Zuoshang Xu

11.8k total citations · 2 hit papers
86 papers, 9.3k citations indexed

About

Zuoshang Xu is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Zuoshang Xu has authored 86 papers receiving a total of 9.3k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Neurology, 46 papers in Molecular Biology and 38 papers in Genetics. Recurrent topics in Zuoshang Xu's work include Amyotrophic Lateral Sclerosis Research (52 papers), Neurogenetic and Muscular Disorders Research (38 papers) and RNA Interference and Gene Delivery (24 papers). Zuoshang Xu is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (52 papers), Neurogenetic and Muscular Disorders Research (38 papers) and RNA Interference and Gene Delivery (24 papers). Zuoshang Xu collaborates with scholars based in United States, China and France. Zuoshang Xu's co-authors include Jiming Kong, Dianne S. Schwarz, Phillip D. Zamore, Neil Aronin, Tingting Du, György Hutvàgner, Cheolwha Jung, Don W. Cleveland, Cynthia Higgins and Michael K. Lee and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Zuoshang Xu

85 papers receiving 9.1k citations

Hit Papers

Asymmetry in the Assembly of the RNAi Enzyme Complex 1998 2026 2007 2016 2003 1998 500 1000 1.5k 2.0k

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Zuoshang Xu United States 46 5.2k 3.6k 1.9k 1.4k 1.3k 86 9.3k
Boris Rogelj Slovenia 36 4.2k 0.8× 4.3k 1.2× 2.6k 1.4× 855 0.6× 578 0.4× 79 7.1k
Paul R. Heath United Kingdom 48 3.3k 0.6× 2.5k 0.7× 1.4k 0.8× 972 0.7× 517 0.4× 131 6.7k
Aaron D. Gitler United States 58 9.1k 1.8× 6.7k 1.8× 2.4k 1.3× 3.0k 2.2× 416 0.3× 118 14.4k
Barry W. Festoff United States 45 2.7k 0.5× 1.3k 0.3× 846 0.5× 1.6k 1.2× 1.1k 0.8× 158 6.6k
Markus A. Rüegg Switzerland 70 10.0k 1.9× 1.8k 0.5× 836 0.4× 3.4k 2.5× 755 0.6× 184 14.8k
Ruth S. Slack Canada 67 8.4k 1.6× 1.9k 0.5× 324 0.2× 2.5k 1.9× 1.0k 0.8× 145 12.6k
Han‐Xiang Deng United States 38 3.0k 0.6× 5.5k 1.5× 3.0k 1.6× 1.4k 1.0× 208 0.2× 107 8.2k
Hemali Phatnani United States 25 4.6k 0.9× 1.2k 0.3× 662 0.4× 1.4k 1.0× 557 0.4× 39 8.3k
Linda Greensmith United Kingdom 47 3.7k 0.7× 3.3k 0.9× 2.0k 1.1× 2.6k 1.9× 139 0.1× 152 7.8k
Vincent Timmerman Belgium 57 5.2k 1.0× 2.7k 0.7× 1.1k 0.6× 6.5k 4.8× 362 0.3× 221 11.8k

Countries citing papers authored by Zuoshang Xu

Since Specialization
Citations

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

Fields of papers citing papers by Zuoshang Xu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zuoshang Xu

