Haining Zhu

10.3k total citations · 1 hit paper
128 papers, 5.7k citations indexed

About

Haining Zhu is a scholar working on Molecular Biology, Neurology and Physiology. According to data from OpenAlex, Haining Zhu has authored 128 papers receiving a total of 5.7k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 41 papers in Neurology and 26 papers in Physiology. Recurrent topics in Haining Zhu's work include Amyotrophic Lateral Sclerosis Research (37 papers), Neurogenetic and Muscular Disorders Research (21 papers) and Alzheimer's disease research and treatments (15 papers). Haining Zhu is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (37 papers), Neurogenetic and Muscular Disorders Research (21 papers) and Alzheimer's disease research and treatments (15 papers). Haining Zhu collaborates with scholars based in United States, China and Brazil. Haining Zhu's co-authors include József Gál, Anna‐Lena Ström, Fujian Zhang, Jianjun Zhai, Xiaoning Lu, Jing Chen, David M. Kwinter, Ping Shi, Kei Fukada and Lisha Kuang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Haining Zhu

123 papers receiving 5.7k citations

Hit Papers

Modeling blood-brain barrier formation and cerebral caver... 2024 2026 2025 2024 20 40 60

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Haining Zhu United States 44 3.4k 1.7k 816 751 559 128 5.7k
Scott Anderson United States 37 5.4k 1.6× 1.0k 0.6× 406 0.5× 465 0.6× 1.7k 3.1× 62 7.2k
Peleg Horowitz United States 36 2.3k 0.7× 624 0.4× 954 1.2× 302 0.4× 598 1.1× 107 4.6k
Jongkyeong Chung South Korea 50 5.0k 1.5× 960 0.6× 814 1.0× 131 0.2× 881 1.6× 119 8.3k
Richard G.H. Cotton Australia 42 3.9k 1.1× 659 0.4× 846 1.0× 228 0.3× 468 0.8× 260 7.3k
Holger Prokisch Germany 54 6.6k 1.9× 842 0.5× 598 0.7× 118 0.2× 490 0.9× 221 8.6k
Deepak Nijhawan United States 19 6.8k 2.0× 392 0.2× 495 0.6× 239 0.3× 749 1.3× 28 9.1k
Sanae M.M. Iguchi‐Ariga Japan 40 3.5k 1.0× 2.2k 1.3× 787 1.0× 88 0.1× 626 1.1× 115 6.3k
Takahiro Taira Japan 37 2.9k 0.8× 2.2k 1.3× 835 1.0× 86 0.1× 505 0.9× 80 5.8k
Hamid Mirzaei United States 38 4.5k 1.3× 500 0.3× 536 0.7× 248 0.3× 409 0.7× 59 5.9k
Barbara A. Spengler United States 42 3.9k 1.1× 2.0k 1.2× 360 0.4× 218 0.3× 685 1.2× 84 6.4k

Countries citing papers authored by Haining Zhu

Since Specialization
Citations

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

Fields of papers citing papers by Haining Zhu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Haining Zhu

