| A familial PLCB4 mutation causing auriculocondylar syndrome 2 with variable severity A Nabil, S El Shafei, NM El Shakankiri, A Habib, H Morsy, S Maddirevula, ... European Journal of Medical Genetics 63 (6), 103917, 2020 | 17 | 2020 |
| MDR1 gene polymorphism and outcome in Egyptian chronic myeloid leukaemia patients O Ghallab, NAM Hamed, S El Shafei, R Abo, S Sherif clinical evidence 8, 9, 2015 | 10 | 2015 |
| Genetic determinants of essential hypertension SA El-Shafei, A Bassili, NM Hassanien, MM Mokhtar J Egypt Public Health Assoc 77 (3-4), 231-46, 2002 | 10 | 2002 |
| CYP1B1 and myocilin gene mutations in Egyptian patients with primary congenital glaucoma MR Fassad, AK Amin, HA Morsy, NM Issa, NH Bayoumi, SA El Shafei, ... Egyptian Journal of Medical Human Genetics 18 (3), 219-224, 2017 | 8 | 2017 |
| The association of angiotensinogen converting enzyme [ACE] insertion/deletion polymorphism with preeclamptic women in Alexandria–Egypt SA El Shafei The Egyptian Journal of Medical Human Genetics 8 (1), 57-67, 2007 | 1 | 2007 |
| Frequency of congenital heart disease in oculoauriculovertebral spectrum and assessment of two biomarkers A Nabil, S El Shafei, N El Shakankiry, A Habib, H Morsy FEBS OPEN BIO 12, 42-43, 2022 | | 2022 |
| Frequency of Arg972-IRS-1 Variant among Type I Diabetic Patients in El-Shatby Patients in El-Shatby Pediatric Hospital, Alexandria, Egypt SA El-Shafei, MF El-Belvesy, MH Zein El-Din, MO Abdou Journal of High Institute of Public Health 34 (3), 641-650, 2004 | | 2004 |
| The benefit of early diagnosis and management of phenylketonuria SA El Shafei Alexandria Journal of Pediatrics 16 (1), 97-102, 2002 | | 2002 |
| Genetic study of glucose-6-phosphate dehydrogenase [G-6-PD] in Alexandria: frequency and variants MM Eissa, SA El Shafei Alexandria Journal of Pediatrics 15 (1), 67-71, 2001 | | 2001 |
| Multidrug resistance 1 gene polymorphism and resistance to tyrosine kinase inhibitors in Egyptian chronic myeloid leukaemia patients O Ghallab, NAM Hamed, S El Shafei, R Abo | | |
