Selected Recent Publications / Contributions to Knowledge
My research and published work in SCD, the most common genetic disorder worldwide include:
Afolabi, B. B., Babah, O. A., Adeyemo, T. A., Balogun, M., Banke-Thomas, A., Abioye, A. I., ... & Umar-Suleiman, S. (2024). Intravenous versus oral iron for anaemia among pregnant women in Nigeria (IVON): an open-label, randomised controlled trial. The Lancet Global Health, 12(10), e1649-e1659.
Ojewunmi, O. O., Adeyemo, T. A., Oyetunji, A. I., Inyang, B., Akinrindoye, A., Mkumbe, B. S., ... & Menzel, S. (2024). The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria. Human Molecular Genetics, 33(10), 919-929.
Ochuwa Adiketu Babah, Opeyemi Rebecca Akinajo, Lenka Beňová, Claudia Hanson, Ajibola Ibraheem Abioye, Victoria Olawunmi Adaramoye, Titilope A. Adeyemo, Mobolanle Rasheedat Balogun, Aduragbemi Banke-Thomas, Hadiza S. Galadanci, Nadia A. Sam-Agudu, Bosede Bukola Afolabi & Elin C. Larsson. (2024). Prevalence of and risk factors for iron deficiency among pregnant women with moderate or severe anaemia in Nigeria: a cross-sectional study. BMC pregnancy and childbirth, 24(1), 39.
Afolabi, B.B., Babah, O.A., Adeyemo, T.A. (2022). Evidence-based obstetric management of women with sickle cell disease in low-income countries. Hematology. American Society of Hematology. Education Program, 2022, 2022(1), pp. 414–420.
Ojewunmi, O. O., Adeyemo, T. A., Oyetunji, A. I., Benn, Y., Ekpo, M. G., & Iwalokun, B. A. (2021). Association of alpha‐thalassemia and Glucose‐6‐Phosphate Dehydrogenase deficiency with transcranial Doppler ultrasonography in Nigerian children with sickle cell anemia. Journal of clinical laboratory analysis, 35(6), e23802.
