Rchr
J-GLOBAL ID:202001016509342512   Update date: Nov. 09, 2020

WANG ZHENG

ワン ジェン | WANG ZHENG
Affiliation and department:
Job title: 研究員
Research field  (3): Molecular biology ,  Genetics ,  Genomics
Research keywords  (1): 遺伝学 骨系統疾患 軟骨 骨 繊毛病
Research theme for competitive and other funds  (2):
  • 2017 - 2019 Analysis on the pathogenesis of idiopathic scoliosis using Gpr126 conditional knock-out mice
  • 2017 - 2019 Systematic sequence analysis for early onset skeletal dysplasia
Papers (20):
  • Mao Lin, Sen Zhao, Gang Liu, Yingzhao Huang, Chenxi Yu, Yanxue Zhao, Lianlei Wang, Yuanqiang Zhang, Zihui Yan, Shengru Wang, et al. Identification of novel FBN1 variations implicated in congenital scoliosis. Journal of Human Genetics. 2020. 65. 3. 221-230
  • Jing-yi Xue, Zheng Wang, Satoshi Shinagawa, Hirofumi Ohashi, Nao Otomo, Nursel H Elcioglu, Tomoki Nakashima, Gen Nishimura, Shiro Ikegawa, Long Guo. TNFRSF11A -Associated Dysosteosclerosis: A Report of the Second Case and Characterization of the Phenotypic Spectrum. Journal of Bone and Mineral Research. 2019. 34. 10. 1873-1879
  • Long Guo, Débora Romeo Bertola, Asako Takanohashi, Asuka Saito, Yuko Segawa, Takanori Yokota, Satoru Ishibashi, Yoichiro Nishida, Guilherme Lopes Yamamoto, José Francisco da Silva Franco, et al. Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain Malformation. The American Journal of Human Genetics. 2019. 104. 5. 925-935
  • Hae Ryung Chang, Sung Yoon Cho, Jae Hoon Lee, Eunkyung Lee, Jieun Seo, Hye Ran Lee, Denise P. Cavalcanti, Outi Mäkitie, Helena Valta, Katta M. Girisha, et al. Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia. The American Journal of Human Genetics. 2019. 104. 3. 439-453
  • Bin Mao, Siyu Chen, Xin Chen, Xiumei Yu, Xiaojia Zhai, Tao Yang, Lulu Li, Zheng Wang, Xiuli Zhao, Xue Zhang. Clinical characteristics and spectrum of NF1 mutations in 12 unrelated Chinese families with neurofibromatosis type 1. BMC Medical Genetics. 2018. 19. 1
more...
Lectures and oral presentations  (3):
  • New Discovery on the Basic Research of Camurati-Engelmann Disease
    (第9回 Orthopedic Research Club 2019)
  • Identification of Disease Genes of Skeletal Dysplasia: Lessons from Skeletal Ciliopathy
    (第8回 Orthopedic Research Club 2017)
  • Identification of disease genes of skeletal dysplasia
    (The 3rd Tsinghua-RIKEN Joint Symposium 2017)
Education (2):
  • 2003 - 2008 Peking Union Medical College, Tsinghua University Medical Genetics
  • 1999 - 2003 Nanjing University
Work history (3):
  • 2016/10 - 現在 RIKEN RIKEN Center for Integrative Medical Sciences
  • 2008/07 - 2016/09 Chinese Academy of Medical Sciences Institute of Basic Medical Sciences
  • 2014/03 - 2016/03 RIKEN RIKEN Center for Integrative Medical Sciences Visiting scholar
Awards (1):
  • 2019/08 - 理化学研究所 桜舞賞・研究奨励賞 遺伝性骨疾患の新しい原因遺伝子の同定
Association Membership(s) (1):
日本人類遺伝学会
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