| 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 | 52 | 2014 |
| 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 |
| 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 | 38 | 2022 |
| 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 | 37 | 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 | 22 | 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 | 20 | 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 | 8 | 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 | 8 | 2020 |
| A clinical study of serum calcium, phosphorus, and alkaline phosphates level in type II Diabetes mellitus among Sudanese population in Khartoum State, 2012 NA Hamad, LB Eltayeb, SL Brair, KH Bakheit, HZ Hamdan, WH Omer جامعة النيلين-مركز النيلين الطبي, 2013 | 8 | 2013 |
| 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), 1-8, 2014 | 5 | 2014 |
| 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 | 4 | 2023 |
| 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 | 3 | 2021 |
| 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 |
| 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 | 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 MedicineBestätigte E-Mail-Adresse bei sidra.org