This figure shows the co-authorship network connecting the top 25 collaborators of Haining Zhu. A scholar is included among the top collaborators of Haining Zhu 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 Haining Zhu. Haining Zhu 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.
Yi, Dong Kee, Julian W. Tang, Fanyi Meng, et al.. (2025). Construction of chiral nitrogen stereocenters via enantioselective C–H activation. Chem. 12(1). 102730–102730.
2.
Carver, Megan, et al.. (2025). The role of stress granules in heavy metal-induced carcinogenesis. 3(1). 43–46. 1 indexed citations
3.
Zhu, Haining, et al.. (2024). Exploring the periodic behavior of a singular predator-prey system. Archiv der Mathematik. 124(1). 99–107.
4.
Shaw, Brian, et al.. (2024). Stress granules play a critical role in hexavalent chromium-induced malignancy in a G3BP1 dependent manner. Environmental Pollution. 362. 124997–124997. 1 indexed citations
6.
Wang, Po‐Shun, Zulong Liu, Jie Xie, et al.. (2024). Long noncoding RNA ABHD11-AS1 interacts with SART3 and regulates CD44 RNA alternative splicing to promote lung carcinogenesis. Environment International. 185. 108494–108494. 14 indexed citations
7.
Zhu, Haining, et al.. (2023). A hydrolyzed casein diet promotes Ngn3 controlling enteroendocrine cell differentiation to increase gastrointestinal motility in mice. Food & Function. 15(3). 1237–1249. 4 indexed citations
8.
Tripathi, R. P., Daheng He, Yuanyuan Wu, et al.. (2023). ABL1/2 and DDR1 Drive MEKi Resistance in NRAS-Mutant Melanomas by Stabilizing RAF/MYC/ETS1 and Promoting RAF Homodimerization. Cancers. 15(3). 954–954. 3 indexed citations
9.
Kuang, Lisha, Lin Yang, Xiu Li, et al.. (2022). Yin and yang regulation of stress granules by Caprin-1. Proceedings of the National Academy of Sciences. 119(44). e2207975119–e2207975119. 42 indexed citations
10.
Gál, József, Yuriko Katsumata, Haining Zhu, et al.. (2021). Apolipoprotein E Proteinopathy Is a Major Dementia-Associated Pathologic Biomarker in Individuals with or without the APOE Epsilon 4 Allele. American Journal Of Pathology. 192(3). 564–578. 6 indexed citations
11.
Xie, Yanqi, Tianxin Yu, Wen Zhang, et al.. (2019). Semisynthetic aurones inhibit tubulin polymerization at the colchicine-binding site and repress PC-3 tumor xenografts in nude mice and myc-induced T-ALL in zebrafish. Scientific Reports. 9(1). 6439–6439. 19 indexed citations
12.
Koren, Shon A., Shelby E. Meier, Jing Chen, et al.. (2019). Tau drives translational selectivity by interacting with ribosomal proteins. Acta Neuropathologica. 137(4). 571–583. 74 indexed citations
13.
Carroll, Dustin, Jing Chen, Luksana Chaiswing, et al.. (2017). Extracellular Vesicles Released by Cardiomyocytes in a Doxorubicin-Induced Cardiac Injury Mouse Model Contain Protein Biomarkers of Early Cardiac Injury. Clinical Cancer Research. 24(7). 1644–1653. 59 indexed citations
14.
Meier, Shelby E., Danielle N. Lyons, Jennifer Rodriguez-Rivera, et al.. (2016). Pathological Tau Promotes Neuronal Damage by Impairing Ribosomal Function and Decreasing Protein Synthesis. Journal of Neuroscience. 36(3). 1001–1007. 128 indexed citations
15.
Jiang, Hong, Lisha Wu, Jing Chen, et al.. (2015). Sulfiredoxin Promotes Colorectal Cancer Cell Invasion and Metastasis through a Novel Mechanism of Enhancing EGFR Signaling. Molecular Cancer Research. 13(12). 1554–1566. 35 indexed citations
16.
Convertini, Paolo, Jia Yu Zhang, Pierre de la Grange, et al.. (2013). Genome wide array analysis indicates that an amyotrophic lateral sclerosis mutation of FUS causes an early increase of CAMK2N2 in vitro. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1832(8). 1129–1135. 9 indexed citations
17.
Shi, Ping, József Gál, David M. Kwinter, Xiaoyan Liu, & Haining Zhu. (2009). Mitochondrial dysfunction in amyotrophic lateral sclerosis. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1802(1). 45–51. 175 indexed citations
18.
Ström, Anna‐Lena, Ping Shi, Fujian Zhang, et al.. (2008). Interaction of Amyotrophic Lateral Sclerosis (ALS)-related Mutant Copper-Zinc Superoxide Dismutase with the Dynein-Dynactin Complex Contributes to Inclusion Formation. Journal of Biological Chemistry. 283(33). 22795–22805. 42 indexed citations
19.
Babu, Jeganathan Ramesh, M. Lamar Seibenhener, Junmin Peng, et al.. (2008). Genetic inactivation of p62 leads to accumulation of hyperphosphorylated tau and neurodegeneration. Journal of Neurochemistry. 106(1). 107–120. 207 indexed citations
20.
Fukada, Kei, et al.. (2006). Prohibitin and Cofilin Are Intracellular Effectors of Transforming Growth Factor β Signaling in Human Prostate Cancer Cells. Cancer Research. 66(17). 8640–8647. 92 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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