Abdullah Tamim
Varendra University(BD)University of Rajshahi(BD)
Publications by Year
Research Areas
Genomics and Rare Diseases, Metabolism and Genetic Disorders, Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Cancer-related gene regulation
Most-Cited Works
- → The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes(2017)300 cited
- → Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy(2020)53 cited
- → Biallelic Loss‐of‐Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh‐Like Syndrome to Isolated Optic Atrophy(2021)16 cited
- → Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders(2023)10 cited
- → Efficacy and Safety of Perampanel in Children with Drug-Resistant Focal-Onset Seizures: A Retrospective Review(2023)6 cited
- → The efficacy of non-fasting ketogenic diet protocol in the management of intractable epilepsy in pediatric patients: a single center study from Saudi Arabia(2022)6 cited
- → Bi-allelic UGGT1 variants cause a congenital disorder of glycosylation(2025)4 cited
- → Biallelic ZBTB11 Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders(2024)3 cited
- → ADAT3 variants disrupt the activity of the ADAT tRNA deaminase complex and impair neuronal migration(2025)2 cited
- → Neurodevelopmental disorders associated variants in ADAT3 disrupt the activity of the ADAT2/ADAT3 tRNA deaminase complex and impair neuronal migration(2024)