Chaoping Hu

473 total citations
16 papers, 90 citations indexed

About

Chaoping Hu is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry. According to data from OpenAlex, Chaoping Hu has authored 16 papers receiving a total of 90 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 4 papers in Clinical Biochemistry. Recurrent topics in Chaoping Hu's work include Mitochondrial Function and Pathology (4 papers), Muscle Physiology and Disorders (4 papers) and Metabolism and Genetic Disorders (4 papers). Chaoping Hu is often cited by papers focused on Mitochondrial Function and Pathology (4 papers), Muscle Physiology and Disorders (4 papers) and Metabolism and Genetic Disorders (4 papers). Chaoping Hu collaborates with scholars based in China. Chaoping Hu's co-authors include Xihua Li, Shuizhen Zhou, Lei Zhao, Bingbing Wu, Yì Wáng, Hui Li, Fang Liu, Lei Zhao, Wenhui Li and Yi Wang and has published in prestigious journals such as Gene Therapy, Human Mutation and Orphanet Journal of Rare Diseases.

In The Last Decade

Chaoping Hu

12 papers receiving 90 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chaoping Hu China	5	75	25	20	17	16	16	90
Claudio Bruno Italy	4	91 1.2×	9 0.4×	21 1.1×	9 0.5×	25 1.6×	12	102
Agnès Guët France	6	53 0.7×	15 0.6×	19 0.9×	4 0.2×	17 1.1×	12	102
Ahlam A. Hamed Sudan	7	33 0.4×	17 0.7×	7 0.3×	4 0.2×	14 0.9×	15	102
Abigail R. Benkert United States	7	72 1.0×	20 0.8×	24 1.2×	3 0.2×	9 0.6×	17	139
Stephen Tennant United Kingdom	4	46 0.6×	21 0.8×	32 1.6×	4 0.2×	5 0.3×	7	90
Şahin Avcı Türkiye	6	83 1.1×	4 0.2×	11 0.6×	14 0.8×	7 0.4×	21	103
Adolfo López de Munaín Arregui Spain	4	42 0.6×	4 0.2×	8 0.4×	7 0.4×	16 1.0×	5	60
Marcos Madruga Garrido Spain	5	45 0.6×	2 0.1×	13 0.7×	9 0.5×	9 0.6×	9	83
Kevin Widjaja United States	4	75 1.0×	20 0.8×	3 0.1×	3 0.2×	15 0.9×	4	99
Carrie Stephan United States	6	119 1.6×	2 0.1×	49 2.5×	35 2.1×	52 3.3×	13	136

Countries citing papers authored by Chaoping Hu

Since Specialization

Citations

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

Fields of papers citing papers by Chaoping Hu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chaoping Hu

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

All Works

Sort: Min cites: Since: Top N: Style:

16 of 16 papers shown

Guan, Jing, Min Zhang, Chaoping Hu, et al.. (2025). Clinical and genetic features of congenital myasthenic syndrome due to the muscle acetylcholine receptor genes. Brain and Development. 47(5). 104412–104412.

Ye, Qun, Bingrui Zhou, Ying Zhang, et al.. (2025). [Analysis of the intervention effects of skill training for parents with autism child on toddlers with autism spectrum disorder].. PubMed. 63(5). 491–497.

Zhao, Lei, et al.. (2024). Two novel deep intronic variants cause Duchenne muscular dystrophy by splice-altering mechanism. Neuromuscular Disorders. 45. 104470–104470. 2 indexed citations

Zhao, Lei, Chaoping Hu, Shuizhen Zhou, et al.. (2024). Comprehensive analysis of 2097 patients with dystrophinopathy based on a database from 2011 to 2021. Orphanet Journal of Rare Diseases. 19(1). 311–311.

Hu, Chaoping, Lei Zhao, Wenhua Zhu, et al.. (2024). Clinical, Pathologic, and Genetic Spectrum of Collagen VI–Related Disorder in China—A Retrospective Observational Multicenter Study. Human Mutation. 2024(1). 3503253–3503253.

Zhu, Xiaomei, et al.. (2023). Spinal muscular atrophy with hypoplasia of the corpus callosum: a case report. BMC Neurology. 23(1). 77–77. 1 indexed citations

Hu, Chaoping, et al.. (2023). PIGW-related glycosylphosphatidylinositol deficiency: A case report and literature review. Neurological Sciences. 45(5). 2253–2260. 3 indexed citations

Hu, Chaoping, Xihua Li, Xiaomei Zhu, et al.. (2022). Comprehensive profile and natural history of pediatric patients with spinal muscular atrophy: A large retrospective study from China. Frontiers in Neurology. 13. 5 indexed citations

Shi, Yuqing, Dan Sun, Chaoping Hu, et al.. (2021). Phenotypes and genotypes of mitochondrial diseases with mtDNA variations in Chinese children: A multi-center study. Mitochondrion. 62. 139–150. 7 indexed citations

10.

Hu, Chaoping, Qiong Xu, Jin Shen, & Yì Wáng. (2021). Clinical and Genetic Characteristics of Mitochondrial Encephalopathy Due to FOXRED1 Mutations: Two Chinese Case Reports and a Review of the Literature. Frontiers in Neurology. 12. 633397–633397. 1 indexed citations

11.

Hu, Chaoping, et al.. (2021). Myotonia Congenita: Clinical Characteristic and Mutation Spectrum of CLCN1 in Chinese Patients. Frontiers in Pediatrics. 9. 759505–759505. 6 indexed citations

12.

Hu, Chaoping, et al.. (2020). Clinical Profile and Outcome of Pediatric Mitochondrial Myopathy in China. Frontiers in Neurology. 11. 1000–1000. 4 indexed citations

13.

Hu, Chaoping & Xihua Li. (2020). Gene therapeutic strategies and relevant clinical trials in neuromuscular disorder in China. Gene Therapy. 27(7-8). 321–328. 1 indexed citations

14.

Hu, Chaoping, et al.. (2020). Clinical and molecular characterization of pediatric mitochondrial disorders in south of China. European Journal of Medical Genetics. 63(8). 103898–103898. 23 indexed citations

15.

Hu, Chaoping, et al.. (2017). [Reducing maternal parenting stress of children with autism spectrum disorder: father's involvement].. PubMed. 55(5). 355–359. 3 indexed citations

16.

Li, Xihua, Lei Zhao, Shuizhen Zhou, et al.. (2015). A comprehensive database of Duchenne and Becker muscular dystrophy patients (0–18 years old) in East China. Orphanet Journal of Rare Diseases. 10(1). 5–5. 34 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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