Xiaoyun Jia

3.6k total citations
115 papers, 2.7k citations indexed

About

Xiaoyun Jia is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Xiaoyun Jia has authored 115 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 83 papers in Molecular Biology, 52 papers in Ophthalmology and 31 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Xiaoyun Jia's work include Retinal Development and Disorders (42 papers), Retinal Diseases and Treatments (36 papers) and Mitochondrial Function and Pathology (25 papers). Xiaoyun Jia is often cited by papers focused on Retinal Development and Disorders (42 papers), Retinal Diseases and Treatments (36 papers) and Mitochondrial Function and Pathology (25 papers). Xiaoyun Jia collaborates with scholars based in China, United States and New Zealand. Xiaoyun Jia's co-authors include Qingjiong Zhang, Shiqiang Li, Xueshan Xiao, Xiangming Guo, Panfeng Wang, Wenmin Sun, Yong‐Gang Yao, A‐Mei Zhang, J. Fielding Hejtmancik and Li Huang and has published in prestigious journals such as PLoS ONE, Brain and Biochemistry.

In The Last Decade

Xiaoyun Jia

112 papers receiving 2.7k citations

Peers

Xiaoyun Jia

OPHTH

RNMI

GENET

EPIDE

Xiangming Guo China

Xueshan Xiao China

Arif O. Khan Saudi Arabia

Gavin Arno United Kingdom

Motokazu Tsujikawa Japan

Alice E. Davidson United Kingdom

Coral G. Chamberlain Australia

Camiel J.F. Boon Netherlands

Jill Urquhart United Kingdom

Jana Zernant United States

Xiangming Guo China

Xiaoyun Jia

2.0k ×1.0

1.4k ×1.2

OPHTH

661 ×1.0

RNMI

612 ×1.1

GENET

528 ×1.1

EPIDE

Citations per year, relative to Xiaoyun Jia Xiaoyun Jia (= 1×) peers Xiangming Guo

Countries citing papers authored by Xiaoyun Jia

Since Specialization

Citations

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

Fields of papers citing papers by Xiaoyun Jia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiaoyun Jia

This figure shows the co-authorship network connecting the top 25 collaborators of Xiaoyun Jia. A scholar is included among the top collaborators of Xiaoyun Jia 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 Xiaoyun Jia. Xiaoyun Jia 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

Zhen, Yi, Yingwei Wang, Jie Liu, et al.. (2025). Retinitis Pigmentosa‐Associated Gene TRIM49 Regulates ULK1‐Mediated Autophagy and Photoreceptor Phagocytosis by the Retinal Pigment Epithelium. Advanced Science. 12(43). e12305–e12305.

Jia, Xiaoyun, et al.. (2025). QTL Mapping and Candidate Gene Analysis for Cotton Fiber Quality and Early Maturity Using F2 and F3 Generations. Plants. 14(7). 1063–1063.

Xiao, Xueshan, Wenmin Sun, Shiqiang Li, et al.. (2024). Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia. Journal of Translational Medicine. 22(1). 75–75. 7 indexed citations

Wang, Panfeng, Shiqiang Li, Yi Jiang, et al.. (2024). Clinical and genetic landscape of optic atrophy in 826 families: insights from 50 nuclear genes. Brain. 148(5). 1604–1620. 2 indexed citations

Wang, Yingwei, Yi Jiang, Shiqiang Li, et al.. (2024). Variant and clinical landscape of Leber hereditary optic neuropathy based on 1516 families with mtDNA variants in a tertiary centre. British Journal of Ophthalmology. 108(9). 1318–1327. 2 indexed citations

Zhen, Yi, Xueshan Xiao, Shiqiang Li, et al.. (2023). Clinical and Genetic Features of NR2E3-Associated Retinopathy: A Report of Eight Families with a Longitudinal Study and Literature Review. Genes. 14(8). 1525–1525. 3 indexed citations

