Author

Julia Platt

Stanford Health CareORCID 0000-0002-2486-9902Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:benchmarking· 1 Assay:electronic health records· 1 Approach:experimental assay· 1 Approach:statistical model· 1

Frequent Co-Authors

Colleen A. CaleshuiD· 2 shared Adam H. BuchananiD· 1 shared Amy Curry SturmiD· 1 shared Archana Natarajan RajaiD· 1 shared Benjamin M. HelmiD· 1 shared Brittney A. MurrayiD· 1 shared Catherine Gordon· 1 shared Cédric EspeneliD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Colleen A. CaleshuORCID

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2 papers

Recent·Most cited

Cardiovascular genetic counseling is associated with improved patient-reported outcomes across clinical indications and settings

Brittney A. Murray, Catherine Gordon, Susan Christian, Tara Dzwiniel, Crystal Tichnell, Emily E. Brown, Gretchen L. MacCarrick, Rebecca McClellan, Chloe M. Reuter, Hannah E. Ison, Jennefer N. Carter, Tia Moscarello, Ryan Murtha, Mitchel J. Pariani, Julia Platt, , Cynthia A. James

This study shows cardiovascular genetic counseling improves patient empowerment and reduces worry, with benefits varying by patient characteristics and the strength of the counselor-patient relationship.

Circulation Genomic and Precision Medicine · Oct 1, 2026Peer-reviewedGenetic & Genomic Medicine

Mono- and bi-allelic protein truncating variants in alpha-actinin 2 cause cardiomyopathy through distinct mechanisms

Maléne E. Lindholm, David Jimenez‐Morales, Han Zhu, Kinya Seo, David Amar, Chunli Zhao, Archana Natarajan Raja, Roshni Madhvani, Sarah Abramowitz, Cédric Espenel, Shirley C. Sutton, Colleen A. Caleshu, Gerald J. Berry, Kara S. Motonaga, Kyla E. Dunn, , Matthew Thomas Wheeler

The paper investigates how mono- and bi-allelic ACTN2 mutations cause cardiomyopathy through distinct mechanisms using patient-derived iPSC-cardiomyocytes and CRISPR-Cas9 editing.

Circulation Genomic and Precision Medicine · Nov 22, 2021Peer-reviewedGenetics