Upload Avatar (500 x 500)
Yu-Fang Zheng
zhengyf@fudan.edu.cn
Chinese, English
Shanghai
Fudan University
Life Sciences
  • 1997 - Bachelor's Degree in Biological Sciences and Technology: Tsinghua University
  • 1999 - Master's Degree in Biophysics: Tsinghua University
  • 2004 - Ph.D. in Physiology, Biophysics, and Molecular Medicine: Cornell University
  • 2004-2007 - Postdoctoral Research: Yale University
  • 2016 - Deputy Researcher PI: Fudan University Affiliated Obstetrics and Gynecology Hospital
  • 2017 - Researcher: Fudan University
  • Award: Shanghai Pujiang Talent Program
  • Award: Fudan University Zhuoxue Talent Program
  • 2004-2007 - Postdoctoral Research: Yale University
  • 2007-Present - Researcher: Fudan University
  • 2016-Present - Deputy Researcher PI: Fudan University Affiliated Obstetrics and Gynecology Hospital
  • Shanghai Pujiang Talent Program
  • Fudan University Zhuoxue Talent Program
Molecular genetics and developmental mechanisms of major neurological diseases caused by abnormal early embryonic development
  • Deficiency of Wdr60 and Wdr34 cause distinct neural tube malformation phenotypes in early embryos, Yan L, Yin H, Mi Y, Wu Y, Zheng Y*, 2023
  • High glucose causes developmental abnormalities in neuroepithelial cysts with actin and HK1 distribution changes, Peng S, Wu Y, Zheng Y*, 2023
  • Parental folate deficiency induces birth defects in mice accompanied with increased de novo mutations, Zhao Y#, Chen D#, Tang J, Zheng Y*, Qi Ji*, Wang H*, 2022
  • MeCP2 duplication causes hyperandrogenism by upregulating LHCGR and downregulating RORα, Wang Y, Wu Y, Zheng Y*, Wang H*, 2021
  • Organoids as a new model system to study neural tube defects, Wu Y, Peng S, Zheng Y*, 2021
  • SRPS Associated Protein WDR60 Regulates the Multipolar-to-Bipolar Transition of Migrating Neurons during Cortical Development, Li C, Zheng Y, Zheng Y*, Xu Z*, 2021
  • WDR34 mutation from anencephaly patients impaired both SHH and PCP signaling pathways, Yin H, Peng R, Chen Z, Wang H, Zhang T, Zheng Y*, 2020
  • Rare mutations of ADAM17 from TOFs induce hypertrophy in human embryonic stem cell-derived cardiomyocytes via HB-EGF signaling, Xie Y, Ma A, Wang B, Peng R, Jing Y, Wang D, Finnell RH., Qiao B, Wang Y*, Wang H*, Zheng Y*, 2019
  • MicroRNA-197 controls ADAM10 expression to mediate MeCP2’s role in the differentiation of neuronal progenitors, Wang Y#, Zheng Y#,*, Yang S, Yang Z, Zhang L, He Y, Gong X, Liu D, Finnell R.H., Qiu Z, Du Y*, Wang H*, 2019
  • Threshold for neural tube defect risk by accumulated singleton loss-of-function variants, Chen Z#, Lei Y#, Zheng Y#, Aguiar-Pulido V, Ross M.E., Peng R, Jin L, Zhang T*, Finnell R.H.*, Wang H*, 2018
Genetics Development Molecular Biochemistry Animal Models Organoid Models Embryonic Development Neurological Diseases Mechanisms Research

Contact us

Let's talk!
* Required
* Required
* Required
* Invalid email address
By submitting this form, you agree that IoT ONE may contact you with insights and marketing messaging.
No thanks, I don't want to receive any marketing emails from IoT ONE.
Submit

Thank you for your message!
We will contact you soon.