Yinghe Hu

3.5k total citations · 2 hit papers
60 papers, 2.9k citations indexed

About

Yinghe Hu is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Yinghe Hu has authored 60 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 25 papers in Cellular and Molecular Neuroscience and 12 papers in Physiology. Recurrent topics in Yinghe Hu's work include Neuroscience and Neuropharmacology Research (15 papers), Neuroinflammation and Neurodegeneration Mechanisms (10 papers) and Alzheimer's disease research and treatments (10 papers). Yinghe Hu is often cited by papers focused on Neuroscience and Neuropharmacology Research (15 papers), Neuroinflammation and Neurodegeneration Mechanisms (10 papers) and Alzheimer's disease research and treatments (10 papers). Yinghe Hu collaborates with scholars based in China, United States and Netherlands. Yinghe Hu's co-authors include Joe Z. Tsien, Cecilia Jiang, Peter G. Schultz, Suzhen Dong, Eric R. Kandel, Robert D. Hawkins, Carsten Schultz, Min Zhuo, Ya‐Ping Tang and Claire Rampon and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Yinghe Hu

60 papers receiving 2.8k citations

Hit Papers

Effects of environmental enrichment on gene expression in... 1994 2026 2004 2015 2000 1994 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yinghe Hu China 24 1.2k 1.1k 695 375 349 60 2.9k
Hiroyuki Watanabe Japan 21 1.3k 1.1× 1.3k 1.2× 408 0.6× 515 1.4× 322 0.9× 85 3.2k
Marcus Rattray United Kingdom 34 1.4k 1.2× 1.9k 1.7× 919 1.3× 241 0.6× 436 1.2× 89 3.6k
Edward L. Spangler United States 35 1.0k 0.8× 1.0k 0.9× 1.1k 1.5× 674 1.8× 397 1.1× 85 3.4k
Paul L. Chazot United Kingdom 40 2.0k 1.6× 1.6k 1.4× 707 1.0× 451 1.2× 281 0.8× 158 4.7k
Károly Gulya Hungary 27 1.8k 1.5× 1.8k 1.6× 787 1.1× 315 0.8× 438 1.3× 107 3.5k
Alexander Zharkovsky Estonia 29 1.1k 0.9× 1.1k 1.0× 397 0.6× 311 0.8× 206 0.6× 99 2.7k
József Toldi Hungary 38 1.2k 1.0× 1.2k 1.1× 839 1.2× 442 1.2× 785 2.2× 165 5.2k
Carlos Fernando Mello Brazil 41 1.7k 1.4× 1.4k 1.2× 858 1.2× 333 0.9× 291 0.8× 164 4.6k
Ann M. Marini United States 33 1.4k 1.1× 1.6k 1.4× 529 0.8× 288 0.8× 497 1.4× 83 4.0k
Yoichiro Kuroda Japan 38 1.6k 1.3× 1.6k 1.4× 1.0k 1.5× 460 1.2× 319 0.9× 125 4.4k

Countries citing papers authored by Yinghe Hu

Since Specialization
Citations

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

Fields of papers citing papers by Yinghe Hu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yinghe Hu

