Yixi Sun

424 total citations
26 papers, 285 citations indexed

About

Yixi Sun is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Yixi Sun has authored 26 papers receiving a total of 285 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 11 papers in Molecular Biology and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Yixi Sun's work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (9 papers) and Genetic Syndromes and Imprinting (4 papers). Yixi Sun is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (9 papers) and Genetic Syndromes and Imprinting (4 papers). Yixi Sun collaborates with scholars based in China, Thailand and New Zealand. Yixi Sun's co-authors include Hefeng Huang, Feng Ma, Li Su, Jun Zhou, Minyue Dong, Yanmei Yang, Jun Zhou, Liya Wang, Yeqing Qian and Fan Jin and has published in prestigious journals such as Human Mutation, Laboratory Investigation and Frontiers in Genetics.

In The Last Decade

Yixi Sun

24 papers receiving 269 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yixi Sun China 8 96 84 78 45 38 26 285
Randolph B. Lyde United States 10 56 0.6× 92 1.1× 35 0.4× 25 0.6× 18 0.5× 14 294
Letizia Galleri Italy 12 148 1.5× 180 2.1× 173 2.2× 39 0.9× 74 1.9× 17 582
Xuye Yuan China 9 50 0.5× 209 2.5× 55 0.7× 34 0.8× 106 2.8× 18 338
Mariateresa Paciolla Italy 11 117 1.2× 206 2.5× 211 2.7× 18 0.4× 83 2.2× 11 423
Yu Hong China 15 123 1.3× 163 1.9× 59 0.8× 17 0.4× 20 0.5× 37 690
Alessandra Bridi Brazil 11 150 1.6× 220 2.6× 50 0.6× 16 0.4× 54 1.4× 36 379
Lisa K. Iwamoto-Stohl United Kingdom 4 24 0.3× 227 2.7× 40 0.5× 73 1.6× 19 0.5× 4 303
Domenico Valerio Italy 11 31 0.3× 78 0.9× 44 0.6× 148 3.3× 22 0.6× 18 321
Zhilong Chen China 9 78 0.8× 182 2.2× 24 0.3× 36 0.8× 44 1.2× 25 417
Leilei Li China 11 37 0.4× 199 2.4× 155 2.0× 87 1.9× 98 2.6× 53 453

