Yulin Zhou

2.0k total citations
80 papers, 1.0k citations indexed

About

Yulin Zhou is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Yulin Zhou has authored 80 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 21 papers in Pediatrics, Perinatology and Child Health and 18 papers in Genetics. Recurrent topics in Yulin Zhou's work include Prenatal Screening and Diagnostics (16 papers), Genomic variations and chromosomal abnormalities (9 papers) and RNA modifications and cancer (8 papers). Yulin Zhou is often cited by papers focused on Prenatal Screening and Diagnostics (16 papers), Genomic variations and chromosomal abnormalities (9 papers) and RNA modifications and cancer (8 papers). Yulin Zhou collaborates with scholars based in China, United States and Australia. Yulin Zhou's co-authors include Qiwei Guo, Chonggang Wang, Zhenghong Zuo, Xingcheng Gao, Kang Chen, Bolan Yu, Kusheng Wu, Xia Huo, Hui Yang and Yuling Zhang and has published in prestigious journals such as Angewandte Chemie International Edition, PLoS ONE and Food Chemistry.

In The Last Decade

Yulin Zhou

67 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
Yulin Zhou China 18 284 186 167 146 134 80 1.0k
Massimo Venditti Italy 27 596 2.1× 317 1.7× 191 1.1× 86 0.6× 217 1.6× 87 2.4k
Xiangjin Kang China 19 632 2.2× 41 0.2× 120 0.7× 139 1.0× 113 0.8× 39 1.1k
Francesca Ietta Italy 27 361 1.3× 422 2.3× 129 0.8× 559 3.8× 177 1.3× 72 2.3k
Sibylle Gröters Germany 16 136 0.5× 308 1.7× 61 0.4× 37 0.3× 62 0.5× 40 1.0k
Birgitta Weijdegård Sweden 25 377 1.3× 54 0.3× 224 1.3× 129 0.9× 103 0.8× 36 1.7k
V. Romano-Spica Italy 16 656 2.3× 279 1.5× 117 0.7× 247 1.7× 104 0.8× 34 1.7k
Xin Ren China 20 379 1.3× 248 1.3× 33 0.2× 34 0.2× 59 0.4× 49 1.7k
Sher Singh Taiwan 12 386 1.4× 358 1.9× 65 0.4× 51 0.3× 30 0.2× 18 960
Liying Gao China 22 342 1.2× 674 3.6× 111 0.7× 111 0.8× 26 0.2× 68 1.4k
Hyunwoong Park South Korea 18 218 0.8× 293 1.6× 95 0.6× 42 0.3× 128 1.0× 75 1.1k

Countries citing papers authored by Yulin Zhou

Since Specialization
Citations

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

Fields of papers citing papers by Yulin Zhou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yulin Zhou

This figure shows the co-authorship network connecting the top 25 collaborators of Yulin Zhou. A scholar is included among the top collaborators of Yulin Zhou 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 Yulin Zhou. Yulin Zhou 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.
Zheng, Yanxin, Li‐Gao Liu, Yulin Zhou, et al.. (2025). Copper‐Catalyzed Asymmetric [2 + 2 + 2] Cycloaddition of Diynes via Vinyl Cations. Angewandte Chemie. 137(38).
2.
Zheng, Yanxin, Li‐Gao Liu, Yulin Zhou, et al.. (2025). Copper‐Catalyzed Asymmetric [2 + 2 + 2] Cycloaddition of Diynes via Vinyl Cations. Angewandte Chemie International Edition. 64(38). e202514641–e202514641.
3.
Hu, Ping, et al.. (2025). Fragile X Syndrome Carrier Screening Using a Nanopore Sequencing Assay. Journal of Molecular Diagnostics. 27(7). 645–656.
4.
Dong, Yi, Tiantian Chen, Mei Lu, et al.. (2025). Assessment of Long-Read Sequencing-Based Congenital Adrenal Hyperplasia Genotyping Assay for Newborns in Fujian, China. International Journal of Neonatal Screening. 11(1). 22–22.
5.
Guo, Jintao, Qiwei Guo, Hongkun Fang, et al.. (2024). Phenome-wide association study in 25,639 pregnant Chinese women reveals loci associated with maternal comorbidities and child health. Cell Genomics. 4(10). 100632–100632. 1 indexed citations
6.
Luo, Zhenyu, et al.. (2024). Development of a low-cost and accurate carrier screening method for spinal muscular atrophy in developing countries. European Journal of Medical Genetics. 68. 104921–104921.
7.
Tang, Chaopeng, Jie Dong, Ping Li, et al.. (2023). Collecting Duct Carcinoma of the Kidney: A Single-Center Retrospective Study of 23 Cases. Technology in Cancer Research & Treatment. 22. 2223907029–2223907029. 4 indexed citations
8.
Zhou, Yulin, et al.. (2023). Current Advances in Genetic Testing for Spinal Muscular Atrophy. Current Genomics. 24(5). 273–286.
9.
10.
Zhou, Yulin, Chaopeng Tang, Jie Dong, et al.. (2023). Establishment and validation of a nomogram to select patients with metastatic sarcomatoid renal cell carcinoma suitable for cytoreductive radical nephrectomy. Frontiers in Oncology. 13. 1239405–1239405. 1 indexed citations
11.
Zhou, Yulin, et al.. (2022). Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China. Cytogenetic and Genome Research. 162(7). 354–364. 3 indexed citations
12.
13.
Ge, Yunsheng, Jia Li, Jian Zhang, et al.. (2021). Expanded noninvasive prenatal testing for fetal aneuploidy and copy number variations and parental willingness for invasive diagnosis in a cohort of 18,516 cases. BMC Medical Genomics. 14(1). 106–106. 24 indexed citations
14.
Sun, Yongpeng, Xinyi Zheng, Zizheng Zheng, et al.. (2021). Epidemiology of Respiratory Pathogens Among Children Hospitalized for Pneumonia in Xiamen: A Retrospective Study. Infectious Diseases and Therapy. 10(3). 1567–1578. 16 indexed citations
15.
Sun, Yu, Jiale Xiang, Sen Chen, et al.. (2019). Increased diagnostic yield by reanalysis of data from a hearing loss gene panel. BMC Medical Genomics. 12(1). 76–76. 22 indexed citations
16.
Zhou, Yulin, et al.. (2019). Carrier screening for spinal muscular atrophy with a simple test based on melting analysis. Journal of Human Genetics. 64(5). 387–396. 9 indexed citations
17.
Guo, Jintao, Jiankun Huang, Ying Zhou, et al.. (2018). Germline and somatic variations influence the somatic mutational signatures of esophageal squamous cell carcinomas in a Chinese population. BMC Genomics. 19(1). 538–538. 17 indexed citations
18.
Jeon, Young Joo, Yulin Zhou, Yihan Li, et al.. (2014). The Feasibility Study of Non-Invasive Fetal Trisomy 18 and 21 Detection with Semiconductor Sequencing Platform. PLoS ONE. 9(10). e110240–e110240. 113 indexed citations
19.
Zhou, Yulin, et al.. (2013). Rapid Prenatal Diagnosis of Common Numerical Chromosomal Abnormalities by High-Resolution Melting Analysis of Segmental Duplications. Genetic Testing and Molecular Biomarkers. 18(3). 141–148. 3 indexed citations
20.
Guo, Qiwei, et al.. (2012). Quadruplex real-time polymerase chain reaction assay for molecular diagnosis of Y-chromosomal microdeletions. Fertility and Sterility. 97(4). 864–869. 5 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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