Wenlan L. Liu

3002 Sungang West Road
Shenzhen, 518035, China

Last Updated: 09/26/2026

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Found 81 publications

Fetal Y chromosome abnormalities cause false-low fetal fraction in NIPT: a retrospective analysis of 24,101 pregnant women.

Fetal Y chromosome abnormalities cause false-low fetal fraction in NIPT: a retrospective analysis of 24,101 pregnant women.

Journal: Frontiers in genetics
Published: April 15, 2026

Machine learning models for reducing false positives in Fluorometric newborn screening of phenylketonuria: Development, validation, and clinical application.

Machine learning models for reducing false positives in Fluorometric newborn screening of phenylketonuria: Development, validation, and clinical application.

Journal: Clinica chimica acta; international journal of clinical chemistry
Published: February 04, 2026

Genetic screening for hearing impairment and the genotype-phenotype correlation of GJB2 c.109G>A variants in 47,729 neonates: a population-based study in southern China.

Genetic screening for hearing impairment and the genotype-phenotype correlation of GJB2 c.109G>A variants in 47,729 neonates: a population-based study in southern China.

Journal: International journal of pediatric otorhinolaryngology
Published: November 10, 2025

A novel HBD gene mutation associated with normal-range hb A2 in β-thalassemia carriers.

A novel HBD gene mutation associated with normal-range hb A2 in β-thalassemia carriers.

Journal: Annals of hematology
Published: November 07, 2025

Genotype Characteristics and Hearing Phenotype Analysis of Newborns with Biallelic GJB2 Mutations: A 652-Case-Cohort Study.

Genotype Characteristics and Hearing Phenotype Analysis of Newborns with Biallelic GJB2 Mutations: A 652-Case-Cohort Study.

Journal: International journal of neonatal screening
Published: November 02, 2025

Comprehensive genotype-phenotype correlation analysis in 11 509 neonates carrying common deafness-associated pathogenic variants.

Comprehensive genotype-phenotype correlation analysis in 11 509 neonates carrying common deafness-associated pathogenic variants.

Journal: Journal of medical genetics
Published: August 10, 2025

N-glycomics profiling reveals alteration of fucosylation in early acute ischemic stroke from mouse brain tissue to human serum.

N-glycomics profiling reveals alteration of fucosylation in early acute ischemic stroke from mouse brain tissue to human serum.

Journal: Clinical proteomics
Published: June 27, 2025

Clinical significance of regions of homozygosity detection in prenatal chromosomal microarray analysis.

Clinical significance of regions of homozygosity detection in prenatal chromosomal microarray analysis.

Journal: HGG advances
Published: April 15, 2025

Mass spectrometry-based spatiotemporal characterization of lipids in early focal cerebral ischemia.

Mass spectrometry-based spatiotemporal characterization of lipids in early focal cerebral ischemia.

Journal: Analytical and bioanalytical chemistry
Published: April 06, 2025

A novel dual-target Septin9 methylation assay for improved detection of early-stage colorectal cancer and high-grade intraepithelial neoplasia.

A novel dual-target Septin9 methylation assay for improved detection of early-stage colorectal cancer and high-grade intraepithelial neoplasia.

Journal: BMC cancer
Published: April 28, 2024

Future Directions of the Prokaryotic Chromosome Field.

Future Directions of the Prokaryotic Chromosome Field.

Journal: Molecular microbiology
Published: March 22, 2024

Adenylate kinase 4 promotes neuronal energy metabolism and mitophagy in early cerebral ischemia via Parkin/PKM2 pathway.

Adenylate kinase 4 promotes neuronal energy metabolism and mitophagy in early cerebral ischemia via Parkin/PKM2 pathway.

Journal: Experimental neurology
Published: March 01, 2024
Showing 1-12 of 81

Last Updated: 09/26/2026