Hongyan Chai

1.2k total citations
48 papers, 949 citations indexed

About

Hongyan Chai is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hongyan Chai has authored 48 papers receiving a total of 949 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 16 papers in Genetics and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hongyan Chai's work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (11 papers) and Cancer-related molecular mechanisms research (6 papers). Hongyan Chai is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (11 papers) and Cancer-related molecular mechanisms research (6 papers). Hongyan Chai collaborates with scholars based in China, United States and Spain. Hongyan Chai's co-authors include Jing Yang, Haixia Zhao, Jiancheng Tu, Austin M. Guo, Jing Wei, Peining Li, Wenyuan Gao, Jiang Yue, Shuli Man and Chunzi Liang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and RSC Advances.

In The Last Decade

Hongyan Chai

46 papers receiving 937 citations

Peers

Hongyan Chai
Lizhu Lin China
Pei Xiao China
Lu Gao China
Bong Whan Ahn South Korea
Maowen Hu United States
Hongyan Chai
Citations per year, relative to Hongyan Chai Hongyan Chai (= 1×) peers Xiangzhong Zhao

Countries citing papers authored by Hongyan Chai

Since Specialization
Citations

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

Fields of papers citing papers by Hongyan Chai

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hongyan Chai

This figure shows the co-authorship network connecting the top 25 collaborators of Hongyan Chai. A scholar is included among the top collaborators of Hongyan Chai 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 Hongyan Chai. Hongyan Chai 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.
Zhang, Wei, Yan Zhang, Xiaowen Yang, & Hongyan Chai. (2025). Harnessing State-of-the-Art Gene Therapy to Transform Oral Cancer Treatment. Biochemical Genetics. 64(1). 1–26. 1 indexed citations
2.
Chai, Hongyan, Mei Ling Chong, Guilin Wang, et al.. (2024). Patterns of Cytogenomic Findings from a Case Series of Recurrent Pregnancy Loss Provide Insight into the Extent of Genetic Defects Causing Miscarriages. SHILAP Revista de lepidopterología. 11(1). 123–131. 1 indexed citations
3.
Peng, Gang, Qinghua Zhou, Hongyan Chai, et al.. (2023). Estimation on risk of spontaneous abortions by genomic disorders from a meta‐analysis of microarray results on large case series of pregnancy losses. Molecular Genetics & Genomic Medicine. 11(8). e2181–e2181. 7 indexed citations
4.
Chong, Mei Ling, James Knight, Gang Peng, et al.. (2023). Integrated exome sequencing and microarray analyses detected genetic defects and underlying pathways of hepatocellular carcinoma. Cancer Genetics. 276-277. 30–35. 1 indexed citations
5.
Chai, Hongyan, et al.. (2022). Genotype–Phenotype Correlations for Putative Haploinsufficient Genes in Deletions of 6q26-q27: Report of Eight Patients and Review of Literature. SHILAP Revista de lepidopterología. 9(2). 166–174. 5 indexed citations
6.
Ordulu, Zehra, Hongyan Chai, Gang Peng, et al.. (2020). Molecular and clinicopathologic characterization of intravenous leiomyomatosis. Modern Pathology. 33(9). 1844–1860. 21 indexed citations
7.
Zhao, Chen, Hongyan Chai, Qinghua Zhou, et al.. (2020). Exome sequencing analysis on products of conception: a cohort study to evaluate clinical utility and genetic etiology for pregnancy loss. Genetics in Medicine. 23(3). 435–442. 33 indexed citations
8.
Chang, Hao, Sean F. Landrette, Sheng Ding, et al.. (2019). Efficient genome-wide first-generation phenotypic screening system in mice using the piggyBac transposon. Proceedings of the National Academy of Sciences. 116(37). 18507–18516. 9 indexed citations
9.
Chai, Hongyan, Fang Xu, Qinghua Zhou, et al.. (2019). A Retrospective Analysis of 10-Year Data Assessed the Diagnostic Accuracy and Efficacy of Cytogenomic Abnormalities in Current Prenatal and Pediatric Settings. Frontiers in Genetics. 10. 1162–1162. 12 indexed citations
11.
Hu, Qiping, Hongyan Chai, Wei Shu, & Peining Li. (2018). Human ring chromosome registry for cases in the Chinese population: re-emphasizing Cytogenomic and clinical heterogeneity and reviewing diagnostic and treatment strategies. Molecular Cytogenetics. 11(1). 19–19. 16 indexed citations
12.
Wei, Jing, Shanshan Gao, Man Zhu, et al.. (2016). Potential diagnostic value of lncRNA SPRY4-IT1 in hepatocellular carcinoma. Oncology Reports. 36(2). 1085–1092. 57 indexed citations
13.
Li, Peining, et al.. (2016). Diagnostic Yield of Cytogenomic Abnormalities in Current Prenatal Diagnosis: A Retrospective Analysis in a Clinical Cytogenetics Laboratory. North American Journal of Medicine and Science. 9(4). 1 indexed citations
14.
Wei, Jing, et al.. (2016). Prognostic and Diagnostic Significance of SDPR-Cavin-2 in Hepatocellular Carcinoma. Cellular Physiology and Biochemistry. 39(3). 950–960. 23 indexed citations
15.
Wang, Chenlong, Xuewei Chen, Chenfan Duan, et al.. (2015). Dopamine induces growth inhibition and vascular normalization through reprogramming M2-polarized macrophages in rat C6 glioma. Toxicology and Applied Pharmacology. 286(2). 112–123. 57 indexed citations
16.
Man, Shuli, Jing Li, Wei Fan, et al.. (2015). Inhibition of pulmonary adenoma in diethylnitrosamine-induced rats by Rhizoma paridis saponins. The Journal of Steroid Biochemistry and Molecular Biology. 154. 62–67. 15 indexed citations
17.
Man, Shuli, Hongyan Chai, Zhen Yu Liu, et al.. (2015). Turmeric enhancing anti-tumor effect of Rhizoma paridis saponins by influencing their metabolic profiling in tumors of H22 hepatocarcinoma mice. Pathology - Research and Practice. 211(12). 948–954. 13 indexed citations
18.
Zhao, Haixia, Xinhua Zhang, Xuewei Chen, et al.. (2014). Isoliquiritigenin, a flavonoid from licorice, blocks M2 macrophage polarization in colitis-associated tumorigenesis through downregulating PGE2 and IL-6. Toxicology and Applied Pharmacology. 279(3). 311–321. 87 indexed citations
19.
Li, Ying, Haixia Zhao, Yuzhong Wang, et al.. (2013). Isoliquiritigenin induces growth inhibition and apoptosis through downregulating arachidonic acid metabolic network and the deactivation of PI3K/Akt in human breast cancer. Toxicology and Applied Pharmacology. 272(1). 37–48. 79 indexed citations
20.
Yu, Wei, Hongyan Chai, Ying Li, et al.. (2012). Increased expression of CYP4Z1 promotes tumor angiogenesis and growth in human breast cancer. Toxicology and Applied Pharmacology. 264(1). 73–83. 72 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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