| Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents D Yan, D Tekin, G Bademci, J Foster, FB Cengiz, A Kannan-Sundhari, ... Human genetics 135, 953-961, 2016 | 131 | 2016 |
| Effects of probiotic Lactobacillus acidophilus and Lactobacillus casei on colorectal tumor cells activity (CaCo-2) MMS Dallal, M Mojarrad, F Baghbani, R Raoofian, J Mardaneh, ... Archives of Iranian medicine 18 (3), 0-0, 2015 | 112 | 2015 |
| AutoMap is a high performance homozygosity mapping tool using next-generation sequencing data M Quinodoz, VG Peter, N Bedoni, B Royer Bertrand, K Cisarova, ... Nature communications 12 (1), 518, 2021 | 80 | 2021 |
| PRUNE is crucial for normal brain development and mutated in microcephaly with neurodevelopmental impairment M Zollo, M Ahmed, V Ferrucci, V Salpietro, F Asadzadeh, M Carotenuto, ... Brain 140 (4), 940-952, 2017 | 73 | 2017 |
| Genetic, phenotypic, and interferon biomarker status in ADAR1-related neurological disease GI Rice, N Kitabayashi, M Barth, TA Briggs, ACE Burton, ML Carpanelli, ... Neuropediatrics 48 (03), 166-184, 2017 | 69 | 2017 |
| Duchenne muscular dystrophy: an updated review of common available therapies A Salmaninejad, SF Valilou, H Bayat, N Ebadi, A Daraei, M Yousefi, ... International Journal of Neuroscience 128 (9), 854-864, 2018 | 63 | 2018 |
| Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases E Perenthaler, A Nikoncuk, S Yousefi, WM Berdowski, M Alsagob, I Capo, ... Acta Neuropathologica 139, 415-442, 2020 | 49 | 2020 |
| Polymorphism of genes and implantation failure M Mojarrad, M Hassanzadeh-Nazarabadi, N Tafazoli International Journal of Molecular and Cellular Medicine 2 (1), 1, 2013 | 40 | 2013 |
| Sensitive and specific clinically diagnosis of SARS-CoV-2 employing a novel biosensor based on boron nitride quantum dots/flower-like gold nanostructures signal amplification B Hatamluyi, M Rezayi, SA Jamehdar, KS Rizi, M Mojarrad, Z Meshkat, ... Biosensors and Bioelectronics 207, 114209, 2022 | 38 | 2022 |
| Analysis of superoxide dismutase 1, dual-specificity phosphatase 1, and transforming growth factor, beta 1 genes expression in keratoconic and non-keratoconic corneas S Saee-Rad, R Raoofian, M Mahbod, M Miraftab, M Mojarrad, S Asgari, ... Molecular vision 19, 2501, 2013 | 37 | 2013 |
| Long non-coding RNAs as the critical factors during tumor progressions among Iranian population: an overview Z Rahmani, M Mojarrad, M Moghbeli Cell & bioscience 10, 1-13, 2020 | 35 | 2020 |
| Mutation spectrum of the PAH gene in the PKU patients from Khorasan Razavi province of Iran T Hamzehloei, SA Hosseini, R Vakili, M Mojarad Gene 506 (1), 230-232, 2012 | 34 | 2012 |
| The role of tumor protein 53 mutations in common human cancers and targeting the murine double minute 2–p53 interaction for cancer therapy T Hamzehloie, M Mojarrad, M Hasanzadeh_Nazarabadi, S Shekouhi Iranian journal of medical sciences 37 (1), 3, 2012 | 33 | 2012 |
| Common therapeutic advances for Duchenne muscular dystrophy (DMD) A Salmaninejad, Y Jafari Abarghan, S Bozorg Qomi, H Bayat, M Yousefi, ... International Journal of Neuroscience 131 (4), 370-389, 2021 | 31 | 2021 |
| Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants C Neuray, R Maroofian, M Scala, T Sultan, GS Pai, M Mojarrad, ... Brain 143 (8), 2388-2397, 2020 | 31 | 2020 |
| MicroRNA-499a-5p promotes differentiation of human bone marrow-derived mesenchymal stem cells to cardiomyocytes V Neshati, S Mollazadeh, BS Fazly Bazzaz, AAF De Vries, M Mojarrad, ... Applied biochemistry and biotechnology 186, 245-255, 2018 | 30 | 2018 |
| Bee venom induces apoptosis and suppresses matrix metaloprotease-2 expression in human glioblastoma cells M Sisakht, B Mashkani, A Bazi, H Ostadi, M Zare, FZ Avval, ... Revista Brasileira de Farmacognosia 27, 324-328, 2017 | 30 | 2017 |
| Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder PE Schneeberger, F Kortüm, GC Korenke, M Alawi, R Santer, M Woidy, ... Brain 143 (8), 2437-2453, 2020 | 28 | 2020 |
| Autocrine human growth hormone expression leads to resistance of MCF-7 cells to tamoxifen M Mojarrad, M Momeny, F Mansuri, Y Abdolazimi, MH Tabrizi, SH Ghaffari, ... Medical oncology 27, 474-480, 2010 | 28 | 2010 |
| Chromosomal study of couples with the history of recurrent spontaneous abortions with diagnosed blightded ovum. HNM Shekoohi S, Mojarrad M, Raoofian R, Ahmadzadeh S Int J Mol Cell Med 2 (4), 164-8, 0 | 25* | |
