| Fetal hemoglobin in sickle cell anemia I Akinsheye, A Alsultan, N Solovieff, D Ngo, CT Baldwin, P Sebastiani, ... Blood, The Journal of the American Society of Hematology 118 (1), 19-27, 2011 | 648 | 2011 |
| Effectiveness of therapeutic heparin versus prophylactic heparin on death, mechanical ventilation, or intensive care unit admission in moderately ill patients with covid-19 … M Sholzberg, GH Tang, H Rahhal, M AlHamzah, LB Kreuziger, FN Áinle, ... bmj 375, 2021 | 364 | 2021 |
| LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency A Alangari, A Alsultan, N Adly, MJ Massaad, IS Kiani, A Aljebreen, ... Journal of Allergy and Clinical Immunology 130 (2), 481-488. e2, 2012 | 285 | 2012 |
| Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked–like disorder caused by loss-of-function mutations in LRBA LM Charbonnier, E Janssen, J Chou, TK Ohsumi, S Keles, JT Hsu, ... Journal of Allergy and Clinical Immunology 135 (1), 217-227. e9, 2015 | 282 | 2015 |
| Fetal hemoglobin in sickle cell anemia: a glass half full? MH Steinberg, DHK Chui, GJ Dover, P Sebastiani, A Alsultan Blood, The Journal of the American Society of Hematology 123 (4), 481-485, 2014 | 276 | 2014 |
| Effective treatment of steroid and therapy-refractory acute graft-versus-host disease with a novel mesenchymal stromal cell product (MSC-FFM) P Bader, Z Kuçi, S Bakhtiar, O Basu, G Bug, M Dennis, J Greil, A Barta, ... Bone Marrow Transplantation 53 (7), 852-862, 2018 | 114 | 2018 |
| Sickle cell disease in S audi A rabia: the phenotype in adults with the A rab‐I ndian haplotype is not benign A Alsultan, MK Alabdulaali, PJ Griffin, AM AlSuliman, HA Ghabbour, ... British journal of haematology 164 (4), 597-604, 2014 | 114 | 2014 |
| Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype D Ngo, H Bae, MH Steinberg, P Sebastiani, N Solovieff, CT Baldwin, ... Blood Cells, Molecules, and Diseases 51 (1), 22-26, 2013 | 80 | 2013 |
| MYSM1 is mutated in a family with transient transfusion-dependent anemia, mild thrombocytopenia, and low NK- and B-cell counts A Alsultan, HE Shamseldin, ME Osman, M Aljabri, FS Alkuraya Blood, The Journal of the American Society of Hematology 122 (23), 3844-3845, 2013 | 63 | 2013 |
| Sickle cell disease subphenotypes in patients from Southwestern Province of Saudi Arabia A Alsultan, A Aleem, H Ghabbour, FH AlGahtani, A Al-Shehri, ME Osman, ... Journal of pediatric hematology/oncology 34 (2), 79-84, 2012 | 62 | 2012 |
| Chronic granulomatous disease presenting with disseminated intracranial aspergillosis A Alsultan, MS Williams, S Lubner, FD Goldman Pediatric blood & cancer 47 (1), 107-110, 2006 | 56 | 2006 |
| Deficiency of ADA2 mimicking autoimmune lymphoproliferative syndrome in the absence of livedo reticularis and vasculitis A Alsultan, E Basher, J Alqanatish, R Mohammed, M Alfadhel Pediatric blood & cancer 65 (4), e26912, 2018 | 54 | 2018 |
| BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia P Sebastiani, JJ Farrell, A Alsultan, S Wang, HL Edward, H Shappell, ... Blood Cells, Molecules, and Diseases 54 (3), 224-230, 2015 | 53 | 2015 |
| Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans A Alsultan, N Solovieff, A Aleem, FH AlGahtani, A Al-Shehri, ME Osman, ... American journal of hematology 86 (7), 612-614, 2011 | 50 | 2011 |
| Clofarabine salvage therapy for refractory high‐risk langerhans cell histiocytosis A Abraham, A Alsultan, M Jeng, C Rodriguez‐Galindo, PK Campbell Pediatric blood & cancer 60 (6), E19-E22, 2013 | 48 | 2013 |
| Children and adults with refractory acute graft-versus-host disease respond to treatment with the mesenchymal stromal cell preparation “MSC-FFM”—outcome report of 92 patients H Bonig, Z Kuçi, S Kuçi, S Bakhtiar, O Basu, G Bug, M Dennis, J Greil, ... Cells 8 (12), 1577, 2019 | 46 | 2019 |
| A comprehensive, ethnically diverse library of sickle cell disease-specific induced pluripotent stem cells S Park, A Gianotti-Sommer, FJ Molina-Estevez, K Vanuytsel, N Skvir, ... Stem Cell Reports 8 (4), 1076-1085, 2017 | 46 | 2017 |
| A phased SNP-based classification of sickle cell anemia HBB haplotypes EM Shaikho, JJ Farrell, A Alsultan, H Qutub, AK Al-Ali, MS Figueiredo, ... BMC genomics 18, 1-7, 2017 | 44 | 2017 |
| Tacrolimus as an alternative to cyclosporine in the maintenance phase of immunosuppressive therapy for severe aplastic anemia in children A Alsultan, NA Goldenberg, N Kaiser, DK Graham, T Hays Pediatric blood & cancer 52 (5), 626-630, 2009 | 36 | 2009 |
| Clinical characteristics and treatment outcome of childhood acute lymphoblastic leukemia in Saudi Arabia: A multi‐institutional retrospective national collaborative study R Al‐Sudairy, A Al‐Nasser, A Alsultan, AA Ahmari, I Abosoudah, ... Pediatric blood & cancer 61 (1), 74-80, 2014 | 35 | 2014 |