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Coilin phosphomutants disrupt Cajal body formation, reduce cell proliferation and produce a distinct coilin degradation product.
Ostertagia
Co-Principal Investigator
Mutations in LAMA1 cause cerebellar dysplasia and cysts with and without retinal dystrophy.
An automated electronic health-record derived frailty index is associated with adverse events after endoscopy.
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Soliman, Elsayed
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Soliman, Elsayed
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Academic Article
Impact of ancestry and common genetic variants on QT interval in African Americans.
Academic Article
Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: a genome-wide association study of 13,372 participants.
Concept
Genetic Variation
Academic Article
Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.
Academic Article
A common SCN5A variant is associated with PR interval and atrial fibrillation among African Americans.
Academic Article
Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval.
Academic Article
Multiple SCN5A variant enhancers modulate its cardiac gene expression and the QT interval.
Academic Article
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.
Academic Article
Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis.
Search Criteria
Genetic Variation