| Genetics of intellectual disability in consanguineous families H Hu, K Kahrizi, L Musante, Z Fattahi, R Herwig, M Hosseini, C Oppitz, ... Molecular psychiatry 24 (7), 1027-1039, 2019 | 194 | 2019 |
| Iranome: A catalogue of genomic variations in the Iranian population Human mutation 40 (11), 1968-1984, 2019 | 142* | 2019 |
| Distinct genetic variation and heterogeneity of the Iranian population Z Mehrjoo, Z Fattahi, M Beheshtian, M Mohseni, H Poustchi, F Ardalani, ... PLoS genetics 15 (9), e1008385, 2019 | 48 | 2019 |
| Evaluation of cytokeratin 19 as a prognostic tumoral and metastatic marker with focus on improved detection methods M Mehrpouya, Z Pourhashem, N Yardehnavi, M Oladnabi Journal of cellular physiology 234 (12), 21425-21435, 2019 | 36 | 2019 |
| Mapping local patterns of childhood overweight and wasting in low-and middle-income countries between 2000 and 2017 Nature medicine 26 (5), 750-759, 2020 | 29 | 2020 |
| Core promoter STRs: novel mechanism for inter-individual variation in gene expression in humans A Heidari, ZNS Fam, E Esmaeilzadeh-Gharehdaghi, M Banan, ... Gene 492 (1), 195-198, 2012 | 24 | 2012 |
| Exceptional human core promoter nucleotide compositions OM Darvish H, Oladnabi M, Firouzabadi SG, Karimlou M, Heidari A, Najmabadi H Gene 475 (2), 79-86., 2011 | 24 | 2011 |
| Molecular and biochemical mechanisms of human iris color: A comprehensive review OM Dorgaleleh S, Naghipoor K, Barahouie A, Dastaviz F Journal of Cellular Physiology, 1–11., 2020 | 23* | 2020 |
| Novel evidence of the involvement of calreticulin in major psychiatric disorders M Ohadi, A Mirabzadeh, E Esmaeilzadeh-Gharehdaghi, M Rezazadeh, ... Progress in Neuro-Psychopharmacology and Biological Psychiatry 37 (2), 276-281, 2012 | 22 | 2012 |
| Reversion of the human calreticulin gene promoter to the ancestral type as a result of a novel psychosis-associated mutation OM Farokhashtiani T1, Mirabzadeh A, Oladnabi M, Magham ZG, Khorshid HR ... Prog Neuropsychopharmacol Biol Psychiatry 35 (2), 541-4, 2011 | 20* | 2011 |
| Novel extreme homozygote haplotypes at the human caveolin 1 gene upstream purine complex in sporadic Alzheimer's disease M Zarif Yeganeh, A Mirabzadeh, HR Khorram Khorshid, K Kamali, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153 …, 2010 | 17 | 2010 |
| New evidence for the role of calpain 10 in autosomal recessive intellectual disability: identification of two novel nonsense variants by exome sequencing in Iranian families. NH Oladnabi M, Musante L, Larti F, Hu H, Abedini SS, Wienker T, Ropers HH ... Arch Iran Med 18 (3), 179-84, 2015 | 16 | 2015 |
| Cannabinoid CB2 receptor functional variation (Q63R) is associated with multiple sclerosis in Iranian subjects A Tahamtan, S Rezaiy, S Samadizadeh, A Moradi, A Tabarraei, N Javid, ... Journal of Molecular Neuroscience 70, 26-31, 2020 | 15 | 2020 |
| Novel mutations in the calreticulin gene core promoter and coding sequence in schizoaffective disorder M Olad Nabi, A Mirabzadeh, G Feizzadeh, HR Khorram Khorshid, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153 …, 2010 | 15 | 2010 |
| CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability S Kazeminasab, II Taskiran, Z Fattahi, N Bazazzadegan, M Hosseini, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 …, 2018 | 13 | 2018 |
| Extremely low frequency-pulsed electromagnetic fields affect proangiogenic-related gene expression in retinal pigment epithelial cells K Oladnabi M, Bagheri A, Rezaei Kanavi M, Azadmehr A Iran J Basic Med Sci, 1-6, 2019 | 12* | 2019 |
| Iranome: A human genome variation database of eight major ethnic groups that live in Iran and neighboring countries in the Middle East ASHG Annual Meeting, 2017 | 11 | 2017 |
| Cloning and expression of codon-optimized recombinant darbepoetin alfa in Leishmania tarentolae T7-TR EO Anvarsadat Kianmehr a, *, Raziyeh Golavar b, Mandana Rouintan b ... Protein Expression and Purification 118, 120-125, 2016 | 11 | 2016 |
| The impact of fasting in Ramadan on the risk factors of COVID-19 in adolescents: A brief review E Behboudi, A Shamsi, V Hamidi-Sofiani, M Oladnabi International Journal of Pediatrics, 2021 | 9 | 2021 |
| NF1 mutations analysis using Whole Exome Sequencing technique in 11 Unrelated Iranian families with Neurofibromatosis type 1 S Foji, S Dorgaleleh, M Oladnabi, L Jouybari International Journal of Pediatrics, 2020 | 8 | 2020 |
