Steinberg, Martin H.
Università Cattolica del Sacro Cuore · Morgan Stanley Children's Hospital · St. Jude Children's Research Hospital · University of Toronto · Columbia University Irving Medical Center · University of Illinois Chicago · Children’s Hospital at TriStar Centennial · Sarah Cannon
31 papers on CoChatORCID 0000-0001-8800-8020
Most cited papers
- Verified
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
- Verified
Prevalence and diversity of haplotypes of sickle cell disease in the Eastern Province of Saudi Arabia
Al-Ali, A. K., Alsulaiman, A., Alzahrani, A. J., Obeid, O. T., Vatte, C. B., Cyrus, C., Alnafie, A. N., Alali, R. A., Alfarhan, M., Mozeleski, B., et al. (2020) · Hemoglobin
Hemoglobinopathies and Related DisordersMalaria Research and Control
Cited by 20
- Verified
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
- Verified
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
- Verified
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
- Verified
Comparing Bowtie and BWA to Align Short Reads from a RNA-Seq Experiment
Medina-Medina, N., Broka, A., Lacey, S., Lin, H., Klings, E. S., Baldwin, C. T., Steinberg, M. H., & Sebastiani, P. (2012) · Advances in Intelligent and Soft Computing
Genomics and Phylogenetic StudiesAlgorithms and Data Compression
Cited by 6
- Verified
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
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