Wenjun Xia

524 total citations
20 papers, 275 citations indexed

About

Wenjun Xia is a scholar working on Molecular Biology, Sensory Systems and Cancer Research. According to data from OpenAlex, Wenjun Xia has authored 20 papers receiving a total of 275 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 8 papers in Sensory Systems and 5 papers in Cancer Research. Recurrent topics in Wenjun Xia's work include Hearing, Cochlea, Tinnitus, Genetics (8 papers), Cancer-related molecular mechanisms research (3 papers) and Vestibular and auditory disorders (3 papers). Wenjun Xia is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (8 papers), Cancer-related molecular mechanisms research (3 papers) and Vestibular and auditory disorders (3 papers). Wenjun Xia collaborates with scholars based in China, South Korea and United States. Wenjun Xia's co-authors include Ken McKinnon, J. Kenneth Baillie, Peter Simmonds, Duan Ma, Peng Jiang, Fei Liu, Nan Jiang, Youxiang Mao, Jing Ma and Jianbo Huang and has published in prestigious journals such as Nature Neuroscience, Nature reviews. Immunology and PLoS ONE.

In The Last Decade

Wenjun Xia

17 papers receiving 272 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Wenjun Xia China	10	157	58	34	27	23	20	275
Anwen Bullen United Kingdom	10	135 0.9×	117 2.0×	35 1.0×	23 0.9×	18 0.8×	16	343
Dharmeshkumar Patel United States	10	317 2.0×	164 2.8×	16 0.5×	17 0.6×	31 1.3×	29	549
David Dahan Canada	11	276 1.8×	23 0.4×	11 0.3×	17 0.6×	55 2.4×	14	402
Barbara Hauert Switzerland	8	168 1.1×	54 0.9×	17 0.5×	39 1.4×	31 1.3×	11	372
Zhangfei Shen United States	13	262 1.7×	12 0.2×	30 0.9×	46 1.7×	66 2.9×	25	439
Jonas Åström Sweden	13	635 4.0×	20 0.3×	13 0.4×	17 0.6×	44 1.9×	17	789
Christopher Batters Germany	14	303 1.9×	30 0.5×	16 0.5×	12 0.4×	22 1.0×	24	448
Baptiste Fischer Belgium	6	297 1.9×	6 0.1×	42 1.2×	23 0.9×	36 1.6×	10	415
Karin M. Green United States	12	219 1.4×	38 0.7×	6 0.2×	74 2.7×	51 2.2×	16	448
Yuan Mang Denmark	11	241 1.5×	12 0.2×	45 1.3×	9 0.3×	14 0.6×	17	400

Countries citing papers authored by Wenjun Xia

Since Specialization

Citations

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

Fields of papers citing papers by Wenjun Xia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wenjun Xia

This figure shows the co-authorship network connecting the top 25 collaborators of Wenjun Xia. A scholar is included among the top collaborators of Wenjun Xia 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 Wenjun Xia. Wenjun Xia 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

Mao, Youxiang, et al.. (2026). Metabolites as signalling molecules in the tumour immune microenvironment. Nature reviews. Immunology.

Mao, Youxiang, et al.. (2024). Metabolic reprogramming, sensing, and cancer therapy. Cell Reports. 43(12). 115064–115064. 30 indexed citations

Xia, Wenjun & Peng Jiang. (2024). p53 promotes antiviral innate immunity by driving hexosamine metabolism. Cell Reports. 43(2). 113724–113724. 4 indexed citations

Liu, Xiaojie, et al.. (2024). Brexpiprazole Prevents the Malignant Progression of Human Colorectal Cancer Cells and Increases Its Sensitivity to EGFR Inhibition. Frontiers in Bioscience-Landmark. 29(5). 174–174.