This figure shows the co-authorship network connecting the top 25 collaborators of Yinghe Hu. A scholar is included among the top collaborators of Yinghe Hu 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 Yinghe Hu. Yinghe Hu 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.
Miao, Yang, et al.. (2023). Physiological Сharacteristics and Anthraquinones Accumulation of Rubia yunnanensis Affected by Drought Stress and Re-Watering. Russian Journal of Plant Physiology. 70(6). 1 indexed citations
2.
Luo, Jiancheng, Songtao Ye, Putu Ustriyana, et al.. (2020). Unraveling Chiral Selection in the Self-assembly of Chiral Fullerene Macroions: Effects of Small Chiral Components Including Counterions, Co-ions, or Neutral Molecules. Langmuir. 36(17). 4702–4710. 5 indexed citations
3.
Hu, Yinghe, et al.. (2013). Global view of transcriptome in the brains of aged NR2B transgenic mice.. PubMed Central. 1 indexed citations
4.
Dong, Suzhen, Qingwen Zeng, Ellen Siobhan Mitchell, et al.. (2012). Curcumin Enhances Neurogenesis and Cognition in Aged Rats: Implications for Transcriptional Interactions Related to Growth and Synaptic Plasticity. PLoS ONE. 7(2). e31211–e31211. 139 indexed citations
5.
Lu, Xiaoming, Ning Zhang, Bo Meng, Suzhen Dong, & Yinghe Hu. (2012). Involvement of GPR12 in the regulation of cell proliferation and survival. Molecular and Cellular Biochemistry. 366(1-2). 101–110. 20 indexed citations
6.
Dong, Suzhen, et al.. (2012). Advances in the pathogenesis of Alzheimer’s disease: a re-evaluation of amyloid cascade hypothesis. Translational Neurodegeneration. 1(1). 18–18. 103 indexed citations
7.
Zhang, Zhen, et al.. (2009). The repertoire of G-protein-coupled receptors in Xenopus tropicalis. BMC Genomics. 10(1). 263–263. 33 indexed citations
8.
Shen, Qian, et al.. (2009). Systematic gene expression profile of hypothalamus in calorie-restricted mice implicates the involvement of mTOR signaling in neuroprotective activity. Mechanisms of Ageing and Development. 130(9). 602–610. 30 indexed citations
9.
Wu, Shi‐Biao, Yun Zhao, Yinghe Hu, et al.. (2008). New Guaiane Sesquiterpenes and Furanocoumarins fromNotopterygium incisum. Planta Medica. 74(15). 1812–1817. 17 indexed citations
10.
11.
Shi, Jianting, Ying Wen, Hui Fan, et al.. (2008). Translational responses of NR2B overexpression in the cerebral cortex of transgenic mice: A liquid chromatography-based proteomic approach. Brain Research. 1250. 1–13. 2 indexed citations
12.
Shen, Qian, et al.. (2007). Calorie restriction ameliorates neurodegenerative phenotypes in forebrain-specific presenilin-1 and presenilin-2 double knockout mice. Neurobiology of Aging. 29(10). 1502–1511. 93 indexed citations
13.
Dong, Suzhen, et al.. (2007). Environment enrichment rescues the neurodegenerative phenotypes in presenilins‐deficient mice. European Journal of Neuroscience. 26(1). 101–112. 42 indexed citations
14.
Li, Chunxia, Wenze Niu, Cecilia Jiang, & Yinghe Hu. (2006). Effects of enriched environment on gene expression and signal pathways in cortex of hippocampal CA1 specific NMDAR1 knockout mice. Brain Research Bulletin. 71(6). 568–577. 28 indexed citations
15.
Niu, Wenze, Nan Jiang, & Yinghe Hu. (2006). Detection of proteins based on amino acid sequences by multiple aptamers against tripeptides. Analytical Biochemistry. 362(1). 126–135. 12 indexed citations
16.
Mei, Bing, et al.. (2005). Distinct gene expression profiles in hippocampus and amygdala after fear conditioning. Brain Research Bulletin. 67(1-2). 1–12. 49 indexed citations
17.
Zheng, Xuxu, et al.. (2005). Screening of active compounds as neuromedin U2 receptor agonist from natural products. Bioorganic & Medicinal Chemistry Letters. 15(20). 4531–4535. 17 indexed citations
18.
Wang, Daguang, Chengjun Deng, Christopher J. Leonard, et al.. (2003). Cloning and characterization of novel PDE4D isoforms PDE4D6 and PDE4D7. Cellular Signalling. 15(9). 883–891. 43 indexed citations
19.
Hu, Yinghe, Ari Barzilai, Mary Chen, Craig H. Bailey, & Eric R. Kandel. (1993). 5-HT and cAMP induce the formation of coated pits and vesicles and increase the expression of clathrin light chain in sensory neurons of aplysia. Neuron. 10(5). 921–929. 69 indexed citations
20.
Hu, Yinghe, et al.. (1989). Study on mechanism of micronucleoli formation by laser microirradiation. Cell Biophysics. 14(3). 257–269. 2 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