Yi Dong

755 total citations
44 papers, 463 citations indexed

About

Yi Dong is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Nutrition and Dietetics. According to data from OpenAlex, Yi Dong has authored 44 papers receiving a total of 463 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 28 papers in Cellular and Molecular Neuroscience and 14 papers in Nutrition and Dietetics. Recurrent topics in Yi Dong's work include Genetic Neurodegenerative Diseases (28 papers), Mitochondrial Function and Pathology (21 papers) and Trace Elements in Health (14 papers). Yi Dong is often cited by papers focused on Genetic Neurodegenerative Diseases (28 papers), Mitochondrial Function and Pathology (21 papers) and Trace Elements in Health (14 papers). Yi Dong collaborates with scholars based in China, United States and Switzerland. Yi Dong's co-authors include Zhi‐Ying Wu, Ni Wang, Juan‐Juan Xie, Shi‐Rui Gan, Ning Wang, Yuchao Chen, Yue Zhang, Bo Wan, Jianfeng Xu and Ning Wang and has published in prestigious journals such as PLoS ONE, Neurology and Gene.

In The Last Decade

Yi Dong

41 papers receiving 459 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yi Dong China	13	232	214	168	129	113	44	463
Nadine M. Tassabehji United States	5	77 0.3×	66 0.3×	249 1.5×	21 0.2×	95 0.8×	9	381
Helga Weirich‐Schwaiger Austria	9	159 0.7×	134 0.6×	40 0.2×	101 0.8×	25 0.2×	14	290
Fai Tsang Singapore	10	149 0.6×	87 0.4×	49 0.3×	180 1.4×	21 0.2×	13	414
Yee Kit Tai Singapore	13	123 0.5×	29 0.1×	58 0.3×	89 0.7×	33 0.3×	25	421
C. Whitmore United Kingdom	9	147 0.6×	49 0.2×	33 0.2×	55 0.4×	17 0.2×	14	322
R. Liane Ramirez United States	8	247 1.1×	259 1.2×	34 0.2×	116 0.9×	14 0.1×	11	366
Kazuyuki Nakajima Japan	8	104 0.4×	105 0.5×	68 0.4×	25 0.2×	42 0.4×	10	440
Alejandra Darling Spain	8	78 0.3×	45 0.2×	36 0.2×	42 0.3×	31 0.3×	18	177
Małgorzata Goralska United States	12	242 1.0×	19 0.1×	111 0.7×	40 0.3×	12 0.1×	19	411
Violeta Mihaylova Bulgaria	12	172 0.7×	76 0.4×	19 0.1×	210 1.6×	12 0.1×	22	424

Countries citing papers authored by Yi Dong

Since Specialization

Citations

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

Fields of papers citing papers by Yi Dong

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yi Dong

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

Dong, Yi, et al.. (2024). Genotype-phenotype correlation and founder effect analysis in southeast Chinese patients with sialidosis type I. Orphanet Journal of Rare Diseases. 19(1). 362–362.

Li, Xiaoyan, et al.. (2024). Multi-omics Analysis Reveals Key Gut Microbiota and Metabolites Closely Associated with Huntington’s Disease. Molecular Neurobiology. 62(1). 351–365. 4 indexed citations

Dong, Yi, et al.. (2023). CAT Interruption as a Protective Factor in Chinese Patients with Spinocerebellar Ataxia Type 1. The Cerebellum. 23(3). 1211–1214. 1 indexed citations

Li, Xiaoyan, et al.. (2023). Application Value of Serum Neurofilament Light Protein for Disease Staging in Huntington's Disease. Movement Disorders. 38(7). 1307–1315. 5 indexed citations

Xu, Lingyi, Ziwei Zheng, Shenghai Chang, et al.. (2023). Structures of the human Wilson disease copper transporter ATP7B. Cell Reports. 42(5). 112417–112417. 34 indexed citations

Li, Xiaoyan, et al.. (2023). Loss of CAA interruption and intergenerational CAG instability in Chinese patients with Huntington’s disease. Journal of Molecular Medicine. 101(7). 869–876. 4 indexed citations

Dong, Yi, et al.. (2022). Pathogenicity of Intronic and Synonymous Variants of ATP7B in Wilson Disease. Journal of Molecular Diagnostics. 25(1). 57–67. 6 indexed citations

Zheng, Ziwei, Yi Dong, & Zhi‐Ying Wu. (2022). Latest innovations in the treatment of Wilson's disease. PubMed. 1(3). 181–186. 5 indexed citations

Zheng, Ziwei, et al.. (2022). Serum Neurofilament Light Chain in Wilson's Disease: A Promising Indicator but Unparallel to Real‐Time Treatment Response. Movement Disorders. 37(7). 1531–1535. 4 indexed citations

10.

Zheng, Ziwei, et al.. (2022). Acute-Onset Visual Impairment in Wilson's Disease: A Case Report and Literature Review. Frontiers in Neurology. 13. 911882–911882. 5 indexed citations

11.

Wang, Ni, et al.. (2021). A novel ceruloplasmin mutation identified in a Chinese patient and clinical spectrum of aceruloplasminemia patients. Metabolic Brain Disease. 36(8). 2273–2281. 6 indexed citations

12.

Zhao, Hua, et al.. (2020). Phenotypic variance in monozygotic twins with SCA3. Molecular Genetics & Genomic Medicine. 8(10). e1438–e1438. 3 indexed citations

13.

Yu, Hao, Guo‐Min Yang, Nan Xia, et al.. (2020). Clinical features and outcome of Wilson's disease with generalized epilepsy in Chinese patients. CNS Neuroscience & Therapeutics. 26(8). 842–850. 3 indexed citations

14.

Dong, Yi, et al.. (2020). Clinical features and genetic characteristics of homozygous spinocerebellar ataxia type 3. Molecular Genetics & Genomic Medicine. 8(9). e1314–e1314. 6 indexed citations

15.

Dong, Yi, et al.. (2020). Genetic profile and clinical characteristics of Chinese patients with spinocerebellar ataxia type 2: A multicenter experience over 10 years. European Journal of Neurology. 28(3). 955–964. 7 indexed citations

16.

Gan, Shi‐Rui, et al.. (2020). Factors Associated with Intergenerational Instability of ATXN3 CAG Repeat and Genetic Anticipation in Chinese Patients with Spinocerebellar Ataxia Type 3. The Cerebellum. 19(6). 902–906. 4 indexed citations

17.

Li, Honglei, Yi Dong, Bin Gao, et al.. (2019). Haplotype analysis encompassing HTT gene in Chinese patients with Huntington's disease. European Journal of Neurology. 27(2). 273–279. 6 indexed citations

18.

Dong, Yi, et al.. (2019). Neurofilament light chain is a promising serum biomarker in spinocerebellar ataxia type 3. Molecular Neurodegeneration. 14(1). 39–39. 53 indexed citations

19.

Li, Xiaoyan, Yanbin Zhang, Miao Xu, et al.. (2019). Effect of Apolipoprotein E Genotypes on Huntington’s Disease Phenotypes in a Han Chinese Population. Neuroscience Bulletin. 35(4). 756–762. 4 indexed citations

20.

Chen, Sheng, Shi‐Rui Gan, Pingping Cai, et al.. (2015). Mitochondrial NADH Dehydrogenase Subunit 3 Polymorphism Associated with an Earlier Age at Onset in Male Machado–Joseph disease Patients. CNS Neuroscience & Therapeutics. 22(1). 38–42. 15 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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