Wang, Yingwei, Yi Jiang, Yi Zhen, et al.. (2023). New Insight into the Genotype-Phenotype Correlation of PRPH2-Related Diseases Based on a Large Chinese Cohort and Literature Review. International Journal of Molecular Sciences. 24(7). 6728–6728. 6 indexed citations

Li, Shiqiang, Yi Jiang, Zhen Yi, et al.. (2023). Pathogenic Variants in CEP290 or IQCB1 Cause Earlier-Onset Retinopathy in Senior-Loken Syndrome Compared to Those in INVS, NPHP3, or NPHP4. American Journal of Ophthalmology. 252. 188–204. 8 indexed citations

Wang, Yingwei, Xueshan Xiao, Xueqing Li, et al.. (2022). Genetic and clinical landscape ofARR3-associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritance. British Journal of Ophthalmology. 107(10). 1545–1553. 19 indexed citations

10.

Sun, Wenmin, Xueshan Xiao, Shiqiang Li, et al.. (2021). Clinical and genetic features of retinoschisis in 120 families withRS1mutations. British Journal of Ophthalmology. 107(3). 367–372. 11 indexed citations

11.

Wang, Panfeng, Xiaoyun Jia, Wenmin Sun, et al.. (2021). Pathogenicity evaluation and the genotype–phenotype analysis of OPA1 variants. Molecular Genetics and Genomics. 296(4). 845–862. 5 indexed citations

12.

Xiao, Xueshan, Shiqiang Li, Xiaoyun Jia, et al.. (2021). Severe Exudative Vitreoretinopathy as a Common Feature for CTNNB1, KIF11 and NDP Variants Plus Sector Degeneration for KIF11. American Journal of Ophthalmology. 235. 178–187. 5 indexed citations

13.

Zhen, Yi, Wenmin Sun, Xueshan Xiao, et al.. (2021). Novel variants in GUCY2D causing retinopathy and the genotype-phenotype correlation. Experimental Eye Research. 208. 108637–108637. 7 indexed citations

14.

Sun, Wenmin, Shiqiang Li, Xiaoyun Jia, et al.. (2020). Structural variations in a non-coding region at 1q32.1 are responsible for the NYS7 locus in two large families. Human Genetics. 139(8). 1057–1064. 4 indexed citations

15.

Sun, Wenmin, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, & Qingjiong Zhang. (2020). A novel deep intronic COL2A1 mutation in a family with early‐onset high myopia/ocular‐only Stickler syndrome. Ophthalmic and Physiological Optics. 40(3). 281–288. 13 indexed citations

16.

Sun, Wenmin, Xueshan Xiao, Shiqiang Li, et al.. (2019). CPSF1 mutations are associated with early-onset high myopia and involved in retinal ganglion cell axon projection. Human Molecular Genetics. 28(12). 1959–1970. 29 indexed citations

17.

Xu, Yan, Liping Guan, Xueshan Xiao, et al.. (2015). Mutation analysis in 129 genes associated with other forms of retinal dystrophy in 157 families with retinitis pigmentosa based on exome sequencing.. PubMed. 21. 477–86. 31 indexed citations

18.

Li, Jie, Xiaoyun Jia, Shiqiang Li, Shaohua Fang, & Xiangming Guo. (2014). Mutation survey of candidate genes in 40 Chinese patients with congenital ectopia lentis.. PubMed. 20. 1017–24. 14 indexed citations

19.

Huang, Li, Qingyan Zhang, Shiqiang Li, et al.. (2013). Exome Sequencing of 47 Chinese Families with Cone-Rod Dystrophy: Mutations in 25 Known Causative Genes. PLoS ONE. 8(6). e65546–e65546. 53 indexed citations

20.

Zhang, Qingjiong, Shiqiang Li, Xueshan Xiao, Xiaoyun Jia, & Xiangming Guo. (2007). The 208delG Mutation inFSCN2Does Not Associate with Retinal Degeneration in Chinese Individuals. Investigative Ophthalmology & Visual Science. 48(2). 530–530. 34 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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