Chenming Xu

2.0k total citations
92 papers, 1.1k citations indexed

About

Chenming Xu is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Chenming Xu has authored 92 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Pediatrics, Perinatology and Child Health, 31 papers in Molecular Biology and 31 papers in Genetics. Recurrent topics in Chenming Xu's work include Prenatal Screening and Diagnostics (34 papers), Genomic variations and chromosomal abnormalities (20 papers) and Fetal and Pediatric Neurological Disorders (10 papers). Chenming Xu is often cited by papers focused on Prenatal Screening and Diagnostics (34 papers), Genomic variations and chromosomal abnormalities (20 papers) and Fetal and Pediatric Neurological Disorders (10 papers). Chenming Xu collaborates with scholars based in China, United States and Thailand. Chenming Xu's co-authors include Hefeng Huang, Fan Jin, Songchang Chen, Dahui Wang, Xiangyang Zou, Liya Wang, Yuli Qian, Yanting Wu, Yinghui Ye and Minyue Dong and has published in prestigious journals such as Circulation, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Chenming Xu

80 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chenming Xu China 17 446 321 304 295 205 92 1.1k
Viktoria von Schönfeldt Germany 19 300 0.7× 186 0.6× 475 1.6× 206 0.7× 507 2.5× 49 1.1k
Anish Shah United States 13 263 0.6× 215 0.7× 250 0.8× 59 0.2× 317 1.5× 21 912
Sana M. Salih United States 19 259 0.6× 67 0.2× 379 1.2× 241 0.8× 288 1.4× 34 912
Matthias Ruebner Germany 18 541 1.2× 279 0.9× 73 0.2× 120 0.4× 27 0.1× 54 1.1k
Vivek Dhir United Kingdom 19 607 1.4× 66 0.2× 73 0.2× 220 0.7× 80 0.4× 26 1.0k
W. Hilscher Germany 16 331 0.7× 60 0.2× 285 0.9× 234 0.8× 382 1.9× 62 806
Shauh‐Der Yeh Taiwan 10 517 1.2× 22 0.1× 152 0.5× 318 1.1× 382 1.9× 22 995
Maciej Brązert Poland 15 285 0.6× 61 0.2× 150 0.5× 53 0.2× 124 0.6× 43 594
Minghui Niu China 19 399 0.9× 25 0.1× 276 0.9× 196 0.7× 390 1.9× 25 829
Yong Zhu China 19 546 1.2× 24 0.1× 161 0.5× 180 0.6× 274 1.3× 59 1.1k

Countries citing papers authored by Chenming Xu

Since Specialization
Citations

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

Fields of papers citing papers by Chenming Xu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chenming Xu

This figure shows the co-authorship network connecting the top 25 collaborators of Chenming Xu. A scholar is included among the top collaborators of Chenming Xu 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 Chenming Xu. Chenming Xu 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.
2.
Xu, Chenming, et al.. (2025). Establishment and Evaluation of HepG2 Cell Insulin Resistance Model. Diabetes Metabolic Syndrome and Obesity. Volume 18. 2573–2584. 1 indexed citations
3.
Chen, Songchang, et al.. (2025). Application and clinical utility assessment of natural language processing-based software for copy-number variants interpretation. Journal of Translational Medicine. 23(1). 1052–1052.
4.
Jiang, Yonghong, Zhou Fang, Haokun Zhang, et al.. (2024). Risk factors and birth outcomes of preterm birth subtypes: a case-control study of singleton natural pregnancy. SHILAP Revista de lepidopterología. 4(3). e000027–e000027.
5.
Luo, Qiong, Yanting Wu, Songchang Chen, et al.. (2024). Advancing prenatal diagnosis through comprehensive fetal cell‐free DNA screening. Clinical and Translational Medicine. 14(12). e70129–e70129.
6.
Chen, Yiyao, Bingxin Yang, Xiaoyu Zhang, et al.. (2023). Biallelic variants in RBM42 cause a multisystem disorder with neurological, facial, cardiac, and musculoskeletal involvement. Protein & Cell. 15(1). 52–68. 4 indexed citations
7.
Wang, Jun, Songchang Chen, Minghui Wu, et al.. (2023). Chromosome Detection in Metaphase Cell Images Using Morphological Priors. IEEE Journal of Biomedical and Health Informatics. 27(9). 4579–4590. 4 indexed citations
8.
Lin, Xian-Hua, Mengxi Guo, Yao Lu, et al.. (2022). Preimplantation genetic testing for aneuploidy in severe male factor infertility: protocol for a multicenter randomised controlled trial. BMJ Open. 12(7). e063030–e063030. 1 indexed citations
9.
Zhang, Shuo, Caixia Lei, Jing Zhou, et al.. (2022). Detection of cryptic balanced chromosomal rearrangements using high-resolution optical genome mapping. Journal of Medical Genetics. 60(3). 274–284. 33 indexed citations
10.
Chen, Songchang, Qian Zhang, Yiyao Chen, et al.. (2021). Comprehensive copy number analysis of Y chromosome-linked loci for detection of structural variations and diagnosis of male infertility. Journal of Human Genetics. 67(2). 107–114. 5 indexed citations
11.
12.
Song, Jeffrey, Chenming Xu, Qi Song, et al.. (2020). Association of iodine‐related knowledge, attitudes and behaviours with urinary iodine excretion in pregnant women with mild iodine deficiency. Journal of Human Nutrition and Dietetics. 34(2). 314–323. 7 indexed citations
13.
Chen, Songchang, Yeqing Qian, Liya Wang, et al.. (2020). Preimplantation Genetic Testing for a Chinese Family With X-Linked Lymphoproliferative Syndrome Type 1. Frontiers in Genetics. 11. 550507–550507.
14.
Liu, Bei, Yanmei Yang, Kai Yan, et al.. (2015). Identification of novel PKD1 and PKD2 mutations in a Chinese population with autosomal dominant polycystic kidney disease. Scientific Reports. 5(1). 17468–17468. 20 indexed citations
15.
Wu, Yanting, Tingting Wang, Xijing Chen, et al.. (2012). Bone morphogenetic protein-15 in follicle fluid combined with age may differentiate between successful and unsuccessful poor ovarian responders. Reproductive Biology and Endocrinology. 10(1). 116–116. 22 indexed citations
16.
Wei, Xiaoming, Fan Jin, Yinghui Ye, et al.. (2011). A novel mutation of IDS gene in a Chinese patient with mucopolysaccharidosis II by next-generation sequencing. Clinica Chimica Acta. 412(23-24). 2340–2342. 8 indexed citations
17.
Wang, Liya, Dahui Wang, Xiangyang Zou, & Chenming Xu. (2009). Mitochondrial functions on oocytes and preimplantation embryos. Journal of Zhejiang University SCIENCE B. 10(7). 483–492. 124 indexed citations
18.
Xu, Chenming, Yimin Zhu, Minyue Dong, et al.. (2007). Preimplantation genetic diagnosis for Down syndrome pregnancy. Journal of Zhejiang University SCIENCE B. 8(7). 515–521. 4 indexed citations
19.
Liu, Ai-Xia, Yimin Zhu, Yanting Wu, et al.. (2006). Specific peptide patterns of follicular fluids at different growth stages analyzed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Biochimica et Biophysica Acta (BBA) - General Subjects. 1770(1). 29–38. 23 indexed citations
20.
Ye, Yinghui, et al.. (2004). Identification of embryonic chromosomal abnormality using FISH-based preimplantaion genetic diagnosis. Journal of Zhejiang University. Science A. 5(10). 1249–1254. 1 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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