Qiangge Zhang

2.4k total citations · 1 hit paper
18 papers, 808 citations indexed

About

Qiangge Zhang is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Qiangge Zhang has authored 18 papers receiving a total of 808 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 7 papers in Cell Biology and 5 papers in Genetics. Recurrent topics in Qiangge Zhang's work include Microtubule and mitosis dynamics (5 papers), Cellular transport and secretion (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Qiangge Zhang is often cited by papers focused on Microtubule and mitosis dynamics (5 papers), Cellular transport and secretion (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Qiangge Zhang collaborates with scholars based in United States, China and Czechia. Qiangge Zhang's co-authors include Xueliang Zhu, Guoping Feng, Fubin Wang, Zhenye Yang, Qiongping Huang, Viviana Gradinaru, Yu Chen, Nicholas C. Flytzanis, Yingying Fan and Yijing Chen and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Qiangge Zhang

17 papers receiving 800 citations

Hit Papers

AAV capsid variants with ... 2021 2026 2022 2024 2021 50 100 150 200

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Qiangge Zhang United States 12 509 260 258 151 114 18 808
Caroline Hookway United States 8 485 1.0× 106 0.4× 176 0.7× 193 1.3× 53 0.5× 8 737
Wendy Froehlich United States 7 501 1.0× 197 0.8× 401 1.6× 137 0.9× 151 1.3× 8 956
Yuki Nakazawa Japan 9 566 1.1× 228 0.9× 557 2.2× 284 1.9× 300 2.6× 9 1.0k
John Salogiannis United States 10 614 1.2× 388 1.5× 182 0.7× 163 1.1× 43 0.4× 12 987
Edmund J. Koundakjian United States 8 739 1.5× 344 1.3× 254 1.0× 191 1.3× 96 0.8× 8 1.1k
Dennis A. Ridenour United States 10 571 1.1× 169 0.7× 156 0.6× 247 1.6× 115 1.0× 12 935
Dietmar Schreiner Germany 18 769 1.5× 100 0.4× 194 0.8× 422 2.8× 95 0.8× 31 1.1k
Akishi Onishi Japan 21 1.3k 2.6× 131 0.5× 117 0.5× 438 2.9× 96 0.8× 33 1.6k
Weisheng V. Chen United States 8 750 1.5× 112 0.4× 177 0.7× 447 3.0× 43 0.4× 10 1.0k
Justyna A. Janas United States 12 478 0.9× 118 0.5× 136 0.5× 235 1.6× 75 0.7× 14 716

Countries citing papers authored by Qiangge Zhang

Since Specialization
Citations

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

Fields of papers citing papers by Qiangge Zhang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Qiangge Zhang

