Xinxin Liao

1.6k total citations · 1 hit paper
67 papers, 921 citations indexed

About

Xinxin Liao is a scholar working on Molecular Biology, Physiology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Xinxin Liao has authored 67 papers receiving a total of 921 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 24 papers in Physiology and 16 papers in Cellular and Molecular Neuroscience. Recurrent topics in Xinxin Liao's work include Alzheimer's disease research and treatments (17 papers), Hereditary Neurological Disorders (8 papers) and Genetic Neurodegenerative Diseases (8 papers). Xinxin Liao is often cited by papers focused on Alzheimer's disease research and treatments (17 papers), Hereditary Neurological Disorders (8 papers) and Genetic Neurodegenerative Diseases (8 papers). Xinxin Liao collaborates with scholars based in China, United States and Canada. Xinxin Liao's co-authors include Lu Shen, Bin Jiao, Beisha Tang, Xuewen Xiao, Lina Guo, Yafang Zhou, Junling Wang, Xixi Liu, Qijie Yang and Zhenhua Yuan and has published in prestigious journals such as Scientific Reports, Environmental Pollution and Journal of Hepatology.

In The Last Decade

Xinxin Liao

65 papers receiving 908 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Neural biomarker diagnosis and prediction to mild cognitive impairment and Alzheimer’s disease using EEG technology

2023 81 citations Bin Jiao, Rihui Li et al. Alzheimer s Research & Therapy profile →

Peers

Xinxin Liao

PHYSI

CMN

NEURO

Xiaoying Liu China

Huajun Yang China

Jiaji Lin China

Yuanyuan Ma China

Lingli Yang Japan

Lixian Xu China

Luca Lorenzini Italy

Yin Liu United States

Meng‐Han Tsai Taiwan

Xiaoying Liu China

Xinxin Liao

348 ×1.2

289 ×1.5

PHYSI

157 ×1.2

CMN

72 ×0.6

NEURO

112 ×1.1

NEURO

Citations per year, relative to Xinxin Liao Xinxin Liao (= 1×) peers Xiaoying Liu

Countries citing papers authored by Xinxin Liao

Since Specialization

Citations

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

Fields of papers citing papers by Xinxin Liao

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xinxin Liao

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

Chen, Huaqiu, Yijia Feng, Mingjing Liu, et al.. (2025). Activation of AMPK by GLP-1R agonists mitigates Alzheimer-related phenotypes in transgenic mice. Nature Aging. 5(6). 1097–1113. 12 indexed citations

Liao, Xinxin, et al.. (2024). A Case of a Patient With MYH2-Associated Myopathy Presenting With a Chief Complaint of Hand Tremor. Tremor and Other Hyperkinetic Movements. 14(1). 50–50.

Zhang, Zhongyang, et al.. (2024). Sleeve gastrectomy ameliorates renal injury in obesity-combined hyperuricemic nephropathy mice by modulating the AMPK/Nrf2/ABCG2 pathway. Scientific Reports. 14(1). 3 indexed citations

Yang, Qijie, Bin Jiao, Weiwei Zhang, et al.. (2023). Clinical features of progressive supranuclear palsy. Frontiers in Aging Neuroscience. 15. 1229491–1229491. 5 indexed citations

Jiao, Bin, Rihui Li, Hui Zhou, et al.. (2023). Neural biomarker diagnosis and prediction to mild cognitive impairment and Alzheimer’s disease using EEG technology. Alzheimer s Research & Therapy. 15(1). 32–32. 81 indexed citations breakdown →

Jiang, Yaling, Xuewen Xiao, Xixi Liu, et al.. (2023). GSNgene frameshift mutations in Alzheimer’s disease. Journal of Neurology Neurosurgery & Psychiatry. 94(6). 436–447. 5 indexed citations

Liu, Xixi, Yaling Jiang, Bin Jiao, et al.. (2023). Brain-derived extracellular vesicles promote bone-fat imbalance in Alzheimer's disease. International Journal of Biological Sciences. 19(8). 2409–2427. 23 indexed citations

Xiao, Xuewen, Hui Liu, Lu Zhou, et al.. (2022). The associations of APP, PSEN1, and PSEN2 genes with Alzheimer's disease: A large case–control study in Chinese population. CNS Neuroscience & Therapeutics. 29(1). 122–128. 5 indexed citations

Wang, Xin, Bin Jiao, Hui Liu, et al.. (2022). Machine learning based on Optical Coherence Tomography images as a diagnostic tool for Alzheimer's disease. CNS Neuroscience & Therapeutics. 28(12). 2206–2217. 31 indexed citations

10.

Jiao, Bin, Xuewen Xiao, Lu Zhou, et al.. (2021). Mutations in GBA, SNCA, and VPS35 are not associated with Alzheimer’s disease in a Chinese population: a case-control study. Neural Regeneration Research. 17(3). 682–682. 7 indexed citations

11.

Wu, Jing, Jiayan Li, Yanwei Liu, et al.. (2021). Tannic acid repair of zearalenone-induced damage by regulating the death receptor and mitochondrial apoptosis signaling pathway in mice. Environmental Pollution. 287. 117557–117557. 27 indexed citations

12.

Jiao, Bin, Ling Weng, Yafang Zhou, et al.. (2020). Lack of association between LGMN and Alzheimer’s disease in the Southern Han Chinese population. European Journal of Neuroscience. 52(8). 4009–4017. 5 indexed citations

13.

Liao, Xinxin, Fang Cai, Zhanfang Sun, et al.. (2020). Identification of Alzheimer’s disease–associated rare coding variants in the ECE2 gene. JCI Insight. 5(4). 21 indexed citations

14.

Jiang, Yaling, Bin Jiao, Xinxin Liao, et al.. (2020). Analyses Mutations in GSN, CST3, TTR, and ITM2B Genes in Chinese Patients With Alzheimer’s Disease. Frontiers in Aging Neuroscience. 12. 581524–581524. 6 indexed citations

15.

Jiao, Bin, Zhengmao Hu, Juan Du, et al.. (2020). Homozygosity mapping and next generation sequencing for the genetic diagnosis of hereditary ataxia and spastic paraplegia in consanguineous families. Parkinsonism & Related Disorders. 80. 65–72. 12 indexed citations

16.

Li, Yongyin, Libo Tang, Ling Guo, et al.. (2019). CXCL13-mediated recruitment of intrahepatic CXCR5+CD8+ T cells favors viral control in chronic HBV infection. Journal of Hepatology. 72(3). 420–430. 77 indexed citations

17.

Xing, Wu, Xinxin Liao, Tingting Guan, et al.. (2017). [Value of 1H-MRS on SCA3/MJD diagnosis and clinical course].. PubMed. 42(3). 291–297. 2 indexed citations

18.

Liao, Xinxin, Xinwei Wu, Weihua Liao, et al.. (2017). Resting state fMRI studies in SPG4-linked hereditary spastic paraplegia. Journal of the Neurological Sciences. 384. 1–6. 12 indexed citations

19.

Liao, Xinxin, et al.. (2015). Epigenetic modifications of histone H3 during the transdifferentiation of Thy-1(+) Lin(−) bone marrow cells into hepatocytes. Molecular Medicine Reports. 12(5). 7561–7567. 6 indexed citations

20.

Liao, Xinxin, Juan Du, Yingying Luo, et al.. (2013). Exome sequencing released a case of X-linked adrenoleukodystrophy mimicking recessive hereditary spastic paraplegia. European Journal of Medical Genetics. 56(7). 375–378. 15 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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