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Type I interferon activation and endothelial dysfunction in caveolin-1 insufficiency-associated pulmonary arterial hypertension

Proceedings of the National Academy of Sciences - PNAS, 2021-03, Vol.118 (11), p.1

2021

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Sex-based differences in veterans with pulmonary hypertension: Results from the veterans affairs-clinical assessment reporting and tracking database

PloS one, 2017-11, Vol.12 (11), p.e0187734-e0187734

2017

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Pulmonary hypertension: NHLBI Workshop on the Primary Prevention of Chronic Lung Diseases

Annals of the American Thoracic Society, 2014-04, Vol.11 Suppl 3 (Supplement 3), p.S178-S185

2014

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Abnormal trafficking of endogenously expressed BMPR2 mutant allelic products in patients with heritable pulmonary arterial hypertension

PloS one, 2013-11, Vol.8 (11), p.e80319-e80319

2013

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Translational Advances in the Field of Pulmonary Hypertension Molecular Medicine of Pulmonary Arterial Hypertension. From Population Genetics to Precision Medicine and Gene Editing

American journal of respiratory and critical care medicine, 2017-01, Vol.195 (1), p.23-31

2017

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The genetics of pulmonary arterial hypertension in the post-BMPR2 era

Pulmonary Circulation, 2011-07, Vol.1 (3), p.305-319

2011

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FHIT , a Novel Modifier Gene in Pulmonary Arterial Hypertension

American journal of respiratory and critical care medicine, 2019-01, Vol.199 (1), p.83-98

2019

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Aberrant Caveolin-1-Mediated Smad Signaling and Proliferation Identified by Analysis of Adenine 474 Deletion Mutation (c.474delA) in Patient Fibroblasts: A New Perspective in the Mechanism of Pulmonary Hypertension

Molecular biology of the cell, 2017-05, Vol.28 (9), p.1177-1185

2017

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Aberrant caveolin-1-mediated Smad signaling and proliferation identified by analysis of adenine 474 deletion mutation (c.474delA) in patient fibroblasts: a new perspective on the mechanism of pulmonary hypertension

Molecular biology of the cell, 2018-03, Vol.28 (9), p.1177

2018

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Valsalva Maneuver in Pulmonary Arterial Hypertension

Chest, 2016-05, Vol.149 (5), p.1252-1260

2016

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Synergistic heterozygosity for TGFβ1 SNPs and BMPR2 mutations modulates the age at diagnosis and penetrance of familial pulmonary arterial hypertension

Genetics in medicine, 2008-05, Vol.10 (5), p.359-365

2008

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Valsalva Maneuver in Pulmonary Arterial Hypertension: Hemodynamic Changes and Excessive Systemic Vasodilation

Autonomic neuroscience, 2015-11, Vol.192, p.105-106

2015

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HERITABLE PULMONARY ARTERIAL HYPERTENSION IS ASSOCIATED WITH WORSE PULMONARY CAPACITANCE AND RIGHT VENTRICULAR STROKE WORK INDEX COMPARED TO IDIOPATHIC PULMONARY ARTERIAL HYPERTENSION

Journal of the American College of Cardiology, 2012-03, Vol.59 (13), p.E1600-E1600

2012

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Genetic Testing in Pulmonary Arterial Hypertension Evaluation

Chest, 2024-05, Vol.165 (5), p.1224-1227

2024

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Exploring the Association of Male Sex With Adverse Outcomes in Severe Bronchopulmonary Dysplasia

Chest, 2024-03, Vol.165 (3), p.610-620

2024

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Idiopathic and heritable PAH perturb common molecular pathways, correlated with increased MSX1 expression

Pulmonary circulation, 2011-07, Vol.1 (3), p.389-398

2011

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Abstract 14979: Endostatin as a Predictor of Severity and Survival in Pediatric Congenital Heart Disease Associated Pulmonary Hypertension

Circulation (New York, N.Y.), 2020-11, Vol.142 (Suppl_3 Suppl 3), p.A14979-A14979

2020

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Abstract 11199: Insulin-Like Growth Factor Binding Protein-4 is Associated with Pulmonary Arterial Hypertension Severity and Survival

Circulation (New York, N.Y.), 2021-11, Vol.144 (Suppl_1)

2021

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Abstract 12603: Impaired Coronary Flow Reserve in Athletes With Long-Term Cardiovascular Symptoms After COVID-19

