Works by Cai, Meiying

Results: 45

Fetal agenesis of corpus callosum: chromosomal copy number abnormalities and postnatal follow-up.

Published in:

2024

By:

Cai, Meiying;
Lin, Na;
Fu, Meimei;
Que, Yanting;
Huang, Hailong;
Xu, Liangpu

Publication type:

Case Study

Copy number variations associated with fetal congenital kidney malformations.

Published in:

Molecular Cytogenetics (17558166), 2020, v. 13, n. 1, p. 1, doi. 10.1186/s13039-020-00481-7

By:

Cai, Meiying;
Lin, Na;
Su, Linjuan;
Wu, Xiaoqing;
Xie, Xiaorui;
Li, Ying;
Chen, Xuemei;
Lin, Yuan;
Huang, Hailong;
Xu, Liangpu

Publication type:

Article

Submicroscopic aberrations of chromosome 16 in prenatal diagnosis.

Published in:

Molecular Cytogenetics (17558166), 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13039-019-0448-y

By:

Wu, Xiaoqing;
Xu, Liangpu;
Li, Ying;
Lin, Na;
Su, Linjuan;
Cai, Meiying;
Xie, Xiaorui;
Zheng, Lin;
Huang, Hailong;
Lin, Yuan

Publication type:

Article

Chromosomal abnormalities and copy number variations in fetal ventricular septal defects.

Published in:

Molecular Cytogenetics (17558166), 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13039-018-0408-y

By:

Cai, Meiying;
Huang, Hailong;
Su, Linjuan;
Lin, Na;
Wu, Xiaoqing;
Xie, Xiaorui;
An, Gang;
Li, Ying;
Lin, Yuan;
Xu, Liangpu;
Cao, Hua

Publication type:

Article

Evaluation of chromosomal abnormalities and copy number variations in fetuses with ultrasonic soft markers.

Published in:

BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-00870-w

By:

Cai, Meiying;
Lin, Na;
Chen, Xuemei;
Fu, Meimei;
Guo, Nan;
Xu, Liangpu;
Huang, Hailong

Publication type:

Article

Application of the Single-Molecule Real-Time Technology (SMRT) for Identification of HKαα Thalassemia Allele.

Published in:

Laboratory Medicine, 2023, v. 54, n. 1, p. 65, doi. 10.1093/labmed/lmac065

By:

Zhang, Min;
Lin, Zhaodong;
Chen, Meihuan;
Pan, Yali;
Zhang, Yanhong;
Chen, Lingji;
Lin, Na;
Ren, Yuanyuan;
Jia, Hongjin;
Cai, Meiying;
Xu, Liangpu;
Huang, Hailong

Publication type:

Article

Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center.

Published in:

2022

By:

Cai, Meiying;
Lin, Na;
Su, Linjuan;
Wu, Xiaoqing;
Xie, Xiaorui;
Xu, Shiyi;
Fu, Xianguo;
Xu, Liangpu;
Huang, Hailong

Publication type:

journal article

Molecular genetic analysis of 1,980 cases of male infertility.

Published in:

Experimental & Therapeutic Medicine, 2023, v. 26, n. 1, p. N.PAG, doi. 10.3892/etm.2023.12044

By:

Fu, Meimei;
Chen, Meihuan;
Guo, Nan;
Lin, Min;
Li, Ying;
Huang, Hailong;
Cai, Meiying;
Xu, Liangpu

Publication type:

Article

Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern China.

Published in:

Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-33668-0

By:

Cai, Meiying;
Lin, Na;
Guo, Nan;
Su, Linjuan;
Wu, Xiaoqing;
Xie, Xiaorui;
Li, Ying;
He, Shuqiong;
Fu, Xianguo;
Xu, Liangpu;
Huang, Hailong

Publication type:

Article

Fetal congenital talipes equinovarus: genomic abnormalities and obstetric follow-up results.

Published in:

2024

By:

Cai, Meiying;
Lin, Jiansong;
Que, Yanting;
Xu, Liangpu;
Lin, Na;
Huang, Hailong

Publication type:

Case Study

Different Cutoff Values for Increased Nuchal Translucency in First-Trimester Screening to Predict Fetal Chromosomal Abnormalities.

Published in:

International Journal of General Medicine, 2021, v. 14, p. 8437, doi. 10.2147/IJGM.S330960

By:

Su, Linjuan;
Wu, Xiaoqing;
Lin, Na;
Xie, Xiaorui;
Cai, Meiying;
Wang, Meiying;
Zheng, Lin;
Xu, Liangpu

Publication type:

Article

Application of Single Nucleotide Polymorphism Microarray in Prenatal Diagnosis of Fetuses with Central Nervous System Abnormalities.

