Seo‐Kyung Chung

3.1k total citations
27 papers, 949 citations indexed

About

Seo‐Kyung Chung is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Seo‐Kyung Chung has authored 27 papers receiving a total of 949 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Seo‐Kyung Chung's work include Ion channel regulation and function (9 papers), Cardiac electrophysiology and arrhythmias (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Seo‐Kyung Chung is often cited by papers focused on Ion channel regulation and function (9 papers), Cardiac electrophysiology and arrhythmias (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Seo‐Kyung Chung collaborates with scholars based in United Kingdom, Australia and United States. Seo‐Kyung Chung's co-authors include Mark I. Rees, Jonathan G.L. Mullins, Jonathan R. Skinner, Jackie Crawford, Andrew N. Shelling, Thomas D. Cushion, William B. Dobyns, Victoria L. Harvey, Judith MacCormick and Rhys H. Thomas and has published in prestigious journals such as Nature Genetics, Brain and PEDIATRICS.

In The Last Decade

Seo‐Kyung Chung

26 papers receiving 922 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Seo‐Kyung Chung United Kingdom 16 592 286 243 199 166 27 949
Zaid Afawi Israel 17 442 0.7× 266 0.9× 113 0.5× 63 0.3× 441 2.7× 27 1.1k
Inge A. Meijer Canada 14 369 0.6× 362 1.3× 45 0.2× 138 0.7× 150 0.9× 22 811
I. D. Millar United Kingdom 12 676 1.1× 276 1.0× 49 0.2× 137 0.7× 106 0.6× 21 1.0k
Chihiro Ohba Japan 16 563 1.0× 252 0.9× 32 0.1× 102 0.5× 341 2.1× 26 922
Klaus Rüether Germany 17 1.2k 2.0× 484 1.7× 81 0.3× 207 1.0× 58 0.3× 21 1.5k
Rebecca C. Ahrens‐Nicklas United States 17 406 0.7× 86 0.3× 121 0.5× 72 0.4× 108 0.7× 68 744
Mizue Iai Japan 17 431 0.7× 177 0.6× 27 0.1× 86 0.4× 191 1.2× 48 856
Venkateswaran Ramesh United Kingdom 13 427 0.7× 251 0.9× 32 0.1× 74 0.4× 146 0.9× 20 846
Kathleen J. Sweadner United States 14 606 1.0× 195 0.7× 49 0.2× 37 0.2× 110 0.7× 17 905
Eduardo Pérez‐Palma United States 16 500 0.8× 154 0.5× 70 0.3× 34 0.2× 478 2.9× 38 888

