Leilei Li

714 total citations
53 papers, 453 citations indexed

About

Leilei Li is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Leilei Li has authored 53 papers receiving a total of 453 indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Genetics, 24 papers in Pediatrics, Perinatology and Child Health and 21 papers in Molecular Biology. Recurrent topics in Leilei Li's work include Prenatal Screening and Diagnostics (22 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers) and Genomic variations and chromosomal abnormalities (16 papers). Leilei Li is often cited by papers focused on Prenatal Screening and Diagnostics (22 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers) and Genomic variations and chromosomal abnormalities (16 papers). Leilei Li collaborates with scholars based in China, United States and Germany. Leilei Li's co-authors include Ruizhi Liu, Xiao Hu, Caixia Li, Hongguo Zhang, Ruixue Wang, Yuting Jiang, Qi Xi, Genhua Zhang, Shaoping Deng and Yuan Jiang Pan and has published in prestigious journals such as International Journal of Molecular Sciences, Medicine and BMC Pregnancy and Childbirth.

In The Last Decade

Leilei Li

45 papers receiving 440 citations

Peers

Leilei Li
Lindsay Moritz United States
Qiaoyan Shen China
Letizia Galleri Italy
I. Reima Finland
Souraya Jaroudi United Kingdom
Zhenzhen Hou China
Shepu Xue China
Chan Luo China
Cristina E. Requena United Kingdom
Kaifeng Guan China
Lindsay Moritz United States
Leilei Li
Citations per year, relative to Leilei Li Leilei Li (= 1×) peers Lindsay Moritz

Countries citing papers authored by Leilei Li

Since Specialization
Citations

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

Fields of papers citing papers by Leilei Li

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Leilei Li

This figure shows the co-authorship network connecting the top 25 collaborators of Leilei Li. A scholar is included among the top collaborators of Leilei Li 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 Leilei Li. Leilei Li 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.
2.
Sun, Meiling, Hongguo Zhang, Yuting Jiang, et al.. (2021). Molecular cytogenetic characterization of 1q42.3q44 deletion and 8q24.3 duplication in a fetus with single umbilical artery and ventricular septal defects. Taiwanese Journal of Obstetrics and Gynecology. 60(6). 1126–1133.
3.
Zhang, Zhihong, et al.. (2021). ICSI outcomes of fresh or cryopreserved spermatozoa from micro-TESE in patients with nonobstructive azoospermia. Medicine. 100(12). e25021–e25021. 14 indexed citations
4.
Hu, Xiaonan, Leilei Li, Qingyang Shi, et al.. (2021). Prenatal diagnosis of a fetus with mosaic ring chromosome 13: Case report and review of the literature. Taiwanese Journal of Obstetrics and Gynecology. 60(3). 554–558.
5.
Li, Leilei, et al.. (2021). Genetic diversity and population structure of Tibetan sheep breeds determined by whole genome resequencing. Tropical Animal Health and Production. 53(1). 174–174. 10 indexed citations
6.
Shi, Qingyang, et al.. (2020). Ultrasonographic findings and prenatal diagnosis of complete trisomy 17p syndrome: A case report and review of the literature. Journal of Clinical Laboratory Analysis. 35(1). e23582–e23582. 3 indexed citations
7.
Li, Leilei, Yi Yang, Hongguo Zhang, et al.. (2020). High frequency of Y chromosome microdeletions in male infertility patients with 45,X/46,XY mosaicism. Brazilian Journal of Medical and Biological Research. 53(3). e8980–e8980. 10 indexed citations
8.
Chen, Shuang, Qi Xi, Yuting Jiang, et al.. (2020). Molecular cytogenetic studies of a male carrier with a unique (Y;14) translocation: Case report. Journal of Clinical Laboratory Analysis. 35(2). e23614–e23614. 1 indexed citations
9.
He, Jing, Leilei Li, Yang Yu, et al.. (2020). Two mutations in the axonemal dynein heavy chain gene 5 in a Chinese asthenozoospermia patient. Medicine. 99(28). e20813–e20813. 8 indexed citations
10.
Sun, Meiling, Yang Yu, Leilei Li, et al.. (2020). Prenatal diagnosis of a de novo 15q11.2 microdeletion in a maternal inv(4)(p15q31) fetus with increased nuchal translucency. Medicine. 99(40). e22496–e22496.
11.
Zhao, Haiyue, Hongguo Zhang, Qi Xi, et al.. (2020). Case report: A non-obstructive azoospermia patient with heat shock factor-2 mutation. Medicine. 99(31). e21107–e21107. 8 indexed citations
12.
13.
Chen, Shuang, Ruixue Wang, Leilei Li, et al.. (2020). Ultrasonographic findings and prenatal diagnosis of Jacobsen syndrome. Medicine. 99(1). e18695–e18695. 2 indexed citations
14.
Yu, Yang, Ruixue Wang, Qi Xi, et al.. (2019). Effect of paternal age on intracytoplasmic sperm injection outcomes in cryptozoospermic men. Medicine. 98(26). e16209–e16209. 5 indexed citations
15.
Xi, Qi, Ruixue Wang, Hongguo Zhang, et al.. (2019). Chromosomal copy number variations in products of conception from spontaneous abortion by next-generation sequencing technology. Medicine. 98(47). e18041–e18041. 16 indexed citations
16.
Zhang, Hongguo, Qi Xi, Yuting Jiang, et al.. (2019). Molecular cytogenetic analysis and genetic counseling: a case report of eight 46,XX males and a literature review. Molecular Cytogenetics. 12(1). 44–44. 6 indexed citations
17.
Zhang, Hongguo, Ruixue Wang, Yuan Jiang Pan, et al.. (2018). A report of nine cases and review of the literature of infertile men carrying balanced translocations involving chromosome 5. Molecular Cytogenetics. 11(1). 10–10. 9 indexed citations
18.
Yu, Yang, Qi Xi, Ruixue Wang, et al.. (2018). Intraoperative assessment of tubules in predicting microdissection testicular sperm extraction outcome in men with Sertoli cell-only syndrome. Journal of International Medical Research. 47(2). 722–729. 7 indexed citations
19.
Pan, Yuan Jiang, Hongguo Zhang, Qi Xi, et al.. (2017). Molecular microdeletion analysis of infertile men with karyotypic Y chromosome abnormalities. Journal of International Medical Research. 46(1). 307–315. 13 indexed citations
20.
Jiang, Yuting, et al.. (2012). Impact of chromosomal heteromorphisms on reproductive failure and analysis of 38 heteromorphic pedigrees in Northeast China. Journal of Assisted Reproduction and Genetics. 30(2). 275–281. 21 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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