Pengfei Lin

1.3k total citations
66 papers, 872 citations indexed

About

Pengfei Lin is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Pengfei Lin has authored 66 papers receiving a total of 872 indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 21 papers in Cellular and Molecular Neuroscience and 10 papers in Genetics. Recurrent topics in Pengfei Lin's work include Muscle Physiology and Disorders (12 papers), Mitochondrial Function and Pathology (10 papers) and Hereditary Neurological Disorders (10 papers). Pengfei Lin is often cited by papers focused on Muscle Physiology and Disorders (12 papers), Mitochondrial Function and Pathology (10 papers) and Hereditary Neurological Disorders (10 papers). Pengfei Lin collaborates with scholars based in China, United States and Australia. Pengfei Lin's co-authors include Chuanzhu Yan, Yuying Zhao, Yaoqin Gong, Bing Wen, Kunqian Ji, Weibo Niu, Jiayong Wang, Jun Niu, Huijie Gao and Enyu Liu and has published in prestigious journals such as Brain, Neurology and Annals of Neurology.

In The Last Decade

Pengfei Lin

60 papers receiving 865 citations

Peers

Pengfei Lin

CMN

Xavier Guillonneau France

Sandra Meulemans Belgium

Julien Saint‐Pol France

Matthew Hayden United Kingdom

Olivier R. Baris France

Keiko Fujiki Japan

Juan Amaral United States

M Uyama Japan

José‐Daniel Aroca‐Aguilar Spain

Veronika Boczonadi United Kingdom

Xavier Guillonneau France

Pengfei Lin

1.1k ×2.4

120 ×0.7

CMN

78 ×0.5

65 ×0.5

165 ×1.6

Citations per year, relative to Pengfei Lin Pengfei Lin (= 1×) peers Xavier Guillonneau

Countries citing papers authored by Pengfei Lin

Since Specialization

Citations

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

Fields of papers citing papers by Pengfei Lin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pengfei Lin

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

Feng, Qixiang, He Ping Zhou, Pengfei Lin, et al.. (2025). An Atorvastatin/Ferrostatin-1 Codelivered Hybrid Exosome/Liposome System for Combinational Ferroptosis Inhibition, Inflammation Suppression, Efferocytosis Promotion, and Macrophage Reprogramming in Atherosclerosis Treatment. ACS Applied Materials & Interfaces. 17(25). 36542–36556. 3 indexed citations

Chen, Yujing, Sujuan Sun, Ni Gao, et al.. (2025). CSF Aβ, Tau, Axonal, Synaptic, Glial, Neural, and Inflammatory Biomarkers in Patients With Sporadic Amyotrophic Lateral Sclerosis. Neurology. 105(7). e213914–e213914.

Fu, Lijun, Lining Zhang, Kai Shao, et al.. (2024). Development of differential diagnostic models for distinguishing between limb-girdle muscular dystrophy and idiopathic inflammatory myopathy. Arthritis Research & Therapy. 26(1). 215–215.

Yang, Mengqi, et al.. (2024). Expanding the spectrum of HSPB8-related myopathy: a novel mutation causing atypical pediatric-onset axial and limb-girdle involvement with autophagy abnormalities and molecular dynamics studies. Journal of Human Genetics. 70(3). 159–165. 1 indexed citations

Sun, Sujuan, Yujing Chen, Yan Yun, et al.. (2024). Elevated peripheral inflammation is associated with choroid plexus enlargement in independent sporadic amyotrophic lateral sclerosis cohorts. Fluids and Barriers of the CNS. 21(1). 83–83. 5 indexed citations

Liu, Shuangwu, Qingguo Ren, Yujing Chen, et al.. (2023). Glymphatic dysfunction in patients with early-stage amyotrophic lateral sclerosis. Brain. 147(1). 100–108. 45 indexed citations

Wang, Guangyu, et al.. (2022). A novel mutation in HINT1 gene causes autosomal recessive axonal neuropathy with neuromyotonia, effective treatment with carbamazepine and review of the literature. Acta Neurologica Belgica. 122(5). 1305–1312. 2 indexed citations

Lin, Pengfei, et al.. (2022). Clinical, genetic, and pathological characterization of GNE myopathy in China. Neurological Sciences. 43(7). 4483–4491. 6 indexed citations

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

10.

Zhao, Bing, Wei Jiang, Tingjun Dai, et al.. (2021). Clinical, pathological, and molecular genetic analysis of 7 Chinese patients with hereditary myopathy with early respiratory failure. Neurological Sciences. 43(5). 3371–3380.

11.

Jiang, Wei, et al.. (2020). Idebenone Protects against Atherosclerosis in Apolipoprotein E-Deficient Mice Via Activation of the SIRT3-SOD2-mtROS Pathway. Cardiovascular Drugs and Therapy. 35(6). 1129–1145. 34 indexed citations

12.

Bian, Xianli, Pengfei Lin, Jiangxia Li, et al.. (2018). Whole-Genome Linkage Analysis with Whole-Exome Sequencing Identifies a Novel Frameshift Variant in NEFH in a Chinese Family with Charcot-Marie-Tooth 2: A Novel Variant in NEFH for Charcot-Marie-Tooth 2. Neurodegenerative Diseases. 18(2-3). 74–83. 7 indexed citations

13.

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

14.

Lin, Pengfei, et al.. (2016). DNM2 mutations in Chinese Han patients with centronuclear myopathy. Neurological Sciences. 37(6). 995–998. 6 indexed citations

15.

Lin, Pengfei, Weibo Niu, Cheng Peng, Zhaoyang Zhang, & Jun Niu. (2015). The role of TAK1 expression in thyroid cancer.. PubMed. 8(11). 14449–56. 11 indexed citations

16.

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

17.

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

18.

Gao, Huijie, Cheng Peng, Benjia Liang, et al.. (2014). β6 integrin induces the expression of metalloproteinase-3 and metalloproteinase-9 in colon cancer cells via ERK-ETS1 pathway. Cancer Letters. 354(2). 427–437. 43 indexed citations

19.

Lin, Pengfei, Wei Li, Bing Wen, et al.. (2012). Novel PNPLA2 gene mutations in Chinese Han patients causing neutral lipid storage disease with myopathy. Journal of Human Genetics. 57(10). 679–681. 19 indexed citations

20.

Ju, Shiqiang, et al.. (2009). Experiment on Production in Vitro of Porcine Somatic Cell Cloned Embryos. Zhongguo nongye Kexue. 42(4). 1386–1393. 1 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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