| Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran CM Sloan-Heggen, M Babanejad, M Beheshtian, AC Simpson, KT Booth, ... Journal of medical genetics 52 (12), 823-829, 2015 | 116 | 2015 |
| Association of Polymorphisms at LDLR Locus with Coronary Artery Disease Independently from Lipid Profile. SH Jamaldini, M Babanejad, R Mozaffari, N Nikzat, K Jalalvand, A Badiei, ... Acta Medica Iranica 52 (5), 352-359, 2014 | 28 | 2014 |
| Identification of a founder mutation for Pendred syndrome in families from northwest Iran M Mohseni, A Honarpour, R Mozafari, B Davarnia, H Najmabadi, ... International Journal of Pediatric Otorhinolaryngology 78 (11), 1828-1832, 2014 | 9 | 2014 |
| Prediction of gene expression from regulatory sequence composition enhances transcriptome-wide association studies F Marotta, R Mozafari, E Grassi, A Lussana, E Mariella, P Provero bioRxiv, 2021.05. 11.443571, 2021 | | 2021 |
| 965insA mutation in SLC26A4 gene is a founder effect in North West part of Iran R Mozafari, M Babanejad, H Najmabadi Internatinal Iranian Genetics Congress 13, 2014 | | 2014 |
| A novel variation in 3UTR of SLC26A4 gene in an Iranian family with Pendred Syndrome R Mozafari, B Mojgan, H Najmabadi European Conference on Human Genetics (ESHG) 22, 390, 2014 | | 2014 |
| Association of polymorphisms in CYP2F4 gene with Warfarin Dosage in CAD patients R Mozafari, B Mojgan, H Jamaldini, H Najmabadi Internatinal Iranian Genetics Congress 12, 2013 | | 2013 |
| Prediction of the performance of machine learning methods for screening single nocleotide polymorphisms in coronary artery disease R Mozafari, SH Jamaldini Internatinal Iranian Genetics Congress 12, 2013 | | 2013 |
