Meiying Cai

770 total citations
75 papers, 496 citations indexed

About

Meiying Cai is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Meiying Cai has authored 75 papers receiving a total of 496 indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Pediatrics, Perinatology and Child Health, 39 papers in Genetics and 20 papers in Molecular Biology. Recurrent topics in Meiying Cai's work include Prenatal Screening and Diagnostics (53 papers), Genomic variations and chromosomal abnormalities (31 papers) and Fetal and Pediatric Neurological Disorders (17 papers). Meiying Cai is often cited by papers focused on Prenatal Screening and Diagnostics (53 papers), Genomic variations and chromosomal abnormalities (31 papers) and Fetal and Pediatric Neurological Disorders (17 papers). Meiying Cai collaborates with scholars based in China, Australia and Macao. Meiying Cai's co-authors include Liangpu Xu, Hailong Huang, Na Lin, Xiaoqing Wu, Cai‐Lan Hou, Fu‐Jun Jia, Yu Zang, Yu‐Tao Xiang, Gábor S. Ungvári and Yuan Lin and has published in prestigious journals such as Scientific Reports, Human Molecular Genetics and Human Reproduction.

In The Last Decade

Meiying Cai

67 papers receiving 491 citations

Peers

Countries citing papers authored by Meiying Cai

Since Specialization

Citations

This map shows the geographic impact of Meiying Cai's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Meiying Cai with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Meiying Cai more than expected).

Fields of papers citing papers by Meiying Cai

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Meiying Cai. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Meiying Cai. The network helps show where Meiying Cai may publish in the future.

Co-authorship network of co-authors of Meiying Cai

This figure shows the co-authorship network connecting the top 25 collaborators of Meiying Cai. A scholar is included among the top collaborators of Meiying Cai based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Meiying Cai. Meiying Cai is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Molecular Genetic and Clinical Characteristics of Fetuses With Chromosome 16 Short‐Arm Microdeletions/Microduplications 2024 ·Journal of Clinical Laboratory Analysis ·Meiying Cai, (unknown), (unknown), Hailong Huang, (unknown), (unknown), Min Zhang, Liangpu Xu	1
2	Fetal agenesis of corpus callosum: chromosomal copy number abnormalities and postnatal follow-up 2024 ·Molecular Biology Reports ·Meiying Cai, Na Lin, (unknown), (unknown), Hailong Huang, Liangpu Xu	1
3	Molecular genetic analysis of 1,980 cases of male infertility 2023 ·Experimental and Therapeutic Medicine ·(unknown), Meihuan Chen, (unknown), (unknown), Ying Li, (unknown), Meiying Cai, Liangpu Xu	4
4	Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis 2023 ·BMC Medical Genomics ·(unknown), (unknown), (unknown), Meiying Cai, Yuqin Chen, (unknown), Liangpu Xu	2
5	Non-invasive prenatal testing for the diagnosis of congenital abnormalities: Insights from a large multicenter study in southern China 2023 ·Brazilian Journal of Medical and Biological Research ·Meiying Cai, Na Lin, (unknown), (unknown), (unknown), (unknown), Hailong Huang, (unknown), Liangpu Xu	4
6	Pathogenic copy number variations are associated with foetal short femur length in a tertiary referral centre study 2023 ·Journal of Cellular and Molecular Medicine ·Meiying Cai, (unknown), Meihuan Chen, Min Zhang, Hailong Huang, Liangpu Xu, Na Lin	1
7	Genetic analysis, ultrasound phenotype, and pregnancy outcomes of fetuses with Xp22.33 or Yp11.32 microdeletions 2023 ·Journal of Perinatal Medicine ·Meiying Cai, (unknown), Ying Li, Na Lin, Hailong Huang, Liangpu Xu	0
8	Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center 2022 ·Journal of Translational Medicine ·Meiying Cai, Na Lin, (unknown), Xiaoqing Wu, (unknown), (unknown), (unknown), Liangpu Xu, Hailong Huang	8
9	16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-up 2022 ·BMC Pregnancy and Childbirth ·Meiying Cai, (unknown), Xuemei Chen, Yuqing Chen, (unknown), Hailong Huang, Liangpu Xu, Na Lin	8
10	Chromosomal Microarray Analysis for the Prenatal Diagnosis in Fetuses with Nasal Bone Hypoplasia: A Retrospective Cohort Study 2021 ·Risk Management and Healthcare Policy ·Hailong Huang, Meiying Cai, Wei Ma, Na Lin, Liangpu Xu	8
11	SNP Array as a Tool for Prenatal Diagnosis of Congenital Heart Disease Screened by Echocardiography: Implications for Precision Assessment of Fetal Prognosis 2021 ·Risk Management and Healthcare Policy ·Hailong Huang, Meiying Cai, Yan Wang, (unknown), Na Lin, Liangpu Xu	7
12	Comparative clinical genetic testing in spontaneous miscarriage: Insights from a study in Southern Chinese women 2021 ·Journal of Cellular and Molecular Medicine ·Meiying Cai, Na Lin, Liangpu Xu, Hailong Huang	4
13	Chromosomal microarray analysis for pregnancies with abnormal maternal serum screening who undergo invasive prenatal testing 2021 ·Journal of Cellular and Molecular Medicine ·Xiaoqing Wu, Ying Li, Na Lin, (unknown), (unknown), Meiying Cai, Yuan Lin, (unknown), Meiying Wang, Liangpu Xu, Hailong Huang	7
14	Choroid Plexus Cysts: Single Nucleotide Polymorphism Array Analysis of Associated Genetic Anomalies and Resulting Obstetrical Outcomes 2021 ·Risk Management and Healthcare Policy ·Meiying Cai, Hailong Huang, (unknown), Xiaoqing Wu, (unknown), Liangpu Xu, Na Lin	5
15	Performance of Chromosomal Microarray Analysis for Detection of Copy Number Variations in Fetal Echogenic Bowel 2021 ·Risk Management and Healthcare Policy ·(unknown), Hailong Huang, (unknown), (unknown), Meiying Cai, Na Lin, Liangpu Xu	6
16	Effectiveness of Chromosomal Microarray Analysis for Prenatal Diagnosis of Fetal Echogenic Intracardiac Focus: A Single-Center Experience 2021 ·International Journal of General Medicine ·Hailong Huang, Meiying Cai, (unknown), Liangpu Xu, Na Lin	5
17	Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype 2020 ·Molecular Diagnosis & Therapy ·Xiaoqing Wu, (unknown), (unknown), (unknown), Meiying Cai, Na Lin, Hailong Huang, Lin Yuan, Liangpu Xu	7
18	Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age 2019 ·Journal of Clinical Laboratory Analysis ·(unknown), Gang An, (unknown), (unknown), Meiying Cai, Xuemei Chen, Ying Li, Na Lin, (unknown), Meiying Wang, (unknown), Liangpu Xu	12
19	Submicroscopic aberrations of chromosome 16 in prenatal diagnosis 2019 ·Molecular Cytogenetics ·Xiaoqing Wu, Liangpu Xu, Ying Li, Na Lin, (unknown), Meiying Cai, (unknown), Lin Zheng, Hailong Huang, Lin Yuan	3
20	Antipsychotic-Free Status in Community-Dwelling Patients With Schizophrenia in China 2018 ·The Journal of Clinical Psychiatry ·Cai‐Lan Hou, (unknown), Meiying Cai, (unknown), (unknown), (unknown), Fu‐Jun Jia	10

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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