Huijun Wang

3.3k total citations
160 papers, 2.0k citations indexed

About

Huijun Wang is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Huijun Wang has authored 160 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 87 papers in Molecular Biology, 62 papers in Genetics and 25 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Huijun Wang's work include Congenital heart defects research (29 papers), Genomics and Rare Diseases (21 papers) and Congenital Heart Disease Studies (16 papers). Huijun Wang is often cited by papers focused on Congenital heart defects research (29 papers), Genomics and Rare Diseases (21 papers) and Congenital Heart Disease Studies (16 papers). Huijun Wang collaborates with scholars based in China, United States and United Kingdom. Huijun Wang's co-authors include Wenhao Zhou, Bingbing Wu, Duan Ma, Lin Yang, Yanyan Qian, Yulan Lu, Xinran Dong, Xiaojing Ma, Ping Zhang and Guoying Huang and has published in prestigious journals such as Blood, Bioinformatics and PLoS ONE.

In The Last Decade

Huijun Wang

146 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Huijun Wang China 24 1.1k 650 259 248 227 160 2.0k
Gail E. Graham Canada 23 786 0.7× 549 0.8× 261 1.0× 149 0.6× 258 1.1× 60 1.9k
Stefan Böhringer Netherlands 30 529 0.5× 464 0.7× 197 0.8× 201 0.8× 241 1.1× 110 2.4k
Carl Virtanen Canada 27 1.5k 1.4× 446 0.7× 214 0.8× 244 1.0× 227 1.0× 56 2.7k
Susan M. White Australia 33 1.4k 1.3× 1.6k 2.4× 180 0.7× 221 0.9× 266 1.2× 113 3.5k
Hui‐Teng Cheng Taiwan 23 1.5k 1.4× 409 0.6× 202 0.8× 409 1.6× 360 1.6× 45 2.6k
Matthew S. Lebo United States 27 973 0.9× 1.5k 2.4× 151 0.6× 132 0.5× 172 0.8× 74 2.9k
Jean‐Baptiste Cazier United Kingdom 24 1.1k 1.0× 532 0.8× 155 0.6× 166 0.7× 159 0.7× 76 2.4k
Francesco Marabita Sweden 17 1.6k 1.5× 446 0.7× 239 0.9× 176 0.7× 173 0.8× 24 2.5k
Michael T. Geraghty United States 36 1.9k 1.7× 896 1.4× 176 0.7× 283 1.1× 337 1.5× 121 3.6k
Peter Farndon United Kingdom 24 1.4k 1.3× 969 1.5× 171 0.7× 173 0.7× 272 1.2× 63 3.0k

Countries citing papers authored by Huijun Wang

Since Specialization
Citations

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

Fields of papers citing papers by Huijun Wang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Huijun Wang

