Weiyue Gu

645 total citations
50 papers, 317 citations indexed

About

Weiyue Gu is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Weiyue Gu has authored 50 papers receiving a total of 317 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 22 papers in Genetics and 7 papers in Oncology. Recurrent topics in Weiyue Gu's work include Genetics and Neurodevelopmental Disorders (16 papers), Genomics and Rare Diseases (12 papers) and Ion Transport and Channel Regulation (5 papers). Weiyue Gu is often cited by papers focused on Genetics and Neurodevelopmental Disorders (16 papers), Genomics and Rare Diseases (12 papers) and Ion Transport and Channel Regulation (5 papers). Weiyue Gu collaborates with scholars based in China, United States and United Kingdom. Weiyue Gu's co-authors include Hongyan Liu, Rongrong Wang, Xue Zhang, Jia Huang, Xiao Han, Fuwei Li, Bolin Chen, Ke Xu, Congying Zhao and Xiaolei Tang and has published in prestigious journals such as PEDIATRICS, Scientific Reports and British Journal of Cancer.

In The Last Decade

Weiyue Gu

42 papers receiving 315 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Weiyue Gu China 11 139 101 52 52 47 50 317
Sofía Gouveia Spain 11 152 1.1× 114 1.1× 28 0.5× 38 0.7× 52 1.1× 37 361
Katsura Ishizu Japan 12 213 1.5× 136 1.3× 26 0.5× 32 0.6× 37 0.8× 25 404
Péter Gergics Hungary 14 209 1.5× 134 1.3× 23 0.4× 18 0.3× 28 0.6× 29 501
Jie‐Yuan Jin China 11 170 1.2× 50 0.5× 27 0.5× 27 0.5× 19 0.4× 56 324
Kinga Buraczyńska Poland 12 233 1.7× 47 0.5× 18 0.3× 16 0.3× 26 0.6× 24 414
Monica Piccini Italy 8 240 1.7× 58 0.6× 28 0.5× 20 0.4× 21 0.4× 8 378
Alina Kurolap Israel 12 150 1.1× 118 1.2× 28 0.5× 20 0.4× 89 1.9× 42 399
Aneal Khan Canada 13 305 2.2× 73 0.7× 14 0.3× 24 0.5× 41 0.9× 42 477
Tianming Liu China 4 166 1.2× 76 0.8× 9 0.2× 42 0.8× 30 0.6× 11 363
Francesca Clementina Radio Italy 15 194 1.4× 149 1.5× 90 1.7× 15 0.3× 17 0.4× 40 421

Countries citing papers authored by Weiyue Gu

Since Specialization
Citations

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

Fields of papers citing papers by Weiyue Gu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Weiyue Gu

This figure shows the co-authorship network connecting the top 25 collaborators of Weiyue Gu. A scholar is included among the top collaborators of Weiyue Gu 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 Weiyue Gu. Weiyue Gu 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.
Nie, Xiaojing, Zhihua Yu, Yan Jiang, et al.. (2025). Reanalysis of Whole Genome Sequencing Resolves Genetically Undiagnosed Patients With “ RNUopathies ”. Clinical Genetics. 109(3). 576–580.
2.
Zhong, Wenlong, Ligang Wang, Lihua Zhao, et al.. (2025). Identification of Multi‐Landscape and Cell Interactions in the Tumor Microenvironment Through High‐Coverage Single‐Cell Sequencing. Small Methods. 9(8). e2500241–e2500241. 1 indexed citations
3.
Wan, Xueshuai, Jie Zhao, Xiaobo Yang, et al.. (2025). Therapeutic T cells with 3-in-1 strategy for the treatment of biliary tract cancer. Cell Reports Medicine. 6(10). 102349–102349.
4.
Gao, Kai, Huifang Yan, Jingmin Wang, et al.. (2024). SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathy. PubMed. 6(1). 42–42.
5.
Zhang, Ning, Luopei Guo, Shuai Wang, et al.. (2024). Genetic variation and molecular profiling of congenital malformations of the female genital tract based on whole-genome sequencing. World Journal of Pediatrics. 20(11). 1179–1195. 1 indexed citations
6.
Zhang, Xi, et al.. (2023). De novo variants in MAST4 related to neurodevelopmental disorders with developmental delay and infantile spasms: Genotype-phenotype association. Frontiers in Molecular Neuroscience. 16. 1097553–1097553. 11 indexed citations
7.
Li, Fuwei, et al.. (2023). Hand-foot-genital syndrome due to a duplication variant in the GC-rich region of HOXA13. European Journal of Medical Genetics. 66(3). 104711–104711.
8.
Chen, Bolin, et al.. (2023). Genomic and molecular landscape of homologous recombination deficiency across multiple cancer types. Scientific Reports. 13(1). 8899–8899. 16 indexed citations
9.
Wang, Yuan, Shujuan Zhou, Yanli Zhang, et al.. (2023). Metagenomic next-generation sequencing for detecting lower respiratory tract infections in sputum and bronchoalveolar lavage fluid samples from children. Frontiers in Cellular and Infection Microbiology. 13. 4 indexed citations
10.
11.
Fu, Fang, Ru Li, Qiuxia Yu, et al.. (2022). Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing. Frontiers in Genetics. 13. 951829–951829. 1 indexed citations
12.
13.
Wang, Sumei, et al.. (2022). Emerging evidence of genotype–phenotype associations of developmental and epileptic encephalopathy due to KCNC2 mutation: Identification of novel R405G. Frontiers in Molecular Neuroscience. 15. 950255–950255. 4 indexed citations
14.
Li, Ang, Siwen Liu, Peng Zhang, et al.. (2022). A novel heterozygous SIX1 missense mutation resulted in non-syndromic unilateral hearing loss. Frontiers in Genetics. 13. 1047230–1047230. 1 indexed citations
15.
16.
Zhang, Feng, et al.. (2022). Novel Variant Expands the Clinical Spectrum of CUX2-Associated Developmental and Epileptic Encephalopathies. Frontiers in Genetics. 13. 808181–808181. 3 indexed citations
17.
18.
Xu, Chengxian, Jia Rao, Qing Ye, et al.. (2022). Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemia. JCI Insight. 7(11). 13 indexed citations
19.
Wang, Jingjing, et al.. (2020). Case report: a Chinese girl with dent disease 1 and turner syndrome due to a hemizygous CLCN5 gene mutation and Isochromosome (Xq). BMC Nephrology. 21(1). 171–171. 3 indexed citations
20.
Duan, Chao, Han Wang, Ying Chen, et al.. (2018). Whole exome sequencing reveals novel somatic alterations in neuroblastoma patients with chemotherapy. Cancer Cell International. 18(1). 21–21. 24 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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