles in Kawasaki disease. Scientific Reports. 9: 328. PMID 30674924 DOI: 10.1038/s41598-018-36520-y |
0.44 |
|
| 2018 |
Ko TM, Kiyotani K, Chang JS, Park JH, Yew PY, Chen YT, Wu JY, Nakamura Y. Immunoglobulin profiling identifies unique signatures in patients with Kawasaki disease during intravenous immunoglobulin treatment. Human Molecular Genetics. PMID 29771320 DOI: 10.1093/hmg/ddy176 |
0.44 |
|
| 2018 |
Yang CF, Lin SP, Chiang CP, Wu YH, H'ng WS, Chang CP, Chen YT, Wu JY. Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans. American Journal of Human Genetics. PMID 29336782 DOI: 10.1016/j.ajhg.2017.12.012 |
0.44 |
|
| 2017 |
Lee TH, Ko TM, Chen CH, Chang YJ, Lu LS, Chang CH, Huang KL, Chang TY, Lee JD, Chang KC, Yang JT, Wen MS, Wang CY, Chen YT, Chen TC, ... ... Chen YT, et al. A genome-wide association study links small-vessel ischemic stroke to autophagy. Scientific Reports. 7: 15229. PMID 29123153 DOI: 10.1038/s41598-017-14355-3 |
0.44 |
|
| 2017 |
Chiang HL, Wu JY, Chen YT. Identification of functional single nucleotide polymorphisms in the branchpoint site. Human Genomics. 11: 27. PMID 29121990 DOI: 10.1186/s40246-017-0122-6 |
0.44 |
|
| 2017 |
Shen LF, Chen YJ, Liu KM, Haddad ANS, Song IW, Roan HY, Chen LY, Yen JJY, Chen YJ, Wu JY, Chen YT. Role of S-Palmitoylation by ZDHHC13 in Mitochondrial function and Metabolism in Liver. Scientific Reports. 7: 2182. PMID 28526873 DOI: 10.1038/s41598-017-02159-4 |
0.44 |
|
| 2017 |
Chiang HL, Wang NH, Song IW, Chang CP, Wen MS, Chien YH, Hwu WL, Tsai FJ, Chen YT, Wu JY. Genetic epidemiological study doesn't support GLA IVS4+919G>A variant is a significant mutation in Fabry disease. Molecular Genetics and Metabolism. PMID 28377241 DOI: 10.1016/j.ymgme.2017.03.005 |
0.44 |
|
| 2017 |
Yang CF, Wang CH, Siong H'ng W, Chang CP, De Lin W, Chen YT, Wu JY, Tsai FJ. Filamin B loss-of-Function Mutation in Dimerization Domain Causes Autosomal Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies. Human Mutation. PMID 28145000 DOI: 10.1002/humu.23186 |
0.44 |
|
| 2017 |
Wen MS, Chang KC, Lee TH, Chen YF, Hung KC, Chang YJ, Liou CW, Chen JJ, Chang CH, Wang CY, Jeng JS, Chuang HP, Chen YT, Chen CH, Wu JY, ... Chen YT, et al. Pharmacogenetic dosing of warfarin in the Han-Chinese population: a randomized trial. Pharmacogenomics. PMID 28112575 DOI: 10.2217/pgs-2016-0154 |
0.44 |
|
| 2016 |
Chen CH, Yang JH, Chiang CW, Hsiung CN, Wu PE, Chang LC, Chu HW, Chang J, Song IW, Yang SL, Chen YT, Liu FT, Shen CY. Population structure of Han Chinese in the modern Taiwanese population based on 10,000 participants in the Taiwan Biobank project. Human Molecular Genetics. PMID 27798100 DOI: 10.1093/hmg/ddw346 |
0.32 |
|
| 2016 |
Chen BM, Su YC, Chang CJ, Burnouf PA, Chuang KH, Chen CH, Cheng TL, Chen YT, Wu JY, Roffler SR. Measurement of pre-existing IgG and IgM antibodies against polyethylene glycol in healthy individuals. Analytical Chemistry. PMID 27726379 DOI: 10.1021/acs.analchem.6b03109 |
0.44 |
|
| 2016 |
Song IW, Chen HC, Lin YF, Yang JH, Chang CC, Chou CT, Lee MM, Chou YC, Chen CH, Chen YT, Chen CH, Wu JY. Identification of susceptibility gene associated with female primary Sjögren's syndrome in Han Chinese by genome-wide association study. Human Genetics. PMID 27503288 DOI: 10.1007/s00439-016-1716-0 |
0.44 |
|
| 2016 |
Chuang TP, Wang JY, Jao SW, Wu CC, Chen JH, Hsiao KH, Lin CY, Chen SH, Su SY, Chen YJ, Chen YT, Wu DC, Li LH. Over-expression of AURKA, SKA3 and DSN1 contributes to colorectal adenoma to carcinoma progression. Oncotarget. PMID 27329586 DOI: 10.18632/oncotarget.9960 |
0.4 |
|
| 2016 |
Yin CL, Chen HI, Li LH, Chien YL, Liao HM, Chou MC, Chou WJ, Tsai WC, Chiu YN, Wu YY, Lo CZ, Wu JY, Chen YT, Gau SS. Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder. Molecular Autism. 7: 23. PMID 27042285 DOI: 10.1186/s13229-016-0087-7 |
0.44 |
|
| 2016 |
