A novel nonsense mutation in DNAJC6 expands the phenotype of autosomal-recessive juvenile-onset Parkinson’s disease LE Elsayed, V Drouet, T Usenko, IN Mohammed, AA Hamed, MA Elseed, ... Ann Neurol 79 (2), 335-337, 2016 | 79 | 2016 |
Expanding the phenome and variome of skeletal dysplasia S Maddirevula, S Alsahli, L Alhabeeb, N Patel, F Alzahrani, ... Genetics in Medicine 20 (12), 1609-1616, 2018 | 57 | 2018 |
Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan LEO Elsayed, IN Mohammed, AAA Hamed, MA Elseed, A Johnson, ... European Journal of Human Genetics 25 (1), 100-110, 2017 | 38 | 2017 |
Fragmentation of 28Si nuclei in nuclear emulsion M El-Nadi, MS El-Nagdy, N Ali-Mossa, A Abdelsalam, AM Abdalla, ... Journal of Physics G: Nuclear and Particle Physics 25 (6), 1169, 1999 | 31 | 1999 |
Effect of pasteurization and storage conditions on the microbiological, chemical and organoleptic properties of Domiati cheese during pickling. AI Hamed, NA El-Saify, SI Farag, F Orsi | 27 | 1992 |
Clinical profile of pediatric neurological disorders: Outpatient department, Khartoum, Sudan IN Mohamed, MA Elseed, AA Hamed Child neurology open 3, 2329048X15623548, 2016 | 24 | 2016 |
Diallel analysis for studying heterosis and combining ability of some economical yield traits in pumpkin AH Hussien, AA Hamed Journal of Plant Production 6 (3), 261-270, 2015 | 22 | 2015 |
Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556 ES Cauley, A Hamed, IN Mohamed, M Elseed, S Martinez, A Yahia, ... Neurogenetics 20, 91-98, 2019 | 21 | 2019 |
Impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and Sudan M Saha, HM Reddy, MA Salih, E Estrella, MD Jones, S Mitsuhashi, ... Physiological genomics 50 (11), 929-939, 2018 | 20 | 2018 |
Brain tuberculoma, an unusual cause of stroke in a child with trisomy 21: a case report AEM Kheir, SA Ibrahim, AA Hamed, BM Yousif, FA Hamid Journal of medical case reports 11, 1-4, 2017 | 19 | 2017 |
Prevalence of epilepsy in 74,949 school children in Khartoum State, Sudan IN Mohamed, MA Elseed, AA Hamed, ME Abdel-Rahman, SM El-Sadig, ... Paediatrics and international child health 37 (3), 188-192, 2017 | 17 | 2017 |
The differential effects of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) on seizure frequency in patients with drug-resistant epilepsy—A randomized, double-blind … FAS Ibrahim, K Ghebremeskel, ME Abdel-Rahman, AAM Ahmed, ... Epilepsy & Behavior 87, 32-38, 2018 | 16 | 2018 |
Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family LEO Elsayed, IN Mohammed, AAA Hamed, MA Elseed, MAM Salih, ... BMC medical genetics 19, 1-5, 2018 | 15 | 2018 |
Storm surge generation by winter cyclones at Alexandria, Egypt AA Hamed, AA El Gindy The International Hydrographic Review, 1988 | 14 | 1988 |
Intelligence quotient (IQ) among children with epilepsy: National epidemiological study–Sudan IN Mohamed, AH Osman, S Mohamed, EK Hamid, AA Hamed, A Alsir, ... Epilepsy & Behavior 103, 106813, 2020 | 13 | 2020 |
Effect of Soxhlet method extraction on characterization of pectin of pumpkin peels AAR Hamed, AEE Elkhedir, SE Mustafa Journal of Experimental Food Chemistry 3 (1), 1-3, 2017 | 11 | 2017 |
Novel Homozygous Missense Mutation in the ARG1 Gene in a Large Sudanese Family LEO Elsayed, IN Mohammed, AAA Hamed, MA Elseed, MAM Salih, ... Frontiers in neurology 11, 569996, 2020 | 10 | 2020 |
Novel variants causing megalencephalic leukodystrophy in Sudanese families M Amin, C Vignal, AAA Hamed, IN Mohammed, MA Elseed, S Drunat, ... Journal of Human Genetics 67 (3), 127-132, 2022 | 8 | 2022 |
A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability M Amin, C Vignal, E Eltaraifee, IN Mohammed, AAA Hamed, MA Elseed, ... BMC Medical Genomics 15 (1), 236, 2022 | 7 | 2022 |
Methylation of alpha-synuclein in a Sudanese cohort Y Bakhit, I Schmitt, A Hamed, EAA Ibrahim, IN Mohamed, SM El-Sadig, ... Parkinsonism & Related Disorders 101, 6-8, 2022 | 7 | 2022 |