Xiaofeng Wei

4.7k total citations
42 papers, 798 citations indexed

About

Xiaofeng Wei is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, Xiaofeng Wei has authored 42 papers receiving a total of 798 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 15 papers in Hematology and 14 papers in Molecular Biology. Recurrent topics in Xiaofeng Wei's work include Hemoglobinopathies and Related Disorders (23 papers), Iron Metabolism and Disorders (13 papers) and Prenatal Screening and Diagnostics (6 papers). Xiaofeng Wei is often cited by papers focused on Hemoglobinopathies and Related Disorders (23 papers), Iron Metabolism and Disorders (13 papers) and Prenatal Screening and Diagnostics (6 papers). Xiaofeng Wei collaborates with scholars based in China, Japan and United States. Xiaofeng Wei's co-authors include Xiangmin Xu, Xuan Shang, Yuqiu Zhou, Fu Xiong, Ren Cai, Xinhua Zhang, Jiwei Huang, Jiwu Lou, Manna Sun and Lingwen Zeng and has published in prestigious journals such as Advanced Materials, Blood and Scientific Reports.

In The Last Decade

Xiaofeng Wei

40 papers receiving 787 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Xiaofeng Wei China	16	449	336	259	144	100	42	798
Yunyan He China	12	168 0.4×	131 0.4×	198 0.8×	59 0.4×	78 0.8×	41	512
Christina Gamba‐Vitalo United States	13	62 0.1×	136 0.4×	681 2.6×	24 0.2×	87 0.9×	21	996
Anna Maria Offidani Italy	20	77 0.2×	85 0.3×	115 0.4×	17 0.1×	47 0.5×	51	1.0k
Eun Jung Baek South Korea	14	74 0.2×	134 0.4×	137 0.5×	17 0.1×	21 0.2×	43	569
Maria Vadon Austria	5	53 0.1×	205 0.6×	50 0.2×	33 0.2×	74 0.7×	6	376
Wenting Chen China	14	62 0.1×	68 0.2×	182 0.7×	16 0.1×	17 0.2×	41	648
Sonja Serafini Italy	15	16 0.0×	58 0.2×	391 1.5×	78 0.5×	101 1.0×	27	1.0k
Ilnaz Rahimmanesh Iran	14	53 0.1×	35 0.1×	285 1.1×	17 0.1×	41 0.4×	44	534
Anna Hogan Ireland	14	20 0.0×	60 0.2×	244 0.9×	16 0.1×	96 1.0×	27	766
Maria Pamela Dobay Switzerland	11	51 0.1×	54 0.2×	297 1.1×	11 0.1×	22 0.2×	24	645

Countries citing papers authored by Xiaofeng Wei

Since Specialization

Citations

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

Fields of papers citing papers by Xiaofeng Wei

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiaofeng Wei

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

Wei, Xiaofeng, et al.. (2025). Ultra-sensitive detection of Cu2+ in water and infant formula using a carbon dot-embedded MIL-53 electrochemiluminescence sensor. Food Chemistry. 485. 144338–144338. 1 indexed citations

Zhang, Miao, et al.. (2025). A comprehensive analysis of O3 variation and source contributions of VOCs-oriented to O3 pollution episodes over Jinan city, China. Atmospheric Pollution Research. 16(8). 102552–102552. 1 indexed citations

Wei, Xiaofeng, et al.. (2024). SUPT5H mutations associated with elevation of Hb A2 level: Identification of two novel variants and literature review. Gene. 908. 148294–148294. 3 indexed citations

Wei, Xiaofeng, et al.. (2024). Loss-of-function SLC25A20 variant causes carnitine-acylcarnitine translocase deficiency by reducing SLC25A20 protein stability. Gene. 940. 149201–149201. 1 indexed citations

Zhang, Yanxia, et al.. (2023). A novel gain‐of‐function PIP4K2A mutation elevates the expression of β‐globin and aggravates the severity of α‐thalassemia. British Journal of Haematology. 202(5). 1018–1023. 1 indexed citations

Wei, Xiaofeng, Yanting Zhang, Qian Zhang, et al.. (2023). The Strength of hERG Inhibition by Erythromycin at Different Temperatures Might Be Due to Its Interacting Features with the Channels. Molecules. 28(13). 5176–5176. 1 indexed citations

Wan, Jia, Yongzhi Liang, Xiaofeng Wei, Haiyi Liang, & Xu‐Lin Chen. (2023). Chitosan-based double network hydrogel loading herbal small molecule for accelerating wound healing. International Journal of Biological Macromolecules. 246. 125610–125610. 25 indexed citations

Zhang, Qiyu, et al.. (2023). Itaconate attenuates autoimmune hepatitis via PI3K/AKT/mTOR pathway-mediated inhibition of dendritic cell maturation and autophagy. Heliyon. 9(7). e17551–e17551. 19 indexed citations

Zhang, Qianqian, Peng Lin, Aiping Mao, et al.. (2023). An unusual case of thalassemia intermedia with inheritable complex repeats detected by single-molecule optical mapping. Haematologica. 109(3). 1000–1006. 2 indexed citations

10.

Wei, Xiaofeng, et al.. (2022). A novel splicing mutation of ANK1 is associated with phenotypic heterogeneity of hereditary spherocytosis in a Chinese family. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1869(1). 166595–166595. 3 indexed citations

11.

Ye, Yuhua, et al.. (2021). TEA domain transcription factor 4 modulates repression of fetal haemoglobin by direct binding to the γ‐globin gene promoters. British Journal of Haematology. 195(5). 764–769. 2 indexed citations

12.

Cai, Decheng, Fang Yang, Yi Cheng, et al.. (2020). Unusual survival of a twin with homozygous α<sup>0</sup>-thalassemia due to chimerism. Haematologica. 106(5). 1507–1510.

13.

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

14.

Feng, Liping, Jiawen Zhu, Haitao Chang, et al.. (2016). The CodY regulator is essential for virulence in Streptococcus suis serotype 2. Scientific Reports. 6(1). 21241–21241. 42 indexed citations

15.

Wang, Jin, Youming Chen, Dun Liu, et al.. (2014). DNA hypermethylation and X chromosome inactivation are major determinants of phenotypic variation in women heterozygous for G6PD mutations. Blood Cells Molecules and Diseases. 53(4). 241–245. 13 indexed citations

16.

Huang, Jiwei, Xuan Shang, Ying Zhao, et al.. (2013). A novel fusion gene and a common α0-thalassemia deletion cause hemoglobin H disease in a Chinese family. Blood Cells Molecules and Diseases. 51(1). 31–34. 13 indexed citations

17.

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

18.

Wei, Xiaofeng, et al.. (2010). Molecular characterization of a novel 27.6-kb deletion causing α+ thalassemia in a Chinese family. Annals of Hematology. 90(1). 17–22. 18 indexed citations

19.

Lou, Jiwu, Qian Li, Xiaofeng Wei, Jiwei Huang, & Xiangmin Xu. (2010). Identification of the Linkage of a 1.357 KB β-Globin Gene Deletion and A γ-Globin Gene Triplication in a Chinese Family. Hemoglobin. 34(4). 343–353. 9 indexed citations

20.

Wang, Hongjun, Yuanyuan Jiang, Xiaofeng Wei, et al.. (2009). Silibinin induces protective superoxide generation in human breast cancer MCF-7 cells. Free Radical Research. 44(1). 90–100. 26 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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