| Prevalence of HBV and HCV infection among multi-transfused Egyptian thalassemic patients. DAM Mansour AK, Aly RM, Abdelrazek SY, Elghannam DM, Abdelaziz SM, Shahine ... Hematol Oncol Stem Cell The 5 (1), 54 - 9, 2012 | 86* | 2012 |
| Increased DNA damage in children caused by passive smoking as assessed by comet assay and oxidative stress A Zalata, S Yahia, A El-Bakary, HM Elsheikha Mutation Research/Genetic Toxicology and Environmental Mutagenesis 629 (2 …, 2007 | 82 | 2007 |
| Influence of hyperbilirubinemia and phototherapy on markers of genotoxicity and apoptosis in full-term infants S Yahia, AE Shabaan, M Gouida, D El-Ghanam, H Eldegla, A El-Bakary, ... European journal of pediatrics 174, 459-464, 2015 | 62 | 2015 |
| Predictors of anxiety and depression in Egyptian thalassemic patients: a single center study S Yahia, MA El-Hadidy, AH El-Gilany, R Anwar, A Darwish, AK Mansour International journal of hematology 97, 604-609, 2013 | 60 | 2013 |
| Leptin, insulin and thyroid hormones in a cohort of Egyptian obese Down syndrome children: a comparative study S Yahia, RM El-Farahaty, AK El-Hawary, MA El-Hussiny, H Abdel-Maseih, ... BMC endocrine disorders 12, 1-7, 2012 | 49 | 2012 |
| Interleukin-17A rs2275913, Interleukin-17F rs763780 and rs2397084 gene polymorphisms as possible risk factors in Juvenile lupus and lupus related nephritis A Hammad, YM Mosaad, EM Hammad, S Elhanbly, SR El-Bassiony, ... Autoimmunity 49 (1), 31-40, 2016 | 48 | 2016 |
| Cytogenetic and comorbidity profile of Down syndrome in Mansoura University Children's Hospital, Egypt AH El-Gilany, S Yahia, M Shoker, F El-Dahtory Indian journal of human genetics 17 (3), 157, 2011 | 41 | 2011 |
| A novel homozygous p. Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome M Al-Haggar, A Madej-Pilarczyk, L Kozlowski, JM Bujnicki, S Yahia, ... European journal of human genetics 20 (11), 1134-1140, 2012 | 39 | 2012 |
| Prevalence of congenital heart diseases in children with Down syndrome in Mansoura, Egypt: a retrospective descriptive study AH El-Gilany, S Yahia, Y Wahba Annals of Saudi medicine 37 (5), 386-392, 2017 | 37 | 2017 |
| Sirenomelia (symelia apus) with Potter's syndrome in connection with gestational diabetes mellitus: a case report and literature review M Al-Haggar, S Yahia, D Abdel-Hadi, F Grill, A Al Kaissi African health sciences 10 (4), 2010 | 36 | 2010 |
| Expression of lung resistance protein and multidrug resistance-related protein (MRP1) in pediatric acute lymphoblastic leukemia ER EEl-Sharnouby JA, Abou El-Enein AM, El Ghannam DM, El-Shanshory MR, Hagag ... J Oncol Pharm Pract 16 (3), 179 - 88, 2010 | 31 | 2010 |
| Glucosidase acid beta gene mutations in Egyptian children with Gaucher disease and relation to disease phenotypes Z El-Morsy, MT Khashaba, OES Soliman, S Yahia, DA El-Hady World Journal of Pediatrics 7, 326-330, 2011 | 27 | 2011 |
| Rapunzel syndrome (gastric trichobezoar), a rare presentation with generalised oedema: case report and review of the literature I Nour, M Abd Alatef, A Megahed, S Yahia, Y Wahba, AE Shabaan Paediatrics and International Child Health 39 (1), 76-78, 2019 | 25 | 2019 |
| Low expression of glucocorticoid receptors in children with steroid-resistant nephrotic syndrome A Hammad, S Yahia, MS Gouida, A Bakr, RM El-farahaty Pediatric Nephrology 28, 759-763, 2013 | 25 | 2013 |
| Human Metapneumovirus (hMPV) in acute respiratory infection: a clinic-based study in Egypt S Yahia, AY Kandeel, E Hammad, AH El-Gilany The Indian Journal of Pediatrics 79, 1323-1327, 2012 | 24 | 2012 |
| Prevalence of iron deficiency anemia and beta thalassemia carriers among relatives of beta thalassemia patients in Nile Delta region, Egypt: a multicenter study MR El-Shanshory, LM Sherief, HM Hassab, SM Ragab, S Yahia, ... Journal of the Egyptian Public Health Association 96, 1-8, 2021 | 22 | 2021 |
| Cytoprotective effect of honey against chromosomal breakage in fanconi anemia patients in vitro FAM El-Dahtory, S Yahia Indian journal of human genetics 17 (2), 77, 2011 | 21 | 2011 |
| Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: unusual clinical associations and novel claudin16 mutation in an Egyptian family M Al-Haggar, A Bakr, T Tajima, K Fujieda, A Hammad, O Soliman, ... Clinical and experimental nephrology 13, 288-294, 2009 | 21 | 2009 |
| Optimal method for collection of umbilical cord blood: An E gyptian trial for a public cord blood bank MR Bassiouny, F El‐Chennawi, AK Mansour, S Yahia, A Darwish Transfusion 55 (6), 1263-1268, 2015 | 20 | 2015 |
| Markers of apoptosis and proliferation related gene products as predictors of treatment outcome in childhood acute lymphoblastic leukemia M Hafez, Y Al-Tonbary, MA El-Bayoumi, N Hatem, S Hawas, A Mansour, ... Hematology 12 (3), 209-218, 2007 | 18 | 2007 |