Published in:

International Journal of General Medicine, 2021, v. 14, p. 4239, doi. 10.2147/IJGM.S323899

By:

Xie, Xiaorui;
Wu, Xiaoqing;
Su, Linjuan;
Cai, Meiying;
Li, Ying;
Huang, Hailong;
Xu, Liangpu

Publication type:

Article

Effectiveness of Chromosomal Microarray Analysis for Prenatal Diagnosis of Fetal Echogenic Intracardiac Focus: A Single-Center Experience.

Published in:

International Journal of General Medicine, 2021, v. 14, p. 1991, doi. 10.2147/IJGM.S311800

By:

Huang, Hailong;
Cai, Meiying;
Liu, Linyu;
Xu, Liangpu;
Lin, Na

Publication type:

Article

Molecular Genetic and Clinical Characteristics of Fetuses With Chromosome 16 Short‐Arm Microdeletions/Microduplications.

Published in:

Journal of Clinical Laboratory Analysis, 2024, v. 38, n. 24, p. 1, doi. 10.1002/jcla.25132

By:

Cai, Meiying;
Lin, Na;
Guo, Nan;
Huang, Hailong;
Fan, Xiangqun;
Fu, Meimei;
Zhang, Min;
Xu, Liangpu

Publication type:

Article

Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age.

Published in:

2020

By:

Wu, Xiaoqing;
An, Gang;
Xie, Xiaorui;
Su, Linjuan;
Cai, Meiying;
Chen, Xuemei;
Li, Ying;
Lin, Na;
He, Deqin;
Wang, Meiying;
Huang, Hailong;
Xu, Liangpu

Publication type:

journal article

Detection of copy number disorders associated with congenital anomalies of the kidney and urinary tract in fetuses via single nucleotide polymorphism arrays.

Published in:

2020

By:

Cai, Meiying;
Lin, Na;
Su, Linjuan;
Wu, Xiaoqing;
Xie, Xiaorui;
Li, Ying;
Chen, Xuemei;
Dai, Yifang;
Lin, Yuan;
Huang, Hailong;
Xu, Liangpu

Publication type:

journal article

Ultrasound Phenotype, Genetic Analysis, and Pregnancy Outcomes of Fetuses With 1p36 Deletion Syndrome.

Published in:

Molecular Genetics & Genomic Medicine, 2025, v. 13, n. 5, p. 1, doi. 10.1002/mgg3.70104

By:

Cai, Meiying;
Lin, Na;
Chen, Xuemei;
Huang, Hailong;
Guo, Nan;
Lin, Jiansong;
Xu, Liangpu

Publication type:

Article

Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype.

Published in:

Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 8, p. N.PAG, doi. 10.1002/mgg3.811

By:

Su, Linjuan;
Huang, Hailong;
An, Gang;
Cai, Meiying;
Wu, Xiaoqing;
Li, Ying;
Xie, Xiaorui;
Lin, Yuan;
Wang, Meiying;
Xu, Liangpu

Publication type:

Article

Copy number variations in ultrasonically abnormal late pregnancy fetuses with normal karyotypes.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-72157-6

By:

Cai, Meiying;
Lin, Na;
Su, Linjuan;
Wu, Xiaoqing;
Xie, Xiaorui;
Li, Ying;
Lin, Yuan;
Xu, Liangpu;
Huang, Hailong

Publication type:

Article

Prenatal Diagnosis of 17p11.2 Copy Number Abnormalities Associated With Smith–Magenis and Potocki–Lupski Syndromes in Fetuses.

Published in:

2021

By:

Cai, Meiying;
Fu, Xianguo;
Xu, Liangpu;
Lin, Na;
Huang, Hailong

Publication type:

Case Study

Classifying and Evaluating Fetuses With Ventriculomegaly in Genetic Etiologic Studies.

Published in:

Frontiers in Genetics, 2021, v. 11, p. 1, doi. 10.3389/fgene.2021.682707

By:

Cai, Meiying;
Huang, Hailong;
Xu, Liangpu;
Lin, Na

Publication type:

Article

The role of miR-129-5p in regulating γ-globin expression and erythropoiesis in β-thalassemia.

Published in:

Human Molecular Genetics, 2025, v. 34, n. 4, p. 291, doi. 10.1093/hmg/ddae180

By:

Li, Jingmin;
Chen, Meihuan;
Zhao, Wantong;
Lv, Aixiang;
Lin, Siyang;
Zheng, Yanping;
Cai, Meiying;
Lin, Na;
Xu, Liangpu;
Huang, Hailong

Publication type:

Article

Choroid Plexus Cysts: Single Nucleotide Polymorphism Array Analysis of Associated Genetic Anomalies and Resulting Obstetrical Outcomes.

