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High Res

Erin M. Miller, MS, CGC

Genetic Counselor, Cardiology Clinic

Academic Affiliations

Assistant Professor, N/A

University of Cincinnati

Phone 513-636-4729

Fax 513-636-7297

Email erin.miller@cchmc.org

Clinical Interests
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Cardiovascular genetic counseling; inherited arrhythmias; sudden cardiac arrest/sudden cardiac death; cardiomyopathy; aortopathy; Marfan syndrome; familial hypercholesterolemia
Biography
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Erin Miller is a licensed genetic counselor in the Heart Institute at Cincinnati Children’s Hospital Medical Center. Her clinical activities are focused in the arena of cardiovascular genetics with specific interests in pediatric cardiomyopathy, arrhythmia and aortopathy. Research interests include the impact of clinical genetic testing and cardiac screening recommendations on family members, genotype-phenotype correlations, and the integration of cardiovascular genetic counseling and evaluation into clinical cardiology care. She is currently serving as the lead genetic counselor for the NIH/NHLBI funded study lead by Dr. Steven Lipshultz, ‘Genotype-phenotype correlations in pediatric cardiomyopathy’. Erin also has an interest in training and education and serves as a clinical supervisor and research advisory committee chair for the University of Cincinnati Genetic Counseling Graduate Program. She is a member of the National Society of Genetic Counselors and Cardiovascular Special Interest Group.
Education and Training
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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.

Publications
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View PubMed Publications

Campbell M, Czosek RJ, Hinton RB, Miller EM. Exon 3 Deletion of Ryanodine Receptor Causes Left Ventricular Noncompaction, Worsening Catecholaminergic Polymorphic Ventricular Tachycardia, and Sudden Cardiac Arrest. American Journal of Medical Genetics. 2015;167A:2197-2200.

Boczek NJ, Miller EM, Ye D, Nesterenko V, Tester DJ, Antzelevitch C, Czosek RJ, Ware SM, Ackerman MJ. Novel Timothy Syndrome Mutation Leading to Increase in CACNA1C Window Current. Heart Rhythm. 2015;12:211-219.

Parrott A, James J, Goldenberg P, Hinton RB, Miller EM, Shikany A, Aylsworth AS, Kaiser-Rogers K, Ferns SJ, Lalani SR, Ware SM. Aortopathy in the 7q11.23 microduplication syndrome. American Journal of Medical Genetics. 2015;167(2):363-70.

Somers AE, Ware SM, Collins K, Jefferies JL, He H, Miller EM. Provision of cardiovascular genetic counseling services: current practice and future directions. J Genet Counsel. 2014;23(6):976-83.

Connor J, Hinton RB, Miller EM, Sund K, Ruschman JG, Ware SM. Chromosomal imbalances identified by microarray in infants with congenital heart defects. Congenit. Heart Dis. 2014;9(2):158-67.

Miller EM, Ware SM. Genetic Counseling for Hypertrophic and Dilated Cardiomyopathy: Uptake of genetic testing and cardiac screening among family members. J Genet Couns. 2013;22:258-267.

Kindel SJ, Miller EM, Gupta M, Cripe LH, Hinton RB, Spicer RL, Towbin JA, Ware SM. Pediatric cardiomyopathy: importance of genetic and metabolic evaluation. J Card Fail. 2012 May;18(5):396-403.

Czosek RJ, Miller EM, Goldenberg P, Towbin JA, Ware SM. Cardiac Electrical System Involvement in Alstrom Syndrome: Uncommon Causes of Dilated Cardiomyopathies. Cardiogenetics. 2012;2:(e2)1-10.

Miller E, Hopkin R, Bao L, Ware SM. Implications for genotype-phenotype predictions in Townes Brocks Syndrome: a case report of a novel SALL1 deletion and a review of the literature. Am J Med Genet A. 2012 Mar;158A(3):533-40.

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