Jong‐Min Lee

3.9k total citations
42 papers, 1.5k citations indexed

About

Jong‐Min Lee is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Jong‐Min Lee has authored 42 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 35 papers in Cellular and Molecular Neuroscience and 13 papers in Neurology. Recurrent topics in Jong‐Min Lee's work include Genetic Neurodegenerative Diseases (35 papers), Mitochondrial Function and Pathology (24 papers) and Neurological disorders and treatments (12 papers). Jong‐Min Lee is often cited by papers focused on Genetic Neurodegenerative Diseases (35 papers), Mitochondrial Function and Pathology (24 papers) and Neurological disorders and treatments (12 papers). Jong‐Min Lee collaborates with scholars based in United States, United Kingdom and Germany. Jong‐Min Lee's co-authors include James F. Gusella, Marcy E. MacDonald, Marcy E. MacDonald, Tammy Gillis, Jun Wan Shin, Michael J. Chao, Kyung‐Hee Kim, Vanessa C. Wheeler, Seung Kwak and Peter Holmans and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and PLoS ONE.

In The Last Decade

Jong‐Min Lee

41 papers receiving 1.5k citations

Peers

Jong‐Min Lee
Tammy Gillis United States
Michael Flower United Kingdom
Ralph André United Kingdom
Astrid Lunkes Germany
Mark Kristiansen United Kingdom
Jillian K. Cooper United States
Rim Amouri Tunisia
Stefan Kuemmerle United States
John J. Kleiderlein United States
Elisa Fossale United States
Tammy Gillis United States
Jong‐Min Lee
Citations per year, relative to Jong‐Min Lee Jong‐Min Lee (= 1×) peers Tammy Gillis

Countries citing papers authored by Jong‐Min Lee

Since Specialization
Citations

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

Fields of papers citing papers by Jong‐Min Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jong‐Min Lee

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

All Works

20 of 20 papers shown
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Gao, Dadi, Kevin Correia, Jennie C. L. Roy, et al.. (2024). Splice modulators target PMS1 to reduce somatic expansion of the Huntington’s disease-associated CAG repeat. Nature Communications. 15(1). 3182–3182. 14 indexed citations
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Shin, Jun Wan, Eun Pyo Hong, Ihn Sik Seong, et al.. (2022). Allele-specific silencing of the gain-of-function mutation in Huntington’s disease using CRISPR/Cas9. JCI Insight. 7(19). 17 indexed citations
5.
Neueder, Andreas, Kerstin Kojer, Daniel J. Lavery, et al.. (2022). Abnormal molecular signatures of inflammation, energy metabolism, and vesicle biology in human Huntington disease peripheral tissues. Genome biology. 23(1). 189–189. 10 indexed citations
6.
Shin, Jun Wan, et al.. (2022). PAM-altering SNP-based allele-specific CRISPR-Cas9 therapeutic strategies for Huntington’s disease. Molecular Therapy — Methods & Clinical Development. 26. 547–561. 8 indexed citations
7.
Hong, Eun Pyo, Marcy E. MacDonald, Vanessa C. Wheeler, et al.. (2021). Huntington’s Disease Pathogenesis: Two Sequential Components. Journal of Huntington s Disease. 10(1). 35–51. 54 indexed citations
8.
Lee, Yejin, Douglas Barker, Kevin Correia, et al.. (2021). Mutations causing Lopes-Maciel-Rodan syndrome are huntingtin hypomorphs. Human Molecular Genetics. 30(3-4). 135–148. 20 indexed citations
9.
Lee, Jong‐Min, Jung-hyun Rho, Michael H. A. Roehrl, & Julia Y. Wang. (2021). Dermatan Sulfate Is a Potential Regulator of IgH via Interactions With Pre-BCR, GTF2I, and BiP ER Complex in Pre-B Lymphoblasts. Frontiers in Immunology. 12. 680212–680212. 11 indexed citations
10.
Loupe, Jacob M., Ricardo Mouro Pinto, Kyung‐Hee Kim, et al.. (2020). Promotion of somatic CAG repeat expansion by Fan1 knock-out in Huntington’s disease knock-in mice is blocked by Mlh1 knock-out. Human Molecular Genetics. 29(18). 3044–3053. 50 indexed citations
11.
Oh, Hyejin, Seung Kwak, Susan L. Cotman, et al.. (2018). Novel DNA Aptamers that Bind to Mutant Huntingtin and Modify Its Activity. Molecular Therapy — Nucleic Acids. 11. 416–428. 13 indexed citations
12.
Kovalenko, Marina, Austen J. Milnerwood, Jason St. Claire, et al.. (2018). HttQ111/+ Huntington’s Disease Knock-in Mice Exhibit Brain Region-Specific Morphological Changes and Synaptic Dysfunction. Journal of Huntington s Disease. 7(1). 17–33. 25 indexed citations
13.
Chao, Michael J., Tammy Gillis, Ranjit Singh Atwal, et al.. (2017). Haplotype-based stratification of Huntington's disease. European Journal of Human Genetics. 25(11). 1202–1209. 18 indexed citations
14.
Shin, Aram, Tammy Gillis, Jayalakshmi Srinidhi Mysore, et al.. (2016). The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease. The American Journal of Human Genetics. 98(2). 287–298. 103 indexed citations
15.
Kovalenko, Marina, Ella Dragileva, Jason St. Claire, et al.. (2012). Msh2 Acts in Medium-Spiny Striatal Neurons as an Enhancer of CAG Instability and Mutant Huntingtin Phenotypes in Huntington’s Disease Knock-In Mice. PLoS ONE. 7(9). e44273–e44273. 59 indexed citations
16.
Cao, Yi, John F. Staropoli, Janice A. Espinola, et al.. (2011). Distinct Early Molecular Responses to Mutations Causing vLINCL and JNCL Presage ATP Synthase Subunit C Accumulation in Cerebellar Cells. PLoS ONE. 6(2). e17118–e17118. 49 indexed citations
17.
Wang, Julia Y., Jong‐Min Lee, Ming Yan, Jung-hyun Rho, & Michael H. A. Roehrl. (2011). Dermatan Sulfate Interacts with Dead Cells and Regulates CD5+ B-Cell Fate. American Journal Of Pathology. 178(5). 2168–2176. 16 indexed citations
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Kang, Kihwa, Jennifer Schmahl, Jong‐Min Lee, et al.. (2011). Mouse ghrelin‐ O ‐acyltransferase (GOAT) plays a critical role in bile acid reabsorption. The FASEB Journal. 26(1). 259–271. 25 indexed citations
20.
Seong, Ihn Sik, Elena V. Ivanova, Jong‐Min Lee, et al.. (2005). HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolism. Human Molecular Genetics. 14(19). 2871–2880. 235 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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