William Greenleaf: h-index, Total Citations, and Citation Map
William Greenleaf's h-index is 91 (177 i10-index, 52,642+ total citations across 5+ publications) according to Google Scholar as of May 2026. William Greenleaf is affiliated with Associate Professor of Genetics, Stanford University.
William Greenleaf is a researcher affiliated with Associate Professor of Genetics, Stanford University, specializing in chromatin structure, high-throughput biochemistry, single molecule biophysics. Their work has been cited 52,642 times. This profile visualizes their global influence, highlighting strong citation networks in United States.
William Greenleaf's Citation Metrics
Bibliometric impact based on 5 indexed publications.
- H-Index
- 91
- i10-Index
- 177
- Total Citations
- 52,642
- Citing Countries
- 24
As of May 2026.
William Greenleaf has an h-index of 91 and 52,642 total citations across 5 publications, with research cited by institutions in 24 countries.
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We've mapped 5,000 of 52,642 citations for William Greenleaf
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Top Cited Works
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Transposition of native chromatin for fast and sensitive epigenomic profiling of open chromatin, DNA-binding proteins and nucleosome position
20137,401
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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 established and refined ATAC-seq as a standard method for genome-wide chromatin accessibility analysis, significantly improving protocol robustness and broadening its applicability to frozen tissues.
The researcher developed a transposition-based method for fast, sensitive epigenomic profiling of open chromatin, DNA-binding proteins, and nucleosome positions, as detailed in a seminal 2013 Nature Methods paper.
The researcher established foundational principles of regulatory variation by applying single-cell chromatin accessibility analysis, a contribution recognized as seminal in the field.
Citation trend (last 10 years)Click to expand
Citation Trend (Last 10 Years)
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