Cha Gon Lee
Impact in
- Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders
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- Bacterial Infections and Vaccines
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 10
- Genomics and Rare Diseases 7
- Genetics and Neurodevelopmental Disorders 4
- Genetic Syndromes and Imprinting 3
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- Congenital heart defects research 3
- Epigenetics and DNA Methylation 3
- Co-authors
- Jeehun Lee (9 shared papers)Munhyang Lee (9 shared papers)Hee Joon Yu (6 shared papers)Sang‐Jin Park (5 shared papers)Young Bae Sohn (5 shared papers)Eun Yeon Joo (1 shared paper)Shin-Young Yim (3 shared papers)Hyun‐Seok Jin (3 shared papers)
- Journals
- Brain and Development (4 papers)Korean Journal of Pediatrics (3 papers)European Journal of Medical Genetics (2 papers)PLoS ONE (2 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (1 paper)
- Partner nations
- South KoreaUnited States
In The Last Decade
Cha Gon Lee
31 papers receiving 299 citations
Peers
Comparison fields: 5 of 53
- Clinical Biochemistry 66
- Microbiology 30
- Psychiatry and Mental health 72
- Genetics 126
- Pediatrics, Perinatology and Child Health 72
Countries citing papers authored by Cha Gon Lee
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
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-authors
The 25 scholars most cited alongside Cha Gon Lee, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 35 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 66 | |
| 2 | 2018 | 26 | |
| 3 | 2014 | 24 | |
| 4 | 2012 | 23 | |
| 5 | 2012 | 20 | |
| 6 | 2010 | 17 | |
| 7 | 2012 | 16 | |
| 8 | 2015 | 16 | |
| 9 | Clinical and genetic analysis of three Korean children with pyridoxine-dependent epilepsy. | 2012 | 15 |
| 10 | 2016 | 14 | |
| 11 | 2018 | 13 | |
| 12 | 1970 | 13 | |
| 13 | 2014 | 11 | |
| 14 | 2012 | 11 | |
| 15 | 2013 | 10 | |
| 16 | 2013 | 8 | |
| 17 | Coinheritance of Novel Mutations in SCN1A Causing GEFS+ and in KDM6A Causing Kabuki Syndrome in a Family. | 2017 | 7 |
| 18 | 2017 | 6 | |
| 19 | 2016 | 5 | |
| 20 | 2014 | 5 |
About Cha Gon Lee
Cha Gon Lee is a scholar working on Genetics, Molecular Biology, Surgery, Psychiatry and Mental health and Cellular and Molecular Neuroscience, having authored 35 papers that have together received 353 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Genomics and Rare Diseases (7 papers), Epilepsy research and treatment (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genetic Syndromes and Imprinting (3 papers), Congenital heart defects research (3 papers), Epigenetics and DNA Methylation (3 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Clinical Biochemistry (66 citations), Microbiology (30 citations), Psychiatry and Mental health (72 citations), Genetics (126 citations) and Pediatrics, Perinatology and Child Health (72 citations). Cha Gon Lee has collaborated with scholars based in South Korea and United States. Frequent co-authors include Jeehun Lee, Munhyang Lee, Hee Joon Yu, Sang‐Jin Park, Young Bae Sohn, Eun Yeon Joo, Shin-Young Yim, Hyun‐Seok Jin, Chang‐Seok Ki and Ji Hye Kim. Their work appears in journals such as Brain and Development, Korean Journal of Pediatrics, European Journal of Medical Genetics, PLoS ONE and American Journal of Medical Genetics Part B Neuropsychiatric Genetics.
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.