Xueping Shen

Huzhou, China

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 22 publications

Genetic analysis of a patient with Weiss-Kruszka syndrome due to variant of ZNF462 gene

Genetic analysis of a patient with Weiss-Kruszka syndrome due to variant of ZNF462 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: July 07, 2025

Ras p21 protein activator 1 regulates trophoblast function and its association with preeclampsia through the Ras/mitogen-activated protein kinase pathway.

Ras p21 protein activator 1 regulates trophoblast function and its association with preeclampsia through the Ras/mitogen-activated protein kinase pathway.

Journal: CytoJournal
Published: February 10, 2025

Analysis of the results for genetic disease screening among 1 000 newborns from Huzhou

Analysis of the results for genetic disease screening among 1 000 newborns from Huzhou

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 29, 2024

Dioscin pretreatment ameliorates ferroptosis in cardiomyocytes after myocardial infarction via inhibiting endoplasmic reticulum stress.

Dioscin pretreatment ameliorates ferroptosis in cardiomyocytes after myocardial infarction via inhibiting endoplasmic reticulum stress.

Journal: Molecular medicine (Cambridge, Mass.)
Published: April 15, 2024

Identification of four TTN variants in three families with fetal akinesia deformation sequence.

Identification of four TTN variants in three families with fetal akinesia deformation sequence.

Journal: BMC medical genomics
Published: December 18, 2023

Renal Hypodysplasia/Aplasia 3 Caused by a Rare Variant of GREB1L With Incomplete Penetrance in a Chinese Family.

Renal Hypodysplasia/Aplasia 3 Caused by a Rare Variant of GREB1L With Incomplete Penetrance in a Chinese Family.

Journal: Urology
Published: November 06, 2023

Prenatal diagnosis of recurrent moderate skeletal dysplasias in lamin B receptors.

Prenatal diagnosis of recurrent moderate skeletal dysplasias in lamin B receptors.

Journal: Frontiers in genetics
Published: August 16, 2022

Genetic analysis of a child with XYY syndrome in conjunct with 3-methylglutaenedioic aciduria type I

Genetic analysis of a child with XYY syndrome in conjunct with 3-methylglutaenedioic aciduria type I

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: July 10, 2022

Case Report: Prenatal Diagnosis of Postaxial Polydactyly With Bi-Allelic Variants in Smoothened (SMO).

Case Report: Prenatal Diagnosis of Postaxial Polydactyly With Bi-Allelic Variants in Smoothened (SMO).

Journal: Frontiers in genetics
Published: March 01, 2022

A Novel Mutation c.3392G>T of COL2A1 Causes Spondyloepiphyseal Dysplasia Congenital by Affecting Pre-mRNA Splicing.

A Novel Mutation c.3392G>T of COL2A1 Causes Spondyloepiphyseal Dysplasia Congenital by Affecting Pre-mRNA Splicing.

Journal: Frontiers in genetics
Published: December 02, 2021

Prenatal diagnosis of three fetuses with small supernumerary marker chromosomes

Prenatal diagnosis of three fetuses with small supernumerary marker chromosomes

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

Genetic analysis and prenatal diagnosis of a pregnant woman with Sheldon-Hall syndrome

Genetic analysis and prenatal diagnosis of a pregnant woman with Sheldon-Hall syndrome

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 21, 2020
Showing 1-12 of 22

Last Updated: 09/26/2026