Yu-jin Qu

400 total citations
30 papers, 290 citations indexed

About

Yu-jin Qu is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Yu-jin Qu has authored 30 papers receiving a total of 290 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 25 papers in Genetics and 9 papers in Surgery. Recurrent topics in Yu-jin Qu's work include Neurogenetic and Muscular Disorders Research (25 papers), RNA modifications and cancer (24 papers) and RNA Research and Splicing (11 papers). Yu-jin Qu is often cited by papers focused on Neurogenetic and Muscular Disorders Research (25 papers), RNA modifications and cancer (24 papers) and RNA Research and Splicing (11 papers). Yu-jin Qu collaborates with scholars based in China, Egypt and United States. Yu-jin Qu's co-authors include Fang Song, Jin-li Bai, Yuwei Jin, Hong Wang, Wenhui Zhang, Yanyu Lü, Hong Wang, Yan Li, Juan Du and Yan Li and has published in prestigious journals such as Human Molecular Genetics, Gene and Clinica Chimica Acta.

In The Last Decade

Yu-jin Qu

30 papers receiving 288 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yu-jin Qu China	11	253	242	124	16	9	30	290
Eilidh Somers United Kingdom	6	217 0.9×	185 0.8×	85 0.7×	10 0.6×	14 1.6×	6	232
Matthew Mailman United States	4	273 1.1×	278 1.1×	156 1.3×	15 0.9×	8 0.9×	5	342
Eva Also‐Rallo Spain	10	232 0.9×	213 0.9×	113 0.9×	18 1.1×	8 0.9×	11	298
Adoración Venceslá Spain	7	294 1.2×	276 1.1×	181 1.5×	19 1.2×	16 1.8×	9	370
Loren Price Australia	4	140 0.6×	148 0.6×	43 0.3×	10 0.6×	4 0.4×	4	237
Dongni Zhao China	5	40 0.2×	43 0.2×	78 0.6×	17 1.1×	8 0.9×	10	265
Poh Sim Low Singapore	5	75 0.3×	78 0.3×	28 0.2×	9 0.6×	5 0.6×	5	116
David Valdivia United States	4	90 0.4×	78 0.3×	26 0.2×	7 0.4×	4 0.4×	5	109
Maren Freigang Germany	7	83 0.3×	58 0.2×	31 0.3×	9 0.6×	9 1.0×	12	99
Irene Hadjidemetriou United Kingdom	6	33 0.1×	79 0.3×	51 0.4×	34 2.1×	5 0.6×	9	179

Countries citing papers authored by Yu-jin Qu

Since Specialization

Citations

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

Fields of papers citing papers by Yu-jin Qu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yu-jin Qu. 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 Yu-jin Qu. The network helps show where Yu-jin Qu may publish in the future.

Co-authorship network of co-authors of Yu-jin Qu

This figure shows the co-authorship network connecting the top 25 collaborators of Yu-jin Qu. A scholar is included among the top collaborators of Yu-jin Qu 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 Yu-jin Qu. Yu-jin Qu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

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

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

Ye, Jin, et al.. (2023). Research of pavement crack detection system based on image processing. 4–4. 3 indexed citations

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

Qu, Yu-jin, Xiaohui Li, Junting Liu, et al.. (2021). Bone mineral density and its influencing factors in Chinese children with spinal muscular atrophy types 2 and 3. BMC Musculoskeletal Disorders. 22(1). 729–729. 6 indexed citations

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

Wang, Jia, Jin-li Bai, Hong Wang, et al.. (2021). Antisense oligonucleotides targeting the SMN2 promoter region enhance SMN2 expression in spinal muscular atrophy cell lines and mouse model. Human Molecular Genetics. 31(10). 1635–1650. 8 indexed citations

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

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

10.

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

11.

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

12.

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

13.

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

14.

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

15.

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

16.

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

17.

Qu, Yu-jin, Liwen Wang, Yan Li, et al.. (2014). Subtle Mutation Detection of SMN1 Gene in Chinese Spinal Muscular Atrophy Patients: Implication of Molecular Diagnostic Procedure for SMN1 Gene Mutations. Genetic Testing and Molecular Biomarkers. 18(8). 546–551. 14 indexed citations

18.

Qu, Yu-jin, Jin-li Bai, Liwen Wang, et al.. (2014). Association of Copy Numbers of Survival Motor Neuron Gene 2 and Neuronal Apoptosis Inhibitory Protein Gene With the Natural History in a Chinese Spinal Muscular Atrophy Cohort. Journal of Child Neurology. 30(4). 429–436. 29 indexed citations

19.

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

20.

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

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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