Erin M Miller

Summary

Affiliation: Cincinnati Children's Hospital Medical Center
Country: USA

Publications

  1. doi request reprint A pediatric approach to family history of cardiovascular disease: diagnosis, risk assessment, and management
    Erin M Miller
    Division of Cardiology, The Heart Institute, Cincinnati Children s Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA Electronic address
    Pediatr Clin North Am 61:187-205. 2014
  2. doi request reprint Uptake of cardiac screening and genetic testing among hypertrophic and dilated cardiomyopathy families
    Erin M Miller
    The Heart Institute, Cincinnati Children s Hospital Medical Center, 3333 Burnet Avenue, MLC 7020, Cincinnati, OH 45229 3039, USA
    J Genet Couns 22:258-67. 2013
  3. doi request reprint Genetic testing practices in infants with congenital heart disease
    Jessica A Connor
    Division of Human Genetics, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio, USA
    Congenit Heart Dis 9:158-67. 2014
  4. pmc Pediatric cardiomyopathy: importance of genetic and metabolic evaluation
    Steven J Kindel
    Department of Pediatrics, Heart Institute, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio 45229, USA
    J Card Fail 18:396-403. 2012
  5. doi request reprint Exon 3 deletion of ryanodine receptor causes left ventricular noncompaction, worsening catecholaminergic polymorphic ventricular tachycardia, and sudden cardiac arrest
    Matthew J Campbell
    Department of Pediatrics, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio
    Am J Med Genet A 167:2197-200. 2015
  6. doi request reprint Provision of cardiovascular genetic counseling services: current practice and future directions
    Allyson E Somers
    University of Cincinnati, Cincinnati, OH, USA
    J Genet Couns 23:976-83. 2014

Collaborators

  • Robert B Hinton
  • Richard J Czosek
  • Yu Wang
  • Stephanie M Ware
  • Matthew J Campbell
  • Allyson E Somers
  • Jessica A Connor
  • Steven J Kindel
  • Kathleen Collins
  • John L Jefferies
  • Hua He
  • Kristen L Sund
  • Jennifer G Ruschman
  • Linda H Cripe
  • Jeffrey A Towbin
  • Resmi Gupta
  • Robert L Spicer

Detail Information

Publications6

  1. doi request reprint A pediatric approach to family history of cardiovascular disease: diagnosis, risk assessment, and management
    Erin M Miller
    Division of Cardiology, The Heart Institute, Cincinnati Children s Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA Electronic address
    Pediatr Clin North Am 61:187-205. 2014
    ..Improved understanding of the causes of pediatric cardiovascular disease promises the opportunity to develop new diagnostic and therapeutic strategies. ..
  2. doi request reprint Uptake of cardiac screening and genetic testing among hypertrophic and dilated cardiomyopathy families
    Erin M Miller
    The Heart Institute, Cincinnati Children s Hospital Medical Center, 3333 Burnet Avenue, MLC 7020, Cincinnati, OH 45229 3039, USA
    J Genet Couns 22:258-67. 2013
    ..The approach to cardiac screening and genetic testing should be family-specific and requires expertise in the genetics of cardiomyopathy...
  3. doi request reprint Genetic testing practices in infants with congenital heart disease
    Jessica A Connor
    Division of Human Genetics, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio, USA
    Congenit Heart Dis 9:158-67. 2014
    ..We hypothesized that chromosome microarray analysis (CMA) would identify genetic abnormalities underlying both syndromic and isolated CHD...
  4. pmc Pediatric cardiomyopathy: importance of genetic and metabolic evaluation
    Steven J Kindel
    Department of Pediatrics, Heart Institute, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio 45229, USA
    J Card Fail 18:396-403. 2012
    ..A research-based pediatric cardiomyopathy registry identified familial, syndromic, or metabolic causes in 30% of children. However, these results predated clinical genetic testing...
  5. doi request reprint Exon 3 deletion of ryanodine receptor causes left ventricular noncompaction, worsening catecholaminergic polymorphic ventricular tachycardia, and sudden cardiac arrest
    Matthew J Campbell
    Department of Pediatrics, Cincinnati Children s Hospital Medical Center, Cincinnati, Ohio
    Am J Med Genet A 167:2197-200. 2015
    ..Deletion duplication testing should be considered in the context of CPVT and LVNC or SCA...
  6. doi request reprint Provision of cardiovascular genetic counseling services: current practice and future directions
    Allyson E Somers
    University of Cincinnati, Cincinnati, OH, USA
    J Genet Couns 23:976-83. 2014
    ..These data suggest a growing interest in cardiovascular genetic counseling and need for additional training resources among the NSGC membership...