| Genotype, phenotype and in silico pathogenicity analysis of HEXB mutations: Panel based sequencing for differential diagnosis of gangliosidosis N Mahdieh, S Mikaeeli, AR Tavasoli, Z Rezaei, M Maleki, B Rabbani Clinical Neurology and Neurosurgery 167, 43-53, 2018 | 6 | 2018 |
| PCSK7: A novel regulator of apolipoprotein B and a potential target against non-alcoholic fatty liver disease V Sachan, M Le Dévéhat, A Roubtsova, R Essalmani, JF Laurendeau, ... Metabolism 150, 155736, 2024 | 3 | 2024 |
| COLQ-related congenital myasthenic syndrome: An integrative view T Eshaghian, B Rabbani, RS Badv, S Mikaeeli, B Gharib, S Iyadurai, ... neurogenetics 24 (3), 189-200, 2023 | 1 | 2023 |
| P506: An integrative view of COLQ-related congenital myasthenic syndrome T Eshaghian, B Rabbani, RS Badv, S Mikaeeli, B Gharib, S Iyadurai Genetics in Medicine Open 1 (1), 2023 | | 2023 |
| PCSK7: A Potential Target for Treatment of Non-Alcoholic Fatty Liver Disease (NAFLD) Sahar mikaeeli S Mikaeeli McGill University (Canada), 2021 | | 2021 |
| PCSK7: A potential target for treatment of non-alcoholic fatty liver disease (NAFLD) S Mikaeeli McGill University, 2021 | | 2021 |
| shRNAs: A few keypoints about their applications SA Angaji, S Mikaeeli, S Mikaeeli | | |
