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Author Details

Erin M Miller
College of Medicine, University of Cincinnati
2006
38
16
PMIDPaper TitleJournal TitlePublished Year
37528675Preparedness and training of genetic counselors practicing in inpatient settings.J Genet Couns2024
37226762Left Ventricular Systolic Dysfunction in Patients Diagnosed With Hypertrophic Cardiomyopathy During Childhood: Insights From the SHaRe Registry.Circulation2023
35261109Retrospective comparison of parent-reported genetics knowledge, empowerment, and familial uptake of cardiac screening between parents who received genetic counseling by a certified genetic counselor and those who did not: A single US academic medical center study.J Genet Couns2022
35420547A clinical scoring system for early onset (neonatal) Marfan syndrome.Genet Med2022
36422086Outcomes of Returning Medically Actionable Genomic Results in Pediatric Research.J Pers Med2022
35026164The genetic architecture of pediatric cardiomyopathy.Am J Hum Genet2022
34255550Impact of Genetic Testing for Cardiomyopathy on Emotional Well-Being and Family Dynamics: A Study of Parents and Adolescents.Circ Genom Precis Med2021
33906374Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes Study.J Am Heart Assoc2021
33847800Rotational Position of the Aortic Root is Associated with Increased Aortic Dimensions in Marfan and Loeys-Dietz Syndrome.Pediatr Cardiol2021
34400210Uptake of Screening and Recurrence of Bicuspid Aortic Valve and Thoracic Aortic Aneurysm Among At-Risk Siblings of Pediatric Probands.J Pediatr2021
34712558A novel variant in <i>KCNQ1</i> associated with short QT syndrome.HeartRhythm Case Rep2021
34010605A human importin-β-related disorder: Syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8.Am J Hum Genet2021
31229680Genetic testing and cascade screening in pediatric long QT syndrome and hypertrophic cardiomyopathy.Heart Rhythm2020
31912959Investigation of de novo variation in pediatric cardiomyopathy.Am J Med Genet C Semin Med Genet2020
32717230A Comprehensive Clinical Genetics Approach to Critical Congenital Heart Disease in Infancy.J Pediatr2020
30556322Prevalence of Noonan spectrum disorders in a pediatric population with valvar pulmonary stenosis.Congenit Heart Dis2019
31126764A multi-institutional experience in the aortic and arterial pathology in individuals with genetically confirmed vascular Ehlers-Danlos syndrome.J Vasc Surg2019
30907979Left ventricular outflow tract obstruction: Uptake of familial cardiac screening and parental knowledge from a single tertiary care center.J Genet Couns2019
29362845Hypertrophic Cardiomyopathy Genotype Prediction Models in a Pediatric Population.Pediatr Cardiol2018
30260051Novel pathogenic variants in filamin C identified in pediatric restrictive cardiomyopathy.Hum Mutat2018
28912187Pediatric Cardiomyopathies.Circ Res2017
29212898Genetic Testing in Pediatric Left Ventricular Noncompaction.Circ Cardiovasc Genet2017
27112580Analysis of TGFBR1*6A variant in individuals evaluated for Marfan syndrome.Am J Med Genet A2016
25260352Novel Timothy syndrome mutation leading to increase in CACNA1C window current.Heart Rhythm2015
26018045Exon 3 deletion of ryanodine receptor causes left ventricular noncompaction, worsening catecholaminergic polymorphic ventricular tachycardia, and sudden cardiac arrest.Am J Med Genet A2015
25428557Aortopathy in the 7q11.23 microduplication syndrome.Am J Med Genet A2015
23782710Genetic testing practices in infants with congenital heart disease.Congenit Heart Dis2014
24788056Provision of cardiovascular genetic counseling services: current practice and future directions.J Genet Couns2014
24267465A pediatric approach to family history of cardiovascular disease: diagnosis, risk assessment, and management.Pediatr Clin North Am2014
23054336Uptake of cardiac screening and genetic testing among hypertrophic and dilated cardiomyopathy families.J Genet Couns2013
21842318Barriers to and motivations for physician referral of patients to cancer genetics clinics.J Genet Couns2012
22555271Pediatric cardiomyopathy: importance of genetic and metabolic evaluation.J Card Fail2012
22308078Implications for genotype-phenotype predictions in Townes-Brocks syndrome: case report of a novel SALL1 deletion and review of the literature.Am J Med Genet A2012
20473602Retrospective comparison of patient outcomes after in-person and telephone results disclosure counseling for BRCA1/2 genetic testing.Fam Cancer2010
19188198Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes.J Med Genet2009
19353585High resolution SNP based microarray mapping of mosaic supernumerary marker chromosomes 13 and 17: delineating novel loci for apraxia.Am J Med Genet A2009
18076673Pediatric restrictive cardiomyopathy associated with a mutation in beta-myosin heavy chain.Clin Genet2008
17128474Gene symbol: COL1A2. Disease: osteogenesis imperfecta type II.Hum Genet2006
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Collaborators

Lisa J Martin
Co-authored papers 5
Wendy K Chung
Boston Children's Hospital, Harvard Medical School
Co-authored papers 5
Jeffrey A Towbin
University of Tennessee Health Science Center
Co-authored papers 4
John L Jefferies
University of Tennessee Health Sciences Centre
Co-authored papers 4
Steven E Lipshultz
University at Buffalo Jacobs School of Medicine and Biomedical Sciences
Co-authored papers 3
Jeffrey A Schubert
Co-authored papers 3
Steven D Colan
Boston Children's Hospital, Harvard Medical School
Co-authored papers 3
Charles E Canter
University of Washington
Co-authored papers 2
Bruce J Aronow
Cincinnati Children's Hospital Medical Center
Co-authored papers 2
Melanie F Myers
Cincinnati Children's Hospital Medical Center
Co-authored papers 2
Euan A Ashley
Stanford University
Co-authored papers 1
E Clayton
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
Co-authored papers 1
Dana A Hill
Co-authored papers 1
Seema R Lalani
Co-authored papers 1
Cynthia A Prows
Cincinnati Children's Hospital Medical Center
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James S Ware
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Jeffrey B Anderson
University of Cincinnati College of Medicine
Co-authored papers 1
Karen Uzark
University of Michigan ann arbor
Co-authored papers 1
Victoria N Parikh
Stanford University
Co-authored papers 1
Richard F Ittenbach
Cincinnati Children's Hospital Medical Center, University of Cincinnati
Co-authored papers 1
Yufeng Shen
Columbia University
Co-authored papers 1
Julia Wynn
Vagelos College of Physicians and Surgeons, Columbia University
Co-authored papers 1
Alistair T Pagnamenta
NIHR Biomedical Research Centre, University of Oxford
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John B Harley
US Department of Veterans Affairs Medical Center
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Paul S Appelbaum
Center for Law, Columbia University Irving Medical Center
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Shaine A Morris
Baylor College of Medicine
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Michelle L McGowan
Biomedical Ethics Research Program, Mayo Clinic
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Georgia L Wiesner
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