Author

Amro Alsaid

Geisinger Health SystemORCID 0000-0002-6466-2615Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Amy Curry SturmiD· 1 shared Aris BarasiD· 1 shared Brandon K. FornwaltiD· 1 shared Brittney A. MurrayiD· 1 shared Christopher M. HaggertyiD· 1 shared Crystal TichnelliD· 1 shared Cynthia A. JamesiD· 1 shared Eric D. CarruthiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Amy Curry SturmORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineCirculation Genomic and Precision MedicinePeer-reviewedJun 14, 2022

Loss-of-Function FLNC Variants are Associated with Arrhythmogenic Cardiomyopathy Phenotypes when Identified through Exome Sequencing of a General Clinical Population

Eric D. Carruth, Maria Qureshi, Amro Alsaid…·Christopher M. Haggerty

The paper identifies FLNC loss-of-function variants in a clinical population and finds they are associated with increased odds of arrhythmogenic cardiomyopathy phenotypes.

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humanwhole-exome sequencing

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