Area of research
Genetics · Hematology
Research interest
Research interests include Hemoglobinopathies and Related Disorders, Iron Metabolism and Disorders, Blood groups and transfusion, and Erythrocyte Function and Pathophysiology.
Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations
Editing aberrant splice sites efficiently restores β-globin expression in β-thalassemia
Notch and Aryl Hydrocarbon Receptor Signaling Impact Definitive Hematopoiesis from Human Pluripotent Stem Cells
Induced pluripotent stem cell–based mapping of β-globin expression throughout human erythropoietic development
Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype–phenotype correlation
A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem Cells
A phased SNP-based classification of sickle cell anemia HBB haplotypes
A long noncoding RNA from the HBS1L-MYB intergenic region on chr6q23 regulates human fetal hemoglobin expression
Variants of ZBTB7A (LRF) and its β-globin gene cluster binding motifs in sickle cell anemia
BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia
The genetics of hemoglobin A<sub>2</sub> regulation in sickle cell anemia
Fetal hemoglobin in sickle cell anemia: a glass half full?
The aryl hydrocarbon receptor directs hematopoietic progenitor cell expansion and differentiation
Sickle cell disease in <scp>S</scp>audi <scp>A</scp>rabia: the phenotype in adults with the <scp>A</scp>rab‐<scp>I</scp>ndian haplotype is not benign
Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype
Novel dominant β‐thalassemia: Hb Boston‐Kuwait [Codon 139/140(+T)]