Zirui Dong

3.5k total citations
43 papers, 1.2k citations indexed

About

Zirui Dong is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Zirui Dong has authored 43 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 16 papers in Molecular Biology and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Zirui Dong's work include Genomic variations and chromosomal abnormalities (21 papers), Genomics and Rare Diseases (14 papers) and Prenatal Screening and Diagnostics (12 papers). Zirui Dong is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), Genomics and Rare Diseases (14 papers) and Prenatal Screening and Diagnostics (12 papers). Zirui Dong collaborates with scholars based in China, Hong Kong and United States. Zirui Dong's co-authors include Kwong Wai Choy, Jun Wang, Wenwei Zhang, Zhijian Tian, Xueda Hu, Yuankun Zhu, Lin Kang, Li Bao, Bertrand Chin‐Ming Tan and Zhiyu Peng and has published in prestigious journals such as Nucleic Acids Research, Nature Biotechnology and Genome biology.

In The Last Decade

Zirui Dong

34 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Zirui Dong China 15 631 479 371 215 108 43 1.2k
Megan P. Hall United States 14 686 1.1× 425 0.9× 976 2.6× 153 0.7× 30 0.3× 20 1.6k
Kavita S. Reddy United States 19 254 0.4× 380 0.8× 163 0.4× 62 0.3× 144 1.3× 55 846
Jessica Nordlund Sweden 20 591 0.9× 248 0.5× 157 0.4× 161 0.7× 57 0.5× 57 1.1k
Isabel Lorda‐Sánchez Spain 23 558 0.9× 759 1.6× 689 1.9× 43 0.2× 163 1.5× 67 1.4k
Nathan D. Montgomery United States 17 613 1.0× 201 0.4× 75 0.2× 124 0.6× 37 0.3× 53 1.1k
Marta Rodríguez de Alba Spain 19 285 0.5× 316 0.7× 566 1.5× 62 0.3× 35 0.3× 42 889
M. Mannens Netherlands 15 595 0.9× 314 0.7× 197 0.5× 62 0.3× 38 0.4× 30 836
Anna Almeida France 17 640 1.0× 289 0.6× 33 0.1× 190 0.9× 104 1.0× 24 1.1k
Stephen Laderman United States 4 436 0.7× 541 1.1× 126 0.3× 107 0.5× 211 2.0× 4 783

