Area of research
Pulmonary and Respiratory Medicine · Cardiology and Cardiovascular Medicine
Research interest
Research interests include Pulmonary Hypertension Research and Treatments, Cardiovascular Function and Risk Factors, Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis, and MicroRNA in disease regulation.
Hemodynamics and Phosphodiesterase-5 Inhibitor Treatment Associated with Survival in Pulmonary Hypertension in Interstitial Lung Disease: A PVRI GoDeep Meta-Registry Analysis
Precision Medicine for Pulmonary Vascular Disease: The Future Is Now (2023 Grover Conference Series)
Male survival disadvantage in pulmonary hypertension: independent of aetiology, age, disease severity, comorbidities and treatment
Chronic thromboembolic pulmonary hypertension is an uncommon complication of COVID-19: UK national surveillance and observational screening cohort studies
Wearable technology and the cardiovascular system: the future of patient assessment
Defining the clinical validity of genes reported to cause pulmonary arterial hypertension
Immunogenicity of standard and extended dosing intervals of BNT162b2 mRNA vaccine
Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH
Biological heterogeneity in idiopathic pulmonary arterial hypertension identified through unsupervised transcriptomic profiling of whole blood
Whole-Blood RNA Profiles Associated with Pulmonary Arterial Hypertension and Clinical Outcome
Bayesian Inference Associates Rare <i>KDR</i> Variants With Specific Phenotypes in Pulmonary Arterial Hypertension
Germline selection shapes human mitochondrial DNA diversity
Characterization of <i>GDF2</i> Mutations and Levels of BMP9 and BMP10 in Pulmonary Arterial Hypertension
Loss of Endothelial Endoglin Promotes High-Output Heart Failure Through Peripheral Arteriovenous Shunting Driven by VEGF Signaling
Identification of rare sequence variation underlying heritable pulmonary arterial hypertension
Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data
Loss-of-Function <i>ABCC8</i> Mutations in Pulmonary Arterial Hypertension
Phenotypic Characterization of <i>EIF2AK4</i> Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension
Hypoxia determines survival outcomes of bacterial infection through HIF-1α–dependent reprogramming of leukocyte metabolism
Low-Dose FK506 (Tacrolimus) in End-Stage Pulmonary Arterial Hypertension
P157 Hepatocyte growth factor concentration correlates with haemodynamic severity in connective tissue disease-associated pulmonary arterial hypertension
Reduced MicroRNA-150 Is Associated with Poor Survival in Pulmonary Arterial Hypertension