

Associate Professor of Hematology with more than 20 years of experience in higher education, academic leadership, teaching, research, and quality assurance. Proven expertise in curriculum development, program evaluation, learning outcomes assessment, and academic accreditation. Extensive experience in undergraduate and postgraduate teaching, research supervision, and scholarly publication in hematology and related biomedical sciences. Strong record of academic administration, faculty leadership, and interdisciplinary collaboration, with a commitment to advancing educational excellence, scientific research, and continuous quality improvement.
1. Safia Khalil Ali, Elshazali Widaa Ali. HFE Gene C282Y and E277K Mutations as Possible Genetic Modulators of Iron Overload Severity in Transfusion-Dependent β-Thalassemia Major. Biomedical and Pharmacology Journal 2025;18(4).
2. Samar Ali Osman, Elshazali Widaa Ali, Elamin Abdelkarim Elamin, Osman Mansour. Duffy Antigen Receptor for Chemokines (DARC) Polymorphisms and Susceptibility to Plasmodium Vivax Malaria in Sudan: a Case - Control Study. Mater Sociomed. 2025;37(4):276-280.
3. Mashaer Taha Edris, Maye Mohammad Merghani, Shaza Salih Gafar, Ahmed Mohamed Asmeli, Elrashed B. Yasin, Raed Alserihi, Haitham M.H. Qutob, Aymen Yasin, Elshazali Widaa Ali. Reduced folate carrier 1 (RFC1) gene polymorphisms among acute lymphoblastic leukemia patients. Journal of Biological Research 2025; 98:13105.
4. Adam KM, Ali EW, Elangeeb ME, Abuagla HA, Elamin BK, Ahmed EM, Edris AM, Ahmed AAEM, Eltieb EI. Intelligent Care: A Scientometric Analysis of Artificial Intelligence in Precision Medicine. Med Sci (Basel). 2025;13(2):44.
5. Abuagla HA, Adam KM, Elangeeb ME, Ahmed EM, Ali EW, Edris AM, MohamedAhmed AAE, Eltieb EI, Khalid TBA, Elamin BK, Osman HMA, Idris ES. Impact of nonsynonymous single-nucleotide polymorphisms in PROCR gene on protein stability and thrombotic risk: a molecular dynamics approach. Front Genet. 2025;16:1580993.
6. Ali EW, Adam KM, Elangeeb ME, Ahmed EM, Abuagla HA, MohamedAhmed AAE, Edris AM, Eltieb EI, Osman HMA, Idris ES. Exploring the Structural and Functional Consequences of Deleterious Missense Nonsynonymous SNPs in the EPOR Gene: A Computational Approach. J Pers Med. 2024;14(11):1111.
7. Mohamed Ahmed MA, Ali EW, Alimairi GM. Platelet Glycoprotein IIIa PlA1/PlA2 Polymorphism Modulates the Risk of Myocardial Infarction in Non-Diabetics. J Clin Med Res. 2024 Mar;16(2-3):75-80
8. Ahmed EM, Elangeeb ME, Adam KM, Abuagla HA, MohamedAhmed AAE, Ali EW, Eltieb EI, Edris AM, Ali Osman HM, Idris ES, Khalil KAA. Computational Analysis of Deleterious nsSNPs in INS Gene Associated with Permanent Neonatal Diabetes Mellitus. J Pers Med. 2024;14(4):425.
9. Idriss MI, Hussein AAA, Mussa A, Ali EW, Ibrahim IK, Modawe G, Abdalhabib E, Saboor M, Hajissa K. Prevalence and classification of anemia among children in Sudan: a systematic review and meta-analysis. J Med Life. 2024 Aug;17(8):761-768.
10. Ali EW. Pharmacogenetic And Nanomedicine Perspectives For Optimizing Erythropoietin Therapy In Patients With End-Stage Renal Disease. Nanotechnology Perceptions 2024; 20(S11):1793-1802.
