| New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing A Keller, A Graefen, M Ball, M Matzas, V Boisguerin, F Maixner, ... Nature communications 3 (1), 698, 2012 | 580 | 2012 |
| Ancestry and pathology in King Tutankhamun's family Z Hawass, YZ Gad, S Ismail, R Khairat, D Fathalla, N Hasan, A Ahmed, ... Jama 303 (7), 638-647, 2010 | 539 | 2010 |
| First insights into the metagenome of Egyptian mummies using next-generation sequencing R Khairat, M Ball, CCH Chang, R Bianucci, AG Nerlich, M Trautmann, ... Journal of applied genetics 54, 309-325, 2013 | 90 | 2013 |
| New insights into the Tyrolean Iceman’s origin and phenotype as inferred by whole-genome sequencing. Nat Commun 3: 698 A Keller, A Graefen, M Ball, M Matzas, V Boisguerin, F Maixner, ... | 13 | 2012 |
| Detection of the G34R Mutation in the 5 Alpha Reductase 2 Gene by Allele Specific PCR and Its Linkage to the 89L Allele among Egyptian Cases GYZKRMIO H.G. Sexual Development 1 (5), 293–296, 2007 | 13 | 2007 |
| Epigenetic effects toward new insights as potential therapeutic target in B-thalassemia NH Eltaweel, GY ElKamah, R Khairat, HAE Atia, KS Amr Journal of Genetic Engineering and Biotechnology 19 (1), 51, 2021 | 11 | 2021 |
| Insights from ancient DNA analysis of Egyptian human mummies: clues to disease and kinship YZ Gad, NAM Hassan, DM Mousa, FA Fouad, SG El-Sayed, ... Human Molecular Genetics 30 (R1), R24-R28, 2021 | 10 | 2021 |
| Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1 N N Abdel‐Aziz, G Y El‐Kamah, R A Khairat, H R Mohamed, Y Z Gad, ... Molecular Genetics & Genomic Medicine 9 (12), e1631, 2021 | 9 | 2021 |
| VDR gene expression in asthmatic children patients in relation to vitamin D status and supplementation A Ramadan, SF Sallam, MS Elsheikh, SR Ishak, MGR Abdelsayed, ... Gene Reports 15, 100387, 2019 | 8 | 2019 |
| New insights into the Tyrolean Iceman’s origin and phenotype as inferred by whole-genome sequencing. Nat Commun. 2012; 3: 698 A Keller, A Graefen, M Ball, M Matzas, V Boisguerin, F Maixner | 6 | |
| Expansion of the phenotypic and mutational spectrum of Carpenter syndrome R Khairat, R Elhossini, N Sobreira, E Wohler, G Otaify, AM Mohamed, ... European Journal of Medical Genetics 65 (1), 104377, 2022 | 4 | 2022 |
| Bioarcheology: Medicine, Biology, and forensic sciences O Appenzeller, TG Bromage, R Khairat, AG Nerlich, FJ Rühli BioMed research international 2015, 2015 | 4 | 2015 |
| Maternal and paternal lineages in King Tutankhamun’s family YZ Gad, S Ismail, D Fathalla, R Khairat, S Fares, AZ Gad, R Saad, ... Guardian of Ancient Egypt: Essays in Honor of Zahi Hawass, 2020 | 2 | 2020 |
| Broadening the clinical spectrum of ALGS: an Egyptian cohort with five novel mutations in JAG1 gene R Khairat, H El-Karaksy, HT El-Bassyouni, AK Saad, E Rabie, K Hamed, ... Egyptian Journal of Medical Human Genetics 23 (1), 28, 2022 | 1 | 2022 |
| Association of Adiponectin− 11377 C/G (rs266729) Gene Polymorphism with Nonalcoholic Fatty Liver Disease and Metabolic Features in Egyptian Women M Zaki Al-Azhar University Journal of Virus Researches and Studies 2 (1), 1-10, 2020 | 1 | 2020 |
| Case of autosomal-recessive spinal muscular atrophy with respiratory distress type 1 caused by compound heterozygous mutations in immunoglobulin-binding protein 2 gene … R Khairat, MS Zaki, AI Harkan, H Dawoud Middle East Journal of Medical Genetics 10 (2), 76, 2021 | | 2021 |
| Current Science International Volume: 10| Issue: 04| Oct.–Dec.| 2021 MA Khalifa, IH Zidan, ZM Abdelhakim | | |