This figure shows the co-authorship network connecting the top 25 collaborators of Huijun Wang. A scholar is included among the top collaborators of Huijun Wang 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 Huijun Wang. Huijun Wang 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.
Tang, Tingting, Liyuan Yang, Huijun Wang, et al.. (2025). Stachyose alleviates coronary heart disease by modulating the metabolic pathways influenced by gut microbiota and short-chain fatty acids. Journal of Agriculture and Food Research. 24. 102304–102304.
2.
Yu, Hong, Wenbing Liu, Junping Zhang, et al.. (2025). The Clinical and Molecular Characterization of Distinct Subtypes in Adult T Cell Acute Lymphoblastic Leukemia. Cancer Science. 116(4). 1126–1138.
3.
Wang, Yaqiong, Huijun Wang, Haili Jiang, et al.. (2024). Development and validation of machine-learning models of diet management for hyperphenylalaninemia: a multicenter retrospective study. BMC Medicine. 22(1). 377–377.
4.
Yin, Tingting, Yunfei Liao, Xu Li, et al.. (2024). Characterization of a human induced pluripotent stem cell line (FDCHi015-A) derived from PBMCs of a patient harbouring ALDOB mutation. Stem Cell Research. 78. 103451–103451. 1 indexed citations
5.
Wang, Ji, Gang Li, Bingbing Wu, et al.. (2023). Novel Variants of PPP2R1A in Catalytic Subunit Binding Domain and Genotype–Phenotype Analysis in Neurodevelopmentally Delayed Patients. Genes. 14(9). 1750–1750. 3 indexed citations
6.
Zhang, Ping, Bingbing Wu, Yaqiong Wang, et al.. (2022). Identification of Pathogenic Variants in RPGRIP1L with Meckel Syndrome and Preimplantation Genetic Testing in a Chinese Family. Reproductive Sciences. 29(8). 2200–2207. 5 indexed citations
7.
Zhang, Ping, Wenjing Ying, Yaqiong Wang, et al.. (2022). Intron retention by a novel intronic mutation in DKC1 gene caused recurrent still birth and early death in a Chinese family. Molecular Genetics & Genomic Medicine. 10(6). e1934–e1934. 4 indexed citations
8.
Dong, Xinran, Yulan Lu, Bingbing Wu, et al.. (2021). Genetic etiologies associated with infantile hydrocephalus in a Chinese infantile cohort. World Journal of Pediatrics. 17(3). 305–316. 4 indexed citations
9.
Yu, Sha, Wenxia Chen, Yunfei Zhang, et al.. (2021). Apparent homozygosity for a novel splicing variant in EPS8 causes congenital profound hearing loss. European Journal of Medical Genetics. 64(12). 104362–104362. 3 indexed citations
10.
Yu, Sha, Wenxia Chen, Yun‐Fei Zhang, et al.. (2021). Recessive LOXHD1 variants cause a prelingual down-sloping hearing loss: genotype-phenotype correlation and three additional children with novel variants. International Journal of Pediatric Otorhinolaryngology. 145. 110715–110715. 3 indexed citations
11.
Yu, Sha, Wei Lü, Chao Chen, et al.. (2020). Novel heterozygous GATA3 and SLC34A3 variants in a 6‐year‐old boy with Barakat syndrome and hypercalciuria. Molecular Genetics & Genomic Medicine. 8(5). e1222–e1222. 5 indexed citations
12.
Liu, Bo, Yulan Lu, Bingbing Wu, et al.. (2020). Survival Motor Neuron Gene Copy Number Analysis by Exome Sequencing. Journal of Molecular Diagnostics. 22(5). 619–628. 15 indexed citations
13.
Wang, Huijun, Yulan Lu, Xinran Dong, et al.. (2020). Optimized trio genome sequencing (OTGS) as a first-tier genetic test in critically ill infants: practice in China. Human Genetics. 139(4). 473–482. 40 indexed citations
14.
Liu, Bo, Bingbing Wu, Yi Lu, et al.. (2020). A Novel, Recurrent, 3.6-kb Deletion in the PYGL Gene Contributes to Glycogen Storage Disease Type VI. Journal of Molecular Diagnostics. 22(12). 1373–1382. 4 indexed citations
15.
Yu, Sha, Bingbing Wu, Yanyan Qian, et al.. (2019). Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein–Taybi Syndrome kids with high frequency of polydactyly. Molecular Genetics & Genomic Medicine. 7(12). e1009–e1009. 9 indexed citations
16.
Yang, Lin, et al.. (2018). Evaluation of turn around time and diagnostic accuracy of the next generation sequencing data analysis pipeline version 2 of Children's Hospital of Fudan University. 13(2). 118. 5 indexed citations
17.
Wu, Weiwei, Linli Chen, Changhui Liu, et al.. (2016). Development of the 19 X‐STR loci multiplex system and genetic analysis of a Zhejiang Han population in China. Electrophoresis. 37(15-16). 2260–2272. 25 indexed citations
18.
Huang, Feifei, et al.. (2015). [Pre-packaged foods' nutritional ingredients analysis among 706 adult residents in cities in China].. PubMed. 49(2). 152–5. 2 indexed citations
19.
Wang, Huijun. (2012). Summary on the study of traditional Chinese medicine syndrome based on structural equation model. 1 indexed citations
20.
Sheng, Wei, Huijun Wang, Xiaojing Ma, et al.. (2012). LINE-1 methylation status and its association with tetralogy of fallot in infants. BMC Medical Genomics. 5(1). 20–20. 43 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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