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A Novel Echocardiography Feature-Tracking Algorithm for Stabilized Frame-to-Frame Extraction of Aortic Root Diameters in the Parasternal Long Axis

Journal of the American Society of Echocardiography, 2024-09

2024

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

The Journal of pediatrics, 2020-12, Vol.227, p.231-238.e14

2020

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Early ascertainment of genetic diagnoses clarifies impact on medium-term survival following neonatal congenital heart surgery

The Journal of clinical investigation, 2024-09, Vol.134 (18), p.1-2

2024

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Genetic Testing Guidelines Impact Care in Newborns with Congenital Heart Defects

The Journal of pediatrics, 2023-09, Vol.260, p.113495-113495, Article 113495

2023

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Genotype–phenotype correlations in Marfan syndrome

Heart (British Cardiac Society), 2017-11, Vol.103 (22), p.1750-1752

2017

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Regenerative Effects of Transplanted Mesenchymal Stem Cells in Fracture Healing

Stem cells (Dayton, Ohio), 2009-08, Vol.27 (8), p.1887-1898

2009

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Activation of the Hedgehog signaling pathway leads to fibrosis in aortic valves

Cell & bioscience, 2023-03, Vol.13 (1), p.43-43, Article 43

2023

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Genetic Evaluation of Inpatient Neonatal and Infantile Congenital Heart Defects: New Findings and Review of the Literature

Genes, 2021-08, Vol.12 (8), p.1244

2021

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Serial Magnetic Resonance Imaging for Aortic Dilation in Tetralogy of Fallot With Pulmonary Stenosis

The American journal of cardiology, 2023-03, Vol.191, p.92-100

2023

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Disruption of FBN1 by an Alu element insertion: A novel genetic cause of Marfan syndrome

European journal of medical genetics, 2023-07, Vol.66 (7), p.104775-104775, Article 104775

2023

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Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart Disease

Journal of the American Heart Association, 2022-10, Vol.11 (19), p.e026369-e026369

2022

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Bicuspid Aortic Valve: a Review with Recommendations for Genetic Counseling

Journal of Genetic Counseling, 2016-12, Vol.25 (6), p.1171-1178

2016

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Prenatal Diagnosis of Congenital Heart Disease and Birth Outcomes

Pediatric cardiology, 2013-03, Vol.34 (3), p.597-605

2013

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Insertion of microneedles into skin: measurement and prediction of insertion force and needle fracture force

Journal of biomechanics, 2004-08, Vol.37 (8), p.1155-1163

2004

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A Novel Human Biospecimen Repository for Clinical and Molecular Investigation of Thoracic Aortopathy

Cardiogenetics, 2021-09, Vol.11 (3), p.148-163

2021

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The Journey to Becoming an Adult Learner: From Dependent to Self-Directed Learning

Journal of the American College of Cardiology, 2014-11, Vol.64 (19), p.2066-2068

2014

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Characterization of the Rate of Aortic Dilation in Young Patients with Thoracic Aortic Aneurysm

Pediatric cardiology, 2021-01, Vol.42 (1), p.148-157

2021

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A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease

Journal of the American Heart Association, 2023-09, Vol.12 (18), p.e029340-e029340

2023

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CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes

Cardiology in the young, 2016-01, Vol.26 (1), p.30-52

2016

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Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return

European journal of human genetics : EJHG, 2023-12, Vol.31 (12), p.1430-1439

2023

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Clinical Stratification of Pediatric Patients with Idiopathic Thoracic Aortic Aneurysm

The Journal of pediatrics, 2015-07, Vol.167 (1), p.131-137.e5

2015

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The Journey to Becoming an Adult Learner

Journal of the American College of Cardiology, 2014-11, Vol.64 (19), p.2066-2068

2014

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Clinically relevant variants identified in thoracic aortic aneurysm patients by research exome sequencing

American journal of medical genetics. Part A, 2016-05, Vol.170A (5), p.1288-1294

2016

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Twins with progressive thoracic aortic aneurysm, recurrent dissection and ACTA2 mutation

Pediatrics (Evanston), 2014-10, Vol.134 (4), p.e1218-e1223

2014

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The Current Landscape of Genetic Testing in Cardiovascular Malformations: Opportunities and Challenges

Frontiers in cardiovascular medicine, 2016-07, Vol.3, p.22-22

2016

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A Novel Echocardiography Feature-Tracking Algorithm for Stabilized Frame-to-Frame Extraction of Aortic Root Diameters in the Parasternal Long Axis

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

Early ascertainment of genetic diagnoses clarifies impact on medium-term survival following neonatal congenital heart surgery

Genetic Testing Guidelines Impact Care in Newborns with Congenital Heart Defects

Genotype–phenotype correlations in Marfan syndrome

Regenerative Effects of Transplanted Mesenchymal Stem Cells in Fracture Healing

Activation of the Hedgehog signaling pathway leads to fibrosis in aortic valves

Genetic Evaluation of Inpatient Neonatal and Infantile Congenital Heart Defects: New Findings and Review of the Literature

Serial Magnetic Resonance Imaging for Aortic Dilation in Tetralogy of Fallot With Pulmonary Stenosis

Disruption of FBN1 by an Alu element insertion: A novel genetic cause of Marfan syndrome

Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart Disease

Bicuspid Aortic Valve: a Review with Recommendations for Genetic Counseling

Prenatal Diagnosis of Congenital Heart Disease and Birth Outcomes

Insertion of microneedles into skin: measurement and prediction of insertion force and needle fracture force

A Novel Human Biospecimen Repository for Clinical and Molecular Investigation of Thoracic Aortopathy

The Journey to Becoming an Adult Learner: From Dependent to Self-Directed Learning

Characterization of the Rate of Aortic Dilation in Young Patients with Thoracic Aortic Aneurysm

A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease

CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes

Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return

Clinical Stratification of Pediatric Patients with Idiopathic Thoracic Aortic Aneurysm

The Journey to Becoming an Adult Learner

Clinically relevant variants identified in thoracic aortic aneurysm patients by research exome sequencing

Twins with progressive thoracic aortic aneurysm, recurrent dissection and ACTA2 mutation

The Current Landscape of Genetic Testing in Cardiovascular Malformations: Opportunities and Challenges

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