| Genetic etiology and clinical challenges of phenylketonuria NA Elhawary, IA AlJahdali, IS Abumansour, EN Elhawary Human Genomics 16 (22), 1-17, 2022 | 47 | 2022 |
| Molecular updating of β-thalassemia mutations in the upper Egyptian population EH Jiffri, N Bogari, KH Zidan, S Teama, NA Elhawary Hemoglobin 34 (6), 538-547, 2010 | 41 | 2010 |
| Frameshift Deletion Mechanisms in Egyptian Duchenne and Becker Muscular Dystrophy Families NA Elhawary, RM Shawky, H Nemat Molecules and Cells 18 (2), 141-149, 2004 | 35 | 2004 |
| The MTHFR 677T Allele May Influence the Severity and Biochemical Risk Factors of Alzheimer’s Disease in an Egyptian Population NA Elhawary, D Hewedi, A Arab, S Teama, H Shaibah, MT Tayeb, ... Disease markers 35 (5), 439-446, 2013 | 34 | 2013 |
| The impact of common tumor necrosis factor haplotypes on the development of asthma in children: an Egyptian model EH Jiffri, NA Elhawary Genetic Testing and Molecular Biomarkers 15 (5), 293-299, 2011 | 29 | 2011 |
| TNF‐238 polymorphism may predict bronchopulmonary dysplasia among preterm infants in the Egyptian population NA Elhawary, MT Tayeb, S Abdel‐Ghafar, M Rashad, AA Alkhotani Pediatric Pulmonology 48 (7), 699-706, 2013 | 27 | 2013 |
| Molecular characterization of exonic rearrangements and frame shifts in the dystrophin gene in Duchenne muscular dystrophy patients in a Saudi community NA Elhawary, EH Jiffri, S Jambi, AH Mufti, A Dannoun, H Kordi, A Khogeer, ... Human genomics 12, 1-11, 2018 | 24 | 2018 |
| Association between ANKK1 (rs1800497) and LTA (rs909253) Genetic Variants and Risk of Schizophrenia A Arab, N Elhawary BioMed Research International 2015 (2015), 821827, 2015 | 24 | 2015 |
| Human genome meeting 2016: Houston, TX, USA. 28 February-2 March 2016 AK Srivastava, Y Wang, R Huang, C Skinner, T Thompson, L Pollard, ... Human genomics 10, 1-40, 2016 | 21 | 2016 |
| Methylenetetrahydrofolate reductase gene variants confer potential vulnerability to autism spectrum disorder in a Saudi community AH Arab, NA Elhawary Neuropsychiatric Disease and Treatment, 3569-3581, 2019 | 18 | 2019 |
| Combined Genetic Biomarkers Confer Susceptibility to Risk of Urothelial Bladder Carcinoma in a Saudi Population NA Elhawary, A Nassir, H Saada, A Dannoun, O Qoqandi, A Alsherif, ... Disease Markers 2017 (1474560), 11, 2017 | 16 | 2017 |
| Screening for six Mediterranean mutations in 90 Egyptian patients with phenylketonuria L Effat, M Essawi, M Abd El Hamid, N Hawari, Y Gad Bratisl Lek Listy 109 (1), 17-19, 2008 | 16 | 2008 |
| Mutations in transglutaminase 1 gene in autosomal recessive congenital ichthyosis in Egyptian families RM Shawky, NS Sayed, NA Elhawary Disease markers 20 (6), 325-332, 2004 | 16 | 2004 |
| Genetic biomarkers predict susceptibility to autism spectrum disorder through interactive models of inheritance in a Saudi community NA Elhawary, MT Tayeb, IA Sindi, N Qutub, M Rashad, A Mufti, AH Arab, ... Cogent Biology 5 (1), 1606555, 2019 | 13 | 2019 |
| Common Tag STSs in the AZF region associated with azoospermia and severe oligospermia in infertile Egyptian men N A Elhawary, N S Seif-Eldin, M Zaki, H Diab, S Teama, S A Saleh The Open Andrology Journal 2 (1), 2010 | 13 | 2010 |
| Transporter TAP1-637G and immunoproteasome PSMB9-60H variants influence the risk of developing vitiligo in the Saudi population NA Elhawary, N Bogari, E Jiffri, M Rashad, A Fatani, M Tayeb Disease markers 2014 (260732), 10.1155/2014/260732, 2014 | 12 | 2014 |
| Effect of stem cell therapy on gentamicin induced testicular dysfunction in rats S Mohamed, N ElHawary, S Mohamed, N Hashim, S Saleh, M Bakeer, ... Journal of Health and Medical Informatics 8 (3), 2017 | 9 | 2017 |
| Risk of Colorectal Carcinoma May Predispose to the Genetic Variants of the GST, CYP450, and TP53 Genes Among Nonsmokers in the Saudi Community IA Sindi, AO Babalghith, MT Tayeb, AH Mufti, H Naffadi, SN Ekram, ... International Journal of General Medicine, 1311-1323, 2021 | 8 | 2021 |
| Null genetic risk of ACE gene polymorphisms with nephropathy in type 1 diabetes among Egyptian population NA Elhawary, N Bogari, M Rashad, MT Tayeb Egyptian Journal of Medical Human Genetics 12 (2), 187-192, 2011 | 8 | 2011 |
| Phenotypic variability to medication management: an update on fragile X syndrome NA Elhawary, IA AlJahdali, IS Abumansour, ZA Azher, AH Falemban, ... Human Genomics 17 (1), 60, 2023 | 6 | 2023 |
Rabah M ShawkyProfessor of Pediatrics and Genetics, Ainshams University, Cairo, Egypt在 med.asu.edu.eg 的电子邮件经过验证
