Richard Durbin: h-index, Total Citations, and Citation Map
Richard Durbin's h-index is 165 (326 i10-index, 383,007+ total citations across 5+ publications) according to Google Scholar as of May 2026. Richard Durbin is affiliated with Dept of Genetics, University of Cambridge.
Richard Durbin is a researcher affiliated with Dept of Genetics, University of Cambridge, specializing in Genomics, Human genetics, Bioinformatics. Their work has been cited 383,007 times. This profile visualizes their global influence, highlighting strong citation networks in United States.
Richard Durbin's Citation Metrics
Bibliometric impact based on 5 indexed publications.
- H-Index
- 165
- i10-Index
- 326
- Total Citations
- 383,007
- Citing Countries
- 31
As of May 2026.
Richard Durbin has an h-index of 165 and 383,007 total citations across 5 publications, with research cited by institutions in 31 countries.
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We've mapped 5,000 of 383,007 citations for Richard Durbin
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Top Cited Works
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The Sequence Alignment/Map format and SAMtools
200968,257
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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.
5 citing papers could not be classified (no author data) — excluded from the percentages above.
The researcher developed the Sequence Alignment/Map format and SAMtools, establishing a foundational standard for processing high-throughput sequencing data.
The researcher co-authored the seminal 2001 Nature paper presenting the initial sequencing and analysis of the human genome, a foundational contribution to genomics.
The researcher developed a fast, accurate short-read alignment method using the Burrows–Wheeler transform, establishing a foundational algorithmic standard in bioinformatics.
Citation trend (last 10 years)Click to expand
Citation Trend (Last 10 Years)
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