Chui, David H.K.

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

HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server

Hardison, R. C., Chui, D. H. K., Giardine, B., Riemer, C., Patrinos, G. P., Anagnou, N., Miller, W., & Wajcman, H. (2002) · Human Mutation

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 439

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

Prevalence and Genotypes of α- and β-Thalassemia Carriers in Hong Kong — Implications for Population Screening

Lau, Y.-L., Chan, L.-C., Chan, Y.-Y. A., Ha, S.-Y., Yeung, C.-Y., Waye, J. S., & Chui, D. H. K. (1997) · New England Journal of Medicine

Hemoglobinopathies and Related DisordersBlood groups and transfusion

Cited by 212

BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies

Sedgewick, A. E., Timofeev, N., Sebastiani, P., So, J. C. C., Ma, E. S. K., Chan, L. C., Fucharoen, G., Fucharoen, S., Barbosa, C. G., Vardarajan, B. N., et al. (2008) · Blood Cells, Molecules, and Diseases

Hemoglobinopathies and Related DisordersGenetic Associations and Epidemiology

Cited by 172

Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin

Ngo, D. A., Aygun, B., Akinsheye, I., Hankins, J. S., Bhan, I., Luo, H. Y., Steinberg, M. H., & Chui, D. H. K. (2012) · British Journal of Haematology

Hemoglobinopathies and Related DisordersIron Metabolism and Disorders

Cited by 142

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

A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem Cells

Park, S., Gianotti-Sommer, A., Molina-Estevez, F. J., Vanuytsel, K., Skvir, N., Leung, A., Rozelle, S. S., Shaikho, E. M., Weir, I., Jiang, Z., et al. (2017) · Stem Cell Reports

Hemoglobinopathies and Related DisordersPluripotent Stem Cells Research

Cited by 50

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

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

Cis- and trans-acting expression quantitative trait loci differentially regulate gamma-globin gene expression

Shaikho, E. M., Farrell, J. J., Chui, D. H. K., Sebastiani, P., & Steinberg, M. H. (2018) · bioRxiv (Cold Spring Harbor Laboratory)

Hemoglobinopathies and Related DisordersGenetic Associations and Epidemiology

Cited by 5