Peer Bork: h-index, Total Citations, and Citation Map
Peer Bork's h-index is 261 (691 i10-index, 459,100+ total citations across 5+ publications) according to Google Scholar as of May 2026. Peer Bork is affiliated with Interim Director General of EMBL.
Peer Bork is a researcher affiliated with Interim Director General of EMBL, specializing in biology, computational biology, systems biology. Their work has been cited 459,100 times. This profile visualizes their global influence, highlighting strong citation networks in United States.
Peer Bork's Citation Metrics
Bibliometric impact based on 5 indexed publications.
- H-Index
- 261
- i10-Index
- 691
- Total Citations
- 459,100
- Citing Countries
- 21
As of May 2026.
Peer Bork has an h-index of 261 and 459,100 total citations across 5 publications, with research cited by institutions in 21 countries.
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We've mapped 5,000 of 459,100 citations for Peer Bork
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Global Impact Map
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Top Cited Works
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Initial sequencing and analysis of the human genome
200126,535
Top Citing Countries
Top Citing Institutions
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.
8 citing papers could not be classified (no author data) — excluded from the percentages above.
The researcher contributed to the foundational sequencing and analysis of the human genome, a seminal work that established critical reference standards for genomic science.
The researcher developed a foundational computational method and server for predicting damaging missense mutations, establishing a widely adopted standard in genomic variant analysis.
The researcher published a seminal 2010 paper that has garnered over 15,000 citations, establishing a foundational contribution widely adopted by independent scholars across the field.
Citation trend (last 10 years)Click to expand
Citation Trend (Last 10 Years)
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