Area of research
Genetics · Hematology
Research interest
Research interests include Medicine, Biology, Internal medicine, Disease, Sickle cell anemia, and Anemia.
Ferroportin Q248H mutation is associated with the less weight loss in persons with HIV-1
Riociguat in patients with sickle cell disease and hypertension or proteinuria (STERIO-SCD): a randomised, double-blind, placebo controlled, phase 1–2 trial
Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed
A randomized clinical trial of the efficacy and safety of rivipansel for sickle cell vaso-occlusive crisis
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
Early Initiation of Treatment with Rivipansel for Acute Vaso-Occlusive Crisis in Sickle Cell Disease (SCD) Achieves Earlier Discontinuation of IV Opioids and Shorter Hospital Stay: Reset Clinical Trial Analysis
Real-time, portable genome sequencing for Ebola surveillance
Epidermal devices for noninvasive, precise, and continuous mapping of macrovascular and microvascular blood flow
Frequency of Hospitalizations for Pain and Association With Altered Brain Network Connectivity in Sickle Cell Disease
Risk Factors for Death in 632 Patients with Sickle Cell Disease in the United States and United Kingdom
Iron, Inflammation, and Early Death in Adults With Sickle Cell Disease
Hemodynamic Predictors of Mortality in Adults with Sickle Cell Disease
Genetic determinants of haemolysis in sickle cell anaemia
A GCH1 haplotype confers sex‐specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemia
Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans
The HCV Non-Nucleoside Inhibitor Tegobuvir Utilizes a Novel Mechanism of Action to Inhibit NS5B Polymerase Function
Reduced sensitivity of the ferroportin Q248H mutant to physiological concentrations of hepcidin
Harnessing genomics to identify environmental determinants of heritable disease