Shibo Li

2.2k total citations
87 papers, 1.4k citations indexed

About

Shibo Li is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Shibo Li has authored 87 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 49 papers in Genetics and 15 papers in Plant Science. Recurrent topics in Shibo Li's work include Genomic variations and chromosomal abnormalities (36 papers), Chromosomal and Genetic Variations (13 papers) and DNA Repair Mechanisms (10 papers). Shibo Li is often cited by papers focused on Genomic variations and chromosomal abnormalities (36 papers), Chromosomal and Genetic Variations (13 papers) and DNA Repair Mechanisms (10 papers). Shibo Li collaborates with scholars based in United States, China and South Korea. Shibo Li's co-authors include John J. Mulvihill, Xiaohua Wu, Bin Zheng, Xingwei Wang, Susan J. Hassed, Takuya Chiba, Hailong Wang, Cathy M. Tuck‐Müller, Wladimir Wertelecki and Hong Liu and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Shibo Li

83 papers receiving 1.4k citations

Peers

Shibo Li

GENET

ONCOL

Ivo Renkens Netherlands

Markus J. van Roosmalen Netherlands

Mark S. Lechner United States

J. Vrolijk Netherlands

Anita Göndör Sweden

Dione K. Bailey United States

Roland Green United States

Adam P. Butler United Kingdom

Lisa Ann Cirillo United States

Danny Wangsa United States

Ivo Renkens Netherlands

Shibo Li

894 ×0.9

524 ×0.9

GENET

251 ×1.2

105 ×0.7

ONCOL

306 ×2.2

Citations per year, relative to Shibo Li Shibo Li (= 1×) peers Ivo Renkens

Countries citing papers authored by Shibo Li

Since Specialization

Citations

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

Fields of papers citing papers by Shibo Li

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shibo Li

This figure shows the co-authorship network connecting the top 25 collaborators of Shibo Li. A scholar is included among the top collaborators of Shibo Li 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 Shibo Li. Shibo Li 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:

20 of 20 papers shown

Li, Shibo, et al.. (2024). 53BP1 deficiency leads to hyperrecombination using break-induced replication (BIR). Nature Communications. 15(1). 8648–8648. 2 indexed citations

Wang, Qiujing, Yue Yao, Hangfei Chen, et al.. (2024). Emergence of novel hypervirulent Acinetobacter baumannii strain and herpes simplex type 1 virus in a case of community-acquired pneumonia in China. Journal of Infection and Public Health. 17(7). 102456–102456. 2 indexed citations

Yao, Qigu, et al.. (2023). Pooled Analysis of Mesenchymal Stromal Cell-Derived Extracellular Vesicle Therapy for Liver Disease in Preclinical Models. Journal of Personalized Medicine. 13(3). 441–441. 8 indexed citations

Wang, Xianfu, et al.. (2022). Molecular cytogenetic characterization of partial trisomy of the long arm of chromosome 11 in a patient with multiple congenital anomalies. Molecular Cytogenetics. 15(1). 17–17. 1 indexed citations

Li, Shibo & Xiaohua Wu. (2020). Common fragile sites: protection and repair. Cell & Bioscience. 10(1). 29–29. 34 indexed citations

Ma, Zhikun, Young Kim, Xiaoshan Feng, et al.. (2018). DMBA promotes ErbB2‑mediated carcinogenesis via ErbB2 and estrogen receptor pathway activation and genomic instability. Oncology Reports. 40(3). 1632–1640. 11 indexed citations

Hassed, Susan J., Shibo Li, John J. Mulvihill, Christopher E. Aston, & Susan Palmer. (2017). Adams–Oliver syndrome review of the literature: Refining the diagnostic phenotype. American Journal of Medical Genetics Part A. 173(3). 790–800. 63 indexed citations

Chen, Yuhui, et al.. (2017). An Array-based Comparative Genomic Hybridization Platform for Efficient Detection of Copy Number Variations in Fast Neutron-induced <em>Medicago truncatula</em> Mutants. Journal of Visualized Experiments. 7 indexed citations

Lee, Eunjung, Ji Wook Moon, Xianfu Wang, et al.. (2015). Genomic Copy Number Signatures Uncovered a Genetically Distinct Group from Adenocarcinoma and Squamous Cell Carcinoma in Non–Small Cell Lung Cancer. Human Pathology. 46(8). 1111–1120. 7 indexed citations

10.

Wang, Xianfu, et al.. (2015). Two patients with small chromosome 22q11.21 alterations and central nervous system abnormalities. Molecular Cytogenetics. 8(1). 102–102. 3 indexed citations

11.

Kim, Young Mi, Ji-Yun Lee, Lijun Xia, John J. Mulvihill, & Shibo Li. (2013). Trisomy 8: a common finding in mouse embryonic stem (ES) cell lines. Molecular Cytogenetics. 6(1). 3–3. 14 indexed citations

12.

Zhang, Han, et al.. (2011). Reversed clinical phenotype due to a microduplication of Sotos syndrome region detected by array CGH: Microcephaly, developmental delay and delayed bone age. American Journal of Medical Genetics Part A. 155(6). 1374–1378. 24 indexed citations

13.

Qi, Ling, Anita C. Bellail, Michael R. Rossi, et al.. (2011). Heterogeneity of primary glioblastoma cells in the expression of caspase-8 and the response to TRAIL-induced apoptosis. APOPTOSIS. 16(11). 1150–1164. 21 indexed citations

14.

Wang, Xingwei, et al.. (2008). Automated classification of metaphase chromosomes: Optimization of an adaptive computerized scheme. Journal of Biomedical Informatics. 42(1). 22–31. 51 indexed citations

15.

Wang, Xingwei, et al.. (2007). Automated identification of analyzable metaphase chromosomes depicted on microscopic digital images. Journal of Biomedical Informatics. 41(2). 264–271. 32 indexed citations

16.

Purandare, Smita M., Jiyun Lee, Susan J. Hassed, et al.. (2005). Ring chromosome 9 [r(9)(p24q34)]: A report of two cases. American Journal of Medical Genetics Part A. 138A(3). 229–235. 30 indexed citations

17.

Casas, Kari, Tarja Mononen, Susan J. Hassed, et al.. (2004). Chromosome 2q terminal deletion: Report of 6 new patients and review of phenotype‐breakpoint correlations in 66 individuals. American Journal of Medical Genetics Part A. 130A(4). 331–339. 70 indexed citations

18.

Wang, Jianzhou, et al.. (2003). Uterine Tumor Resembling Ovarian Sex Cord Tumor: Report of a Case With t(X;6)(p22.3;q23.1) and t(4;18)(q21.1;q21.3). Diagnostic Molecular Pathology. 12(3). 174–180. 28 indexed citations

19.

Zhang, Lijun, et al.. (2002). Duplication 15q in a patient with t(8;21) acute myeloblastic leukemia (M2). Cancer Genetics and Cytogenetics. 133(2). 148–151. 4 indexed citations

20.

Tuck‐Müller, Cathy M., Harold Chen, Shibo Li, et al.. (1995). Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature. Human Genetics. 96(1). 119–129. 81 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