Kunqian Ji

1.1k total citations
50 papers, 772 citations indexed

About

Kunqian Ji is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Kunqian Ji has authored 50 papers receiving a total of 772 indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 20 papers in Clinical Biochemistry and 8 papers in Rheumatology. Recurrent topics in Kunqian Ji's work include Mitochondrial Function and Pathology (33 papers), Metabolism and Genetic Disorders (20 papers) and ATP Synthase and ATPases Research (16 papers). Kunqian Ji is often cited by papers focused on Mitochondrial Function and Pathology (33 papers), Metabolism and Genetic Disorders (20 papers) and ATP Synthase and ATPases Research (16 papers). Kunqian Ji collaborates with scholars based in China, United States and Canada. Kunqian Ji's co-authors include Chuanzhu Yan, Kaiming Liu, Wei Wu, Liang Guo, Huixia Lu, Peiyan Shan, Yuying Zhao, Pengfei Lin, Jingwei Lv and Yue‐Bei Luo and has published in prestigious journals such as Journal of the American Chemical Society, Nucleic Acids Research and Neurology.

In The Last Decade

Kunqian Ji

44 papers receiving 764 citations

Peers

Kunqian Ji
Ady Kendler United States
Claudia Morganti Italy
Costanza Lamperti Italy
Dorota Piekutowska‐Abramczuk Poland
Jie Lin China
Rosa Aledo Spain
Emanuela Bottani Italy
Rıza Köksal Özgül Türkiye
Adekunle M. Adesina United States
Edoardo Malfatti France
Ady Kendler United States
Kunqian Ji
Citations per year, relative to Kunqian Ji Kunqian Ji (= 1×) peers Ady Kendler

Countries citing papers authored by Kunqian Ji

Since Specialization
Citations

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

Fields of papers citing papers by Kunqian Ji

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kunqian Ji

This figure shows the co-authorship network connecting the top 25 collaborators of Kunqian Ji. A scholar is included among the top collaborators of Kunqian Ji 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 Kunqian Ji. Kunqian Ji 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.
2.
Li, Yuxuan, Xinchen Lv, Xu Liu, et al.. (2025). Computational design of a high-precision mitochondrial DNA cytosine base editor. Nature Structural & Molecular Biology. 32(12). 2575–2586.
3.
Lin, Yan, et al.. (2024). Queuine ameliorates impaired mitochondrial function caused by mt-tRNAAsn variants. Journal of Translational Medicine. 22(1). 780–780. 1 indexed citations
4.
Ji, Kunqian, Junling Wang, Yuying Zhao, et al.. (2024). The clinical and genetic spectrum of mitochondrial diseases in China: A multicenter retrospective cross‐sectional study. Clinical Genetics. 106(6). 733–744. 2 indexed citations
5.
Lin, Yan, Dongdong Wang, Busu Li, et al.. (2024). Targeting DRP1 with Mdivi-1 to correct mitochondrial abnormalities in ADOA+ syndrome. JCI Insight. 9(15). 16 indexed citations
6.
Lin, Yan, Bin Wang, Fuchen Liu, et al.. (2023). A Missense Variant in AIFM1 Caused Mitochondrial Dysfunction and Intolerance to Riboflavin Deficiency. NeuroMolecular Medicine. 25(4). 489–500. 4 indexed citations
7.
Long, Yuxin, Qiang Li, Zidong Zhang, et al.. (2023). Coupling MoSe2 with Non‐Stoichiometry Ni0.85Se in Carbon Hollow Nanoflowers for Efficient Electrocatalytic Synergistic Effect on Li‐O2 Batteries. Small. 20(10). e2304882–e2304882. 10 indexed citations
8.
Zhao, Yuying, Xiaotian Ma, Yuan Sun, et al.. (2023). A different pattern of clinical, muscle pathology and brain MRI findings in MELAS with mt‐ND variants. Annals of Clinical and Translational Neurology. 10(6). 1035–1045. 6 indexed citations
9.
10.
Yan, Chuanzhu, et al.. (2021). Late-Onset Leukodystrophy Mimicking Hereditary Spastic Paraplegia without Diffuse Leukodystrophy on Neuroimaging. Neuropsychiatric Disease and Treatment. Volume 17. 1451–1458. 7 indexed citations
11.
Lin, Yan, Hong Ren, Dandan Zhao, et al.. (2021). Novel biallelic mutations in POLG gene: large deletion and missense variant associated with PEO. Neurological Sciences. 42(10). 4271–4280. 3 indexed citations
12.
Sun, Yuan, Yan Lin, Dandan Zhao, et al.. (2021). A novel nonsense variant in MT-CO3 causes MELAS syndrome. Neuromuscular Disorders. 31(6). 558–565. 9 indexed citations
13.
Ji, Kunqian, et al.. (2020). “Myo-neuropathy” is commonly associated with mitochondrial tRNALysine mutation. Journal of Neurology. 267(11). 3319–3328. 5 indexed citations
14.
Sun, Yuan‐Ting, et al.. (2019). Clinical research of two cases of late-onset ornithine carbamoyltransferase deficiency. Chin J Neurol. 52(5). 399–405. 1 indexed citations
15.
Ji, Kunqian, Shu Zhang, Chang Liu, et al.. (2019). Late-onset mitochondrial disease in a patient with MELAS and mitochondrial DNA T14487C mutation. Chinese Medical Journal. 132(6). 716–718. 2 indexed citations
16.
Lv, Jingwei, Ling Li, Kunqian Ji, et al.. (2018). Role of the chemokine receptors CXCR3, CXCR4 and CCR7 in the intramuscular recruitment of plasmacytoid dendritic cells in dermatomyositis. Journal of Neuroimmunology. 319. 142–148. 13 indexed citations
17.
Yu, Xiaolin, Chuanzhu Yan, Kunqian Ji, et al.. (2018). Clinical, Neuroimaging, and Pathological Analyses of 13 Chinese Leigh Syndrome Patients with Mitochondrial DNA Mutations. Chinese Medical Journal. 131(22). 2705–2712. 13 indexed citations
18.
Zhao, Lizhen, Kunqian Ji, Yuying Zhao, et al.. (2016). Growth Differentiation Factor 15 Is a Novel Diagnostic Biomarker of Mitochondrial Diseases. Molecular Neurobiology. 54(10). 8110–8116. 45 indexed citations
19.
Lin, Pengfei, Junling Liu, Ming Ren, et al.. (2015). Idebenone protects against oxidized low density lipoprotein induced mitochondrial dysfunction in vascular endothelial cells via GSK3β/β-catenin signalling pathways. Biochemical and Biophysical Research Communications. 465(3). 548–555. 35 indexed citations
20.
Shan, Jingli, Bin Chen, Pengfei Lin, et al.. (2014). Oculopharyngeal Muscular Dystrophy: Phenotypic and Genotypic Studies in a Chinese Population. NeuroMolecular Medicine. 16(4). 782–786. 12 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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