|
| 37998513 | <i>TGFBR1</i> Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy. | J Cardiovasc Dev Dis | 2023 |
| 34929414 | Association of KIR gene polymorphisms with COVID-19 disease. | Clin Immunol | 2022 |
| 36145626 | Reply to Zandi, M.; Soltani, S. Comment on "Alfassam et al. Development of a Colorimetric Tool for SARS-CoV-2 and Other Respiratory Viruses Detection Using Sialic Acid Fabricated Gold Nanoparticles. <i>Pharmaceutics</i> 2021, <i>13</i>, 502". | Pharmaceutics | 2022 |
| 36035137 | Analysis of chronic kidney disease patients by targeted next-generation sequencing identifies novel variants in kidney-related genes. | Front Genet | 2022 |
| 36327219 | Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. | PLoS Genet | 2022 |
| 34978705 | Correlation between ABO Blood Group Phenotype and the Risk of COVID-19 Infection and Severity of Disease in a Saudi Arabian Cohort. | J Epidemiol Glob Health | 2022 |
| 35214093 | Fast-Dissolving Nifedipine and Atorvastatin Calcium Electrospun Nanofibers as a Potential Buccal Delivery System. | Pharmaceutics | 2022 |
| 35205398 | Consanguinity and Congenital Heart Disease Susceptibility: Insights into Rare Genetic Variations in Saudi Arabia. | Genes (Basel) | 2022 |
| 35205281 | The Role of the Disrupted Podosome Adaptor Protein (SH3PXD2B) in Frank-Ter Haar Syndrome. | Genes (Basel) | 2022 |
| 32402091 | Role of sphingolipid metabolism in neurodegeneration. | J Neurochem | 2021 |
| 33919081 | Novel Autosomal Recessive Splice-Altering Variant in <i>PRKD1</i> Is Associated with Congenital Heart Disease. | Genes (Basel) | 2021 |
| 33918625 | Development of Epirubicin-Loaded Biocompatible Polymer PLA-PEG-PLA Nanoparticles: Synthesis, Characterization, Stability, and In Vitro Anticancerous Assessment. | Polymers (Basel) | 2021 |
| 33917625 | Development of a Colorimetric Tool for SARS-CoV-2 and Other Respiratory Viruses Detection Using Sialic Acid Fabricated Gold Nanoparticles. | Pharmaceutics | 2021 |
| 33838280 | Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortality. | Genomics | 2021 |
| 34043590 | Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19. | J Clin Invest | 2021 |
| 33398468 | A cell-based drug delivery platform for treating central nervous system inflammation. | J Mol Med (Berl) | 2021 |
| 32286682 | PDCD6IP, encoding a regulator of the ESCRT complex, is mutated in microcephaly. | Clin Genet | 2020 |
| 33398295 | Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19. | medRxiv | 2020 |
| 32679809 | Optimized Polyethylene Glycolylated Polymer-Lipid Hybrid Nanoparticles as a Potential Breast Cancer Treatment. | Pharmaceutics | 2020 |
| 32734812 | Novel Self-Assembled Polycaprolactone-Lipid Hybrid Nanoparticles Enhance the Antibacterial Activity of Ciprofloxacin. | SLAS Technol | 2020 |
| 32323311 | ADAMTS19-associated heart valve defects: Novel genetic variants consolidating a recognizable cardiac phenotype. | Clin Genet | 2020 |
| 31068897 | A Novel Homozygous Non-sense Mutation in the Catalytic Domain of MTHFR Causes Severe 5,10-Methylenetetrahydrofolate Reductase Deficiency. | Front Neurol | 2019 |
| 29564125 | Therapeutics discovery: From bench to first in-human trials. | Biomed Rep | 2018 |
| 29343958 | Preparation of anastrozole loaded PEG-PLA nanoparticles: evaluation of apoptotic response of breast cancer cell lines. | Int J Nanomedicine | 2017 |
| 28143899 | A missense mutation in the <i>CRBN</i> gene that segregates with intellectual disability and self-mutilating behaviour in a consanguineous Saudi family. | J Med Genet | 2017 |
| 19756532 | Electrophoretic properties of BSA-coated quantum dots. | Anal Bioanal Chem | 2010 |