Author

Lily Hoffman‐Andrews

University of PennsylvaniaORCID 0000-0001-8021-8306Unclaimed 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 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

ANJALI TIKU OWENSiD· 2 shared C. Anwar A. ChahaliD· 2 shared Elizabeth M. McNallyiD· 2 shared Jessica L. Chowns· 2 shared Ajit KoduriiD· 1 shared Ajith Nair· 1 shared Amber WaddelliD· 1 shared Ana MoralesiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

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2 papers

Recent·Most cited

Genetic & Genomic MedicineJournal of Cardiac FailurePeer-reviewedJan 1, 2026

Impact of Cardiomyopathy and Arrhythmia Genetic Testing on Clinical Management Decisions

Ana Morales, Yi-Lee Ting, Brianna A. Bucknor…·Elizabeth M. McNally

This study examines how genetic testing results for cardiomyopathy and arrhythmia influence clinical management decisions, finding that positive results lead to more management changes.

DOI 10.1016/j.cardfail.2025.11.066

humanstatistical model

𝕏 PostBluesky

Genetic & Genomic MedicineCirculation Genomic and Precision MedicinePeer-reviewedApr 21, 2025

Clinical Validity of Autosomal Dominant ALPK3 Loss-of-function Variants as a Cause of Hypertrophic Cardiomyopathy

Sophie Hespe, Emma S. Singer, Chloe M. Reuter…·Jodie Ingles

The paper evaluates the clinical validity of heterozygous ALPK3 loss-of-function variants as a cause of hypertrophic cardiomyopathy, finding strong gene-disease association with reduced penetrance.

3 citations

humanstatistical model

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