This figure shows the co-authorship network connecting the top 25 collaborators of Qiangge Zhang. A scholar is included among the top collaborators of Qiangge Zhang 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 Qiangge Zhang. Qiangge Zhang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Chen, Yefei, William Menegas, Qiangge Zhang, & Guoping Feng. (2025). Common marmoset: An emerging non-human primate model for translational applications in brain disorders. Current Opinion in Neurobiology. 92. 102998–102998. 1 indexed citations
2.
Kang, Jinyoung, Kenneth K. W. Li, Eunah Yu, et al.. (2025). A transcriptomic atlas of astrocyte heterogeneity across space and time in mouse and marmoset. Neuron. 113(23). 3942–3965.e19.
3.
Wang, Junqiang, et al.. (2024). Evolutionary and developmental specialization of foveal cell types in the marmoset. Proceedings of the National Academy of Sciences. 121(16). e2313820121–e2313820121. 7 indexed citations
4.
Prager, Eric M., et al.. (2023). Pathway-specific alterations in striatal excitability and cholinergic modulation in a SAPAP3 mouse model of compulsive motor behavior. Cell Reports. 42(11). 113384–113384. 9 indexed citations
5.
Fass, Daniel M., Michael C. Lewis, Rushdy Ahmad, et al.. (2022). Brain-specific deletion of GIT1 impairs cognition and alters phosphorylation of synaptic protein networks implicated in schizophrenia susceptibility. Molecular Psychiatry. 27(8). 3272–3285. 7 indexed citations
6.
Lea, Nicholas E., Qiangge Zhang, Martin Wienisch, et al.. (2022). 341 Repeats Is Not Enough for Methylation in a New Fragile X Mouse Model. eNeuro. 9(5). ENEURO.0142–22.2022. 4 indexed citations
7.
Park, Joha, Joha Park, Dae Hee Yun, et al.. (2021). Epitope-preserving magnified analysis of proteome (eMAP). Science Advances. 7(46). eabf6589–eabf6589. 25 indexed citations
8.
Goertsen, David, Nicholas C. Flytzanis, Nick Goeden, et al.. (2021). AAV capsid variants with brain-wide transgene expression and decreased liver targeting after intravenous delivery in mouse and marmoset. Nature Neuroscience. 25(1). 106–115. 229 indexed citations breakdown →
9.
Wilde, Jonathan J., Tomomi Aida, Ricardo C.H. del Rosario, et al.. (2021). Efficient embryonic homozygous gene conversion via RAD51-enhanced interhomolog repair. Cell. 184(12). 3267–3280.e18. 40 indexed citations
10.
Wang, Wenting, Chenchen Li, Qian Chen, et al.. (2017). Striatopallidal dysfunction underlies repetitive behavior in Shank3-deficient model of autism. Journal of Clinical Investigation. 127(5). 1978–1990. 122 indexed citations
11.
Zhang, Qiangge, Xianhua Gao, Chenchen Li, et al.. (2016). Impaired Dendritic Development and Memory inSorbs2Knock-Out Mice. Journal of Neuroscience. 36(7). 2247–2260. 48 indexed citations
12.
Wan, Yihan, Zhenye Yang, Jing Guo, et al.. (2012). Misfolded Gβ is recruited to cytoplasmic dynein by Nudel for efficient clearance. Cell Research. 22(7). 1140–1154. 13 indexed citations
13.
Shan, Yongli, Yan Li, Youdong Pan, et al.. (2009). Nudel and FAK as Antagonizing Strength Modulators of Nascent Adhesions through Paxillin. PLoS Biology. 7(5). e1000116–e1000116. 44 indexed citations
14.
Zhang, Qiangge, Fubin Wang, Jingli Cao, et al.. (2009). Nudel Promotes Axonal Lysosome Clearance and Endo‐lysosome Formation via Dynein‐Mediated Transport. Traffic. 10(9). 1337–1349. 30 indexed citations
15.
Shen, Yidong, Ning Li, Shuang Wu, et al.. (2008). Nudel Binds Cdc42GAP to Modulate Cdc42 Activity at the Leading Edge of Migrating Cells. Developmental Cell. 14(3). 342–353. 60 indexed citations
16.
Liang, Yun, Wei Yu, Yan Li, et al.. (2007). Nudel Modulates Kinetochore Association and Function of Cytoplasmic Dynein in M Phase. Molecular Biology of the Cell. 18(7). 2656–2666. 68 indexed citations
17.
Wang, Fubin, Qiangge Zhang, Jingli Cao, Qiongping Huang, & Xueliang Zhu. (2007). The microtubule plus end-binding protein EB1 is involved in Sertoli cell plasticity in testicular seminiferous tubules. Experimental Cell Research. 314(1). 213–226. 26 indexed citations
18.
Guo, Jing, Zhenye Yang, Wei Song, et al.. (2005). Nudel Contributes to Microtubule Anchoring at the Mother Centriole and Is Involved in Both Dynein-dependent and -independent Centrosomal Protein Assembly. Molecular Biology of the Cell. 17(2). 680–689. 75 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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