Yifeng Zhou

3.5k total citations
97 papers, 2.7k citations indexed

About

Yifeng Zhou is a scholar working on Cognitive Neuroscience, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Yifeng Zhou has authored 97 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Cognitive Neuroscience, 32 papers in Cellular and Molecular Neuroscience and 25 papers in Molecular Biology. Recurrent topics in Yifeng Zhou's work include Visual perception and processing mechanisms (60 papers), Neural dynamics and brain function (42 papers) and Retinal Development and Disorders (22 papers). Yifeng Zhou is often cited by papers focused on Visual perception and processing mechanisms (60 papers), Neural dynamics and brain function (42 papers) and Retinal Development and Disorders (22 papers). Yifeng Zhou collaborates with scholars based in China, United States and Canada. Yifeng Zhou's co-authors include Audie G. Leventhal, Zhong‐Lin Lu, Chang‐Bing Huang, Yongchang Wang, Yuanye Ma, Mingliang Pu, Tianmiao Hua, Yong Wang, Zhen Liang and Xiangrui Li and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Yifeng Zhou

96 papers receiving 2.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yifeng Zhou China 26 1.9k 594 521 433 265 97 2.7k
Duje Tadin United States 31 2.5k 1.3× 332 0.6× 348 0.7× 230 0.5× 231 0.9× 117 2.9k
Janine D. Mendola United States 19 2.5k 1.3× 189 0.3× 344 0.7× 341 0.8× 239 0.9× 48 2.9k
David C. Bradley United States 20 3.0k 1.6× 663 1.1× 209 0.4× 439 1.0× 173 0.7× 32 3.6k
Tom C. A. Freeman United Kingdom 21 1.4k 0.7× 224 0.4× 269 0.5× 144 0.3× 228 0.9× 58 1.7k
David P. Crewther Australia 35 2.0k 1.0× 327 0.6× 932 1.8× 723 1.7× 747 2.8× 176 4.0k
K.H. Ruddock United Kingdom 24 1.5k 0.8× 272 0.5× 211 0.4× 401 0.9× 237 0.9× 85 2.1k
Peter Hallett Canada 20 2.3k 1.2× 312 0.5× 159 0.3× 490 1.1× 399 1.5× 54 3.1k
Walter Makous United States 25 1.3k 0.7× 383 0.6× 194 0.4× 397 0.9× 223 0.8× 69 2.0k
Michael A. Paradiso United States 23 2.2k 1.1× 810 1.4× 94 0.2× 369 0.9× 99 0.4× 47 2.9k
Tatiana Pasternak United States 25 3.2k 1.6× 757 1.3× 123 0.2× 290 0.7× 86 0.3× 48 3.4k

Countries citing papers authored by Yifeng Zhou

Since Specialization
Citations

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

Fields of papers citing papers by Yifeng Zhou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yifeng Zhou