11. Elnageeb ME, Elfaki I, Adam KM, Ahmed EM, Elkhalifa EM, Abuagla HA, Ahmed AAEM, Ali EW, Eltieb EI, Edris AM. In Silico Evaluation of the Potential Association of the Pathogenic Mutations of Alpha Synuclein Protein with Induction of Synucleinopathies. Diseases. 2023; 11(3):115.
12. Ali EW, Ibrahim IK. Multi-factorial Mechanism Behind COVID-19 Related Thrombosis. Med Arch. 2022; 76(1): 62-65.
13. Noha Alnair Abdelrhman, Elshazali Widaa Ali. The association of interleukin-6 (−174 G/C) polymorphism with risk of chronic kidney disease and erythropoietin hyporesponsiveness. J Nephropathol. 2022; 11(2): e12914.
14. Al Romisa Ahmed Abdulaziz, Elshazali Widaa Ali. Angiotensin-converting Enzyme Insertion/Deletion Polymorphism(rs4646994) and Susceptibility to Acute Lymphoblastic Leukemia: A Case–control Study. Open Access Maced J Med Sci. 2022; 10(B):997-1001.
15. Marwa Abdelmonem Ibrahim, Elshazali Widda Ali, NasrEldeen Ali Mohammed Gaufri. Endothelial Nitric Oxide Synthase Gene Polymorphism (T786C) among Sudanese Sickle Cell Disease Patients: Disease Prognostics and Response to Hydroxyurea. Al Jouf University Medical Journal 2021; 8(1): 7-14.
16. Safaa Awad Mohammed Ibrahim, Elshazali Widaa Ali. Lack of Association between Angiotensin-Converting Enzyme (ACE) Insertion/Deletion Polymorphism (rs4340) and Risk of Myocardial Infarction. Medical Science 2020; 24(106): 3987-93.
17. Aisha M Adam, Ibrahim Khidir Ibrahim, Elshazli Widaa Ali, Rosline Hassan. Angiotensin-Converting Enzyme Insertion/Deletion Gene Polymorphisms in Sudanese Patients with Chronic Lymphocytic Leukaemia. International Journal of Hematology and Oncology 2019; 29(1): 46-50.
18. Ibrahim IK, Hassan R, Ali EW, Omer A. Polycythaemia Vera among Sudanese Patients with Special Emphasis on JAK2 Mutations. Asian Pacific Journal of Cancer Prevention 2019; 20(1): 41-44
19. Elham Ali Ibrahim Elamin, Mohammed Ahmed Suliman, Mohammed Eltoum Azoz, Elshazali Widaa Ali, Livesey David Olerile, Yulian Jiao, Yueran Zhao. Effect of Helicobacter pylori Infection on Haematological Parameters in Kosti Teaching Hospital, Sudan. Iranian Red Crescent Medical Journal 2018; 20 (2): e58276
20. Sana Abass Mahjoub, Enaam Abdelrhman, Mohammed Elfatih Mohy El-Deen, Mustafa Sharf Eldin Mustafa, Elshazali Widaa Ali. Angiotensin-converting enzyme insertion/deletion polymorphism is not associated with vaso-occlusive complications of sickle cell anaemia. International journal of applied and basic medical research 2016; 6:267-270.
21. Elshazali Widaa Ali, Emad Eldean Mohammed Ahmed. The role of erythrocyte enzyme Glucose-6-phosphate dehydrogenase deficiency in the pathogenesis of anaemia of patients on haemodialysis. Saudi Journal of Kidney Diseases and Transplantation 2013; 24(6):1153-1156.
22. Khalid M. Osman, Elshazali W. Ali, El Sir A. Abugroun. Assessment of Quality Systems Adoption Levels in Blood Transfusion Services in Sudan. Graduate College Neelain University Journal 2018; 11(44-1):222-230.
