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Nature Medicine|November 14, 2017
Enhancing the precision of genetic lineage tracing using dual recombinasesLingjuan He, Yan Li, Yi Li, et al.Nature Medicine|January 22, 2024
Prospective prenatal cell-free DNA screening for genetic conditions of heterogenous etiologiesJinglan Zhang, Yanting Wu, Songchang Chen, et al.Nature|May 18, 2022
Maternal inheritance of glucose intolerance via oocyte TET3 insufficiencyBin Chen, Ya-Rui Du, Hong Zhu, et al.Human Molecular Genetics|July 17, 2018
Basonuclin 1 deficiency is a cause of primary ovarian insufficiencyDan Zhang, Yifeng Liu, Zhou Zhang, et al.Prenatal Diagnosis|November 10, 2012
Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factorsShan Dan, Wei Wang, Jinghui Ren, et al.Nature Communications|May 2, 2026
Cell-free DNA fragmentomics for preeclampsia risk assessmentWenqiu Xu, Songchang Chen, Jia Li, et al.Methodsx|July 21, 2025
A stepwise approach to designing and delivering the SCHeLTI trial community-family-mother-child obesity prevention interventionOlivia De-Jongh González, Jianxia Fan, Isabelle Marc, et al.Nature|May 27, 2026
Spatiotemporal transcriptome atlas of human embryos after gastrulationJiexue Pan, Yuejiao Li, Zhongliang Lin, et al.Maturitas|February 7, 2024
Practice guideline on ovarian tissue cryopreservation and transplantation in the prevention and treatment of iatrogenic premature ovarian insufficiencyXiangyan Ruan, Che Xu, Hefeng Huang, et al.Maturitas|December 25, 2025
Practice guideline for the treatment and management of iatrogenic premature ovarian insufficiencyXiangyan Ruan, Che Xu, Hefeng Huang, et al.Pageof 25