Erik P. Garrison
University of Tennessee Health Science Center
Affiliation University of Tennessee Health Science Center Top Publications A global reference for human genetic variation (2015) – 20,527 citations A map of human genome variation from population-scale sequencing (2010) – 8,192 citations Haplotype-based variant detection from short-read sequencing (2012) – 4,126 citations The repertoire of mutational signatures in human cancer (2020) – 3,865 citations ... <a title="Erik P. Garrison" class="read-more" href="https://journalsworld.com/researchers/erik-p-garrison/" aria-label="Read more about Erik P. Garrison">Read more</a>
Read biography ↓Biography, research & contributions
Affiliation
University of Tennessee Health Science Center
Top Publications
- A global reference for human genetic variation (2015) - 20,527 citations
- A map of human genome variation from population-scale sequencing (2010) - 8,192 citations
- Haplotype-based variant detection from short-read sequencing (2012) - 4,126 citations
- The repertoire of mutational signatures in human cancer (2020) - 3,865 citations
- The complete sequence of a human genome (2022) - 3,499 citations
At a glance
- Full name
- Erik P. Garrison
- ORCID
- 0000-0003-3821-631X
- OpenAlex ID
- https://openalex.org/A5008992371
Research interests
- Genomics and Phylogenetic Studies, Genomic variations and chromosomal abnormalities, Algorithms and Data Compression, Chromosomal and Genetic Variations, Cancer Genomics and Diagnostics
Research topics
Education
Not yet documented in this profile.
Selected research & further reading
A curated reading list, not a ranking by citation count. References use DOI metadata, matching public scholarly records or authoritative lecture sources.
See the source-linked reading and original works in the research guide above.
Citation & publication trends
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Source: OpenAlex · Retrieved 2026-10-07. Metrics are database-specific and are not a scientific ranking.
Most-cited linked publications
Publications matched across ORCID and OpenAlex. Citation counts are source-specific.
- A global reference for human genetic variation ↗2015 · Nature20,527OpenAlex citations
- 8,192OpenAlex citations
- Haplotype-based variant detection from short-read sequencing ↗2012 · arXiv (Cornell University)4,126OpenAlex citations
- 3,865OpenAlex citations
- The complete sequence of a human genome ↗2022 · Science3,499OpenAlex citations
Recent linked publications
Publications matched across ORCID and OpenAlex. Citation counts are source-specific.
- A global reference for human genetic variation ↗2015 · Nature
- Haplotype-based variant detection from short-read sequencing ↗2012 · arXiv (Cornell University)
- The complete sequence of a human genome ↗2022 · Science
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Institutions
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Awards & honors
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Career timeline
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Co-authors
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Education & career institution links
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Sign in to claim this profileSources & data information
Editorial review: 2026-10-07 · Last data update: 2026-10-07 21:37:58
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