23. Wafaa Salah Aldeen Khogaly, Mohamed El-Fatih Mohy El-Deen, Enaam Abdelrhman Abdelgader, Eldirdiri Mohamed Abdelrahman, Elshazali Widaa Ali. Hematological findings in Sudanese patients with lymphoid leukemias with relation to p53 arginine/proline polymorphism. International Journal of Information Research and Review 2016; 2(9): 1192-1194.
24. Aisha Mahmood Fageer Hussian, Nasr Eldeen Ali Mohammed, Mohanad Altayeb Mohamed Ahmed, Elshazali Widaa Ali. Angiotensin-Converting Enzyme Insertion/Deletion (I/D) Polymorphism and Risk of Recurrent Pregnancy Loss among Sudanese Women. Research in Obstetrics and Gynecology 2016; 4(1): 7-10.
25. Samia Ali Gafar, Elshazali Widaa Ali. Janus Kinase2 V617F Mutation in Sudanese Patients with Essential Thrombocythemia. Laboratory medicine journal2016; 2(1):1-5
26. Rania Ahmed Elmubarak, Ebtihal Ahmed Babiker, Elshazali Widaa Ali. Angiotensin-Converting Enzyme I/D Polymorphism and Risk of Acute Myeloid Leukemia among Sudanese Population. Laboratory medicine journal 2016; 2(1): 10-14.
27. Emtenan Hassan Alamas, Sana Abass Mahjoub, Elshazali Widaa Ali. Genotyping of P53 Gene Exon 4 Codon 72 in Sudanese Patients with Essential Thrombocythemia. Journal of Science 2016; 6(3): 187-190.
28. Sheraz Fathi Saeed, Elshazali Widaa Ali, Hiba Abbas Elamin, Mohanad Altayeb Mohamed Ahmed, Ebtihal Ahmed Babekir, Lubna Babiker. Association of vitamin-D receptor (VDR) start codon FOK-I polymorphism with chronic myeloid leukaemiaInternational journal of advances in pharmacy, biology and chemistry 2015; 4(1): 228-232.
29. Abdelrahman Fakey Abdelrahman, Ibrahim Khider Ibrahim, Safa Mhammed Omer, Hadeel Ibrahim Mohammed Noor, Mohanad Altayeb Mohamed Ahmed, Elshazali Widaa Ali. A minisatellite tandem repeat of human telomerase reverse transcriptase (MNS16A) in Sudanese patients with acute lymphoblastic leukaemia. Americam journal of research communication 2015; 3(2):89-96.
30. Tsabeeh Eltayeb Mohamed, Elshazali Widaa Ali, Leena Babiker Mirghani, Enaam Abdelrhman Abdelgader. Frequency of FLT3-Internal Tandem Duplication (FLT3-ITD) Mutation among Sudanese Patients with Acute Myeloblastic Leukemia. American Journal of Medicine and Medical Sciences 2014, 4(2): 47-50.
31. Salma Salim Hamad, Ibrahim Khider Ibrahim, Elshazali Widaa Ali, Omer Ali Eisawi. Evaluation of serum erythropoietin level in Sudanese patients with polycythaemia. Laboratory medicine journal 2013; 1(1): 36-42.
32. Nada Salih Badreldin, Elshazali Widaa Ali. Effectiveness of iron replacement therapy in Sudanese haemodialysis patients treated with recombinant erythropoietin. Laboratory Medicine Journal 2013; 1(2):15-21
33. Nsma Ali Hassan, Elshazali Widaa Ali, Nasreldin Ali Mohammed, Ibrahim Khider Ibrahim, Hiba Badreldin Khalil. The effect of freezing storage of citrated plasma on prothrombin time and activated partial thromboplastin time. Asian journal of biomedical and pharmaceutical sciences 2013; 3(23): 18-19.
· Bernard-Houwen travel award, the 29th conference of the International Society of Laboratory Haematology, Milano, Italy (2016).
· Young Investigators travel award, the 35th Congress of the International Society of Hematology, Beijing, China (2014).
Registered by Sudan National Council for Medical and Health Professions as Medical Laboratory First Consultant- Haematology & Immunohaematology,