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Maosheng Gu
Observed name:
Gu, Maosheng
Institutions:
Chuzhou University,
Maternal and Child Health Hospital of Xuzhou
Observed institutions:
Xuzhou Medical College,
Chuzhou University,
Maternal and Child Health Hospital of Xuzhou
ORCID:
0000-0002-6595-9090
Observed ORCID:
0000-0002-6595-9090
OpenAlex ID:
A5109390190
Newborn Screening for Methylmalonic Acidemia in a Chinese Population: Molecular Genetic Confirmation and Genotype Phenotype Correlations
2019
·
Wei Zhou
, Huizhong Li
, et al.
·
Frontiers in Genetics
·
57
PDF
Non-invasive prenatal testing in detecting sex chromosome aneuploidy: A large-scale study in Xuzhou area of China
2018
·
Feng Suo
, Chuangxia Wang
, et al.
·
Clinica Chimica Acta
·
40
Next-generation sequencing of NKX2.1 , FOXE1 , PAX8 , NKX2.5 , and TSHR in 100 Chinese patients with congenital hypothyroidism and athyreosis
2017
·
Fang Wang
, Chang Liu
, et al.
·
Clinica Chimica Acta
·
26
Clinical utilization of chromosomal microarray analysis for the genetic analysis in subgroups of pregnancy loss
2020
·
Lingshan Gou
, Tianya Liu
, et al.
·
The Journal of Maternal-Fetal & Neonatal Medicine
·
24
Biochemical, Molecular, and Clinical Characterization of Patients With Primary Carnitine Deficiency via Large-Scale Newborn Screening in Xuzhou Area
2019
·
Wei Zhou
, Huizhong Li
, et al.
·
Frontiers in Pediatrics
·
22
PDF
GJB2 as Well as SLC26A4 Gene Mutations are Prominent Causes for Congenital Deafness
2015
·
Yuan Fang
, Maosheng Gu
, et al.
·
Cell Biochemistry and Biophysics
·
19
Reference Standards for Newborn Screening of Metabolic Disorders by Tandem Mass Spectrometry: A Nationwide Study on Millions of Chinese Neonatal Populations
2021
·
Falin He
, Rulai Yang
, et al.
·
Frontiers in Molecular Biosciences
·
18
Targeted exome sequencing strategy ( NeoEXOME ) for Chinese newborns using a pilot study with 3423 neonates
2024
·
Lin Zou
, Ziyang Cao
, et al.
·
Molecular Genetics & Genomic Medicine
·
14
Development of a fast and robust liquid chromatography-mass spectrometry-based metabolomics analysis method for neonatal dried blood spots
2023
·
Xingyu Guo
, Lina Zhou
, et al.
·
Journal of Pharmaceutical and Biomedical Analysis
·
14
Clinical management of pregnancies with positive screening results for rare autosomal aneuploidies at a single center
2020
·
Lingshan Gou
, Yuan Fang
, et al.
·
Journal of International Medical Research
·
14
Application of karyotype analysis combined with BACs-on-Beads for prenatal diagnosis
2018
·
Yuan Fang
, Guangming Wang
, et al.
·
Experimental and Therapeutic Medicine
·
13
PDF
Chinese expert brief consensus on newborn screening of inherited metabolic disorders during the novel coronavirus infection epidemic
2020
·
Shan Liu
, Dongjuan Wang
, et al.
·
Annals of Translational Medicine
·
12
Hepatic protein phosphatase 1 regulatory subunit 3G alleviates obesity and liver steatosis by regulating the gut microbiota and bile acid metabolism
2024
·
Chu Zhang
, Gui Wang
, et al.
·
Journal of Pharmaceutical Analysis
·
10
Quantification of Differential Metabolites in Dried Blood Spots Using Second-Tier Testing for SCADD/IBDD Disorders Based on Large-Scale Newborn Screening in a Chinese Population
2021
·
Wei Zhou
, Heng Cai
, et al.
·
Frontiers in Pediatrics
·
10
Gut microbiota-bile acid metabolic disorder involved in the cognitive impairments in epilepsy through HO-1 dependent ferroptosis
2025
·
Xinyu Li
, Jia Ji
, et al.
·
Journal of Pharmaceutical Analysis
·
9
Clinical value for the detection of fetal chromosomal deletions/duplications by noninvasive prenatal testing in clinical practice
2021
·
Lingshan Gou
, Feng Suo
, et al.
·
Molecular Genetics & Genomic Medicine
·
7
PDF
Decreased PPP1R3G in pre-eclampsia impairs human trophoblast invasion and migration via Akt/MMP-9 signaling pathway
2023
·
Huimin Shi
, Renyu Kong
, et al.
·
Experimental Biology and Medicine
·
6
PDF
Healthy Plasma Exosomes Exert Potential Neuroprotective Effects against Methylmalonic Acid-Induced Hippocampal Neuron Injury
2024
·
Wei Zhou
, Huizhong Li
, et al.
·
ACS Chemical Neuroscience
·
5
Identification and analyzes of DUOX2 mutations in two familial congenital hypothyroidism cases
2020
·
Liangshan Li
, Wenmiao Liu
, et al.
·
Endocrine
·
5
Metabolite biomarkers of screening neonatal congenital hypothyroidism based on dried blood spot metabolomics
2025
·
Xingyu Guo
, Feng Suo
, et al.
·
Analytical and Bioanalytical Chemistry
·
4
The Diagnosis Pattern of Mid-Trimester Fetal Chromosomal Aneuploidy in Xuzhou and the Clinical Applications
2015
·
Yuan Fang
, Guangming Wang
, et al.
·
Cell Biochemistry and Biophysics
·
4
Discordant performances of non-invasive prenatal testing for foetal trisomy 21 screening in subgroups of pregnancies
2023
·
Feng Suo
, Yi Wang
, et al.
·
Journal of Obstetrics and Gynaecology
·
3
PDF
Establishment and evaluation of rapid detection of AZFc deletion on Y chromosome based on multienzyme isothermal rapid amplification
2024
·
Yan Zhang
, Fang Shao
, et al.
·
Microchemical Journal
·
2
Corrigendum: Decreased PPP1R3G in pre-eclampsia impairs human trophoblast invasion and migration via Akt/MMP-9 signaling pathway
2024
·
Huimin Shi
, Renyu Kong
, et al.
·
Experimental Biology and Medicine
·
2
PDF
Newborn Screening for Isovaleric Acidemia: Treatment With Pivalate‐Generating Antibiotics Contributed to False C5 ‐Carnitine Positivity in a Chinese Population
2024
·
Wei Zhou
, Ting Huang
, et al.
·
Molecular Genetics & Genomic Medicine
·
2
PDF
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Works count:
36
Citation count:
342
H-index:
12
I10-index:
14
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