Dae‐Seong Kim

1.5k total citations
55 papers, 915 citations indexed

About

Dae‐Seong Kim is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Dae‐Seong Kim has authored 55 papers receiving a total of 915 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 13 papers in Cellular and Molecular Neuroscience and 13 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Dae‐Seong Kim's work include Muscle Physiology and Disorders (12 papers), Neurogenetic and Muscular Disorders Research (9 papers) and Genetic Neurodegenerative Diseases (7 papers). Dae‐Seong Kim is often cited by papers focused on Muscle Physiology and Disorders (12 papers), Neurogenetic and Muscular Disorders Research (9 papers) and Genetic Neurodegenerative Diseases (7 papers). Dae‐Seong Kim collaborates with scholars based in South Korea, Finland and Sudan. Dae‐Seong Kim's co-authors include Jin‐Hong Shin, Young‐Chul Choi, Hyang-Sook Kim, Kyu-Hyun Park, Sun‐Young Kim, Arash Minai‐Tehrani, Soon‐Kyung Hwang, Myung‐Haing Cho, Jung‐Taek Kwon and Young-Eun Park and has published in prestigious journals such as Hepatology, Scientific Reports and ChemSusChem.

In The Last Decade

Dae‐Seong Kim

49 papers receiving 903 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dae‐Seong Kim South Korea 18 375 232 168 133 129 55 915
Junhee Park South Korea 18 594 1.6× 239 1.0× 94 0.6× 61 0.5× 24 0.2× 52 1.3k
Xue Yao China 23 825 2.2× 261 1.1× 140 0.8× 32 0.2× 29 0.2× 65 1.9k
Be׳eri Niego Australia 18 239 0.6× 73 0.3× 179 1.1× 100 0.8× 31 0.2× 35 913
Emilia Manole Romania 12 580 1.5× 127 0.5× 53 0.3× 95 0.7× 20 0.2× 35 909
Jiangang Wang China 21 347 0.9× 113 0.5× 165 1.0× 398 3.0× 25 0.2× 119 1.2k
Xiaobo Han China 17 384 1.0× 68 0.3× 126 0.8× 48 0.4× 80 0.6× 52 1.0k
Yifei Miao United States 22 627 1.7× 48 0.2× 140 0.8× 131 1.0× 96 0.7× 36 1.4k
J. Jasmin Brazil 16 247 0.7× 71 0.3× 70 0.4× 209 1.6× 27 0.2× 37 881
Shailendra Joshi United States 24 227 0.6× 82 0.4× 117 0.7× 77 0.6× 43 0.3× 74 1.6k
Christine Cheung Singapore 18 563 1.5× 51 0.2× 81 0.5× 117 0.9× 16 0.1× 47 1.2k

Countries citing papers authored by Dae‐Seong Kim

Since Specialization
Citations

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

Fields of papers citing papers by Dae‐Seong Kim

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dae‐Seong Kim. 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 Dae‐Seong Kim. The network helps show where Dae‐Seong Kim may publish in the future.

