Can Liao

No. 9 Jinsui Road
Guangzhou, 510623, China

Last Updated: 09/26/2026

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Found 28 publications

Genetic architecture and prognostic significance of suspected fetal microcephaly: evidence from prenatal exome sequencing in a large prospective cohort.

Genetic architecture and prognostic significance of suspected fetal microcephaly: evidence from prenatal exome sequencing in a large prospective cohort.

Journal: Human genomics

Published: August 30, 2025

Genetic burden and multidimensional predictors in prenatal diagnosis of fetal congenital diaphragmatic hernia.

Genetic burden and multidimensional predictors in prenatal diagnosis of fetal congenital diaphragmatic hernia.

Journal: Human genetics

Published: March 04, 2025

Inhibition of the NLR pathway alleviates MAPK1 mutation-driven proliferation and differentiation deficits and enhanced apoptosis in P19 cells.

Inhibition of the NLR pathway alleviates MAPK1 mutation-driven proliferation and differentiation deficits and enhanced apoptosis in P19 cells.

Journal: Tissue & cell

Published: February 16, 2025

MiR-424-5p Inhibits Proliferation, Migration, Invasion and Angiogenesis of the HTR-8/SVneo Cells Through Targeting LRP6 Mediated β-catenin.

MiR-424-5p Inhibits Proliferation, Migration, Invasion and Angiogenesis of the HTR-8/SVneo Cells Through Targeting LRP6 Mediated β-catenin.

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: January 15, 2024

Association of prenatal Cleft Lip and Palate ultrasound abnormalities with copy number variants at a single Chinese tertiary center.

Association of prenatal Cleft Lip and Palate ultrasound abnormalities with copy number variants at a single Chinese tertiary center.

Journal: Italian journal of pediatrics

Published: January 07, 2024

Prenatal diagnosis of polycystic renal diseases: diagnostic yield, novel disease-causing variants, and genotype-phenotype correlations.

Prenatal diagnosis of polycystic renal diseases: diagnostic yield, novel disease-causing variants, and genotype-phenotype correlations.

Journal: American journal of obstetrics & gynecology MFM

Published: August 06, 2023

Single-cell RNA sequencing reveals cellular and molecular landscape of fetal cystic hygroma.

Single-cell RNA sequencing reveals cellular and molecular landscape of fetal cystic hygroma.

Journal: BMC medical genomics

Published: June 27, 2023

Prenatal diagnosis and perinatal outcomes of twin pregnancies disharmonious for one fetus with nuchal translucency above the 95th percentile.

Prenatal diagnosis and perinatal outcomes of twin pregnancies disharmonious for one fetus with nuchal translucency above the 95th percentile.

Journal: Molecular cytogenetics

Published: April 27, 2023

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

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

Journal: Human genetics

Published: January 13, 2023

Whole exome sequencing improves genetic diagnosis of fetal clubfoot.

Whole exome sequencing improves genetic diagnosis of fetal clubfoot.

Journal: Human genetics

Published: October 23, 2022

Clinical impacts of genome-wide noninvasive prenatal testing for rare autosomal trisomy.

Clinical impacts of genome-wide noninvasive prenatal testing for rare autosomal trisomy.

Journal: American journal of obstetrics & gynecology MFM

Published: October 20, 2022

Germline mosaicism for a disease-causing mutation in the ATP1A3 gene in a Chinese family.

Germline mosaicism for a disease-causing mutation in the ATP1A3 gene in a Chinese family.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: September 04, 2022

Showing 1-12 of 28

Last Updated: 09/26/2026