Huang MC, Chuang TP, Chen CH, Wu JY, Chen YT, Li LH, Yang HC. An integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays. Bmc Genomics. 17: 266. PMID 27029637 DOI: 10.1186/s12864-016-2478-8 |
0.52 |
|
| 2016 |
Ko TM, Wong CS, Wu JY, Chen YT. Pharmacogenomics for personalized pain medicine. Acta Anaesthesiologica Taiwanica : Official Journal of the Taiwan Society of Anesthesiologists. PMID 26976339 DOI: 10.1016/j.aat.2016.02.001 |
0.44 |
|
| 2016 |
Chan R, Wei CY, Chen YT, Benet LZ. Use of the Biopharmaceutics Drug Disposition Classification System (BDDCS) to Help Predict the Occurrence of Idiosyncratic Cutaneous Adverse Drug Reactions Associated with Antiepileptic Drug Usage. The Aaps Journal. PMID 26951484 DOI: 10.1208/s12248-016-9898-x |
0.36 |
|
| 2016 |
Song IW, Sung CC, Chen CH, Cheng CJ, Yang SS, Chou YC, Yang JH, Chen YT, Wu JY, Lin SH. Novel susceptibility gene for nonfamilial hypokalemic periodic paralysis. Neurology. PMID 26935888 DOI: 10.1212/WNL.0000000000002524 |
0.44 |
|
| 2016 |
Chen B, Chen Y, Shao Z, Tong T, Luo L. Blood vessel enhancement via multi-dictionary and sparse coding: Application to retinal vessel enhancing Neurocomputing. 200: 110-117. DOI: 10.1016/j.neucom.2016.03.012 |
0.36 |
|
| 2016 |
Yang F, Chen Y, Kang R, Ma J. Truss transformation method to obtain the non-overconstrained forms of 3D overconstrained linkages Mechanism and Machine Theory. 102: 149-166. DOI: 10.1016/j.mechmachtheory.2016.04.005 |
0.48 |
|
| 2016 |
Chen YJ, Yang HC, Pai PF. Design and kinematics evaluation of a gear pair with asymmetric parabolic teeth Mechanism and Machine Theory. 101: 140-157. DOI: 10.1016/j.mechmachtheory.2016.03.008 |
0.52 |
|
| 2016 |
Gong X, Yang XF, Zhong Y, Chen Y, Li Z. A mitochondria-targetable near-infrared fluorescent probe for imaging nitroxyl (HNO) in living cells Dyes and Pigments. 131: 24-32. DOI: 10.1016/j.dyepig.2016.03.046 |
0.56 |
|
| 2016 |
Xia J, Zhang S, Zhao X, Liu J, Chen Y. Effects of different groundwater depths on the distribution characteristics of soil-Tamarix water contents and salinity under saline mineralization conditions Catena. 142: 166-176. DOI: 10.1016/j.catena.2016.03.005 |
0.56 |
|
| 2016 |
Chen Y, Liu J, Li Z. Synthesis and properties of new water-soluble copolymers based on methyl acrylic acid sucrose ester and methyl acrylic acid Journal of Applied Polymer Science. 133. DOI: 10.1002/app.43627 |
0.56 |
|
| 2015 |
Hsueh PT, Liu JK, Chen YL, Liu PJ, Ni WF, Chen YS, Wu KM, Lin HH. Genomic Sequence of Burkholderia multivorans NKI379, a Soil Bacterium That Inhibits the Growth of Burkholderia pseudomallei. Genome Announcements. 3. PMID 26586873 DOI: 10.1128/genomeA.01294-15 |
0.4 |
|
| 2015 |
Lin CW, Chen YS, Lin CC, Chen YJ, Lo GH, Lee PH, Kuo PL, Dai CY, Huang JF, Chung WL, Yu ML. Amiodarone as an autophagy promoter reduces liver injury and enhances liver regeneration and survival in mice after partial hepatectomy. Scientific Reports. 5: 15807. PMID 26515640 DOI: 10.1038/srep15807 |
0.4 |
|
| 2015 |
Hsueh PT, Chen YS, Lin HH, Liu PJ, Ni WF, Liu MC, Chen YL. Comparison of Whole-Genome Sequences from Two Colony Morphovars of Burkholderia pseudomallei. Genome Announcements. 3. PMID 26472836 DOI: 10.1128/genomeA.01194-15 |
0.4 |
|
| 2015 |
Sampson JN, Wheeler WA, Yeager M, Panagiotou O, Wang Z, Berndt SI, Lan Q, Abnet CC, Amundadottir LT, Figueroa JD, Landi MT, Mirabello L, Savage SA, Taylor PR, Vivo ID, ... Chen Y, ... Chen YH, ... Chen YS, ... Chen YM, et al. Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types. Journal of the National Cancer Institute. 107. PMID 26464424 DOI: 10.1093/jnci/djv279 |
0.4 |
|
| 2015 |
Chen MH, Lan WH, Hsu JW, Huang KL, Chen YS, Li CT, Lin WC, Chang WH, Chen TJ, Pan TL, Su TP, Bai YM. Risk of bipolar disorder among adolescents with allergic rhinitis: A nationwide longitudinal study. Journal of Psychosomatic Research. PMID 26363680 DOI: 10.1016/j.jpsychores.2015.08.009 |
0.36 |
|
| 2015 |
