Linyan Zhu

Ningbo, China

Last Updated: 09/26/2026

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Found 13 publications

Research progress on risk factors and clinical management of Ureaplasma Species infection in preterm infants.

Research progress on risk factors and clinical management of Ureaplasma Species infection in preterm infants.

Journal: Frontiers in pediatrics

Published: April 02, 2026

Case Report: Prenatal imaging and genetic integrated diagnosis of SCN2A encephalopathy-a case of cryptical cortical dysplasia caused by a loss-of-function frameshift genetic variant.

Case Report: Prenatal imaging and genetic integrated diagnosis of SCN2A encephalopathy-a case of cryptical cortical dysplasia caused by a loss-of-function frameshift genetic variant.

Journal: Frontiers in neuroscience

Published: September 03, 2025

Prenatal Diagnosis of Shwachman-Diamond Syndrome: Fetal Compound Heterozygous Variants in the SBDS Gene Associated With Mildly Straight Ribs.

Prenatal Diagnosis of Shwachman-Diamond Syndrome: Fetal Compound Heterozygous Variants in the SBDS Gene Associated With Mildly Straight Ribs.

Journal: Prenatal diagnosis

Published: October 25, 2024

A novel variant c.7104 + 6T > A of ABCA12 linked to autosomal recessive congenital ichthyosis verified by minigene splicing assay.

A novel variant c.7104 + 6T > A of ABCA12 linked to autosomal recessive congenital ichthyosis verified by minigene splicing assay.

Journal: Frontiers in pediatrics

Published: October 04, 2024

Prenatal detection of novel compound heterozygous variants of the PLD1 gene in a fetus with congenital heart disease.

Prenatal detection of novel compound heterozygous variants of the PLD1 gene in a fetus with congenital heart disease.

Journal: Frontiers in genetics

Published: September 19, 2024

Case report: A compound heterozygous mutations in ASNS broadens the spectrum of asparagine synthetase deficiency in the prenatal diagnosis.

Case report: A compound heterozygous mutations in ASNS broadens the spectrum of asparagine synthetase deficiency in the prenatal diagnosis.

Journal: Frontiers in pediatrics

Published: August 07, 2023

Limb girdle muscular dystrophy 23 caused by compound heterozygous mutations of LAMA2 gene.

Limb girdle muscular dystrophy 23 caused by compound heterozygous mutations of LAMA2 gene.

Journal: Frontiers in pediatrics

Published: March 21, 2023

RTN2, a new member of circadian clock genes identified by database mining and bioinformatics prediction, is highly expressed in ovarian cancer.

RTN2, a new member of circadian clock genes identified by database mining and bioinformatics prediction, is highly expressed in ovarian cancer.

Journal: Molecular medicine reports

Published: March 09, 2022

Prenatal diagnosis of Walker-Warburg syndrome due to compound mutations in the B3GALNT2 gene.

Prenatal diagnosis of Walker-Warburg syndrome due to compound mutations in the B3GALNT2 gene.

Journal: The journal of gene medicine

Published: December 28, 2021

The Circadian Gene NPAS2 Act as a Putative Tumor Stimulative Factor for Uterine Corpus Endometrial Carcinoma.

The Circadian Gene NPAS2 Act as a Putative Tumor Stimulative Factor for Uterine Corpus Endometrial Carcinoma.

Journal: Cancer management and research

Published: October 09, 2021

MiR-486-5p Act as a Biomarker in Endometrial Carcinoma: Promotes Cell Proliferation, Migration, Invasion by Targeting MARK1.

MiR-486-5p Act as a Biomarker in Endometrial Carcinoma: Promotes Cell Proliferation, Migration, Invasion by Targeting MARK1.

Journal: OncoTargets and therapy

Published: June 18, 2020

Matrix metalloproteinase-7 may serve as a novel biomarker for cervical cancer.

Matrix metalloproteinase-7 may serve as a novel biomarker for cervical cancer.

Journal: OncoTargets and therapy

Published: July 28, 2018

Showing 1-12 of 13

Last Updated: 09/26/2026