Author

Micaela Eisenberg

University of LeicesterORCID 0000-0002-4051-3674Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:electronic health records· 1 Organism:human· 1 Research Focus:software / tool· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Edward J. HolloxiD· 2 shared Katherine A. FawcettiD· 2 shared Nick R. G. ShrineiD· 2 shared Richard J. PackeriD· 2 shared Ahmed EdrisiD· 1 shared Alex Williams· 1 shared Anna L. GuyattiD· 1 shared Balasubramanya Seetharama Rao· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Edward J. HolloxORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJun 4, 2026

Phenome-wide association of multiallelic copy number variation in 422,170 UK Biobank individuals reveals novel genetic loci associated with disease

Micaela Eisenberg, Richard J. Packer, Nick R. G. Shrine…·Katherine A. Fawcett

This paper identifies novel associations between multiallelic copy number variations and disease traits using UK Biobank data, highlighting potential causal variants and mechanisms.

1 citation

humanwhole-exome sequencing

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Genetic & Genomic MedicineBioinformaticsPeer-reviewedFeb 4, 2023

DeepPheWAS: an R package for phenotype generation and association analysis for phenome-wide association studies.

Richard J. Packer, Alex Williams, William Hennah…·Martin D. Tobin

DeepPheWAS creates composite phenotypes and performs association analysis for phenome-wide studies using genetic inputs and various models.

24 citations

electronic health recordsstatistical model

𝕏 PostBluesky