Fatao Li

548 total citations
20 papers, 326 citations indexed

About

Fatao Li is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Fatao Li has authored 20 papers receiving a total of 326 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Pediatrics, Perinatology and Child Health, 9 papers in Molecular Biology and 9 papers in Genetics. Recurrent topics in Fatao Li's work include Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (7 papers) and Congenital Heart Disease Studies (5 papers). Fatao Li is often cited by papers focused on Prenatal Screening and Diagnostics (10 papers), Genomic variations and chromosomal abnormalities (7 papers) and Congenital Heart Disease Studies (5 papers). Fatao Li collaborates with scholars based in China and Syria. Fatao Li's co-authors include Min Pan, Can Liao, Yongling Zhang, Dong‐Zhi Li, Zhen Li, Fang Fu, Can Liao, Xiangyi Jing, Jin Han and Zhiqiang Nie and has published in prestigious journals such as Gene, Human Genetics and Ultrasound in Obstetrics and Gynecology.

In The Last Decade

Fatao Li

20 papers receiving 320 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fatao Li China 10 185 157 120 60 40 20 326
Grétel Oudesluijs Netherlands 5 153 0.8× 155 1.0× 106 0.9× 23 0.4× 43 1.1× 9 281
Laura J. C. M. van Zutven Netherlands 11 76 0.4× 113 0.7× 192 1.6× 26 0.4× 23 0.6× 19 351
Emily Hardisty United States 8 239 1.3× 147 0.9× 80 0.7× 14 0.2× 29 0.7× 17 301
Elizabeth Scotchman United Kingdom 9 255 1.4× 166 1.1× 104 0.9× 10 0.2× 35 0.9× 12 335
Rhiannon Mellis United Kingdom 11 349 1.9× 250 1.6× 107 0.9× 13 0.2× 53 1.3× 17 456
Angela Elvira Covone Italy 8 146 0.8× 47 0.3× 137 1.1× 12 0.2× 39 1.0× 14 319
Erika Biral Italy 10 84 0.5× 94 0.6× 118 1.0× 19 0.3× 22 0.6× 14 363
Ning He Canada 11 59 0.3× 441 2.8× 443 3.7× 41 0.7× 66 1.6× 16 610
Rebeca Caze United States 6 59 0.3× 59 0.4× 68 0.6× 23 0.4× 9 0.2× 9 464

Countries citing papers authored by Fatao Li

Since Specialization
Citations

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

Fields of papers citing papers by Fatao Li

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fatao Li

This figure shows the co-authorship network connecting the top 25 collaborators of Fatao Li. A scholar is included among the top collaborators of Fatao 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 Fatao Li. Fatao 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.
Zhang, Lu, Hang Zhou, Fei Guo, et al.. (2024). Prenatal diagnosis in fetal right aortic arch using chromosomal microarray analysis and whole exome sequencing: a Chinese single-center retrospective study. Molecular Cytogenetics. 17(1). 22–22. 1 indexed citations
2.
Zhou, Jianying, Xuewei Tang, Li J, et al.. (2023). Utilization of multiple genetic methods for prenatal diagnosis of rare thalassemia variants. Frontiers in Genetics. 14. 1208102–1208102. 3 indexed citations
3.
Huang, Qiong, Yongling Zhang, Xiangyi Jing, et al.. (2023). Association of prenatal thoracic ultrasound abnormalities with copy number variants at a single Chinese tertiary center. International Journal of Gynecology & Obstetrics. 164(2). 770–777. 3 indexed citations
4.
Fu, Fang, Ru Li, Qiuxia Yu, et al.. (2022). Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing. Frontiers in Genetics. 13. 951829–951829. 1 indexed citations
5.
Mao, Aiping, Fengzhi Liu, Yan-Lin Li, et al.. (2022). Detection of rare thalassemia mutations using long-read single-molecule real-time sequencing. Gene. 825. 146438–146438. 23 indexed citations
6.
Li, Ru, Fatao Li, Qiuxia Yu, et al.. (2022). Contribution of maternal mosaicism to false-positive chromosome X loss associated with noninvasive prenatal testing. The Journal of Maternal-Fetal & Neonatal Medicine. 35(25). 9647–9653. 4 indexed citations
7.
Li, Ru, Qiuxia Yu, Dan Wang, et al.. (2021). Evaluation of the Z‐score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18 and 21 at a single center. Prenatal Diagnosis. 41(6). 690–696. 22 indexed citations
8.
Fu, Fang, Ru Li, Tingying Lei, et al.. (2020). Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease. Human Genetics. 140(2). 333–348. 20 indexed citations
9.
Li, Ru, Fang Fu, Qiuxia Yu, et al.. (2020). Prenatal exome sequencing in fetuses with congenital heart defects. Clinical Genetics. 98(3). 215–230. 32 indexed citations
10.
Deng, Qiong, Lihua Huang, Juan Liu, et al.. (2019). Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with congenital cystic adenomatoid malformation by chromosomal microarray analysis. The Journal of Maternal-Fetal & Neonatal Medicine. 34(16). 2623–2629. 4 indexed citations
11.
Li, Ru, Yongling Zhang, Xiangyi Jing, et al.. (2018). Pregnancy outcome of autosomal aneuploidies other than common trisomies detected by noninvasive prenatal testing in routine clinical practice. Prenatal Diagnosis. 38(11). 849–857. 25 indexed citations
12.
Duan, Li, Yunting Lin, Yonglan Huang, et al.. (2018). Early prenatal diagnosis of lysosomal storage disorders by enzymatic and molecular analysis. Prenatal Diagnosis. 38(10). 779–787. 7 indexed citations
13.
Jin, Yulin, Qihua Liang, Jie Tang, et al.. (2018). Altered expression of circular RNAs in human placental chorionic plate‐derived mesenchymal stem cells pretreated with hypoxia. Journal of Clinical Laboratory Analysis. 33(3). e22825–e22825. 9 indexed citations
14.
Su, Ling, et al.. (2017). Two homozygous mutations in the exon 5 of BCKDHB gene that may cause the classic form of maple syrup urine disease. Metabolic Brain Disease. 32(3). 765–772. 10 indexed citations
15.
Wu, Xiaoli, Ru Li, Fang Fu, et al.. (2017). Chromosome microarray analysis in the investigation of children with congenital heart disease. BMC Pediatrics. 17(1). 117–117. 31 indexed citations
16.
Fu, Fang, Zhiqiang Nie, Lei Tang, et al.. (2017). Whole exome sequencing as a diagnostic adjunct to clinical testing in fetuses with structural abnormalities. Ultrasound in Obstetrics and Gynecology. 51(4). 493–502. 112 indexed citations
17.
Bao, Junjie, Yong Zou, Fei Gao, et al.. (2015). [Deep sequencing of the T cell receptor Vb CDR3 repertoire of peripheral CD4+T cells in primary biliary cirrhosis].. PubMed. 23(8). 580–5. 5 indexed citations
18.
Wu, Xiaoli, Fang Fu, Ru Li, et al.. (2014). [Clinical value of genome-wide high resolution chromosomal microarray analysis in etiological study of fetuses with congenital heart defects].. PubMed. 49(12). 893–8. 3 indexed citations
19.
20.
Liao, Can, et al.. (2009). The detection of aneuploidy and maternal contamination by QF-PCR in samples undergoing prenatal diagnosis for thalassemia in Southern China. European Journal of Obstetrics & Gynecology and Reproductive Biology. 144(2). 149–152. 10 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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