Yi‐Chung Lee

5.8k total citations · 1 hit paper
179 papers, 3.4k citations indexed

About

Yi‐Chung Lee is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Yi‐Chung Lee has authored 179 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Neurology, 68 papers in Cellular and Molecular Neuroscience and 47 papers in Molecular Biology. Recurrent topics in Yi‐Chung Lee's work include Genetic Neurodegenerative Diseases (41 papers), Hereditary Neurological Disorders (34 papers) and Neurological diseases and metabolism (24 papers). Yi‐Chung Lee is often cited by papers focused on Genetic Neurodegenerative Diseases (41 papers), Hereditary Neurological Disorders (34 papers) and Neurological diseases and metabolism (24 papers). Yi‐Chung Lee collaborates with scholars based in Taiwan, United States and South Korea. Yi‐Chung Lee's co-authors include Bing‐Wen Soong, Yi‐Chu Liao, Pei‐Chien Tsai, Kon‐Ping Lin, Zoë Morris, W.T. Longstreth, Hannah H. Alphs, C Warlow, S. Ladd and Rustam Al‐Shahi Salman and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Brain.

In The Last Decade

Yi‐Chung Lee

166 papers receiving 3.4k citations

Hit Papers

align trajectories

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.

Incidental findings on brain magnetic resonance imaging: systematic review and meta-analysis

2009 519 citations Yi‐Chung Lee et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yi‐Chung Lee Taiwan	32	1.3k	922	841	555	403	179	3.4k
Fiore Manganelli Italy	33	1.3k 1.0×	642 0.7×	937 1.1×	680 1.2×	317 0.8×	204	3.6k
Marco Locatelli Italy	39	1.7k 1.3×	853 0.9×	1.1k 1.3×	356 0.6×	249 0.6×	207	5.2k
David Lacomis United States	38	2.3k 1.8×	918 1.0×	603 0.7×	225 0.4×	441 1.1×	139	4.6k
Marianne Juhler Denmark	35	2.0k 1.5×	471 0.5×	1.3k 1.6×	365 0.7×	148 0.4×	174	4.0k
Yadollah Harati United States	32	2.1k 1.6×	926 1.0×	856 1.0×	333 0.6×	185 0.5×	71	3.8k
Koji Iihara Japan	38	2.5k 1.9×	947 1.0×	693 0.8×	418 0.8×	505 1.3×	328	6.3k
Ronen R. Leker Israel	35	1.4k 1.1×	1.4k 1.5×	643 0.8×	561 1.0×	167 0.4×	181	4.7k
Takayoshi Shimohata Japan	34	1.7k 1.3×	1.4k 1.5×	1.2k 1.4×	906 1.6×	147 0.4×	198	3.9k
Mark A. Ross United States	40	806 0.6×	1.2k 1.3×	301 0.4×	260 0.5×	227 0.6×	109	4.4k
Meiping Ding China	28	669 0.5×	376 0.4×	472 0.6×	320 0.6×	814 2.0×	151	2.7k

Countries citing papers authored by Yi‐Chung Lee

Since Specialization

Citations

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

Fields of papers citing papers by Yi‐Chung Lee

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yi‐Chung Lee

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

Lee, Cheng‐Chia, Yi‐Chu Liao, Joseph Jen‐Tse Huang, et al.. (2024). The role of adiponectin-AMPK axis in TDP-43 mislocalization and disease severity in ALS. Neurobiology of Disease. 202. 106715–106715. 1 indexed citations

Tsai, Yao‐Chou, Yu-Chien Hsu, Yiru Huang, et al.. (2024). PIAS1 S510G variant acts as a genetic modifier of spinocerebellar ataxia type 3 by selectively impairing mutant ataxin-3 proteostasis. The International Journal of Biochemistry & Cell Biology. 176. 106662–106662. 1 indexed citations

Chen, Wenjie, Yi‐Chu Liao, Yu‐Chun Lin, et al.. (2024). A missense mutation in human INSC causes peripheral neuropathy. EMBO Molecular Medicine. 16(5). 1091–1114.

Liao, Yi‐Chu, et al.. (2024). Characterization of a novel TFG variant causing autosomal recessive pure hereditary spastic paraplegia. Annals of Clinical and Translational Neurology. 11(7). 1909–1920.

