Lushan Li

发表

Whole‐exome sequencing in the evaluation of fetal congenital anomalies of the kidney and urinary tract detected by ultrasonography

C. Liao, Dongzhi Li, T. Lei, 2020, Prenatal diagnosis.

Microarray screening for key genes and prognosis factors in interferon regulatory factor 1-silenced ovarian cancer SKOV-3 cells

F. Wang, C. Liao, T. Lei, 2018 .

Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis

C. Liao, Dongzhi Li, T. Lei, 2022, Molecular Cytogenetics.

Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses

C. Liao, P. Fang, Dongzhi Li, 2022, Genome Medicine.

Identification of differential microRNAs and messenger RNAs resulting from ASXL transcriptional regulator 3 knockdown during during heart development

C. Liao, Dongzhi Li, T. Lei, 2022, Bioengineered.

Prenatal Diagnosis of PPP2R1A-Related Neurodevelopmental Disorders Using Whole Exome Sequencing: Clinical Report and Review of Literature

C. Liao, T. Lei, F. Fu, 2023, Genes.

Genetic Analysis and Sonography Characteristics in Fetus with SHOX Haploinsufficiency

C. Liao, F. Fu, Ru Li, 2023, Genes.

Prenatal diagnosis and pregnancy outcome analysis of thickened nuchal fold in the second trimester

C. Liao, F. Fu, Ru Li, 2018, Medicine.

Genetic tests aid in counseling of fetuses with cerebellar vermis defects

C. Liao, Ru Li, Qiuxia Yu, 2020, Prenatal diagnosis.

Genetic diagnosis of fetal microcephaly at a single tertiary center in China

C. Liao, T. Lei, F. Fu, 2023, Frontiers in Genetics.

All‐trans‐retinoid acid induces the differentiation of P19 cells into neurons involved in the PI3K/Akt/GSK3β signaling pathway

C. Liao, Dongzhi Li, T. Lei, 2020, Journal of cellular biochemistry.

ASXL3 gene mutations inhibit cell proliferation and promote cell apoptosis in mouse cardiomyocytes by upregulating lncRNA NONMMUT063967.2

C. Liao, Dongzhi Li, T. Lei, 2023, Biochemistry and biophysics reports.

Ndufa4 Regulates the Proliferation and Apoptosis of Neurons via miR-145a-5p/Homer1/Ccnd2

C. Liao, Dongzhi Li, T. Lei, 2023, Molecular Neurobiology.

Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencing

C. Liao, T. Lei, F. Fu, 2023, Human Genetics.

Prenatal diagnosis and outcomes in fetuses with duplex kidney

F. Fu, Ru Li, Lushan Li, 2024, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

Prenatal diagnosis of 17q12 copy number variants in fetuses via chromosomal microarray analysis - a retrospective cohort study and literature review.

F. Fu, Lushan Li, Ruibin Huang, 2024, Heliyon.