Dr. Wu, Jer-Yuarn 's publons link picture

Dr. Wu, Jer-Yuarn

Research Fellow
  • 02-27899075 (Lab) (Room No: N520)
  • 02-27824066 (Fax)
Specialty:
  • Human Genetics
  • Pharmacogenetics
  • Genome Medicine
Education and Positions:

  • Ph.D, Duke University, USA

Dr. Wu, Jer-Yuarn 's
Publications

Journal 83 Book 0

  1. Wong Henry Sung-Ching, Lin Ying-Ju, Lu Hsing-Fang, Liao Wen-Ling, Chen Chien-Hsiun, Wu Jer-Yuarn, Chang Wei-Chiao, Tsai Fuu-Jen Genomic interrogation of familial short stature contributes to the discovery of the pathophysiological mechanisms and pharmaceutical drug repositioning. Journal of Biomedical Science 26(1), 91 (2019) [JCR] [WOS]
  2. 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 27(15), 2671-2677 (2018-05-16) [JCR] [WOS]
  3. Takeuchi F, Akiyama M, Matoba N, Katsuya T, Nakatochi M, Tabara Y, Narita A, Saw WY, Moon S, Spracklen CN, Chai JF, Kim YJ, Zhang L, Wang C, Li H, Li H, Wu JY, Dorajoo R, Nierenberg JL, Wang YX, He J, Bennett DA, Takahashi A, Momozawa Y, Hirata M, Matsuda K, Rakugi H, Nakashima E, Isono M, Shirota M, Hozawa A, Ichihara S, Matsubara T, Yamamoto K, Kohara K, Igase M, Han S, Gordon-Larsen P, Huang W, Lee NR, Adair LS, Hwang MY, Lee J, Chee ML, Sabanayagam C, Zhao W, Liu J, Reilly DF, Sun L, Huo S, Edwards TL, Long J, Chang LC, Chen CH, Yuan JM, Koh WP, Friedlander Y, Kelly TN, Bin Wei W, Xu L, Cai H, Xiang YB, Lin K, Clarke R, Walters RG, Millwood IY, Li L, Chambers JC, Kooner JS, Elliott P, van der Harst P, Chen Z, Sasaki M, Shu XO, Jonas JB, He J, Heng CK, Chen YT, Zheng W, Lin X, Teo YY, Tai ES, Cheng CY, Wong TY, Sim X, Mohlke KL, Yamamoto M, Kim BJ, Miki T, Nabika T, Yokota M, Kamatani Y, Kubo M, Kato N Interethnic analyses of blood pressure loci in populations of East Asian and European descent.. Nature communications 9(1), 5052 (2018) [JCR] [WOS]
  4. 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 102(2), 219-232 (2018) [JCR] [WOS]
  5. 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, Chou SY, Lee MM, Chen YT*, (Wu JY)* A genome-wide association study links small-vessel ischemic stroke to autophagy.. Scientific reports 7(1), 15229 (2017) [JCR] [WOS]
  6. Spracklen CN, Chen P, Kim YJ, Wang X, Cai H, Li S, Long J, Wu Y, Wang YX, Takeuchi F, Wu JY, Jung KJ, Hu C, Akiyama K, Zhang Y, Moon S, Johnson TA, Li H, Dorajoo R, He M, Cannon ME, Roman TS, Salfati E, Lin KH, Guo X, Sheu WHH, Absher D, Adair LS, Assimes TL, Aung T, Cai Q, Chang LC, Chen CH, Chien LH, Chuang LM, Chuang SC, Du S, Fan Q, Fann CSJ, Feranil AB, Friedlander Y, Gordon-Larsen P, Gu D, Gui L, Guo Z, Heng CK, Hixson J, Hou X, Hsiung CA, Hu Y, Hwang MY, Hwu CM, Isono