Charles Lee, PhD, DSc, FACMG, FRSC: h-index, Total Citations, and Citation Map
Charles Lee, PhD, DSc, FACMG, FRSC's h-index is 103 (205 i10-index, 116,527+ total citations across 3+ publications) according to Google Scholar as of May 2026. Charles Lee, PhD, DSc, FACMG, FRSC is affiliated with The Jackson Laboratory for Genomic Medicine.
Charles Lee, PhD, DSc, FACMG, FRSC is a researcher affiliated with The Jackson Laboratory for Genomic Medicine, specializing in Structural Genomic Variation, Cytogenetics, Genomic Medicine. Their work has been cited 116,527 times. This profile visualizes their global influence, highlighting strong citation networks in United States.
Charles Lee, PhD, DSc, FACMG, FRSC's Citation Metrics
Bibliometric impact based on 3 indexed publications.
- H-Index
- 103
- i10-Index
- 205
- Total Citations
- 116,527
- Citing Countries
- 13
As of May 2026.
Charles Lee, PhD, DSc, FACMG, FRSC has an h-index of 103 and 116,527 total citations across 3 publications, with research cited by institutions in 13 countries.
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We've mapped 5,000 of 116,527 citations for Charles Lee, PhD, DSc, FACMG, FRSC
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Global Impact Map
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Top Cited Works
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A global reference for human genetic variation
201519,394
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Visa Evidence Package
Views and exports tuned for EB-1A, O-1A, and EB-2 NIW petitions. Sustained acclaim, geographic reach, and independent-citation filtering are the strongest evidence categories immigration adjudicators look for.
Significant Contributions
Auto-detected research lines — a seminal paper and the follow-up work building on it. Review and edit before using in a petition. Each Free PDF opens in a new tab — EB-1A organises this into the structure USCIS applies to Criterion 5 of 8 CFR § 204.5(h)(3)(v); EB-1B re-frames it under § 204.5(i)(3) (outstanding researcher); NIW presents it under prong 2 of Matter of Dhanasar.
The researcher produced a seminal, highly cited study mapping human genome variation through population-scale sequencing, establishing a foundational resource for genetic research.
The researcher established a foundational global reference for human genetic variation, a seminal contribution that has become a standard resource in the field.
The researcher produced a seminal, highly cited integrated map of genetic variation from over 1,000 human genomes, establishing a foundational resource for understanding human genomic diversity.
Citation trend (last 10 years)Click to expand
Citation Trend (Last 10 Years)
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