Qian Shen

2.5k total citations
118 papers, 1.2k citations indexed

About

Qian Shen is a scholar working on Molecular Biology, Nephrology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Qian Shen has authored 118 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 39 papers in Nephrology and 31 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Qian Shen's work include Renal Diseases and Glomerulopathies (28 papers), Renal and related cancers (25 papers) and Pediatric Urology and Nephrology Studies (18 papers). Qian Shen is often cited by papers focused on Renal Diseases and Glomerulopathies (28 papers), Renal and related cancers (25 papers) and Pediatric Urology and Nephrology Studies (18 papers). Qian Shen collaborates with scholars based in China, United States and United Kingdom. Qian Shen's co-authors include Hong Xu, Yu Fang, Yihui Zhai, Jing Chen, Xiaoyan Fang, Haimei Liu, Jia Rao, Shimin Yang, Xiaoding Xu and Bing Lv and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Biomaterials.

In The Last Decade

Qian Shen

106 papers receiving 1.2k citations

Peers

Qian Shen

PPCH

NEPHR

PRM

Daniel Shepshelovich Israel

Sezaneh Haghpanah Iran

Bonnie Lau United States

Claudia Langebrake Germany

Gary C. Yee United States

Félix Couture Canada

Suad Hannawi United Arab Emirates

Yahya Mahamat‐Saleh France

Deirdré Hahn Australia

Joseph M. Messana United States

Daniel Shepshelovich Israel

Qian Shen

171 ×0.5

73 ×0.2

PPCH

79 ×0.3

NEPHR

204 ×1.6

PRM

117 ×1.0

Citations per year, relative to Qian Shen Qian Shen (= 1×) peers Daniel Shepshelovich

Countries citing papers authored by Qian Shen

Since Specialization

Citations

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

Fields of papers citing papers by Qian Shen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Qian Shen

This figure shows the co-authorship network connecting the top 25 collaborators of Qian Shen. A scholar is included among the top collaborators of Qian Shen 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 Qian Shen. Qian Shen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Wang, Chunyan, et al.. (2025). Maternal Exposure to 2,4-Di-tert-butylphenol During Pregnancy in a Mouse Model Leads to Abnormal Development of the Urinary System in Offspring. Toxics. 13(11). 991–991.

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.

Wang, Chunyan, Jing Chen, Xiaoyan Fang, et al.. (2024). Protein-losing enteropathy as a new phenotype in atypical hemolytic uremic syndrome caused by CD46 gene mutation. Pediatric Nephrology. 39(12). 3513–3520. 1 indexed citations

Chen, Jing, et al.. (2024). Vitamin A Deficiency Disturbs Ret Expression and Induces Urinary Tract Developmental Abnormalities in Mice. American Journal of Nephrology. 56(2). 1–11. 2 indexed citations

Wang, Yong, Xiaojing Ye, Xiaojun Chen, et al.. (2023). Maturity-onset diabetes of the young type 7 (MODY7) and mutation in the Krüppel-like transcription factor 11 (KLF11) gene. QJM. 117(3). 219–222.

Liu, Junchao, et al.. (2023). Minnelide combined with Angptl3 knockout completely protects mice with adriamycin nephropathy via suppression of TGF-β1-Smad2 and p53 pathways. International Immunopharmacology. 115. 109656–109656. 6 indexed citations

Li, Senlin, Ziqi Huang, Chunfang Wei, et al.. (2023). Remodeling Serine Synthesis and Metabolism via Nanoparticles (NPs)‐Mediated CFL1 Silencing to Enhance the Sensitivity of Hepatocellular Carcinoma to Sorafenib. Advanced Science. 10(19). e2207118–e2207118. 27 indexed citations

Liu, Haimei, Rufeng Dai, Jiaojiao Liu, et al.. (2021). PPARα agonist exerts protective effects in podocyte injury via inhibition of the ANGPTL3 pathway. Experimental Cell Research. 407(2). 112753–112753. 2 indexed citations

Li, Yaxin, Lihong Tan, Shanshan Xue, et al.. (2021). Disruption of Gen1 causes ectopic budding and kidney hypoplasia in mice. Biochemical and Biophysical Research Communications. 589. 173–179. 3 indexed citations

10.

Shen, Qian, Jiemei Chen, Zhi Lin, et al.. (2020). Multi‐centre study of the clinical features and gene variant spectrum of Gitelman syndrome in Chinese children. Clinical Genetics. 99(4). 558–564. 11 indexed citations

11.

Zhao, Rui, Ying Gu, Xia Shen, et al.. (2020). Money matters: a multicenter cross-sectional study of depressive symptoms among the caregivers of children on peritoneal dialysis in Mainland China. BMC Nephrology. 21(1). 472–472. 6 indexed citations

12.

Zhang, Ya, Xin Zhang, Xiaowen Wang, et al.. (2019). Gen1 Modulates Metanephric Morphology Through Retinoic Acid Signaling. DNA and Cell Biology. 38(3). 263–271. 5 indexed citations

13.

Xu, Hong, Yuqing Zhou, Qian Shen, et al.. (2019). Exploration of postnatal integrated management for prenatal renal and urinary tract anomalies in China. The Journal of Maternal-Fetal & Neonatal Medicine. 34(3). 360–365. 3 indexed citations

14.

Dong, Shuangshuang, Chunyan Wang, Xueping Li, et al.. (2019). Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tract. Molecular Genetics and Genomics. 294(2). 493–500. 6 indexed citations

15.

Shen, Qian, Li Sun, Qi Cao, et al.. (2017). Clinical and genetic characters of 8 Chinese children with ADCK4-associated glomerulopathy. 33(1). 22–29. 1 indexed citations

16.

Zhang, Ya, Xiaoyan Fang, Hong Xu, & Qian Shen. (2017). Genetic Analysis of Dent's Disease and Functional Research of CLCN5 Mutations. DNA and Cell Biology. 36(12). 1151–1158. 9 indexed citations

17.

Yang, Caijun, et al.. (2016). Current Situation, Determinants, and Solutions to Drug Shortages in Shaanxi Province, China: A Qualitative Study. PLoS ONE. 11(10). e0165183–e0165183. 46 indexed citations

18.

Xu, Jing, Wei Guo, Hong Xu, et al.. (2015). The significance of Pax2 expression in the ureter epithelium of children with vesicoureteric reflux. Human Pathology. 46(7). 963–970. 6 indexed citations

19.

Sun, Li, Hong Xu, Haimei Liu, et al.. (2011). [Long-term follow-up of 101 cases with pediatric lupus nephritis in a single center in Shanghai].. PubMed. 49(11). 819–24. 5 indexed citations

20.

Mak, Robert H., Wai W. Cheung, Jianying Zhan, Qian Shen, & Bethany J. Foster. (2011). Cachexia and protein-energy wasting in children with chronic kidney disease. Pediatric Nephrology. 27(2). 173–181. 62 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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