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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 19, 2023
The epileptology of Wiedemann-Steiner syndrome: Electroclinical findings in five patients with KMT2A pathogenic variantsAhmed N Sahly, Myriam Srour, Daniela Buhas, et al.
Clinical and Experimental Obstetrics & Gynecology|April 7, 2016
Experience of assisted reproductive technology at King Abdulaziz University HospitalH S O Abduljabbar, S T Djamil, N N Sahly, et al.
Saudi Journal of Biological Sciences|January 1, 2020
Whole exome sequencing identifies rare biallelic ALMS1 missense and stop gain mutations in familial Alström syndrome patientsNaglaa M Kamal, Ahmed N Sahly, Babajan Banaganapalli, et al.
Systems Biology in Reproductive Medicine|March 9, 2021
Molecular differential analysis of uterine leiomyomas and leiomyosarcomas through weighted gene network and pathway tracing approachesNora Naif Sahly, Babajan Banaganapalli, Ahmed N Sahly, et al.
Human Genetics|April 5, 2024
Genotype-phenotype correlation in CLCN4-related developmental and epileptic encephalopathyAhmed N Sahly, Juan Sierra-Marquez, Stefanie Bungert-Plümke, et al.
Seizure|March 17, 2023
Epilepsy surgery outcomes in patients with GATOR1 gene complex variants: Report of new cases and review of literatureAhmed N Sahly, Robyn Whitney, Gregory Costain, et al.
Frontiers in Pediatrics|May 13, 2021
Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi FamiliesOmar I Saadah, Babajan Banaganapalli, Naglaa M Kamal, et al.
Plos One|May 16, 2017
Whole exome sequencing of a consanguineous family identifies the possible modifying effect of a globally rare AK5 allelic variant in celiac disease development among Saudi patientsJumana Yousuf Al-Aama, Noor Ahmad Shaik, Babajan Banaganapalli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 5, 2024
Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected IndividualsMeagan L Collins Hutchinson, Judith St-Onge, Sabrina Schlienger, et al.
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