Author

Gregory M. Cooper

University of PittsburghPrimary ORCID profile (0000-0001-5509-9923 · 24 papers)Unclaimed ORCID profile · follow to get notified of new preprints

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Same name, identified by ORCID

Gregory M. CooperiD24 papers · HudsonAlpha Institute for Biotechnology

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Assay:ChIP-seq· 1 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Andrew A. HardiganiD· 1 shared Anju Shukla· 1 shared Ashwin Dalal· 1 shared Ayman W. El-Hattab· 1 shared Benjamin Cogné· 1 shared Bertrand Isidor· 1 shared Edward J. Lose· 1 shared Fanny Kortüm· 1 shared

Activity by Year

2016-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetics

Andrew A. HardiganORCID

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2 papers

Recent·Most cited

Retrospective analysis of The Two Sister Study using haplotype-based association testing to identify loci associated with early-onset breast cancer

James R. Gilbert, James Cray, Joseph E. Losee, Gregory M. Cooper

The paper uses haplotype-based association testing in The Two Sister Study to identify genetic loci associated with early-onset breast cancer and validates findings using TCGA data.

medRxiv · Dec 4, 2020 · PreprintGenetic & Genomic Medicine

Mutations in EBF3 disturb transcriptional profiles and underlie a novel syndrome of intellectual disability, ataxia and facial dysmorphism

Frederike Leonie Harms, Katta Mohan Girisha, Andrew A. Hardigan, Fanny Kortüm, Anju Shukla, Malik Alawi, Ashwin Dalal, Lauren Brady, Mark Tarnopolsky, Lynne M. Bird, Sophia Ceulemans, Martina Bebin, Kevin M. Bowling, Susan M. Hiatt, Edward J. Lose, , Kerstin Kutsche

The paper identifies EBF3 mutations in individuals with intellectual disability, ataxia, and facial dysmorphism, showing they impair transcriptional regulation and neuronal development.

bioRxiv · Aug 3, 2016 · PreprintGenetics