Tao LS, Tao LJ, Chen YS, Zou B, Zhu GB, Wang JW, Liang CZ. [TURP plus endocrine therapy (ET) versus α1A-blockers plus ET for bladder outlet obstruction in advanced prostate cancer]. Zhonghua Nan Ke Xue = National Journal of Andrology. 21: 626-9. PMID 26333225 |
0.32 |
|
| 2015 |
Tu PC, Hsu JW, Lan CC, Liu CC, Su TP, Chen YS. Structural and functional correlates of a quantitative autistic trait measured using the social responsive scale in neurotypical male adolescents. Autism Research : Official Journal of the International Society For Autism Research. PMID 26284955 DOI: 10.1002/aur.1535 |
0.36 |
|
| 2015 |
Lee SS, Lin HH, Tsai HC, Su IJ, Yang CH, Sun HY, Hung CC, Sy CL, Wu KS, Chen JK, Chen YS, Fang CT. A Clinical Algorithm to Identify HIV Patients at High Risk for Incident Active Tuberculosis: A Prospective 5-Year Cohort Study. Plos One. 10: e0135801. PMID 26280669 DOI: 10.1371/journal.pone.0135801 |
0.4 |
|
| 2015 |
Chen KC, Hsueh WT, Ou CY, Huang CC, Lee WT, Fang SY, Tsai ST, Huang JS, Wong TY, Wu JL, Yen CJ, Wu YH, Lin FC, Yang MW, Chang JY, ... ... Chen YS, et al. Alcohol Drinking Obliterates the Inverse Association Between Serum Retinol and Risk of Head and Neck Cancer. Medicine. 94: e1064. PMID 26131827 DOI: 10.1097/MD.0000000000001064 |
0.52 |
|
| 2015 |
Ju DT, Kuo WW, Ho TJ, Paul CR, Kuo CH, Viswanadha VP, Lin CC, Chen YS, Chang YM, Huang CY. Protocatechuic Acid from Alpinia oxyphylla Induces Schwann Cell Migration via ERK1/2, JNK and p38 Activation. The American Journal of Chinese Medicine. 1-13. PMID 26119854 DOI: 10.1142/S0192415X15500408 |
0.4 |
|
| 2015 |
Chen YL, Chen YS, Hung YC, Liu PJ, Tasi HY, Ni WF, Hseuh PT, Lin HH. Improvement of the Th1-related immune response in BALB/c mice immunized with an HIV-1 gag plasmid combined with a chimeric plasmid encoding IL-18 and flagellin. Microbiology and Immunology. PMID 26094825 DOI: 10.1111/1348-0421.12274 |
0.4 |
|
| 2015 |
Tu PC, Lee YC, Chen YS, Hsu JW, Li CT, Su TP. Network-specific cortico-thalamic dysconnection in schizophrenia revealed by intrinsic functional connectivity analyses. Schizophrenia Research. 166: 137-43. PMID 26081977 DOI: 10.1016/j.schres.2015.05.023 |
0.36 |
|
| 2015 |
Chen PS, Chen YS, Lin HH, Liu PJ, Ni WF, Hsueh PT, Liang SH, Chen C, Chen YL. Airborne Transmission of Melioidosis to Humans from Environmental Aerosols Contaminated with B. pseudomallei. Plos Neglected Tropical Diseases. 9: e0003834. PMID 26061639 DOI: 10.1371/journal.pntd.0003834 |
0.4 |
|
| 2015 |
Zhou Z, Wu S, Chang KJ, Chen WR, Chen YS, Kuo WH, Lin CC, Tsui PH. Classification of Benign and Malignant Breast Tumors in Ultrasound Images with Posterior Acoustic Shadowing Using Half-Contour Features. Journal of Medical and Biological Engineering. 35: 178-187. PMID 25960706 DOI: 10.1007/s40846-015-0031-x |
0.4 |
|
| 2015 |
Chen YS, Lin HH, Hsueh PT, Liu PJ, Ni WF, Chung WC, Lin CP, Chen YL. Whole-Genome Sequence of an Epidemic Strain of Burkholderia pseudomallei vgh07 in Taiwan. Genome Announcements. 3. PMID 25931599 DOI: 10.1128/genomeA.00345-15 |
0.4 |
|
| 2015 |
Sudhir PR, Lin ST, Chia-Wen C, Yang SH, Li AF, Lai RH, Wang MJ, Chen YT, Chen CF, Jou YS, Chen JY. Loss of PTPRM associates with the pathogenic development of colorectal adenoma-carcinoma sequence. Scientific Reports. 5: 9633. PMID 25910225 DOI: 10.1038/srep09633 |
0.36 |
|
| 2015 |
Chen YS, Shen PC, Su BS, Liu TC, Lin CC, Lee LH. Avian reovirus replication in mononuclear phagocytes in chicken footpad and spleen after footpad inoculation. Canadian Journal of Veterinary Research = Revue Canadienne De Recherche VéTéRinaire. 79: 87-94. PMID 25852223 |
0.4 |
|
| 2015 |
Ko TM, Kuo HC, Chang JS, Chen SP, Liu YM, Chen HW, Tsai FJ, Lee YC, Chen CH, Wu JY, Chen YT. CXCL10/IP-10 is a biomarker and mediator for Kawasaki disease. Circulation Research. 116: 876-83. PMID 25605650 DOI: 10.1161/CIRCRESAHA.116.305834 |
0.36 |
|
| 2015 |
