Xiong Deng

4.0k total citations
116 papers, 3.1k citations indexed

About

Xiong Deng is a scholar working on Molecular Biology, Plant Science and Neurology. According to data from OpenAlex, Xiong Deng has authored 116 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Molecular Biology, 26 papers in Plant Science and 24 papers in Neurology. Recurrent topics in Xiong Deng's work include Parkinson's Disease Mechanisms and Treatments (22 papers), Cholesterol and Lipid Metabolism (16 papers) and RNA regulation and disease (10 papers). Xiong Deng is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (22 papers), Cholesterol and Lipid Metabolism (16 papers) and RNA regulation and disease (10 papers). Xiong Deng collaborates with scholars based in China, United States and Canada. Xiong Deng's co-authors include Marshall B. Elam, Rajendra Raghow, Edwards A. Park, Chandrahasa R. Yellaturu, Henry G. Wilcox, Hao Deng, Lauren M. Cagen, Zhi Song, Lamei Yuan and Dongmiao Liu and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Scientific Reports.

In The Last Decade

Xiong Deng

113 papers receiving 3.0k citations

Peers

Xiong Deng
Bin Liang China
Kenneth N. Maclean United States
Charles Affourtit United Kingdom
Irfan J. Lodhi United States
Xiong Deng
Citations per year, relative to Xiong Deng Xiong Deng (= 1×) peers Anna Signorile

Countries citing papers authored by Xiong Deng

Since Specialization
Citations

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

Fields of papers citing papers by Xiong Deng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiong Deng

This figure shows the co-authorship network connecting the top 25 collaborators of Xiong Deng. A scholar is included among the top collaborators of Xiong Deng 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 Xiong Deng. Xiong Deng 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.
Huang, Yanxia, et al.. (2023). Novel compound heterozygous variants in the USH2A gene associated with autosomal recessive retinitis pigmentosa without hearing loss. Frontiers in Cell and Developmental Biology. 11. 1129862–1129862.
2.
Xu, Shan, Yongchao Tian, Zhaofeng Li, et al.. (2022). Proximal and remote sensing in plant phenomics: 20 years of progress, challenges, and perspectives. Plant Communications. 3(6). 100344–100344. 73 indexed citations
3.
Chen, Han, Lamei Yuan, Zhi Song, et al.. (2018). Genetic Analysis of LRRK1 and LRRK2 Variants in Essential Tremor Patients. Genetic Testing and Molecular Biomarkers. 22(6). 398–402. 8 indexed citations
4.
Qin, Xiang, Yi Guo, Wei Xiong, et al.. (2018). Identification of a CNGB1 Frameshift Mutation in a Han Chinese Family with Retinitis Pigmentosa. Optometry and Vision Science. 95(12). 1155–1161. 4 indexed citations
6.
Chen, Qian, Lamei Yuan, Xiong Deng, et al.. (2017). A Missense Variant p.Ala117Ser in the Transthyretin Gene of a Han Chinese Family with Familial Amyloid Polyneuropathy. Molecular Neurobiology. 55(6). 4911–4917. 18 indexed citations
7.
Deng, Hao, Sheng Deng, Hongbo Xu, et al.. (2016). Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly. PLoS ONE. 11(5). e0155180–e0155180. 8 indexed citations
8.
Yuan, Lamei, et al.. (2016). Association of the MTHFR rs1801131 and rs1801133 variants in sporadic Parkinson’s disease patients. Neuroscience Letters. 616. 26–31. 21 indexed citations
9.
Lü, Qian, Zhi Song, Xiong Deng, et al.. (2016). SLC6A3 rs28363170 and rs3836790 variants in Han Chinese patients with sporadic Parkinson’s disease. Neuroscience Letters. 629. 48–51. 4 indexed citations
10.
Zhen, Shoumin, Xiong Deng, Jian Wang, et al.. (2016). First Comprehensive Proteome Analyses of Lysine Acetylation and Succinylation in Seedling Leaves of Brachypodium distachyon L.. Scientific Reports. 6(1). 31576–31576. 62 indexed citations
11.
Yuan, Lamei, Xiong Deng, Zhi Song, et al.. (2015). Genetic analysis of the RAB39B gene in Chinese Han patients with Parkinson's disease. Neurobiology of Aging. 36(10). 2907.e11–2907.e12. 40 indexed citations
12.
Zheng, Wen, Han Chen, Xiong Deng, et al.. (2015). Identification of a Novel Mutation in the Titin Gene in a Chinese Family with Limb-Girdle Muscular Dystrophy 2J. Molecular Neurobiology. 53(8). 5097–5102. 27 indexed citations
13.
Deng, Xiong, Hongbo Xu, Song Wu, et al.. (2015). Identification of a Novel Mutation in the COL2A1 Gene in a Chinese Family with Spondyloepiphyseal Dysplasia Congenita. PLoS ONE. 10(6). e0127529–e0127529. 17 indexed citations
14.
Dong, Qingming, Francesco Giorgianni, Xiong Deng, et al.. (2014). Phosphorylation of sterol regulatory element binding protein-1a by protein kinase A (PKA) regulates transcriptional activity. Biochemical and Biophysical Research Communications. 449(4). 449–454. 20 indexed citations
15.
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
16.
Guo, Yi, Hua Lin, Kai Gao, et al.. (2011). Genetic analysis of IREB2, FAM13A and XRCC5 variants in Chinese Han patients with chronic obstructive pulmonary disease. Biochemical and Biophysical Research Communications. 415(2). 284–287. 22 indexed citations
17.
Deng, Xiong, Xuguang Zhai, Ming‐Ming Zhou, et al.. (2011). p38 Mitogen-Activated Protein Kinase and Liver X Receptor-α Mediate the Leptin Effect on Sterol Regulatory Element Binding Protein-1c Expression in Hepatic Stellate Cells. Molecular Medicine. 18(1). 10–18. 44 indexed citations
18.
Lei, Jing, Xiong Deng, Jie Zhang, et al.. (2011). Mutation screening of the HDC gene in Chinese Han patients with Tourette syndrome. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(1). 72–76. 33 indexed citations
19.
Raghow, Rajendra, Chandrahasa R. Yellaturu, Xiong Deng, Edwards A. Park, & Marshall B. Elam. (2008). SREBPs: the crossroads of physiological and pathological lipid homeostasis. Trends in Endocrinology and Metabolism. 19(2). 65–73. 254 indexed citations
20.
Elam, Marshall B., Henry G. Wilcox, Lauren M. Cagen, et al.. (2001). Increased hepatic VLDL secretion, lipogenesis, and SREBP-1 expression in the corpulent JCR:LA-cp rat. Journal of Lipid Research. 42(12). 2039–2048. 60 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026