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Xiaorui Xie

Observed names: Xiaorui xie, Xie Xiaorui, Xie, Xiaorui
ORCID: 0000-0002-9965-2791
Observed ORCID: 0000-0002-9965-2791
OpenAlex ID: A5020093786
Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype
2019 · Linjuan Su, Hailong Huang, et al. · Molecular Genetics & Genomic Medicine · 30
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Downregulation of miR-146b-3p Inhibits Proliferation and Migration and Modulates the Expression and Location of Sodium/Iodide Symporter in Dedifferentiated Thyroid Cancer by Potentially Targeting MUC20
2021 · Shasha Hou, Xiaorui Xie, et al. · Frontiers in Oncology · 21
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Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age
2019 · Xiaoqing Wu, Gang An, et al. · Journal of Clinical Laboratory Analysis · 19
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Prenatal diagnosis of Pallister‐Killian syndrome and literature review
2021 · Xiaoqing Wu, Xiaorui Xie, et al. · Journal of Cellular and Molecular Medicine · 18
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Chromosomal abnormalities and copy number variations in fetal ventricular septal defects
2018 · Meiying Cai, Hailong Huang, et al. · Molecular Cytogenetics · 16
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Clinical Review of Noninvasive Prenatal Testing
2020 · Xiaoqing Wu, Ying Li, et al. · Journal of Molecular Diagnostics · 15
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Copy number variations in ultrasonically abnormal late pregnancy fetuses with normal karyotypes
2020 · Meiying Cai, Na Lin, et al. · Scientific Reports · 15
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Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype
2020 · Xiaoqing Wu, Ying Li, et al. · Molecular Diagnosis & Therapy · 15
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Detection of copy number disorders associated with congenital anomalies of the kidney and urinary tract in fetuses via single nucleotide polymorphism arrays
2019 · Meiying Cai, Na Lin, et al. · Journal of Clinical Laboratory Analysis · 15
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Copy number variations associated with fetal congenital kidney malformations
2020 · Meiying Cai, Na Lin, et al. · Molecular Cytogenetics · 13
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Fetal congenital heart disease
2018 · Meiying Cai, Hailong Huang, et al. · Medicine · 13
Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center
2022 · Meiying Cai, Na Lin, et al. · Journal of Translational Medicine · 12
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Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center
2021 · Xiaoqing Wu, Linjuan Su, et al. · Molecular Cytogenetics · 11
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Application of Single Nucleotide Polymorphism Microarray in Prenatal Diagnosis of Fetuses with Central Nervous System Abnormalities
2021 · Xiaorui Xie, Xiaoqing Wu, et al. · International Journal of General Medicine · 11
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Chromosomal microarray analysis for pregnancies with abnormal maternal serum screening who undergo invasive prenatal testing
2021 · Xiaoqing Wu, Ying Li, et al. · Journal of Cellular and Molecular Medicine · 11
Different Cutoff Values for Increased Nuchal Translucency in First-Trimester Screening to Predict Fetal Chromosomal Abnormalities
2021 · Linjuan Su, Xiaoqing Wu, et al. · International Journal of General Medicine · 10
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Choroid Plexus Cysts: Single Nucleotide Polymorphism Array Analysis of Associated Genetic Anomalies and Resulting Obstetrical Outcomes
2021 · Meiying Cai, Hailong Huang, et al. · Risk Management and Healthcare Policy · 10
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Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern China
2023 · Meiying Cai, Na Lin, et al. · Scientific Reports · 7
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Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramnios
2022 · Xiaoqing Wu, Ying Li, et al. · BMC Medical Genomics · 7
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Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array
2020 · Meiying Cai, Na Lin, et al. · Molecular Biology Reports · 7
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Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis
2023 · Xiaorui Xie, Baojia Huang, et al. · BMC Medical Genomics · 5
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Single nucleotide polymorphism array (SNP-array) analysis for fetuses with abnormal nasal bone
2023 · Xiaorui Xie, Linjuan Su, et al. · Archives of Gynecology and Obstetrics · 5
Submicroscopic aberrations of chromosome 16 in prenatal diagnosis
2019 · Xiaoqing Wu, Liangpu Xu, et al. · Molecular Cytogenetics · 5
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Fetal mosaicism, should conventional karyotype always be performed?
2023 · Linjuan Su, Xiaoqing Wu, et al. · Journal of obstetrics and gynaecology research · 3
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[Prenatal ultrasonographic manifestations and genetic analysis of eight fetuses with 16p11.2 microdeletions].
2022 · Meiying Cai, Hailong Huang, et al. · PubMed · 3
Works count: 43
Citation count: 300
H-index: 12
I10-index: 17
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