Xia Zhan

623 total citations
39 papers, 376 citations indexed

About

Xia Zhan is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Xia Zhan has authored 39 papers receiving a total of 376 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 13 papers in Clinical Biochemistry and 12 papers in Physiology. Recurrent topics in Xia Zhan's work include Metabolism and Genetic Disorders (13 papers), Lysosomal Storage Disorders Research (8 papers) and Folate and B Vitamins Research (8 papers). Xia Zhan is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Lysosomal Storage Disorders Research (8 papers) and Folate and B Vitamins Research (8 papers). Xia Zhan collaborates with scholars based in China and United States. Xia Zhan's co-authors include Huiwen Zhang, Xuefan Gu, Wenfu Tan, Lianshu Han, Wenjuan Qiu, Yuan Liu, Ying Kong, Hong Xin, Xiaolan Gao and Lili Liang and has published in prestigious journals such as American Journal of Obstetrics and Gynecology, Stem Cells and Molecular Cancer.

In The Last Decade

Xia Zhan

33 papers receiving 369 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Xia Zhan China 13 181 127 69 62 52 39 376
Gülden Gökçay Türkiye 13 277 1.5× 100 0.8× 213 3.1× 86 1.4× 34 0.7× 30 492
Shigeki Fujisawa Japan 13 134 0.7× 120 0.9× 71 1.0× 59 1.0× 11 0.2× 26 653
Antonio Velázquez Mexico 12 173 1.0× 53 0.4× 92 1.3× 178 2.9× 10 0.2× 26 477
Lynwen A. James United Kingdom 9 80 0.4× 67 0.5× 50 0.7× 16 0.3× 18 0.3× 11 404
Meiyuan Huang China 11 158 0.9× 60 0.5× 25 0.4× 41 0.7× 24 0.5× 27 351
Nishan Guha United Kingdom 12 136 0.8× 40 0.3× 20 0.3× 101 1.6× 40 0.8× 31 382
F. Van Hoof Belgium 11 156 0.9× 230 1.8× 41 0.6× 69 1.1× 39 0.8× 14 483
Usue Ariz Spain 11 318 1.8× 61 0.5× 48 0.7× 60 1.0× 46 0.9× 14 652
Marine Berquez Switzerland 8 116 0.6× 76 0.6× 52 0.8× 47 0.8× 5 0.1× 11 333
Karianne Solaas Norway 8 242 1.3× 80 0.6× 65 0.9× 32 0.5× 100 1.9× 9 432

Countries citing papers authored by Xia Zhan

Since Specialization
Citations

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

Fields of papers citing papers by Xia Zhan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xia Zhan

This figure shows the co-authorship network connecting the top 25 collaborators of Xia Zhan. A scholar is included among the top collaborators of Xia Zhan 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 Xia Zhan. Xia Zhan 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, Ping, Yuanhang Zhang, Miaomiao Zhang, et al.. (2025). Identification and characterization of the first G8P[1] sheep rotavirus strain in China: Genetic similarity to human rotavirus and zoonotic potential. Veterinary Microbiology. 310. 110711–110711.
2.
Hao, Lili, Wenjuan Qiu, Huiwen Zhang, et al.. (2025). Variable phenotypes and outcomes associated with the MMACHC c.1A>G variant in Chinese patients with combined methylmalonic acidemia and homocystinuria cblC type. Molecular Genetics and Metabolism. 145(4). 109182–109182.
3.
Hao, Lili, et al.. (2025). Long-term outcome of CblC deficiency complicated with pulmonary hypertension. Orphanet Journal of Rare Diseases. 20(1). 276–276.
4.
Liang, Huan, Xia Zhan, Yu Wang, Gustavo Maegawa, & Huiwen Zhang. (2023). Development and validation of a new genotype–phenotype correlation for Niemann‐Pick disease type C1. Journal of Inherited Metabolic Disease. 47(2). 317–326. 1 indexed citations
5.
Qiu, Wenjuan, Huiwen Zhang, Lili Liang, et al.. (2023). Clinical, biochemical, and genetic analysis of 28 Chinese patients with holocarboxylase synthetase deficiency. Orphanet Journal of Rare Diseases. 18(1). 48–48. 6 indexed citations
6.
Xu, Feng, Wenjun Ji, Xia Zhan, et al.. (2023). Newborn screening of maple syrup urine disease and the effect of early diagnosis. Clinica Chimica Acta. 548. 117483–117483. 12 indexed citations
7.
Hao, Lili, Lili Liang, Xiaolan Gao, et al.. (2023). Screening of 1.17 million newborns for inborn errors of metabolism using tandem mass spectrometry in Shanghai, China: A 19-year report. Molecular Genetics and Metabolism. 141(1). 108098–108098. 4 indexed citations
8.
Zhan, Xia, Huiwen Zhang, Gustavo Maegawa, et al.. (2023). Use of Ambroxol as Therapy for Gaucher Disease. JAMA Network Open. 6(6). e2319364–e2319364. 13 indexed citations
9.
Wu, Shengnan, Yue Yu, Wenjuan Qiu, et al.. (2022). The Follow-Up of Chinese Patients in cblC Type Methylmalonic Acidemia Identified Through Expanded Newborn Screening. Frontiers in Genetics. 13. 805599–805599. 12 indexed citations
10.
11.
Yang, Yi, Feng Xu, Wenjun Ji, et al.. (2022). Clinical, biochemical, and molecular genetic characteristics of patients with primary carnitine deficiency identified by newborn screening in Shanghai, China. Frontiers in Genetics. 13. 1062715–1062715. 5 indexed citations
12.
Hu, Jiayue, Gustavo Maegawa, Xia Zhan, et al.. (2021). Clinical, biochemical, and genotype‐phenotype correlations of 118 patients with Niemann‐Pick disease Types A/B. Human Mutation. 42(5). 614–625. 20 indexed citations
13.
Zhu, Tianwen, Simin Zheng, Xia Zhan, et al.. (2021). Gene expression profiles in the brain of phenylketonuria mouse model reversed by the low phenylalanine diet therapy. Metabolic Brain Disease. 36(8). 2405–2414. 5 indexed citations
14.
15.
Xun, Tianrong, et al.. (2020). Advanced oxidation protein products upregulate efflux transporter expression and activity through activation of the Nrf-2-mediated signaling pathway in vitro and in vivo. European Journal of Pharmaceutical Sciences. 149. 105342–105342. 10 indexed citations
16.
Liang, Lili, Jun Ye, Wenjuan Qiu, et al.. (2019). Examining the blood amino acid status in pretherapeutic patients with  hyperphenylalaninemia. Journal of Clinical Laboratory Analysis. 34(3). e23106–e23106. 6 indexed citations
17.
Zhan, Xia, Jun Ye, Lianshu Han, et al.. (2017). A rare form of Gaucher disease resulting from saposin C deficiency. Blood Cells Molecules and Diseases. 68. 60–65. 24 indexed citations
18.
Zhan, Xia, et al.. (2017). Successful newborn screening for Gaucher disease using fluorometric assay in China. Journal of Human Genetics. 62(8). 763–768. 28 indexed citations
19.
Li, Qian, et al.. (2016). Association between the maternal serum levels of 19 eicosanoids and pre‐eclampsia. International Journal of Gynecology & Obstetrics. 133(3). 291–296. 17 indexed citations
20.
Zhan, Xia, Xiaobin Feng, Ying Kong, Yi Chen, & Wenfu Tan. (2013). JNK signaling maintains the mesenchymal properties of multi-drug resistant human epidermoid carcinoma KB cells through snail and twist1. BMC Cancer. 13(1). 180–180. 20 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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