Ethan O. Perlstein: h-index, Total Citations, and Citation Map
Ethan O. Perlstein's h-index is 20 (28 i10-index, 2,886+ total citations across 5+ publications) according to Google Scholar as of May 2026. Ethan O. Perlstein is affiliated with Perlara PBC.
Ethan O. Perlstein is a researcher affiliated with Perlara PBC, specializing in Rare diseases. Their work has been cited 2,886 times. This profile visualizes their global influence, highlighting strong citation networks in United States.
Ethan O. Perlstein's Citation Metrics
Bibliometric impact based on 5 indexed publications.
- H-Index
- 20
- i10-Index
- 28
- Total Citations
- 2,886
- Citing Countries
- 18
As of May 2026.
Ethan O. Perlstein has an h-index of 20 and 2,886 total citations across 5 publications, with research cited by institutions in 18 countries.
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Global Impact Map
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Top Cited Works
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Small molecules enhance autophagy and reduce toxicity in Huntington's disease models
2007737
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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 identified small molecules that enhance autophagy and reduce toxicity in Huntington's disease models, establishing a foundational therapeutic strategy widely adopted by independent scientists.
The researcher established a foundational framework for understanding global nucleosome occupancy in yeast, a seminal contribution that has been widely adopted by the independent scientific community.
The researcher developed a stereoselective three-component coupling method to synthesize spirooxindole libraries, establishing a foundational protocol for accessing these complex heterocyclic scaffolds with high stereocontrol.
Citation trend (last 10 years)Click to expand
Citation Trend (Last 10 Years)
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