Leping Shao

780 total citations
54 papers, 572 citations indexed

About

Leping Shao is a scholar working on Molecular Biology, Genetics and Nephrology. According to data from OpenAlex, Leping Shao has authored 54 papers receiving a total of 572 indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 15 papers in Genetics and 10 papers in Nephrology. Recurrent topics in Leping Shao's work include Ion Transport and Channel Regulation (25 papers), Ion channel regulation and function (9 papers) and Genetic Syndromes and Imprinting (7 papers). Leping Shao is often cited by papers focused on Ion Transport and Channel Regulation (25 papers), Ion channel regulation and function (9 papers) and Genetic Syndromes and Imprinting (7 papers). Leping Shao collaborates with scholars based in China, Italy and Lebanon. Leping Shao's co-authors include Deyang Zhang, Jie Xu, Xiang‐Ping Hu, Xiangzhong Zhao, Hong Ren, Irene Bottillo, Yan Xu, Yue Han, Nan Chen and Yanxia Gao and has published in prestigious journals such as Angewandte Chemie International Edition, SHILAP Revista de lepidopterología and Scientific Reports.

In The Last Decade

Leping Shao

49 papers receiving 567 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Leping Shao China 15 375 117 114 85 80 54 572
Gaëlle Lenglet France 12 192 0.5× 91 0.8× 32 0.3× 79 0.9× 17 0.2× 23 425
J. M. MCGILL United States 10 158 0.4× 34 0.3× 169 1.5× 25 0.3× 27 0.3× 15 501
Etsuro Onuma United States 13 117 0.3× 39 0.3× 60 0.5× 38 0.4× 16 0.2× 26 372
Yonglan Huang China 13 215 0.6× 38 0.3× 23 0.2× 11 0.1× 34 0.4× 72 473
Jong Woo Kim South Korea 14 134 0.4× 19 0.2× 29 0.3× 17 0.2× 60 0.8× 41 624
N Hayakawa Japan 9 127 0.3× 64 0.5× 81 0.7× 7 0.1× 15 0.2× 37 390
Minami Watanabe Japan 9 171 0.5× 10 0.1× 67 0.6× 88 1.0× 11 0.1× 15 380
Xiangxiao Li China 7 208 0.6× 47 0.4× 28 0.2× 53 0.6× 9 0.1× 15 417
Anthony W. Norman United States 12 171 0.5× 21 0.2× 14 0.1× 32 0.4× 81 1.0× 22 467

Countries citing papers authored by Leping Shao

Since Specialization
Citations

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

Fields of papers citing papers by Leping Shao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Leping Shao

This figure shows the co-authorship network connecting the top 25 collaborators of Leping Shao. A scholar is included among the top collaborators of Leping Shao 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 Leping Shao. Leping Shao 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.
Qiao, Dan, Xuyan Liu, Irene Bottillo, Ran Zhang, & Leping Shao. (2025). Three intronic variants altering RNA splicing were identified in the CLCN5 gene by minigene assay. BMC Medical Genomics. 18(1). 158–158.
2.
Shen, Qian, Zhengkun Xia, Jialu Liu, et al.. (2025). Clinical practice guidelines for rituximab treatment in children with steroid-sensitive nephrotic syndrome. World Journal of Pediatrics. 21(8). 775–791.
3.
Chen, Xing, et al.. (2025). Novel clinical and genetic insights into Gitelman syndrome from 95 Chinese patients. Human Genomics. 19(1). 114–114. 1 indexed citations
4.
Qiao, Dan, et al.. (2024). Three exonic variants in the COL4A5 gene alter RNA splicing in a minigene assay. Molecular Genetics & Genomic Medicine. 12(2). e2395–e2395. 1 indexed citations
5.
Xin, Qing, et al.. (2023). Four novel variants identified in primary hyperoxaluria and genotypic and phenotypic analysis in 21 Chinese patients. Frontiers in Genetics. 14. 1124745–1124745. 4 indexed citations
6.
Pan, Fengjiao, Xin Qing, Wencong Guo, et al.. (2023). Functional analysis of the CTNS gene exonic variants predicted to affect splicing. Clinical Genetics. 105(3). 323–328. 1 indexed citations
7.
Zhao, Xiangzhong, et al.. (2022). A novel WDR60 variant contributes to a late diagnosis of Jeune asphyxiating thoracic dystrophy in a Chinese patient: A case report. SHILAP Revista de lepidopterología. 10(11). e6561–e6561. 1 indexed citations
8.
Liu, Zhiying, Aihua Sui, Sai Wang, et al.. (2022). Double synonymous mutations in exon 9 of the Cullin3 gene restore exon inclusion by abolishing hnRNPs inhibition. Human Molecular Genetics. 31(23). 4006–4018. 1 indexed citations
9.
Xin, Qing, et al.. (2022). Twelve exonic variants in the SLC12A1 and CLCNKB genes alter RNA splicing in a minigene assay. Frontiers in Genetics. 13. 961384–961384. 8 indexed citations
10.
Guo, Wencong, et al.. (2021). Genotypic and phenotypic analysis in 51 Chinese patients with primary distal renal tubular acidosis. Clinical Genetics. 100(4). 440–446. 6 indexed citations
11.
Guo, Wencong, Shujuan Wang, Sai Wang, et al.. (2020). Eight novel KCNJ1 variants and parathyroid hormone overaction or resistance in 5 probands with Bartter syndrome type 2. Clinica Chimica Acta. 511. 248–254. 6 indexed citations
12.
Wang, Cui, et al.. (2018). Five Novel Mutations in Chinese Children with Primary Distal Renal Tubular Acidosis. Genetic Testing and Molecular Biomarkers. 22(10). 599–606. 4 indexed citations
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15.
Shao, Leping, et al.. (2017). Genotype, phenotype, and follow-up of Chinese patients with Gitelman′s syndrome. Zhonghua neifenmi daixie zazhi. 33(1). 40–46. 1 indexed citations
16.
17.
Gao, Yanxia, et al.. (2014). Mutation analysis and audiologic assessment in six Chinese children with primary distal renal tubular acidosis. Renal Failure. 36(8). 1226–1232. 21 indexed citations
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19.
Dong, Hui, Lin Li, & Leping Shao. (2010). Coexistence of Gitelman's syndrome and thyroid disease: SLC12A3 gene analysis in two patients. Zhonghua neifenmi daixie zazhi. 26(5). 395–398. 5 indexed citations
20.
Shao, Leping, Liqiu Liu, Zhimin Miao, et al.. (2008). A Novel SLC12A3 Splicing Mutation Skipping of Two Exons and Preliminary Screening for Alternative Splice Variants in Human Kidney. American Journal of Nephrology. 28(6). 900–907. 22 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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