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Stephany El-Hayek
Stephany El-Hayek
Centre for Arab Genomic Studies
Dirección de correo verificada de hmaward.org.ae
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Año
Mammalian oocytes locally remodel follicular architecture to provide the foundation for germline-soma communication
S El-Hayek, Q Yang, L Abbassi, G FitzHarris, HJ Clarke
Current Biology 28 (7), 1124-1131. e3, 2018
1272018
Follicle-stimulating hormone regulates expression and activity of epidermal growth factor receptor in the murine ovarian follicle
S El-Hayek, I Demeestere, HJ Clarke
Proceedings of the National Academy of Sciences 111 (47), 16778-16783, 2014
1012014
Kefir exhibits anti‑proliferative and pro‑apoptotic effects on colon adenocarcinoma cells with no significant effects on cell migration and invasion
N Khoury, S El‑Hayek, O Tarras, M El‑Sabban, M El‑Sibai, S Rizk
International journal of oncology 45 (5), 2117-2127, 2014
852014
Control of oocyte growth and development by intercellular communication within the follicular niche
S El-Hayek, HJ Clarke
Molecular Mechanisms of Cell Differentiation in Gonad Development, 191-224, 2016
702016
Follicle-stimulating hormone increases gap junctional communication between somatic and germ-line follicular compartments during murine oogenesis
S El-Hayek, HJ Clarke
Biology of reproduction 93 (2), 47, 1-10, 2015
602015
Active fluctuations of the nuclear envelope shape the transcriptional dynamics in oocytes
M Almonacid, A Al Jord, S El-Hayek, A Othmani, F Coulpier, S Lemoine, ...
Developmental Cell 51 (2), 145-157. e10, 2019
462019
Epidermal growth factor receptor signaling uncouples germ cells from the somatic follicular compartment at ovulation
L Abbassi, S El-Hayek, KF Carvalho, W Wang, Q Yang, ...
Nature communications 12 (1), 1438, 2021
452021
Antiproliferative and proapoptotic effects of topotecan in combination with thymoquinone on acute myelogenous leukemia
R Khalife, EH Stephany, O Tarras, MH Hodroj, S Rizk
Clinical Lymphoma Myeloma and Leukemia 14, S46-S55, 2014
352014
Contribution of next generation sequencing in pediatric practice in Lebanon. A Study on 213 cases
P Nair, S Sabbagh, H Mansour, A Fawaz, G Hmaimess, P Noun, ...
Molecular Genetics & Genomic Medicine 6 (6), 1041-1052, 2018
322018
A 20-year clinical and genetic neuromuscular cohort analysis in Lebanon: an international effort
A Megarbane, S Bizzari, A Deepthi, S Sabbagh, H Mansour, E Chouery, ...
Journal of Neuromuscular Diseases 9 (1), 193-210, 2022
212022
COQ8A and MED25 mutations in a child with intellectual disability, microcephaly, seizures, and spastic ataxia: synergistic effect of digenic variants
P Nair, M Lama, S El-Hayek, G Abou Sleymane, S Stora, M Obeid, ...
Molecular syndromology 9 (6), 319-323, 2019
132019
Catalogue for transmission genetics in Arabs (CTGA) database: analysing Lebanese data on genetic disorders
S Bizzari, P Nair, A Deepthi, S Hana, MT Al-Ali, A Megarbané, S El-Hayek
Genes 12 (10), 1518, 2021
112021
Homozygous deletion of exons 2–7 within TGFB3 gene in a child with severe Loeys‐Dietz syndrome and Marfan‐like features
A Mégarbané, A Deepthi, M Obeid, M T. Al‐Ali, A Gambarini, S El‐Hayek
American Journal of Medical Genetics Part A 182 (5), 1230-1235, 2020
102020
Recessive marfanoid syndrome with herniation associated with a homozygous mutation in Fibulin-3
S Bizzari, L El-Bazzal, P Nair, A Younan, S Stora, C Mehawej, S El-Hayek, ...
European journal of medical genetics 63 (5), 103869, 2020
102020
SOX11-related syndrome: report on a new case and review
V Wakim, P Nair, V Delague, S Bizzari, MT Al-Ali, C Castro, A Gambarini, ...
Clinical Dysmorphology 30 (1), 44-49, 2021
92021
The Lebanese allele in the PET100 gene: report on two new families with cytochrome c oxidase deficiency
H Mansour, S Sabbagh, S Bizzari, S El-Hayek, E Chouery, A Gambarini, ...
Journal of Pediatric Genetics 8 (03), 172-178, 2019
82019
Growth In Vitro of Granulosa Cell–Oocyte Complexes of the Mouse
S El-Hayek, Q Yang, HJ Clarke
Mouse Oocyte Development: Methods and Protocols, 1-11, 2018
62018
The Pro-apoptotic effect of kefir in Malignant T-lymphocytes Involves a p53 Dependent Pathway
S Rizk, K Maalouf, H Nasser, S El-Hayek
Clinical Lymphoma, Myeloma and Leukemia 13, S367, 2013
62013
Further delineation of the TRAPPC6B disorder: report on a new family and review
P Nair, L El-Bazzal, H Mansour, S Sabbagh, MT Al-Ali, A Gambarini, ...
Journal of Pediatric Genetics 8 (04), 252-256, 2019
52019
A novel PDE6D mutation in a patient with Joubert syndrome type 22 (JBTS22)
A Mégarbané, G Hmaimess, S Bizzari, L El-Bazzal, MT Al-Ali, S Stora, ...
European Journal of Medical Genetics 62 (11), 103576, 2019
52019
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