G.-J. Lee-Chen

413 total citations
14 papers, 326 citations indexed

About

G.-J. Lee-Chen is a scholar working on Molecular Biology, Neurology and Physiology. According to data from OpenAlex, G.-J. Lee-Chen has authored 14 papers receiving a total of 326 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Neurology and 7 papers in Physiology. Recurrent topics in G.-J. Lee-Chen's work include Parkinson's Disease Mechanisms and Treatments (6 papers), Lysosomal Storage Disorders Research (5 papers) and Mitochondrial Function and Pathology (4 papers). G.-J. Lee-Chen is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (6 papers), Lysosomal Storage Disorders Research (5 papers) and Mitochondrial Function and Pathology (4 papers). G.-J. Lee-Chen collaborates with scholars based in Taiwan, United States and Switzerland. G.-J. Lee-Chen's co-authors include Yih‐Ru Wu, Kuo‐Hsuan Chang, Chien‐Ming Chen, Rong-Kuo Lyu, Hon‐Chung Fung, L.‐S. Ro, Chuan‐Mu Chen, Yi‐Ching Wang, Kailun Fang and Wuh‐Liang Hwu and has published in prestigious journals such as Journal of Neurology Neurosurgery & Psychiatry, Neurobiology of Aging and Journal of Neural Transmission.

In The Last Decade

G.-J. Lee-Chen

14 papers receiving 319 citations

Peers

G.-J. Lee-Chen
Shalini Padmanabhan United States
Jenny Do United States
Outi Heinonen Finland
M. Kéfi Tunisia
Miriam Kolníková Slovakia
Carlos Bessa Portugal
Celeste Sassi United States
Maya Ando Japan
Barbara Wilmarth United States
Hermann Josef Gertz Germany
Shalini Padmanabhan United States
G.-J. Lee-Chen
Citations per year, relative to G.-J. Lee-Chen G.-J. Lee-Chen (= 1×) peers Shalini Padmanabhan

Countries citing papers authored by G.-J. Lee-Chen

Since Specialization
Citations

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

Fields of papers citing papers by G.-J. Lee-Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by G.-J. Lee-Chen. 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 G.-J. Lee-Chen. The network helps show where G.-J. Lee-Chen may publish in the future.

Co-authorship network of co-authors of G.-J. Lee-Chen

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

All Works

14 of 14 papers shown
1.
Tan, Eng‐King, Chin-Song Lu, Rong Peng, et al.. (2009). Analysis of the UCHL1 genetic variant in Parkinson's disease among Chinese. Neurobiology of Aging. 31(12). 2194–2196. 14 indexed citations
2.
Hsu, Wen-Wei, Hon‐Chung Fung, Jian Lin, et al.. (2008). Promoter polymorphisms modulating HSPA5 expression may increase susceptibility to Taiwanese Alzheimer’s disease. Journal of Neural Transmission. 115(11). 1537–1543. 25 indexed citations
3.
Wu, Yih‐Ru, et al.. (2007). Glucocerebrosidase gene mutation is a risk factor for early onset of Parkinson disease among Taiwanese. Journal of Neurology Neurosurgery & Psychiatry. 78(9). 977–979. 75 indexed citations
4.
Wu, Yih‐Ru, J. C. Hwang, Hsiu-Chuan Hsu, et al.. (2007). Interleukin-1α polymorphism has influence on late-onset sporadic Parkinson’s disease in Taiwan. Journal of Neural Transmission. 114(9). 1173–1177. 12 indexed citations
5.
Lee-Chen, G.-J., et al.. (2007). Mitochondrial DNA polymorphisms and the risk of Parkinson’s disease in Taiwan. Journal of Neural Transmission. 114(8). 1017–1021. 12 indexed citations
6.
Fung, Hon‐Chung, Yah-Yuan Wu, Wen-Wei Hsu, et al.. (2005). Heat Shock Protein 70 and Tumor Necrosis Factor Alpha in Taiwanese Patients with Dementia. Dementia and Geriatric Cognitive Disorders. 20(1). 1–7. 17 indexed citations
7.
Wu, Yah-Yuan, Wuh‐Liang Hwu, C.M. Chen, et al.. (2004). DNA Haplotype Analysis of CAG Repeat in Taiwanese Huntington’s Disease Patients. European Neurology. 52(2). 96–100. 18 indexed citations
8.
Wu, Yih‐Ru, Hon‐Chung Fung, G.-J. Lee-Chen, et al.. (2004). Analysis of polyglutamine-coding repeats in the TATA-binding protein in different neurodegenerative diseases. Journal of Neural Transmission. 112(4). 539–546. 21 indexed citations
9.
10.
Lee-Chen, G.-J., et al.. (2002). Identification and characterization of mutations underlying Sanfilippo syndrome type A (mucopolysaccharidosis type IIIA). Clinical Genetics. 61(3). 192–197. 17 indexed citations
11.
12.
Lee-Chen, G.-J., et al.. (1999). Romano-Ward long QT syndrome: identification of a HERG mutation in a Taiwanese kindred.. PubMed. 98(9). 649–52. 2 indexed citations
13.
Lee-Chen, G.-J., et al.. (1999). Mucopolysaccharidosis type I: Characterization of novel mutations affecting α‐ l‐iduronidase activity. Clinical Genetics. 56(1). 66–70. 22 indexed citations
14.
Lee-Chen, G.-J., et al.. (1998). Human alpha-L-iduronidase (IDUA) gene: correlation of polymorphic DNA haplotype and IDUA activity in Chinese population.. PubMed. 22(1). 31–8. 3 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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