| Expression analysis of MiR-21, MiR-205, and MiR-342 in breast cancer in Iran S Savad, P Mehdipour, M Miryounesi, R Shirkoohi, F Fereidooni, ... Asian Pacific Journal of Cancer Prevention 13 (3), 873-877, 2012 | 84 | 2012 |
| Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease M Sharma, D Leung, M Momenilandi, LCW Jones, L Pacillo, AE James, ... Journal of Experimental Medicine 220 (5), e20221755, 2023 | 45 | 2023 |
| Co-culture of mouse embryonic stem cells with sertoli cells promote in vitro generation of germ cells M Miryounesi, K Nayernia, M Dianatpour, F Mansouri, MH Modarressi Iranian journal of basic medical sciences 16 (6), 779, 2013 | 29 | 2013 |
| The spectrum of beta-thalassemia mutations in Isfahan Province of Iran PP DERAKHSHANDEH, FARH HOUR, M Heydari, EM KHEYR, YM MIR IRANIAN JOURNAL OF PUBLIC HEALTH 37 (2), 106-111, 2008 | 27 | 2008 |
| Evaluation of in vitro spermatogenesis system effectiveness to study genes behavior: monitoring the expression of the testis specific 10 (Tsga10) gene as a model M Miryounesi, K Nayernia, MB Mobasheri, M Dianatpour, R Oko, S Savad, ... Archives of Iranian medicine 17 (10), 0-0, 2014 | 23 | 2014 |
| Novel LAMA2 gene mutations associated with merosin-deficient congenital muscular dystrophy F Hashemi-Gorji, VR Yassaee, P Dashti, M Miryounesi Iranian Biomedical Journal 22 (6), 408, 2018 | 21 | 2018 |
| A novel homozygous LRRK1 stop gain mutation in a patient suspected with osteosclerotic metaphyseal dysplasia M Miryounesi, A Nikfar, M Changi‐Ashtiani, M Shahrooei, ... Annals of Human Genetics 84 (1), 102-106, 2020 | 16 | 2020 |
| Report of a case with trisomy 9 mosaicism M Miryounesi, M Dianatpour, Z Shadmani, S Ghafouri-Fard Iranian Journal of Medical Sciences 41 (3), 249, 2016 | 16 | 2016 |
| Clinical, biochemical and molecular features of Iranian families with mucopolysaccharidosis: A case series VR Yassaee, F Hashemi-Gorji, M Miryounesi, A Rezayi, Z Ravesh, ... Clinica chimica acta 474, 88-95, 2017 | 15 | 2017 |
| A case report: Autosomal recessive microcephaly caused by a novel mutation in MCPH1 gene S Ghafouri-Fard, M Fardaei, M Gholami, M Miryounesi Gene 571 (1), 149-150, 2015 | 15 | 2015 |
| Mutations in the VPS13B Gene in Iranian Patients with Different Phenotypes of Cohen Syndrome N Alipour, S Salehpour, SH Tonekaboni, M Rostami, S Bahari, V Yassaee, ... Journal of Molecular Neuroscience 70, 21-25, 2020 | 13 | 2020 |
| Genetic analysis of iranian patients with familial hypercholesterolemia M Ekrami, M Torabi, S Ghafouri-Fard, J Mowla, BM Soltani, ... Iranian biomedical journal 22 (2), 117, 2018 | 13 | 2018 |
| Homozygosity for a Robertsonian translocation (13q; 14q) in a phenotypically normal 44, xx female with a history of recurrent abortion and a normal pregnancy outcome M Miryounesi, M Diantpour, E Motevaseli, S Ghafouri-Fard Journal of Reproduction & Infertility 17 (3), 184, 2016 | 13 | 2016 |
| Leigh syndrome associated with a novel mutation in the COX15 gene M Miryounesi, M Fardaei, SM Tabei, S Ghafouri-Fard Journal of Pediatric Endocrinology and Metabolism 29 (6), 741-744, 2016 | 13 | 2016 |
| ELMO Domain Containing 1 (ELMOD1) Gene Mutation Is Associated with Mental Retardation and Autism Spectrum Disorder M Miryounesi, S Bahari, S Salehpour, N Alipour, S Ghafouri-Fard Journal of Molecular Neuroscience 69, 312-315, 2019 | 12 | 2019 |
| A new missense mutation in the BCKDHB gene causes the classic form of maple syrup urine disease (MSUD) M Miryounesi, S Ghafouri-Fard, H Goodarzi, M Fardaei Journal of Pediatric Endocrinology and Metabolism 28 (5-6), 673-675, 2015 | 12 | 2015 |
| Autosomal recessive nonsyndromic hearing loss: a case report with a mutation in TRIOBP gene M Fardaei, S Sarrafzadeh, S Ghafouri-Fard, M Miryounesi International journal of molecular and cellular medicine 4 (4), 245, 2015 | 11 | 2015 |
| Association of a novel nonsense mutation in KIAA1279 with Goldberg-Shprintzen syndrome S Salehpour, F Hashemi-Gorji, Z Soltani, S Ghafouri-Fard, M Miryounesi Iranian journal of child neurology 11 (1), 70, 2017 | 10 | 2017 |
| Expression analysis of PAWP during mouse embryonic stem cell-based spermatogenesis in vitro S Nourashrafeddin, M Aarabi, M Miryounesi, R Ebrahimzadeh-Vesal, ... In Vitro Cellular & Developmental Biology-Animal 50, 475-481, 2014 | 10 | 2014 |
| Analysis of SPATA19 gene expression during male germ cells development, lessons from in vivo and in vitro study S Nourashrafeddin, R Ebrahimzadeh‐Vesal, M Miryounesi, M Aarabi, ... Cell biology international reports 21 (1), 1-7, 2014 | 8 | 2014 |