Lin CH, Chen JK, Ko TM, Wei CY, Wu JY, Chung WH, Chen SY, Liao YD, Hung SI, Chen YT. Immunologic basis for allopurinol-induced severe cutaneous adverse reactions: HLA-B*58:01-restricted activation of drug-specific T cells and molecular interaction. The Journal of Allergy and Clinical Immunology. 135: 1063-5.e5. PMID 25458913 DOI: 10.1016/j.jaci.2014.09.041 |
0.36 |
|
| 2015 |
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, et al. Association of circadian genes with diurnal blood pressure changes and non-dipper essential hypertension: a genetic association with young-onset hypertension. Hypertension Research : Official Journal of the Japanese Society of Hypertension. 38: 155-62. PMID 25410879 DOI: 10.1038/hr.2014.152 |
0.36 |
|
| 2014 |
Liu KM, Wu JY, Chen YT. Mouse model of glycogen storage disease type III. Molecular Genetics and Metabolism. 111: 467-76. PMID 24613482 DOI: 10.1016/j.ymgme.2014.02.005 |
0.36 |
|
| 2014 |
Hsieh AR, Chang SW, Chen PL, Chu CC, Hsiao CL, Yang WS, Chang CC, Wu JY, Chen YT, Chang TC, Fann CS. Predicting HLA genotypes using unphased and flanking single-nucleotide polymorphisms in Han Chinese population. Bmc Genomics. 15: 81. PMID 24476119 DOI: 10.1186/1471-2164-15-81 |
0.36 |
|
| 2014 |
Chen CH, Lee CS, Lee MT, Ouyang WC, Chen CC, Chong MY, Wu JY, Tan HK, Lee YC, Chuo LJ, Chiu NY, Tsang HY, Chang TJ, Lung FW, Chiu CH, ... ... Chen YS, ... ... Chen YT, et al. Variant GADL1 and response to lithium therapy in bipolar I disorder. The New England Journal of Medicine. 370: 119-28. PMID 24369049 DOI: 10.1056/NEJMoa1212444 |
0.44 |
|
| 2014 |
Wang TH, Hsiong CH, Ho HT, Shih TY, Yen SJ, Wang HH, Wu JY, Kuo BP, Chen YT, Ho ST, Hu OY. Genetic polymorphisms of metabolic enzymes and the pharmacokinetics of indapamide in Taiwanese subjects. The Aaps Journal. 16: 206-13. PMID 24357089 DOI: 10.1208/s12248-013-9535-x |
0.36 |
|
| 2014 |
Chiu LY, Kishnani PS, Chuang TP, Tang CY, Liu CY, Bali D, Koeberl D, Austin S, Boyette K, Weinstein DA, Murphy E, Yao A, Chen YT, Li LH. Identification of differentially expressed microRNAs in human hepatocellular adenoma associated with type I glycogen storage disease: a potential utility as biomarkers. Journal of Gastroenterology. 49: 1274-84. PMID 24129885 DOI: 10.1007/s00535-013-0890-2 |
0.36 |
|
| 2014 |
Lin DS, Chuang TP, Chiang MF, Ho CS, Hsiao CD, Huang YW, Wu TY, Wu JY, Chen YT, Chen TC, Li LH. De novo MECP2 duplication derived from paternal germ line result in dysmorphism and developmental delay. Gene. 533: 78-85. PMID 24129071 DOI: 10.1016/j.gene.2013.10.001 |
0.44 |
|
| 2013 |
Cornejo-García JA, Liou LB, Blanca-López N, Doña I, Chen CH, Chou YC, Chuang HP, Wu JY, Chen YT, Plaza-Serón Mdel C, Mayorga C, Guéant-Rodríguez RM, Lin SC, Torres MJ, Campo P, et al. Genome-wide association study in NSAID-induced acute urticaria/angioedema in Spanish and Han Chinese populations. Pharmacogenomics. 14: 1857-69. PMID 24236485 DOI: 10.2217/pgs.13.166 |
0.44 |
|
| 2013 |
Chou CH, Wu CC, Song IW, Chuang HP, Lu LS, Chang JH, Kuo SY, Lee CH, Wu JY, Chen YT, Kraus VB, Lee MT. Genome-wide expression profiles of subchondral bone in osteoarthritis. Arthritis Research & Therapy. 15: R190. PMID 24229462 DOI: 10.1186/ar4380 |
0.44 |
|
| 2013 |
Chang CJ, Kuo HC, Chang JS, Lee JK, Tsai FJ, Khor CC, Chang LC, Chen SP, Ko TM, Liu YM, Chen YJ, Hong YM, Jang GY, Hibberd ML, Kuijpers T, ... ... Chen YT, et al. Replication and meta-analysis of GWAS identified susceptibility loci in Kawasaki disease confirm the importance of B lymphoid tyrosine kinase (BLK) in disease susceptibility. Plos One. 8: e72037. PMID 24023612 DOI: 10.1371/journal.pone.0072037 |
0.36 |
|
| 2013 |
Wang CW, Chung WH, Cheng YF, Ying NW, Peck K, Chen YT, Hung SI. A new nucleic acid-based agent inhibits cytotoxic T lymphocyte-mediated immune disorders. The Journal of Allergy and Clinical Immunology. 132: 713-722.e11. PMID 23791505 DOI: 10.1016/j.jaci.2013.04.036 |
