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Genetic Epidemiology|November 5, 2024
A Novel One-Sample Mendelian Randomization Approach for Count-Type Outcomes That Is Robust to Correlated and Uncorrelated Pleiotropic EffectsJanaka S S Liyanage, Jane S Hankins, Jeremie H Estepp, et al.British Journal of Haematology|May 21, 2025
Long-term efficacy and safety of mitapivat in non-transfusion-dependent α- or β-thalassaemia: An open-label phase 2 studyKevin H M Kuo, D Mark Layton, Ashutosh Lal, et al.Ejhaem|July 18, 2022
A meta-analysis of toxicities related to hydroxycarbamide dosing strategiesJoacy G Mathias, Vikki G Nolan, Meghan Meadows-Taylor, et al.JMIR Mhealth and Uhealth|May 9, 2020
Development of the InCharge Health Mobile App to Improve Adherence to Hydroxyurea in Patients With Sickle Cell Disease: User-Centered Design ApproachNicole M Alberts, Sherif M Badawy, Jason Hodges, et al.Pediatric Blood & Cancer|December 31, 2021
Neurocognitive functioning in preschool children with sickle cell diseaseAndrew M Heitzer, Diana L Cohen, Victoria I Okhomina, et al.Pediatric Neurology|September 21, 2020
Cancer and Tumor-Associated Childhood Stroke: Results From the International Pediatric Stroke StudyLisa R Sun, Alexandra Linds, Mukta Sharma, et al.Current Research in Translational Medicine|March 18, 2022
Fetal hemoglobin modulates neurocognitive performance in sickle cell anemia✰,✰✰Andrew M Heitzer, Jennifer Longoria, Evadnie Rampersaud, et al.Experimental Biology and Medicine (Maywood, N.J.)|August 19, 2021
Progression of central nervous system disease from pediatric to young adulthood in sickle cell anemiaGrace Champlin, Scott N Hwang, Andrew Heitzer, et al.Journal of Pediatric Hematology/Oncology|July 26, 2023
Barriers and Facilitators of Premarital Genetic Counseling for Sickle Cell Disease in Northern NigeriaAisha A Galadanci, Jeremie H Estepp, Hamda Khan, et al.Pediatrics|June 24, 2016
Pharmacogenetics for Safe Codeine Use in Sickle Cell DiseaseRoseann S Gammal, Kristine R Crews, Cyrine E Haidar, et al.Pageof 5