Author

Megan E. Grove

Stanford Health CareORCID 0000-0002-7972-0005Unclaimed 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· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Euan Angus AshleyiD· 3 shared Jason D. MerkeriD· 2 shared Kevin S. SmithiD· 2 shared Laure FrésardiD· 2 shared Matthew Thomas WheeleriD· 2 shared Sowmi UtirameruriD· 2 shared Stephen B. MontgomeryiD· 2 shared Zachary ZappalaiD· 2 shared

Activity by Year

2017-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 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

3 shared papersGenomics

Euan Angus AshleyORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

GenomicsbioRxivPreprintOct 7, 2025

Spatial genomics of the cardiac sarcomere

Christian Cadisch, Victoria Nicole Parikh, Megan E. Grove…·Euan Angus Ashley

The paper integrates genomic and structural data to identify variant intolerance regions in cardiac sarcomere genes and links them to disease mechanisms in hypertrophic cardiomyopathy.

DOI 10.1101/2025.10.07.680947

humanDNA methylation

𝕏 PostBluesky

GenomicsbioRxivPreprintSep 4, 2018

Identification of rare-disease genes in diverse undiagnosed cases using whole blood transcriptome sequencing and large control cohorts

Laure Frésard, Craig Smail, Kevin S. Smith…·Stephen B. Montgomery

This study evaluates the use of whole blood transcriptome sequencing for diagnosing rare diseases, finding an 8.5% diagnostic rate across 56 undiagnosed cases.

10 citations

humanwhole-exome sequencing

𝕏 PostBluesky

GenomicsGenetics in MedicinePeer-reviewedJun 22, 2017

Long-read whole genome sequencing identifies causal structural variation in a Mendelian disease

Jason D. Merker, Aaron M. Wenger, Tam P. Sneddon…·Euan Angus Ashley

The paper uses long-read whole genome sequencing to identify a pathogenic structural variant in a patient with Carney complex, demonstrating the potential of LRS in diagnosing Mendelian diseases.

252 citationstop 1%

humanwhole-genome sequencing

𝕏 PostBluesky