0.36 |
|
| 2013 |
Sun B, Fredrickson K, Austin S, Tolun AA, Thurberg BL, Kraus WE, Bali D, Chen YT, Kishnani PS. Alglucosidase alfa enzyme replacement therapy as a therapeutic approach for glycogen storage disease type III. Molecular Genetics and Metabolism. 108: 145-7. PMID 23318145 DOI: 10.1016/j.ymgme.2012.12.002 |
0.36 |
|
| 2012 |
Wei CY, Lee MT, Chen YT. Pharmacogenomics of adverse drug reactions: implementing personalized medicine. Human Molecular Genetics. 21: R58-65. PMID 22907657 DOI: 10.1093/hmg/dds341 |
0.36 |
|
| 2012 |
Okada Y, Sim X, Go MJ, Wu JY, Gu D, Takeuchi F, Takahashi A, Maeda S, Tsunoda T, Chen P, Lim SC, Wong TY, Liu J, Young TL, Aung T, ... ... Chen YT, et al. Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations. Nature Genetics. 44: 904-9. PMID 22797727 DOI: 10.1038/ng.2352 |
0.36 |
|
| 2012 |
Cheng YC, Hsiao FC, Yeh EC, Lin WJ, Tang CY, Tseng HC, Wu HT, Liu CK, Chen CC, Chen YT, Yao A. VarioWatch: providing large-scale and comprehensive annotations on human genomic variants in the next generation sequencing era. Nucleic Acids Research. 40: W76-81. PMID 22618869 DOI: 10.1093/nar/gks397 |
0.36 |
|
| 2012 |
Liou YJ, Wang HH, Lee MT, Wang SC, Chiang HL, Chen CC, Lin CH, Chung MS, Kuo CC, Liao DL, Wu CK, Liu CM, Liu YL, Hwu HG, Lai IC, ... ... Chen YT, et al. Genome-wide association study of treatment refractory schizophrenia in Han Chinese. Plos One. 7: e33598. PMID 22479419 DOI: 10.1371/journal.pone.0033598 |
0.44 |
|
| 2012 |
Wei CY, Chung WH, Huang HW, Chen YT, Hung SI. Direct interaction between HLA-B and carbamazepine activates T cells in patients with Stevens-Johnson syndrome. The Journal of Allergy and Clinical Immunology. 129: 1562-9.e5. PMID 22322005 DOI: 10.1016/j.jaci.2011.12.990 |
0.36 |
|
| 2012 |
Wei CY, Ko TM, Shen CY, Chen YT. A recent update of pharmacogenomics in drug-induced severe skin reactions. Drug Metabolism and Pharmacokinetics. 27: 132-41. PMID 22041139 DOI: 10.2133/dmpk.DMPK-11-RV-116 |
0.36 |
|
| 2011 |
Ko TM, Chung WH, Wei CY, Shih HY, Chen JK, Lin CH, Chen YT, Hung SI. Shared and restricted T-cell receptor use is crucial for carbamazepine-induced Stevens-Johnson syndrome. The Journal of Allergy and Clinical Immunology. 128: 1266-1276.e11. PMID 21924464 DOI: 10.1016/j.jaci.2011.08.013 |
0.44 |
|
| 2011 |
Mu SC, Lin YJ, Liu HC, Wu JY, Li SC, Michael Lee MT, Chou CH, Chen LK, Chen YT. A mutation in cartilage oligomeric matrix protein (COMP) causes early-onset osteoarthritis in a large kindred study. Annals of Human Genetics. 75: 575-83. PMID 21834907 DOI: 10.1111/j.1469-1809.2011.00667.x |
0.44 |
|
| 2011 |
Chung CM, Lin TH, Chen JW, Leu HB, Yang HC, Ho HY, Ting CT, Sheu SH, Tsai WC, Chen JH, Lin SJ, Chen YT, Pan WH. A genome-wide association study reveals a quantitative trait locus of adiponectin on CDH13 that predicts cardiometabolic outcomes. Diabetes. 60: 2417-23. PMID 21771975 DOI: 10.2337/db10-1321 |
0.52 |
|
| 2011 |
Sabbagha NG, Kao HJ, Yang CF, Huang CC, Lin WD, Tsai FJ, Chen TH, Tarn WY, Wu JY, Chen YT. Alternative splicing in Acad8 resulting a mitochondrial defect and progressive hepatic steatosis in mice. Pediatric Research. 70: 31-6. PMID 21659959 DOI: 10.1203/PDR.0b013e31821b89ee |
0.44 |
|
| 2011 |
Lin CH, Lin JK, Chang SC, Chang YH, Chang HM, Liu JH, Li LH, Chen YT, Tsai SF, Chen WS. Molecular profile and copy number analysis of sporadic colorectal cancer in Taiwan. Journal of Biomedical Science. 18: 36. PMID 21645411 DOI: 10.1186/1423-0127-18-36 |
0.44 |
|
| 2011 |
Banugaria SG, Prater SN, Ng YK, Kobori JA, Finkel RS, Ladda RL, Chen YT, Rosenberg AS, Kishnani PS. The impact of antibodies on clinical outcomes in diseases treated with therapeutic protein: lessons learned from infantile Pompe disease. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 13: 729-36. PMID 21637107 DOI: 10.1097/GIM.0b013e3182174703 |
0.36 |
|
| 2011 |
