Associated Papers
Global analysis of suppressor mutations that rescue human genetic defects.
Ünlü B et al.
Genome Medicine, 2023
37821946 (PubMed )
Supplement: 13073_2023_1232_MOESM3_ESM.xlsx › Data
Do Genetic Polymorphisms Affect Fetal Hemoglobin (HbF) Levels in Patients With Sickle Cell Anemia Treated With Hydroxyurea? A Systematic Review and Pathway Analysis.
Sales RR et al.
Frontiers in Pharmacology, 2021
Pharmacogenomics of sickle cell disease: steps toward personalized medicine.
Husain M et al.
Pharmacogenomics and Personalized Medicine, 2017
Disease burden and the role of pharmacogenomics in African populations.
Mpye KL et al.
Global Health, Epidemiology and Genomics, 2017
Whole exome sequencing identifies novel genes for fetal hemoglobin response to hydroxyurea in children with sickle cell anemia.
Sheehan VA et al.
Plos One, 2014
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