Changhong Ding

901 total citations
71 papers, 611 citations indexed

About

Changhong Ding is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Changhong Ding has authored 71 papers receiving a total of 611 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 14 papers in Neurology and 14 papers in Genetics. Recurrent topics in Changhong Ding's work include Metabolism and Genetic Disorders (12 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomics and Rare Diseases (9 papers). Changhong Ding is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomics and Rare Diseases (9 papers). Changhong Ding collaborates with scholars based in China, United States and Germany. Changhong Ding's co-authors include Renlong Xin, Changfa Guo, Qing Liu, Bo Song, Bingshu Wang, Yingchun Liang, Fang Fang, Li‐Ping Zou, Jiuwei Li and Qing Liu and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Annals of Neurology.

In The Last Decade

Changhong Ding

63 papers receiving 606 citations

Peers

Countries citing papers authored by Changhong Ding

Since Specialization

Citations

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

Fields of papers citing papers by Changhong Ding

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Changhong Ding

This figure shows the co-authorship network connecting the top 25 collaborators of Changhong Ding. A scholar is included among the top collaborators of Changhong Ding 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 Changhong Ding. Changhong Ding 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:

20 of 20 papers shown

#	Work	Indexed citations
1	How does hydropower station construction reshape the geomorphology of downstream mid-channel bars? 2025 ·Geomorphology ·(unknown), Shengjun Wu, Changhong Ding, Zhaofei Wen	1
2	4-Phenylbutyrate restored GABA uptake, mitigated seizures in SLC6A1 and SLC6A11 microdeletions/3p- syndrome: From cellular models to human patients 2025 ·Epilepsy Research ·(unknown), Wangzhen Shen, (unknown), Changhong Ding, (unknown), Jing‐Qiong Kang	2
3	Deep brain stimulation for pediatric pantothenate kinase-associated neurodegeneration with status dystonicus: A case report and literature review 2024 ·Clinical Neurology and Neurosurgery ·(unknown), Ke Sun, (unknown), Shuli Liang, Changhong Ding, (unknown), (unknown), Feng Zhai, Guojun Zhang	1
4	Causal relationship between the composition of the Gut Microbiota and central precocious puberty: a two-sample Mendelian randomization study 2024 ·Frontiers in Pediatrics ·Ming‐Hong Chen, Xueqin Huang, Wuqing Huang, Changhong Ding	2
5	Basal nuclei lesions and cholecystitis as initial findings of late infantile metachromatic leukodystrophy 2022 ·Clinical Neurology and Neurosurgery ·(unknown), Changhong Ding, (unknown), (unknown)	0
6	Chinese patients with p.Arg756 mutations of ATP1A3: Clinical manifestations, treatment, and follow‐up 2022 ·Pediatric Investigation ·(unknown), Jiuwei Li, (unknown), (unknown), Weixing Feng, Shuai Gong, (unknown), Changhong Ding, (unknown), Fang Fang	3
7	Novel Loss-of-Function Variants in CHD2 Cause Childhood-Onset Epileptic Encephalopathy in Chinese Patients 2022 ·Genes ·(unknown), (unknown), Di Cui, Changhong Ding, Chun‐Hong Chen, Xiaohui Wang, Fang Fang, Hong Jin, (unknown)	2
8	Genotype–phenotype correlation of CACNA1A variants in children with epilepsy 2021 ·Developmental Medicine & Child Neurology ·(unknown), Ying Yang, (unknown), (unknown), Ming Liu, Changhong Ding, (unknown), Zhixian Yang, Yuwu Jiang, Yuehua Zhang	11
9	Clinical Features and Outcomes of Anti-N-Methyl-d-Aspartate Receptor Encephalitis in Infants and Toddlers 2021 ·Pediatric Neurology ·Changhong Ren, Weihua Zhang, (unknown), Jiuwei Li, Changhong Ding, Xiaohui Wang, Haitao Ren, Fang Fang	5
10	Phenotypes and genotypes of mitochondrial diseases with mtDNA variations in Chinese children: A multi-center study 2021 ·Mitochondrion ·Yuqing Shi, (unknown), Dan Sun, Chaoping Hu, Zhimei Liu, Danmin Shen, Junling Wang, Tianyu Song, Weihua Zhang, Jiuwei Li, (unknown), (unknown), Changhong Ding, Yi Wang, Fang Fang	7
11	Altered inhibitory synapses in de novo GABRA5 and GABRA1 mutations associated with early onset epileptic encephalopathies 2019 ·Brain ·Ciria C. Hernández, Wenshu XiangWei, Ningning Hu, Dingding Shen, Wangzhen Shen, Andre H. Lagrange, Yujia Zhang, (unknown), Changhong Ding, Zhaohui Sun, (unknown), Hongmin Zhu, Yuwu Jiang, Robert L. Macdonald	31
12	Large-single scale mitochondrial DNA deletions in different tissues in Kearns-Sayre syndrome 2019 ·Zhonghua shiyong erke linchuang zazhi ·Yuqing Shi, Fang Fang, Zhimei Liu, Weihua Zhang, Jiuwei Li, (unknown), (unknown), Changhong Ding, (unknown)	1
13	Two Chinese siblings with two novel KCTD7 mutations have dystonia or seizures and epileptic discharge on electroencephalograms 2019 ·Seizure ·(unknown), Changhong Ding, Fang Fang	3
14	Next-Generation Sequencing Analysis Reveals Novel Pathogenic Variants in Four Chinese Siblings With Late-Infantile Neuronal Ceroid Lipofuscinosis 2019 ·Frontiers in Genetics ·(unknown), Xiaohui Wang, Changhong Ding, Xiang Shen, Hao Zhang, Weihua Zhang, Jiuwei Li, Changhong Ren, Fang Fang	11
15	Phenotype-Driven Virtual Panel Is an Effective Method to Analyze WES Data of Neurological Disease 2019 ·Frontiers in Pharmacology ·Xu Wang, Xiang Shen, Fang Fang, Changhong Ding, Hao Zhang, Zhenhua Cao, (unknown)	20
16	Clinical analysis of 25 children with mild encephalitis/encephalopathy with a reversible splenial lesion 2017 ·Zhonghua shiyong erke linchuang zazhi ·(unknown), Changhong Ding, (unknown), (unknown), Xiaohui Wang, Weihua Zhang, Xinying Yang, Fang Fang	1
17	Acute autonomic neuropathy with severe gastrointestinal symptoms in children: a case series 2017 ·BMC Neurology ·(unknown), Changhong Ding, Yangyang Wang, Liying Liu, (unknown), Li‐Ping Zou	6
18	Stevens–Johnson syndrome induced by levetiracetam 2012 ·Seizure ·Li‐Ping Zou, Changhong Ding, (unknown), Xiaofeng Li	24
19	Ultrastructural Characterization of the Mature Embryo Sac in the Chromosome-9 Monosomic Addition Line of Beta corolliflora in Sugar Beet 2009 ·Chinese Bulletin of Botany ·(unknown), (unknown), (unknown), Changhong Ding, Wei Li, (unknown)	0
20	Effectiveness of the First Antiepileptic Drug in the Treatment of Pediatric Epilepsy 2009 ·Pediatric Neurology ·(unknown), (unknown), Ying Wang, Fang Fang, Changhong Ding, Li‐Ping Zou	10

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.

Explore authors with similar magnitude of impact