Area of research
Physiology · Genetics
Research interest
Research interests include Erythrocyte Function and Pathophysiology, Hemoglobinopathies and Related Disorders, Blood groups and transfusion, and Blood properties and coagulation.
Slowing the cell cycle to increase fetal hemoglobin
Comprehensive phenotypic and proteomic analyses of human reticulocyte maturation
A mouse model for hemoglobin SC disease recapitulates characteristic human pathologies.
A novel isoform of tensin-1 promotes actin filament assembly for efficient erythroblast enucleation.
Welcome to Blood Red Cells & Iron
Diagnosis and management of pyruvate kinase deficiency: international expert guidelines
The diagnostic utility of obtaining two blood cultures for the diagnosis of early onset sepsis in neonates
Joint bleeds in mild hemophilia: Prevalence and clinical characteristics
Survey research in perinatal medicine
Epigenetic Remodeling in Human Coronary Artery Smooth Muscle Cell Phenotypic Switching
Phenotypic and proteomic characterization of the human erythroid progenitor continuum reveal dynamic changes in cell cycle and in metabolic pathways
HEXIM1 is an essential transcription regulator during human erythropoiesis.
A Novel β-Globin Locus Deletional Syndrome: εγ-Thalassemia
Phase 3, multicentre, randomised, placebo-controlled study evaluating the efficacy and safety of ustekinumab in patients with systemic lupus erythematosus
HMGB1-mediated restriction of EPO signaling contributes to anemia of inflammation
Gender analysis of Journal of Perinatology authorship during COVID-19
Extramedullary hematopoietic stem cells
Gender Analysis of Journal of Perinatology Authorship During COVID-19
Recommendations for diagnosis and treatment of methemoglobinemia
Comprehensive phenotyping of erythropoiesis in human bone marrow: Evaluation of normal and ineffective erythropoiesis
The Journal of Perinatology: looking forward
Genotype‐phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency
Comprehensive proteomic analysis of murine terminal erythroid differentiation
Aberrant splicing contributes to severe α-spectrin–linked congenital hemolytic anemia
Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study
Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency
Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype–phenotype correlation
Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis
A Pediatrician’s Practical Guide to Diagnosing and Treating Hereditary Spherocytosis in Neonates
Isolation and transcriptome analyses of human erythroid progenitors: BFU-E and CFU-E