Xiang Lin

653 total citations
33 papers, 369 citations indexed

About

Xiang Lin is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Xiang Lin has authored 33 papers receiving a total of 369 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 9 papers in Genetics. Recurrent topics in Xiang Lin's work include Hereditary Neurological Disorders (9 papers), Neurogenetic and Muscular Disorders Research (9 papers) and Neurological diseases and metabolism (6 papers). Xiang Lin is often cited by papers focused on Hereditary Neurological Disorders (9 papers), Neurogenetic and Muscular Disorders Research (9 papers) and Neurological diseases and metabolism (6 papers). Xiang Lin collaborates with scholars based in China, United States and Czechia. Xiang Lin's co-authors include Wan‐Jin Chen, En‐Lin Dong, Ning Wang, Miao Zhao, Xiao-Hong Lin, J. He, Lixiang Ma, Ying‐Qian Lu, Lianyun Li and Min Wu and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Xiang Lin

29 papers receiving 367 citations

Peers

Xiang Lin

CMN

GENET

NEURO

Yumiko Azuma Japan

Jacek Pilch Poland

Israel Ben‐Dor Israel

Mark Greenslade United Kingdom

Seyedmehdi Shojaee United States

Stephanie N. Oprescu United States

Francesca Tagliavini Italy

Thomas Palm Germany

Bing Lu-jun China

Sabrina A. Volpi United States

Yumiko Azuma Japan

Xiang Lin

233 ×1.1

77 ×0.6

CMN

84 ×1.0

GENET

47 ×0.6

NEURO

53 ×1.4

Citations per year, relative to Xiang Lin Xiang Lin (= 1×) peers Yumiko Azuma

Countries citing papers authored by Xiang Lin

Since Specialization

Citations

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

Fields of papers citing papers by Xiang Lin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiang Lin

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

Zhang, Tongtong, Hui‐Zhen Su, Shuyuan Wang, et al.. (2025). Lysosomal and mTORC1 signaling dysregulation underpin the pathology of spastic paraplegia type 80. Nature Communications. 16(1). 9833–9833.

Yu, Sulan, Meiling Wu, Philip H. Li, et al.. (2025). Calycosin synergizes with methotrexate in the treatment of Sjögren’s disease by targeting BATF in T follicular helper cells. Acta Pharmacologica Sinica. 46(7). 1990–2005.

Lin, Xiang, et al.. (2025). USP10-mediated Ku70/80 stabilization inhibits PANoptosis and promotes chemoresistance in colorectal cancer. Oncogene. 44(44). 4239–4253.

Liu, Songyi, et al.. (2024). Modulation of YBX1-mediated PANoptosis inhibition by PPM1B and USP10 confers chemoresistance to oxaliplatin in gastric cancer. Cancer Letters. 587. 216712–216712. 30 indexed citations

Jiang, Junyi, et al.. (2024). A pseudo‐homozygous missense variant and Alu‐mediated exon 5 deletion in FARS2 causing spastic paraplegia 77. Annals of Clinical and Translational Neurology. 11(11). 3019–3024.

Su, Hui‐Zhen, Xiang Lin, Yan Shi, et al.. (2024). ESCRT-I protein UBAP1 controls ventricular expansion and cortical neurogenesis via modulating adherens junctions of radial glial cells. Cell Reports. 43(3). 113818–113818. 2 indexed citations

Wang, Chenyu, Qiaoyun Long, Zhuo Cao, et al.. (2024). The roles of nuclear orphan receptor NR2F6 in anti-viral innate immunity. PLoS Pathogens. 20(6). e1012271–e1012271. 1 indexed citations

Lin, Xiang, Junyi Jiang, Daojun Hong, et al.. (2023). Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular Characterization. Movement Disorders. 39(1). 152–163. 3 indexed citations

Mao, Shiqi, Shuo Yang, Xinyu Liu, et al.. (2023). Molecular correlation of response to pyrotinib in advanced NSCLC with HER2 mutation: biomarker analysis from two phase II trials. Experimental Hematology and Oncology. 12(1). 53–53. 5 indexed citations

10.

Shi, Yan, Shi‐Rui Gan, Xiang Lin, et al.. (2023). Clinical and genetic heterogeneity of adult polyglucosan body disease caused by GBE1 biallelic mutations in China. Genes & Diseases. 11(5). 101140–101140. 1 indexed citations

11.

Li, Qinglan, Xiang Lin, Yali Yu, et al.. (2021). Genome-wide profiling in colorectal cancer identifies PHF19 and TBC1D16 as oncogenic super enhancers. Nature Communications. 12(1). 6407–6407. 63 indexed citations

12.

Chen, Yijun, Mengwen Wang, En‐Lin Dong, et al.. (2019). Chinese patients with adrenoleukodystrophy and Zellweger spectrum disorder presenting with hereditary spastic paraplegia. Parkinsonism & Related Disorders. 65. 256–260. 10 indexed citations

13.

Ju, Lingao, et al.. (2018). Characterization of WDR20: A new regulator of the ERAD machinery. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1865(7). 970–980. 4 indexed citations

14.

Ju, Lingao, Yuan Zhu, Qiaoyun Long, et al.. (2018). SPOP suppresses prostate cancer through regulation of CYCLIN E1 stability. Cell Death and Differentiation. 26(6). 1156–1168. 39 indexed citations

15.

Dong, En‐Lin, Chong Wang, Shuang Wu, et al.. (2018). Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China. Molecular Neurodegeneration. 13(1). 36–36. 55 indexed citations

16.

Zhang, Qi‐Jie, Jin-Jing Li, Xiang Lin, et al.. (2017). Modeling the phenotype of spinal muscular atrophy by the direct conversion of human fibroblasts to motor neurons. Oncotarget. 8(7). 10945–10953. 21 indexed citations

17.

Zhang, Qi‐Jie, Xiang Lin, Jin-Jing Li, et al.. (2017). Application of urine cells in drug intervention for spinal muscular atrophy. Experimental and Therapeutic Medicine. 14(3). 1993–1998. 5 indexed citations

18.

Zhang, Qijie, J. He, Ni Wang, et al.. (2013). Noninvasive urine-derived cell lines derived from neurological genetic patients. Neuroreport. 24(4). 161–166. 5 indexed citations

19.

Zhou, Hao, Zhixian Wu, Longteng Ma, et al.. (2011). Assessing Immunologic Function Through CD4 T-lymphocyte Ahenosine Triphosphate Levels by ImmuKnow Assay in Chinese Patients Following Renal Transplantation. Transplantation Proceedings. 43(7). 2574–2578. 9 indexed citations

20.

Gao, Peng, et al.. (2007). Selection of antisense oligonucleotides for reversal of multidrug resistance in breast carcinoma cells. Cytotherapy. 9(8). 795–801. 5 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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