Author

Olivia R. Kalash

Vanderbilt University Medical Center

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· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant effect prediction· 2 Assay:electronic health records· 1 Approach:experimental assay· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Andrew Michael GlazeriD· 2 shared Ayesha MuhammadiD· 2 shared Brett M. KronckeiD· 2 shared Dan M. RodeniD· 2 shared Yuko WadaiD· 2 shared Adam S. Gordon· 1 shared Alfred L. GeorgeiD· 1 shared Ashutosh SinghaliD· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Andrew Michael GlazerORCID

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2 papers

Recent·Most cited

Arrhythmia variant associations and reclassifications in the eMERGE-III sequencing study

Andrew Michael Glazer, Giovanni Davogustto, Christian M. Shaffer, Carlos G. Vanoye, Reshma R. Desai, Eric H. Farber‐Eger, Ozan Dikilitas, Ning Shang, Jennifer A. Pacheco, Tao Yang, Ayesha Muhammad, Jonathan D. Mosley, Sara L. Van Driest, Quinn Stanton Wells, Lauren Lee Shaffer, , Dan M. Roden

The paper identifies pathogenic variants in arrhythmia genes in eMERGE-III participants and reclassifies variants of uncertain significance using functional studies.

Circulation · Dec 21, 2021Peer-reviewedGenetic & Genomic Medicine

High-throughput reclassification of SCN5A variants

Andrew Michael Glazer, Yuko Wada, Bian Li, Ayesha Muhammad, Olivia R. Kalash, Matthew J. O’Neill, Tiffany Shields, Lynn D. Hall, Laura L Short, Marcia A. Blair, Brett M. Kroncke, John A. Capra, Dan M. Roden

This study reclassifies SCN5A variants using high-throughput patch clamping, finding most variants of uncertain significance are either benign or pathogenic.

The American Journal of Human Genetics · Jun 12, 2020Peer-reviewedGenetics