E. Miller

发表

Cardiac electrical system involvement in Alström syndrome: uncommon causes of dilated cardiomyopathies

J. Towbin, S. Ware, R. Spicer, 2012 .

Left Ventricular Noncompaction in Noonan Syndrome

R. Hinton, S. Ware, Richard C Godby, 2016 .

Retrospective comparison of patient outcomes after in-person and telephone results disclosure counseling for BRCA1/2 genetic testing

Lisa J. Martin, E. Miller, Courtney Doughty Rice, 2010, Familial Cancer.

A Comprehensive Clinical Genetics Approach to Critical Congenital Heart Disease in Infancy.

R. Hinton, B. Landis, S. Ware, 2020, The Journal of pediatrics.

Left ventricular outflow tract obstruction: Uptake of familial cardiac screening and parental knowledge from a single tertiary care center

P. Khoury, E. Miller, Ashley Parrott, 2019, Journal of genetic counseling.

Aortopathy in the 7q11.23 microduplication syndrome

S. Lalani, R. Hinton, S. Ware, 2015, American journal of medical genetics. Part A.

Analysis of TGFBR1*6A variant in individuals evaluated for Marfan syndrome

R. Hinton, S. Ware, V. Pilipenko, 2016, American journal of medical genetics. Part A.

Provision of Cardiovascular Genetic Counseling Services: Current Practice and Future Directions

S. Ware, J. Jefferies, Kathleen Collins, 2014, Journal of Genetic Counseling.

A human importin-β-related disorder: Syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8.

Anthony R. Dallosso, J. Rosenfeld, A. Pagnamenta, 2021, American journal of human genetics.

Uptake of Cardiac Screening and Genetic Testing Among Hypertrophic and Dilated Cardiomyopathy Families

S. Ware, Yu Wang, E. Miller, 2013, Journal of Genetic Counseling.

A multi-institutional experience in vascular Ehlers-Danlos syndrome diagnosis.

P. Byers, D. Milewicz, D. Coleman, 2019, Journal of vascular surgery.

A multi-institutional experience in the aortic and arterial pathology in individuals with genetically confirmed vascular Ehlers-Danlos syndrome.

P. Byers, D. Milewicz, D. Coleman, 2019, Journal of vascular surgery.

Genetic testing practices in infants with congenital heart disease.

R. Hinton, K. Sund, S. Ware, 2014, Congenital heart disease.

Exon 3 deletion of ryanodine receptor causes left ventricular noncompaction, worsening catecholaminergic polymorphic ventricular tachycardia, and sudden cardiac arrest

R. Hinton, M. Campbell, R. Czosek, 2015, American journal of medical genetics. Part A.

Pediatric cardiomyopathy: importance of genetic and metabolic evaluation.

J. Towbin, R. Hinton, S. Ware, 2012, Journal of cardiac failure.

Implications for genotype–phenotype predictions in Townes–Brocks syndrome: Case report of a novel SALL1 deletion and review of the literature

S. Ware, R. Hopkin, E. Miller, 2012, American journal of medical genetics. Part A.

Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes

W. Craigen, S. Ware, R. Spicer, 2009, Journal of Medical Genetics.

High resolution SNP based microarray mapping of mosaic supernumerary marker chromosomes 13 and 17: Delineating novel loci for apraxia

S. Ware, E. Miller, J. Kogan, 2009, American journal of medical genetics. Part A.

Novel Timothy syndrome mutation leading to increase in CACNA1C window current.

Michael J Ackerman, Charles Antzelevitch, C. Antzelevitch, 2015, Heart rhythm.

Outcomes of Returning Medically Actionable Genomic Results in Pediatric Research

John J. Connolly, H. Hakonarson, E. Clayton, 2022, Journal of personalized medicine.

Investigation of de novo variation in pediatric cardiomyopathy

A. Lorts, C. Villa, P. Khoury, 2020, American journal of medical genetics. Part C, Seminars in medical genetics.

Prevalence of Noonan spectrum disorders in a pediatric population with valvar pulmonary stenosis

J. Cnota, V. Pilipenko, K. Weaver, 2018, Congenital heart disease.

The genetic architecture of pediatric cardiomyopathy.

S. Colan, Yufeng Shen, B. Aronow, 2022, American journal of human genetics.

Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes Study

Lisa J. Martin, W. Chung, S. Colan, 2021, Journal of the American Heart Association.

Genetic Testing in Pediatric Left Ventricular Noncompaction

R. Hinton, S. Ware, R. Ittenbach, 2017, Circulation. Cardiovascular genetics.

A pediatric approach to family history of cardiovascular disease: diagnosis, risk assessment, and management.

R. Hinton, E. Miller, 2014, Pediatric clinics of North America.

A clinical scoring system for early onset (neonatal) Marfan syndrome.

S. Morris, K. Yutzey, A. J. Kim, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Novel pathogenic variants in filamin C identified in pediatric restrictive cardiomyopathy

S. Ware, G. Geddes, M. Tariq, 2018, Human mutation.

Pediatric Cardiomyopathies.

W. Chung, S. Colan, J. Towbin, 2017, Circulation research.

A novel variant in KCNQ1 associated with short QT syndrome

T. Knilans, R. Czosek, E. Miller, 2021, HeartRhythm case reports.

Genetic Testing and Cascade Screening in Pediatric Long QT Syndrome and Hypertrophic Cardiomyopathy.

S. Ware, S. Etheridge, C. Travers, 2019, Heart rhythm.

Barriers to and Motivations for Physician Referral of Patients to Cancer Genetics Clinics

Lisa J. Martin, E. Miller, Sara C. Knapke, 2012, Journal of Genetic Counseling.

Impact of Genetic Testing for Cardiomyopathy on Emotional Well-Being and Family Dynamics

W. Chung, P. Appelbaum, J. Wynn, 2021, Circulation. Genomic and precision medicine.

Hypertrophic Cardiomyopathy Genotype Prediction Models in a Pediatric Population

Clifford Chin, J. Jefferies, E. Miller, 2018, Pediatric Cardiology.

Retrospective 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

V. Pilipenko, Justin T. Tretter, K. Weaver, 2022, Journal of genetic counseling.

Pediatric restrictive cardiomyopathy associated with a mutation in β‐myosin heavy chain

K. Uzark, M. Quinn, E. Miller, 2007, Clinical genetics.

Rotational Position of the Aortic Root is Associated with Increased Aortic Dimensions in Marfan and Loeys–Dietz Syndrome

T. Alsaied, Justin T. Tretter, Nicole M Brown, 2021, Pediatric Cardiology.

Left Ventricular Systolic Dysfunction in Patients Diagnosed With Hypertrophic Cardiomyopathy During Childhood: Insights From the SHaRe Registry

E. Ashley, J. Ware, I. Olivotto, 2023, Circulation.

Uptake of Screening and Recurrence of Bicuspid Aortic Valve and Thoracic Aortic Aneurysm Among At-Risk Siblings of Pediatric Probands.

Lisa J. Martin, J. Cnota, Justin T. Tretter, 2021, The Journal of pediatrics.