Siyuan Linpeng

500 total citations
26 papers, 319 citations indexed

About

Siyuan Linpeng is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Siyuan Linpeng has authored 26 papers receiving a total of 319 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Pediatrics, Perinatology and Child Health, 10 papers in Molecular Biology and 9 papers in Genetics. Recurrent topics in Siyuan Linpeng's work include Prenatal Screening and Diagnostics (12 papers), Fetal and Pediatric Neurological Disorders (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Siyuan Linpeng is often cited by papers focused on Prenatal Screening and Diagnostics (12 papers), Fetal and Pediatric Neurological Disorders (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Siyuan Linpeng collaborates with scholars based in China, France and United States. Siyuan Linpeng's co-authors include Lingqian Wu, Hu Tan, Huaiyu Sun, Hua Wang, David S. Cram, Yingdi Liu, Hongmin Zhu, Yu Zhang, Fuli Yu and Mengnan Xu and has published in prestigious journals such as Scientific Reports, Gene and Medicine.

In The Last Decade

Siyuan Linpeng

23 papers receiving 314 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Siyuan Linpeng China 8 197 131 116 58 25 26 319
Hu Tan China 8 184 0.9× 148 1.1× 74 0.6× 51 0.9× 30 1.2× 30 304
Elizabeth Scotchman United Kingdom 9 255 1.3× 166 1.3× 104 0.9× 31 0.5× 35 1.4× 12 335
Ivy Ng Singapore 10 141 0.7× 147 1.1× 120 1.0× 52 0.9× 17 0.7× 19 375
Ioannis Papoulidis Greece 13 195 1.0× 251 1.9× 116 1.0× 24 0.4× 40 1.6× 52 388
Kyra E. Stuurman Netherlands 8 76 0.4× 72 0.5× 137 1.2× 38 0.7× 64 2.6× 18 274
Nicholas J. Ahn United States 5 39 0.2× 91 0.7× 194 1.7× 20 0.3× 35 1.4× 9 277
Yunli Lai China 12 103 0.5× 99 0.8× 157 1.4× 22 0.4× 14 0.6× 15 351
George Rebello South Africa 10 106 0.5× 67 0.5× 158 1.4× 25 0.4× 62 2.5× 25 316
Amy Y. Y. Chan Hong Kong 8 181 0.9× 61 0.5× 76 0.7× 64 1.1× 10 0.4× 26 379
Carole Goumy France 11 100 0.5× 185 1.4× 125 1.1× 7 0.1× 75 3.0× 36 324

Countries citing papers authored by Siyuan Linpeng

Since Specialization
Citations

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

Fields of papers citing papers by Siyuan Linpeng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Siyuan Linpeng

This figure shows the co-authorship network connecting the top 25 collaborators of Siyuan Linpeng. A scholar is included among the top collaborators of Siyuan Linpeng 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 Siyuan Linpeng. Siyuan Linpeng 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, Hongyun, Jun He, Yanling Teng, et al.. (2025). Non-invasive prenatal testing for dominant single-gene disorders using targeted next-generation sequencing. QJM. 118(5). 344–353. 1 indexed citations
2.
Jing, Liu, Shunyao Wang, Shihao Zhou, et al.. (2025). Cost-effectiveness of different screening strategies for Down syndrome: a real-world analysis in 140,472 women. Frontiers in Public Health. 13. 1535381–1535381.
3.
Peng, Can, et al.. (2024). The genetics and clinical outcomes in 151 cases of fetal growth restriction: A Chinese single-center study. European Journal of Obstetrics & Gynecology and Reproductive Biology. 298. 128–134. 1 indexed citations
4.
Li, Xu, et al.. (2023). Case report: Paternal uniparental disomy on chromosome 7 and homozygous SUGCT mutation in a fetus with overweight after birth. Frontiers in Genetics. 14. 1272028–1272028. 1 indexed citations
5.
Xu, Zhen, Lanping Hu, Yinyin Liu, et al.. (2023). Comparison of Third-Generation Sequencing and Routine Polymerase Chain Reaction in Genetic Analysis of Thalassemia. Archives of Pathology & Laboratory Medicine. 148(3). 336–344. 1 indexed citations
6.
7.
Zhang, Hongyun, Siyuan Linpeng, Yanling Teng, et al.. (2023). A de novo heterozygous POU3F3 genotype for the p.(Q214*) variant in a fetus with transient isolated bilateral mild ventriculomegaly: a case report and review of the literature. Frontiers in Pediatrics. 11. 1177137–1177137. 1 indexed citations
8.
Peng, Can, et al.. (2022). Prenatal genetic diagnosis of tetrasomy 18p from maternal trisomy 18p: a case report. Molecular Cytogenetics. 15(1). 25–25.
9.
10.
Linpeng, Siyuan, et al.. (2022). Cell-Free DNA Screening for Sex Chromosome Abnormalities and Pregnancy Outcomes, 2018–2020: A Retrospective Analysis. Journal of Personalized Medicine. 12(1). 48–48. 8 indexed citations
11.
Liu, Yingdi, Zhuo Li, Siyuan Linpeng, et al.. (2020). A novel GJB1 mutation associated with X‐linked Charcot–Marie–Tooth disease in a large Chinese family pedigree. Molecular Genetics & Genomic Medicine. 8(3). e1127–e1127. 3 indexed citations
12.
13.
Luo, Dan, et al.. (2019). Molecular genetic study of 59 Chinese Oculocutaneous albinism families. European Journal of Medical Genetics. 62(10). 103709–103709. 5 indexed citations
14.
Cram, David S., Hu Tan, Siyuan Linpeng, et al.. (2019). Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes. Genetics in Medicine. 21(9). 1998–2006. 167 indexed citations
15.
Tang, Hui, et al.. (2019). Next generation sequencing identified two novel mutations in NIPBL and a frame shift mutation in CREBBP in three Chinese children. Orphanet Journal of Rare Diseases. 14(1). 45–45. 7 indexed citations
16.
Tan, Hu, Xin Chen, Weigang Lv, et al.. (2018). Truncating mutations of HIBCH tend to cause severe phenotypes in cases with HIBCH deficiency: a case report and brief literature review. Journal of Human Genetics. 63(7). 851–855. 10 indexed citations
17.
Tan, Hu, et al.. (2018). Three Novel Mutations in <i>FBN1</i> and <i>TGFBR2</i> in Patients with the Syndromic Form of Thoracic Aortic Aneurysms and Dissections. International Heart Journal. 59(5). 1059–1068. 6 indexed citations
18.
19.
Zhang, Rundong, Siyuan Linpeng, Yihua Huang, et al.. (2017). Novel variants in PAX6 gene caused congenital aniridia in two Chinese families. Eye. 31(6). 956–961. 13 indexed citations
20.
Wu, Yong, Zhiqing Hu, Zhuo Li, et al.. (2016). In situ genetic correction of F8 intron 22 inversion in hemophilia A patient-specific iPSCs. Scientific Reports. 6(1). 18865–18865. 43 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Hu Tan Breakdown of academic impact, for papers by Elizabeth Scotchman Breakdown of academic impact, for papers by Ivy Ng Breakdown of academic impact, for papers by Ioannis Papoulidis Breakdown of academic impact, for papers by Kyra E. Stuurman Breakdown of academic impact, for papers by Nicholas J. Ahn Breakdown of academic impact, for papers by Yunli Lai Breakdown of academic impact, for papers by George Rebello Breakdown of academic impact, for papers by Amy Y. Y. Chan Breakdown of academic impact, for papers by Carole Goumy
Rankless by CCL
2026