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.
Novel pathogenic variants in filamin C identified in pediatric restrictive cardiomyopathy.
Schubert, J; Tariq, M; Geddes, G; Kindel, S; Miller, EM; Ware, SM.
Human Mutation.
2018;
39:2083-2096.
Hypertrophic Cardiomyopathy Genotype Prediction Models in a Pediatric Population.
Newman, R; Jefferies, JL; Chin, C; He, H; Shikany, A; Miller, EM; Parrott, A.
Pediatric Cardiology.
2018;
39:709-717.
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.
Pediatric Cardiomyopathies.
Lee, TM; Hsu, DT; Kantor, P; Towbin, JA; Ware, SM; Colan, SD; Chung, WK; Jefferies, JL; Rossano, JW; Castleberry, CD; et al.
Circulation Research.
2017;
121:855-873.
Analysis of TGFBR1*6A Variant in Individuals Evaluated for Marfan Syndrome.
Somers, AE; Hinton, RB; Pilipenko, V; Miller, E; Ware, SM.
American Journal of Medical Genetics, Part A.
2016;
170:1786-1790.
Left Ventricular Noncompaction in Noonan Syndrome.
Hinton, RB; Goldenberg, P.
Journal of Genetic Disorders and Genetic Reports.
2016;
05:1-1.
Exon 3 Deletion of Ryanodine Receptor Causes Left Ventricular Noncompaction, Worsening Catecholaminergic Polymorphic Ventricular Tachycardia, and Sudden Cardiac Arrest.
Campbell, MJ; Czosek, RJ; Hinton, RB; Miller, EM.
American Journal of Medical Genetics, Part A.
2015;
167A:2197-2200.
Aortopathy in the 7q11.23 Microduplication Syndrome.
Parrott, A; James, J; Goldenberg, P; Hinton, RB; Miller, E; Shikany, A; Aylsworth, AS; Kaiser-Rogers, K; Ferns, SJ; Lalani, SR; et al.
American Journal of Medical Genetics, Part A.
2015;
167A:363-370.