Zhubo Wei

1.3k total citations
17 papers, 919 citations indexed

About

Zhubo Wei is a scholar working on Molecular Biology, Cell Biology and Cancer Research. According to data from OpenAlex, Zhubo Wei has authored 17 papers receiving a total of 919 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 8 papers in Cell Biology and 5 papers in Cancer Research. Recurrent topics in Zhubo Wei's work include Microtubule and mitosis dynamics (6 papers), Ubiquitin and proteasome pathways (4 papers) and DNA Repair Mechanisms (3 papers). Zhubo Wei is often cited by papers focused on Microtubule and mitosis dynamics (6 papers), Ubiquitin and proteasome pathways (4 papers) and DNA Repair Mechanisms (3 papers). Zhubo Wei collaborates with scholars based in United States, Japan and China. Zhubo Wei's co-authors include Min Li, Xiao Fang, Pumin Zhang, Pumin Zhang, Neal G. Copeland, Nancy A. Jenkins, Shuhua Han, Darren J. Baker, J. Philippe York and Linjie Guo and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and The Journal of Cell Biology.

In The Last Decade

Zhubo Wei

17 papers receiving 913 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Zhubo Wei United States	12	639	373	228	199	96	17	919
Irina Matos Portugal	13	546 0.9×	384 1.0×	173 0.8×	162 0.8×	56 0.6×	17	853
Monideepa Roy United States	11	779 1.2×	206 0.6×	251 1.1×	113 0.6×	87 0.9×	18	1.1k
Wei-Chien Yuan United States	9	821 1.3×	407 1.1×	200 0.9×	161 0.8×	67 0.7×	9	1.1k
Ju He United States	14	606 0.9×	206 0.6×	238 1.0×	97 0.5×	65 0.7×	21	880
Lai Xu China	14	939 1.5×	262 0.7×	438 1.9×	243 1.2×	72 0.8×	67	1.4k
Kathleen L. Pfaff United States	12	686 1.1×	478 1.3×	288 1.3×	71 0.4×	68 0.7×	27	956
Viola Nähse Norway	13	859 1.3×	371 1.0×	266 1.2×	109 0.5×	124 1.3×	17	1.2k
Richard J. Austin United States	14	1.1k 1.7×	257 0.7×	340 1.5×	107 0.5×	192 2.0×	22	1.4k
Evguenia M. Alexandrova United States	12	804 1.3×	245 0.7×	449 2.0×	189 0.9×	74 0.8×	18	1.1k
Samrat T. Kundu United States	15	599 0.9×	257 0.7×	160 0.7×	187 0.9×	35 0.4×	26	938

Countries citing papers authored by Zhubo Wei

Since Specialization

Citations

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

Fields of papers citing papers by Zhubo Wei

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zhubo Wei

This figure shows the co-authorship network connecting the top 25 collaborators of Zhubo Wei. A scholar is included among the top collaborators of Zhubo Wei 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 Zhubo Wei. Zhubo Wei is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

17 of 17 papers shown

1.

Thakur, Abhimanyu, Amanda Johnson, Emily G. Jacobs, et al.. (2022). Energy Sources for Exosome Communication in a Cancer Microenvironment. Cancers. 14(7). 1698–1698. 41 indexed citations

2.

Kodama, Takahiro, Michiko Kodama, Nancy A. Jenkins, et al.. (2022). Ring Finger Protein 125 Is an Anti-Proliferative Tumor Suppressor in Hepatocellular Carcinoma. Cancers. 14(11). 2589–2589. 9 indexed citations

3.

Kodama, Michiko, Jean C. Tien, Justin Y. Newberg, et al.. (2021). Sleeping Beauty Transposon Mutagenesis Identifies Genes Driving the Initiation and Metastasis of Uterine Leiomyosarcoma. Cancer Research. 81(21). 5413–5424. 7 indexed citations

4.

Wei, Zhubo, et al.. (2019). ZFR promotes cell proliferation and tumor development in colorectal and liver cancers. Biochemical and Biophysical Research Communications. 513(4). 1027–1034. 8 indexed citations

5.

Kodama, Takahiro, Michiko Kodama, Jian Li, et al.. (2019). MRTFB suppresses colorectal cancer development through regulating SPDL1 and MCAM. Proceedings of the National Academy of Sciences. 116(47). 23625–23635. 22 indexed citations

6.

Yu, Tianyu, Zhigang He, Muqing Yang, et al.. (2018). The development of methods for primary mast cells in vitro and ex vivo: An historical review. Experimental Cell Research. 369(2). 179–186. 8 indexed citations

7.

Kodama, Takahiro, Jing Yi, Justin Y. Newberg, et al.. (2018). Molecular profiling of nonalcoholic fatty liver disease-associated hepatocellular carcinoma using SB transposon mutagenesis. Proceedings of the National Academy of Sciences. 115(44). E10417–E10426. 46 indexed citations

8.

Kodama, Michiko, Takahiro Kodama, Justin Y. Newberg, et al.. (2017). In vivo loss-of-function screens identify KPNB1 as a new druggable oncogene in epithelial ovarian cancer. Proceedings of the National Academy of Sciences. 114(35). E7301–E7310. 86 indexed citations

9.

Chen, Huanhuan Joyce, Zhubo Wei, Jian Sun, et al.. (2016). A recellularized human colon model identifies cancer driver genes. Nature Biotechnology. 34(8). 845–851. 76 indexed citations

10.

Takeda, Haruna, Zhubo Wei, Hideto Koso, et al.. (2015). Transposon mutagenesis identifies genes and evolutionary forces driving gastrointestinal tract tumor progression. Nature Genetics. 47(2). 142–150. 89 indexed citations

11.

Peddibhotla, Sirisha, et al.. (2011). The DNA damage effector Chk1 kinase regulates Cdc14B nucleolar shuttling during cell cycle progression. Cell Cycle. 10(4). 671–679. 14 indexed citations

12.

Wei, Zhubo, Sirisha Peddibhotla, Lin Han, et al.. (2011). Early-Onset Aging and Defective DNA Damage Response in Cdc14b-Deficient Mice. Molecular and Cellular Biology. 31(7). 1470–1477. 32 indexed citations

13.

Li, Min, Xiao Fang, Darren J. Baker, et al.. (2010). The ATM–p53 pathway suppresses aneuploidy-induced tumorigenesis. Proceedings of the National Academy of Sciences. 107(32). 14188–14193. 195 indexed citations

14.

Chao, Wei‐Ting, Felicity Ashcroft, Alexes C. Daquinag, et al.. (2010). Type I Phosphatidylinositol Phosphate Kinase Beta Regulates Focal Adhesion Disassembly by Promoting β1 Integrin Endocytosis. Molecular and Cellular Biology. 30(18). 4463–4479. 50 indexed citations

15.

Li, Min, Xiao Fang, Zhubo Wei, J. Philippe York, & Pumin Zhang. (2009). Loss of spindle assembly checkpoint–mediated inhibition of Cdc20 promotes tumorigenesis in mice. The Journal of Cell Biology. 185(6). 983–994. 102 indexed citations

16.

Li, Min, Xiao Fang, Zhubo Wei, J. Philippe York, & Pumin Zhang. (2009). Loss of spindle assembly checkpoint–mediated inhibition of Cdc20 promotes tumorigenesis in mice. The Journal of Cell Biology. 186(1). 161–161. 6 indexed citations

17.

Li, Min, Lingfei Hou, Xingxu Huang, et al.. (2008). The adaptor protein of the anaphase promoting complex Cdh1 is essential in maintaining replicative lifespan and in learning and memory. Nature Cell Biology. 10(9). 1083–1089. 128 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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