Author

Megan A. Lewis

RTI InternationalORCID 0000-0002-1670-9298Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Ali G. GharaviiD· 1 shared Alicia BrandtiD· 1 shared Alicia Yiran ZhouiD· 1 shared Amy TayloriD· 1 shared Andreas A. Theodorou· 1 shared Andrew HaddadiD· 1 shared Anjene Musick· 1 shared Ann Katherine M. ForemaniD· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Ali G. GharaviORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

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

Eric Venner, Karynne Patterson, Divya Kalra, Marsha M. Wheeler, Yi–Ju Chen, Sara E. Kalla, Bo Yuan, Jason H. Karnes, Kimberly Walker, Joshua D. Smith, Sean R. McGee, Aparna Radhakrishnan, Andrew Haddad, Philip E. Empey, Qiaoyan Wang, , May Okihiro

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

Communications Biology · Feb 19, 2024Peer-reviewedGenetic & Genomic Medicine

Genomic sequencing for newborn screening: Results of the NC NEXUS project

Tamara S. Roman, Stephanie B. Crowley, Myra I. Roche, Ann Katherine M. Foreman, Julianne M. O’Daniel, Bryce A. Seifert, Kristy Lee, Alicia Brandt, Chelsea E. Gustafson, Daniela M. DeCristo, Natasha T. Strande, Lori A. Ramkissoon, Laura V. Milko, Phillips Owen, Sayanty Roy, , Jonathan S. Berg

The paper evaluates exome sequencing in newborn screening, finding high diagnostic yield for metabolic disorders but limited actionable results for hearing loss and identifying carrier status variants.

The American Journal of Human Genetics · Aug 26, 2020Peer-reviewedGenetic & Genomic Medicine