Circulation (New York, N.Y.), 2021-11, Vol.144 (Suppl_1)

2021

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Abstract 12424: A Non-Invasive Proteomic Model Predicts Pulmonary Arterial Hypertension Survival

Circulation (New York, N.Y.), 2021-11, Vol.144 (Suppl_1)

2021

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T ranslational A dvances in the F ield of P ulmonary H ypertension Molecular Medicine of Pulmonary Arterial Hypertension. From Population Genetics to Precision Medicine and Gene Editing

American journal of respiratory and critical care medicine, 2017-01, Vol.195 (1), p.23-31

2017

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Career Development of Young Physician–Scientists in the Cardiovascular Sciences

Circulation research, 2018-05, Vol.122 (10), p.1330-1333

2018

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Letter to the Editor, in response to: “Iron Homeostasis and Pulmonary Hypertension: Iron Deficiency Leads to Pulmonary Vascular Remodeling in the Rat”

Circulation research, 2015-08, Vol.117 (6), p.e56-e57

2015

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Pulmonary hypertension's variegated landscape: a snapshot

Pulmonary circulation, 2016-12, Article 690552

2016

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Type I interferon activation and endothelial dysfunction in caveolin-1 insufficiency-associated pulmonary arterial hypertension

Sex-based differences in veterans with pulmonary hypertension: Results from the veterans affairs-clinical assessment reporting and tracking database

Pulmonary hypertension: NHLBI Workshop on the Primary Prevention of Chronic Lung Diseases

Abnormal trafficking of endogenously expressed BMPR2 mutant allelic products in patients with heritable pulmonary arterial hypertension

Translational Advances in the Field of Pulmonary Hypertension Molecular Medicine of Pulmonary Arterial Hypertension. From Population Genetics to Precision Medicine and Gene Editing

The genetics of pulmonary arterial hypertension in the post-BMPR2 era

FHIT , a Novel Modifier Gene in Pulmonary Arterial Hypertension

Aberrant Caveolin-1-Mediated Smad Signaling and Proliferation Identified by Analysis of Adenine 474 Deletion Mutation (c.474delA) in Patient Fibroblasts: A New Perspective in the Mechanism of Pulmonary Hypertension

Aberrant caveolin-1-mediated Smad signaling and proliferation identified by analysis of adenine 474 deletion mutation (c.474delA) in patient fibroblasts: a new perspective on the mechanism of pulmonary hypertension

Valsalva Maneuver in Pulmonary Arterial Hypertension

Synergistic heterozygosity for TGFβ1 SNPs and BMPR2 mutations modulates the age at diagnosis and penetrance of familial pulmonary arterial hypertension

Valsalva Maneuver in Pulmonary Arterial Hypertension: Hemodynamic Changes and Excessive Systemic Vasodilation

HERITABLE PULMONARY ARTERIAL HYPERTENSION IS ASSOCIATED WITH WORSE PULMONARY CAPACITANCE AND RIGHT VENTRICULAR STROKE WORK INDEX COMPARED TO IDIOPATHIC PULMONARY ARTERIAL HYPERTENSION

Genetic Testing in Pulmonary Arterial Hypertension Evaluation

Exploring the Association of Male Sex With Adverse Outcomes in Severe Bronchopulmonary Dysplasia

Idiopathic and heritable PAH perturb common molecular pathways, correlated with increased MSX1 expression

Abstract 14979: Endostatin as a Predictor of Severity and Survival in Pediatric Congenital Heart Disease Associated Pulmonary Hypertension

Abstract 11199: Insulin-Like Growth Factor Binding Protein-4 is Associated with Pulmonary Arterial Hypertension Severity and Survival

Abstract 12603: Impaired Coronary Flow Reserve in Athletes With Long-Term Cardiovascular Symptoms After COVID-19

Abstract 12424: A Non-Invasive Proteomic Model Predicts Pulmonary Arterial Hypertension Survival

T ranslational A dvances in the F ield of P ulmonary H ypertension Molecular Medicine of Pulmonary Arterial Hypertension. From Population Genetics to Precision Medicine and Gene Editing

United States Pulmonary Hypertension Scientific Registry

Career Development of Young Physician–Scientists in the Cardiovascular Sciences

Letter to the Editor, in response to: “Iron Homeostasis and Pulmonary Hypertension: Iron Deficiency Leads to Pulmonary Vascular Remodeling in the Rat”

Pulmonary hypertension's variegated landscape: a snapshot

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