Author

Kelsey Mayo

Vanderbilt University Medical CenterORCID 0000-0002-2382-1376Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 2 Organism:human· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Approach:benchmark study· 1 Research Focus:benchmarking· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Henry Robert Condon· 2 shared Alexander G. BickiD· 1 shared Andrea H. RamireziD· 1 shared Anjene Musick· 1 shared Anthony PhilippakisiD· 1 shared Chris LuntiD· 1 shared Dan M. RodeniD· 1 shared David GlazeriD· 1 shared

Activity by Year

2022-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenetics

Henry Robert Condon

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2 papers

Recent·Most cited

Cloud gazing: demonstrating paths for unlocking the value of cloud genomics through cross-cohort analysis

Nicole A. Deflaux, Margaret Sunitha Selvaraj, Henry Robert Condon, Kelsey Mayo, Sara Haidermota, Melissa Basford, Chris Lunt, Anthony Philippakis, Dan M. Roden, Joshua C. Denny, Anjene Musick, Rory Collins, Naomi E. Allen, Mark Effingham, David Glazer, , Alexander G. Bick

This study compares meta-analysis and pooled analysis approaches in cross-cohort GWAS of lipid measures, finding method-specific variants and implications for TRE design and analysis.

bioRxiv · Nov 29, 2022 · PreprintGenetics

Common and Rare Variants Associated with Cardiometabolic Traits across 98,622 Whole-Genome Sequences in the All of Us Research Program

Xin Wang, Justine H. Ryu, Jihoon Kim, Andrea H. Ramirez, Kelsey Mayo, Henry Robert Condon, Nataraja Sarma Vaitinadin, Lucila Ohno-machado A, Greg A. Talavera, Patrick T. Ellinor, Steven A. Lubitz, Seung Hoan Choi

The paper analyzes whole-genome sequences from 98,622 participants to identify common and rare variants associated with cardiometabolic traits, replicating known associations and finding new loci.

medRxiv · Nov 23, 2022 · PreprintGenetic & Genomic Medicine