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Journal of Child Psychology and Psychiatry, and Allied Disciplines|May 16, 2019
Retraction: Randomized controlled trial of vitamin D supplementation in children with autism spectrum disorderK Saad, A Abdel-Rahman, Y Elserogy, et al.
American Journal of Medical Genetics. Part A|February 5, 2021
Neurodevelopmental disorder in an Egyptian family with a biallelic ALKBH8 variantAhmed K Saad, Dana Marafi, Tadahiro Mitani, et al.
Frontiers in Public Health|September 15, 2025
The role of public health networks in strengthening public health systems: the case of EMPHNET in the Eastern Mediterranean regionYousef Khader, Dana Shalabi, Leen Daoud, et al.
Biomaterials|December 21, 2021
Perspectives on scaling production of adipose tissue for food applicationsJohn S K Yuen, Andrew J Stout, N Stephanie Kawecki, et al.
Medrxiv : the Preprint Server for Health Sciences|January 8, 2026
Expanding the Clinical and Molecular Spectrum of TUBB2B Through Distinct Variants Identified Across Multiple FamiliesShaghayegh T Beheshti, Angad Jolly, Ahmed K Saad, et al.
Frontiers in Cellular and Infection Microbiology|June 16, 2015
Epidemiology and characteristics of urinary tract infections in children and adolescentsRima H Hanna-Wakim, Soha T Ghanem, Mona W El Helou, et al.
HGG Advances|July 18, 2026
Expanding the clinical and molecular spectrum of TUBB2B through distinct variants identified across multiple familiesShaghayegh T Beheshti, Angad Jolly, Ahmed K Saad, et al.
The International Journal of Cardiovascular Imaging|December 14, 2022
Abnormal echocardiographic findings after COVID-19 infection: a multicenter registrySebastián Garcia-Zamora, José M Picco, Augusto J Lepori, et al.
Clinical Genetics|February 1, 2025
Integrating Prenatal Exome Sequencing and Ultrasonographic Fetal Phenotyping for Assessment of Congenital Malformations: High Molecular Diagnostic Yield and Novel Phenotypic Expansions in a Consanguineous CohortSara H El-Dessouky, Wessam E Sharaf-Eldin, Mona M Aboulghar, et al.
Journal of Inherited Metabolic Disease|September 15, 2023
Biallelic missense variants in COG3 cause a congenital disorder of glycosylation with impairment of retrograde vesicular traffickingRuizhi Duan, Dana Marafi, Zhi-Jie Xia, et al.
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