Tingying Lei

565 total citations
39 papers, 314 citations indexed

About

Tingying Lei is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Tingying Lei has authored 39 papers receiving a total of 314 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Pediatrics, Perinatology and Child Health, 20 papers in Molecular Biology and 11 papers in Genetics. Recurrent topics in Tingying Lei's work include Prenatal Screening and Diagnostics (24 papers), Genomic variations and chromosomal abnormalities (9 papers) and Congenital heart defects research (8 papers). Tingying Lei is often cited by papers focused on Prenatal Screening and Diagnostics (24 papers), Genomic variations and chromosomal abnormalities (9 papers) and Congenital heart defects research (8 papers). Tingying Lei collaborates with scholars based in China and Russia. Tingying Lei's co-authors include Xin Yang, Fang Fu, Can Liao, Xiangyi Jing, Qiong Deng, Ru Li, Dong‐Zhi Li, Can Liao, Ru Li and Qiuxia Yu and has published in prestigious journals such as Gene, Energy and Buildings and Journal of Cellular Biochemistry.

In The Last Decade

Tingying Lei

37 papers receiving 312 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tingying Lei China 10 157 148 128 47 33 39 314
Mary Ann Thomas Canada 10 126 0.8× 123 0.8× 180 1.4× 45 1.0× 41 1.2× 46 361
Chunyu Luo China 8 82 0.5× 138 0.9× 61 0.5× 40 0.9× 55 1.7× 35 258
Koumudi Godbole India 10 82 0.5× 102 0.7× 36 0.3× 48 1.0× 32 1.0× 22 295
Jacob S. Hogue United States 9 50 0.3× 186 1.3× 119 0.9× 118 2.5× 14 0.4× 21 340
Claire Bénéteau France 10 97 0.6× 117 0.8× 155 1.2× 43 0.9× 11 0.3× 30 278
Hu Tan China 8 184 1.2× 74 0.5× 148 1.2× 30 0.6× 18 0.5× 30 304
Selahattin Tekeş Türkiye 12 35 0.2× 104 0.7× 146 1.1× 56 1.2× 83 2.5× 33 364
M. Barr United States 6 93 0.6× 199 1.3× 144 1.1× 62 1.3× 11 0.3× 6 346
Padmanabhan Rengasamy United Arab Emirates 10 139 0.9× 70 0.5× 61 0.5× 106 2.3× 8 0.2× 16 381
Nathalie Rives France 12 94 0.6× 133 0.9× 158 1.2× 51 1.1× 6 0.2× 40 540

Countries citing papers authored by Tingying Lei

Since Specialization
Citations

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

Fields of papers citing papers by Tingying Lei

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tingying Lei

This figure shows the co-authorship network connecting the top 25 collaborators of Tingying Lei. A scholar is included among the top collaborators of Tingying Lei 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 Tingying Lei. Tingying Lei 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.
Lei, Tingying, et al.. (2025). KRT14 knockdown reduces cisplatin resistance by lowering LRP11 expression levels in cisplatin-resistant ovarian cancer cell lines. Translational Cancer Research. 14(3). 1786–1798. 1 indexed citations
2.
Fu, Fang, Xin Yang, Ru Li, et al.. (2024). Single-cell RNA sequencing reveals cellular and molecular landscape of fetal cystic hygroma. BMC Medical Genomics. 17(1). 96–96. 1 indexed citations
3.
Liu, Lei, Tingying Lei, Fei Guo, et al.. (2024). Prenatal diagnosis of the recurrent 1q21.1 microdeletions in fetuses with ultrasound anomalies and review of the literature. Frontiers in Genetics. 15. 1448341–1448341. 1 indexed citations
4.
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6.
Liu, Liyuan, Fang Fu, Ru Li, et al.. (2023). Chromosome Microarray Analysis and Exome Sequencing: Implementation in Prenatal Diagnosis of Fetuses with Digestive System Malformations. Genes. 14(10). 1872–1872. 2 indexed citations
7.
Lei, Tingying, Zhen Li, Xin Yang, et al.. (2023). Prenatal Diagnosis of PPP2R1A-Related Neurodevelopmental Disorders Using Whole Exome Sequencing: Clinical Report and Review of Literature. Genes. 14(1). 126–126. 7 indexed citations
8.
Fu, Fang, Ru Li, Jin Han, et al.. (2023). ASXL3 gene mutations inhibit cell proliferation and promote cell apoptosis in mouse cardiomyocytes by upregulating lncRNA NONMMUT063967.2. Biochemistry and Biophysics Reports. 35. 101505–101505. 2 indexed citations
9.
Fu, Fang, Tingying Lei, Zhen Li, et al.. (2023). Genetic diagnosis of fetal microcephaly at a single tertiary center in China. Frontiers in Genetics. 14. 1112153–1112153. 5 indexed citations
10.
Fu, Fang, Hang Zhou, Lu Zhang, et al.. (2023). Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencing. Human Genetics. 142(6). 835–847. 6 indexed citations
11.
Lei, Tingying, Fang Fu, Zhen Li, et al.. (2022). Prenatal exome sequencing in fetuses with callosal anomalies. Prenatal Diagnosis. 42(6). 744–752. 13 indexed citations
12.
Zhou, Hang, Fang Fu, You Wang, et al.. (2022). Whole exome sequencing improves genetic diagnosis of fetal clubfoot. Human Genetics. 142(3). 407–418. 8 indexed citations
13.
Zhou, Hang, Fang Fu, Ru Li, et al.. (2022). Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis. Molecular Cytogenetics. 15(1). 27–27. 6 indexed citations
14.
Zhou, Hang, Fang Fu, Tingying Lei, et al.. (2022). Should prenatal chromosomal microarray analysis be offered for isolated ventricular septal defect? A single-center retrospective study from China. Frontiers in Cardiovascular Medicine. 9. 988438–988438. 6 indexed citations
15.
Wang, Rongyue, Tingying Lei, Fang Fu, et al.. (2018). Application of chromosome microarray analysis in patients with unexplained developmental delay/intellectual disability in South China. Pediatrics & Neonatology. 60(1). 35–42. 22 indexed citations
16.
Fu, Fang, Qiong Deng, Tingying Lei, et al.. (2017). Clinical application of SNP array analysis in fetuses with ventricular septal defects and normal karyotypes. Archives of Gynecology and Obstetrics. 296(5). 929–940. 23 indexed citations
17.
Lei, Tingying, Fang Fu, Ru Li, et al.. (2017). Whole-exome sequencing for prenatal diagnosis of fetuses with congenital anomalies of the kidney and urinary tract. Nephrology Dialysis Transplantation. 32(10). 1665–1675. 50 indexed citations
18.
Lei, Tingying, Hongtao Wang, Fan Li, et al.. (2016). Application of high resolution SNP arrays in patients with congenital oral clefts in south China. Journal of Genetics. 95(4). 801–809. 6 indexed citations
19.
Chen, Feifei, Tingying Lei, Fang Fu, et al.. (2016). [Application of chromosome microarray analysis for fetuses with multicystic dysplastic kidney].. PubMed. 33(6). 752–757. 1 indexed citations
20.
Fu, Fang, Ru Li, Jin Han, et al.. (2014). Prenatal diagnosis of foetuses with congenital abnormalities and duplication of the MECP2 region. Gene. 546(2). 222–225. 13 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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