Yuwei Jin

436 total citations
27 papers, 307 citations indexed

About

Yuwei Jin is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Yuwei Jin has authored 27 papers receiving a total of 307 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 20 papers in Genetics and 7 papers in Surgery. Recurrent topics in Yuwei Jin's work include Neurogenetic and Muscular Disorders Research (19 papers), RNA modifications and cancer (19 papers) and RNA Research and Splicing (9 papers). Yuwei Jin is often cited by papers focused on Neurogenetic and Muscular Disorders Research (19 papers), RNA modifications and cancer (19 papers) and RNA Research and Splicing (9 papers). Yuwei Jin collaborates with scholars based in China and Ecuador. Yuwei Jin's co-authors include Fang Song, Yu-jin Qu, Jin-li Bai, Hong Wang, Hong Wang, Ting Zhang, Xiaoying Zheng, Wenhui Zhang, Hong Wang and Yan Li and has published in prestigious journals such as Human Molecular Genetics, Gene and Clinica Chimica Acta.

In The Last Decade

Yuwei Jin

26 papers receiving 306 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yuwei Jin China 10 260 200 94 55 26 27 307
Ons Mamaï Tunisia 7 91 0.3× 29 0.1× 27 0.3× 5 0.1× 26 1.0× 11 161
Aoi Wakabayashi United States 7 146 0.6× 46 0.2× 24 0.3× 3 0.1× 15 0.6× 9 211
José Luis Vázquez Rojas Spain 7 127 0.5× 122 0.6× 99 1.1× 2 0.0× 4 0.2× 21 237
Colleen M. Carlston United States 8 122 0.5× 20 0.1× 12 0.1× 20 0.4× 7 0.3× 13 234
Catena Kresbach Germany 6 114 0.4× 54 0.3× 48 0.5× 2 0.0× 6 0.2× 13 188
Karolina Antosik Poland 13 135 0.5× 12 0.1× 149 1.6× 7 0.1× 9 0.3× 28 305
Colleen Macmurdo United States 4 84 0.3× 24 0.1× 48 0.5× 8 0.1× 8 0.3× 9 183
Irene Hadjidemetriou United Kingdom 6 79 0.3× 33 0.2× 51 0.5× 6 0.1× 2 0.1× 9 179
Patricia Bretones France 8 165 0.6× 14 0.1× 21 0.2× 11 0.2× 6 0.2× 14 301
Korbinian M. Riedhammer Germany 10 134 0.5× 14 0.1× 17 0.2× 5 0.1× 5 0.2× 26 231

Countries citing papers authored by Yuwei Jin

Since Specialization
Citations

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

Fields of papers citing papers by Yuwei Jin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yuwei Jin

