Stephanie M Ware
15PUBLICATIONS
53CO-AUTHORS
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Publications (15)
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|Apr 10, 2026
Rapid Genome Sequencing Shows Diagnostic Utility in Infants With Congenital Heart Defects.Matthew D Durbin, Lindsey R Helvaty, Alyx Posorske
|Dec 05, 2025
Cardiomyopathy-Associated Pathogenic Variants in Pediatric Myocarditis: A Study From the Pediatric Cardiomyopathy Registry.Alicia M Kamsheh, Stephanie M Ware, Surbhi Bhatnagar
|Jun 24, 2025
Evaluating first-line genetic testing strategies for inpatients with congenital heart defects.Al Lindstrom, Amy Breman, Sara Fitzgerald-Butt
|Mar 28, 2025
Dysmorphology-Based Prediction Model for Genetic Disorders in Infants With Congenital Heart Disease.Benjamin M Helm, Leah Wetherill, Benjamin J Landis
|Mar 13, 2025
Identification of Long Noncoding RNA Candidate Disease Genes Associated With Clinically Reported Copy Number Variants in Congenital Heart Disease.Jacqueline S Penaloza, Blythe Moreland, Jeffrey B Gaither
|Feb 06, 2025
A CRISPR mis-insertion in the Zic3 5'UTR inhibits in vivo translation and is predicted to result in formation of an mRNA stem-loop hairpin.Helen M Bellchambers, Maria B Padua, Stephanie M Ware
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Frequent Collaborators
5 joint publications
Benjamin J Landis
4 joint publications
Benjamin M Helm
3 joint publications
Lindsey R Helvaty
2 joint publications
Katherine G Spoonamore
2 joint publications
Steven D Colan
2 joint publications
Manyan Huang
2 joint publications
Paul F Kantor
2 joint publications
Sara M Fitzgerald-Butt
2 joint publications
Maria B Padua
2 joint publications
Helen M Bellchambers
