| 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 |
| A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran M Babanejad, Z Fattahi, N Bazazzadegan, C Nishimura, N Meyer, ... American journal of medical genetics Part A 158 (10), 2485-2492, 2012 | 71 | 2012 |
| Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population Z Fattahi, AE Shearer, M Babanejad, N Bazazzadegan, SN Almadani, ... American Journal of Medical Genetics Part A 158 (8), 1857-1864, 2012 | 65 | 2012 |
| The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss—a twelve year study N Bazazzadegan, N Nikzat, Z Fattahi, C Nishimura, N Meyer, S Sahraian, ... International journal of pediatric otorhinolaryngology 76 (8), 1164-1174, 2012 | 63 | 2012 |
| PDZD7 and hearing loss: More than just a modifier KT Booth, H Azaiez, K Kahrizi, AC Simpson, WTA Tollefson, CM Sloan, ... American Journal of Medical Genetics Part A 167 (12), 2957-2965, 2015 | 59 | 2015 |
| Variants in CIB2 cause DFNB48 and not USH1J KT Booth, K Kahrizi, M Babanejad, H Daghagh, G Bademci, S Arzhangi, ... Clinical genetics 93 (4), 812-821, 2018 | 54 | 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 | 36 | 2016 |
| Mutations in TMC1 are a Common Cause of DFNB7/11 Hearing Loss in the Iranian Population MS Hildebrand, K Kahrizi, CJ Bromhead, AE Shearer, JA Webster, ... Annals of otology, rhinology & laryngology 119 (12), 830-835, 2010 | 36 | 2010 |
| 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 |
| 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, 352-359, 2014 | 28 | 2014 |
| Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss B Davarnia, M Babanejad, Z Fattahi, N Nikzat, N Bazazzadegan, ... International journal of pediatric otorhinolaryngology 76 (2), 268-271, 2012 | 28 | 2012 |
| Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases K Najafi, S Gholami, A Moshtagh, M Bazrgar, N Sadatian, G Abbasi, ... Molecular Genetics & Genomic Medicine 7 (8), e820, 2019 | 23 | 2019 |
| Investigating the CFH Gene Polymorphisms as a Risk Factor for Age-related Macular Degeneration in an Iranian Population M Babanejad, H Moein, MR Akbari, A Badiei, M Yaseri, M Soheilian, ... Ophthalmic genetics 37 (2), 144-149, 2016 | 19 | 2016 |
| 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 | 18 | 2022 |
| Two novel mutations in ILDR1 gene cause autosomal recessive nonsyndromic hearing loss in consanguineous Iranian families Z Mehrjoo, M Babanejad, K Kahrizi, H Najmabadi Journal of genetics 94, 483-487, 2015 | 17 | 2015 |
| Investigation of the asporin gene polymorphism as a risk factor for knee osteoarthritis in Iran R Jazayeri, M Qoreishi, HR Hoseinzadeh, M Babanejad, E Bakhshi, ... Am J Orthop 42 (7), 313-6, 2013 | 16* | 2013 |
| 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 |
| Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran M Mohseni, M Babanejad, KT Booth, P Jamali, K Jalalvand, B Davarnia, ... Clinical genetics 100 (1), 59-78, 2021 | 9 | 2021 |
| Analysis of the association Hind III Polymorphism of Lipoprotein Lipase gene on the risk of coronary artery disease M Imeni, M Hasanzad, T Naji, B Poopak, M Babanejad, HR Sanati, ... Research in Molecular Medicine 1 (3), 18-23, 2013 | 8 | 2013 |
| When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS) M Mohseni, M Akbari, KT Booth, M Babanejad, H Azaiez, F Ardalani, ... Journal of human genetics 65 (7), 609-617, 2020 | 6 | 2020 |