Lee, Yi‐Chung, et al.. (2024). Psychometric Evaluation of the Chinese Version of the Vulvovaginal Symptom Questionnaire in Women With Breast Cancer. Journal of Advanced Nursing. 81(7). 3904–3928.

Yu, Kai‐Wei, et al.. (2023). Biallelic DDHD2 mutations in patients with adult‐onset complex hereditary spastic paraplegia. Annals of Clinical and Translational Neurology. 10(9). 1603–1612. 4 indexed citations

Lin, Xiang, Junyi Jiang, Daojun Hong, et al.. (2023). Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular Characterization. Movement Disorders. 39(1). 152–163. 3 indexed citations

Lai, Kuan‐Lin, et al.. (2023). Identification of m.3243A>G mitochondrial DNA mutation in patients with cerebellar ataxia. Journal of the Formosan Medical Association. 122(10). 1028–1034. 1 indexed citations

Yamamoto, Yumi, Yi‐Chu Liao, Yi‐Chung Lee, Masafumi Ihara, & Jay Chol Choi. (2023). Update on the Epidemiology, Pathogenesis, and Biomarkers of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy. Journal of Clinical Neurology. 19(1). 12–12. 19 indexed citations

10.

Liao, Yi‐Chu, Chia‐Hung Wu, Feng‐Chi Chang, et al.. (2023). Impaired cerebral interstitial fluid dynamics in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy. Brain Communications. 6(1). fcad349–fcad349. 9 indexed citations

11.

Lai, Kuan‐Lin, et al.. (2022). Clinical and genetic characterization of NEFL-related neuropathy in Taiwan. Journal of the Formosan Medical Association. 122(2). 132–138. 2 indexed citations

12.

Liu, Yi‐Hong, Wei‐Ju Lee, Takeshi Mizuguchi, et al.. (2022). Neuronal intranuclear inclusion disease in patients with adult-onset non-vascular leukoencephalopathy. Brain. 145(9). 3010–3021. 39 indexed citations

13.

Liao, Yi‐Chu, Kon‐Ping Lin, Po‐Yu Lin, et al.. (2022). Investigating KIF1A mutations in a Taiwanese cohort with hereditary spastic paraplegia. Parkinsonism & Related Disorders. 103. 144–149. 3 indexed citations

14.

Liao, Yi‐Chu, et al.. (2021). Intracerebral Hemorrhage in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy. Stroke. 52(3). 985–993. 29 indexed citations

15.

Tsai, Pei‐Chien, Kang‐Yang Jih, Yi‐Hong Liu, et al.. (2021). Genetic and Functional Analysis of Glycosyltransferase 8 Domain–Containing Protein 1 in Taiwanese Patients With Amyotrophic Lateral Sclerosis. Neurology Genetics. 7(6). e627–e627. 4 indexed citations

16.

Hsueh, Hsueh‐Wen, Shih‐Ying Chen, Yung‐Yee Chang, et al.. (2021). Clinical and genetic characterization of hereditary spastic paraplegia type 3A in Taiwan. Parkinsonism & Related Disorders. 87. 87–91. 8 indexed citations

17.

Liu, Yi‐Hong, Yuh‐Cherng Guo, Ching‐Piao Tsai, et al.. (2021). Treatment response, risk of relapse and clinical characteristics of Taiwanese patients with neuromyelitis optica spectrum disorder. Journal of the Formosan Medical Association. 121(9). 1647–1656. 9 indexed citations

18.

Jih, Kang‐Yang, et al.. (2020). Rapid progressive ALS in a patient with a DNAJC7 loss-of-function mutation. Neurology Genetics. 6(5). e503–e503. 11 indexed citations

19.

Tsai, Pei‐Chien, Yi‐Chu Liao, Kang‐Yang Jih, et al.. (2018). Genetic analysis of ANXA11 variants in a Han Chinese cohort with amyotrophic lateral sclerosis in Taiwan. Neurobiology of Aging. 72. 188.e1–188.e2. 9 indexed citations

20.

Lee, Yi‐Chung, et al.. (2010). Methyl Palmitate: A Potent Vasodilator Released in the Retina. Investigative Ophthalmology & Visual Science. 51(9). 4746–4753. 33 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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