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Transplantation and Cellular Therapy|July 22, 2021
Hematopoietic Stem Cell Transplantation for Patients with Autosomal Recessive Complete INF-λ Receptor 2 Deficiency: Experience in OmanHanan F Nazir, Abdulhakim Al Rawas, Salem Al Tamemi, et al.Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|December 11, 2025
Atypical teratoid rhabdoid tumor with extraneural metastases: a case report with genomic analysisNausheen Yaqoob, Boris Itkin, Syeda Sara Tajammul, et al.Hemoglobin|April 1, 2010
Forecasting hemoglobinopathy burden through neonatal screening in Omani neonatesSalam Alkindi, Shoaib Al Zadjali, Ali Al Madhani, et al.Clinical Immunology (Orlando, Fla.)|May 20, 2023
A homozygous loss-of-function C1S mutation is associated with Kikuchi-Fujimoto diseaseJalila Alshekaili, Iman Nasr, Mohammed Al-Rawahi, et al.Vox Sanguinis|October 14, 2021
Molecular blood group screening in Omani blood donorsArwa Z Al-Riyami, Dina Al Hinai, Mohammed Al-Rawahi, et al.American Journal of Human Genetics|March 25, 2026
Adaptive admixture at ACKR1, the Duffy blood group locus, may have shaped Plasmodium vivax prevalence in OmanPaige E Haffener, Arwa Z Al-Riyami, Shoaib Al-Zadjali, et al.Journal of Clinical Immunology|November 3, 2022
Genetic Causes, Clinical Features, and Survival of Underlying Inborn Errors of Immunity in Omani Patients: a Single-Center StudySalem Al-Tamemi, Shoaib Al-Zadjali, Zandre Bruwer, et al.European Journal of Haematology|December 1, 2011
dRTA and hemolytic anemia: first detailed description of SLC4A1 A858D mutation in homozygous stateNaglaa A Fawaz, Ismail O Beshlawi, Shoaib Al Zadjali, et al.Pageof 4