Lingji Chen

1.5k total citations
72 papers, 1.0k citations indexed

About

Lingji Chen is a scholar working on Artificial Intelligence, Control and Systems Engineering and Genetics. According to data from OpenAlex, Lingji Chen has authored 72 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Artificial Intelligence, 18 papers in Control and Systems Engineering and 13 papers in Genetics. Recurrent topics in Lingji Chen's work include Hemoglobinopathies and Related Disorders (13 papers), Target Tracking and Data Fusion in Sensor Networks (12 papers) and Prenatal Screening and Diagnostics (12 papers). Lingji Chen is often cited by papers focused on Hemoglobinopathies and Related Disorders (13 papers), Target Tracking and Data Fusion in Sensor Networks (12 papers) and Prenatal Screening and Diagnostics (12 papers). Lingji Chen collaborates with scholars based in China, United States and Sweden. Lingji Chen's co-authors include Kumpati S. Narendra, R.К. Mehra, P.O. Arambel, Raman K. Mehra, Jovan Boskovic, Chihoon Lee, Amarjit Budhiraja, Liangpu Xu, Meihuan Chen and Min Zhang and has published in prestigious journals such as PLoS ONE, IEEE Transactions on Automatic Control and Scientific Reports.

In The Last Decade

Lingji Chen

72 papers receiving 1.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Lingji Chen China 14 459 360 177 139 117 72 1.0k
Nick J. Pizzi Canada 18 55 0.1× 273 0.8× 62 0.4× 15 0.1× 53 0.5× 72 822
Μ. Zeitz Germany 24 1.8k 3.8× 107 0.3× 131 0.7× 6 0.0× 6 0.1× 109 2.5k
Bernd Tibken Germany 15 556 1.2× 36 0.1× 12 0.1× 12 0.1× 25 0.2× 116 976
Hongwei Chen China 19 230 0.5× 237 0.7× 283 1.6× 2 0.0× 14 0.1× 49 1.4k
F. Lampariello Italy 12 268 0.6× 263 0.7× 26 0.1× 8 0.1× 7 0.1× 26 1.5k
Élisa Fromont France 14 28 0.1× 185 0.5× 34 0.2× 5 0.0× 59 0.5× 36 695
John B. Anderson Sweden 25 31 0.1× 421 1.2× 1.5k 8.8× 20 0.1× 3 0.0× 107 3.1k
Shankar Vembu United States 15 39 0.1× 366 1.0× 162 0.9× 10 0.1× 9 0.1× 24 1.5k
Marc Sebban France 16 24 0.1× 393 1.1× 42 0.2× 4 0.0× 59 0.5× 55 763
Jean Gao United States 16 42 0.1× 150 0.4× 65 0.4× 3 0.0× 4 0.0× 114 935

Countries citing papers authored by Lingji Chen

Since Specialization
Citations

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

Fields of papers citing papers by Lingji Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lingji Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Lingji Chen. A scholar is included among the top collaborators of Lingji 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 Lingji Chen. Lingji 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.
Chen, Lingji, et al.. (2024). Prenatal diagnosis of fetal skeletal anomalies via whole-exome sequencing in a tertiary referral center. Scientific Reports. 14(1). 27371–27371. 1 indexed citations
3.
Chen, Lingji, et al.. (2024). Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center. Scientific Reports. 14(1). 16266–16266. 1 indexed citations
4.
Zhang, Lin, et al.. (2024). Genetic testing for fetal loss of heterozygosity using single nucleotide polymorphism array and whole-exome sequencing. Scientific Reports. 14(1). 2190–2190. 2 indexed citations
5.
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
6.
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
7.
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
8.
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
9.
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
10.
Wang, Yan, et al.. (2021). [Prenatal diagnosis of five fetuses with 7q11.23 microdeletion or microduplication].. PubMed. 38(11). 1064–1067. 1 indexed citations
11.
Wang, Yan, Na Lin, Hailong Huang, et al.. (2020). Single nucleotide polymorphism array analysis of 102 patients with developmental delay and/or intellectual disability from Fujian, China. Clinica Chimica Acta. 510. 638–643. 2 indexed citations
12.
Xu, Liangpu, Aiping Mao, Hui Liu, et al.. (2020). Long-Molecule Sequencing. Journal of Molecular Diagnostics. 22(8). 1087–1095. 64 indexed citations
13.
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
14.
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
15.
Chen, Lingji, et al.. (2016). On path cover problems with positive and negative constraints for graph-based multitarget tracking. International Conference on Information Fusion. 402–408. 2 indexed citations
16.
Chen, Lingji, et al.. (2015). A maximum weight constrained path cover algorithm for graph-based multitarget tracking. International Conference on Information Fusion. 2073–2077. 2 indexed citations
17.
Kandula, Sasikiran, et al.. (2011). A bootstrapping algorithm to improve cohort identification using structured data. Journal of Biomedical Informatics. 44. S63–S68. 16 indexed citations
18.
Chen, Lingji, et al.. (2010). Vision: towards real time epidemic vigilance through online social networks. 2 indexed citations
19.
Ding, Jian, et al.. (1999). Synthesis and antitumour activity of novel diterpenequinone salvicine and the analogs. Bioorganic & Medicinal Chemistry Letters. 9(18). 2731–2736. 41 indexed citations
20.
Li, Song, et al.. (1990). Preparation of antigastric cancer monoclonal antibody MGb2-mitomycin C conjugate with improved antitumor activity. Bioconjugate Chemistry. 1(4). 245–250. 6 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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