Chae-Seok Lim

874 total citations
18 papers, 502 citations indexed

About

Chae-Seok Lim is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Chae-Seok Lim has authored 18 papers receiving a total of 502 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 4 papers in Genetics. Recurrent topics in Chae-Seok Lim's work include Neuroscience and Neuropharmacology Research (6 papers), Neurobiology and Insect Physiology Research (3 papers) and Neurogenesis and neuroplasticity mechanisms (3 papers). Chae-Seok Lim is often cited by papers focused on Neuroscience and Neuropharmacology Research (6 papers), Neurobiology and Insect Physiology Research (3 papers) and Neurogenesis and neuroplasticity mechanisms (3 papers). Chae-Seok Lim collaborates with scholars based in South Korea, United States and United Kingdom. Chae-Seok Lim's co-authors include Bong‐Kiun Kaang, Yong‐Seok Lee, Nam‐Kyung Yu, Daekwan Seo, Joseph Bakes, Hye Jin Nam, Jin‐Hee Han, Sung Hee Baek, Jin‐A Lee and Deok-Jin Jang and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neuroscience and Genes & Development.

In The Last Decade

Chae-Seok Lim

17 papers receiving 495 citations

Peers

Chae-Seok Lim

CMN

GENET

Elissa D. Pastuzyn United States

Luoxiu Huang United States

Andrew Taibi United States

Magali Hennion France

Jennifer Spaethling United States

Madeleine Kyrke‐Smith New Zealand

Nataša Savić Switzerland

Yi‐Wen Hsieh United States

Corinna Giorgi Italy

Ovidiu D. Iancu United States

Elissa D. Pastuzyn United States

Chae-Seok Lim

507 ×1.6

205 ×1.3

CMN

106 ×0.8

GENET

67 ×0.9

81 ×1.2

Citations per year, relative to Chae-Seok Lim Chae-Seok Lim (= 1×) peers Elissa D. Pastuzyn

Countries citing papers authored by Chae-Seok Lim

Since Specialization

Citations

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

Fields of papers citing papers by Chae-Seok Lim

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chae-Seok Lim. 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 Chae-Seok Lim. The network helps show where Chae-Seok Lim may publish in the future.

Co-authorship network of co-authors of Chae-Seok Lim

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

18 of 18 papers shown

Lim, Chae-Seok, et al.. (2025). Circadian Rhythm Dysfunction in Neurodegenerative Diseases: A Bidirectional Perspective and Therapeutic Potential. Nature and Science of Sleep. Volume 17. 2969–2989.

Lim, Chae-Seok, Min Jung Kim, Ja Eun Choi, et al.. (2021). Dysfunction of NMDA receptors in neuronal models of an autism spectrum disorder patient with a DSCAM mutation and in Dscam-knockout mice. Molecular Psychiatry. 26(12). 7538–7549. 18 indexed citations

Lee, Yong‐Seok, Nam‐Kyung Yu, Jae‐Kyung Jung, et al.. (2020). Identification of a novel Shank2 transcriptional variant in Shank2 knockout mouse model of autism spectrum disorder. Molecular Brain. 13(1). 54–54. 11 indexed citations

Huh, Yang Hoon, Yong‐Seok Lee, Deok-Jin Jang, et al.. (2020). Autophagy pathway upregulation in a human iPSC-derived neuronal model of Cohen syndrome with VPS13B missense mutations. Molecular Brain. 13(1). 69–69. 11 indexed citations

Ryu, Hyun-Hee, TaeHyun Kim, Jung-Woong Kim, et al.. (2019). Excitatory neuron–specific SHP2-ERK signaling network regulates synaptic plasticity and memory. Science Signaling. 12(571). 35 indexed citations

Kim, Min Jung, Jihae Oh, Ja Eun Choi, et al.. (2019). Spatial Learning and Motor Deficits in Vacuolar Protein Sorting-associated Protein 13b (Vps13b) Mutant Mouse. Experimental Neurobiology. 28(4). 485–494. 12 indexed citations

Lim, Chae-Seok, Xi Kang, Vincent R. Mirabella, et al.. (2017). BRaf signaling principles unveiled by large-scale human mutation analysis with a rapid lentivirus-based gene replacement method. Genes & Development. 31(6). 537–552. 12 indexed citations

Hwang, Su‐Kyeong, Jae‐Hyung Lee, Jae‐Kyung Jung, et al.. (2016). Everolimus improves neuropsychiatric symptoms in a patient with tuberous sclerosis carrying a novel TSC2 mutation. Molecular Brain. 9(1). 56–56. 26 indexed citations

Lee, Seung‐Hee, Jaehoon Shim, Sue‐Hyun Lee, et al.. (2016). ApCPEB4, a non-prion domain containing homolog of ApCPEB, is involved in the initiation of long-term facilitation. Molecular Brain. 9(1). 91–91. 4 indexed citations

10.

Lim, Chae-Seok, Jae‐Ick Kim, Daekwan Seo, et al.. (2016). The Brain-Enriched MicroRNA miR-9-3p Regulates Synaptic Plasticity and Memory. Journal of Neuroscience. 36(33). 8641–8652. 92 indexed citations

11.

Yu, Nam‐Kyung, Hyoung F. Kim, Jae-Hoon Shim, et al.. (2016). A transducible nuclear/nucleolar protein, mLLP, regulates neuronal morphogenesis and synaptic transmission. Scientific Reports. 6(1). 22892–22892. 14 indexed citations

12.

Kim, Kun Hyung, Yongsoo Park, Jin‐A Lee, et al.. (2014). Intracellular Membrane Association of the Aplysia cAMP Phosphodiesterase Long and Short Forms via Different Targeting Mechanisms. Journal of Biological Chemistry. 289(37). 25797–25811. 13 indexed citations

13.

Yu, Nam‐Kyung, Joseph Bakes, Daekwan Seo, et al.. (2014). Optimization of AAV expression cassettes to improve packaging capacity and transgene expression in neurons. Molecular Brain. 7(1). 17–17. 124 indexed citations

14.

Park, Pojeong, et al.. (2014). Effects of PI3Kβ overexpression in the hippocampus on synaptic plasticity and spatial learning. Molecular Brain. 7(1). 78–78. 28 indexed citations

15.

Han, Jin‐Hee, Chae-Seok Lim, Yong‐Seok Lee, Eric R. Kandel, & Bong‐Kiun Kaang. (2004). Role ofAplysiaCell Adhesion Molecules During 5-HT-Induced Long-Term Functional and Structural Changes. Learning & Memory. 11(4). 421–435. 19 indexed citations

16.

Lee, Yong Rok, Jin‐Hee Han, Chae-Seok Lim, et al.. (2003). Impairment of a parabolic bursting rhythm by the ectopic expression of a small conductance Ca2+-activated K+ channel in Aplysia neuron R15. Neuroscience Letters. 349(1). 53–57. 3 indexed citations

17.

Lim, Chae-Seok, et al.. (2002). Hydrogen peroxide-induced cell death in cultured Aplysia sensory neurons. Brain Research. 941(1-2). 137–145. 14 indexed citations

18.

Kim, Hyong Kyu, Kyung‐Hee Kim, Jin‐Hee Han, et al.. (2001). Overexpression of and RNA Interference with the CCAAT Enhancer-Binding Protein on Long-Term Facilitation ofAplysiaSensory to Motor Synapses. Learning & Memory. 8(4). 220–226. 66 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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