Yu-Fang Zheng (Yufang Zheng)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 17

Top Venues

Cell death & disease

Birth defects research

Journal of human genetics

International journal of molecular sciences

Obstetrics and Gynecology Hospital of Fudan University

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Obstetrics and Gynecology Hospital of Fudan University Mar 01 2016

China

Professor

Fudan University Nov 08 2007

China

Professor

Publications

Bing Yan, Baoming Gong, Yu-Fang Zheng, Lei Sun, Xiaohui Wu
Embryonic Lethal Phenotyping to Identify Candidate Genes Related with Birth Defects. International journal of molecular sciences 25 (16) (2024)
Bing Yan, Baoming Gong, Yu-Fang Zheng, Lei Sun, Xiaohui Wu
Embryonic Lethal Phenotyping to Identify Candidate Genes Related with Birth Defects. International journal of molecular sciences 25 (16) (2024)
Ying Zhao, Duoyuan Chen, Jianping Tang, Yu-Fang Zheng, Ji Qi, Hongyan Wang
Parental folate deficiency induces birth defects in mice accompanied with increased de novo mutations. Cell discovery 8 (1) (2022)
Cui Li, Yu Zheng, Yu-Fang Zheng, Zhiheng Xu
SRPS associated protein WDR60 regulates the multipolar-to-bipolar transition of migrating neurons during cortical development. Cell death & disease 12 (1) (2021)
Yu Wu, Sisi Peng, Richard H Finnell, Yu-Fang Zheng
Organoids as a new model system to study neural tube defects. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 35 (4) (2021)
Yu-Meng Wang, Yu Wu, Yu-Fang Zheng, Hong-Yan Wang
MeCP2 duplication causes hyperandrogenism by upregulating LHCGR and downregulating RORα. Cell death & disease 12 (11) (2021)
Jianhong Ye, Youli Tong, Jiashun Lv, Rui Peng, Shuxia Chen, Lele Kuang, Ke Su, Yu-Fang Zheng, Ting Zhang, Feng Zhang, Li Jin, Xueyan Yang, Hongyan Wang
Rare mutations in the autophagy-regulating gene AMBRA1 contribute to human neural tube defects. Human mutation 41 (8) (2020)
Hailing Yin, Rui Peng, Zhongzhong Chen, Hongyan Wang, Ting Zhang, Yu-Fang Zheng
WDR34 mutation from anencephaly patients impaired both SHH and PCP signaling pathways. Journal of human genetics 65 (11) (2020)
Yifang Xie, Anyun Ma, Boshi Wang, Rui Peng, Yingchun Jing, Deqian Wang, Richard H Finnell, Bin Qiao, Yongming Wang, Hongyan Wang, Yu-Fang Zheng
Rare mutations of ADAM17 from TOFs induce hypertrophy in human embryonic stem cell-derived cardiomyocytes via HB-EGF signaling. Clinical science (London, England : 1979) 133 (2) (2019)
Meng-Jiao Zhu, Xiao-Yun Ma, Pei-Cheng Ding, Han-Fei Tang, Rui Peng, Lei Lu, Pei-Qiang Li, Bin Qiao, Xue-Yan Yang, Yu-Fang Zheng, Hong-Yan Wang, Yun-Qian Gao, Feng-Shan Chen
Novel mutations of AXIN2 identified in a Chinese Congenital Heart Disease Cohort. Journal of human genetics 64 (5) (2019)
Linna Zhang, Yue Qin, Xiaohong Gong, Rui Peng, Chunquan Cai, Yu-Fang Zheng, Yasong Du, Hongyan Wang
A promoter variant in ZNF804A decreasing its expression increases the risk of autism spectrum disorder in the Han Chinese population. Translational psychiatry 9 (1) (2019)
Bin Wang, Yingying Zhang, Hongli Dong, Siyi Gong, Bin Wei, Man Luo, Hongyan Wang, Xiaohui Wu, Wei Liu, Xingshun Xu, Yu-Fang Zheng, Miao Sun
Loss of Tctn3 causes neuronal apoptosis and neural tube defects in mice. Cell death & disease 9 (5) (2018)
Yu-Meng Wang, Yu-Fang Zheng, Si-Yu Yang, Zhang-Min Yang, Lin-Na Zhang, Yan-Qin He, Xiao-Hong Gong, Dong Liu, Richard H Finnell, Zi-Long Qiu, Ya-Song Du, Hong-Yan Wang
MicroRNA-197 controls ADAM10 expression to mediate MeCP2's role in the differentiation of neuronal progenitors. Cell death and differentiation 26 (10) (2018)
Zhongzhong Chen, Yunping Lei, Yu-Fang Zheng, Vanessa Aguiar-Pulido, M Elizabeth Ross, Rui Peng, Li Jin, Ting Zhang, Richard H Finnell, Hongyan Wang
Threshold for neural tube defect risk by accumulated singleton loss-of-function variants. Cell research 28 (10) (2018)
Xiaoya Gao, Richard H Finnell, Hongyan Wang, Yu-Fang Zheng
Network correlation analysis revealed potential new mechanisms for neural tube defects beyond folic acid. Birth defects research 110 (12) (2018)
Jimi Kim, Yunping Lei, Jin Guo, Sung-Eun Kim, Bogdan J Wlodarczyk, Robert M Cabrera, Ying Linda Lin, Torbjorn K Nilsson, Ting Zhang, Aiguo Ren, Linlin Wang, Zhengwei Yuan, Yu-Fang Zheng, Hong-Yan Wang, Richard H Finnell
Formate rescues neural tube defects caused by mutations in Slc25a32. Proceedings of the National Academy of Sciences of the United States of America 115 (18) (2018)
Zhiwen Shi, Xueyan Yang, Bin-Bin Li, Shuxia Chen, Luming Yang, Liangping Cheng, Ting Zhang, Hongyan Wang, Yu-Fang Zheng
Novel Mutation of LRP6 Identified in Chinese Han Population Links Canonical WNT Signaling to Neural Tube Defects. Birth defects research 110 (1) (2017)

Yu-Fang Zheng.css-eqlu8i{font-size:small;padding-left:4px;} (Yufang Zheng)

Publication Activity (10 Years)

Top Topics

Top Venues

Yu-Fang Zheng (Yufang Zheng)