Qingrun Zhang

15.1k total citations
23 papers, 745 citations indexed

About

Qingrun Zhang is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Qingrun Zhang has authored 23 papers receiving a total of 745 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Genetics and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Qingrun Zhang's work include Genetic Associations and Epidemiology (10 papers), Genetic Mapping and Diversity in Plants and Animals (5 papers) and Genetic and phenotypic traits in livestock (4 papers). Qingrun Zhang is often cited by papers focused on Genetic Associations and Epidemiology (10 papers), Genetic Mapping and Diversity in Plants and Animals (5 papers) and Genetic and phenotypic traits in livestock (4 papers). Qingrun Zhang collaborates with scholars based in United States, Canada and China. Qingrun Zhang's co-authors include Quan Long, Jürg Ott, Changqing Zeng, Wen Tan, Yang Gao, Tong Sun, Dongxin Lin, Sufang Ma, Magnus Nordborg and Yongli Guo and has published in prestigious journals such as Nature Genetics, Bioinformatics and PLoS ONE.

In The Last Decade

Qingrun Zhang

22 papers receiving 727 citations

Peers

Qingrun Zhang

GENET

ONCOL

Arunkanth Ankala United States

Manqiu Cao United States

Andy Rimmer United Kingdom

Andrew Crenshaw United States

Genqing Liang United States

Mathew A. Sloane Australia

Carol Jones United States

Jairo Navarro Gonzalez United States

W. T. Schroeder United States

Galt P Barber United States

Arunkanth Ankala United States

Qingrun Zhang

635 ×1.5

436 ×1.8

GENET

288 ×1.5

105 ×1.3

21 ×0.3

ONCOL

Citations per year, relative to Qingrun Zhang Qingrun Zhang (= 1×) peers Arunkanth Ankala

Countries citing papers authored by Qingrun Zhang

Since Specialization

Citations

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

Fields of papers citing papers by Qingrun Zhang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Qingrun Zhang

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

All Works

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20 of 20 papers shown

Su, Liya, Timothy J. Purwin, Sophia Ran, et al.. (2025). Selective USP7 Inhibition Synergizes with MEK1/2 Inhibitor to Enhance Immune Responses and Potentiate Anti–PD-1 Therapy in NRAS-Mutant Melanoma. Journal of Investigative Dermatology. 145(10). 2549–2561.e11. 3 indexed citations

Ghoreishi, Seyed Kamran, et al.. (2025). Using penalized-distance likelihood functions to analyze high-dimensional sparse/non-sparse data. AStA Advances in Statistical Analysis. 109(3). 509–528.

Yang, Yang, Biao Ma, Qingrun Zhang, et al.. (2023). ING1 inhibits Twist1 expression to block EMT and is antagonized by the HDAC inhibitor vorinostat. European Journal of Cell Biology. 102(3). 151341–151341. 6 indexed citations

Li, Qing, et al.. (2023). rvTWAS: identifying gene–trait association using sequences by utilizing transcriptome-directed feature selection. Genetics. 226(2). 3 indexed citations

Zhang, Qingrun, et al.. (2023). A multi-threaded approach to genotype pattern mining for detecting digenic disease genes. Frontiers in Genetics. 14. 1222517–1222517. 1 indexed citations

Cao, Chen, Devin Kwok, Qing Li, et al.. (2021). Disentangling genetic feature selection and aggregation in transcriptome-wide association studies. Genetics. 220(2). 19 indexed citations

Chen, Xin, Qingrun Zhang, & Thierry Chekouo. (2021). Filtering High-Dimensional Methylation Marks With Extremely Small Sample Size: An Application to Gastric Cancer Data. Frontiers in Genetics. 12. 705708–705708. 6 indexed citations

Mansoor, Adnan, et al.. (2019). Expression Profiling Reveals Involvement of WNT Pathway in the Malignant Progression of Sessile Serrated Adenomas. American Journal Of Pathology. 189(9). 1732–1743. 3 indexed citations

Zhang, Qingrun, Chris Tyler‐Smith, & Quan Long. (2015). An extended Tajima’s D neutrality test incorporating SNP calling and imputation uncertainties. Statistics and Its Interface. 8(4). 447–456. 6 indexed citations

10.

Zhang, Qingrun, Quan Long, & Jürg Ott. (2014). AprioriGWAS, a New Pattern Mining Strategy for Detecting Genetic Variants Associated with Disease through Interaction Effects. PLoS Computational Biology. 10(6). e1003627–e1003627. 25 indexed citations

11.

Long, Quan, Fernando A. Rabanal, Dazhe Meng, et al.. (2013). Massive genomic variation and strong selection in Arabidopsis thaliana lines from Sweden. Nature Genetics. 45(8). 884–890. 272 indexed citations

12.

Long, Quan, et al.. (2013). JAWAMix5: an out-of-core HDF5-based java implementation of whole-genome association studies using mixed models. Bioinformatics. 29(9). 1220–1222. 9 indexed citations

13.

Long, Quan, Daniel Jeffares, Qingrun Zhang, et al.. (2011). PoolHap: Inferring Haplotype Frequencies from Pooled Samples by Next Generation Sequencing. PLoS ONE. 6(1). e15292–e15292. 27 indexed citations

14.

Long, Quan, Qingrun Zhang, & Jürg Ott. (2009). Detecting disease-associated genotype patterns. BMC Bioinformatics. 10(S1). S75–S75. 25 indexed citations

15.

Shaaban, Sherin, Toshihiko Matsuo, Satoshi Hasebe, et al.. (2009). Chromosomes 4q28.3 and 7q31.2 as New Susceptibility Loci for Comitant Strabismus. Investigative Ophthalmology & Visual Science. 50(2). 654–654. 30 indexed citations

16.

Zhang, Qingrun, Shuang Wang, & Jürg Ott. (2008). Combining identity by descent and association in genetic case-control studies. BMC Genetics. 9(1). 42–42. 7 indexed citations

17.

Sun, Tong, Yang Gao, Wen Tan, et al.. (2008). Reply to ”A promoter polymorphism in the CASP8 gene is not associated with cancer risk”. Nature Genetics. 40(3). 260–261. 2 indexed citations

18.

Kim, Ivana K., Fei Ji, Margaux A. Morrison, et al.. (2008). Comprehensive analysis of CRP, CFH Y402H and environmental risk factors on risk of neovascular age-related macular degeneration.. PubMed. 14. 1487–95. 35 indexed citations

19.

Sun, Tong, Yang Gao, Wen Tan, et al.. (2007). A six-nucleotide insertion-deletion polymorphism in the CASP8 promoter is associated with susceptibility to multiple cancers. Nature Genetics. 39(5). 605–613. 218 indexed citations

20.

Sun, Tong, Yang Gao, Wen Tan, et al.. (2006). Haplotypes in Matrix Metalloproteinase Gene Cluster on Chromosome 11q22 Contribute to the Risk of Lung Cancer Development and Progression. Clinical Cancer Research. 12(23). 7009–7017. 36 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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