Yulan Chen

1.2k total citations
58 papers, 721 citations indexed

About

Yulan Chen is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Yulan Chen has authored 58 papers receiving a total of 721 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 12 papers in Molecular Biology and 9 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Yulan Chen's work include Genomics and Rare Diseases (6 papers), Epilepsy research and treatment (4 papers) and Metabolism and Genetic Disorders (4 papers). Yulan Chen is often cited by papers focused on Genomics and Rare Diseases (6 papers), Epilepsy research and treatment (4 papers) and Metabolism and Genetic Disorders (4 papers). Yulan Chen collaborates with scholars based in China, United States and Taiwan. Yulan Chen's co-authors include Xiaoning Li, Li Luo, Zheng‐Hong Qin, Yan Wang, An Hong, Juan Hu, Jianguo Zhang, Lanlan Dai, Zhi‐Ying Wu and Hong‐Fu Li and has published in prestigious journals such as Blood, PLoS ONE and Diabetes.

In The Last Decade

Yulan Chen

53 papers receiving 716 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yulan Chen China 14 328 160 137 98 63 58 721
Naoki Minami Japan 16 218 0.7× 143 0.9× 157 1.1× 141 1.4× 42 0.7× 50 694
Francesca Menni Italy 17 271 0.8× 208 1.3× 115 0.8× 162 1.7× 50 0.8× 46 1.0k
Jessica L. Costa New Zealand 13 267 0.8× 148 0.9× 190 1.4× 93 0.9× 33 0.5× 23 718
Serbülent Yi̇ği̇t Türkiye 17 324 1.0× 83 0.5× 61 0.4× 57 0.6× 62 1.0× 114 925
Lisa C. Jones United States 18 440 1.3× 171 1.1× 99 0.7× 57 0.6× 87 1.4× 23 1.1k
Huimin Yu United States 16 524 1.6× 143 0.9× 40 0.3× 256 2.6× 71 1.1× 32 918
Naomi Hino‐Fukuyo Japan 17 454 1.4× 129 0.8× 77 0.6× 137 1.4× 168 2.7× 59 901
Hao Feng China 16 295 0.9× 69 0.4× 69 0.5× 56 0.6× 35 0.6× 36 660
Susanna Kullberg Sweden 20 403 1.2× 843 5.3× 176 1.3× 46 0.5× 46 0.7× 58 1.3k
Koichi Yano Japan 17 276 0.8× 82 0.5× 108 0.8× 148 1.5× 17 0.3× 80 946

Countries citing papers authored by Yulan Chen

Since Specialization
Citations

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

Fields of papers citing papers by Yulan Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yulan Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Yulan Chen. A scholar is included among the top collaborators of Yulan Chen 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 Yulan Chen. Yulan Chen 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.
Xu, Jiaojiao, Yulan Chen, Hao Yu, et al.. (2025). Genetic and Clinical Features of SLC2A1-Related Paroxysmal Exercise-Induced Dyskinesia. Pediatric Neurology. 170. 31–37.
2.
Jiang, Yangfu, Qiong Zhao, Zhen Su, et al.. (2025). Chronic exposure to environmental concentrations of enrofloxacin impairs neutrophil function in zebrafish via HPT axis disruption and hematopoietic dysregulation. Journal of Hazardous Materials. 495. 138885–138885. 1 indexed citations
3.
Wei, Nan, et al.. (2025). Global and China burden of ectopic pregnancy (1990–2021): Trends, patterns, and future projections. Journal of obstetrics and gynaecology research. 51(7). e70005–e70005. 1 indexed citations
4.
Fu, Chung-Pei, Shih-Min A. Huang, Yi–Ju Chen, et al.. (2024). Developing an entrustable professional activity for providing health education and consultation in occupational therapy and examining its validity. BMC Medical Education. 24(1). 705–705. 1 indexed citations
5.
Qiu, Xuan, et al.. (2024). Associations of TyG index with coronary heart disease risk and coronary artery sclerosis severity in OSA. Diabetology & Metabolic Syndrome. 16(1). 301–301. 2 indexed citations
6.
Chen, Yulan, et al.. (2024). Both gain- and loss-of-function variants of KCNA1 are associated with paroxysmal kinesigenic dyskinesia. Journal of genetics and genomics. 51(8). 801–810. 1 indexed citations
7.
Yu, Li, et al.. (2024). TRPC5-mediated NLRP3 inflammasome activation contributes to myocardial cell pyroptosis in chronic intermittent hypoxia rats. Acta cardiologica. Supplementum. 79(7). 796–804. 3 indexed citations
8.
9.
Chen, Yulan, Xueyuan Bai, Jianwen Chen, et al.. (2023). Pyruvate kinase M2 regulates kidney fibrosis through pericyte glycolysis during the progression from acute kidney injury to chronic kidney disease. Cell Proliferation. 57(2). e13548–e13548. 22 indexed citations
10.
Gao, Yonghui, et al.. (2023). Aal-circRNA-407 regulates ovarian development of Aedes albopictus, a major arbovirus vector, via the miR-9a-5p/Foxl axis. PLoS Pathogens. 19(5). e1011374–e1011374. 6 indexed citations
11.
Chen, Yulan, et al.. (2022). Novel stop‐gain RNF170 variation detected in a Chinese family with adolescent‐onset hereditary spastic paraplegia. Clinical Genetics. 103(1). 87–92. 2 indexed citations
12.
Chen, Yulan, et al.. (2022). Features Differ Between Paroxysmal Kinesigenic Dyskinesia Patients with PRRT2 and TMEM151A Variants. Movement Disorders. 37(3). 608–613. 16 indexed citations
13.
14.
Chen, Yulan, et al.. (2021). Penetrance estimation of PRRT2 variants in paroxysmal kinesigenic dyskinesia and infantile convulsions. Frontiers of Medicine. 15(6). 877–886. 8 indexed citations
15.
Li, Lixi, Yulan Chen, Yijun Chen, et al.. (2019). Functional study and pathogenicity classification of PRRT2 missense variants in PRRT2‐related disorders. CNS Neuroscience & Therapeutics. 26(1). 39–46. 13 indexed citations
16.
Deng, Hao, Sheng Deng, Hongbo Xu, et al.. (2016). Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly. PLoS ONE. 11(5). e0155180–e0155180. 8 indexed citations
17.
Lee, Chia‐Yi, et al.. (2015). Developing a short form of the Psychoeducational Profile-Third Edition for children with autism spectrum disorder. Research in autism spectrum disorders. 21. 37–50. 2 indexed citations
18.
Gao, Xue, Yu Su, Yulan Chen, et al.. (2015). Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family. PLoS ONE. 10(4). e0124757–e0124757. 11 indexed citations
19.
Guo, Yiran, Jiankang Li, Hilda A. Pickett, et al.. (2014). Inherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1. Blood. 124(18). 2767–2774. 71 indexed citations
20.
Wang, Zhiqing, et al.. (2011). A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Chinese patients. BMC Medical Genetics. 12(1). 161–161. 8 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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