Shengnan Wu

3.0k total citations · 1 hit paper
86 papers, 2.2k citations indexed

About

Shengnan Wu is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Shengnan Wu has authored 86 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Molecular Biology, 19 papers in Genetics and 10 papers in Clinical Biochemistry. Recurrent topics in Shengnan Wu's work include Mitochondrial Function and Pathology (12 papers), Metabolism and Genetic Disorders (10 papers) and Genomics and Rare Diseases (7 papers). Shengnan Wu is often cited by papers focused on Mitochondrial Function and Pathology (12 papers), Metabolism and Genetic Disorders (10 papers) and Genomics and Rare Diseases (7 papers). Shengnan Wu collaborates with scholars based in China, United States and France. Shengnan Wu's co-authors include Ming‐Hui Zou, Da Xing, Zhonglin Xie, Gloria Torres, Changhan Ouyang, Miao Zhang, Qilong Wang, Xuejuan Gao, Qiulun Lu and Kai Huang and has published in prestigious journals such as Circulation, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Shengnan Wu

78 papers receiving 2.2k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Non-invasive modulation of meningeal lymphatics ameliorates ageing and Alzheimer’s disease-associated pathology and cognition in mice

2024 48 citations Congcong Yan, Shengnan Wu et al. Nature Communications profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Shengnan Wu China	26	1.2k	303	278	276	276	86	2.2k
Wenxin Ma United States	29	1.5k 1.3×	277 0.9×	358 1.3×	156 0.6×	594 2.2×	56	3.8k
Gaofeng Wang United States	27	1.1k 0.9×	201 0.7×	292 1.1×	131 0.5×	322 1.2×	50	2.5k
Aqeela Afzal United States	27	1.1k 0.9×	520 1.7×	129 0.5×	206 0.7×	328 1.2×	54	2.6k
Jena J. Steinle United States	30	1.5k 1.3×	349 1.2×	353 1.3×	114 0.4×	264 1.0×	125	2.9k
Sayon Roy United States	40	2.1k 1.8×	762 2.5×	130 0.5×	204 0.7×	335 1.2×	101	3.9k
Yaoming Wang United States	28	1.1k 0.9×	108 0.4×	613 2.2×	332 1.2×	490 1.8×	47	3.2k
Yehong Zhuo China	27	1.7k 1.5×	493 1.6×	324 1.2×	213 0.8×	158 0.6×	169	3.0k
Pawel Kermer Germany	30	1.5k 1.3×	249 0.8×	999 3.6×	380 1.4×	226 0.8×	80	2.9k
Simone Wagner Germany	23	998 0.9×	94 0.3×	362 1.3×	627 2.3×	279 1.0×	48	3.3k
Tsunehiko Ikeda Japan	31	1.0k 0.9×	1.2k 3.9×	251 0.9×	153 0.6×	287 1.0×	247	3.5k

Countries citing papers authored by Shengnan Wu

Since Specialization

Citations

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

Fields of papers citing papers by Shengnan Wu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shengnan Wu

This figure shows the co-authorship network connecting the top 25 collaborators of Shengnan Wu. A scholar is included among the top collaborators of Shengnan Wu 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 Shengnan Wu. Shengnan Wu 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

Liu, Zhixue, Xiaoxu Zheng, Shengnan Wu, et al.. (2025). MFN2-mediated decrease in mitochondria-associated endoplasmic reticulum membranes contributes to sunitinib-induced endothelial dysfunction and hypertension. Journal of Molecular and Cellular Cardiology. 200. 45–60. 2 indexed citations

Zhang, Yuanfeng, Jianjun Huang, Chunmei Wang, et al.. (2025). Genotypic and Phenotypic Characteristics of Pediatric X-Adrenoleukodystrophy in a Chinese Cohort. Neuropsychiatric Disease and Treatment. Volume 21. 677–687.

Yang, Yang, et al.. (2025). Provincial border effects on capital flows in China: A study based on enterprise cross-regional investment data. Cities. 162. 105984–105984. 1 indexed citations

Weng, Wenhao, et al.. (2025). Diagnostic Utility of Trio–Exome Sequencing for Children With Neurodevelopmental Disorders. JAMA Network Open. 8(3). e251807–e251807. 4 indexed citations

Zhao, Tingting, et al.. (2024). Clinical and genetic characterization of 47 Chinese pediatric patients with Pitt–Hopkins syndrome: a retrospective study. Orphanet Journal of Rare Diseases. 19(1). 51–51.

