Author

Oyediran Akinrinade

St. George's UniversityORCID 0000-0002-6797-6353Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:whole-genome sequencing· 3 Research Focus:differential expression· 2 Research Focus:variant calling· 2 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Adam P GiessiD· 2 shared Afshan SiddiqiD· 2 shared Alexander SieghartiD· 2 shared Alona SosinskyiD· 2 shared Anna C. NeediD· 2 shared Athanasios KousathanasiD· 2 shared Christine PatchiD· 2 shared Christopher R. BoustrediD· 2 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Adam P GiessORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineJournal of Cardiovascular Translational ResearchPeer-reviewedJul 21, 2023

Age and Sex Differences in the Genetics of Cardiomyopathy

Oyediran Akinrinade, Robert Lesurf, John C. Ambrose…·Seema R. Mital

This study identifies genetic differences between pediatric and adult cardiomyopathy, finding more constrained variants in childhood cases and female patients.

32 citationstop 3%

humanwhole-genome sequencing

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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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GenomicsBMC Medical GenomicsPeer-reviewedJan 29, 2020

Quality of Whole Genome Sequencing from Blood versus Saliva Derived DNA in Cardiac Patients

Roderick Yao, Oyediran Akinrinade, Marie Chaix, Seema R. Mital

The paper compares the quality of whole-genome sequencing from blood and saliva samples in cardiac patients, finding saliva is a viable alternative for detecting sequence variants.

44 citations

humanwhole-genome sequencing

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