Weibin Zhou

7.0k total citations · 1 hit paper
71 papers, 2.8k citations indexed

About

Weibin Zhou is a scholar working on Molecular Biology, Nephrology and Genetics. According to data from OpenAlex, Weibin Zhou has authored 71 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 13 papers in Nephrology and 13 papers in Genetics. Recurrent topics in Weibin Zhou's work include Renal and related cancers (20 papers), Renal Diseases and Glomerulopathies (12 papers) and Genetic and Kidney Cyst Diseases (11 papers). Weibin Zhou is often cited by papers focused on Renal and related cancers (20 papers), Renal Diseases and Glomerulopathies (12 papers) and Genetic and Kidney Cyst Diseases (11 papers). Weibin Zhou collaborates with scholars based in United States, China and Japan. Weibin Zhou's co-authors include Friedhelm Hildebrandt, John Y. Kuwada, Hiromi Hirata, Louis Saint‐Amant, Wilson W. Cui, Bin Liu, Na Fu, Qi Deng, Junping Hu and Xiongwei Wu and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Weibin Zhou

69 papers receiving 2.8k citations

Hit Papers

Comprehensive review onzinc‐ionbattery anode: Challenges ... 2022 2026 2023 2024 2022 50 100 150 200 250

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Weibin Zhou United States 27 1.6k 725 428 302 297 71 2.8k
Hideshi Yagi Japan 22 3.9k 2.5× 563 0.8× 350 0.8× 186 0.6× 105 0.4× 69 5.9k
Kei‐ichiro Nakamura Japan 33 1.8k 1.1× 237 0.3× 390 0.9× 48 0.2× 146 0.5× 127 4.1k
Takahiro Sato Japan 33 834 0.5× 256 0.4× 158 0.4× 80 0.3× 64 0.2× 145 3.2k
Gary Davidson Germany 30 3.5k 2.2× 757 1.0× 664 1.6× 22 0.1× 631 2.1× 63 5.2k
Herbert Schulz Germany 36 2.3k 1.4× 459 0.6× 280 0.7× 25 0.1× 66 0.2× 121 4.2k
Tian Yu China 26 2.5k 1.6× 264 0.4× 636 1.5× 219 0.7× 21 0.1× 96 3.5k
Mitsuru Nakazawa Japan 35 1.7k 1.1× 153 0.2× 428 1.0× 187 0.6× 45 0.2× 239 4.5k
Francis J. Alenghat United States 17 1.6k 1.0× 1.5k 2.0× 882 2.1× 20 0.1× 89 0.3× 32 3.1k
Keisuke Sekine Japan 28 4.0k 2.5× 1.0k 1.4× 519 1.2× 24 0.1× 86 0.3× 65 7.1k
Jason R. Rock United States 43 4.9k 3.0× 448 0.6× 428 1.0× 146 0.5× 23 0.1× 69 9.9k

Countries citing papers authored by Weibin Zhou

Since Specialization
Citations

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

Fields of papers citing papers by Weibin Zhou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Weibin Zhou

