Author

Andrew Haddad

University of PittsburghORCID 0009-0003-4279-9367Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Assay:electronic health records· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Research Focus:phylogenetics / evolution· 1

Frequent Co-Authors

Anjene Musick· 2 shared Aparna RadhakrishnaniD· 2 shared Divya KalraiD· 2 shared Eric VenneriD· 2 shared Gail Pairitz JarvikiD· 2 shared Jason H. KarnesiD· 2 shared Karynne PattersoniD· 2 shared Kimberly WalkeriD· 2 shared

Activity by Year

2024-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Anjene Musick

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJun 12, 2024

Frequency of pharmacogenomic variation and medication exposures among All of Us Participants

Andrew Haddad, Aparna Radhakrishnan, Sean R. McGee…·Philip E. Empey

The paper assesses pharmacogenomic variation and medication exposures in a diverse cohort using whole genome sequencing and EHR data, finding high prevalence of actionable variants and previously unreported alleles.

13 citations

humanwhole-genome sequencing

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Genetic & Genomic MedicineCommunications BiologyPeer-reviewedFeb 19, 2024

The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

Eric Venner, Karynne Patterson, Divya Kalra…·May Okihiro

The paper analyzes pathogenic variant frequencies in the All of Us cohort by ancestry, revealing disparities and potential biases in genomic data.

61 citationstop 1%

humanwhole-genome sequencing

𝕏 PostBluesky