Alsultan, Abdulrahman

Fetal hemoglobin in sickle cell anemia

Akinsheye, I., Alsultan, A., Solovieff, N., Ngo, D., Baldwin, C. T., Sebastiani, P., Chui, D. H. K., & Steinberg, M. H. (2011) · Blood

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 553

Fetal hemoglobin in sickle cell anemia: a glass half full?

Steinberg, M. H., Chui, D. H. K., Dover, G. J., Sebastiani, P., & Alsultan, A. (2014) · Blood

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 267

Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab‐Indian haplotype is not benign

Alsultan, A., Alabdulaali, M. K., Griffin, P. J., AlSuliman, A. M., Ghabbour, H. A., Sebastiani, P., Albuali, W. H., Al‐Ali, A. K., Chui, D. H. K., & Steinberg, M. H. (2014) · British Journal of Haematology

Hemoglobinopathies and Related DisordersBlood groups and transfusion

Cited by 95

Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans

Alsultan, A., Solovieff, N., Aleem, A., AlGahtani, F. H., Al‐Shehri, A., Elfaki Osman, M., Kurban, K., Bahakim, H., Kareem Al‐Momen, A., Baldwin, C. T., et al. (2011) · American Journal of Hematology

Hemoglobinopathies and Related DisordersGenetic Associations and Epidemiology

Cited by 32

Variants of ZBTB7A (LRF) and its β-globin gene cluster binding motifs in sickle cell anemia

Shaikho, E. M., Habara, A. H., Alsultan, A., Al-Rubaish, A. M., Al-Muhanna, F., Naserullah, Z., Alsuliman, A., Qutub, H. O., Patra, P. K., Sebastiani, P., et al. (2016) · Blood Cells, Molecules, and Diseases

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 20

A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia

Vathipadiekal, V., Farrell, J. J., Wang, S., Edward, H. L., Shappell, H., Al‐Rubaish, A. M., Al‐Muhanna, F., Naserullah, Z., Alsuliman, A., Qutub, H. O., et al. (2016) · American Journal of Hematology

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 20

Homozygosity for a haplotype in the HBG2‐OR51B4 region is exclusive to Arab‐Indian haplotype sickle cell anemia

Vathipadiekal, V., Alsultan, A., Baltrusaitis, K., Farrell, J. J., Al‐Rubaish, A. M., Al‐Muhanna, F., Naserullah, Z., Suliman, A., Patra, P. K., Milton, J. N., et al. (2016) · American Journal of Hematology

Hemoglobinopathies and Related DisordersGenetic Associations and Epidemiology

Cited by 15