Meihuan Chen

434 total citations
49 papers, 257 citations indexed

About

Meihuan Chen is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Meihuan Chen has authored 49 papers receiving a total of 257 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 18 papers in Hematology and 16 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Meihuan Chen's work include Hemoglobinopathies and Related Disorders (23 papers), Prenatal Screening and Diagnostics (14 papers) and Iron Metabolism and Disorders (13 papers). Meihuan Chen is often cited by papers focused on Hemoglobinopathies and Related Disorders (23 papers), Prenatal Screening and Diagnostics (14 papers) and Iron Metabolism and Disorders (13 papers). Meihuan Chen collaborates with scholars based in China, United States and Hong Kong. Meihuan Chen's co-authors include Liangpu Xu, Lingji Chen, Na Lin, Hailong Huang, Min Zhang, Yuan Lin, Yan Wang, Dan Li, Donghong Lin and Zhaolei Cui and has published in prestigious journals such as PLoS ONE, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Meihuan Chen

42 papers receiving 255 citations

Peers

Meihuan Chen
Anindita Basak Türkiye
Cong Peng China
Maria Suciu United Kingdom
Amy Y. Y. Chan Hong Kong
Shu Yau United Kingdom
Jessica Goodman United States
Н.С. Сметанина Russia
Kristen S. Jahn United States
Wattanan Makarasara Thailand
Konstantinos Varvagiannis Greece
Anindita Basak Türkiye
Meihuan Chen
Citations per year, relative to Meihuan Chen Meihuan Chen (= 1×) peers Anindita Basak

Countries citing papers authored by Meihuan Chen

Since Specialization
Citations

This map shows the geographic impact of Meihuan Chen'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 Meihuan Chen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Meihuan Chen more than expected).

Fields of papers citing papers by Meihuan Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Meihuan Chen. 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 Meihuan Chen. The network helps show where Meihuan Chen may publish in the future.

Co-authorship network of co-authors of Meihuan Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Meihuan Chen. A scholar is included among the top collaborators of Meihuan Chen 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 Meihuan Chen. Meihuan Chen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Mao, Bin, Xiaoling Cai, Na Lin, et al.. (2025). Congenital muscular dystrophies and myopathies: the leading cause of genetic muscular disorders in eleven Chinese families. BMC Musculoskeletal Disorders. 26(1). 51–51. 1 indexed citations
2.
3.
Zhang, Siwen, Meihuan Chen, Junhao Zheng, et al.. (2025). Upregulation of miR-17-3p is associated with HbF in patients with β-thalassemia and induces γ-globin expression by targeting BCL11A. Orphanet Journal of Rare Diseases. 20(1). 260–260.
4.
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Li, Jingmin, et al.. (2024). Global Trends on β-Thalassemia Research Over 10 Years: A Bibliometric Analysis. International Journal of General Medicine. Volume 17. 3989–4001.
6.
Chen, Meihuan, et al.. (2024). IL-37 Inhibits Inflammation of Lacrimal Gland in Dry Eye Mice via the IL-37-PTEN-NFκB Signaling Pathway. Ocular Immunology and Inflammation. 32(10). 2449–2458. 1 indexed citations
7.
Zheng, Yanping, et al.. (2024). Regulation of N 6 ‐methyladenosine modification in erythropoiesis and thalassemia. Clinical Genetics. 106(1). 3–12. 1 indexed citations
8.
Chen, Meihuan, et al.. (2023). Molecular genetic analysis of 1,980 cases of male infertility. Experimental and Therapeutic Medicine. 26(1). 345–345. 4 indexed citations
9.
Cai, Meiying, Meihuan Chen, Min Zhang, et al.. (2023). Pathogenic copy number variations are associated with foetal short femur length in a tertiary referral centre study. Journal of Cellular and Molecular Medicine. 27(16). 2354–2361. 1 indexed citations
10.
Chen, Meihuan, et al.. (2023). Mutation analysis of GJB2, SLC26A4, GJB3 and mtDNA12SrRNA genes in 251 non-syndromic hearing loss patients in Fujian, China. International Journal of Pediatric Otorhinolaryngology. 176. 111777–111777. 2 indexed citations
11.
Li, Jingmin, et al.. (2023). Activating transcription factor 4 in erythroid development and $$\beta $$-thalassemia: a powerful regulator with therapeutic potential. Annals of Hematology. 103(8). 2659–2670. 3 indexed citations
12.
Xu, Liangpu, Xinrui Wang, Jia Li, et al.. (2022). A novel PLS1 c.981+ 1G >A variant causes autosomal‐dominant hereditary hearing loss in a family. Clinical Genetics. 103(4). 413–423. 2 indexed citations
13.
Chen, Meihuan, Yanhong Zhang, Min Zhang, et al.. (2022). Analysis of genotype–phenotype correlation in patients with α‐thalassemia from Fujian province, Southeastern China. Journal of Clinical Laboratory Analysis. 36(10). e24696–e24696. 4 indexed citations
14.
Wang, Yan, Xinrui Wang, Xiaoqing Wu, et al.. (2022). Prenatal diagnosis of fetuses with region of homozygosity detected by single nucleotide polymorphism array: a retrospective cohort study. Journal of Human Genetics. 67(11). 629–638. 3 indexed citations
15.
Huang, Hailong, Meihuan Chen, Lingji Chen, et al.. (2021). Prenatal diagnosis of thalassemia in 695 pedigrees from southeastern China: a 10‐year follow‐up study. Journal of Clinical Laboratory Analysis. 35(10). e23982–e23982. 8 indexed citations
16.
Wang, Haiwei, et al.. (2021). Abnormal regulation of microRNAs and related genes in pediatric β‐thalassemia. Journal of Clinical Laboratory Analysis. 35(9). e23945–e23945. 11 indexed citations
17.
Xu, Liangpu, Min Zhang, Hailong Huang, et al.. (2020). The Comprehensive Comparison of Bacterial Artificial Chromosomes (BACs)–on-Beads Assay and Copy Number Variation Sequencing in Prenatal Diagnosis of Southern Chinese Women. Journal of Molecular Diagnostics. 22(11). 1324–1332. 3 indexed citations
18.
Huang, Hailong, Liangpu Xu, Meihuan Chen, et al.. (2019). Molecular characterization of thalassemia and hemoglobinopathy in Southeastern China. Scientific Reports. 9(1). 3493–3493. 45 indexed citations
19.
Xu, Liangpu, Min Zhang, Yan Wang, et al.. (2018). Genetic testing and prenatal diagnosis of X-linked ichthyosis in two pedigrees. Zhonghua weichan yixue zazhi. 21(5). 293–300. 1 indexed citations
20.
Cui, Zhaolei, et al.. (2014). Diagnostic value of circulating microRNAs as biomarkers for breast cancer: a meta-analysis study. Tumor Biology. 36(2). 829–839. 22 indexed citations

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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