Countries citing papers authored by Seo‐Kyung Chung

Since Specialization
Citations

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

Fields of papers citing papers by Seo‐Kyung Chung

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Seo‐Kyung Chung

This figure shows the co-authorship network connecting the top 25 collaborators of Seo‐Kyung Chung. A scholar is included among the top collaborators of Seo‐Kyung Chung 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 Seo‐Kyung Chung. Seo‐Kyung Chung 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.
Nash, Benjamin M., Milan Fernando, James P. Robinson, et al.. (2021). Evaluation for Retinal Therapy for RPE65 Variation Assessed in hiPSC Retinal Pigment Epithelial Cells. Stem Cells International. 2021. 1–12. 4 indexed citations
2.
Piard, Juliette, George K. E. Umanah, Frederike L. Harms, et al.. (2017). A homozygous ATAD1 mutation impairs postsynaptic AMPA receptor trafficking and causes a lethal encephalopathy. Brain. 141(3). 651–661. 35 indexed citations
3.
Oegema, Renske, Thomas D. Cushion, Ian G. Phelps, et al.. (2015). Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes. Human Molecular Genetics. 24(18). 5313–5325. 61 indexed citations
4.
Thomas, Rhys H., et al.. (2014). Ethnicity can predict GLRA1 genotypes in hyperekplexia. Journal of Neurology Neurosurgery & Psychiatry. 86(3). 341–343. 8 indexed citations
5.
Kang, Jing‐Qiong, Wangzhen Shen, William Owen Pickrell, et al.. (2014). A Novel GABRG2 mutation, p.R136*, in a family with GEFS+ and extended phenotypes. Neurobiology of Disease. 64. 131–141. 31 indexed citations
6.
Cushion, Thomas D., William B. Dobyns, Jonathan G.L. Mullins, et al.. (2013). Overlapping cortical malformations and mutations in TUBB2B and TUBA1A. Brain. 136(2). 536–548. 101 indexed citations
7.
Thomas, Rhys H., Seo‐Kyung Chung, Thomas D. Cushion, et al.. (2013). Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delay. Brain. 136(10). 3085–3095. 54 indexed citations
8.
James, Victoria M., Anna Bode, Seo‐Kyung Chung, et al.. (2012). Novel missense mutations in the glycine receptor β subunit gene (GLRB) in startle disease. Neurobiology of Disease. 52. 137–149. 46 indexed citations
9.
Pickrell, William Owen, Mark I. Rees, & Seo‐Kyung Chung. (2012). Next Generation Sequencing Methodologies - An Overview. Advances in protein chemistry and structural biology. 89. 1–26. 13 indexed citations
10.
Thomas, Rhys H., Seo‐Kyung Chung, Khalid Hamandi, Mark I. Rees, & Michael Kerr. (2012). Translation of genetic findings to clinical practice in juvenile myoclonic epilepsy. Epilepsy & Behavior. 26(3). 241–246. 4 indexed citations
11.
Gill, Jennifer, Jean-François Vanbellinghen, Seo‐Kyung Chung, et al.. (2011). Startle disease in Irish wolfhounds associated with a microdeletion in the glycine transporter GlyT2 gene. Neurobiology of Disease. 43(1). 184–189. 40 indexed citations
12.
MacCormick, Judith, Jackie Crawford, Seo‐Kyung Chung, et al.. (2011). Symptoms and Signs Associated with Syncope in Young People with Primary Cardiac Arrhythmias. Heart Lung and Circulation. 20(9). 593–598. 26 indexed citations
13.
Lane, M. R., Jackie Crawford, Seo‐Kyung Chung, et al.. (2010). Elevated serum gastrin levels in Jervell and Lange-Nielsen syndrome: A marker of severe KCNQ1 dysfunction?. Heart Rhythm. 8(4). 551–554. 23 indexed citations
14.
Mullins, Jonathan G.L., Seo‐Kyung Chung, & Mark I. Rees. (2010). Fine architecture and mutation mapping of human brain inhibitory system ligand gated ion channels by high-throughput homology modeling. Advances in protein chemistry and structural biology. 80. 117–152. 5 indexed citations
15.
Gladding, Patrick, Jackie Crawford, Seo‐Kyung Chung, et al.. (2010). Posthumous diagnosis of long QT syndrome from neonatal screening cards. Heart Rhythm. 7(4). 481–486. 43 indexed citations
16.
Eddy, Carey-Anne, Judith MacCormick, Seo‐Kyung Chung, et al.. (2008). Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome. Heart Rhythm. 5(9). 1275–1281. 62 indexed citations
17.
Skinner, Jonathan R., et al.. (2007). Coinheritance of long QT syndrome and Kearns-Sayre syndrome. Heart Rhythm. 4(12). 1568–1572. 10 indexed citations
18.
Chung, Seo‐Kyung, Judith MacCormick, Caroline McCulley, et al.. (2007). Long QT and Brugada syndrome gene mutations in New Zealand. Heart Rhythm. 4(10). 1306–1314. 31 indexed citations
19.
Skinner, Jonathan R., Seo‐Kyung Chung, Andrew N. Shelling, et al.. (2007). Brugada Syndrome Masquerading as Febrile Seizures. PEDIATRICS. 119(5). e1206–e1211. 46 indexed citations
20.
Rees, Mark I., Kirsten Harvey, Brian R. Pearce, et al.. (2006). Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease. Nature Genetics. 38(7). 801–806. 174 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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