Tsai FJ, Lee YC, Chang JS, Huang LM, Huang FY, Chiu NC, Chen MR, Chi H, Lee YJ, Chang LC, Liu YM, Wang HH, Chen CH, Chen YT, Wu JY. Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study. Plos One. 6: e16853. PMID 21326860 DOI: 10.1371/journal.pone.0016853 |
0.44 |
|
| 2011 |
Lee YC, Chang CJ, Bali D, Chen YT, Yan YT. Glycogen-branching enzyme deficiency leads to abnormal cardiac development: novel insights into glycogen storage disease IV. Human Molecular Genetics. 20: 455-65. PMID 21075835 DOI: 10.1093/hmg/ddq492 |
0.32 |
|
| 2011 |
Lin CT, Wu CC, Chen YS, Lai YC, Chi C, Lin JC, Chen Y, Peng HL. Fur regulation of the capsular polysaccharide biosynthesis and iron-acquisition systems in Klebsiella pneumoniae CG43. Microbiology (Reading, England). 157: 419-29. PMID 21071493 DOI: 10.1099/mic.0.044065-0 |
0.4 |
|
| 2010 |
Akgül B, Lin KW, Ou Yang HM, Chen YH, Lu TH, Chen CH, Kikuchi T, Chen YT, Tu CP. Garlic accelerates red blood cell turnover and splenic erythropoietic gene expression in mice: evidence for erythropoietin-independent erythropoiesis. Plos One. 5: e15358. PMID 21206920 DOI: 10.1371/journal.pone.0015358 |
0.32 |
|
| 2010 |
Chang CF, Li LH, Wang CH, Tsai FJ, Chen TC, Wu JY, Chen YT, Tsai AC. 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. 152: 2365-71. PMID 20803649 DOI: 10.1002/ajmg.a.33580 |
0.44 |
|
| 2010 |
Lee YC, Huang HY, Chang CJ, Cheng CH, Chen YT. Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome. Human Molecular Genetics. 19: 3721-33. PMID 20639396 DOI: 10.1093/hmg/ddq286 |
0.32 |
|
| 2010 |
Lee MT, Hung SI, Wei CY, Chen YT. Pharmacogenetics of toxic epidermal necrolysis. Expert Opinion On Pharmacotherapy. 11: 2153-62. PMID 20536296 DOI: 10.1517/14656566.2010.495120 |
0.44 |
|
| 2010 |
Cheng HY, Chen YS, Wu CY, Chang HY, Lai YC, Peng HL. RmpA regulation of capsular polysaccharide biosynthesis in Klebsiella pneumoniae CG43. Journal of Bacteriology. 192: 3144-58. PMID 20382770 DOI: 10.1128/JB.00031-10 |
0.4 |
|
| 2010 |
Tsai FJ, Yang CF, Chen CC, Chuang LM, Lu CH, Chang CT, Wang TY, Chen RH, Shiu CF, Liu YM, Chang CC, Chen P, Chen CH, Fann CS, Chen YT, et al. A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. Plos Genetics. 6: e1000847. PMID 20174558 DOI: 10.1371/journal.pgen.1000847 |
0.44 |
|
| 2010 |
Li SC, Chen CM, Goldstein JL, Wu JY, Lemyre E, Burrow TA, Kang PB, Chen YT, Bali DS. Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder. Journal of Inherited Metabolic Disease. 33: S83-90. PMID 20058079 DOI: 10.1007/s10545-009-9026-5 |
0.36 |
|
| 2009 |
Abdulla MA, Ahmed I, Assawamakin A, Bhak J, Brahmachari SK, Calacal GC, Chaurasia A, Chen CH, Chen J, Chen YT, Chu J, Cutiongco-de la Paz EM, De Ungria MC, Delfin FC, et al. Mapping human genetic diversity in Asia. Science (New York, N.Y.). 326: 1541-5. PMID 20007900 DOI: 10.1126/science.1177074 |
0.36 |
|
| 2009 |
Lee MJ, Chang CP, Lee YH, Wu YC, Tseng HW, Tung YY, Wu MT, Chen YH, Kuo LT, Stephenson D, Hung SI, Wu JY, Chang C, Chen YT, Chern Y. Longitudinal evaluation of an N-ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus. Plos One. 4: e7868. PMID 19924295 DOI: 10.1371/journal.pone.0007868 |
0.36 |
|
| 2009 |
Kishnani PS, Chuang TP, Bali D, Koeberl D, Austin S, Weinstein DA, Murphy E, Chen YT, Boyette K, Liu CH, Chen YT, Li LH. Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage disease. Human Molecular Genetics. 18: 4781-90. PMID 19762333 DOI: 10.1093/hmg/ddp441 |
0.4 |
|
| 2009 |
Yang HC, Liang YJ, Wu YL, Chung CM, Chiang KM, Ho HY, Ting CT, Lin TH, Sheu SH, Tsai WC, Chen JH, Leu HB, Yin WH, Chiu TY, Chen CI, ... ... Chen YT, et al. Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan. Plos One. 4: e5459. PMID 19421330 DOI: 10.1371/journal.pone.0005459 |
0.52 |
|
| 2009 |
Wang HH, Liao YW, Chiang HL, Wu JY, Chen YT. Novel DNA sequence variations of cytochrome P450 genes in the Han Chinese population Pharmacogenomics. 10: 359-374. PMID 19290787 DOI: 10.2217/14622416.10.3.359 |
