Min Chen

发表

Prenatal diagnosis of complete maternal uniparental isodisomy of chromosome 4 in a fetus without congenital abnormality or inherited disease-associated variations

K. Choy, WeiQiang Liu, Huimin Zhang, 2015, Molecular Cytogenetics.

Noninvasive prenatal testing for β-thalassemia by targeted nanopore sequencing combined with relative haplotype dosage (RHDO): a feasibility study

WeiQiang Liu, Min Chen, Xiaofang Sun, 2021, Scientific Reports.

Knowledge, attitudes, practices, and influencing factors of anxiety among pregnant women in Wuhan during the outbreak of COVID-19: a cross-sectional study

Min Chen, W. Ding, J. Lu, 2021, BMC Pregnancy and Childbirth.

Ultrasound Screening of Fetal Anomalies at 11–13+6 Weeks

Min Chen, W. Ding, Nan Li, 2020 .

Identify Down syndrome transcriptome associations using integrative analysis of microarray database and correlation-interaction network

Min Chen, Yingjun Luo, Dunjin Chen, 2018, Human Genomics.

Identification of Adrenomedullin-Induced S-Nitrosylated Proteins in JEG-3 Placental Cells

Min Chen, P. Chiu, Cheuk-Lun Lee, 2021, Reproductive Sciences.

Implementation of a High-Resolution Single-Nucleotide Polymorphism Array in Analyzing the Products of Conception.

WeiQiang Liu, Huimin Zhang, Zhihua Li, 2016, Genetic testing and molecular biomarkers.

Contribution of genomic copy-number variations in prenatal oral clefts: a multicenter cohort study

J. Rosenfeld, Ankita Patel, S. Cheung, 2016, Genetics in Medicine.

Prenatal diagnosis of Roberts syndrome in a Chinese family based on ultrasound findings and whole exome sequencing: a case report

WeiQiang Liu, Huimin Zhang, Min Chen, 2022, BMC Medical Genomics.

Novel and recurrent variants identified in fetuses with central nervous system abnormalities by trios-medical exome sequencing.

Min Chen, Jingsi Chen, Dunjin Chen, 2020, Clinica chimica acta; international journal of clinical chemistry.

Clinical application of cervical shear wave elastography in predicting the risk of preterm delivery in DCDA twin pregnancy

Min Chen, Nan Li, D. Cao, 2022, BMC Pregnancy and Childbirth.

Monozygotic twins discordant for homologous Robertsonian translocation trisomy 21 of 46, XX, + 21, der (21;21) (q10; q10) in a twin-to-twin transfusion syndrome, case report

WeiQiang Liu, Zhihua Li, Min Chen, 2021, BMC Pregnancy and Childbirth.

Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing Analysis

K. Choy, T. Leung, Min Chen, 2019, Frontiers in genetics.

Noninvasive Prenatal Diagnosis for Duchenne Muscular Dystrophy Based on the Direct Haplotype Phasing

Zhiyu Peng, Min Chen, C. Yin, 2019, bioRxiv.

Noninvasive prenatal sequencing for multiple Mendelian monogenic disorders among fetuses with skeletal dysplasia or increased nuchal translucency

K. Choy, T. Leung, Min Chen, 2020, Prenatal diagnosis.

Rapid Diagnosis of Imprinting Disorders Involving Copy Number Variation and Uniparental Disomy Using Genome-Wide SNP Microarrays

WeiQiang Liu, Huimin Zhang, Guojiu Yu, 2015, Cytogenetic and Genome Research.

The application of late amniocentesis: a retrospective study in a tertiary fetal medicine center in China

Min Chen, Jingsi Chen, Yufan Li, 2020, BMC Pregnancy and Childbirth.

Prenatal diagnosis of complete maternal uniparental isodisomy of chromosome 4 in a fetus without congenital abnormality or inherited disease-associated variations

K. Choy, WeiQiang Liu, Huimin Zhang, 2015, Molecular Cytogenetics.

Modification of PCR Conditions and Design of Exon-Specific Primers for the Efficient Molecular Diagnosis of PKD1 Mutations

WeiQiang Liu, Zhihua Li, Min Chen, 2014, Kidney and Blood Pressure Research.

