Author

JoEllen Weaver

University of PennsylvaniaORCID 0000-0002-0596-0188Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Approach:Bayesian inference· 1 Research Focus:benchmarking· 1 Research Focus:gene regulatory network inference· 1 Assay:GWAS summary statistics· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Anurag VermaiD· 2 shared Daniel James RaderiD· 2 shared Marylyn DeRiggi RitchieiD· 2 shared Renae JudyiD· 2 shared Scott M. DamraueriD· 2 shared Theodore G. DrivasiD· 2 shared Yuki Bradford· 2 shared Afiya Poindexter· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 43 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

2 shared papersGenetic & Genomic Medicine

Anurag VermaORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Genetic & Genomic MedicineJAMAPeer-reviewedNov 16, 2024

Population Performance and Individual Agreement of Coronary Artery Disease Polygenic Risk Scores

Sarah A. Abramowitz, Kristin M. Boulier, Karl Keat…·Theodore G. Drivas

This study evaluates the reliability of coronary artery disease polygenic risk scores across diverse populations, finding poor individual agreement despite equivalent population-level performance.

67 citationstop 1%

humanGWAS summary statistics

𝕏 PostBluesky

GenomicsNature MedicinePeer-reviewedJan 1, 2021

Exome-by-phenome-wide rare variant gene burden association with electronic health record phenotypes

Joseph Park, Anastasia Lucas, Xinyuan Zhang…·Daniel James Rader

This study identifies robust gene-phenotype associations by analyzing rare loss-of-function variants in exome-wide data linked to electronic health records.

58 citationstop 2%

humanwhole-exome sequencing

𝕏 PostBluesky