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Frontiers in Neurology|May 10, 2019
A Novel Homozygous Non-sense Mutation in the Catalytic Domain of MTHFR Causes Severe 5,10-Methylenetetrahydrofolate Reductase DeficiencySalam Massadeh, Muhammad Umair, Manal Alaamery, et al.Genes|February 25, 2022
Consanguinity and Congenital Heart Disease Susceptibility: Insights into Rare Genetic Variations in Saudi ArabiaNour Albesher, Salam Massadeh, Sabah M Hassan, et al.Journal of Epidemiology and Global Health|January 3, 2022
Correlation between ABO Blood Group Phenotype and the Risk of COVID-19 Infection and Severity of Disease in a Saudi Arabian CohortDunia Jawdat, Ali Hajeer, Salam Massadeh, et al.Journal of Medical Genetics|February 2, 2017
A missense mutation in the <i>CRBN</i> gene that segregates with intellectual disability and self-mutilating behaviour in a consanguineous Saudi familyAtia Sheereen, Manal Alaamery, Shahad Bawazeer, et al.Journal of Medical Case Reports|May 7, 2026
Jagged-1 mutation is associated with congenital heart defects: a case reportOthman Alahmed, Manal Alaamery, Fahad Alhabshan, et al.Polymers|April 30, 2021
Development of Epirubicin-Loaded Biocompatible Polymer PLA-PEG-PLA Nanoparticles: Synthesis, Characterization, Stability, and In Vitro Anticancerous AssessmentSalam Massadeh, Iman Almohammed, Eman Barhoush, et al.Clinical Genetics|April 15, 2020
PDCD6IP, encoding a regulator of the ESCRT complex, is mutated in microcephalyAmjad Khan, Manal Alaamery, Salam Massadeh, et al.Clinical Immunology (Orlando, Fla.)|December 20, 2021
Association of KIR gene polymorphisms with COVID-19 diseaseAli Hajeer, Dunia Jawdat, Salam Massadeh, et al.Journal of Infection and Public Health|August 22, 2024
Association between human leukocyte antigen alleles and COVID-19 disease severityAli Hajeer, Dunia Jawdat, Salam Massadeh, et al.Genes|February 25, 2022
The Role of the Disrupted Podosome Adaptor Protein (SH3PXD2B) in Frank-Ter Haar SyndromeSalam Massadeh, Fahad Alhabshan, Hadeel N AlSudairi, et al.Pageof 4