| Novel PITX 2 gene mutations in patients with Axenfeld‐Rieger syndrome M Seifi, T Footz, SAM Taylor, GM Elhady, EM Abdalla, MA Walter Acta Ophthalmologica 94 (7), e571-e579, 2016 | 23 | 2016 |
| De novo EDA mutations: Variable expression in two Egyptian families A Gaczkowska, EM Abdalla, KML Dowidar, GM Elhady, PP Jagodzinski, ... Archives of Oral Biology 68, 21-28, 2016 | 19 | 2016 |
| The association between interleukin 1 beta promoter polymorphisms and keratoconus incidence and severity in an Egyptian population KM Nabil, GM Elhady, H Morsy Clinical Ophthalmology, 2217-2223, 2019 | 11 | 2019 |
| Chromosomal aberrations in 224 couples with recurrent pregnancy loss GM Elhady, S Kholeif, N Nazmy Journal of Human Reproductive Sciences 13 (4), 340-348, 2020 | 10 | 2020 |
| The effect of teratozoospermia on sex chromosomes in human embryos DM Nayel, HSED Mahrous, EED Khalifa, S Kholeif, GM Elhady The application of clinical genetics 14, 125, 2021 | 5 | 2021 |
| Familial reciprocal non robertsonian translocation t (14; 22) resulting in 22q11. 2 deletion syndrome N Nazmy, G Elhady, E Refaat, S Kholeif The Turkish Journal of Pediatrics 61 (5), 780-785, 2019 | 1 | 2019 |
| The Use of Fluorescence In situ Hybridisation in the Diagnosis of Hidden Mosaicism in Egyptian Patients with Turner Syndrome HM Ossama, S Kholeif, GM Elhady Journal of Human Reproductive Sciences 16 (4), 286-298, 2023 | | 2023 |
| Sperm chromosomal abnormalities in infertile men with failed intracytoplasmic sperm injection (ICSI) RF Elnahas, AK Behery, S Kholeif, YI Orief, GM Elhady Middle East Fertility Society Journal 28 (1), 18, 2023 | | 2023 |
| Cytogenetic abnormalities in a sample of females with premature ovarian failure NM Issa, GM Elhady Middle East Fertility Society Journal 27 (1), 7, 2022 | | 2022 |
| Association of CHEK2 I157T and SULT1A1 R213H genetic variants with risk of sporadic colorectal cancer in a sample of Egyptian patients GM Elhady, MA Elnaggar, LM Desouky Egyptian Journal of Medical Human Genetics 23 (1), 18, 2022 | | 2022 |
| Discovery of a novel deletion in PITX2 by dye-based quantitative PCR confirms that haploinsufficiency is a disease-causing mechanism for Axenfeld-Rieger Syndrome M Seifi, T Footz, EM Abdalla, KM Nabil, GM Elhady, R Ritch, MA Walter Investigative Ophthalmology & Visual Science 55 (13), 6416-6416, 2014 | | 2014 |
