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Transcriptomic Profiling Maps Anatomically Patterned Subpopulations among Single Embryonic Cardiac Cells

Developmental cell, 2016-11, Vol.39 (4), p.491-507

2016

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Maternal Obesity and Diabetes Mellitus as Risk Factors for Congenital Heart Disease in the Offspring

Journal of the American Heart Association, 2020-04, Vol.9 (8), p.e011541-e011541

2020

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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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Weakly supervised classification of aortic valve malformations using unlabeled cardiac MRI sequences

Nature communications, 2019-07, Vol.10 (1), p.3111-10, Article 3111

2019

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Single-Cell RNA-Seq of the Developing Cardiac Outflow Tract Reveals Convergent Development of the Vascular Smooth Muscle Cells

Cell reports (Cambridge), 2019-07, Vol.28 (5), p.1346-1361.e4

2019

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Exome-Based Case-Control Analysis Highlights the Pathogenic Role of Ciliary Genes in Transposition of the Great Arteries

Circulation research, 2020-03, Vol.126 (7), p.811-821

2020

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A phenome-wide association study of 26 mendelian genes reveals phenotypic expressivity of common and rare variants within the general population

PLoS genetics, 2020-11, Vol.16 (11), p.e1008802-e1008802

2020

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De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects

PLoS genetics, 2016-04, Vol.12 (4), p.e1005963-e1005963

2016

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Medical implications of technical accuracy in genome sequencing

Genome medicine, 2016-03, Vol.8 (1), p.24-24, Article 24

2016

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Targeting HDAC6 to treat heart failure with preserved ejection fraction in mice

Nature communications, 2024-02, Vol.15 (1), p.1352-1352, Article 1352

2024

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Leveraging Machine Learning for Translational Genetics of Cardiovascular Imaging

Journal of the American College of Cardiology, 2022-08, Vol.80 (5), p.498-499

Priest, James R.

2022

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Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing

Heart rhythm, 2014-10, Vol.11 (10), p.1707-1713

2014

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Birthweight, Type 2 Diabetes Mellitus, and Cardiovascular Disease: Addressing the Barker Hypothesis With Mendelian Randomization

Circulation. Genomic and precision medicine, 2018-06, Vol.11 (6), p.e002054-e002054

2018

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Adults With Mild-to-Moderate Congenital Heart Disease Demonstrate Measurable Neurocognitive Deficits

Journal of the American Heart Association, 2020-10, Vol.9 (19), p.e015379-e015379

2020

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Genomic Sequencing of Pleistocene Cave Bears

Science (American Association for the Advancement of Science), 2005-07, Vol.309 (5734), p.597-600

2005

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Maternal first trimester metabolic profile in pregnancies with transposition of the great arteries

Birth defects research, 2023-03, Vol.115 (5), p.517-524

2023

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A primer to clinical genome sequencing

Current opinion in pediatrics, 2017-10, Vol.29 (5), p.513-519

Priest, James R

2017

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Triiodothyronine supplementation and cytokines during cardiopulmonary bypass in infants and children

The Journal of thoracic and cardiovascular surgery, 2012-10, Vol.144 (4), p.938-943.e2

2012

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Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data

PLoS genetics, 2015-10, Vol.11 (10), p.e1005496-e1005496

2015

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AAV9:PKP2 improves heart function and survival in a Pkp2-deficient mouse model of arrhythmogenic right ventricular cardiomyopathy

Communications medicine, 2024-03, Vol.4 (1), p.38-38, Article 38

2024

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Polymorphisms in hypoxia inducible factor 1 and the initial clinical presentation of coronary disease

The American heart journal, 2007-12, Vol.154 (6), p.1035-1042

2007

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Relationships of the location and content of rounds to specialty, institution, patient-census, and team size

PloS one, 2010-06, Vol.5 (6), p.e11246-e11246

2010

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Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease

JCI insight, 2022-02, Vol.7 (3)

2022

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Single‐cell transcriptomic landscape of cardiac neural crest cell derivatives during development

EMBO reports, 2021-11, Vol.22 (11), p.e52389-n/a

2021

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Self-reported history of childhood smoking is associated with an increased risk for peripheral arterial disease independent of lifetime smoking burden

PloS one, 2014-02, Vol.9 (2), p.e88972-e88972

2014

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Transcriptomic Profiling Maps Anatomically Patterned Subpopulations among Single Embryonic Cardiac Cells

Maternal Obesity and Diabetes Mellitus as Risk Factors for Congenital Heart Disease in the Offspring

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

Weakly supervised classification of aortic valve malformations using unlabeled cardiac MRI sequences

Single-Cell RNA-Seq of the Developing Cardiac Outflow Tract Reveals Convergent Development of the Vascular Smooth Muscle Cells

Exome-Based Case-Control Analysis Highlights the Pathogenic Role of Ciliary Genes in Transposition of the Great Arteries

A phenome-wide association study of 26 mendelian genes reveals phenotypic expressivity of common and rare variants within the general population

De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects

Medical implications of technical accuracy in genome sequencing

Targeting HDAC6 to treat heart failure with preserved ejection fraction in mice

Leveraging Machine Learning for Translational Genetics of Cardiovascular Imaging

Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing

Birthweight, Type 2 Diabetes Mellitus, and Cardiovascular Disease: Addressing the Barker Hypothesis With Mendelian Randomization

Adults With Mild-to-Moderate Congenital Heart Disease Demonstrate Measurable Neurocognitive Deficits

Genomic Sequencing of Pleistocene Cave Bears

Maternal first trimester metabolic profile in pregnancies with transposition of the great arteries

A primer to clinical genome sequencing

Triiodothyronine supplementation and cytokines during cardiopulmonary bypass in infants and children

Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data

AAV9:PKP2 improves heart function and survival in a Pkp2-deficient mouse model of arrhythmogenic right ventricular cardiomyopathy

Polymorphisms in hypoxia inducible factor 1 and the initial clinical presentation of coronary disease

Relationships of the location and content of rounds to specialty, institution, patient-census, and team size

Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease

Single‐cell transcriptomic landscape of cardiac neural crest cell derivatives during development

Self-reported history of childhood smoking is associated with an increased risk for peripheral arterial disease independent of lifetime smoking burden

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