Prof. Antonis C. Antoniou: h-index, Total Citations, and Citation Map
Prof. Antonis C. Antoniou's h-index is 109 (292 i10-index, 58,995+ total citations across 5+ publications) according to Google Scholar as of May 2026. Prof. Antonis C. Antoniou is affiliated with Professor of Cancer Risk Prediction, University of Cambridge.
Prof. Antonis C. Antoniou is a researcher affiliated with Professor of Cancer Risk Prediction, University of Cambridge, specializing in genetic epidemiology, cancer genetics, cancer epidemiology. Their work has been cited 58,995 times. This profile visualizes their global influence, highlighting strong citation networks in United States.
Prof. Antonis C. Antoniou's Citation Metrics
Bibliometric impact based on 5 indexed publications.
- H-Index
- 109
- i10-Index
- 292
- Total Citations
- 58,995
- Citing Countries
- 30
As of May 2026.
Prof. Antonis C. Antoniou has an h-index of 109 and 58,995 total citations across 5 publications, with research cited by institutions in 30 countries.
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We've mapped 5,000 of 58,995 citations for Prof. Antonis C. Antoniou
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Top Cited Works
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Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies
20035,217
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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 foundational, large-scale risk estimates for BRCA1/2 mutations, later refining these metrics to guide clinical management of breast and ovarian cancer.
The researcher established a prospective evidence base for cancer risks in BRCA1/2 mutation carriers through the seminal EMBRACE study, providing critical data for clinical risk assessment.
The researcher identified 65 new breast cancer risk loci through association analysis, establishing a foundational genetic framework for understanding breast cancer susceptibility.
Citation trend (last 10 years)Click to expand
Citation Trend (Last 10 Years)
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