Stephanie M. Ware
Biochemistry, Genetics and Molecular Biology · Indiana University
Publications
255
Citations
8,597
Est. group size
~3
Recurring co-author estimate
Active years
25
Publishing since 2002
Stephanie M. Ware studies the genetics of heart conditions that are present from birth or early childhood, including congenital heart defects, pediatric cardiomyopathy (diseases of the heart muscle), and heterotaxy (abnormal arrangement of internal organs). Her work links specific gene variants to disease severity and outcomes, and develops guidelines for when and how to perform genetic testing in infants, including those in intensive care. She also uses laboratory and computational tools to understand how particular gene changes affect biological function.
Publication activity has been relatively steady over the past five years (about 12-13 papers per year), after a higher output earlier in the decade.
Generated by claude-opus-4-8 from public bibliographic data · Jul 11, 2026
- Variant burden and severity of cardiomyopathy in patients with DMD-related Duchenne muscular dystrophy
Pediatric Research · 2026
- Taxonomic synthesis of the eastern North American millipede genus Pseudopolydesmus (Diplopoda: Polydesmida: Polydesmidae), utilizing high-detail ultraviolet fluorescence imaging
The Catalogue of Life · 2026
- First record of the genus Touranella Attems, 1937 (Diplopoda, Polydesmida, Paradoxosomatidae) from Laos, with a description of a new species
The Catalogue of Life · 2026
- First record of the genus Touranella Attems, 1937 (Diplopoda, Polydesmida, Paradoxosomatidae) from Laos, with a description of a new species
The Catalogue of Life · 2026
- MAVIS: Multimer-Aware Variant Impact Scoring
Zenodo (CERN European Organization for Nuclear Research) · 2026
- MAVIS: Multimer-Aware Variant Impact Scoring
Zenodo (CERN European Organization for Nuclear Research) · 2026
- Body Region Dysmorphology Is Predictive of Genetic Diagnoses in Infants With Congenital Heart Disease
Molecular Genetics & Genomic Medicine · 2026
- Genomics of pediatric cardiomyopathy
Pediatric Research · 2025
- Zic3 enables bimodal regulation of tyrosine hydroxylase expression in olfactory bulb and midbrain-derived neurons
Cell Death Discovery · 2025
- A CRISPR mis-insertion in the <i>Zic3</i> 5′UTR inhibits <i>in vivo</i> translation and is predicted to result in formation of an mRNA stem-loop hairpin
Biology Open · 2025
- Report of Facing Heterotaxy Together 2024: A Virtual, Multidisciplinary Scientific Conference
World Journal for Pediatric and Congenital Heart Surgery · 2025
- Abstract 4346181: The Impact of Genotype on Phenotypic Severity and Survival in Pediatric Dilated Cardiomyopathy: a report from the Pediatric Cardiomyopathy Registry
Circulation · 2025
- Abstract 4346346: Biomarkers in Patients with Newly Diagnosed Dilated Cardiomyopathy: A Study from the Pediatric Cardiomyopathy Registry
Circulation · 2025
- Gpr101 expression during early stages of murine development
Gene Expression Patterns · 2025
- Cardiomyopathy-Associated Pathogenic Variants in Pediatric Myocarditis: A Study From the Pediatric Cardiomyopathy Registry
Circulation Heart Failure · 2025
- Circulation×15
- PMC×11
- Genetics in Medicine×6
- Journal of the American Heart Association×6
- Journal of Genetic Counseling×6
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 11, 2026.
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