Zhao, Lina, Wenjun Xia, & Peng Jiang. (2021). CREB1 and ATF1 Negatively Regulate Glutathione Biosynthesis Sensitizing Cells to Oxidative Stress. Frontiers in Cell and Developmental Biology. 9. 698264–698264. 5 indexed citations

Liu, Yun-Tao, Chang-Lu Tao, Xiaokang Zhang, et al.. (2020). Mesophasic organization of GABAA receptors in hippocampal inhibitory synapses. Nature Neuroscience. 23(12). 1589–1596. 52 indexed citations

Xia, Wenjun, Jing Ma, Jianbo Huang, et al.. (2019). Novel TRRAP mutation causes autosomal dominant non‐syndromic hearing loss. Clinical Genetics. 96(4). 300–308. 13 indexed citations

Xia, Wenjun, Jing Ma, Jianbo Huang, et al.. (2019). Mutations in TOP 2B cause autosomal‐dominant hereditary hearing loss via inhibition of the PI 3K‐Akt signalling pathway. FEBS Letters. 593(15). 2008–2018. 17 indexed citations

Huang, Jianbo, Xiaogang Bao, Wenjun Xia, et al.. (2019). Functional analysis of a de novo mutation c.1692 del A of the PHEX gene in a Chinese family with X-linked hypophosphataemic rickets. Bone and Joint Research. 8(8). 405–413. 1 indexed citations

10.

Yang, Jichun, Jing Ma, Yu Xiong, et al.. (2018). Epigenetic regulation of megakaryocytic and erythroid differentiation by PHF2 histone demethylase. Journal of Cellular Physiology. 233(9). 6841–6852. 10 indexed citations

11.

Ma, Jing, Xianming Wang, Deyong Xiao, et al.. (2017). A novel loss-of-function heterozygous BRCA2 c.8946_8947delAG mutation found in a Chinese woman with family history of breast cancer. Journal of Cancer Research and Clinical Oncology. 143(4). 631–637. 4 indexed citations

12.

Xia, Wenjun & Jinzhi Lei. (2017). Formulation of the protein synthesis rate with sequence information. Mathematical Biosciences & Engineering. 15(2). 507–522.

13.

Xia, Wenjun, Fei Liu, Jing Ma, et al.. (2017). New role of LRP5, associated with nonsyndromic autosomal-recessive hereditary hearing loss. Human Mutation. 38(10). 1421–1431. 9 indexed citations

14.

Liu, Fei, Wenjun Xia, Lili Hao, et al.. (2016). Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss. Journal of Translational Medicine. 14(1). 29–29. 11 indexed citations

15.

Xia, Wenjun, Fei Liu, Jing Ma, et al.. (2016). SLC44A4mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss. Human Molecular Genetics. 26(16). ddw394–ddw394. 12 indexed citations

16.

Xia, Wenjun, Fei Liu, & Duan Ma. (2016). Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness. Frontiers of Medicine. 10(2). 137–142. 12 indexed citations

17.

Shen, Xiaofang, Fei Liu, Yingzhi Wang, et al.. (2015). Down-regulation of msrb3 and destruction of normal auditory system development through hair cell apoptosis in zebrafish. The International Journal of Developmental Biology. 59(4-5-6). 195–203. 16 indexed citations

18.

Liu, Fei, Wenjun Xia, Yingzhi Wang, et al.. (2015). Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in Zebrafish. PLoS ONE. 10(9). e0136832–e0136832. 8 indexed citations

19.

Liu, Fei, Fan Yang, Wenjun Xia, et al.. (2015). Grhl1 deficiency affects inner ear development in zebrafish. The International Journal of Developmental Biology. 59(10-11-12). 417–423. 8 indexed citations

20.

Simmonds, Peter, Wenjun Xia, J. Kenneth Baillie, & Ken McKinnon. (2013). Modelling mutational and selection pressures on dinucleotides in eukaryotic phyla –selection against CpG and UpA in cytoplasmically expressed RNA and in RNA viruses. BMC Genomics. 14(1). 610–610. 63 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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