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Genetic Counselor, Cardiology Clinic
Associate Professor, University of Cincinnati
erin.miller@cchmc.org
513-636-4729
513-636-7297
Understanding why certain health conditions develop has always been an interest of mine. I was drawn to genetics because our DNA is often a significant part of our personal health risks. Genetic information can seem very complicated and be overwhelming to patients and families. I want to make genetic and medical information accessible so that patients and families can make the best healthcare decisions.
Genetic counseling is for anyone interested in personalized information about their genetic health. As a genetic counselor at the Heart Institute, I’m very interested in understanding what patients and families need. For example, what are their motivations for seeking care and how can I provide them with the information and support that’s most important to them? The Heart Institute Genetic Counseling Clinic is a resource for individuals of all ages.
I gather detailed information about medical and family history and may talk with patients about questions such as:
In my research, I’m interested in gathering evidence to guide genetic counseling, genetic testing and cardiac screening. This information includes a better understanding of specific disease risks, such as:
My colleagues and I are looking at how patients and families understand and feel about these risks. I'm also interested in learning about how families communicate regarding health information and how genetic counseling affects patient and family outcomes.
During my free time, I enjoy running, yoga and hiking. I'm interested in architecture and interior design, and my husband and I renovate homes in the Cincinnati area. The most fun I have by far is watching our four children grow!
Cardiovascular genetic counseling; inherited arrhythmias; sudden cardiac arrest/sudden cardiac death; cardiomyopathy; aortopathy; Marfan syndrome; familial hypercholesterolemia
Genetics, Cardiovascular Genetics, Cardiomyopathy
By Erin M. Miller, MS, LGC11/27/2019
By Erin M. Miller, MS, LGC11/26/2019
BS: Psychology, The University of Arizona, Tucson, AZ, 2003.
MSc: Medical Genetics, Indiana Univeristy, Indianapolis, IN, 2005.
Board Certification: American Board of Genetic Counseling, 2007.
Investigation of de novo variation in pediatric cardiomyopathy. Parrott, A; Khoury, PR; Shikany, AR; Lorts, A; Villa, CR; Miller, EM. American Journal of Medical Genetics, Part C: Seminars in Medical Genetics. 2020; 184:116-123.
Left ventricular outflow tract obstruction: Uptake of familial cardiac screening and parental knowledge from a single tertiary care center. Shikany, AR; Parrott, A; James, J; Madueme, P; Weaver, KN; Cassidy, C; Khoury, PR; Miller, EM. Journal of Genetic Counseling. 2019; 28:779-789.
Prevalence of Noonan spectrum disorders in a pediatric population with valvar pulmonary stenosis. Anderson, K; Cnota, J; James, J; Miller, EM; Parrott, A; Pilipenko, V; Weaver, KN; Shikany, A. Congenital Heart Disease. 2019; 14:264-273.
Genetic Testing in Pediatric Left Ventricular Noncompaction. Miller, EM; Hinton, RB; Czosek, R; Lorts, A; Parrott, A; Shikany, AR; Ittenbach, RF; Ware, SM. Circulation: Cardiovascular Genetics. 2017; 10.
Uptake of cardiac screening and genetic testing among hypertrophic and dilated cardiomyopathy families. Miller, EM; Wang, Y; Ware, SM. Journal of Genetic Counseling. 2013; 22:258-267.
Pediatric cardiomyopathy: importance of genetic and metabolic evaluation. Kindel, SJ; Miller, EM; Gupta, R; Cripe, LH; Hinton, RB; Spicer, RL; Towbin, JA; Ware, SM. Journal of Cardiac Failure. 2012; 18:396-403.
A human importin-β-related disorder: Syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8. Van Gucht, I; Meester, JA N; Bento, JR; Bastiaansen, M; Bastianen, J; Luyckx, I; Van Den Heuvel, L; Neutel, CH G; Guns, PJ; Vermont, M; et al. American Journal of Human Genetics. 2021; 108:1115-1125.
Rotational Position of the Aortic Root is Associated with Increased Aortic Dimensions in Marfan and Loeys-Dietz Syndrome. Powell, SK; Almeneisi, H; Alsaied, T; Shikany, A; Riley, L; Miller, E; Belonis, A; Weaver, KN; Brown, N; Mori, S; et al. Pediatric Cardiology. 2021; 42:1157-1161.
Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes Study. Ware, SM; Wilkinson, JD; Tariq, M; Schubert, JA; Sridhar, A; Colan, SD; Shi, L; Canter, CE; Hsu, DT; Webber, SA; et al. Journal of the American Heart Association. 2021; 10.
A Comprehensive Clinical Genetics Approach to Critical Congenital Heart Disease in Infancy. Shikany, AR; Landis, BJ; Parrott, A; Miller, EM; Coyan, A; Walters, L; Hinton, RB; Goldenberg, P; Ware, SM. Journal of Pediatrics. 2020; 227:231-238.e14.