0.36 |
|
| 2009 |
Mu SC, Liu HC, Wu JY, Lee MT, Chuang HP, Chen LK, Chen YT. A large kindred of early-onset osteoarthritis of the knee and hip: excluding the link to COL2A1 gene. Rheumatology (Oxford, England). 48: 371-4. PMID 19223283 DOI: 10.1093/rheumatology/kep010 |
0.44 |
|
| 2008 |
Lin CH, Li LH, Ho SF, Chuang TP, Wu JY, Chen YT, Fann CS. A large-scale survey of genetic copy number variations among Han Chinese residing in Taiwan. Bmc Genetics. 9: 92. PMID 19108714 DOI: 10.1186/1471-2156-9-92 |
0.44 |
|
| 2008 |
Chung WH, Hung SI, Yang JY, Su SC, Huang SP, Wei CY, Chin SW, Chiou CC, Chu SC, Ho HC, Yang CH, Lu CF, Wu JY, Liao YD, Chen YT. Granulysin is a key mediator for disseminated keratinocyte death in Stevens-Johnson syndrome and toxic epidermal necrolysis. Nature Medicine. 14: 1343-50. PMID 19029983 DOI: 10.1038/nm.1884 |
0.44 |
|
| 2008 |
Lee MT, Tsai AC, Chou CH, Sun FM, Huang LC, Yen P, Lin CC, Liu CY, Wu JY, Chen YT, Tsai FJ. Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia. Genomic Medicine. 2: 45-9. PMID 18696259 DOI: 10.1007/s11568-008-9024-y |
0.44 |
|
| 2008 |
Lin CH, Huang MC, Li LH, Wu JY, Chen YT, Fann CS. Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling. Human Mutation. 29: 1055-62. PMID 18470944 DOI: 10.1002/humu.20760 |
0.44 |
|
| 2008 |
Yang HC, Huang MC, Li LH, Lin CH, Yu AL, Diccianni MB, Wu JY, Chen YT, Fann CS. MPDA: microarray pooled DNA analyzer. Bmc Bioinformatics. 9: 196. PMID 18412951 DOI: 10.1186/1471-2105-9-196 |
0.52 |
|
| 2008 |
Koeberl DD, Pinto C, Sun B, Li S, Kozink DM, Benjamin DK, Demaster AK, Kruse MA, Vaughn V, Hillman S, Bird A, Jackson M, Brown T, Kishnani PS, Chen YT. AAV vector-mediated reversal of hypoglycemia in canine and murine glycogen storage disease type Ia. Molecular Therapy : the Journal of the American Society of Gene Therapy. 16: 665-72. PMID 18362924 DOI: 10.1038/mt.2008.15 |
0.36 |
|
| 2007 |
Chiang MC, Chen HM, Lee YH, Chang HH, Wu YC, Soong BW, Chen CM, Wu YR, Liu CS, Niu DM, Wu JY, Chen YT, Chern Y. Dysregulation of C/EBPalpha by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease. Human Molecular Genetics. 16: 483-98. PMID 17213233 DOI: 10.1093/hmg/ddl481 |
0.36 |
|
| 2006 |
Kao HJ, Cheng CF, Chen YH, Hung SI, Huang CC, Millington D, Kikuchi T, Wu JY, Chen YT. ENU mutagenesis identifies mice with cardiac fibrosis and hepatic steatosis caused by a mutation in the mitochondrial trifunctional protein beta-subunit. Human Molecular Genetics. 15: 3569-77. PMID 17116638 DOI: 10.1093/hmg/ddl433 |
0.36 |
|
| 2006 |
Li LH, Ho SF, Chen CH, Wei CY, Wong WC, Li LY, Hung SI, Chung WH, Pan WH, Lee MT, Tsai FJ, Chang CF, Wu JY, Chen YT. Long contiguous stretches of homozygosity in the human genome. Human Mutation. 27: 1115-21. PMID 16955415 DOI: 10.1002/humu.20399 |
0.44 |
|
| 2006 |
Niu DM, Hwang B, Hwang HW, Wang NH, Wu JY, Lee PC, Chien JC, Shieh RC, Chen YT. 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. 43: 817-21. PMID 16707561 DOI: 10.1136/jmg.2006.042192 |
0.36 |
|
| 2006 |
Yang HC, Lin CH, Hsu CL, Hung SI, Wu JY, Pan WH, Chen YT, Fann CS. A comparison of major histocompatibility complex SNPs in Han Chinese residing in Taiwan and Caucasians. Journal of Biomedical Science. 13: 489-98. PMID 16544196 DOI: 10.1007/s11373-006-9077-7 |
0.52 |
|
| 2006 |
Pan WH, Fann CS, Wu JY, Hung YT, Ho MS, Tai TH, Chen YJ, Liao CJ, Yang ML, Cheng AT, Chen YT. Han Chinese cell and genome bank in Taiwan: purpose, design and ethical considerations. Human Heredity. 61: 27-30. PMID 16534213 DOI: 10.1159/000091834 |
0.44 |
|
| 2005 |
Hung SI, Chung WH, Chen YT. HLA-B genotyping to detect carbamazepine-induced Stevens-Johnson syndrome: implications for personalizing medicine. Personalized Medicine. 2: 225-237. PMID 29793265 DOI: 10.2217/17410541.2.3.225 |
0.44 |
|
| 2005 |