This figure shows the co-authorship network connecting the top 25 collaborators of Yuwei Jin. A scholar is included among the top collaborators of Yuwei Jin 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 Yuwei Jin. Yuwei Jin 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.
Chen, Peipei, Yuwei Jin, Xinfang Ma, & Yan Lin. (2024). Public perception on active aging after COVID-19: an unsupervised machine learning analysis of 44,343 posts. Frontiers in Public Health. 12. 1329704–1329704.
2.
Jin, Yuwei, et al.. (2024). Circ_0038718 augments colorectal cancer progression through mediating the miR-761/miR-214–3p/ITGA6 axis. Pathology - Research and Practice. 263. 155649–155649. 1 indexed citations
3.
Qu, Yu-jin, Jin-li Bai, Hong Qi, et al.. (2024). Variants located in intron 6 of SMN1 lead to misdiagnosis in genetic detection and screening for SMA. Heliyon. 10(6). e28015–e28015. 1 indexed citations
4.
Bai, Jin-li, Yu-jin Qu, Wen‐Chen Huang, et al.. (2023). A high-fidelity long-read sequencing-based approach enables accurate and effective genetic diagnosis of spinal muscular atrophy. Clinica Chimica Acta. 553. 117743–117743. 6 indexed citations
5.
Zhu, Lin, et al.. (2023). IKBKE regulates angiogenesis by modulating VEGF expression and secretion in glioblastoma. Tissue and Cell. 84. 102180–102180. 1 indexed citations
6.
Bai, Jin-li, Yu-jin Qu, Jingjing Li, et al.. (2023). Novel Alu-mediated deletions of the SMN1 gene were identified by ultra-long read sequencing technology in patients with spinal muscular atrophy. Neuromuscular Disorders. 33(5). 382–390. 6 indexed citations
7.
Fan, Hong, et al.. (2021). Long non-coding RNA ROR recruits histone transmethylase MLL1 to up-regulate TIMP3 expression and promote breast cancer progression. Journal of Translational Medicine. 19(1). 95–95. 23 indexed citations
8.
Cao, Yanyan, Yu-jin Qu, Jin-li Bai, et al.. (2021). Factors associated with delayed diagnosis of spinal muscular atrophy in China and changes in diagnostic delay. Neuromuscular Disorders. 31(6). 519–527. 8 indexed citations
9.
Bai, Jin-li, et al.. (2020). Dual Mechanism of a New SMN1 Variant (c.835G>C, p.Gly279Arg) by Interrupting Exon 7 Skipping and YG Oligomerization in Causation of Spinal Muscular Atrophy. Journal of Molecular Neuroscience. 71(1). 112–121. 1 indexed citations
10.
Cao, Yanyan, Yu-jin Qu, Jin-li Bai, et al.. (2020). Transmission characteristics of SMN from 227 spinal muscular atrophy core families in China. Journal of Human Genetics. 65(5). 469–473. 2 indexed citations
11.
Cao, Yanyan, Wenhui Zhang, Yu-jin Qu, et al.. (2018). Diagnosis of Spinal Muscular Atrophy. Chinese Medical Journal. 131(24). 2921–2929. 11 indexed citations
12.
Bai, Jin-li, Yu-jin Qu, Lan Yang, et al.. (2017). The SMN1 common variant c.22 dupA in Chinese patients causes spinal muscular atrophy by nonsense-mediated mRNA decay in humans. Gene. 644. 49–55. 11 indexed citations
13.
Qu, Yu-jin, Ge Lin, Jin-li Bai, et al.. (2017). p.Val19Glyfs*21 and p.Leu228* variants in the survival of motor neuron 1 trigger nonsense-mediated mRNA decay causing the SMN1 PTC+ transcripts degradation. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 806. 31–38. 4 indexed citations
14.
Qu, Yu-jin, Jin-li Bai, Hong Wang, et al.. (2016). Mutation Spectrum of the Survival of Motor Neuron 1 and Functional Analysis of Variants in Chinese Spinal Muscular Atrophy. Journal of Molecular Diagnostics. 18(5). 741–752. 42 indexed citations
15.
Qu, Yu-jin, Yan Li, Jin-li Bai, et al.. (2016). Association between SMN2 methylation and disease severity in Chinese children with spinal muscular atrophy. Journal of Zhejiang University SCIENCE B. 17(1). 76–82. 16 indexed citations
16.
Gao, Ying, Xiaoyan Liu, Yu-jin Qu, et al.. (2015). A novel large deletion mutation of FERMT1 gene in a Chinese patient with Kindler syndrome. Journal of Zhejiang University SCIENCE B. 16(11). 957–962. 5 indexed citations
17.
Qu, Yu-jin, Jin-li Bai, Wenhui Zhang, et al.. (2015). A rare variant (c.863G>T) in exon 7 of SMN1 disrupts mRNA splicing and is responsible for spinal muscular atrophy. European Journal of Human Genetics. 24(6). 864–870. 10 indexed citations
18.
Qu, Yu-jin, et al.. (2013). Correlation of PLS3 expression with disease severity in children with spinal muscular atrophy. Journal of Human Genetics. 59(1). 24–27. 33 indexed citations
19.
Qu, Yu-jin, Juan Du, Erzhen Li, et al.. (2012). Subtle mutations in the SMN1 gene in Chinese patients with SMA: p.Arg288Met mutation causing SMN1 transcript exclusion of exon7. BMC Medical Genetics. 13(1). 86–86. 23 indexed citations
20.
Song, Fang, et al.. (2005). Phenylketonuria mutations in Northern China. Molecular Genetics and Metabolism. 86. 107–118. 55 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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