Author

Abdelrahman Said

Hospital for Sick ChildrenORCID 0000-0002-3960-6670Unclaimed 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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Research Focus:differential expression· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Assay:scRNA-seq· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Guoliang Meng· 2 shared A. Orioli· 1 shared Adam P GiessiD· 1 shared Afshan SiddiqiD· 1 shared Alex Stuckey· 1 shared Alexander SieghartiD· 1 shared Alona SosinskyiD· 1 shared Anastasia Miron· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Guoliang Meng

Mutual co-authors in cluster

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2 papers

Recent·Most cited

GeneticsCell Reports MedicinePeer-reviewedApr 19, 2024

Myosin inhibitor reverses hypertrophic cardiomyopathy in pediatric iPSC-cardiomyocytes to mirror variant correction

Caroline Kinnear, Abdelrahman Said, Guoliang Meng…·Seema R. Mital

This study shows that a myosin ATPase inhibitor reverses HCM phenotypes in pediatric iPSC-cardiomyocytes, with effects dependent on the underlying genetic variant.

20 citationstop 3%

humanscRNA-seq

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Genetic & Genomic Medicinenpj Genomic MedicinePeer-reviewedMar 14, 2022

Whole genome sequencing delineates regulatory and novel genic variants in childhood cardiomyopathy

Robert Lesurf, Abdelrahman Said, Oyediran Akinrinade…·R. Sultana

This study uses whole-genome sequencing to identify regulatory and novel genic variants contributing to childhood cardiomyopathy.

46 citationstop 2%

humanwhole-genome sequencing

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