Author

Hunter R. Underhill

University of UtahORCID 0000-0002-7389-1487Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Research Focus:variant calling· 2 Research Focus:batch correction / integration· 1 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Aaron R. QuinlaniD· 1 shared Anne O’Donnell‐LuriaiD· 1 shared Ben WeisburdiD· 1 shared Beryl B. CummingsiD· 1 shared Brandon A. Zielinski· 1 shared Brent S. PederseniD· 1 shared Carrie BaileyiD· 1 shared Colleen M. CarlstoniD· 1 shared

Activity by Year

2017-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperBioinformatics

Aaron R. QuinlanORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

GeneticsPLoS ONEPeer-reviewedNov 17, 2025

The insidious degeneration of white matter and cognitive decline in Fabry disease

Jacob W. Johnson, Hediyeh Baradaran, Jubel Morgan…·Hunter R. Underhill

This study compares cognitive decline and white matter changes in Fabry disease patients to typical aging, finding microstructural damage in younger patients and progressive tissue damage with age.

3 citations

humanbulk RNA-seq

𝕏 PostBluesky

BioinformaticsGenome MedicinePeer-reviewedJul 14, 2020

Somalier: rapid relatedness estimation for cancer and germline studies using efficient genome sketches

Brent S. Pedersen, Preetida J. Bhetariya, Joe Brown…·Aaron R. Quinlan

Somalier estimates sample relatedness and detects swaps in cancer and germline studies using efficient genome sketches without requiring germline variant calls.

137 citations

humanwhole-genome sequencing

𝕏 PostBluesky

GeneticsHuman MutationPeer-reviewedFeb 23, 2017

Pathogenic ASXL1 somatic variants in reference databases complicate germline variant interpretation for Bohring-Opitz Syndrome

Colleen M. Carlston, Anne O’Donnell‐Luria, Hunter R. Underhill…·Rong Mao

56 citations

humanwhole-exome sequencing

𝕏 PostBluesky