Liu YF, Chen WM, Lin YF, Yang RC, Lin MW, Li LH, Chang YH, Jou YS, Lin PY, Su JS, Huang SF, Hsiao KJ, Fann CS, Hwang HW, Chen YT, et al. Type II collagen gene variants and inherited osteonecrosis of the femoral head. The New England Journal of Medicine. 352: 2294-301. PMID 15930420 DOI: 10.1056/NEJMoa042480 |
0.36 |
|
| 2005 |
Yuan HY, Chen JJ, Lee MT, Wung JC, Chen YF, Charng MJ, Lu MJ, Hung CR, Wei CY, Chen CH, Wu JY, Chen YT. A novel functional VKORC1 promoter polymorphism is associated with inter-individual and inter-ethnic differences in warfarin sensitivity. Human Molecular Genetics. 14: 1745-51. PMID 15888487 DOI: 10.1093/hmg/ddi180 |
0.44 |
|
| 2005 |
An Y, Young SP, Kishnani PS, Millington DS, Amalfitano A, Corz D, Chen YT. Glucose tetrasaccharide as a biomarker for monitoring the therapeutic response to enzyme replacement therapy for Pompe disease. Molecular Genetics and Metabolism. 85: 247-54. PMID 15886040 DOI: 10.1016/j.ymgme.2005.03.010 |
0.36 |
|
| 2005 |
Hung SI, Chung WH, Liou LB, Chu CC, Lin M, Huang HP, Lin YL, Lan JL, Yang LC, Hong HS, Chen MJ, Lai PC, Wu MS, Chu CY, Wang KH, ... ... Chen YT, et al. 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. 102: 4134-9. PMID 15743917 DOI: 10.1073/pnas.0409500102 |
0.44 |
|
| 2005 |
Xu F, Ding E, Migone F, Serra D, Schneider A, Chen YT, Amalfitano A. Glycogen storage in multiple muscles of old GSD-II mice can be rapidly cleared after a single intravenous injection with a modified adenoviral vector expressing hGAA. The Journal of Gene Medicine. 7: 171-8. PMID 15515143 DOI: 10.1002/jgm.660 |
0.36 |
|
| 2004 |
Hunley TE, Corzo D, Dudek M, Kishnani P, Amalfitano A, Chen YT, Richards SM, Phillips JA, Fogo AB, Tiller GE. Nephrotic syndrome complicating alpha-glucosidase replacement therapy for Pompe disease. Pediatrics. 114: e532-5. PMID 15466083 DOI: 10.1542/peds.2003-0988-L |
0.36 |
|
| 2004 |
Wu JY, Kao HJ, Li SC, Stevens R, Hillman S, Millington D, Chen YT. ENU mutagenesis identifies mice with mithochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease Journal of Clinical Investigation. 113: 434-440. PMID 14755340 DOI: 10.1172/JCI19574 |
0.36 |
|
| 2003 |
Young SP, Stevens RD, An Y, Chen YT, Millington DS. Analysis of a glucose tetrasaccharide elevated in Pompe disease by stable isotope dilution-electrospray ionization tandem mass spectrometry. Analytical Biochemistry. 316: 175-80. PMID 12711338 DOI: 10.1016/S0003-2697(03)00056-3 |
0.36 |
|
| 2002 |
Ding E, Hu H, Hodges BL, Migone F, Serra D, Xu F, Chen YT, Amalfitano A. Efficacy of gene therapy for a prototypical lysosomal storage disease (GSD-II) is critically dependent on vector dose, transgene promoter, and the tissues targeted for vector transduction. Molecular Therapy : the Journal of the American Society of Gene Therapy. 5: 436-46. PMID 11945071 DOI: 10.1006/mthe.2002.0563 |
0.36 |
|
| 2001 |
Santer R, Kinner M, Steuerwald U, Kjaergaard S, Skovby F, Simonsen H, Shaiu WL, Chen YT, Schneppenheim R, Schaub J. Molecular genetic basis and prevalence of glycogen storage disease type IIIA in the Faroe Islands. European Journal of Human Genetics : Ejhg. 9: 388-91. PMID 11378828 DOI: 10.1038/sj.ejhg.5200632 |
0.36 |
|
| 1997 |
Van Hove JL, Yang HW, Oliver LM, Pennybacker MF, Chen YT. Purification of recombinant human precursor acid alpha-glucosidase. Biochemistry and Molecular Biology International. 43: 613-23. PMID 9352080 DOI: 10.1080/15216549700204421 |
0.36 |
|
| 1996 |
Svetkey LP, Timmons PZ, Emovon O, Anderson NB, Preis L, Chen YT. Association of hypertension with beta2- and alpha2c10-adrenergic receptor genotype. Hypertension (Dallas, Tex. : 1979). 27: 1210-5. PMID 8641726 DOI: 10.1161/01.HYP.27.6.1210 |
0.36 |
|
| 1994 |
Tang TT, Segura AD, Chen YT, Ricci LM, Franciosi RA, Splaingard ML, Lubinsky MS. Neonatal hypotonia and cardiomyopathy secondary to type IV glycogenosis. Acta Neuropathologica. 87: 531-6. PMID 8059607 DOI: 10.1007/BF00294181 |
0.36 |
|
| Show low-probability matches. |