Liangjie H. Guo

No. 7 Weiwu Road
Zhengzhou, 450003, China

Last Updated: 09/26/2026

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Found 19 publications

Gestational age-associated differences in amniotic fluid extracellular vesicle-enriched preparations during mid-pregnancy: an exploratory proteomic study.

Gestational age-associated differences in amniotic fluid extracellular vesicle-enriched preparations during mid-pregnancy: an exploratory proteomic study.

Journal: Journal of proteomics
Published: May 29, 2026

Integrated multiomics profiling of amniotic fluid exosomes reveals dysregulated lipid and protein signatures in fetal 22q11.2 deletion syndrome.

Integrated multiomics profiling of amniotic fluid exosomes reveals dysregulated lipid and protein signatures in fetal 22q11.2 deletion syndrome.

Journal: Human genomics
Published: January 24, 2026

Prenatal Diagnosis of COQ2 Variants in Suspected Coenzyme Q10 Deficiency.

Prenatal Diagnosis of COQ2 Variants in Suspected Coenzyme Q10 Deficiency.

Journal: Kidney international reports
Published: April 08, 2025

Correlation between maternal serum biomarkers and the risk of fetal chromosome copy number variants: a single-center retrospective study.

Correlation between maternal serum biomarkers and the risk of fetal chromosome copy number variants: a single-center retrospective study.

Journal: Archives of gynecology and obstetrics
Published: February 07, 2024

Genetic analysis of a Chinese pedigree with Cohen syndrome due to compound heterozygous variants of VPS13B gene

Genetic analysis of a Chinese pedigree with Cohen syndrome due to compound heterozygous variants of VPS13B gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 02, 2023

Identification of a novel de novo mutation of SETBP1 and new findings of SETBP1 in tumorgenesis.

Identification of a novel de novo mutation of SETBP1 and new findings of SETBP1 in tumorgenesis.

Journal: Orphanet journal of rare diseases
Published: June 22, 2022

Expert consensus on the application of prenatal exome sequencing for fetal structural anomalies

Expert consensus on the application of prenatal exome sequencing for fetal structural anomalies

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 22, 2022

A gonadal mosaicism novel KMT2D mutation identified by haplotype construction and clone sequencing strategy.

A gonadal mosaicism novel KMT2D mutation identified by haplotype construction and clone sequencing strategy.

Journal: Clinica chimica acta; international journal of clinical chemistry
Published: March 18, 2022

METTL3-Mediated m6A RNA Methylation of ZBTB4 Interferes With Trophoblast Invasion and Maybe Involved in RSA.

METTL3-Mediated m6A RNA Methylation of ZBTB4 Interferes With Trophoblast Invasion and Maybe Involved in RSA.

Journal: Frontiers in cell and developmental biology
Published: March 12, 2022

A novel mutation within intron 17 of the CUL7 gene results in appearance of premature termination codon.

A novel mutation within intron 17 of the CUL7 gene results in appearance of premature termination codon.

Journal: Clinica chimica acta; international journal of clinical chemistry
Published: March 06, 2020

Hereditary spherocytosis due to a novel c.5798+1G>A variant of the SPTB gene

Hereditary spherocytosis due to a novel c.5798+1G>A variant of the SPTB gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: January 11, 2020

Prenatal diagnosis of a fetus affected with Finnish type congenital nephrotic syndrome

Prenatal diagnosis of a fetus affected with Finnish type congenital nephrotic syndrome

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: October 11, 2019
Showing 1-12 of 19

Last Updated: 09/26/2026