Yan, Congcong, et al.. (2024). Non-invasive modulation of meningeal lymphatics ameliorates ageing and Alzheimer’s disease-associated pathology and cognition in mice. Nature Communications. 15(1). 1453–1453. 48 indexed citations breakdown →

Wang, Xueqian, Shengnan Wu, Qing Wang, et al.. (2024). UBTF haploinsufficiency associated with UBTF-related global developmental delay and distinctive facial features without neuroregression. Journal of Medical Genetics. 61(12). 1089–1095. 1 indexed citations

Du, Mengmeng, Shengnan Wu, Chang Su, et al.. (2023). Serum vitamin B12 is a promising auxiliary index for the diagnosis of methylmalonic acidemia in children: A single center study in China. Clinica Chimica Acta. 546. 117409–117409.

Xiao, Man, Yanfen Lu, Xiaojun Tang, et al.. (2022). Two novel heterozygous truncating variants in NR4A2 identified in patients with neurodevelopmental disorder and brief literature review. Frontiers in Neuroscience. 16. 956429–956429. 6 indexed citations

10.

Liu, Meiyan, et al.. (2022). Clinical characteristics and genetics of ten Chinese children with PRRT2-associated neurological diseases. Frontiers in Pediatrics. 10. 997088–997088. 2 indexed citations

11.

Miller, Cassandra, Bin Dong, Atit A. Patel, et al.. (2021). Rapid subcellular calcium responses and dynamics by calcium sensor G-CatchER+. iScience. 24(3). 102129–102129. 24 indexed citations

12.

Dong, Fang, Fangfei Xiao, Ting Ge, et al.. (2021). Case Report: A Novel Compound Heterozygous Mutation in IL-10RA in a Chinese Child With Very Early-Onset Inflammatory Bowel Disease. Frontiers in Pediatrics. 9. 678390–678390. 4 indexed citations

13.

Wang, Cheng, Xiaoyan Dai, Shengnan Wu, et al.. (2021). FUNDC1-dependent mitochondria-associated endoplasmic reticulum membranes are involved in angiogenesis and neoangiogenesis. Nature Communications. 12(1). 2616–2616. 80 indexed citations

14.

Tian, Danbi, Shengnan Wu, Hao Zhang, Lingxiang Jiang, & Fengwei Huo. (2019). Application of Inner Filter Effect Technology in Biological Detection and Disease Markers. Huaxue jinzhan. 31. 413. 2 indexed citations

15.

Chen, Qiong, et al.. (2019). Clinical and molecular genetic characterizations of 7 children with X-linked adrenal hypoplasia congenital. Zhonghua shiyong erke linchuang zazhi. 34(8). 595–598. 2 indexed citations

16.

Chen, Qiong, Shengnan Wu, Yongxing Chen, et al.. (2019). A novel missense COL10A1 mutation: c.2020G>A; p. Gly674Arg linked with the bowed legs stature in the Schmid metaphyseal chondrodysplasia-affected Chinese lineage. Bone Reports. 12. 100240–100240. 4 indexed citations

17.

Lu, Qiulun, Zhonglin Xie, Chenghui Yan, et al.. (2017). SNRK (Sucrose Nonfermenting 1-Related Kinase) Promotes Angiogenesis In Vivo. Arteriosclerosis Thrombosis and Vascular Biology. 38(2). 373–385. 29 indexed citations

18.

Li, Weiwei, Wenquan Niu, Yi Zhang, et al.. (2009). Family-based analysis of apelin and AGTRL1 gene polymorphisms with hypertension in Han Chinese. Journal of Hypertension. 27(6). 1194–1201. 44 indexed citations

19.

Wu, Shengnan, Rui Gao, Qinghe Xing, et al.. (2006). Association of DRD2 polymorphisms and chlorpromazine-induced extrapyramidal syndrome in Chinese schizophrenic patients1. Acta Pharmacologica Sinica. 27(8). 966–970. 17 indexed citations

20.

Wu, Shengnan. (2005). Risk factors of Iatrogenic Fungal Infection in Intensive Care Unit. 1 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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