Furu Zhang

882 total citations
24 papers, 608 citations indexed

About

Furu Zhang is a scholar working on Ophthalmology, Biomedical Engineering and Molecular Biology. According to data from OpenAlex, Furu Zhang has authored 24 papers receiving a total of 608 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Ophthalmology, 14 papers in Biomedical Engineering and 11 papers in Molecular Biology. Recurrent topics in Furu Zhang's work include Optical Coherence Tomography Applications (14 papers), Retinal Development and Disorders (11 papers) and Glaucoma and retinal disorders (9 papers). Furu Zhang is often cited by papers focused on Optical Coherence Tomography Applications (14 papers), Retinal Development and Disorders (11 papers) and Glaucoma and retinal disorders (9 papers). Furu Zhang collaborates with scholars based in United States and China. Furu Zhang's co-authors include Donald T. Miller, Kazuhiro Kurokawa, Zhuolin Liu, James A. Crowell, John J. Lee, Daniel X. Hammer, Omer P. Kocaoglu, Ravi S. Jonnal, Anant Agrawal and Marcel T. Bernucci and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Sensors.

In The Last Decade

Furu Zhang

24 papers receiving 596 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Furu Zhang United States 10 404 260 258 218 75 24 608
Drew Scoles United States 14 770 1.9× 185 0.7× 478 1.9× 337 1.5× 72 1.0× 40 990
Phillip Bedggood Australia 16 489 1.2× 237 0.9× 419 1.6× 76 0.3× 59 0.8× 49 717
William S. Fischer United States 9 258 0.6× 72 0.3× 128 0.5× 146 0.7× 43 0.6× 16 392
Omer P. Kocaoglu United States 16 856 2.1× 602 2.3× 596 2.3× 366 1.7× 126 1.7× 35 1.2k
B. Masella United States 9 339 0.8× 55 0.2× 145 0.6× 367 1.7× 65 0.9× 18 575
Xiang-Run Huang United States 15 665 1.6× 307 1.2× 458 1.8× 173 0.8× 54 0.7× 21 791
Ratheesh K. Meleppat United States 14 224 0.6× 175 0.7× 234 0.9× 115 0.5× 57 0.8× 30 503
Koji Nozato United States 7 275 0.7× 107 0.4× 171 0.7× 104 0.5× 44 0.6× 13 377
Zhangyi Zhong United States 9 541 1.3× 143 0.6× 410 1.6× 115 0.5× 37 0.5× 12 691
Stacey S. Choi United States 18 906 2.2× 464 1.8× 675 2.6× 247 1.1× 88 1.2× 53 1.2k

Countries citing papers authored by Furu Zhang

Since Specialization
Citations

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

Fields of papers citing papers by Furu Zhang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Furu Zhang

This figure shows the co-authorship network connecting the top 25 collaborators of Furu Zhang. A scholar is included among the top collaborators of Furu 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 Furu Zhang. Furu Zhang 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.
Das, Vineeta, Furu Zhang, Andrew J. Bower, et al.. (2024). Revealing speckle obscured living human retinal cells with artificial intelligence assisted adaptive optics optical coherence tomography. SHILAP Revista de lepidopterología. 4(1). 68–68. 7 indexed citations
2.
Zhang, Furu, et al.. (2024). In vivo imaging of human retinal ganglion cells using optical coherence tomography without adaptive optics. Biomedical Optics Express. 15(8). 4675–4675. 2 indexed citations
3.
Liu, Zhuolin, et al.. (2022). Ultrahigh-speed multimodal adaptive optics system for microscopic structural and functional imaging of the human retina. Biomedical Optics Express. 13(11). 5860–5860. 26 indexed citations
4.
Bernucci, Marcel T., Kazuhiro Kurokawa, Yan Liu, et al.. (2021). Measuring S, M, and L cone sensitivities in the living human eye using phase-sensitive AO-OCT. Investigative Ophthalmology & Visual Science. 62(8). 52–52. 2 indexed citations
5.
Kurokawa, Kazuhiro, Zhuolin Liu, Furu Zhang, et al.. (2021). Weakly supervised individual ganglion cell segmentation from adaptiveoptics OCT images for glaucomatous damage assessment. Optica. 8(5). 642–642. 32 indexed citations
6.
Zhang, Furu, Kazuhiro Kurokawa, Marcel T. Bernucci, et al.. (2021). Revealing How Color Vision Phenotype and Genotype Manifest in Individual Cone Cells. Investigative Ophthalmology & Visual Science. 62(2). 8–8. 19 indexed citations
7.
Zhang, Furu, et al.. (2020). Measuring dysfunction of cone photoreceptors in retinitis pigmentosa with phase-sensitive AO-OCT. 52. 40–40. 3 indexed citations
8.
Kurokawa, Kazuhiro, James A. Crowell, Furu Zhang, & Donald T. Miller. (2020). Suite of methods for assessing inner retinal temporal dynamics across spatial and temporal scales in the living human eye. Neurophotonics. 7(1). 1–1. 35 indexed citations
9.
10.
Kurokawa, Kazuhiro, et al.. (2019). Method to track and measure loss of inner retinal neurons in the living human eye. 41. 19–19. 3 indexed citations
11.
Zhang, Furu, et al.. (2019). Cone photoreceptor classification in the living human eye from photostimulation-induced phase dynamics. Proceedings of the National Academy of Sciences. 116(16). 7951–7956. 121 indexed citations
12.
Kurokawa, Kazuhiro, et al.. (2019). Measuring neuron loss in the retinal ganglion cell layer in healthy subjects. 60(9). 1781–1781. 1 indexed citations
13.
Liu, Zhuolin, James A. Crowell, Furu Zhang, Donald T. Miller, & Kazuhiro Kurokawa. (2018). Method to investigate temporal dynamics of ganglion and other retinal cells in the living human eye. 58. 31–31. 6 indexed citations
14.
Liu, Zhuolin, Kazuhiro Kurokawa, Furu Zhang, John J. Lee, & Donald T. Miller. (2017). Imaging and quantifying ganglion cells and other transparent neurons in the living human retina. Proceedings of the National Academy of Sciences. 114(48). 12803–12808. 165 indexed citations
15.
Liu, Zhuolin, Kazuhiro Kurokawa, Furu Zhang, & Donald T. Miller. (2017). In vivo imaging of human retinal ganglion cells with AO-OCT. 58(8). 3430–3430. 2 indexed citations
16.
Zhang, Furu, Zhuolin Liu, Kazuhiro Kurokawa, & Donald T. Miller. (2017). Tracking dynamics of photoreceptor disc shedding with adaptive optics-optical coherence tomography. Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE. 10045. 1004517–1004517. 1 indexed citations
17.
Liu, Zhuolin, Kazuhiro Kurokawa, Furu Zhang, & Donald T. Miller. (2017). Characterizing motility dynamics in human RPE cells. Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE. 10045. 1004515–1004515. 5 indexed citations
18.
Liu, Zhuolin, Kazuhiro Kurokawa, Omer P. Kocaoglu, Furu Zhang, & Donald T. Miller. (2016). Measuring organelle motility in RPE cells in the living human retina. Investigative Ophthalmology & Visual Science. 57(12). 1 indexed citations
19.
Kocaoglu, Omer P., Zhuolin Liu, Furu Zhang, et al.. (2016). Photoreceptor disc shedding in the living human eye. Biomedical Optics Express. 7(11). 4554–4554. 74 indexed citations
20.
Xu, Jia, et al.. (2016). SAR Ground Moving Target Indication Based on Relative Residue of DPCA Processing. Sensors. 16(10). 1676–1676. 10 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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