Gregory M. Cooper
HudsonAlpha Institute for Biotechnology
Affiliation HudsonAlpha Institute for Biotechnology Top Publications A general framework for estimating the relative pathogenicity of human genetic variants (2014) – 6,741 citations Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) – 5,327 citations CADD: predicting the deleteriousness of variants throughout the human genome (2018) ... <a title="Gregory M. Cooper" class="read-more" href="https://journalsworld.com/researchers/gregory-m-cooper/" aria-label="Read more about Gregory M. Cooper">Read more</a>
Read biography ↓Biography, research & contributions
Affiliation
HudsonAlpha Institute for Biotechnology
Top Publications
- A general framework for estimating the relative pathogenicity of human genetic variants (2014) - 6,741 citations
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) - 5,327 citations
- CADD: predicting the deleteriousness of variants throughout the human genome (2018) - 4,026 citations
- Genome sequence of the Brown Norway rat yields insights into mammalian evolution (2004) - 2,221 citations
- Identifying a High Fraction of the Human Genome to be under Selective Constraint Using GERP++ (2010) - 1,941 citations
At a glance
- Full name
- Gregory M. Cooper
- ORCID
- 0000-0001-5509-9923
- OpenAlex ID
- https://openalex.org/A5027561780
Research interests
- Genomics and Rare Diseases, Craniofacial Disorders and Treatments, Genetics and Neurodevelopmental Disorders, Genetic Associations and Epidemiology, Genomic variations and chromosomal abnormalities
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 2026-10-08. 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.
- 6,741OpenAlex citations
- 5,327OpenAlex citations
- CADD: predicting the deleteriousness of variants throughout the human genome ↗2018 · Nucleic Acids Research4,026OpenAlex citations
- 2,221OpenAlex citations
- Identifying a High Fraction of the Human Genome to be under Selective Constraint Using GERP++ ↗2010 · PLoS Computational Biology1,941OpenAlex citations
Recent linked publications
Publications matched across ORCID and OpenAlex. Citation counts are source-specific.
- CADD: predicting the deleteriousness of variants throughout the human genome ↗2018 · Nucleic Acids Research
- Identifying a High Fraction of the Human Genome to be under Selective Constraint Using GERP++ ↗2010 · PLoS Computational Biology
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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: 2026-10-08 · Last data update: 2026-10-08 00:10:26
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