Author

Jessica L. Chowns

University of Pennsylvania

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2

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 Lily Hoffman‐AndrewsiD· 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

Impact of Cardiomyopathy and Arrhythmia Genetic Testing on Clinical Management Decisions

Ana Morales, Yi-Lee Ting, Brianna A. Bucknor, Mohamad A. Alkhayat, Naomi Barker, Megan N. Betts, C. Anwar A. Chahal, Jessica L. Chowns, Rebecca Eberly, Emily Higgs, Lily Hoffman‐Andrews, Emily A. Huth, Daniel Philip Judge, Ajit Koduri, Ajith Nair, , 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.

Journal of Cardiac Failure · Jan 1, 2026Peer-reviewedGenetic & Genomic Medicine

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

Sophie Hespe, Emma S. Singer, Chloe M. Reuter, Brittney A. Murray, Elizabeth Jordan, Jessica L. Chowns, Stacey A. Peters, Megan Mayers, Belinda R. Gray, Ray E. Hershberger, ANJALI TIKU OWENS, Christopher Semsarian, Amber Waddell, Babken Asatryan, Emma Owens, , 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.

Circulation Genomic and Precision Medicine · Apr 21, 2025Peer-reviewedGenetic & Genomic Medicine