Co-authorship network of co-authors of Dae‐Seong Kim

This figure shows the co-authorship network connecting the top 25 collaborators of Dae‐Seong Kim. A scholar is included among the top collaborators of Dae‐Seong Kim 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 Dae‐Seong Kim. Dae‐Seong Kim 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
1.
2.
Park, Young-Eun, Dae‐Seong Kim, & Jin‐Hong Shin. (2022). A novel nonsense mutation in the dimerization domain of FLNC causing mild myofibrillar myopathy. Clinical Neurology and Neurosurgery. 221. 107386–107386. 3 indexed citations
3.
Ullah, H. M. Arif, Sunyoung Park, Yong Deuk Kim, et al.. (2021). Nogo-A Is Critical for Pro-Inflammatory Gene Regulation in Myocytes and Macrophages. Cells. 10(2). 282–282. 27 indexed citations
4.
Shin, Jin‐Hong, Young-Eun Park, & Dae‐Seong Kim. (2021). Nomenclature of emerging therapeutics in neurology. 23(1). 29–34.
5.
Shin, Jin‐Hong & Dae‐Seong Kim. (2020). Focal eosinophilic myositis presenting with leg pain and tenderness. 22(2). 125–128. 1 indexed citations
6.
Park, Young-Eun, Jin‐Hong Shin, & Dae‐Seong Kim. (2020). Muscle pathology in neuromuscular disorders. 22(2). 51–60. 1 indexed citations
7.
Jung, Na‐Yeon, Eun Soo Kim, Hyang-Sook Kim, et al.. (2020). Comparison of Diagnostic Performances Between Cerebrospinal Fluid Biomarkers and Amyloid PET in a Clinical Setting. Journal of Alzheimer s Disease. 74(2). 473–490. 16 indexed citations
8.
Shin, Jin‐Hong, et al.. (2018). Characterization of congenital myopathies at a Korean neuromuscular center. Muscle & Nerve. 58(2). 235–244. 6 indexed citations
9.
Jung, Jae Ho, Eun Hye Oh, Jin‐Hong Shin, et al.. (2018). Atypical clinical manifestations of Miller Fisher syndrome. Neurological Sciences. 40(1). 67–73. 22 indexed citations
10.
Choi, Kwang‐Dong, Ji‐Soo Kim, Hyo‐Jung Kim, et al.. (2017). Genetic Variants Associated with Episodic Ataxia in Korea. Scientific Reports. 7(1). 13855–13855. 58 indexed citations
11.
Lee, Jung Hwan, Jin‐Hong Shin, Hyung Jun Park, et al.. (2017). Targeted population screening of late onset Pompe disease in unspecified myopathy patients for Korean population. Neuromuscular Disorders. 27(6). 550–556. 11 indexed citations
12.
Seo, Jiwon, Minji Kim, Geu‐Ru Hong, et al.. (2016). Fabry disease in patients with hypertrophic cardiomyopathy: a practical approach to diagnosis. Journal of Human Genetics. 61(9). 775–780. 19 indexed citations
13.
Shin, Ha Young, Hoon Jang, Hyung Jun Park, et al.. (2015). Targeted next-generation sequencing for the genetic diagnosis of dysferlinopathy. Neuromuscular Disorders. 25(6). 502–510. 17 indexed citations
14.
Kim, Hyang-Sook, et al.. (2012). Autonomic dysfunction in SCN9A-associated primary erythromelalgia. Clinical Autonomic Research. 23(2). 105–107. 9 indexed citations
15.
Jeon, Hyun‐Kyu, Junho Kim, Jung‐Hwan Choi, et al.. (2010). 6.4: A Clockembedded Voltage Differential Signaling CVDS for the ChipOnGlass Application of TFTLCD. SID Symposium Digest of Technical Papers. 41(1). 66–69. 1 indexed citations
16.
Lee, Jae‐Hyeok, et al.. (2009). Disabling Head Tremor in a Patient with DYT1 Mutation. Journal of Movement Disorders. 2(2). 86–87. 1 indexed citations
17.
Choi, Byung‐Ok, Jong‐Min Kim, Jeeyoung Oh, et al.. (2006). Clinical and Genetic Characteristics in Patients of Charcot-Marie-Tooth type 2A with Mitofusin 2 (MFN2) Mutations. Journal of the Korean Neurological Association. 24(2). 131–140. 1 indexed citations
18.
Park, Young-Eun, et al.. (2006). Two new missense mutations of GAA in late onset glycogen storage disease type II. Journal of the Neurological Sciences. 251(1-2). 113–117. 14 indexed citations
19.
Shin, Jin‐Hong, et al.. (2002). A Case of Anti-Hu Associated Paraneoplastic Subacute Sensory Neuronopathy.. Journal of the Korean Neurological Association. 20(1). 89–92.
20.
Choi, Kwang‐Dong, et al.. (2002). Electrophysiological Classification of Guillain-Barre Syndrome - Sequential Changes in Electrophysiologic Findings -. Journal of the Korean Neurological Association. 20(6). 630–633. 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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