Xiaoliu Shi

1.6k total citations
64 papers, 1.2k citations indexed

About

Xiaoliu Shi is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Xiaoliu Shi has authored 64 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 11 papers in Physiology and 8 papers in Genetics. Recurrent topics in Xiaoliu Shi's work include Ion channel regulation and function (8 papers), Pain Mechanisms and Treatments (5 papers) and Genetic factors in colorectal cancer (4 papers). Xiaoliu Shi is often cited by papers focused on Ion channel regulation and function (8 papers), Pain Mechanisms and Treatments (5 papers) and Genetic factors in colorectal cancer (4 papers). Xiaoliu Shi collaborates with scholars based in China, United States and Canada. Xiaoliu Shi's co-authors include Wen Yi, Xiaotao Duan, Zhiguo Zheng, Yaxian Cheng, Hao Nie, Jiayi Fan, Xiaohui Cang, Haixing Ju, Wei Xie and Kun Xia and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Nature Genetics.

In The Last Decade

Xiaoliu Shi

59 papers receiving 1.1k citations

Peers

Xiaoliu Shi

IMMUN

GENET

Joana Neves United States

John J. Kelly Canada

Dongmei Tang China

Nicholas Matigian Australia

Nicolas Bourmeyster France

Elaine Y.M. Wong United States

Sami S. Amr United States

Francesca Di Leva Italy

Teruhiko Okada Japan

Sonja J. McKeown Australia

Joana Neves United States

Xiaoliu Shi

766 ×1.0

365 ×1.3

133 ×1.0

IMMUN

137 ×1.0

50 ×0.4

GENET

Citations per year, relative to Xiaoliu Shi Xiaoliu Shi (= 1×) peers Joana Neves

Countries citing papers authored by Xiaoliu Shi

Since Specialization

Citations

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

Fields of papers citing papers by Xiaoliu Shi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiaoliu Shi

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

Huang, Hui, et al.. (2025). Clinical and radiological characteristics of adult-onset X-linked adrenoleukodystrophy: a Chinese cohort study and review of the literature. BMC Neurology. 25(1). 428–428.

Peng, Ying, Liangjie Jia, Hu Xiao, et al.. (2025). Cellular Feimin enhances exercise performance by suppressing muscle thermogenesis. Nature Metabolism. 7(1). 84–101. 4 indexed citations

Li, Zhiyuan, Zheng Tian, Xiaoliu Shi, et al.. (2025). Adipose tissue-derived PRXL2A suppresses hepatic lipogenesis in a study with male mice. Nature Communications. 16(1). 6567–6567. 1 indexed citations

Shi, Xiaoliu, et al.. (2024). Perinatal exposure to PBEB aggravates liver injury via macrophage-derived TWEAK in male adult offspring mice under western diet. Journal of Hazardous Materials. 479. 135735–135735. 2 indexed citations

Huang, Hui, et al.. (2022). Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case report. BMC Neurology. 22(1). 168–168. 1 indexed citations

He, Miao, Jia Fang, Weiqian Yan, et al.. (2021). Clinical Presentations and Genetic Characteristics of Late-Onset MADD Due to ETFDH Mutations in Five Patients: A Case Series. Frontiers in Neurology. 12. 747360–747360. 1 indexed citations

Jin, Tao, Xiaoliu Shi, Lingling Lv, et al.. (2020). Preliminary Findings on Proline-Rich Protein 14 as a Diagnostic Biomarker for Parkinson’s Disease. NeuroMolecular Medicine. 23(2). 285–291. 7 indexed citations

Wang, Yongjun, Liang‐Liang Fan, Hui Huang, et al.. (2020). Clinical and Genetic Analyses of 38 Chinese Patients with Peutz‐Jeghers Syndrome. BioMed Research International. 2020(1). 9159315–9159315. 13 indexed citations

Huang, Hui, et al.. (2020). Four Variants of SLCO2A1 Identified in Three Chinese Patients with Chronic Enteropathy Associated with the SLCO2A1 Gene. Digestive Diseases and Sciences. 66(9). 2992–3001. 11 indexed citations

10.

Tang, Dongfang, Hui Huang, Haiyan Tang, et al.. (2020). Myotonia congenita and periodic hypokalemia paralysis in a consanguineous marriage pedigree: Coexistence of a novel CLCN1 mutation and an SCN4A mutation. PLoS ONE. 15(5). e0233017–e0233017. 5 indexed citations

11.

Zhou, Junfeng, Guiying Zhang, Meng Shi, et al.. (2019). A novel splicing mutation of PTCH1 in a Chinese family with nevoid basal cell carcinoma syndrome. Medical Molecular Morphology. 52(4). 235–237. 3 indexed citations

12.

Yang, Zhihui, et al.. (2017). Effects of aspirin and enoxaparin in a rat model of liver fibrosis. World Journal of Gastroenterology. 23(35). 6412–6419. 37 indexed citations

13.

Guo, Yalin, Meng Shi, Zhiping Tan, & Xiaoliu Shi. (2014). Possible anticipation in familial epidermolytic palmoplantar keratoderma with the p.R163W mutation of Keratin 9. Genetics and Molecular Research. 13(4). 8089–8093. 3 indexed citations

14.

Yang, Huarong, Yong Qi, Xiong Deng, et al.. (2013). Novel ATPase Cu2+ Transporting Beta Polypeptide Mutations in Chinese Families with Wilson's Disease. PLoS ONE. 8(7). e66526–e66526. 6 indexed citations

15.

Wang, Yongjun, Fan Zhang, Fan Wang, et al.. (2013). Beneficial Effects of Trypsin Inhibitors Derived from a Spider Venom Peptide in L-Arginine-Induced Severe Acute Pancreatitis in Mice. PLoS ONE. 8(4). e61049–e61049. 8 indexed citations

16.

Long, Yang, Tiejun Zhao, Xiaoliu Shi, et al.. (2009). Functional Analysis of a Dominant Negative Mutation of Interferon Regulatory Factor 5. PLoS ONE. 4(5). e5500–e5500. 22 indexed citations

17.

Ling, Jie, Hua Xiong, Xiaoliu Shi, et al.. (2009). Mutation L437P in the 2B domain of keratin 1 causes diffuse palmoplantar keratoderma in a Chinese pedigree. Journal of the European Academy of Dermatology and Venereology. 23(9). 1079–1082. 4 indexed citations

18.

Shi, Xiaoliu, Zhiping Tan, Haiyan Fang, et al.. (2002). [Translational frameshift may be occur in p11, an interaction protein of Cx31, in yeast].. PubMed. 34(2). 219–24. 2 indexed citations

19.

Fan, Xiao‐Yong, Xiaoliu Shi, Yun Zhao, Ruipeng Zhao, & Fan Yan. (1999). Insecticidal activity of transgenic tobacco plants expressing both Bt and CpTI genes on cotton bollworm (Helicoverpa armigera).. PubMed. 15(1). 1–5. 12 indexed citations

20.

Liu, Chunyu, Qian Pan, Lei Huang, et al.. (1998). Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment. Nature Genetics. 20(4). 370–373. 336 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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