Jiexia Yang

587 total citations
21 papers, 280 citations indexed

About

Jiexia Yang is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Infectious Diseases. According to data from OpenAlex, Jiexia Yang has authored 21 papers receiving a total of 280 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Pediatrics, Perinatology and Child Health, 7 papers in Genetics and 6 papers in Infectious Diseases. Recurrent topics in Jiexia Yang's work include Prenatal Screening and Diagnostics (17 papers), Fetal and Pediatric Neurological Disorders (10 papers) and Genomic variations and chromosomal abnormalities (7 papers). Jiexia Yang is often cited by papers focused on Prenatal Screening and Diagnostics (17 papers), Fetal and Pediatric Neurological Disorders (10 papers) and Genomic variations and chromosomal abnormalities (7 papers). Jiexia Yang collaborates with scholars based in China, United States and Germany. Jiexia Yang's co-authors include Haishan Peng, Yaping Hou, Fangfang Guo, Jing Wu, Aihua Yin, Yiming Qi, Yixia Wang, Dongmei Wang, Xiaozhuang Zhang and Yang‐Yi Chen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Scientific Reports.

In The Last Decade

Jiexia Yang

19 papers receiving 271 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jiexia Yang China 8 229 104 74 52 25 21 280
Francesca Dulcetti Italy 10 301 1.3× 203 2.0× 84 1.1× 83 1.6× 28 1.1× 12 387
Maurizio Travi Italy 10 161 0.7× 54 0.5× 33 0.4× 108 2.1× 49 2.0× 16 312
Simona De Toffol Italy 11 303 1.3× 216 2.1× 79 1.1× 84 1.6× 26 1.0× 15 412
Matthew Hoi Kin Chau Hong Kong 13 271 1.2× 250 2.4× 41 0.6× 93 1.8× 38 1.5× 28 387
Eva Pompilii Italy 7 245 1.1× 145 1.4× 50 0.7× 50 1.0× 34 1.4× 13 298
Elizabeth Scotchman United Kingdom 9 255 1.1× 166 1.6× 31 0.4× 104 2.0× 35 1.4× 12 335
Cristina González-González Spain 10 209 0.9× 93 0.9× 85 1.1× 51 1.0× 13 0.5× 12 253
Pere Mir Spain 11 291 1.3× 136 1.3× 18 0.2× 84 1.6× 35 1.4× 16 392
M.T. Jones United Kingdom 4 271 1.2× 55 0.5× 89 1.2× 100 1.9× 21 0.8× 5 317

Countries citing papers authored by Jiexia Yang

Since Specialization
Citations

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

Fields of papers citing papers by Jiexia Yang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jiexia Yang

