Charles Lee
Impact in
- Genetics top 0.05%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Cancer Research top 0.1%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 102
- Genomic variations and chromosomal abnormalities 69
- Genomics and Rare Diseases 32
- Genetic Associations and Epidemiology 11
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- Genomics and Phylogenetic Studies 17
- CRISPR and Genetic Engineering 13
- Co-authors
- Stephen W. Scherer (11 shared papers)A. John Iafrate (3 shared papers)Lars Feuk (5 shared papers)Mark A. Rubin (6 shared papers)Patricia K. Donahoe (3 shared papers)Pasi A. Jänne (6 shared papers)Marc Listewnik (2 shared papers)Miguel N. Rivera (1 shared paper)
- Journals
- Proceedings of the National Academy of Sciences (10 papers)Nature Genetics (9 papers)Blood (6 papers)Chromosoma (5 papers)Genome Research (5 papers)
- Partner nations
- United StatesSouth KoreaUnited Kingdom
In The Last Decade
Charles Lee
262 papers receiving 26.7k citations
Charles Lee's Hit Papers
Peers
Comparison fields: 5 of 200
- Genetics 8.3k
- Cancer Research 3.9k
- Molecular Biology 13.0k
- Pulmonary and Respiratory Medicine 5.6k
- Oncology 4.5k
Countries citing papers authored by Charles Lee
This map shows the geographic impact of Charles 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 Charles Lee with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Charles Lee more than expected).
Fields of papers citing papers by Charles Lee
This network shows the impact of papers produced by Charles 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 Charles Lee. The network helps show where Charles Lee may publish in the future.
Co-authors
The 25 scholars most cited alongside Charles 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 274 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | MET Amplification Leads to Gefitinib Resistance in Lung Cancer by Activating ERBB3 Signaling Hit paper breakdown → | 2007 | 3694 |
| 2 | Recurrent Fusion of TMPRSS2 and ETS Transcription Factor Genes in Prostate Cancer Hit paper breakdown → | 2005 | 2976 |
| 3 | Detection of large-scale variation in the human genome Hit paper breakdown → | 2004 | 2215 |
| 4 | Relative Impact of Nucleotide and Copy Number Variation on Gene Expression Phenotypes Hit paper breakdown → | 2007 | 1327 |
| 5 | Integrative genomic analyses identify MITF as a lineage survival oncogene amplified in malignant melanoma Hit paper breakdown → | 2005 | 1157 |
| 6 | Diet and the evolution of human amylase gene copy number variation Hit paper breakdown → | 2007 | 1049 |
| 7 | EML4-ALK Fusion Gene and Efficacy of an ALK Kinase Inhibitor in Lung Cancer Hit paper breakdown → | 2008 | 825 |
| 8 | Copy number variation: New insights in genome diversity Hit paper breakdown → | 2006 | 636 |
| 9 | Landscape of Somatic Retrotransposition in Human Cancers Hit paper breakdown → | 2012 | 562 |
| 10 | Common deletion polymorphisms in the human genome Hit paper breakdown → | 2005 | 554 |
| 11 | BRAF Mutations Are Sufficient to Promote Nevi Formation and Cooperate with p53 in the Genesis of Melanoma Hit paper breakdown → | 2005 | 520 |
| 12 | Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs Hit paper breakdown → | 2008 | 519 |
| 13 | 2003 | 417 | |
| 14 | 2006 | 408 | |
| 15 | 2002 | 358 | |
| 16 | 2003 | 329 | |
| 17 | 2007 | 300 | |
| 18 | 2007 | 295 | |
| 19 | 2008 | 273 | |
| 20 | 2013 | 249 |
About Charles Lee
Charles Lee is a scholar working on Genetics, Molecular Biology, Plant Science, Pulmonary and Respiratory Medicine and Oncology, having authored 274 papers that have together received 27.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (69 papers), Chromosomal and Genetic Variations (49 papers), Genomics and Rare Diseases (32 papers), Prenatal Screening and Diagnostics (17 papers), Genomics and Phylogenetic Studies (17 papers), Cancer Genomics and Diagnostics (14 papers), CRISPR and Genetic Engineering (13 papers) and Genetic Associations and Epidemiology (11 papers). The work is most often cited by research in Genetics (8.3k citations), Cancer Research (3.9k citations), Molecular Biology (13.0k citations), Pulmonary and Respiratory Medicine (5.6k citations) and Oncology (4.5k citations). Charles Lee has collaborated with scholars based in United States, South Korea and United Kingdom. Frequent co-authors include Stephen W. Scherer, A. John Iafrate, Lars Feuk, Mark A. Rubin, Patricia K. Donahoe, Pasi A. Jänne, Marc Listewnik, Miguel N. Rivera, Ying Qi and Neal I. Lindeman. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics, Blood, Chromosoma and Genome Research.
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.