Alsuliman, A.

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

BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia

Sebastiani, P., Farrell, J. J., Alsultan, A., Wang, S., Edward, H. L., Shappell, H., Bae, H., Milton, J. N., Baldwin, C. T., Al-Rubaish, A. M., et al. (2015) · Blood Cells, Molecules, and Diseases

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 41

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

ANTXR1 Intronic Variants Are Associated with Fetal Hemoglobin in the Arab-Indian Haplotype of Sickle Cell Disease

Al-Ali, Z. A., Fallatah, R. K., Aljaffer, E. A., Albukhari, E. R., Sadek Al-Ali, N., Al-Ghannam, Z. T., Sayeb Al-Atrash, R., Alsuliman, A., & Vatte, C. (2018) · Acta Haematologica

Hemoglobinopathies and Related DisordersBlood groups and transfusion

Cited by 13