Author

Sara M. Fitzgerald‐Butt

Indiana University IndianapolisORCID 0000-0003-2316-2486Unclaimed 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 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Adam H. BuchananiD· 1 shared Aïda Masmoudi· 1 shared Amy Curry SturmiD· 1 shared Benjamin M. HelmiD· 1 shared Brittney A. MurrayiD· 1 shared Catherine Gordon· 1 shared Chloe M. ReuteriD· 1 shared Christina M. Rigelsky· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Adam H. BuchananORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineCirculation Genomic and Precision MedicinePeer-reviewedOct 1, 2026

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

Brittney A. Murray, Catherine Gordon, Susan Christian…·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.

2 citationstop 4%

humanelectronic health records

𝕏 PostBluesky

GeneticsPLoS GeneticsPeer-reviewedMay 26, 2020

Novel frameshift variant in MYL2 reveals molecular differences between dominant and recessive forms of hypertrophic cardiomyopathy

Sathiyanarayanan Manivannan, Sihem Darouich, Aïda Masmoudi…·Vidu Garg

The paper identifies a novel recessive frameshift variant in MYL2 causing severe infantile-onset HCM and shows molecular differences between recessive and dominant MYL2 variants.

26 citations

humanwhole-exome sequencing

𝕏 PostBluesky