| Overt and occult hepatitis B virus infection in adult Sudanese HIV patients H Mudawi, W Hussein, M Mukhtar, M Yousif, O Nemeri, D Glebe, ... International Journal of Infectious Diseases 29, 65-70, 2014 | 56 | 2014 |
| Qatar Genome: insights on genomics from the Middle East H Mbarek, G Devadoss Gandhi, S Selvaraj, W Al‐Muftah, R Badji, ... Human Mutation 43 (4), 499-510, 2022 | 53 | 2022 |
| Allelic imbalance in regulation of ANRIL through chromatin interaction at 9p21 endometriosis risk locus H Nakaoka, A Gurumurthy, T Hayano, S Ahmadloo, WH Omer, ... PLoS genetics 12 (4), e1005893, 2016 | 45 | 2016 |
| Genotyping and virological characteristics of hepatitis B virus in HIV-infected individuals in Sudan M Yousif, H Mudawi, W Hussein, M Mukhtar, O Nemeri, D Glebe, ... International Journal of Infectious Diseases 29, 125-132, 2014 | 43 | 2014 |
| Thousands of Qatari genomes inform human migration history and improve imputation of Arab haplotypes RM Razali, J Rodriguez-Flores, M Ghorbani, H Naeem, W Aamer, ... Nature Communications 12 (1), 5929, 2021 | 29 | 2021 |
| PGAP3 Associated with Hyperphosphatasia with Mental Retardation Plays a Novel Role in Brain Morphogenesis and Neuronal Wiring at Early Development SI Da’as, W Aamer, W Hasan, A Al-Maraghi, A Al-Kurbi, H Kilani, ... Cells 9 (8), 1782, 2020 | 22 | 2020 |
| Prevalence of Hepatitis B surface antigen and Hepatitis C virus antibodies among pre-surgery screened patients in Khartoum, Central Sudan EA Osman, NA Abdulrahman, O Abbass, WH Omer, HA Saad, ... Journal of General and Molecular Virology 4 (1), 6-9, 2012 | 18 | 2012 |
| Comparison of different diagnostic methodsof Helicobacter pylori infection in Sudanese patients N Abdalsadeg, AA Adam, H Abdul-Aziz, WH Omer, HA Osman, AK Bolad Al Neelain Med J 2 (4), 27-34, 2012 | 18 | 2012 |
| Ethnic-specific association of amylase gene copy number with adiposity traits in a large Middle Eastern biobank N Rossi, E Aliyev, A Visconti, ASA Akil, N Syed, W Aamer, SS Padmajeya, ... NPJ Genomic Medicine 6 (1), 8, 2021 | 9 | 2021 |
| Association of HLA‐DR‐DQ alleles, haplotypes, and diplotypes with type 1 diabetes in Saudis N Eltayeb‐Elsheikh, E Khalil, M Mubasher, A AlJurayyan, H AlHarthi, ... Diabetes/Metabolism Research and Reviews 36 (8), e3345, 2020 | 9 | 2020 |
| Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study M Abdi, E Aliyev, B Trost, M Kohailan, W Aamer, N Syed, R Shaath, ... Genome Medicine 15 (1), 81, 2023 | 6 | 2023 |
| Genome-wide linkage and exome analyses identify variants of HMCN1for splenic epidermoid cyst WH Omer, A Narita, K Hosomichi, S Mitsunaga, Y Hayashi, A Yamashita, ... BMC Medical Genetics 15, 1-8, 2014 | 6 | 2014 |
| A novel STK4 mutation impairs T cell immunity through dysregulation of cytokine-induced adhesion and chemotaxis genes A Guennoun, S Bougarn, T Khan, R Mackeh, M Rahman, F Al-Ali, M Ata, ... Journal of Clinical Immunology 41 (8), 1839-1852, 2021 | 5 | 2021 |
| Molecular characterization and genotyping of hepatitis C virus from Sudanese end-stage renal disease patients on haemodialysis T Zitha, CY Chen, H Mudawi, W Hussein, M Mukhtar, M Shigidi, ... BMC Infectious Diseases 22 (1), 848, 2022 | 3 | 2022 |
| Distribution of erythrocyte binding antigen 175 (EBA-175) gene dimorphic alleles in Plasmodium falciparumfield isolates from Sudan AAM Adam, AAA Amine, DA Hassan, WH Omer, BY Nour, AZ Jebakumar, ... BMC Infectious Diseases 13, 1-6, 2013 | 3 | 2013 |
| Assessing the genetic burden of familial hypercholesterolemia in a large middle eastern biobank GD Gandhi, W Aamer, N Krishnamoorthy, N Syed, E Aliyev, A Al-Maraghi, ... Journal of Translational Medicine 20 (1), 502, 2022 | 2 | 2022 |
| Patterns and distribution of de novo mutations in multiplex Middle Eastern families M Kohailan, W Aamer, N Syed, S Padmajeya, S Hussein, A Sayed, ... Journal of Human Genetics 67 (10), 579-588, 2022 | 2 | 2022 |
| A de novo start-loss in EFTUD2 associated with mandibulofacial dysostosis with microcephaly: case report M Kohailan, O Al-Saei, S Padmajeya, W Aamer, N Elbashir, AAS Akil, ... Molecular Case Studies 8 (4), a006206, 2022 | 2 | 2022 |
| A recessive variant in SIM2 in a child with complex craniofacial anomalies and global developmental delay AA Al-Kurbi, SI Da'as, W Aamer, N Krishnamoorthy, I Poggiolini, ... European Journal of Medical Genetics 65 (4), 104455, 2022 | 2 | 2022 |
| Analysis of HLA gene polymorphisms in East Africans reveals evidence of gene flow in two Semitic populations from Sudan W Aamer, HY Hassan, H Nakaoka, K Hosomichi, M Jaeger, H Tahir, ... European Journal of Human Genetics 29 (8), 1259-1271, 2021 | 2 | 2021 |
Elbay AliyevSidra Medicine在 sidra.org 的电子邮件经过验证
