StephanieMWareMD
Medical Genetics • Indianapolis, INClinical Genetics
Professor, Departments of Pediatrics and Medical and Molecular Genetics, Indiana University School of Medicine; Vice Chair of Clinical Affairs, Medical and Molecular Genetics; Director of Cardiovascular Genetics
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Office
705 Riley Hospital Dr
Indianapolis, IN 46202Phone+1 317-944-3966Fax+1 317-278-0936
Education & Training
Baylor College of MedicineResidency, Medical Genetics and Genomics, 2000 - 2002- Baylor College of Medicine (Houston)Residency, Pediatrics, 1997 - 2000
University of Cincinnati College of MedicineClass of 1997
Certifications & Licensure
IN State Medical License 2014 - 2025
OH State Medical License 2004 - 2017
TX State Medical License 2002 - 2005- American Board of Pediatrics Pediatrics
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Clinical Trials
- Molecular Genetics of Heterotaxy and Related Congenital Heart Defects Start of enrollment: 2009 Jul 01
Roles: Principal Investigator, Contact
- Pediatric Cardiomyopathy Mutation Analysis Start of enrollment: 2014 Apr 01
Roles: Contact, Principal Investigator
- Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases Network Start of enrollment: 2015 Sep 16
Roles: Contact
Publications & Presentations
PubMed
- 97 citationsGenetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, Daniel P Judge, Paul F Kantor
Genetics in Medicine. 2018-09-01 - 33 citationsPediatric restrictive cardiomyopathy associated with a mutation in β-myosin heavy chainStephanie M. Ware, M. E. Quinn, E. T. Ballard, Erin M. Miller, Karen Uzark
Clinical Genetics. 2007-12-12 - 66 citationsInfantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genesStephanie M. Ware, Nahed O. ElHassan, Stephen G. Kahler, Q. Zhang, Y. W. Ma
Journal of Medical Genetics. 2009-05-01
Journal Articles
- Nonreentrant Atrial Tachycardia Occurs Independently of Hypertrophic Cardiomyopathy in RASopathy PatientsKaren W Gripp, Rosemarie Smith, Stephanie M Ware, Paula Goldenberg, Kathryn C Chatfield, Mark D Levin, Richard J Czosek, Elaine H Zackai, Angela E Lin, Tara L Wenger, ..., American Journal of Medical Genetics Part A
- Genetic Evaluation of Cardiomyopathy: A Clinical Practice Resource of the American College of Medical Genetics and Genomics (ACMG)Kim L McBride, Stephanie M Ware, Ray E Hershberger, Michael M Givertz, Nature
Press Mentions
Study Maps Genetic Causes of Pediatric CardiomyopathyMarch 28th, 2022- Teens Knowing Results of Their Cardiomyopathy Genetic Tests May Improve Family FunctionJuly 13th, 2021
- Campus Lights Highlight Rare Diseases on Leap DayMarch 5th, 2024
Grant Support
- Role Of The Embryonic Node In Cardiac Development And Congenital Heart DiseaseNational Heart, Lung, And Blood Institute2010–2011
- Role Of The Embryonic Node In Cardiac Development And Congenital Heart DiseaseNational Heart, Lung, And Blood Institute2007–2009
- ZIC3 And The Control Of Body Pattern FormationNational Heart, Lung, And Blood Institute2004–2005
- ZIC3 And The Control Of Body Pattern FormationNational Heart, Lung, And Blood Institute2001–2003
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