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Tissue & Cell|June 4, 2025
Inhibition of the NLR pathway alleviates MAPK1 mutation-driven proliferation and differentiation deficits and enhanced apoptosis in P19 cellsTingying Lei, Lei Liu, Fei Guo, et al.
Pediatrics and Neonatology|November 14, 2024
Genetic burden in neonatal and pediatric-onset pulmonary hypertension: A single-center retrospective study using exome sequencing in a Chinese populationChen Chen, Hang Zhou, Fang Fu, et al.
Genes|September 23, 2022
Prenatal Diagnosis and Outcomes in Fetuses with HemivertebraHang Zhou, You Wang, Ruibin Huang, et al.
Molecular Cytogenetics|June 28, 2022
Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysisRuibin Huang, Hang Zhou, Fang Fu, et al.
Frontiers in Genetics|May 25, 2023
Genetic diagnosis of fetal microcephaly at a single tertiary center in ChinaYou Wang, Fang Fu, Tingying Lei, et al.
BMC Medical Genomics|April 22, 2024
Single-cell RNA sequencing reveals cellular and molecular landscape of fetal cystic hygromaFang Fu, Xin Yang, Ru Li, et al.
Human Genetics|April 24, 2023
Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencingRuibin Huang, Fang Fu, Hang Zhou, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 6, 2021
[Application of whole exome sequencing technology in fetuses with congenital structural abnormalities]Lushan Li, Fang Fu, Ru Li, et al.
Nature Communications|March 2, 2025
Targeting the ceramidase ACER3 attenuates cholestasis in mice by mitigating bile acid overload via unsaturated ceramide-mediated LXRβ signaling transductionLeyi Liao, Ziying Liu, Lei Liu, et al.
Prenatal Diagnosis|May 22, 2025
Prenatal Exome Sequencing for Fetal Macrocephaly: A Large Prospective Observational Cohort StudyHang Zhou, Fang Fu, Ruibin Huang, et al.
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