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Nuclear import and export signals are essential for proper cellular trafficking and function of ZIC3

Human molecular genetics, 2007-01, Vol.16 (2), p.187-198

2007

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Approaches to Studying Outcomes in Patients With Congenital Heart Disease With Genetic Syndromes: What Down Syndrome Can Teach Us

Journal of the American Heart Association, 2024-01, Vol.13 (2), p.e033193-e033193

Ware, Stephanie M

2024

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Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association

Circulation (New York, N.Y.), 2018-11, Vol.138 (21), p.e653-e711

2018

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Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of America Practice Guideline

Journal of cardiac failure, 2018-05, Vol.24 (5), p.281-302

2018

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Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2018-09, Vol.20 (9), p.899-909

2018

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Pediatric Cardiomyopathies

Circulation research, 2017-09, Vol.121 (7), p.855-873

2017

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Genetics and genetic testing in congenital heart disease

Clinics in perinatology, 2015-06, Vol.42 (2), p.373

2015

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Disorders of left-right asymmetry: Heterotaxy and situs inversus

American journal of medical genetics. Part C, Seminars in medical genetics, 2009-11, Vol.151C (4), p.307-317

2009

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Single cell RNA analysis of the left-right organizer transcriptome reveals potential novel heterotaxy genes

Scientific reports, 2023-07, Vol.13 (1), p.10688-10688, Article 10688

2023

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Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning

Proceedings of the National Academy of Sciences - PNAS, 2011-02, Vol.108 (7), p.2915-2920

2011

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Congenital heart defects caused by FOXJ1

Human molecular genetics, 2023-07, Vol.32 (14), p.2335-2346

2023

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DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia

PLoS genetics, 2016-02, Vol.12 (2), p.e1005821-e1005821

2016

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High prevalence of eosinophilic esophagitis in patients with inherited connective tissue disorders

Journal of allergy and clinical immunology, 2013-08, Vol.132 (2), p.378-386

2013

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Genetic Testing in Pediatric Left Ventricular Noncompaction

Circulation. Cardiovascular genetics, 2017-12, Vol.10 (6)

2017

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Pediatric Cardiomyopathy: Importance of Genetic and Metabolic Evaluation

Journal of cardiac failure, 2012-05, Vol.18 (5), p.396-403

2012

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Genetic architecture of laterality defects revealed by whole exome sequencing

European journal of human genetics : EJHG, 2019-04, Vol.27 (4), p.563-573

2019

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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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Cardiac Disease in Patients With Mitochondrial Defects: 2 Steps Forward and 1 Step Back

Journal of the American College of Cardiology, 2022-10, Vol.80 (15), p.1444-1446

Ware, Stephanie M

2022

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Genetic testing and genetic counseling in patients with sudden death risk due to heritable arrhythmias

Heart rhythm, 2016-03, Vol.13 (3), p.789-797

2016

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Novel Timothy syndrome mutation leading to increase in CACNA1C window current

Heart rhythm, 2015-01, Vol.12 (1), p.211-219

2015

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Genetic and Developmental Basis of Cardiovascular Malformations

Clinics in perinatology, 2016-03, Vol.43 (1), p.39

2016

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Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association

Circulation. Genomic and precision medicine, 2021-10, Vol.14 (5), p.e000086-e000086

2021

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Molecular Characterization of Pediatric Restrictive Cardiomyopathy from Integrative Genomics

Scientific reports, 2017-01, Vol.7 (1), p.39276-39276, Article 39276

2017

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Heart Failure in Pediatric Patients With Congenital Heart Disease

Circulation research, 2017-03, Vol.120 (6), p.978-994

2017

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A multi-disciplinary, comprehensive approach to management of children with heterotaxy

Orphanet journal of rare diseases, 2022-09, Vol.17 (1), p.1-351, Article 351

2022

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Nuclear import and export signals are essential for proper cellular trafficking and function of ZIC3

Approaches to Studying Outcomes in Patients With Congenital Heart Disease With Genetic Syndromes: What Down Syndrome Can Teach Us

Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association

Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of America Practice Guideline

Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

Pediatric Cardiomyopathies

Genetics and genetic testing in congenital heart disease

Disorders of left-right asymmetry: Heterotaxy and situs inversus

Single cell RNA analysis of the left-right organizer transcriptome reveals potential novel heterotaxy genes

Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning

Congenital heart defects caused by FOXJ1

DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia

High prevalence of eosinophilic esophagitis in patients with inherited connective tissue disorders

Genetic Testing in Pediatric Left Ventricular Noncompaction

Pediatric Cardiomyopathy: Importance of Genetic and Metabolic Evaluation

Genetic architecture of laterality defects revealed by whole exome sequencing

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

Cardiac Disease in Patients With Mitochondrial Defects: 2 Steps Forward and 1 Step Back

Genetic testing and genetic counseling in patients with sudden death risk due to heritable arrhythmias

Novel Timothy syndrome mutation leading to increase in CACNA1C window current

Genetic and Developmental Basis of Cardiovascular Malformations

Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association

Molecular Characterization of Pediatric Restrictive Cardiomyopathy from Integrative Genomics

Heart Failure in Pediatric Patients With Congenital Heart Disease

A multi-disciplinary, comprehensive approach to management of children with heterotaxy

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