Cha Gon Lee

566 total citations
35 papers, 353 citations indexed

About

Cha Gon Lee is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Cha Gon Lee has authored 35 papers receiving a total of 353 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 15 papers in Molecular Biology and 5 papers in Surgery. Recurrent topics in Cha Gon Lee's work include Genomic variations and chromosomal abnormalities (10 papers), Genomics and Rare Diseases (7 papers) and Epilepsy research and treatment (4 papers). Cha Gon Lee is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Genomics and Rare Diseases (7 papers) and Epilepsy research and treatment (4 papers). Cha Gon Lee collaborates with scholars based in South Korea and United States. Cha Gon Lee's co-authors include Munhyang Lee, Jeehun Lee, Hee Joon Yu, Sang‐Jin Park, Young Bae Sohn, Eun Yeon Joo, Shin-Young Yim, Hyun‐Seok Jin, Chang‐Seok Ki and Eun‐Hae Cho and has published in prestigious journals such as PLoS ONE, Stroke and Epilepsia.

In The Last Decade

Cha Gon Lee

31 papers receiving 299 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cha Gon Lee South Korea 12 126 117 72 72 66 35 353
Manami Akasaka Japan 10 109 0.9× 110 0.9× 84 1.2× 81 1.1× 42 0.6× 41 341
Kiyokuni Miura Japan 12 141 1.1× 133 1.1× 77 1.1× 100 1.4× 75 1.1× 29 444
Jehan Suleiman United Arab Emirates 13 137 1.1× 231 2.0× 44 0.6× 96 1.3× 35 0.5× 25 610
Tommy Stödberg Sweden 14 162 1.3× 169 1.4× 69 1.0× 174 2.4× 59 0.9× 22 625
Keitaro Yamada Japan 11 57 0.5× 189 1.6× 25 0.3× 37 0.5× 85 1.3× 31 347
Muddathir H. Hamad Saudi Arabia 9 51 0.4× 105 0.9× 37 0.5× 52 0.7× 27 0.4× 44 274
Simona Domenica Marino Italy 9 82 0.7× 68 0.6× 80 1.1× 130 1.8× 24 0.4× 39 287
Victoria Rodriguez‐Casero Australia 5 177 1.4× 142 1.2× 64 0.9× 241 3.3× 43 0.7× 7 380
Carmen Gómez‐Lado Spain 11 70 0.6× 55 0.5× 67 0.9× 64 0.9× 18 0.3× 31 223
Jianmin Zhong China 10 54 0.4× 107 0.9× 34 0.5× 68 0.9× 31 0.5× 27 216

Countries citing papers authored by Cha Gon Lee

Since Specialization
Citations

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

Fields of papers citing papers by Cha Gon Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cha Gon 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 Cha Gon Lee. The network helps show where Cha Gon Lee may publish in the future.

Co-authorship network of co-authors of Cha Gon Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Cha Gon Lee. A scholar is included among the top collaborators of Cha Gon 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 Cha Gon Lee. Cha Gon 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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Lee, Woong‐Woo, Cha Gon Lee, & Chang‐Seok Ki. (2024). KCNJ3 is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia identified using whole genome sequencing. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 195(7). e32984–e32984.
3.
Kang, Kyusik, Cha Gon Lee, & Byung‐Kun Kim. (2023). Intracranial Vessel Wall Magnetic Resonance Imaging of Middle Cerebral Artery Dissection in Neurofibromatosis Type 1. Stroke. 54(9). e419–e420. 2 indexed citations
4.
Seo, Ji Young, Cha Gon Lee, Hoon Choi, et al.. (2023). Effects of once-weekly dulaglutide on juvenile type 2 diabetes mellitus and obesity in Korea: a pilot study. Annals of Pediatric Endocrinology & Metabolism. 28(4). 296–301. 3 indexed citations
5.
Lee, Cha Gon & Chang‐Seok Ki. (2020). A Novel De Novo Heterozygous ARID1A Missense Variant Cluster in cis c.[5954C>G;6314C>T;6334C>T;6843G>C] causes a Coffin–Siris Syndrome. Annals of Laboratory Medicine. 41(3). 350–353. 4 indexed citations
6.
Lee, Cha Gon, et al.. (2020). The first familial case of inherited intellectual developmental disorder with dysmorphic facies and behavioral abnormalities (IDDFBA) with a novel FBXO11 variant. American Journal of Medical Genetics Part A. 182(11). 2788–2792. 3 indexed citations
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Lee, Dohwan, Ja‐Hyun Jang, & Cha Gon Lee. (2019). Smith-Kingsmore syndrome: The first report of a Korean patient with the MTOR germline mutation c.5395G>A p.(Glu1799Lys). 16(1). 27–30. 4 indexed citations
9.
Lee, Cha Gon, Ja‐Hyun Jang, & Ji Young Seo. (2019). First identified Korean family with Tatton-Brown-Rahman Syndrome caused by the novel DNMT3A variant c.118G>C p.(Glu40Gln). Annals of Pediatric Endocrinology & Metabolism. 24(4). 253–256. 1 indexed citations
10.
Lee, Cha Gon, et al.. (2018). A novel missense mutation in the ACTG1 gene in a family with congenital autosomal dominant deafness: A case report. Molecular Medicine Reports. 17(6). 7611–7617. 13 indexed citations
11.
Lee, Cha Gon, Jeehun Lee, & Munhyang Lee. (2018). Multi-gene panel testing in Korean patients with common genetic generalized epilepsy syndromes. PLoS ONE. 13(6). e0199321–e0199321. 26 indexed citations
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Cho, Eun‐Hae, et al.. (2016). Temple syndrome: A patient with maternal hetero-UPD14, mixed iso- and hetero-disomy detected by SNP microarray typing of patient-father duos. Brain and Development. 38(7). 669–673. 5 indexed citations
15.
Lee, Cha Gon, Eun‐Hae Cho, & Young Min Ahn. (2016). Maternally inherited autosomal dominant intellectual disability caused by 16p13.3 microduplication. European Journal of Medical Genetics. 59(4). 210–214. 14 indexed citations
16.
Lee, Cha Gon, et al.. (2014). The natural course of clinically isolated syndrome in pediatric patients. Brain and Development. 37(4). 432–438. 11 indexed citations
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Yu, Hee Joon, et al.. (2013). Clinical and ictal characteristics of infantile seizures: EEG correlation via long-term video EEG monitoring. Brain and Development. 35(8). 771–777. 8 indexed citations
19.
Kim, Hee Su, Jeehun Lee, Cha Gon Lee, et al.. (2011). Early Diagnosis of Perinatal Ischemic Stroke Based on Clinical and Radiological Characteristics. 19(2). 131–141.
20.
Lee, Cha Gon, et al.. (2011). The role of ketogenic diet in the treatment of refractory status epilepticus. Epilepsia. 52(11). e181–e184. 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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