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Alternative Therapies in Health and Medicine|October 27, 2022
Random Forest Model for Labor Induction in Pregnant Women With Hypertensive Disorders Using a Cervical Double BalloonKehua Huang, Zhaozhen Liu, Jinying Luo, et al.
Journal of Cellular Biochemistry|December 31, 2019
Identification of hub-methylated differentially expressed genes in patients with gestational diabetes mellitus by multi-omic WGCNA basing epigenome-wide and transcriptome-wide profilingMin Chen, Jianying Yan, Qing Han, et al.
The Journal of International Medical Research|November 23, 2018
Expression of β-catenin in human trophoblast and its role in placenta accreta and placenta previaQing Han, Lianghui Zheng, Zhaodong Liu, et al.
Frontiers in Medicine|December 10, 2025
Hepcidin, ferroportin, and hemoglobin as predictors of iron deficiency anemia risk and perinatal outcomes in twin pregnancyYanling Zhong, Lin Deng, Xingyan Xu, et al.
Frontiers in Nutrition|September 4, 2025
The influence of hypertensive disorders in pregnancy on neonatal amino acid and acylcarnitine levelsShiyi Xu, Fei Kong, Shuting Huang, et al.
Pakistan Journal of Medical Sciences|December 5, 2024
A nested case-control study of circular ribonucleic acid expression profiles in the peripheral blood of pregnant women with pre-eclampsiaQiuping Liao, Lin Zheng, Liangpu Xu, et al.
Clinics (Sao Paulo, Brazil)|August 21, 2023
Characteristics of the oral glucose tolerance test in women with different pre-pregnancy body mass index and the effect of gestational diabetes mellitus on twin pregnancy outcomesJinying Luo, Xiaoyan Geng, Jinfu Zhou, et al.
Molecular Biology Reports|June 28, 2023
Expression profiling of N6-methyladenosine-modified mRNA in PC12 cells in response to unconjugated bilirubinJinfu Zhou, Sining Liao, Chenran Zhang, et al.
Medicine|June 27, 2020
Perinatal risk factors for congenital hypothyroidism: A retrospective cohort study performed at a tertiary hospital in ChinaJinfu Zhou, Jinying Luo, Junyu Lin, et al.
Molecular Biology Reports|September 14, 2022
Characterization of phenylalanine hydroxylase gene variants and analysis of genotype-phenotype correlation in patients with phenylalanine hydroxylase deficiency from Fujian Province, Southeastern ChinaJinfu Zhou, Yinglin Zeng, Xiaolong Qiu, et al.
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