Wanjun Zhou

850 total citations
36 papers, 406 citations indexed

About

Wanjun Zhou is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Wanjun Zhou has authored 36 papers receiving a total of 406 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 13 papers in Hematology and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Wanjun Zhou's work include Hemoglobinopathies and Related Disorders (19 papers), Prenatal Screening and Diagnostics (11 papers) and Iron Metabolism and Disorders (7 papers). Wanjun Zhou is often cited by papers focused on Hemoglobinopathies and Related Disorders (19 papers), Prenatal Screening and Diagnostics (11 papers) and Iron Metabolism and Disorders (7 papers). Wanjun Zhou collaborates with scholars based in China, Malaysia and India. Wanjun Zhou's co-authors include Ling Xia, Gongke Li, Xiangmin Xu, Yanlong Chen, Jiani Yang, Yanhui Zhong, Simin Huang, Yanshu Zhang, Tizhen Yan and Fu Xiong and has published in prestigious journals such as PLoS ONE, Analytical Chemistry and Analytical Biochemistry.

In The Last Decade

Wanjun Zhou

35 papers receiving 395 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wanjun Zhou China 11 154 141 76 72 66 36 406
Paromita Dey United States 9 35 0.2× 312 2.2× 85 1.1× 53 0.7× 9 0.1× 15 509
Kittiphong Paiboonsukwong Thailand 11 203 1.3× 180 1.3× 50 0.7× 159 2.2× 35 0.5× 37 440
Deborah Chen Canada 10 50 0.3× 50 0.4× 29 0.4× 88 1.2× 32 0.5× 20 369
Paraskevi Diamanti United Kingdom 9 27 0.2× 108 0.8× 22 0.3× 110 1.5× 22 0.3× 24 333
Christopher M. Williams United Kingdom 10 15 0.1× 104 0.7× 24 0.3× 52 0.7× 7 0.1× 14 312
Raheleh Torabi Iran 10 12 0.1× 159 1.1× 84 1.1× 89 1.2× 23 0.3× 17 429
A. N. Lestas United Kingdom 10 60 0.4× 90 0.6× 10 0.1× 118 1.6× 91 1.4× 20 348
Christoph Grabmer Austria 12 81 0.5× 96 0.7× 229 3.0× 103 1.4× 4 0.1× 25 563
В. А. Сергунова Russia 12 27 0.2× 110 0.8× 34 0.4× 37 0.5× 53 0.8× 52 392
Christelle Machon France 14 14 0.1× 238 1.7× 29 0.4× 9 0.1× 26 0.4× 44 526

Countries citing papers authored by Wanjun Zhou

Since Specialization
Citations

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

Fields of papers citing papers by Wanjun Zhou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wanjun Zhou

This figure shows the co-authorship network connecting the top 25 collaborators of Wanjun Zhou. A scholar is included among the top collaborators of Wanjun 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 Wanjun Zhou. Wanjun 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
1.
Li, Xue, Shanshan Luo, Wanjun Zhou, et al.. (2024). Cav3.2 deletion attenuates nonalcoholic fatty liver disease in mice. Gene. 929. 148812–148812. 1 indexed citations
2.
Li, Xue, Zhetao Zhang, Hongtao Wang, et al.. (2023). Cav3.2 channel regulates cerebral ischemia/reperfusion injury: a promising target for intervention. Neural Regeneration Research. 19(11). 2480–2487. 9 indexed citations
3.
4.
He, Jun, et al.. (2022). One-step genotyping of α-thalassaemia by multiplex symmetric PCR melting curve. Journal of Clinical Pathology. 76(9). 632–636.
5.
Zhang, Qiang, Xiaojun Wen, Sheng He, et al.. (2020). A Nested Asymmetric PCR Melting Curve Assay for One-Step Genotyping of Nondeletional α-Thalassemia Mutations. Journal of Molecular Diagnostics. 22(6). 794–800. 5 indexed citations
6.
Li, Zhiming, Fei Zhu, Xiaofeng Wei, et al.. (2020). Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α0-thalassemia by targeted next-generation sequencing. Molecular Genetics and Genomics. 295(2). 505–514. 8 indexed citations
7.
He, Fei, Wanjun Zhou, Ren Cai, Tizhen Yan, & Xiangmin Xu. (2018). Systematic assessment of the performance of whole-genome amplification for SNP/CNV detection and β-thalassemia genotyping. Journal of Human Genetics. 63(4). 407–416. 20 indexed citations
8.
9.
Zhang, Qiang, et al.. (2017). α+-Thalassemia Caused by an 811 bp Deletion in Individuals from Nanning, Guangxi: A Report of Two Cases. Hemoglobin. 41(3). 185–188. 1 indexed citations
10.
Zhou, Wanjun, Hao Shuxian, Laihao Li, et al.. (2016). Research of Purification and Antioxidant Function of the Chondroitin Sulfate Extracted from Sturgeon. 1 indexed citations
11.
Lin, Li, Danna Chen, Jing Guo, Wanjun Zhou, & Xiangmin Xu. (2015). Development of a capillary zone electrophoresis method for rapid determination of human globin chains in α and β-thalassemia subjects. Blood Cells Molecules and Diseases. 55(1). 62–67. 1 indexed citations
12.
Fang, Ping, Liang Li, Jian Zeng, et al.. (2015). Molecular characterization and copy number of SMN1, SMN2 and NAIP in Chinese patients with spinal muscular atrophy and unrelated healthy controls. BMC Musculoskeletal Disorders. 16(1). 11–11. 34 indexed citations
13.
He, Sheng, Qian Qin, Shang Yi, et al.. (2015). First Description of aβ-Thalassemia Mutation, −86 (C > G) (HBB: c.−136C > G), in a Chinese Family. Hemoglobin. 39(6). 448–450. 4 indexed citations
14.
15.
Zhou, Wanjun, Ge Wang, Fu Xiong, et al.. (2013). A Multiplex qPCR Gene Dosage Assay for Rapid Genotyping and Large-Scale Population Screening for Deletional α-Thalassemia. Journal of Molecular Diagnostics. 15(5). 642–651. 22 indexed citations
16.
Xiong, Fu, Qian Li, Cuimei Zhang, et al.. (2012). Analyses of GATA4, NKX2.5, and TFAP2B genes in subjects from southern China with sporadic congenital heart disease. Cardiovascular Pathology. 22(2). 141–145. 33 indexed citations
17.
Luo, Weihao, Bingyi Wu, Fu Xiong, et al.. (2012). Rapid determination of human globin chains using reversed-phase high-performance liquid chromatography. Journal of Chromatography B. 901. 53–58. 14 indexed citations
18.
Wu, Heming, et al.. (2011). Rapid, accurate detection of TMPRSS6 gene causative mutations with a high-resolution melting assay. Blood Cells Molecules and Diseases. 47(3). 198–204. 2 indexed citations
19.
Yan, Tizhen, Qiuhua Mo, Ren Cai, et al.. (2011). Reliable Detection of Paternal SNPs within Deletion Breakpoints for Non-Invasive Prenatal Exclusion of Homozygous α0-Thalassemia in Maternal Plasma. PLoS ONE. 6(9). e24779–e24779. 14 indexed citations
20.
Li, Qiang, Liyan Li, Sheng‐Wen Huang, et al.. (2008). Rapid genotyping of known mutations and polymorphisms in β-globin gene based on the DHPLC profile patterns of homoduplexes and heteroduplexes. Clinical Biochemistry. 41(9). 681–687. 23 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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2026