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生物醫學科學研究所 - 陳垣崇 CHEN, YUAN-TSONG 期刊著作 (專書著作)
** 此資料只顯示近五年的期刊著作,如欲查詢以外的年份,請善用年份查詢 **


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共 47 筆資料 / 4 頁

  • Song IW, Chen HC, Lin YF, Yang JH, Chang CC, Chou CT, Lee MTM, 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. 135(11), 1287-1294, 2016-11. [JCR] [WOS]
  • 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. 88(21), 10661-10666, 2016-10. [JCR] [WOS]
  • Chen CH, Yang JH, Chiang CWK, 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. doi:10.1093/hmg/ddw346, 2016-10. [JCR] [WOS]
  • Kubo K, Ohara M, Tachikawa M, Cavallari LH, Lee MTM, Wen MS, Scordo MG, Nutescue EA, Perera MA, Miyajima A, Kaneko N, Pengo V, Padrini R, (Chen YT), Takahashi H . Population differences in S-warfarin pharmacokinetics among African Americans, Asians and whites: their influence on pharmacogenetic dosing algorithms. PHARMACOGENOMICS JOURNAL. doi:10.1038/tpj.2016.57, 2016-08. [JCR] [WOS]
  • Wang NHH, Chen SJ, Yang CF, Chen HW, Chuang HP, Lu YH, Chen CH, Wu JY, Niu DM, (Chen YT)*. Homozygosity mapping and whole-genome sequencing links a missense mutation in POMGNT1 to autosomal recessive retinitis pigmentosa. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 57(8), 3601-3609, 2016-07. [JCR] [WOS]
  • Wei HM, Lin LC, Wang CF, Lee YJ, (Chen YT) and Liao YD. Antimicrobial Properties of An Immunomodulator - 15 kDa Human Granulysin. PLoS One. 11(6), e0156321, 2016-06. [JCR] [WOS]
  • 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. 7(29), 45803-45818, 2016-06. [JCR] [WOS]
  • 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 drun usage. AAPS Journal. 18(3), 757-766, 2016-05. [JCR] [WOS]
  • Yin CL, Chen H, Li LH, Chien YL, Liao HM, Chou MC, Chou WJ, Tsai WC, Chiu YN, Wu YY, Lo CZ, Wu JY, (Chen YT), Gau SSF. Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder. Molecular Autism. 7, 23, 2016-04. [JCR] [WOS]
  • 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, 2016-03. [JCR] [WOS]
  • Lee TH, Ko TM, Chen CH, Lee MTM, Chang YJ, Chang CH, Huang KL, Chang TY, Lee JD, Chang KC, Yang JT, Wen MS, Wang CY, Chen YT, Hsieh CS, Chou SY, Liu YM, Chen HW, Liao HT, Wang CW, Chen SP, Lu LS, (Chen YT)*, and Wu JY. Identification of PTCSC3 as a novel locus for large-vessel ischemic stroke: A Genome-Wide Association Study. Journal of the American Heart Association. 5(3), e003003, 2016-03. [JCR] [WOS]
  • 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. 86(13), 1190-1198, 2016-03. [JCR] [WOS]
  • Ko TM, Wong CS, Wu JY, (Chen YT)*. Pharmacogenomics for personalized pain medicine.. Acta Anaesthesiologic Taiwanica. 54, 24-30, 2016-03. [JCR] [WOS]
  • W WQ et al. Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference. Scientific Reprots. 6, 17958, 2016-01. [JCR] [WOS]
  • Kato N et al. Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. NATURE GENETICS. 47(11), 1282-1292, 2015-09. [JCR] [WOS]

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