Muntaser Ibrahim

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个人简介

Muntaser Ibrahim currently works at the Institute of Endemic Diseases, Department of Molecular Biology, University of Khartoum. Their current projects includei ' Sudan Genome Project' 'Curing cancer.' and others

研究兴趣

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Bi-allelic PRRT2 Variants May Predispose to Self-limited Familial Infantile Epilepsy

European journal of human genetics EJHGno. 10 (2024): 1338-1342

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Extensive Genetic Diversity in Plasmodium Vivax from Sudan and Its Genetic Relationships with Other Geographical Isolates

Musab M. Ali Albsheer, Alfred Hubbard,Cheikh Cambel Dieng, Eyoab Iyasu Gebremeskel, Safaa Ahmed,Virginie Rougeron,Muntaser E. Ibrahim,Eugenia Lo,Muzamil M. Abdel Hamid

INFECTION GENETICS AND EVOLUTION (2024)

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The rural urban divide, insights from immuno-genetic profiles and implications for health

Reem Hamad,Nahid A Eid, Safa A.E Aboswar, Azza Saeed,Ayman A Hussein,Ibrahim M Elhassan,Kirk A Rockett,Dominic P Kwiatkowski,Muntaser E Ibrahim,Ahmed M Elhassan

bioRxiv (Cold Spring Harbor Laboratory) (2023)

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"The outcome of COVID-19 patients in the intensive care unit in Sudan: A cross-sectional study" (vol 6, e1161, 2023)

M. A. O. Ali,N. A. Abdalrahman,E. A. Shanab,M. M. A. Mohammed,M. M. Ibrahim,I. B. Abdalrahman

HEALTH SCIENCE REPORTSno. 4 (2023)

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Knowledge, Attitudes, and Practices (KAP) During the Malaria Elimination Phase: A Household-Based Cross-Sectional Survey

Siddig Ibrahim Abdelwahab,Ibrahim M. Elhassan,Osama Albasheer,Manal Mohamed Elhassan Taha,Nasir Ahmed Ali,Yahya Salem Al-Jabiri,Waleed Madkhali,Ahmad A. Sahly,Bassem Oraibi,Ahmed Abdallah Ahmed Altraifi,Nasser Hakami,Mohammed M. Alshehri,Mohammad Abu Shaphe,Rashid Ali Beg,Meshal Alshamrani

MEDICINEno. 22 (2023)

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Smell Impairmet and Schizophrania: Genotypic and Phenotypc Correlates in a Familial Cohort

Azza Saeed, Nada Ibraheim,K. Mohamed Ahmed Abbasher,Elfatih A. Hasabo, Roaa Alnour,Reem Hamad, Lamees Ahmed, Safa Abuswar, Amel Eltigani,Ayman A. Hussein,Muntaser E. Ibrahim

Research Square (Research Square) (2023)

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Clinical Phenotyping and Genetic Diagnosis of a Large Cohort of Sudanese Families with Hereditary Spinocerebellar Degenerations

Ashraf Yahia,Ahlam A. A. Hamed,Inaam N. Mohamed,Maha A. Elseed,Mustafa A. Salih,Sarah M. El-sadig, Hassab Elrasoul Siddig, Ali Elsir Musa Nasreldien,Mohamed Ahmed Abdullah, Maha Elzubair, Farouk Yassen Omer,Aisha Motwakil Bakhiet,Rayan Abubaker,Fatima Abozar,Rawaa Adil,Sara Emad,Mhammed Alhassan Musallam,Isra Z. M. Eltazi,Zulfa Omer,Hiba Malik,Mayada O. E. Mohamed,Ali A. Elhassan, Eman O. E. Mohamed,Ahmed K. M. A. Ahmed,Elhami A. A. Ahmed,Esraa Eltaraifee, Bidour K. Hussein,Amal S. I. Abd Allah, Lina Salah,Mohamed Nimir, Omnia M. Tag Elseed, Tasneem E. A. Elhassan, Abubakr Elbashier,Esraa S. A. Alfadul, Moneeb Fadul, Khalil F. Ali,Shaimaa Omer M. A. Taha, Elfatih E. Bushara,Mutaz Amin,Mahmoud Koko,Muntaser E. Ibrahim,Ammar E. Ahmed,Liena E. O. Elsayed,Giovanni Stevanin

European journal of human genetics EJHGno. 10 (2023): 1214-1226

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Editorial: The path towards precision health: Prospects and challenges

Muntaser E. Ibrahim,Ayman Hussein,Maria G. Stathopoulou,Sophie Visvikis-Siest

Frontiers in Medicine (2022): 989746

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