This figure shows the co-authorship network connecting the top 25 collaborators of Jiexia Yang. A scholar is included among the top collaborators of Jiexia Yang 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 Jiexia Yang. Jiexia Yang 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.
Gong, Xiaoli, Wei He, Wan Jin, et al.. (2024). Disruption of maternal vascular remodeling by a fetal endoretrovirus-derived gene in preeclampsia. Genome biology. 25(1). 117–117. 5 indexed citations
2.
Yang, Jiexia, Jing Wu, Dongmei Wang, et al.. (2023). Combined fetal fraction to analyze the Z-score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18, and 21. Journal of Assisted Reproduction and Genetics. 40(4). 803–810. 5 indexed citations
3.
Hou, Yaping, Jiexia Yang, Fanghua Wang, et al.. (2023). Association between cell-free DNA fetal fraction and pregnant character: a retrospective cohort study of 27,793 maternal plasmas. Scientific Reports. 13(1). 11420–11420. 3 indexed citations
4.
Tang, Hui, Jingjing Hu, Lijuan Lv, et al.. (2023). Prenatal diagnosis of Down syndrome combined with transient abnormal myelopoiesis in foetuses with a GATA1 gene variant: two case reports. Molecular Cytogenetics. 16(1). 27–27. 1 indexed citations
5.
He, Wei, Yi Zhang, Yunan Wang, et al.. (2023). Epigenetic phenotype of plasma cell-free DNA in the prediction of early-onset preeclampsia. Journal of Obstetrics and Gynaecology. 43(2). 2282100–2282100. 8 indexed citations
6.
7.
Peng, Haishan, et al.. (2021). Outcomes of pregnancies with trisomy 16 mosaicism detected by NIPT: a series of case reports. Molecular Cytogenetics. 14(1). 44–44. 7 indexed citations
8.
Yang, Jiexia, Yaping Hou, Fangfang Guo, et al.. (2021). Noninvasive prenatal detection of fetal sex chromosome abnormalities using the semiconductor sequencing platform (SSP) in Southern China. Journal of Assisted Reproduction and Genetics. 38(3). 727–734. 11 indexed citations
9.
Yang, Jiexia, Jing Wu, Haishan Peng, et al.. (2021). Performances of NIPT for copy number variations at different sequencing depths using the semiconductor sequencing platform. Human Genomics. 15(1). 41–41. 16 indexed citations
10.
Wang, Dongmei, Jiexia Yang, Haishan Peng, Yaping Hou, & Yixia Wang. (2021). [Analysis of the results of chromosomal trisomies 21, 18 and 13 screening among 40 628 women by non-invasive prenatal testing].. PubMed. 38(11). 1045–1050.
11.
Qi, Yiming, Jiexia Yang, Yaping Hou, et al.. (2020). Potential influence of parental copy number variations on noninvasive prenatal testing (NIPT): two case reports. Molecular Cytogenetics. 13(1). 18–18. 2 indexed citations
12.
Yang, Jiexia, Chunfang Peng, Yiming Qi, et al.. (2019). Noninvasive prenatal detection of hemoglobin Bart hydrops fetalis via maternal plasma dispensed with parental haplotyping using the semiconductor sequencing platform. American Journal of Obstetrics and Gynecology. 222(2). 185.e1–185.e17. 5 indexed citations
13.
Hou, Yaping, Jiexia Yang, Yiming Qi, et al.. (2019). Factors affecting cell-free DNA fetal fraction: statistical analysis of 13,661 maternal plasmas for non-invasive prenatal screening. Human Genomics. 13(1). 62–62. 45 indexed citations
14.
Qi, Yiming, Jiexia Yang, Yaping Hou, et al.. (2019). The significance of trisomy 7 mosaicism in noninvasive prenatal screening. Human Genomics. 13(1). 18–18. 19 indexed citations
15.
Yang, Jiexia, Yiming Qi, Yaping Hou, et al.. (2018). Performance of non-invasive prenatal testing for trisomies 21 and 18 in twin pregnancies. Molecular Cytogenetics. 11(1). 47–47. 15 indexed citations
16.
Yang, Jiexia, Yiming Qi, Fangfang Guo, et al.. (2017). A case of placental trisomy 18 mosaicism causing a false negative NIPT result. Molecular Cytogenetics. 10(1). 40–40. 6 indexed citations
17.
Yin, Aihua, Chang Liu, Yan Zhang, et al.. (2014). Genetic counseling and prenatal diagnosis for hereditary hearing loss in high-risk families. International Journal of Pediatric Otorhinolaryngology. 78(8). 1356–1359. 7 indexed citations
18.
Yang, Jiexia, Jing Wu, Fangfang Guo, et al.. (2014). Maternal Serum Disintegrin and Metalloprotease Protein-12 in Early Pregnancy as a Potential Marker of Adverse Pregnancy Outcomes. PLoS ONE. 9(5). e97284–e97284. 7 indexed citations
19.
Liao, Can, Aihua Yin, Chunfang Peng, et al.. (2014). Noninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencing. Proceedings of the National Academy of Sciences. 111(20). 7415–7420. 97 indexed citations
20.
Yin, Aihua, Chang Liu, Yan Zhang, et al.. (2013). The carrier rate and mutation spectrum of genes associated with hearing loss in South China hearing female population of childbearing age. BMC Medical Genetics. 14(1). 57–57. 20 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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