Area of research
Genetics · Hematology
Research interest
Research focused on Disease and Acute chest syndrome, with related work in Vaso-occlusive crisis, Emergency department, Pregnancy. Notable publications include 'Effect of Anticoagulant Therapy for 6 Weeks vs 3 Months on Recurrence and Bleeding Events in Patients Younger Than 21 Years of Age With Provoked Venous Thromboembolism', 'The sickle cell disease implementation consortium: Translating evidence‐based guidelines into practice for sickle cell disease', and 'Pregnancy outcomes with hydroxyurea use in women with sickle cell disease'.
Mortality in adults with sickle cell disease: Results from the sickle cell disease implementation consortium (SCDIC) registry
The clinical spectrum of <scp>HbSC</scp> sickle cell disease‐not a benign condition
Digital cognitive behavioral therapy vs education for pain in adults with sickle cell disease
Barriers and Facilitators to Integrating Acupuncture into the U.S. Health Care System: A Scoping Review
Pharmacokinetics, pharmacodynamics, safety, and efficacy of crizanlizumab in patients with sickle cell disease: final results from the phase II SOLACE-adults study
Depression, sleep and pain affect instrumental activities of daily living through cognitive functioning in adults with sickle cell disease: A report from the Sickle Cell Disease Implementation Consortium
Patient‐reported pregnancy loss and maternal complications: Insights from the sickle cell disease implementation consortium
Biopsychosocial Factors Associated With Pain and Pain-Related Outcomes in Adults and Children With Sickle Cell Disease: A Multivariable Analysis of the GRNDaD Multicenter Registry
A multilevel mHealth intervention boosts adherence to hydroxyurea in individuals with sickle cell disease
Hybrid effectiveness-implementation trial of guided relaxation and acupuncture for chronic sickle cell disease pain (GRACE): A protocol
Infertility and treatment‐seeking practices among females and males with sickle cell disease in the Sickle Cell Disease Implementation Consortium registry
Effect of Anticoagulant Therapy for 6 Weeks vs 3 Months on Recurrence and Bleeding Events in Patients Younger Than 21 Years of Age With Provoked Venous Thromboembolism
Pregnancy outcomes with hydroxyurea use in women with sickle cell disease
Perspectives of individuals with sickle cell disease on barriers to care
Real-world effectiveness of voxelotor for treating sickle cell disease in the US: a large claims data analysis
Pharmacokinetics, pharmacodynamics, safety, and efficacy of crizanlizumab in patients with sickle cell disease
Consensus definition of essential, optimal, and suggested components of a pediatric sickle cell disease center
An evaluation of patient-reported outcomes in sickle cell disease within a conceptual model
Characterising the prevalence of overweight and obese status among adults with sickle cell disease
Sex-based differences in the manifestations and complications of sickle cell disease: Report from the Sickle Cell Disease Implementation Consortium
Effect of Poloxamer 188 vs Placebo on Painful Vaso-Occlusive Episodes in Children and Adults With Sickle Cell Disease
Comparing the Effectiveness of Education Versus Digital Cognitive Behavioral Therapy for Adults With Sickle Cell Disease: Protocol for the Cognitive Behavioral Therapy and Real-time Pain Management Intervention for Sickle Cell via Mobile Applications (CaRISMA) Study
Patient‐reported outcomes in sickle cell disease and association with clinical and psychosocial factors: Report from the sickle cell disease implementation consortium
<p>Development of a Severity Classification System for Sickle Cell Disease</p>
Publication of data collection forms from NHLBI funded sickle cell disease implementation consortium (SCDIC) registry
Effective Recruitment Strategies for a Sickle Cell Patient Registry Across Sites from the Sickle Cell Disease Implementation Consortium (SCDIC)
Integration of Mobile Health Into Sickle Cell Disease Care to Increase Hydroxyurea Utilization: Protocol for an Efficacy and Implementation Study
Sex Based Differences in Sickle Cell Disease
The sickle cell disease implementation consortium: Translating evidence‐based guidelines into practice for sickle cell disease
Sickle cell disease is associated with iron mediated hypercoagulability