Qingwei Qi

568 total citations
40 papers, 351 citations indexed

About

Qingwei Qi is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Qingwei Qi has authored 40 papers receiving a total of 351 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Pediatrics, Perinatology and Child Health, 15 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in Qingwei Qi's work include Prenatal Screening and Diagnostics (25 papers), Genomic variations and chromosomal abnormalities (11 papers) and Fetal and Pediatric Neurological Disorders (9 papers). Qingwei Qi is often cited by papers focused on Prenatal Screening and Diagnostics (25 papers), Genomic variations and chromosomal abnormalities (11 papers) and Fetal and Pediatric Neurological Disorders (9 papers). Qingwei Qi collaborates with scholars based in China, United States and Philippines. Qingwei Qi's co-authors include Yulin Jiang, Xiya Zhou, Juntao Liu, David S. Cram, Jinlin Hou, Yang Xiang, Xirun Wan, Mengnan Xu, Xiu-yu Yang and Xu-ming Bian and has published in prestigious journals such as Scientific Reports, Medicine and Clinica Chimica Acta.

In The Last Decade

Qingwei Qi

36 papers receiving 344 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Qingwei Qi China 10 238 118 75 56 52 40 351
Jin Han China 13 246 1.0× 160 1.4× 179 2.4× 51 0.9× 34 0.7× 74 551
Joaquín Diaz-Recasens Spain 11 337 1.4× 162 1.4× 98 1.3× 145 2.6× 31 0.6× 14 488
Andrea Nuccitelli Italy 10 446 1.9× 256 2.2× 104 1.4× 69 1.2× 104 2.0× 16 593
Yvonne Cheng Hong Kong 9 233 1.0× 103 0.9× 151 2.0× 44 0.8× 18 0.3× 17 408
Molka Kammoun Tunisia 9 144 0.6× 128 1.1× 86 1.1× 16 0.3× 126 2.4× 18 368
Anjeung Kang Switzerland 9 284 1.2× 100 0.8× 138 1.8× 100 1.8× 20 0.4× 11 463
Pamela Renwick United Kingdom 9 237 1.0× 124 1.1× 121 1.6× 48 0.9× 40 0.8× 10 363
Ana Bustamante‐Aragonés Spain 10 246 1.0× 142 1.2× 72 1.0× 100 1.8× 10 0.2× 17 347

Countries citing papers authored by Qingwei Qi

Since Specialization
Citations

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

Fields of papers citing papers by Qingwei Qi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Qingwei Qi

This figure shows the co-authorship network connecting the top 25 collaborators of Qingwei Qi. A scholar is included among the top collaborators of Qingwei Qi 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 Qingwei Qi. Qingwei Qi 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.
Lü, Yan, Yulin Jiang, Xiya Zhou, et al.. (2025). Incidental Identification of Potentially Affected Individuals Through Expanded Carrier Screening During Preconception or Early Pregnancy. Prenatal Diagnosis. 45(9). 1151–1159. 1 indexed citations
2.
Ren, Yuan, Yulin Jiang, Qingwei Qi, et al.. (2025). Clinical Implications of Noninvasive Prenatal Testing Failures Due to Low Fetal Fraction: Associations With Adverse Maternal and Fetal Outcomes. Prenatal Diagnosis. 45(11). 1417–1425. 1 indexed citations
3.
Li, Mengmeng, Yulin Jiang, Xiya Zhou, et al.. (2025). Prenatal diagnosis and pregnancy outcomes of mosaicism detected by CMA-seq. BMC Pregnancy and Childbirth. 25(1). 912–912.
4.
Jiang, Yulin, Xiya Zhou, Yiqi Yu, et al.. (2025). Deep insights and clinical benefits from the comprehensive cohort of fetal skeletal dysplasia in China. Journal of genetics and genomics. 52(12). 1524–1536.
5.
Lü, Yan, Yi Yu, Mengmeng Li, et al.. (2024). Genetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia. Prenatal Diagnosis. 45(12). 1651–1659. 1 indexed citations
6.
Li, Mengmeng, Na Hao, Yulin Jiang, et al.. (2024). Contribution of uniparental disomy to fetal growth restriction: a whole-exome sequencing series in a prenatal setting. Scientific Reports. 14(1). 238–238. 1 indexed citations
7.
Qi, Qingwei, Yulin Jiang, Xiangqin Zhou, et al.. (2023). Whole‐genome sequencing analysis in fetal structural anomalies: novel phenotype–genotype discoveries. Ultrasound in Obstetrics and Gynecology. 63(5). 664–671. 8 indexed citations
8.
9.
Lü, Yan, Yulin Jiang, Xiya Zhou, et al.. (2023). Detection of Mosaic Absence of Heterozygosity (AOH) Using Low-Pass Whole Genome Sequencing in Prenatal Diagnosis: A Preliminary Report. Diagnostics. 13(18). 2895–2895. 5 indexed citations
10.
Hao, Na, Mengmeng Li, Hanzhe Zhang, et al.. (2023). Analysis of complex chromosomal rearrangement involving chromosome 6 via the integration of optical genomic mapping and molecular cytogenetic methodologies. Journal of Human Genetics. 69(1). 3–11. 4 indexed citations
11.
Lü, Yan, Yulin Jiang, Huanwen Wu, et al.. (2023). Prenatal genetic diagnosis of disseminated infantile myofibromatosis: a case report and literature review. BMC Medical Genomics. 16(1). 185–185. 1 indexed citations
12.
Chen, Xinlin, Yulin Jiang, Qingwei Qi, et al.. (2022). Clinical efficiency of simultaneous CNV-seq and whole-exome sequencing for testing fetal structural anomalies. Journal of Translational Medicine. 20(1). 10–10. 21 indexed citations
13.
Wang, Ying, Yulin Jiang, Shan Jian, et al.. (2022). Ex utero intrapartum therapy in infants with congenital diaphragmatic hernia: a propensity score matching analysis. World Journal of Pediatric Surgery. 5(4). e000425–e000425. 2 indexed citations
14.
Qi, Qingwei, et al.. (2021). Factors associated with test failure in pregnant women undergoing cell-free DNA-based testing for fetal trisomy. Journal of Medical Screening. 28(4). 411–418. 2 indexed citations
15.
Ma, Li, Qingwei Qi, Na Hao, et al.. (2018). Trisomy 22 with long spina bifida occulta. Medicine. 97(39). e12306–e12306. 4 indexed citations
16.
Meng, Hua, et al.. (2018). Adducted thumb as an isolated morphologic finding. Medicine. 97(38). e12437–e12437. 3 indexed citations
17.
Liu, Wenyu, Yijun Song, Xiya Zhou, et al.. (2017). Pregnancy Combined with Epilepsy and Cerebral Cavernous Malformation. Chinese Medical Journal. 130(5). 619–620. 4 indexed citations
18.
Song, Yijun, Xiya Zhou, Xiaohong Li, et al.. (2016). Quantitation of fetal DNA fraction in maternal plasma using circulating single molecule amplification and re-sequencing technology (cSMART). Clinica Chimica Acta. 456. 151–156. 18 indexed citations
20.
Bian, Xu-ming, Qi Guo, & Qingwei Qi. (2010). Current situation and development of prenatal diagnosis in China. Frontiers of Medicine in China. 4(3). 271–274. 8 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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