This figure shows the co-authorship network connecting the top 25 collaborators of Weibin Zhou. A scholar is included among the top collaborators of Weibin 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 Weibin Zhou. Weibin 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
3.
Zang, Liqing, Sei Saitoh, Kan Katayama, et al.. (2024). A zebrafish model of diabetic nephropathy shows hyperglycemia, proteinuria and activation of the PI3K/Akt pathway. Disease Models & Mechanisms. 17(5). 3 indexed citations
4.
Liu, Zheng, Keli Liu, Xun Chen, et al.. (2024). Alkali injury–induced pathological lymphangiogenesis in the iris facilitates the infiltration of T cells and ocular inflammation. JCI Insight. 9(7). 4 indexed citations
5.
Cai, Hong, Jiayi Yan, Shang Liu, et al.. (2023). Paxlovid for hospitalized COVID-19 patients with chronic kidney disease. Antiviral Research. 216. 105659–105659. 12 indexed citations
6.
Nishimura, Yusuke, Koji Ando, Shinya Yuge, et al.. (2022). Blood Flow Regulates Glomerular Capillary Formation in Zebrafish Pronephros. Kidney360. 3(4). 700–713. 8 indexed citations
7.
Hu, Junping, Na Fu, Weibin Zhou, et al.. (2022). Comprehensive review onzinc‐ionbattery anode: Challenges and strategies. InfoMat. 4(7). 273 indexed citations breakdown →
8.
Ya, Chen, Lewis Kaufman, Kyung Lee, et al.. (2022). SARS-CoV-2 viral protein ORF3A injures renal tubules by interacting with TRIM59 to induce STAT3 activation. Molecular Therapy. 31(3). 774–787. 17 indexed citations
9.
Schulz, Angela, Andreas Eisenreich, Andrei Barysenka, et al.. (2019). Analysis of the genomic architecture of a complex trait locus in hypertensive rat models links Tmem63c to kidney damage. eLife. 8. 23 indexed citations
10.
Lee, Mi‐Sun, Julien Philippe, Nicholas Katsanis, & Weibin Zhou. (2019). Polyketide Synthase Plays a Conserved Role in Otolith Formation. Zebrafish. 16(4). 363–369. 5 indexed citations
11.
Ogino, Kazutoyo, Sean E. Low, Kenta Yamada, et al.. (2015). RING finger protein 121 facilitates the degradation and membrane localization of voltage-gated sodium channels. Proceedings of the National Academy of Sciences. 112(9). 2859–2864. 19 indexed citations
12.
Zhao, Ming, Xiaoyang Wan, Yu Li, Weibin Zhou, & Leilei Peng. (2015). Multiplexed 3D FRET imaging in deep tissue of live embryos. Scientific Reports. 5(1). 13991–13991. 18 indexed citations
13.
Huang, Liwei, An Xiao, Soo Young Choi, et al.. (2014). Wnt5a Is Necessary for Normal Kidney Development in Zebrafish and Mice. Nephron Experimental Nephrology. 128(1-2). 80–88. 25 indexed citations
14.
Miller, Douglas L. & Weibin Zhou. (2013). A System for Investigation of Biological Effects of Diagnostic Ultrasound on Development of Zebrafish Embryos. Zebrafish. 10(4). 459–465. 2 indexed citations
15.
Li, X., Z. Li, Weibin Zhou, et al.. (2013). Overexpression of 4EBP1, p70S6K, Akt1 or Akt2 differentially promotes Coxsackievirus B3-induced apoptosis in HeLa cells. Cell Death and Disease. 4(9). e803–e803. 21 indexed citations
16.
Hirata, Hiromi, Hua Wen, Yu Kawakami, et al.. (2011). Connexin 39.9 Protein Is Necessary for Coordinated Activation of Slow-twitch Muscle and Normal Behavior in Zebrafish. Journal of Biological Chemistry. 287(2). 1080–1089. 12 indexed citations
17.
Low, Sean E., Kimberly Amburgey, Eric J. Horstick, et al.. (2011). TRPM7 Is Required within Zebrafish Sensory Neurons for the Activation of Touch-Evoked Escape Behaviors. Journal of Neuroscience. 31(32). 11633–11644. 46 indexed citations
18.
Otto, Edgar A., Kálmán Tory, Massimo Attanasio, et al.. (2009). Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11). Journal of Medical Genetics. 46(10). 663–670. 98 indexed citations
19.
Otto, Edgar A., Juliana Helou, Susan J. Allen, et al.. (2007). Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencing. Human Mutation. 29(3). 418–426. 60 indexed citations
20.
Hirata, Hiromi, Louis Saint‐Amant, Gerald B. Downes, et al.. (2005). Zebrafish bandoneon mutants display behavioral defects due to a mutation in the glycine receptor β-subunit. Proceedings of the National Academy of Sciences. 102(23). 8345–8350. 77 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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