Clinical application of medical exome sequencing for prenatal diagnosis of fetal structural anomalies.

Min Chen, V. Zhang, Jingsi Chen, 2020, European journal of obstetrics, gynecology, and reproductive biology.

Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing Analysis

K. Choy, T. Leung, Min Chen, 2019, bioRxiv.

Temporal persistence of residual fetal cell‐free DNA from a deceased cotwin after selective fetal reduction in dichorionic diamniotic twin pregnancies

Yanyan Zhang, Fang Chen, Min Chen, 2021, Prenatal diagnosis.

Prenatal diagnosis of hemivertebrae--A likely association with 7q deletion.

Y. Li, Min Chen, Wei-qiang Liu, 2016, Taiwanese journal of obstetrics & gynecology.

Noninvasive prenatal diagnosis of monogenic disorders based on direct haplotype phasing through targeted linked-read sequencing

Zhiyu Peng, Min Chen, Jia Li, 2021, BMC medical genomics.

Identification of copy number variants by NGS-based NIPT at low sequencing depth.

Huimin Zhang, Min Chen, Meihua Tan, 2020, European journal of obstetrics, gynecology, and reproductive biology.

Validation of fetal DNA fraction estimation and its application in noninvasive prenatal testing for aneuploidy detection in multiple pregnancies

Min Chen, Dunjin Chen, F. Jiang, 2019, Prenatal diagnosis.

Identify Down syndrome transcriptome associations using integrative analysis of microarray database and correlation-interaction network

Min Chen, Yingjun Luo, Dunjin Chen, 2018, Human Genomics.

An induced pluripotent stem cell line (GZHMCi003-A) derived from a fetus with exon 3 heterozygous deletion in RUNX2 gene causing cleidocranial dysplasia.

Min Chen, Yufan Li, Nan Li, 2021, Stem cell research.

Effects of HAR1 on cognitive function in mice and the regulatory network of HAR1 determined by RNA sequencing and applied bioinformatics analysis

Min Chen, Xiaoshun Shi, Kailing Huang, 2023, Frontiers in Genetics.

Prenatal diagnose of a fetus with Harlequin ichthyosis in a Chinese family.

Min Chen, Jingsi Chen, Dunjin Chen, 2018, Taiwanese journal of obstetrics & gynecology.

Clinical Outcome: A Monosomy 18p is Better than a Tetrasomy 18p

WeiQiang Liu, Min Chen, Xiaofang Sun, 2015, Cytogenetic and Genome Research.

Clinical utility of expanded non‐invasive prenatal screening and chromosomal microarray analysis in high‐risk pregnancy

K. Choy, T. Leung, Min Chen, 2020, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Noninvasive prenatal diagnosis of β‐thalassemia by relative haplotype dosage without analyzing proband

WeiQiang Liu, Min Chen, Haoxian Li, 2019, Molecular genetics & genomic medicine.

Genetic Examination for Fetuses with Increased Fetal Nuchal Translucency by Genomic Technology

Huimin Zhang, Min Chen, Jingsi Chen, 2020, Cytogenetic and Genome Research.

Identifying occult maternal malignancies from 1.93 million pregnant women undergoing noninvasive prenatal screening tests

Huanming Yang, Jian Wang, J. Cigudosa, 2019, Genetics in Medicine.

Selective termination of the fetus in multiple pregnancies using ultrasound-guided radiofrequency ablation

Min Chen, Dunjin Chen, Yufan Li, 2021, BMC Pregnancy and Childbirth.

Haplotype-Based Noninvasive Prenatal Diagnosis for Duchenne Muscular Dystrophy: A pilot study in South China

R. Wu, Zhiyu Peng, Min Chen, 2019, bioRxiv.

Prenatal diagnosis of Noonan syndrome in a set of monozygotic twins- a case report

Min Chen, Yufan Li, Huizhen Yuan, 2023, BMC Pregnancy and Childbirth.

Identifying occult maternal malignancies from 1.93 million pregnant women undergoing noninvasive prenatal screening tests

Tengyu Ma, Huanming Yang, Jian Wang, 2019, Genetics in Medicine.