Yayun Qin

585 total citations
17 papers, 283 citations indexed

About

Yayun Qin is a scholar working on Molecular Biology, Cell Biology and Ophthalmology. According to data from OpenAlex, Yayun Qin has authored 17 papers receiving a total of 283 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 6 papers in Cell Biology and 4 papers in Ophthalmology. Recurrent topics in Yayun Qin's work include Retinal Development and Disorders (9 papers), Zebrafish Biomedical Research Applications (5 papers) and Retinal Diseases and Treatments (4 papers). Yayun Qin is often cited by papers focused on Retinal Development and Disorders (9 papers), Zebrafish Biomedical Research Applications (5 papers) and Retinal Diseases and Treatments (4 papers). Yayun Qin collaborates with scholars based in China, United Kingdom and United States. Yayun Qin's co-authors include Mugen Liu, Fei Liu, Shanshan Yu, Zhaohui Tang, Xuebin Hu, Xinhua Shu, Zhaojing Lu, Jingzhen Li, Xiliang Liu and Yuwen Huang and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Scientific Reports.

In The Last Decade

Yayun Qin

16 papers receiving 283 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yayun Qin China	11	221	76	68	44	42	17	283
Amna Z. Shah United Kingdom	8	270 1.2×	65 0.9×	98 1.4×	67 1.5×	24 0.6×	10	312
María Isabel López-Molina Spain	12	287 1.3×	41 0.5×	130 1.9×	70 1.6×	45 1.1×	18	351
Irene Marcos Spain	11	212 1.0×	42 0.6×	53 0.8×	85 1.9×	37 0.9×	21	290
Divya Ail France	9	278 1.3×	43 0.6×	83 1.2×	67 1.5×	65 1.5×	14	338
Zixi Sun China	11	224 1.0×	32 0.4×	110 1.6×	67 1.5×	40 1.0×	37	304
Gregory B. Willer United States	10	345 1.6×	175 2.3×	43 0.6×	53 1.2×	44 1.0×	12	438
África Sandonís Spain	7	204 0.9×	34 0.4×	21 0.3×	46 1.0×	65 1.5×	9	264
Lisette Hetterschijt Netherlands	10	339 1.5×	92 1.2×	51 0.8×	95 2.2×	34 0.8×	12	381
Holly Y. Chen United States	10	292 1.3×	26 0.3×	44 0.6×	81 1.8×	110 2.6×	14	333
Christy Stotler United States	5	234 1.1×	41 0.5×	24 0.4×	98 2.2×	23 0.5×	8	329

Countries citing papers authored by Yayun Qin

Since Specialization

Citations

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

Fields of papers citing papers by Yayun Qin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yayun Qin

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

All Works

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17 of 17 papers shown

Hu, Hualei, Yayun Qin, Zhen Qu, et al.. (2024). The Zpr-3 Antibody Recognizes the 320–354 Region of Rho and Labels Both Rods and Green Cones in Zebrafish. Zebrafish. 21(6). 394–400.

Li, Hui, Chengcheng Zhang, Yayun Qin, et al.. (2023). Prenatal diagnosis and outcomes in 320 fetuses with nasal bone anomalies. Frontiers in Genetics. 14. 1170720–1170720. 1 indexed citations

Qin, Yayun, Nian Liu, Lijun Liu, et al.. (2023). Prenatal whole-exome sequencing for fetal structural anomalies: a retrospective analysis of 145 Chinese cases. BMC Medical Genomics. 16(1). 262–262. 10 indexed citations

Li, Hui, Yi Song, Jun Du, et al.. (2023). Identification of a novel 10.3 kb deletion causing α0-thalassemia by third-generation sequencing: Pedigree analysis and genetic diagnosis. Clinical Biochemistry. 113. 64–69. 4 indexed citations

Liu, Xiliang, Shanshan Han, Fei Liu, et al.. (2023). Retinal degeneration in rpgra mutant zebrafish. Frontiers in Cell and Developmental Biology. 11. 1169941–1169941. 1 indexed citations

Liu, Fei, Yayun Qin, Yuwen Huang, et al.. (2022). Rod genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor composition and progressive retinal degeneration. PLoS Genetics. 18(3). e1009841–e1009841. 13 indexed citations

Qin, Yayun, Hui Xu, H. J. Yang, et al.. (2022). A feasibility study of noninvasive prenatal diagnosis in facioscapulohumeral muscular dystrophy type 1 in a Chinese family. Frontiers in Genetics. 13. 1046096–1046096. 2 indexed citations

Li, Jingzhen, Fei Liu, Yuexia Lv, et al.. (2021). Prpf31 is essential for the survival and differentiation of retinal progenitor cells by modulating alternative splicing. Nucleic Acids Research. 49(4). 2027–2043. 28 indexed citations

Qin, Yayun, Shanshan Yu, Jingzhen Li, et al.. (2020). A large deletion spanning PITX2 and PANCR in a Chinese family with Axenfeld-Rieger syndrome.. PubMed. 26. 670–678. 7 indexed citations

10.

Lu, Zhaojing, Xuebin Hu, James Reilly, et al.. (2019). Deletion of the transmembrane protein Prom1b in zebrafish disrupts outer-segment morphogenesis and causes photoreceptor degeneration. Journal of Biological Chemistry. 294(38). 13953–13963. 27 indexed citations

11.

Qu, Zhen, Fulton Wong, Shanshan Yu, et al.. (2019). Knocking out lca5 in zebrafish causes cone-rod dystrophy due to impaired outer segment protein trafficking. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1865(10). 2694–2705. 23 indexed citations

12.

Hu, Xuebin, Zhaojing Lu, Shanshan Yu, et al.. (2018). CERKL regulates autophagy via the NAD-dependent deacetylase SIRT1. Autophagy. 15(3). 453–465. 51 indexed citations

13.

Liu, Fei, Yayun Qin, Shanshan Yu, et al.. (2017). Pathogenic mutations in retinitis pigmentosa 2 predominantly result in loss of RP2 protein stability in humans and zebrafish. Journal of Biological Chemistry. 292(15). 6225–6239. 13 indexed citations

14.

Lu, Zhaojing, Xuebin Hu, Fei Liu, et al.. (2017). Ablation of EYS in zebrafish causes mislocalisation of outer segment proteins, F-actin disruption and cone-rod dystrophy. Scientific Reports. 7(1). 46098–46098. 49 indexed citations

15.

Liu, Ying, Jiuxiang Wang, Yayun Qin, et al.. (2016). Identification of three mutations in the MVK gene in six patients associated with disseminated superficial actinic porokeratosis. Clinica Chimica Acta. 454. 124–129. 10 indexed citations

16.

Gao, Meng, Su Zhang, Chunjie Liu, et al.. (2016). Whole exome sequencing identifies a novel NRL mutation in a Chinese family with autosomal dominant retinitis pigmentosa.. PubMed. 22. 234–42. 12 indexed citations

17.

Liu, Fei, Jiaxiang Chen, Shanshan Yu, et al.. (2015). Knockout ofRP2decreases GRK1 and rod transducin subunits and leads to photoreceptor degeneration in zebrafish. Human Molecular Genetics. 24(16). 4648–4659. 32 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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