Molecular blood group screening in Omani blood donors von Al‐Riyami, Arwa Z., Al Hinai, Dina, Al‐Rawahi, Mohammed, Al‐Hosni, Saif, Al‐Zadjali, Shoaib, Al‐Marhoobi, Ali, Al‐Khabori, Murtadha, Al‐Riyami, Hamad, Denomme, Gregory A.

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Warfarin pharmacogenetics: development of a dosing algorithm for Omani patients von Pathare, Anil, Al Khabori, Murtadha, Alkindi, Salam, Al Zadjali, Shoaib, Misquith, Rhea, Khan, Hammad, Lapoumeroulie, Claudine, Paldi, Andras, Krishnamoorthy, Rajagopal

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Analyzing Cancer Incidence Trends in Oman From 1996 to 2019: A Comprehensive Study of the National Cancer Annual Reports von Al-Sayegh, Hasan, Al-Zadjali, Shoaib, Al-Moundhri, Mansour

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IDH1 and IDH2 gene mutations in Omani patients with acute myeloid leukemia: Prognostic significance and clinic-pathologic features von Al Abri, Yusra, Al Huneini, Mohammed, Al Zadjali, Shoaib, Al Rawahi, Mohammed

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T2 cardiovascular magnetic resonance in the management of thalassemia patients in Oman von Daar, Shahina, Pathare, Anil V, Jain, Rajeev, Zadjali, Shoaib Al, Pennell, Dudley J

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Thiamine responsive megaloblastic anemia: The puzzling phenotype von Beshlawi, Ismail, Zadjali, Shoaib Al, Bashir, Wafa, Elshinawy, Mohamed, Alrawas, Abdulhakim, Wali, Yasser

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First reported case of compound heterozygosity for HbA2-Yialousa (HBD: c.82 G>C) and HbA2-Wrens (HBD: c.295 G>A) in Oman von Al Zadjali, Shoaib, Bashir, Wafa, Gravell, David, Al Riyami, Arwa Z., Wali, Yasser, Daar, Shahina

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Targeted next generation sequencing identifies a novel β-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis von Al-Riyami, Arwa Z, Iolascon, Achille, Al-Zadjali, Shoaib, Andolfo, Immacolata, Al-Mammari, Sahima, Manna, Francesco, Al Rawas, AbdulHakim, King, May-Jean, Russo, Roberta

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Cytogenetic Profile of Adult and Pediatric Acute Myeloid Leukemia in Oman: 10-Year Data From a Tertiary Care University Referral Hospital von Riyami, Arwa Al, Bakri, Nooh Al, Salmi, Humoud Al, Zadjali, Shoaib Al, Huneini, Mohammed Al, Khabori, Murtadha Al, Farsi, Khalil Al, Rawas, AbdulHakim Al, Lamki, Zakia Al, Wali, Yasser, Alkindi, Salam

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Impact of Mannose-Binding Protein Gene Polymorphisms in Omani Sickle Cell Disease Patients von Zachariah, Mathew, Al Zadjali, Shoaib, Bashir, Wafa, Al Ambusaidi, Rahma, Misquith, Rhea, Wali, Yasser, Pathare, Anil

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Severity ranking of non-deletional alpha thalassemic alleles: insights from an Omani family study von Wali, Yasser, Zadjali, Shoaib Al, Elshinawy, Mohamed, Beshlawi, Ismail, Fawaz, Naglaa, AlKindi, Salam, Rawas, Abdulhakim, Alsinani, Siham, Daar, Shahina, Krishnamoorthy, Rajagopal

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Warfarin Pharmacogenetics: Polymorphisms of the CYP2C9, CYP4F2, and VKORC1 Loci in a Genetically Admixed Omani Population von Pathare, Anil V., Zadjali, Shoaib Al, Misquith, Rhea, Alkindi, Salam S., Panjwani, Vinodh, Lapoumeroulie, Claudine, Pravin, Sahaya, Paldi, Andras, Krishnamoorthy, Rajagopal

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CD34+CD38-CD123+ Cells Are Present in Virtually All Acute Myeloid Leukaemia Blasts: A Promising Single Unique Phenotype for Minimal Residual Disease Detection von Al-Mawali, Adhra, Pinto, Avinash Daniel, Al-Zadjali, Shoaib

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The Optimal Cut-Off Level for Hemoglobin A2 to Differentiate between Sickle Cell Disease Genotypes von Al Shueili, Fayiz, Al-Khabori, Murtadha K., Al-Kindi, Salam, Wali, Yasser, Al-Zadjali, Shoaib

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A homozygous loss-of-function C1S mutation is associated with Kikuchi-Fujimoto disease von Alshekaili, Jalila, Nasr, Iman, Al-Rawahi, Mohammed, Ansari, Zainab, Al Rahbi, Nasser, Al Balushi, Hamed, Al-Zadjali, Shoaib, Al Kindi, Mahmood, Al-Maawali, Almundher, Cook, Matthew C.

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Neonatal screening : mean haemoglobin and red cell indices in cord blood from Omani neonates von al-Kindi, Salam M. Z., al-Zadjali, Shuayb, al-Madhani, Ali, Pathare, Anil V., al-Abri, Qamariya, al-Haddabi, Hammud, Gravell, David, Mathew, Maryam, Krishnamoorthy, Rajagopal

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Deciphering Urogenital Cancers through Proteomic Biomarkers: A Systematic Review and Meta-Analysis von Khan, Aafaque Ahmad, Al-Mahrouqi, Nahad, Al-Yahyaee, Aida, Al-Sayegh, Hasan, Al-Harthy, Munjid, Al-Zadjali, Shoaib

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Genetic Causes, Clinical Features, and Survival of Underlying Inborn Errors of Immunity in Omani Patients: a Single-Center Study von Al-Tamemi, Salem, Al-Zadjali, Shoaib, Bruwer, Zandre, Naseem, Shafiq-Ur-Rehman, Al-Siyabi, Nabila, ALRawahi, Mohammed, Alkharusi, Khalsa, Al-Thihli, Khalid, Al-Murshedi, Fathiya, AlSayegh, Abeer, Al-Maawali, Almundher, Dennison, David

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Elevated levels of circulating invariant natural killer cell subsets are skewed toward Th2-like phenotype in children with sickle cell disease von Boulassel, Mohamed-Rachid, Al-Zubaidi, Abeer, Al-Zadjali, Shoaib, Al-Qarni, Zahra, Al-Naamany, Nidaa, Al-Yarabi, Ahmed, Elshinawy, Mohamed, Wali, Yasser

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Cardio-protective effect of regular transfusion in children with non-transfusion dependent thalassemia (NTDT): A cohort study von Al Senaidi, Khalfan, Maveda, Surekha Tony, Joshi, Niranjan, Nazir, Hanan, Elshinawy, Mohamed, AL Zadjali, Shoaib, Al Rawas, Abdulhakim, Elghamry, Islam, Wali, Yasser, Khater, Doaa

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