Author

Aneel A. Ashrani

Mayo ClinicORCID 0000-0002-6126-2528Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Allison E. Ashley‐KochiD· 2 shared Braxton D. MitchelliD· 2 shared Christine M. AlbertiD· 2 shared Donna K. ArnettiD· 2 shared Kathleen C. BarnesiD· 2 shared Scott T. WeissiD· 2 shared Susan S RedlineiD· 2 shared Abraham AviviD· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Allison E. Ashley‐KochORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintNov 19, 2023

Whole genome association testing in 333,100 individuals across three biobanks identifies rare non-coding single variant and genomic aggregate associations with height

Gareth Hawkes, Robin N. Beaumont, Zilin Li…·Michael N. Weedon

9 citations

humanwhole-genome sequencing

𝕏 PostBluesky

GeneticsProceedings of the National Academy of SciencesPeer-reviewedJan 21, 2020

De novo mutations across 1,465 diverse genomes reveal novel mutational insights and reductions in the Amish founder population.

Michael D. Kessler, Douglas P. Loesch, James A. Perry…·Mary Lou Biggs

The paper analyzes de novo mutations in 1,465 genomes to show similar mutation rates across ancestries but reduced rates in the Amish population, with environmental factors possibly influencing mutation rates.

92 citationstop 1%

humanwhole-genome sequencing

𝕏 PostBluesky