Published in:

Risk Management & Healthcare Policy, 2021, n. 14, p. 2491, doi. 10.2147/RMHP.S312813

By:

Cai, Meiying;
Huang, Hailong;
Su, Linjuan;
Wu, Xiaoqing;
Xie, Xiaorui;
Xu, Liangpu;
Lin, Na

Publication type:

Article

Performance of Chromosomal Microarray Analysis for Detection of Copy Number Variations in Fetal Echogenic Bowel.

Published in:

Risk Management & Healthcare Policy, 2021, v. 14, p. 1431, doi. 10.2147/RMHP.S299806

By:

Fan, Xiangqun;
Huang, Hailong;
Lin, Xiyao;
Xue, Huili;
Cai, Meiying;
Lin, Na;
Xu, Liangpu

Publication type:

Article

Chromosomal Microarray Analysis for the Prenatal Diagnosis in Fetuses with Nasal Bone Hypoplasia: A Retrospective Cohort Study.

Published in:

Risk Management & Healthcare Policy, 2021, v. 14, p. 1533, doi. 10.2147/RMHP.S286038

By:

Huang, Hailong;
Cai, Meiying;
Ma, Wei;
Lin, Na;
Xu, Liangpu

Publication type:

Article

SNP Array as a Tool for Prenatal Diagnosis of Congenital Heart Disease Screened by Echocardiography: Implications for Precision Assessment of Fetal Prognosis.

Published in:

Risk Management & Healthcare Policy, 2021, v. 14, p. 345, doi. 10.2147/RMHP.S286001

By:

Huang, Hailong;
Cai, Meiying;
Wang, Yan;
Liang, Bin;
Lin, Na;
Xu, Liangpu

Publication type:

Article

Classifying and evaluating fetuses with multicystic dysplastic kidney in etiologic studies.

Published in:

Experimental Biology & Medicine, 2023, v. 248, n. 10, p. 858, doi. 10.1177/15353702231164933

By:

Cai, Meiying;
Guo, Chong;
Wang, Xinrui;
Lin, Min;
Xu, Shiyi;
Huang, Hailong;
Lin, Na;
Xu, Liangpu

Publication type:

Article

Positive predictive value of noninvasive prenatal testing for sex chromosome abnormalities.

Published in:

Molecular Biology Reports, 2022, v. 49, n. 10, p. 9251, doi. 10.1007/s11033-022-07754-x

By:

Guo, Nan;
Cai, Meiying;
Lin, Min;
Xue, Huili;
Huang, Hailong;
Xu, Liangpu

Publication type:

Article

Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism array.

Published in:

Molecular Biology Reports, 2020, v. 47, n. 10, p. 7529, doi. 10.1007/s11033-020-05815-7

By:

Cai, Meiying;
Lin, Na;
Su, Linjuan;
Wu, Xiaoqing;
Xie, Xiaorui;
Li, Ying;
Lin, Yuan;
Huang, Hailong;
Xu, Liangpu

Publication type:

Article

Pathogenic copy number variations are associated with foetal short femur length in a tertiary referral centre study.

Published in:

Journal of Cellular & Molecular Medicine, 2023, v. 27, n. 16, p. 2354, doi. 10.1111/jcmm.17821

By:

Cai, Meiying;
Que, Yanting;
Chen, Meihuan;
Zhang, Min;
Huang, Hailong;
Xu, Liangpu;
Lin, Na

Publication type:

Article

Chromosomal microarray analysis for pregnancies with abnormal maternal serum screening who undergo invasive prenatal testing.

Published in:

Journal of Cellular & Molecular Medicine, 2021, v. 25, n. 13, p. 6271, doi. 10.1111/jcmm.16589

By:

Xiaoqing Wu;
Ying Li;
Na Lin;
Xiaorui Xie;
Linjuan Su;
Meiying Cai;
Yuan Lin;
Linshuo Wang;
Meiying Wang;
Liangpu Xu;
Hailong Huang

Publication type:

Article

Comparative clinical genetic testing in spontaneous miscarriage: Insights from a study in Southern Chinese women.

Published in:

Journal of Cellular & Molecular Medicine, 2021, v. 25, n. 12, p. 5721, doi. 10.1111/jcmm.16588

By:

Cai, Meiying;
Lin, Na;
Xu, Liangpu;
Huang, Hailong

Publication type:

Article

Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype.

Published in:

Molecular Diagnosis & Therapy, 2020, v. 24, n. 5, p. 611, doi. 10.1007/s40291-020-00474-7

By:

Wu, Xiaoqing;
Li, Ying;
Su, Linjuan;
Xie, Xiaorui;
Cai, Meiying;
Lin, Na;
Huang, Hailong;
Lin, Yuan;
Xu, Liangpu

Publication type:

Article

16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-up.

