| 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 | 568 | 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 | 93 | 2013 |
| Revisiting the harem conspiracy and death of Ramesses III: anthropological, forensic, radiological, and genetic study Z Hawass, S Ismail, A Selim, SN Saleem, D Fathalla, S Wasef, AZ Gad, ... BMJ 345, 2012 | 80 | 2012 |
| Molecular analysis of 5α‐reductase type 2 gene in eight unrelated Egyptian children with suspected 5α‐reductase deficiency: prevalence of the G34R mutation I Mazen, YZ Gad, M Hafez, C Sultan, S Lumbroso Clinical endocrinology 58 (5), 627-631, 2003 | 72 | 2003 |
| DNA copy number changes in Schistosoma-associated and non-Schistosoma-associated bladder cancer D Kamel, ML Larramendy, S Shoman, Y Gad, S Baithun, M El-Awady, ... The American journal of pathology 156 (3), 871-878, 2000 | 54 | 2000 |
| Extracellular miR-145, miR-223 and miR-326 expression signature allow for differential diagnosis of immune-mediated neuroinflammatory diseases WE Sharaf-Eldin, NA Kishk, YZ Gad, H Hassan, MAM Ali, MS Zaki, ... Journal of the Neurological Sciences 383, 188-198, 2017 | 47 | 2017 |
| 5α-Reductase deficiency in patients with micropenis YZ Gad, H Nasr, I Mazen, N Salah, R El-Ridi Journal of inherited metabolic disease 20, 95-101, 1997 | 37 | 1997 |
| Familial Leydig cell hypoplasia as a cause of male pseudohermaphroditism MK El-Awady, SA Temtamy, MA Salam, YZ Gad Human heredity 37 (1), 36-40, 1987 | 36 | 1987 |
| Studies of up-regulation of androgen receptors in genital skin fibroblasts YZ Gad, GD Berkovitz, CJ Migeon, TR Brown Molecular and cellular endocrinology 57 (3), 205-213, 1988 | 31 | 1988 |
| Schistosoma hematobium soluble egg antigens induce proliferation of urothelial and endothelial cells MK El-Awady, YZ Gad, Y Wen, M Eassawi, L Effat, KS Amr, S Ismail, ... World journal of urology 19, 263-266, 2001 | 22 | 2001 |
| A novel double mutation in the luteinizing hormone receptor in a kindred with familial Leydig cell hypoplasia and male pseudohermaphroditism R Pals-Rylaarsdam, G Liu, W Brickman, L Duranteau, J Monroe, ... Endocrine research 31 (4), 307-323, 2005 | 19 | 2005 |
| Screening for six Mediterranean mutations in 90 Egyptian patients with phenylketonuria LK Effat, ML Essawi, MS Abd El Hamid, N Hawari, YZ Gad Bratislavske lekarske listy 109 (1), 17, 2008 | 16 | 2008 |
| Dihydrotestosterone regulates plasma sex‐hormone‐binding globulin in prepubertal males MK EL‐AWADY, MA Salam, YZ Gad, J El‐Saban Clinical endocrinology 30 (3), 279-284, 1989 | 16 | 1989 |
| 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 | 15 | 2021 |
| Biochemical Analysis of Four Missense Mutations in the HSD17B3 Gene Associated with 46, XY Disorders of Sex Development in Egyptian Patients RT Engeli, M Tsachaki, HA Hassan, CP Sager, ML Essawi, YZ Gad, ... The journal of sexual medicine 14 (9), 1165-1174, 2017 | 15 | 2017 |
| 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 YZ Gad, R Khairt, I Mazen, HG Osman Sexual Development 1 (5), 293-296, 2007 | 13 | 2007 |
| Molecular analysis of androgen resistance syndromes in Egyptian patients. M Essawi, YZ Gad, O El-Rouby, SA Temtamy, YA Sabour, MK El-Awady Disease markers 13 (2), 99-105, 1997 | 13 | 1997 |
| Intersex disorders among Egyptian patients I Mazen, Y Gad, A Khalil J Arab Child 7, 607-625, 1996 | 13 | 1996 |
| A Novel Nonsense Mutation in Exon 1 of HSD17B3 Gene in an Egyptian 46,XY Adult Female Presenting with Primary Amenorrhea HA Hassan, I Mazen, YZ Gad, OSM Ali, M Mekkawy, ML Essawi Sexual Development 7 (6), 277-281, 2013 | 11 | 2013 |
| The milder phenotype of the dystrophin gene double deletions AA El‐Harouni, KS Amr, LK Effat, ML Eassawi, S Ismail, YZ Gad, ... Acta neurologica scandinavica 107 (6), 400-404, 2003 | 11 | 2003 |
Rabab KhairatAssociate professor, National Research Centrenrc.sci.eg의 이메일 확인됨