Countries citing papers authored by Zirui Dong

Since Specialization
Citations

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

Fields of papers citing papers by Zirui Dong

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zirui Dong

This figure shows the co-authorship network connecting the top 25 collaborators of Zirui Dong. A scholar is included among the top collaborators of Zirui Dong 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 Zirui Dong. Zirui Dong 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.
Lam, King H., Lin Chen, Mingyang Yu, et al.. (2025). TEDD 2.0: an advanced temporal gene expression database enabled by in-silico functional analyses for developmental mechanism investigation. Science China Life Sciences. 69(3). 993–1007.
2.
Liu, Qiqi, Zhuo Song, Simin Liu, et al.. (2025). 3D visualization of uterus and ovary: tissue clearing techniques and biomedical applications. Frontiers in Bioengineering and Biotechnology. 13. 1610539–1610539.
3.
Dong, Zirui. (2024). A method of financial risk assessment for enterprises based on BP algorithm. Procedia Computer Science. 247. 1349–1358.
4.
Chau, Matthew Hoi Kin, Mahesh Choolani, Zirui Dong, Ye Cao, & Kwong Wai Choy. (2024). Genome sequencing in the prenatal diagnosis of structural malformations in the fetus. Best Practice & Research Clinical Obstetrics & Gynaecology. 97. 102539–102539. 3 indexed citations
5.
Zheng, Yu, Lo Wong, Angel Hoi Wan Kwan, et al.. (2023). Prenatal diagnosis of polycystic kidney caused by biallelic hypomorphic variants in the PKD1 gene. Prenatal Diagnosis. 44(2). 247–250. 1 indexed citations
6.
Zhang, Yalan, et al.. (2023). Visual perception of fluid viscosity: Toward realistic fluid simulation. Computers & Graphics. 117. 13–19.
7.
Li, Ying, Matthew Hoi Kin Chau, Tin Chiu Li, et al.. (2023). A pilot investigation of low-pass genome sequencing identifying site-specific variation in chromosomal mosaicisms by a multiple site sampling approach in first-trimester miscarriages. Human Reproduction. 38(8). 1628–1642. 4 indexed citations
8.
Li, Keying, Matthew Hoi Kin Chau, Ye Cao, et al.. (2023). Low-Pass Genome Sequencing-Based Detection of Paternity: Validation in Clinical Cytogenetics. Genes. 14(7). 1357–1357. 3 indexed citations
9.
Chen, Lin, Zirui Dong, & Xiaoyan Chen. (2023). Fertility preservation in pediatric healthcare: a review. Frontiers in Endocrinology. 14. 1147898–1147898. 13 indexed citations
10.
Zhou, Ziheng, Shuguang Wang, Dengwei Zhang, et al.. (2023). Single-cell analysis reveals specific neuronal transition during mouse corticogenesis. Frontiers in Cell and Developmental Biology. 11. 1209320–1209320. 1 indexed citations
11.
Dong, Zirui, Matthew Hoi Kin Chau, Ye Cao, et al.. (2022). Mate-pair genome sequencing reveals structural variants for idiopathic male infertility. Human Genetics. 142(3). 363–377. 3 indexed citations
12.
Cao, Ye, Ho‐Ming Luk, Yanyan Zhang, et al.. (2022). Investigation of Chromosomal Structural Abnormalities in Patients With Undiagnosed Neurodevelopmental Disorders. Frontiers in Genetics. 13. 803088–803088. 2 indexed citations
13.
Chau, Matthew Hoi Kin, Ying Li, Peng Dai, et al.. (2022). Investigation of the genetic etiology in male infertility with apparently balanced chromosomal structural rearrangements by genome sequencing. Asian Journal of Andrology. 24(3). 248–254. 12 indexed citations
14.
Li, Ying, Zirui Dong, Kwong Wai Choy, & Jacqueline Pui Wah Chung. (2021). LOW-PASS GENOME SEQUENCING IDENTIFIED MACROSCOPIC AND MICROSCOPIC CHROMOSOMAL MOSAICISMS TO EXPLAIN FIRST-TRIMESTER MISCARRIAGE. Fertility and Sterility. 116(3). e6–e6.
15.
Marques, Bárbara, et al.. (2021). SVInterpreter: A Comprehensive Topologically Associated Domain-Based Clinical Outcome Prediction Tool for Balanced and Unbalanced Structural Variants. Frontiers in Genetics. 12. 757170–757170. 6 indexed citations
16.
Dong, Zirui, Matthew Hoi Kin Chau, Yanyan Zhang, et al.. (2021). Low-pass genome sequencing–based detection of absence of heterozygosity: validation in clinical cytogenetics. Genetics in Medicine. 23(7). 1225–1233. 23 indexed citations
17.
Chau, Matthew Hoi Kin, Huilin Wang, Yunli Lai, et al.. (2020). Low-pass genome sequencing: a validated method in clinical cytogenetics. Human Genetics. 139(11). 1403–1415. 36 indexed citations
18.
Choy, Kwong Wai, Huilin Wang, Mengmeng Shi, et al.. (2019). Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing Analysis. Frontiers in Genetics. 10. 761–761. 51 indexed citations
19.
Zhang, Jinliang, et al.. (2013). Diagenesis of Clastic Reservoirs: Advances and Prospects. Diqiu kexue jinzhan. 28(9). 957–967. 10 indexed citations
20.
Peng, Zhiyu, Yanbing Cheng, Bertrand Chin‐Ming Tan, et al.. (2012). Comprehensive analysis of RNA-Seq data reveals extensive RNA editing in a human transcriptome. Nature Biotechnology. 30(3). 253–260. 416 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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