| Deep sequencing reveals 50 novel genes for recessive cognitive disorders H Najmabadi, H Hu, M Garshasbi, T Zemojtel, SS Abedini, W Chen, ... Nature 478 (7367), 57-63, 2011 | 763 | 2011 |
| 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 | 87* | 2019 |
| 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 | 60 | 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 | 51 | 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 | 43 | 2012 |
| The role of a novel TRMT1 gene mutation and rare GRM1 gene defect in intellectual disability in two Azeri families B Davarniya, H Hu, K Kahrizi, L Musante, Z Fattahi, M Hosseini, ... PLoS One 10 (8), e0129631, 2015 | 42 | 2015 |
| Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation MS Hildebrand, NP Thorne, CJ Bromhead, K Kahrizi, JA Webster, ... Clinical genetics 77 (6), 563-571, 2010 | 35 | 2010 |
| 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 | 28 | 2019 |
| A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disability F Larti, K Kahrizi, L Musante, H Hu, E Papari, Z Fattahi, N Bazazzadegan, ... European Journal of Human Genetics 23 (3), 331-336, 2015 | 26 | 2015 |
| 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 | 25 | 2019 |
| 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 | 25 | 2012 |
| 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 | 24 | 2017 |
| 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 | 22 | 2017 |
| Mutation profile of BBS genes in Iranian patients with Bardet–Biedl syndrome: genetic characterization and report of nine novel mutations in five BBS genes Z Fattahi, P Rostami, A Najmabadi, M Mohseni, K Kahrizi, MR Akbari, ... Journal of human genetics 59 (7), 368-375, 2014 | 18 | 2014 |
| Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegeneration Z Iqbal, L Püttmann, L Musante, A Razzaq, MY Zahoor, H Hu, TF Wienker, ... European Journal of Human Genetics 24 (3), 392-399, 2016 | 14 | 2016 |
| Report of a patient with limb-girdle muscular dystrophy, ptosis and ophthalmoparesis caused by plectinopathy Z Fattahi, K Kahrizi, S Nafissi, M Fadaee, SS Abedini, A Kariminejad, ... Archives of Iranian medicine 18 (1), 0-0, 2015 | 12 | 2015 |
| Prevalence of ACTN3 (the athlete gene) R577X polymorphism in Iranian population Z Fattahi, H Najmabadi Iranian Red Crescent Medical Journal 14 (10), 617, 2012 | 12 | 2012 |
| Did the GJB2 35delG mutation originate in Iran? V Norouzi, H Azizi, Z Fattahi, F Esteghamat, N Bazazzadegan, ... American journal of medical genetics Part A 155 (10), 2453-2458, 2011 | 12 | 2011 |
| 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 | 9 | 2019 |
| Whole Genome Linkage Analysis Followed by Whole Exome Sequencing Identifies Nicastrin (NCSTN) as a Causative Gene in a Multiplex Family with γ-Secretase Spectrum of … ZM Faraji, F Sabbagh-Kermani, Z Fattahi, M Fadaee, MR Akbari, R Amiri, ... The Journal of investigative dermatology 136 (6), 1283, 2016 | 8 | 2016 |
