Shaoke Chen

1.7k total citations
69 papers, 778 citations indexed

About

Shaoke Chen is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Shaoke Chen has authored 69 papers receiving a total of 778 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 24 papers in Genetics and 15 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Shaoke Chen's work include Thyroid Disorders and Treatments (8 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomic variations and chromosomal abnormalities (7 papers). Shaoke Chen is often cited by papers focused on Thyroid Disorders and Treatments (8 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomic variations and chromosomal abnormalities (7 papers). Shaoke Chen collaborates with scholars based in China, United States and United Kingdom. Shaoke Chen's co-authors include Xin Fan, Yiping Shen, Jingsi Luo, Xuyun Hu, Chunyun Fu, Jiasun Su, Jin Wang, Shiyu Luo, Bobo Xie and Rongyu Chen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Scientific Reports.

In The Last Decade

Shaoke Chen

65 papers receiving 752 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shaoke Chen China 17 326 254 238 171 87 69 778
Manuela Caruso‐Nicoletti Italy 12 259 0.8× 432 1.7× 257 1.1× 105 0.6× 86 1.0× 41 876
Amnon Cohen Italy 11 178 0.5× 146 0.6× 147 0.6× 178 1.0× 44 0.5× 16 745
Carles Zafón Spain 18 252 0.8× 518 2.0× 139 0.6× 40 0.2× 44 0.5× 73 968
Nicoletta Masera Italy 14 108 0.3× 88 0.3× 101 0.4× 138 0.8× 246 2.8× 37 547
Carine Courtillot France 13 206 0.6× 243 1.0× 226 0.9× 93 0.5× 58 0.7× 32 774
Ergül Tunçbılek Türkiye 20 274 0.8× 29 0.1× 254 1.1× 188 1.1× 61 0.7× 55 831
C. P. Schwarze Germany 15 234 0.7× 325 1.3× 249 1.0× 173 1.0× 6 0.1× 26 671
D. Évain-Brion France 15 302 0.9× 153 0.6× 90 0.4× 298 1.7× 10 0.1× 29 875
P. S. N. Menon India 15 205 0.6× 148 0.6× 142 0.6× 65 0.4× 17 0.2× 67 672
Carol A. Blanchong United States 10 150 0.5× 61 0.2× 139 0.6× 27 0.2× 62 0.7× 16 738

Countries citing papers authored by Shaoke Chen

Since Specialization
Citations

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

Fields of papers citing papers by Shaoke Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shaoke Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Shaoke Chen. A scholar is included among the top collaborators of Shaoke 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 Shaoke Chen. Shaoke 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.
Cheng, Zhen, et al.. (2025). High-speed recognition of orbital angular momentum modes under coordinate misalignment. Chinese Optics Letters. 23(10). 100014–100014.
2.
Xie, Bobo, Xiaoyun Lei, Shaoke Chen, et al.. (2024). The cryptic complex rearrangements involving the DMD gene: etiologic clues about phenotypical differences revealed by optical genome mapping. Human Genomics. 18(1). 103–103. 1 indexed citations
3.
Liu, Lian, Li‐Ying Sun, Yujun Chen, et al.. (2022). Delineation of dual molecular diagnosis in patients with skeletal deformity. Orphanet Journal of Rare Diseases. 17(1). 139–139. 1 indexed citations
4.
Huang, Ke, Shuting Si, Ruimin Chen, et al.. (2021). Preterm Birth and Birth Weight and the Risk of Type 1 Diabetes in Chinese Children. Frontiers in Endocrinology. 12. 603277–603277. 8 indexed citations
5.
Chen, Fei, Shaoke Chen, Qi Yang, et al.. (2019). Three additional de novo CTCF mutations in Chinese patients help to define an emerging neurodevelopmental disorder. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 181(2). 218–225. 18 indexed citations
6.
Liang, Li, Chunxiu Gong, Feng Xiong, et al.. (2019). Parental Perceptions of Obesity in School Children and Subsequent Action. Childhood Obesity. 15(7). 459–467. 12 indexed citations
7.
Lai, Chong, Di He, Li Liang, et al.. (2019). U-shaped relationship between birth weight and childhood blood pressure in China. BMC Pediatrics. 19(1). 264–264. 18 indexed citations
8.
Zhang, Shujie, Shaoke Chen, Yu Yang, et al.. (2019). Novel genotypes and phenotypes among Chinese patients with Floating-Harbor syndrome. Orphanet Journal of Rare Diseases. 14(1). 144–144. 12 indexed citations
9.
Fu, Chunyun, Shiyu Luo, Yingfeng Li, et al.. (2017). Mutation screening of the GLIS3 gene in a cohort of 592 Chinese patients with congenital hypothyroidism. Clinica Chimica Acta. 476. 38–43. 16 indexed citations
10.
Hu, Xuyun, Baoheng Gui, Yufei Xu, et al.. (2017). Prenatal and early diagnosis of Chinese 3-M syndrome patients with novel pathogenic variants. Clinica Chimica Acta. 474. 159–164. 11 indexed citations
11.
Fu, Chunyun, Bobo Xie, Shujie Zhang, et al.. (2016). Mutation screening of the TPO gene in a cohort of 192 Chinese patients with congenital hypothyroidism. BMJ Open. 6(5). e010719–e010719. 22 indexed citations
12.
Zhang, Shujie, Jin Wang, Shiyu Luo, et al.. (2016). Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability. Molecular Cytogenetics. 9(1). 66–66. 10 indexed citations
13.
Fu, Chunyun, Jin Wang, Shiyu Luo, et al.. (2016). Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients. Clinica Chimica Acta. 462. 127–132. 25 indexed citations
14.
Xie, Bobo, Xin Fan, Rongyu Chen, et al.. (2016). A novel de novo microdeletion at 17q11.2 adjacent to NF1 gene associated with developmental delay, short stature, microcephaly and dysmorphic features. Molecular Cytogenetics. 9(1). 41–41. 12 indexed citations
15.
Wang, Jin, Chunyun Fu, Shujie Zhang, et al.. (2016). A rare occurrence of two large de novo duplications on 1q42-q44 and 9q21.12-q21.33. Gene. 594(1). 59–65. 3 indexed citations
16.
17.
Fu, Junfen, Li Liang, Chunxiu Gong, et al.. (2014). [A proposal for the cutoff point of waist-to-height for the diagnosis of metabolic syndrome in children and adolescents in six areas of China].. PubMed. 35(8). 882–5. 4 indexed citations
18.
Chen, Shaoke, Jingsi Luo, Yingfen Qin, et al.. (2011). [Epidemiological study on the association between obesity with metabolic syndrome in obese children and adolescents of Nanning city, Guangxi].. PubMed. 32(10). 969–72. 4 indexed citations
19.
Chen, Shaoke. (2011). Research on Properties of Ni/TiC on 45 Steel Surface Prepared by Laser Cladding. Equipment Manufacturing Technology. 1 indexed citations
20.
Chen, Shaoke. (2006). A New Method of the CMM Probe Radius Compensation. Modular Machine Tool & Automatic Manufacturing Technique. 2 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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2026