Area of research
Genetics · Hematology
Research interest
Research interests include Medicine, Internal medicine, Disease, Anemia, Sickle cell anemia, and Immunology.
Iron restriction in sickle cell disease: When less is more
Riociguat in patients with sickle cell disease and hypertension or proteinuria (STERIO-SCD): a randomised, double-blind, placebo controlled, phase 1–2 trial
Effect of Poloxamer 188 vs Placebo on Painful Vaso-Occlusive Episodes in Children and Adults With Sickle Cell Disease
Tricuspid regurgitation velocity and other biomarkers of mortality in children, adolescents and young adults with sickle cell disease in the United States: The <scp>PUSH</scp> study
The <scp><i>CYB5R3</i><sup>c</sup></scp><sup>.<scp>350C</scp>>G</sup> and <scp><i>G6PD</i></scp> A alleles modify severity of anemia in malaria and sickle cell disease
Serum albumin is independently associated with higher mortality in adult sickle cell patients: Results of three independent cohorts
Platelet Extracellular Vesicles Drive Inflammasome–IL-1β–Dependent Lung Injury in Sickle Cell Disease
End points for sickle cell disease clinical trials: renal and cardiopulmonary, cure, and low-resource settings
Clinical Outcomes Associated With Sickle Cell Trait
Simultaneous polymerization and adhesion under hypoxia in sickle cell disease
Intravascular hemolysis and the pathophysiology of sickle cell disease
Kinetics of sickle cell biorheology and implications for painful vasoocclusive crisis
Risk Factors for Death in 632 Patients with Sickle Cell Disease in the United States and United Kingdom
Elevated sphingosine-1-phosphate promotes sickling and sickle cell disease progression
Iron, Inflammation, and Early Death in Adults With Sickle Cell Disease
Hemodynamic Predictors of Mortality in Adults with Sickle Cell Disease
Abnormal Pulmonary Function and Associated Risk Factors in Children and Adolescents With Sickle Cell Anemia
A GCH1 haplotype confers sex‐specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemia
Clinical correlates of acute pulmonary events in children and adolescents with sickle cell disease
The relationship between the severity of hemolysis, clinical manifestations and risk of death in 415 patients with sickle cell anemia in the US and Europe
Mortality in Adults With Sickle Cell Disease and Pulmonary Hypertension
Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans
A Novel Molecular Signature for Elevated Tricuspid Regurgitation Velocity in Sickle Cell Disease
Reduced sensitivity of the ferroportin Q248H mutant to physiological concentrations of hepcidin
Atorvastatin reduces serum cholesterol and triglycerides with limited improvement in vascular function in adults with sickle cell anemia