| 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 | 193 | 2019 |
| Iranome: A catalog of genomic variations in the Iranian population Z Fattahi, M Beheshtian, M Mohseni, H Poustchi, E Sellars, SH Nezhadi, ... Human mutation 40 (11), 1968-1984, 2019 | 139 | 2019 |
| 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 |
| Iran's multiple indicator demographic and health survey-2010: Study protocol A Rashidian, A Karimi-Shahanjarini, A Khosravi, E Elahi, M Beheshtian, ... International journal of preventive medicine 5 (5), 632, 2014 | 87 | 2014 |
| Effect of inbreeding on intellectual disability revisited by trio sequencing K Kahrizi, H Hu, M Hosseini, VM Kalscheuer, Z Fattahi, M Beheshtian, ... Clinical genetics 95 (1), 151-159, 2019 | 67 | 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 | 47 | 2019 |
| Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population Z Fattahi, Z Kalhor, M Fadaee, R Vazehan, E Parsimehr, A Abolhassani, ... Clinical Genetics 91 (3), 386-402, 2017 | 47 | 2017 |
| Effects of cerebrolysin on functional outcome of patients with traumatic brain injury: a systematic review and meta-analysis F Ghaffarpasand, S Torabi, A Rasti, MH Niakan, S Aghabaklou, F Pakzad, ... Neuropsychiatric Disease and Treatment, 127-135, 2018 | 46 | 2018 |
| Heterogeneity of hereditary hearing loss in Iran: a comprehensive review M Beheshtian, M Babanejad, H Azaiez, N Bazazzadegan, D Kolbe, ... Archives of Iranian medicine 19 (10), 720, 2016 | 35 | 2016 |
| Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping JS Amos, L Huang, J Thevenon, A Kariminedjad, CL Beaulieu, ... Clinical genetics 91 (1), 92-99, 2017 | 34 | 2017 |
| Prevalence of common MEFV mutations and carrier frequencies in a large cohort of Iranian populations M Beheshtian, N Izadi, G Kriegshauser, K Kahrizi, EP Mehr, M Rostami, ... Journal of genetics 95, 667-674, 2016 | 34 | 2016 |
| Progress towards health equity in IR of Iran through last three decades MA OULIAEI, ALIA HAGHDOUST, M Beheshtian, BA TEHRANI, ... Iranian Journal of Public Health 38 (1), 130-135, 2009 | 34 | 2009 |
| Impact of whole exome sequencing among Iranian patients with autosomal recessive retinitis pigmentosa M Beheshtian, SS Rad, M Babanejad, M Mohseni, H Hashemi, ... Archives of Iranian Medicine 18 (11), 0-0, 2015 | 30 | 2015 |
| The role of ATP-binding cassette transporters in the chemoresistance of anaplastic thyroid cancer: a systematic review E Abbasifarid, SM Sajjadi-Jazi, M Beheshtian, H Samimi, B Larijani, ... Endocrinology 160 (8), 2015-2023, 2019 | 27 | 2019 |
| Intersectoral collaboration to develop health equity indicators in Iran M Beheshtian, AO Manesh, SH Bonakdar, HM Afzali, B Larijani, ... Iranian journal of public health 42 (Supple1), 31, 2013 | 23 | 2013 |
| Genetic etiology of hearing loss in Iran M Babanejad, M Beheshtian, F Jamshidi, M Mohseni, KT Booth, K Kahrizi, ... Human genetics 141 (3), 623-631, 2022 | 15 | 2022 |
| Health and social determinants M Motlagh, A Oliya Manesh, M Beheshtian Successful publication, 2008 | 12 | 2008 |
| SLC52A2 mutations cause SCABD2 phenotype: a second report M Babanejad, OA Adeli, N Nikzat, M Beheshtian, H Azarafra, F Sadeghnia, ... International Journal of Pediatric Otorhinolaryngology 104, 195-199, 2018 | 11 | 2018 |
| Iranome: A human genome variation database of eight major ethnic groups that live in Iran and neighboring countries in the Middle East MR Akbari, Z Fattahi, M Beheshtian, M Mohseni, H Poustchi, E Sellars, ... ASHG Annual Meeting, 2017 | 11 | 2017 |
| Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum. S Taghizadeh, R Vazehan, M Beheshtian, F Sadeghinia, Z Fattahi, ... Archives of Iranian Medicine (AIM), 2020 | 8 | 2020 |
Mohammadreza ZakeriHealth policy Research Center, Institute of Health, Shiraz University of Medical Sciences, ShirazVerified email at sums.ac.ir
