LabCompass

Publications

255

Citations

8,597

Est. group size

~3

Recurring co-author estimate

Active years

25

Publishing since 2002

Research summary
AI-generated

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.

Congenital heart defects geneticsPediatric cardiomyopathyHeterotaxy and organ lateralityClinical genetic testing in newbornsGene variant interpretation

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

Publication cadence
Publications per year over the last 10 years — averaging 12.6/year recently
2017: 26 publications26172018: 16 publications182019: 13 publications192020: 9 publications202021: 12 publications212022: 12 publications222023: 13 publications232024: 14 publications242025: 16 publications252026: 8 publications26
Recent publications
Publishes in
  • 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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