This figure shows the co-authorship network connecting the top 25 collaborators of Yifeng Zhou. A scholar is included among the top collaborators of Yifeng Zhou 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 Yifeng Zhou. Yifeng Zhou 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.
Zhou, Yifeng, D. Hu, M. Shao, et al.. (2023). R & D of prototype iTOF-MRPC at CEE. Nuclear Instruments and Methods in Physics Research Section A Accelerators Spectrometers Detectors and Associated Equipment. 1054. 168455–168455. 5 indexed citations
2.
Zhuo, Lu, Yufeng Huang, Qilin Lu, et al.. (2019). Abnormal intra-network architecture in extra-striate cortices in amblyopia: a resting state fMRI study. Eye and Vision. 6(1). 20–20. 10 indexed citations
3.
Wang, Zhengchun, et al.. (2018). Near- and Far-Surround Suppression in Human Motion Discrimination. Frontiers in Neuroscience. 12. 206–206. 2 indexed citations
4.
Wang, Zhengchun, et al.. (2018). Aging Potentiates Lateral but Not Local Inhibition of Orientation Processing in Primary Visual Cortex. Frontiers in Aging Neuroscience. 10. 14–14. 9 indexed citations
5.
Liu, Jiachen, et al.. (2018). Globally Normal Bistable Motion Perception of Anisometropic Amblyopes May Profit From an Unusual Coding Mechanism. Frontiers in Neuroscience. 12. 391–391. 2 indexed citations
6.
Xu, Guangwei, Fan Hu, Xuan Wang, Bing Zhang, & Yifeng Zhou. (2017). Bisphenol A exposure perturbs visual function of adult cats by remodeling the neuronal activity in the primary visual pathway. Archives of Toxicology. 92(1). 455–468. 12 indexed citations
7.
Li, Xiaoming, Ru Ma, Ying Chen, et al.. (2017). Delta coherence in resting-state EEG predicts the reduction in cigarette craving after hypnotic aversion suggestions. Scientific Reports. 7(1). 2430–2430. 27 indexed citations
8.
Wang, Xiaoxiao, et al.. (2017). Bayesian Inference of Two-Dimensional Contrast Sensitivity Function from Data Obtained with Classical One-Dimensional Algorithms Is Efficient. Frontiers in Neuroscience. 10. 616–616. 2 indexed citations
9.
Zhou, Yifeng, et al.. (2016). Examining the standard model of signal detection theory in motion discrimination. Journal of Vision. 16(7). 9–9. 2 indexed citations
10.
Liao, Meng, Longqian Liu, Qian Li, et al.. (2016). Training to improve contrast sensitivity in amblyopia: correction of high-order aberrations. Scientific Reports. 6(1). 35702–35702. 15 indexed citations
11.
Reynaud, Alexandre, Yong Tang, Yifeng Zhou, & R. F. Hess. (2014). A unified framework and normative dataset for second-order sensitivity using the quick Contrast Sensitivity Function (qCSF). Journal of Vision. 14(10). 1428–1428. 3 indexed citations
12.
Li, Ya, Feng Gu, Xiliang Zhang, et al.. (2014). Cerebral Activity to Opposite-Sex Voices Reflected by Event-Related Potentials. PLoS ONE. 9(4). e94976–e94976. 5 indexed citations
13.
Liu, Rong, Jiawei Zhou, Yun Dai, et al.. (2014). Immature visual neural system in children reflected by contrast sensitivity with adaptive optics correction. Scientific Reports. 4(1). 4687–4687. 8 indexed citations
14.
Reynaud, Alexandre, et al.. (2014). The amblyopic deficit for 2nd order processing: Generality and laterality. Vision Research. 114. 111–121. 16 indexed citations
15.
Baker, Curtis L., Zhili Wang, Zhimo Yao, et al.. (2013). Second-order neuronal responses to contrast modulation stimuli in primate visual cortex. Journal of Vision. 13(9). 41–41. 4 indexed citations
16.
Li, Guorong, et al.. (2011). Contrast adaptation in cat lateral geniculate nucleus and influence of corticothalamic feedback. European Journal of Neuroscience. 34(4). 622–631. 11 indexed citations
17.
Niu, Lei, Bing Cao, Hong Zhu, et al.. (2008). Impaired in vivo synaptic plasticity in dentate gyrus and spatial memory in juvenile rats induced by prenatal morphine exposure. Hippocampus. 19(7). 649–657. 72 indexed citations
18.
Lu, Hongjing, et al.. (2007). Motion perceptual learning: When only task-relevant information is learned. Journal of Vision. 7(10). 14–14. 27 indexed citations
19.
Guang-xing, LI, et al.. (2005). Chronic morphine exposure induces degradation of receptive field properties of LGN cells in cats1. Acta Pharmacologica Sinica. 26(9). 1034–1038. 4 indexed citations
20.
Li, Xiangrui, et al.. (2005). Degradation of response modulation of visual cortical cells in cats with chronic exposure to morphine. Neuroscience Letters. 384(1-2). 168–171. 6 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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