Published in:

BMC Pregnancy & Childbirth, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12884-022-05267-w

By:

Cai, Meiying;
Que, Yanting;
Chen, Xuemei;
Chen, Yuqing;
Liang, Bin;
Huang, Hailong;
Xu, Liangpu;
Lin, Na

Publication type:

Article

Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis.

Published in:

BMC Medical Genomics, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s12920-023-01733-2

By:

Xie, Xiaorui;
Huang, Baojia;
Su, Linjuan;
Cai, Meiying;
Chen, Yuqin;
Wu, Xiaoqing;
Xu, Liangpu

Publication type:

Article

Genetic and ultrasonographic analyses of fetuses with 1q21.1q21.2 microdeletion/microduplication: a retrospective study.

Published in:

2023

By:

Guo, Nan;
Xue, Huili;
Liang, Bin;
Huang, Hailong;
Cai, Meiying;
Xu, Liangpu

Publication type:

Case Study

Prenatal diagnosis of genetic aberrations in fetuses with pulmonary stenosis in southern China: a retrospective analysis.

Published in:

BMC Medical Genomics, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s12920-023-01548-1

By:

Cai, Meiying;
Guo, Nan;
Fu, Meimei;
Chen, Yuqing;
Liang, Bin;
Que, Yanting;
Ji, Qingqiang;
Huang, Hailong;
Xu, Liangpu;
Lin, Na

Publication type:

Article

Incidental finding of a DMD exons 48–55 deletion during prenatal diagnosis.

Published in:

Frontiers in Pediatrics, 2025, p. 1, doi. 10.3389/fped.2025.1541468

By:

Zhang, Min;
Lin, Zhaodong;
Chen, Meihuan;
Guo, Danhua;
Yang, Qiaomei;
He, Qianqian;
Mao, Bin;
Liang, Bin;
Chen, Lingji;
Cai, Meiying;
Huang, Hailong;
Xu, Liangpu

Publication type:

Article

Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective clinical study.

Published in:

BMC Pregnancy & Childbirth, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12884-023-06223-y

By:

Cai, Meiying;
Lv, Aixiang;
Zhao, Wantong;
Xu, Liangpu;
Lin, Na;
Huang, Hailong

Publication type:

Article

Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective clinical study.

Published in:

BMC Pregnancy & Childbirth, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12884-023-06223-y

By:

Cai, Meiying;
Lv, Aixiang;
Zhao, Wantong;
Xu, Liangpu;
Lin, Na;
Huang, Hailong

Publication type:

Article

Ultrasonographic characteristics, genetic features, and maternal and fetal outcomes in fetuses with omphalocele in China: a single tertiary center study.

Published in:

BMC Pregnancy & Childbirth, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12884-023-05999-3

By:

Que, Yanting;
Cai, Meiying;
Yang, Fang;
Ji, Qingqiang;
Zhang, Shuqi;
Huang, Wenhui;
Gao, Yashi;
Zhou, Bojing;
Huang, Hailong;
Cao, Hua;
Lin, Na

Publication type:

Article

Genetic analysis, ultrasound phenotype, and pregnancy outcomes of fetuses with Xp22.33 or Yp11.32 microdeletions.

Published in:

Journal of Perinatal Medicine, 2024, v. 52, n. 1, p. 96, doi. 10.1515/jpm-2023-0190

By:

Cai, Meiying;
Chen, Xuemei;
Li, Ying;
Lin, Na;
Huang, Hailong;
Xu, Liangpu

Publication type:

Article

Prenatal diagnosis of non-mosaic sex chromosome abnormalities: a 10-year experience from a tertiary referral center.

Published in:

Journal of Perinatal Medicine, 2023, v. 51, n. 7, p. 904, doi. 10.1515/jpm-2022-0552

By:

Wu, Xiaoqing;
Guo, Danhua;
Li, Ying;
Xie, Xiaorui;
Su, Linjuan;
Cai, Meiying;
Zheng, Lin;
Lin, Na;
Liang, Bin;
Huang, Hailong;
Xu, Liangpu

Publication type:

Article

Fetal mosaicism, should conventional karyotype always be performed?

Published in:

Journal of Obstetrics & Gynaecology Research, 2023, v. 49, n. 12, p. 2836, doi. 10.1111/jog.15804

By:

Su, Linjuan;
Wu, Xiaoqing;
Liang, Bin;
Lin, Na;
Xie, Xiaorui;
Cai, Meiying;
Zheng, Lin;
Wang, Meiying;
Xu, Liangpu

Publication type:

Article

Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramnios.

Published in:

BMC Medical Genomics, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s12920-022-01224-w

By:

Wu, Xiaoqing;
Li, Ying;
Lin, Na;
Su, Linjuan;
Xie, Xiaorui;
Liang, Bing;
Shen, Qingmei;
Cai, Meiying;
Guo, Danhua;
Huang, Hailong;
Xu, Liangpu

Publication type:

Article