Countries citing papers authored by Yixi Sun

Since Specialization
Citations

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

Fields of papers citing papers by Yixi Sun

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yixi Sun

This figure shows the co-authorship network connecting the top 25 collaborators of Yixi Sun. A scholar is included among the top collaborators of Yixi Sun 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 Yixi Sun. Yixi Sun 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.
Tan, Meihua, Jiao Liu, Yanmei Yang, et al.. (2024). An efficient molecular genetic testing strategy for incontinentia pigmenti based on single-tube long fragment read sequencing. npj Genomic Medicine. 9(1). 32–32. 2 indexed citations
2.
Qian, Yeqing, Yongfeng Liu, Kai Yan, et al.. (2023). Noninvasive Prenatal Screening for Common Fetal Aneuploidies Using Single-Molecule Sequencing. Laboratory Investigation. 103(4). 100043–100043.
3.
Wang, Zhengrong, Yuqing Xu, Yixi Sun, Shuang Wang, & Minyue Dong. (2023). Novel homozygous silent mutation of ITGB3 gene caused Glanzmann thrombasthenia. Frontiers in Pediatrics. 10. 1062900–1062900. 4 indexed citations
4.
Zhu, Linyan, et al.. (2023). Case report: A compound heterozygous mutations in ASNS broadens the spectrum of asparagine synthetase deficiency in the prenatal diagnosis. Frontiers in Pediatrics. 11. 1273789–1273789. 4 indexed citations
5.
Sun, Yixi, Yangwen Qian, Hai‐Xi Sun, et al.. (2022). Case Report: De novo DDX3X mutation caused intellectual disability in a female with skewed X-chromosome inactivation on the mutant allele. Frontiers in Genetics. 13. 999442–999442. 1 indexed citations
6.
Yan, Kai, Yixi Sun, Yanmei Yang, Bei Liu, & Minyue Dong. (2022). Case Report: Identification Pathogenic Abnormal Splicing of BBS1 Causing Bardet–Biedl Syndrome Type I (BBS1) due to Missense Mutation. Frontiers in Genetics. 13. 849562–849562. 2 indexed citations
7.
Hu, Junjie, et al.. (2022). Case report: Prenatal diagnosis of Kagami–Ogata syndrome in a Chinese family. Frontiers in Genetics. 13. 959666–959666. 1 indexed citations
8.
Hu, Junjie, et al.. (2022). Prenatal diagnosis of trisomy 8 mosaicism, initially identified by cffDNA screening. Molecular Cytogenetics. 15(1). 39–39. 3 indexed citations
9.
Sun, Yixi, Yeqing Qian, Na Chen, et al.. (2022). Case report: FOXP1 syndrome caused by a de novo splicing variant (c.1652+5 G>A) of the FOXP1 gene. Frontiers in Genetics. 13. 926070–926070. 2 indexed citations
10.
Dong, Minyue, et al.. (2020). The association between the two more common genetic causes of spermatogenic failure: a 7-year retrospective study. Asian Journal of Andrology. 22(6). 642–642. 1 indexed citations
11.
Zhang, Min, Yeqing Qian, Yanmei Yang, et al.. (2020). Identification of a likely pathogenic structural variation in the LAMA1 gene by Bionano optical mapping. npj Genomic Medicine. 5(1). 31–31. 16 indexed citations
12.
Lin, Jie, Yixi Sun, Yeqing Qian, et al.. (2020). Non-invasive prenatal screening for Emanuel syndrome. Molecular Cytogenetics. 13(1). 9–9. 5 indexed citations
13.
Sun, Yixi, Yeqing Qian, Liya Wang, et al.. (2019). Heterozygous Deletion of the SHOX Gene Enhancer in two Females With Clinical Heterogeneity Associating With Skewed XCI and Escaping XCI. Frontiers in Genetics. 10. 1086–1086. 6 indexed citations
14.
Sun, Yixi, Yanfeng Li, Min Chen, et al.. (2019). A Novel Silent Mutation in the L1CAM Gene Causing Fetal Hydrocephalus Detected by Whole-Exome Sequencing. Frontiers in Genetics. 10. 817–817. 12 indexed citations
15.
Yang, Yanmei, Kai Yan, Bei Liu, et al.. (2019). Comprehensive genetic diagnosis of patients with Duchenne/Becker muscular dystrophy (DMD/BMD) and pathogenicity analysis of splice site variants in the DMD gene. Journal of Zhejiang University SCIENCE B. 20(9). 753–765. 14 indexed citations
16.
Yu, Jialing, et al.. (2019). [Single nucleotide polymorphism microarray in prenatal diagnosis of fetuses with absent nasal bone].. PubMed. 48(4). 414–419. 1 indexed citations
17.
Wang, Liya, Chunfang Peng, Dan Chen, et al.. (2019). Preimplantation genetic diagnosis and screening (PGD/S) using a semiconductor sequencing platform. Human Genomics. 13(1). 1–1. 8 indexed citations
18.
Xu, Chenming, et al.. (2014). Different segregation patterns in five carriers due to a pericentric inversion of chromosome 1. Systems Biology in Reproductive Medicine. 60(6). 367–372. 16 indexed citations
19.
Sun, Yixi, et al.. (2012). miR-155 mediates suppressive effect of progesterone on TLR3, TLR4-triggered immune response. Immunology Letters. 146(1-2). 25–30. 56 indexed citations
20.

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 Randolph B. Lyde Breakdown of academic impact, for papers by Letizia Galleri Breakdown of academic impact, for papers by Xuye Yuan Breakdown of academic impact, for papers by Mariateresa Paciolla Breakdown of academic impact, for papers by Yu Hong Breakdown of academic impact, for papers by Alessandra Bridi Breakdown of academic impact, for papers by Lisa K. Iwamoto-Stohl Breakdown of academic impact, for papers by Domenico Valerio Breakdown of academic impact, for papers by Zhilong Chen Breakdown of academic impact, for papers by Leilei Li
Rankless by CCL
2026