This figure shows the co-authorship network connecting the top 25 collaborators of Zuoshang Xu. A scholar is included among the top collaborators of Zuoshang Xu 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 Zuoshang Xu. Zuoshang Xu 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.
Link, Christopher D., et al.. (2022). TDP-43 knockdown in mouse model of ALS leads to dsRNA deposition, gliosis, and neurodegeneration in the spinal cord. Cerebral Cortex. 33(10). 5808–5816. 9 indexed citations
2.
Yang, Chunxing, Tao Qiao, Jia Yu, et al.. (2022). Low-level overexpression of wild type TDP-43 causes late-onset, progressive neurodegeneration and paralysis in mice. PLoS ONE. 17(2). e0255710–e0255710. 19 indexed citations
3.
Qiao, Tao, et al.. (2022). Protein citrullination marks myelin protein aggregation and disease progression in mouse ALS models. Acta Neuropathologica Communications. 10(1). 135–135. 15 indexed citations
4.
Boopathy, Sivakumar, Melissa Rotunno, Catherine Douthwright, et al.. (2022). Anti-SOD1 Nanobodies That Stabilize Misfolded SOD1 Proteins Also Promote Neurite Outgrowth in Mutant SOD1 Human Neurons. International Journal of Molecular Sciences. 23(24). 16013–16013. 2 indexed citations
5.
Li, Dongxiao, et al.. (2019). Direct Intrathecal Injection of Recombinant Adeno-associated Viruses in Adult Mice. Journal of Visualized Experiments. 13 indexed citations
6.
Yang, Chunxing, Eric Danielson, Tao Qiao, et al.. (2016). Mutant PFN1 causes ALS phenotypes and progressive motor neuron degeneration in mice by a gain of toxicity. Proceedings of the National Academy of Sciences. 113(41). E6209–E6218. 76 indexed citations
7.
An, Ting, Weisong Duan, Zhongyao Li, et al.. (2014). Oxidative Stress and Autophagic Alteration in Brainstem of SOD1-G93A Mouse Model of ALS. Molecular Neurobiology. 49(3). 1435–1448. 51 indexed citations
8.
Zhang, Hongwei, Bin Yang, Xin Mu, et al.. (2011). Several rAAV Vectors Efficiently Cross the Blood–brain Barrier and Transduce Neurons and Astrocytes in the Neonatal Mouse Central Nervous System. Molecular Therapy. 19(8). 1440–1448. 235 indexed citations
9.
Qiu, Linghua, Jaime A. Rivera‐Pérez, & Zuoshang Xu. (2011). A Non-Specific Effect Associated with Conditional Transgene Expression Based on Cre-loxP Strategy in Mice. PLoS ONE. 6(5). e18778–e18778. 20 indexed citations
10.
Yang, Chunxing, Catheryne Whittle, Linghua Qiu, et al.. (2010). The C-Terminal TDP-43 Fragments Have a High Aggregation Propensity and Harm Neurons by a Dominant-Negative Mechanism. PLoS ONE. 5(12). e15878–e15878. 148 indexed citations
11.
Wang, Hongyan, Huricha Baigude, Chao‐Shun Yang, et al.. (2008). Therapeutic Gene Silencing Delivered by a Chemically Modified Small Interfering RNA against Mutant SOD1 Slows Amyotrophic Lateral Sclerosis Progression. Journal of Biological Chemistry. 283(23). 15845–15852. 51 indexed citations
12.
Xu, Zuoshang, et al.. (2004). Mitochondrial Degeneration in Amyotrophic Lateral Sclerosis. Journal of Bioenergetics and Biomembranes. 36(4). 395–399. 46 indexed citations
13.
Ding, Hongliu, Dianne S. Schwarz, Alex C. Keene, et al.. (2003). Selective silencing by RNAi of a dominant allele that causes amyotrophic lateral sclerosis. Aging Cell. 2(4). 209–217. 133 indexed citations
14.
Higgins, Cynthia, Cheolwha Jung, Hongliu Ding, & Zuoshang Xu. (2002). Mutant Cu, Zn Superoxide Dismutase that Causes Motoneuron Degeneration Is Present in Mitochondria in the CNS. Journal of Neuroscience. 22(6). RC215–RC215. 204 indexed citations
15.
Jung, Cheolwha, Cynthia Higgins, & Zuoshang Xu. (2000). Measuring the Quantity and Activity of Mitochondrial Electron Transport Chain Complexes in Tissues of Central Nervous System Using Blue Native Polyacrylamide Gel Electrophoresis. Analytical Biochemistry. 286(2). 214–223. 82 indexed citations
16.
Bogdanov, Mikhail B., et al.. (1998). Elevated “Hydroxyl Radical” Generation In Vivo in an Animal Model of Amyotrophic Lateral Sclerosis. Journal of Neurochemistry. 71(3). 1321–1324. 138 indexed citations
17.
Bruijn, Lucie, et al.. (1996). Sequence variants in human neurofilament proteins: Absence of linkage to familial amyotrophic lateral sclerosis. Annals of Neurology. 40(4). 603–610. 57 indexed citations
18.
Marszalek, Joseph R., Toni Williamson, Michael K. Lee, et al.. (1996). Neurofilament subunit NF-H modulates axonal diameter by selectively slowing neurofilament transport.. The Journal of Cell Biology. 135(3). 711–724. 150 indexed citations
19.
Wong, Philip C., Thomas O. Crawford, Zuoshang Xu, et al.. (1995). Increasing neurofilament subunit NF-M expression reduces axonal NF-H, inhibits radial growth, and results in neurofilamentous accumulation in motor neurons.. The Journal of Cell Biology. 130(6). 1413–1422. 129 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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