| 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 | 1026 | 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 | 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 |
| 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 | 78 | 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 |
| 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 |
| 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 |
| 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 |
| 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 | 44 | 2010 |
| 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 | 36 | 2014 |
| 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 |
| 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 |
| 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 | 27 | 2015 |
| SARS‐CoV‐2 outbreak in Iran: The dynamics of the epidemic and evidence on two independent introductions Z Fattahi, M Mohseni, K Jalalvand, F Aghakhani Moghadam, ... Transboundary and emerging diseases 69 (3), 1375-1386, 2022 | 23 | 2022 |
| Biallelic missense variants in ZBTB11 can cause intellectual disability in humans Z Fattahi, TI Sheikh, L Musante, M Rasheed, II Taskiran, R Harripaul, ... Human molecular genetics 27 (18), 3177-3188, 2018 | 20 | 2018 |
| 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 | 20 | 2016 |
| 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 … MF Zonooz, F Sabbagh-Kermani, Z Fattahi, M Fadaee, MR Akbari, R Amiri, ... The Journal of investigative dermatology 136 (6), 1283-1286, 2016 | 19 | 2016 |
| 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 | 19 | 2011 |
