Angham Abdulrahman Abdulkareem

Whole Exome Sequencing Identifies Three Novel Mutations in the ASPM Gene From Saudi Families Leading to Primary Microcephaly

Muhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Osama Y. Muthaffar et al. · Frontiers in Pediatrics · 2021 · 21 citations · Full text

Identification of Novel Gene Signatures using Next-Generation Sequencing Data from COVID-19 Infection Models: Focus on Neuro-COVID and Potential Therapeutics

Peter Natesan Pushparaj, Angham Abdulrahman Abdulkareem, Muhammad Imran Naseer · Frontiers in Pharmacology · 2021 · 21 citations · Full text

Experimental manipulations of the subthalamic nucleus fail to suppress tonic seizures in the electroshock model of epilepsy

Safa Shehab, Miloš Ljubisavljević, F. Al-Halhali et al. · Experimental Brain Research · 2006 · 18 citations

Neurodynamics, Neurophysiology, Neuroanatomy +11

A novel homozygous mutation in SZT2 gene in Saudi family with developmental delay, macrocephaly and epilepsy

Muhammad Imran Naseer, Mohammad Khalid Alwasiyah, Angham Abdulrahman Abdulkareem et al. · Genes & Genomics · 2018 · 18 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

Exome Analysis Identified Novel Homozygous Splice Site Donor Alteration in NT5C2 Gene in a Saudi Family Associated With Spastic Diplegia Cerebral Palsy, Developmental Delay, and Intellectual Disability

Muhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Peter Natesan Pushparaj et al. · Frontiers in Genetics · 2020 · 18 citations · Full text