M, Juang JJ, Khor CC, Kim YK, Koh WP, Kubo M, Lee IT, Lee SJ, Lee WJ, Liang KW, Lim B, Lim SH, Liu J, Nabika T, Pan WH, Peng H, Quertermous T, Sabanayagam C, Sandow K, Shi J, Sun L, Tan PC, Tan SP, Taylor KD, Teo YY, Toh SA, Tsunoda T, van Dam RM, Wang A, Wang F, Wang J, Wei WB, Xiang YB, Yao J, Yuan JM, Zhang R, Zhao W, Chen YI, Rich SS, Rotter JI, Wang TD, Wu T, Lin X, Han BG, Tanaka T, Cho YS, Katsuya T, Jia W, Jee SH, Chen YT, Kato N, Jonas JB, Cheng CY, Shu XO, He J, Zheng W, Wong TY, Huang W, Kim BJ, Tai ES, Mohlke KL, Sim X Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.. Human molecular genetics 26(9), 1770-1784 (2017) [JCR] [WOS]
  7. Yang CF, Wang CH, Siong H\'ng W, Chang CP, Lin WD, 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 38(5), 540-547 (2017) [JCR] [WOS]
  8. 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 121(1), 22-27 (2017) [JCR] [WOS]
  9. Li C, Kim YK, Dorajoo R, Li H, Lee IT, Cheng CY, He M, Sheu WH, Guo X, Ganesh SK, He J, Lee J, Liu J, Hu Y, Rao DC, Tsai FJ, Koh JY, Hu H, Liang KW, Palmas W, Hixson JE, Han S, Teo YY, Wang Y, Chen J, Lu CH, Zheng Y, Gui L, Lee WJ, Yao J, Gu D, Han BG, Sim X, Sun L, Zhao J, Chen CH, Kumari N, He Y, Taylor KD, Raffel LJ, Moon S, Rotter JI, Ida Chen YD, Wu T, Wong TY, (Wu JY), Lin X, Tai ES, Kim BJ, Kelly TN Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians.. Circulation-Cardiovascular Genetics 10(2), e001527 (2017) [JCR] [WOS]
  10. van Rooij FJ, Qayyum R, Smith AV, Zhou Y, Trompet S, Tanaka T, Keller MF, Chang LC, Schmidt H, Yang ML, Chen MH, Hayes J, Johnson AD, Yanek LR, Mueller C, Lange L, Floyd JS, Ghanbari M, Zonderman AB, Jukema JW, Hofman A, van Duijn CM, Desch KC, Saba Y, Ozel AB, Snively BM, (Wu JY), Schmidt R, Fornage M, Klein RJ, Fox CS, Matsuda K, Kamatani N, Wild PS, Stott DJ, Ford I, Slagboom PE, Yang J, Chu AY, Lambert AJ, Uitterlinden AG, Franco OH, Hofer E, Ginsburg D, Hu B, Keating B, Schick UM, Brody JA, Li JZ, Chen Z, Zeller T, Guralnik JM, Chasman DI, Peters LL, Kubo M, Becker DM, Li J, Eiriksdottir G, Rotter JI, Levy D, Grossmann V, Patel KV, Chen CH, Ridker PM, Tang H, Launer LJ, Rice KM, Li-Gao R, Ferrucci L, Evans MK, Choudhuri A, Trompouki E, Abraham BJ, Yang S, Takahashi A, Kamatani Y, Kooperberg C, Harris TB, Jee SH, Coresh J, Tsai FJ, Longo DL, Chen YT, Felix JF, Yang Q, Psaty BM, Boerwinkle E, Becker LC, Mook-Kanamori DO, Wilson JG, Gudnason V, O\'Donnell CJ, Dehghan A, Cupples LA, Nalls MA, Morris AP, Okada Y, Reiner AP, Zon LI, Ganesh SK Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis.. American journal of human genetics 100(1), 51-63 (2017) [JCR] [WOS]
Dr. Chern, Yijuang's Lab